Bad Diets For DogsEndoscopic images Copyright © Atlanta South Gastroenterology, P.C. All rights reserved. Logo is Registered Trademark ® of Atlanta South Gastroenterology, P.C. Low-carb diets may be good for your waistline, but you might not be able to say the same for your breath. Low-carb lifestyle junkies are more likely to suffer from a. Bad dog diets are instantly converted into wind, bad breath and that unmistakable doggy smell. That’s why our recipes include both wet and dry foods are made with. FadDiet.com has compiled all of the fad diets. If you are looking for a fad diet, it is probably here. Some weight loss relate humor and analysis of popular diet. Too much protein in middle age 'as bad as smoking'This page was printed from: http: //www. Visit www. medicalnewstoday. Healthline Media UK Ltd. All rights reserved. MNT is the registered trade mark of Healthline Media. Any medical information published on this website is not intended as a substitute for informed medical advice and you should not take any action before consulting with a healthcare professional. ![]() Gluten-free eating has a basis in science, and it does help a genuine health problem. To people with a chronic digestive disorder called celiac disease, gluten is. Bad Diets Don\u0027t Work![]() If you are counting carbs, or at least paying attention to the amount and type of carbs you eat, it can help to understand the difference between "good" and "bad" carbs. The Worst Diets Ever: Diets That Don't Work. Avoid these 5 types of diets for best weight loss results, experts say. Cambridge Diet is a 20-year old liquid diet with a loyal following. This low-fat, low-calorie weight loss program has critics on both sides of the fence. ![]()
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ABO blood group system - Wikipedia. For use in inflammation, see histamine. For hydrogen atom, see hydrogen. The ABO blood group system is the most important blood type system (or blood group system) in human blood transfusion. Found on platelets, epithelium, and cells other than erythrocytes, AB antigens (as with other serotypes) can also cause an adverse immune response to organ transplantation. ABO blood types are also present in some other animals, for example rodents and apes, such as chimpanzees, bonobos, and gorillas. Landsteiner was awarded the Nobel Prize in Physiology or Medicine in 1. However, in 1. 92. American medical commission acknowledged Jansk. In Russia and states of the former USSR blood types O, A, B, and AB are respectively designated I, II, III, and IV. Moss published his own (very similar) work in 1. Felix Bernstein demonstrated the correct blood group inheritance pattern of multiple alleles at one locus in 1. Three drops of blood are mixed with anti- B (left) and anti- A (right) serum. Agglutination on the right side indicates blood type A. Red circles show where there are differences in chemical structure in the antigen- binding site (sometimes called the antibody- combining site) of human immunoglobulin. Notice the O- type antigen does not have a binding site. The removal of A and B antigens still does not address the problem of the Rh blood group antigen on the blood cells of Rh positive individuals, and so blood from Rh negative donors must be used. Patient trials will be conducted before the method can be relied on in live situations. Another approach to the blood antigen problem is the manufacture of artificial blood, which could act as a substitute in emergencies. The ABO blood type is controlled by a single gene (the ABO gene) with three types of alleles inferred from classical genetics: i, IA, and IB. The I designation stands for isoagglutinogen, another term for antigen. The gene is located on the long arm of the ninth chromosome (9q. The IA allele gives type A, IB gives type B, and i gives type O. As a B Positive donor, you are very important to maintaining the blood supply in our community. B+ is the third most common occurring blood type. As both IA and IB are dominant over i, only ii people have type O blood. Individuals with IAIA or IAi have type A blood, and individuals with IBIB or IBi have type B. IAIB people have both phenotypes, because A and B express a special dominance relationship: codominance, which means that type A and B parents can have an AB child. A couple with type A and type B can also have a type O child if they are both heterozygous (IBi,IAi) The cis- AB phenotype has a single enzyme that creates both A and B antigens. The resulting red blood cells do not usually express A or B antigen at the same level that would be expected on common group A1 or B red blood cells, which can help solve the problem of an apparently genetically impossible blood group. The four possibilities represent the combinations obtained when one allele is taken from each parent; each has a 2. Blood group inheritance by phenotype only.
The blood group diet says you should eat right for your blood type. Here's dietitian Juliette Kellow's review of the Blood Type Diet.![]() Blood type. OABABOOO or AO or BA or BAO or AO or AO, A, B or ABA, B or ABBO or BO, A, B or ABO or BA, B or ABABA or BA, B or ABA, B or ABA, B or ABHistorically, ABO blood tests were used in paternity testing, but in 1. American men falsely accused were able to use them as evidence against paternity. A1 makes up about 8. A- type blood, with A2 making up almost all of the rest. Complications can sometimes arise in rare cases when typing the blood. There are six common alleles in white individuals of the ABO gene that produce one's blood type. People with weak alleles of A can sometimes express anti- A antibodies, though these are usually not clinically significant as they do not stably interact with the antigen at body temperature. There are also variations in blood type distribution within human subpopulations. In the UK, the distribution of blood type frequencies through the population still shows some correlation to the distribution of placenames and to the successive invasions and migrations including Norsemen, Danes, Saxons, Celts, and Normans who contributed the morphemes to the placenames and the genes to the population. A premature stop codon results from this frame- shift mutation. This variant is found worldwide, and likely predates human migration from Africa. The O0. 1 allele is considered to predate the O0. It is consistent with the accepted patterns of early population movements and varying prevalent blood types in different parts of the world: for instance, B is very common in populations of Asian descent, but rare in ones of Western European descent. Another theory states that there are four main lineages of the ABO gene and that mutations creating type O have occurred at least three times in humans. The continued presence of the O alleles is hypothesized to be the result of balancing selection. The antibodies created against these environmental antigens in the first years of life can cross- react with ABO- incompatible red blood cells that it comes in contact with during blood transfusion later in life. Anti- A antibodies are hypothesized to originate from immune response towards influenza virus, whose epitopes are similar enough to the . Anti- B antibodies are hypothesized to originate from antibodies produced against Gram- negative bacteria, such as E. Thus, individuals possessing rare types are better equipped to detect pathogens. The high within- population diversity observed in human populations would, then, be a consequence of natural selection on individuals. ABO antigens are found having similar roles on epithelial cells as well as red blood cells. In fact, having type O blood predisposes to bleeding. Higher levels of v. WF are more common amongst people who have had ischemic stroke (from blood clotting) for the first time. The mechanisms behind this association with cholera are unclear in the literature. However, in an O- type mother, Ig. G ABO antibodies are produced and the baby can potentially develop ABO hemolytic disease of the newborn. Clinical applications. In most human carcinomas, including oral carcinoma, a significant event as part of the underlying mechanism is decreased expression of the A and B antigens. The study was based on a community cohort study (the Malmo Diet and Cancer study) and four additional randomized controlled trials of primary prevention cohorts (JUPITER and ASCOT) and secondary prevention cohorts (CARE and PROVE IT- TIMI 2. Scientific evidence in support of these concepts is nonexistent. WORLD JOURNAL OF TRANSPLANTATION. PMC 3. 96. 41. 93 . PMID 2. 46. 69. 36. Wright (1. 99. 3). Human Biology and Health. Englewood Cliffs, New Jersey, USA: Prentice Hall. ISBN 0- 1. 3- 9. 81. Singapore medical journal. PMID 2. 37. 16. 14. Zentralblatt Bakteriologie. Mfinch med Wschr. Klinick (in Czech). Canadian Medical Association Journal. PMC 5. 37. 90. 7 . PMID 2. 03. 21. 69. Bulletin Johns Hopkins Hospital. PMC 1. 20. 52. 97 . PMID 8. 41. 79. 88. J.; Watkins, W. PMID 5. Advances in Human Genetics Vol. Harris, H. M.; Morgan, W. Characterisation of a Novel Type of Glycoprotein Saccharides from Human Erythrocyte Membrane. PMID 7. 11. 73. 3. Kabat, Eds.) Plenum Publishing Corporation, N. Y. NY (1. 98. 8)^Finne (1. PMID 2. 33. 30. 95. Nat Biotechnol. 2. PMID 1. 74. 01. 36. Concepts of Genetics (5th ed.). Upper Saddle River, NJ: Prentice Hall. ISBN 0. 13. 53. 10. Transfus Med Rev. PMID 1. 67. 87. 82. Inheritance patterns of blood groups. Australian Red Cross Blood Service. Retrieved 3. 0 October 2. Abobloodtypes. webnode. Retrieved 2. 01. 5- 0. Retrieved 1 July 2. Seltsam A, Hallensleben M, Kollmann A, Blasczyk R (2. PMID 1. 28. 29. 58. Human Genetics. 9. PMID 8. 64. 16. 96. Blood Transfusion. PMC 2. 95. 74. 92 . PMID 2. 09. 67. 16. In Sawyer PH. English Medieval Settlement. Martin's Press. ISBN 0- 7. Human Genetics. 1. PMID 1. 86. 29. 53. Retrieved 2. 4 September 2. The Protein Journal. PMID 1. 55. 17. 98. M.; Allan, M. J.; Pomiankowski, A; Gustafsson, K (2. Proceedings of the Royal Society B: Biological Sciences. PMC 1. 69. 16. 87 . PMID 1. 52. 93. 86. PMID 1. 71. 18. 64. PMID 1. 57. 28. 12. Seminars in hematology. PMID 1. 50. 71. 78. Current Opinion in Hematology. PMID 1. 57. 25. 90. Br J Haematol. 1. PMID 1. 09. 29. 04. Transfus Med. 1. 1 (4): 3. PMID 1. 15. 32. 18. Arterioscler Thromb Vasc Biol. American Heart Association, Inc. PMID 1. 18. 34. 53. PMID 3. 49. 53. 04. PMID 7. 66. 06. 43. Br J Haematol. Blackwell Synergy. PMID 1. 57. 55. 28. PMID 1. 69. 90. 57. Bibcode: 2. 01. 0PLo. SO.. 5. 11. 97. 2X. M.; Kraft, P.; Gross, M.; Helzlsouer, K.; Bueno- De- Mesquita, H. B.; Steplowski, E.; Stolzenberg- Solomon, R. Z.; Arslan, A. A.; Jacobs, E. J.; Lacroix, A.; Petersen, G.; Zheng, W.; Albanes, D.; Allen, N. E.; Amundadottir, L.; Anderson, G.; Boutron- Ruault, M. E.; Canzian, F.; Chanock, S. J.; Clipp, S.; Gaziano, J. M.; Giovannucci, E. L.; Hallmans, G.; Hankinson, S. E.; Hoover, R. N.; Hunter, D. J.; Hutchinson, A.; Jacobs, K.; Kooperberg, C. Cancer Research. 7. PMC 2. 94. 37. 35 . PMID 2. 01. 03. 62. Z.; Fuchs, C. S.; Petersen, G. M.; Arslan, A. A.; Bueno- De- Mesquita, H. B.; Gross, M.; Helzlsouer, K.; Jacobs, E. J.; Lacroix, A.; Zheng, W.; Albanes, D.; Bamlet, W.; Berg, C. D.; Berrino, F.; Bingham, S.; Buring, J. E.; Bracci, P. M.; Canzian, F.; Clavel- Chapelon, F. O.; Clipp, S.; Cotterchio, M.; De Andrade, M.; Duell, E. J.; Fox Jr, J. W.; Gallinger, S.; Gaziano, J. M.; Giovannucci, E. L.; Goggins, M. Nature Genetics. PMC 2. 83. 98. 71 . PMID 1. 96. 48. 91. International Journal of Cancer. Journal International Du Cancer. PMC 2. 94. 69. 62 . PMID 2. 03. 09. 93. British Medical Journal. PMC 2. 01. 59. 95 . PMID 1. 30. 32. 50. Possible evolutionary significance. American Journal of Epidemiology. PMID 4. 01. 41. 72. Retrieved 2. 0 August 2. Clinical and Experimental Immunology. ISSN 0. 00. 9- 9. PMC 1. 81. 04. 67 . PMID 1. 72. 23. 96. British Medical Journal (Clinical research ed.). ISSN 0. 26. 7- 0. PMC 1. 50. 02. 29 . PMID 6. 81. 26. 84. Biochimica et Biophysica Acta. ISSN 0. 00. 6- 3. PMID 1. 05. 80. 14. Journal of Dental Research. ISSN 0. 02. 2- 0. PMID 1. 56. 15. 87. The Blood Group Diet Review. By Dietitian, Juliette Kellow BSc RDFollow a diet that’s designed specifically for your blood group and you’ll lose weight, feel healthier and lower your risk of many diseases. At least, that’s what Dr Peter D’Adamo, naturopath and creator of the Blood Type Diet claims in his book Eat Right For Your Blood Type. No wonder then, that it’s been a hit with Hollywood stars like Liz Hurley and Courtney Cox- Arquette, as well as closer- to- home celebrities, like Cheryl Cole, Martine Mc. Cutcheon & Sir Cliff Richard. Cheryl says that it has made such a difference, not so much to her shape, but to how she feels and to her energy levels. Having tried the diet, she now believes that it works, and now watches what she eats, not to stay slim but to feel good. But while Cheryl might be a fan of the Blood Type Diet, most medical and nutrition experts aren’t, and agree that the theory is complete nonsense. So what is the theory? Prepare to be blinded by science! Dr D’Adamo believes our blood group determines how our bodies deal with different nutrients. His theory is based on the idea that each blood group has its own unique antigen marker (a substance that the body recognises as being alien) and this marker reacts badly with certain foods, leading to all sorts of potential health problems. Furthermore, Dr D’Adamo believes that levels of stomach acidity and digestive enzymes are linked with your blood type. Consequently, he says, by following a diet designed specifically for your blood type, your body digests and absorbs food more efficiently, with the result that you lose weight. But here’s where the theory becomes even more weird and wonderful. Dr D’Adamo believes that because blood types evolved at different times throughout history, we should eat a diet based on the types of foods our ancestors typically ate at the time when our blood type was first recognised! When did the blood types evolve? Blood Group O was the first blood type to be identified, although how we know this is anyone’s guess – we’re talking about our hunter- gatherer ancestors who were around in 5. B. C! Nevertheless, Dr D’Adamo believes because our type O ancestors survived and thrived on a high- protein, meat- based diet, that’s the type of diet blood group Os should follow in the 2. Next came the emergence of blood type A, sometime around 1. B. C! By this time, our ancestors’ hunter- gathering days were over and instead they started to settle into farming- type communities. The creation of blood type A around this time meant our ancestors did well on a vegetarian- based diet. And again, Dr D’Adamo recommends that blood group A’s should today follow a veggie diet. Blood type B supposedly evolved around 1. B. C thanks to our nomadic ancestors. They left their farms and started wandering the land, constantly moving from place to place. Consequently, Dr D'Adamo's theory goes, blood group B’s today can get away with eating a varied diet that consists of most foods including meat, dairy, grains and vegetables. Finally, came blood type AB, which evolved just 1,0. Dr D'Adamo thinks this blood type helped our ancestors make the transition to modern times. Meaning that people with blood group AB can eat a mixture of the foods suitable for both blood group A and blood group B. That gives me a good idea, but can you be more specific about what you can and can’t eat? Each of the four blood types has a detailed list of foods that should be avoided and those that can be included. Here’s the lowdown. Dr D’Adamo says that our digestive tract retains the memory of ancient times, and so type Os need to eat a typical hunter- gatherer type diet. In other words, type Os should follow a high- protein, low- carb diet with lots of meat and fish but no dairy products, wheat or grains. If that sounds familiar, it’s because it is – the diet recommended for people with blood type O is simply a variation on many of the typical high- protein, low- carb diets that are currently popular, such as the Atkins diet. Foods you can eat freely include meat, fish and olive oil; foods you can eat in moderation include eggs, nuts, seeds, certain vegetables and fruits; and foods to avoid include dairy products, beans, cereals, bread, pasta and rice. To complement your food intake, Dr D’Adamo recommends lots of vigorous aerobic exercise such as aerobics and running – just like our hunter- gatherer ancestors did! Blood Group AThis is the second most common blood type in the UK. Again according to Dr D'Adamo, digestive system is apparently very good at remembering that our ancestors had settled, farming lifestyles, which included eating lots of grains and vegetables but little meat. Consequently, blood type A’s should follow a vegetarian diet but still avoid dairy products. This means nuts, seeds, beans, cereals, pasta, rice, fruit and veg are all on the . Meanwhile, calming exercises are thought to be best for blood type A’s such as yoga or golf. Blood Group BOnly one person in 1. B – a real shame when you consider this blood group has the least dietary restrictions! As our type B ancestors were able to thrive on all sorts of foods, thanks to all that travelling, very few foods need to be avoided and this is the closest you’ll get to a healthy, balanced diet from Dr D'Adamo. The only foods that need to be avoided are processed foods, although nuts and seeds aren’t recommended and only small amounts of carb- rich foods should be eaten. When it comes to exercise, Dr D’Adamo recommends activities that have mental component, such as hiking, tennis and swimming – clearly our ancestors did a lot of thinking while they were walking! Blood Group ABPeople with this rare blood type should eat a combination of the foods recommended for blood groups A and B. Somewhat confusing when type B allows you to eat most foods, while type A suggests a vegetarian diet! Dr D’Adamo gets around this by suggesting that type ABs follow a veggie diet most of the time with some meat, fish and dairy products occasionally. It’s the same when it comes to exercise too – blood type ABs should combine calming exercises with moderately intense activities. What do the experts say? Medical experts universally agree that the theory is nonsense, and say there is absolutely no link between our blood group and the diet we eat. Consequently you won’t find qualified nutritionists or dietitians recommending this diet. There are also several concerns, namely that the diets recommended for blood groups O and A are considerably limited and cut out major groups of foods. In the long term, this can result in a poor intake of nutrients needed for good health. Cutting out dairy products, for example, will lead to poor intakes of calcium, which can put you at risk of osteoporosis (brittle bone disease), while avoiding meat can result in low intakes of iron, which can lead to anaemia. This is even more worrying in view of the fact that most people in the UK are blood group O or A. But will the diet help me lose weight? Almost certainly, but this is because each of the diets for the four blood types eliminates specific groups of food such as bread and cereals, dairy products or meat and fish. Dr D’Adamo doesn’t give any indication about how much weight you’ll lose, it will depend on how much you restrict your food intake. Are there any pros? There are not many positive things to say about this diet, which is clearly based on science fiction rather than science fact. However, as with any diet, it will get you thinking about what you are currently eating, with the result that you may start to make changes to your diet. Added to this, the blood type diet recommends eating fresh, natural foods and so can help you de- junk your diet by cutting out processed foods, takeaways, booze, chocolate and too many cups of coffee – all of which our ancestors missed out on! And the cons? There are plenty. On a practical level, you may need a blood test to discover your blood group if you don’t already know it – and this will mean a trip to your local health centre! Mealtimes may also be impossible if everyone in the family wants to follow the diet, but has a different blood group! But most importantly, it’s just another cranky way of getting people to cut calories – and the most worrying thing about this is that while you’ll probably lose weight, it could also affect your health in the long term. Nevertheless, if you’re still adamant about giving it a go, it’s best to follow it for just a short time (one week or less) and use it to kick- start a longer- term, healthy, weight- loss plan. Juliette’s verdict. I’m really not a fan of this diet. It’s filled with pseudo- science and has the potential to scare people into avoiding many nutritious foods in an effort to lose weight. It’s also worth bearing in mind that although the diet gives the impression that it’s based on sound scientific research this is, in fact, far from the case. Ultimately, the theory is nonsense. Nevertheless, based on Dr D’Adamo’s theory, I’m looking forward to the evolution of blood type F! People with blood type F will need lots of fast food, takeaways, pizza, sugary snacks, crisps and chocolate to remain in tune with their environment. After all, if the theory is correct, surely that’s what we can expect, based on what many of us now eat in the 2. Weight Loss Resources has a great set of tools to help you find a way of dieting you can live with. Find out how to achieve the calorie balance that is going to get you to your ideal weight without a list of forbidden foods. You can access the tools free for 2. 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Besides the obvious health reasons of gaining excess fat, here are six more reasons why conventional bulking is a bad approach to trying to achieve your physique goals: Most bulk up diets involve junk food that floods your body with trans fats, corn syrup and unhealthy amounts of salt, sugars and fats. The idea that a “calorie is a calorie” is nonsense. It’s because they understand this one fact: Muscle growth occurs in SPURTS. Now granted they will make some fast muscle gains initially when starting the program, but they quickly get to the point where the gains in body fat are greater than the gains in lean muscle mass. Not cool. The Solution To Bulking Up Your Muscles, Not Your Waist Line: THE ANABOLIC AMPLIFIER EFFECT! The Anabolic Amplifier Effect is also known as the “Rebound” effect, which we’ll explain shortly. We’ll make it crystal clear why natural bodybuilders hit the gym hard after months of dieting instead of taking time off! Why Is The Anabolic Amplifier Effect So Effective? It’s because when they begin . Just like you, we always want to see proof. I wasn’t in “bad” shape, but certainly not lean enough to compete in a bodybuilding competition. The second picture was taken on stage at the competition. After 1. 2 weeks of strict dieting I got my body weight down to a ripped 1. Then right after the competition was over, the post contest pig out began.. It started off with an “All U Can Eat” Italian buffet with endless amounts of pizza, pasta, and desserts. And for the entire week after the show I pretty much ate whatever I wanted in rather large quantities.. The third picture above was taken within 1 week after the show. And as you can clearly see I was up 2. Vince’s 2. 1- day results.. When Vince and Lee announced that they had a diet that can make you avoid the fat gain and maximize the muscle gain, I decided in the moment that it was the right time to test it. After 2. 1 days I managed to gain 8 pounds and lost 2 pounds of fat. So this diet was the best solution to my problem, and I will use it in the future. Thank you one more time, and I hope you like the results.”Kind Regards,Peter Kingz Faro, Portugal “I went from 1. Strength is through the roof, personal bests in everything. Barbell shrugs= 4. Plate loaded incline chest press 3. Alternating dumbbell curls 5. Basically every exercise has gone way up. I feel way better, more energy, and it's like I always have a pump. Only thing I didn't like was I got pain in my legs where they were growing so fast and stretching.”Brandon Green. St. John's, Newfoundland“Man, I just loved this program! I gained 7. 6 pounds of muscle in 2. I think that this diet is perfect if you're hitting a plateau. I didn't expect to make the gains I did in such a short time, let alone such clean gains. This is definitely something I'll be using in the future.”Dietrich Marquardt. Hobart, Australia“I did the 2. This is great because I'm short. My chest went from 9. My bicep from 3. 3 to 3. My midsection stayed the way it was. This program is amazing and it can help everyone to gain muscle mass in a short amount of time. I say go for it!”Bj. I am a previous customer of Vince's and I trust him completely! I'm happy with the results and will be repeating this programme in the future! I started at 8. 2. BF and finished at 7. BF. My chest measurement has increased 2. My metabolism seemed to have stalled while bulking over the last several months so I wanted to see if there was a way to . I found a side benefit from this strategy was an increased appetite! Previously, my appetite was almost nonexistent and I had issues trying to consume the amount of food needed to bulk. I did one cycle of FMB. My stats: Before: 1. These are the best gains I've had in a long time. I would walk around the four seasons resort and women would be eying me up and down. All and all I highly recommend FMB! You won't regret your results.”Sheldon Ortiz. Wailuku, Hawaii USA“I just wanted to say thanks. I finished the 2. I used to weigh 1. I started your program and now just tipped the scale at 1. My max bench press was 1. I after just 2. 1 days I maxed out at 1. My chin- ups increased by 9 and now can literally do 1. I have been following the program exactly as outlined right from the start and it works awesome. I am supper happy and very grateful that I used it. Thanks again.”Michael Di. Nardo. Snellville, Georgia“The program looks great man! It's something that I haven't really seen before and it definitely works for putting on size, that is for sure. Anyhow, this is how my rebound gains has gone so far.. Saturday November 2. Tuesday November 3. That's up 2. 6 pounds gained since the show! My rebound has been excellent so I can definitely say the Anabolic Amplifier theory works! My strength has been great in the gym as well. After just 2. 1 days I'm up 5 pounds and I've actually lost more fat while gaining solid muscle! All my weights in the gym have gone up by 1. Overall I felt great, especially with all the compliments I got ha! I've been recommending this to all my friends and I will definitely do it again!”Cody Clark. California“Thanks for coming out with this program it's a brilliant system, In fact I actually used this style of training and nutrition cycling to prepare for my most recent fitness model competition in Toronto Canada. I feel great with the results my body feels bigger and stronger than ever before, I am more vascular than I have ever been, and I am still quite lean. I have been able to add an extra at least 1. Thanks.”Jon Chafe. St. John's, Newfoundland“I gained 1. The best part is that normally while bulking continuously, I find it hard to constantly consume excess calories and my body starts to feel slightly sluggish after about 2- 3 weeks, but I felt great cycling calories over the weeks and it kept my metabolism in muscle building mode. My biggest fear was losing size or my metabolism slowing down during the fat loss week, but I actually looked better and bigger! Without a doubt, this program is the perfect strategy for staying lean while gaining lean muscle.”Joey Vaillancourt. Author, Bones To Buff. Quebec, Canada. So how did the 2. Day Fast Mass Building Program work so insanely fast for us & our test group? Simple! One- week of following our Primer Phase – a low calorie nutrition plan immediately followed by two- weeks of our Overload Phase – a high calorie nutrition plan focusing on the most cutting- edge nutrient timing strategies and best muscle- building foods of all time. Research confirms that an increase of muscle- building hormones peak out after 1. Then they start to decline back to base levels. Now you understand why bodybuilders “eat everything in sight” after a bodybuilding contest. They know they are about to make the most incredible muscle gains for TWO WEEKS before things start to plateau. After that if they continue eating excessive amounts of calories beyond the 2 week mark those extra calories will get stored as bodyfat, and NOT as lean muscle mass. That’s why our plan is 2. Imagine brand new eye- popping muscle building results every 2. WITHOUT The Unwanted Fat! Why are guys and gals struggling to gain muscle at a painfully slow rate? Maybe because they are taking advice from guys who don't know what we know. Maybe because they have taken too much advice from people saying what they can't do instead of what they can do! Don't let others sad and slow reality become your sad and slow reality. And if you have.. Today that all changes! Simply put, 2. 1- Day Fast Mass Building is the ONLY program that allows you to pack on 5. Introducing! No stone is left unturned and no background in advanced exercise degrees are required to understand and implement the program. Get the facts, get the plans and then get to work! We're all about simplicity. The best part is you don't have to wait for this manual to arrive in the mail, or drive to a store to get it. You can download it to your computer right now and start making the fastest and easiest muscle gains of your life starting today. Part 2: The 2. 1- Day Fast Mass Building Nutrition Guide ($9. Value)This is the complete 2. We'll tell you exactly what foods to eat, how much and how often. Plus, we'll reveal how to customize the 2. Whether your body fat is 5%.. Part 3: The Bodyweight 5. Fat- Cutting Workout DVD ($4. Value)We included the Bodyweight 5. Primer Phase to capitalize on the maximal fat loss experience. Part 4: The 2. 1- Day Fitness Model Physique 4- Hour Workout DVD ($9. Value)Male fitness models are built like Hollywood sex symbols, and if you're after that look; then look no further. Women are attracted to men with above- average builds with mind- blowing muscle definition. If you're not into the ! Part 5: The 2. 1- Day Muscle Model Physique 4- Hour Workout DVD ($9. Value)Muscle models are the Gods of Aesthetics and if boasting around 2. DVD is our gift to you. Adipose tissue - Wikipedia. In biology, adipose tissue ( listen), body fat, or simply fat is a loose connective tissue composed mostly of adipocytes. Adipose tissue is derived from preadipocytes. Its main role is to store energy in the form of lipids, although it also cushions and insulates the body. Far from being hormonally inert, adipose tissue has, in recent years, been recognized as a major endocrine organ. The two types of adipose tissue are white adipose tissue (WAT), which stores energy, and brown adipose tissue (BAT), which generates body heat. ![]() The formation of adipose tissue appears to be controlled in part by the adipose gene. Adipose tissue – more specifically brown adipose tissue – was first identified by the Swiss naturalist Conrad Gessner in 1. Adipose tissue is found in specific locations, which are referred to as adipose depots. Apart from adipocytes, which comprise the highest percentage of cells within adipose tissue, other cell types are present, collectively termed stromal vascular fraction (SVF) of cells. SVF includes preadipocytes, fibroblasts, adipose tissue macrophages, and endothelial cells. Adipose tissue contains many small blood vessels. In the integumentary system, which includes the skin, it accumulates in the deepest level, the subcutaneous layer, providing insulation from heat and cold. Around organs, it provides protective padding. However, its main function is to be a reserve of lipids, which can be burned to meet the energy needs of the body and to protect it from excess glucose by storing triglycerides produced by the liver from sugars, although some evidence suggests that most lipid synthesis from carbohydrates occurs in the adipose tissue itself. Under normal conditions, it provides feedback for hunger and diet to the brain. For comparison, a mouse with a normal amount of adipose tissue is shown on the right. Mice have eight major adipose depots, four of which are within the abdominal cavity. The mesenteric depot forms a glue- like web that supports the intestines and the omental depot (which originates near the stomach and spleen) and - when massive - extends into the ventral abdomen. Both the mesenteric and omental depots incorporate much lymphoid tissue as lymph nodes and milky spots, respectively. Body weight loss, reduced urge for palatable food and increased release of GLP-1 through daily supplementation with green-plant membranes for three months in.After weight loss, changes in the circulating levels of several peripheral hormones involved in the homeostatic regulation of body weight occur. Unintentional Weight Loss 720. American Family Physician. Volume 89, Number 9 May 1, 2014. If no baseline weight is available, evidence of. Weight loss and fluctuations in weight have been associated with increased risks of death from cardiovascular disease and from all causes. The two superficial depots are the paired inguinal depots, which are found anterior to the upper segment of the hind limbs (underneath the skin) and the subscapular depots, paired medial mixtures of brown adipose tissue adjacent to regions of white adipose tissue, which are found under the skin between the dorsal crests of the scapulae. The layer of brown adipose tissue in this depot is often covered by a . February 2009 Issue. Nutrition and COPD - Dietary Considerations for Better Breathing By Ilaria St. Florian, MS, RD Today’s Dietitian Vol. ![]() The inguinal depots enclose the inguinal group of lymph nodes. Minor depots include the pericardial, which surrounds the heart, and the paired popliteal depots, between the major muscles behind the knees, each containing one large lymph node. A panniculus complicates surgery of the morbidly obese individual. It may remain as a literal . This condition cannot be effectively corrected through diet and exercise alone, as the panniculus consists of adipocytes and other supporting cell types shrunken to their minimum volume and diameter. Visceral fat is different from subcutaneous fat underneath the skin, and intramuscular fat interspersed in skeletal muscles. Fat in the lower body, as in thighs and buttocks, is subcutaneous and is not consistently spaced tissue, whereas fat in the abdomen is mostly visceral and semi- fluid. Visceral fat is often expressed in terms of its area in cm. VFA, visceral fat area). New developments such as the Body Volume Index (BVI) are specifically designed to measure abdominal volume and abdominal fat. Excess visceral fat is also linked to type 2 diabetes. Female sex hormone causes fat to be stored in the buttocks, thighs, and hips in women. The most popular of these equations was formed by Durnin and Wormersley, who rigorously tested many types of skinfold, and, as a result, created two formulae to calculate the body density of both men and women. These equations present an inverse correlation between skinfolds and body density—as the sum of skinfolds increases, the body density decreases. New formulae are still being created. The cause is likely a combination of genetic, environmental, and behavioral factors that are involved in excess energy intake and decreased physical activity. Substantial weight loss can reduce ectopic fat stores in all organs and this is associated with an improvement of the function of that organ. Human fat tissue contains about 8. The net direction of this flux is controlled by insulin and leptin—if insulin is elevated, then there is a net inward flux of FFA, and only when insulin is low can FFA leave adipose tissue. Insulin secretion is stimulated by high blood sugar, which results from consuming carbohydrates. In humans, lipolysis (hydrolysis of triglycerides into free fatty acids) is controlled through the balanced control of lipolytic B- adrenergic receptors and a. A- adrenergic receptor- mediated antilipolysis. Fat cells have an important physiological role in maintaining triglyceride and free fatty acid levels, as well as determining insulin resistance. Abdominal fat has a different metabolic profile—being more prone to induce insulin resistance. This explains to a large degree why central obesity is a marker of impaired glucose tolerance and is an independent risk factor for cardiovascular disease (even in the absence of diabetes mellitus and hypertension). This suggests a possible cause- and- effect link between the two, wherein stress promotes the accumulation of visceral fat, which in turn causes hormonal and metabolic changes that contribute to heart disease and other health problems. In addition, adipose- derived stem cells from both human and animals reportedly can be efficiently reprogrammed into induced pluripotent stem cells without the need for feeder cells. Perivascular adipose tissue releases adipokines such as adiponectin that affect the contractile function of the vessels that they surround. This specialized tissue can generate heat by . The process of uncoupling means that when protons transit down the electrochemical gradient across the inner mitochondrial membrane, the energy from this process is released as heat rather than being used to generate ATP. This thermogenic process may be vital in neonates exposed to cold, which then require this thermogenesis to keep warm, as they are unable to shiver, or take other actions to keep themselves warm. Techniques to manipulate the differentiation of . Metabolically active tissue with temperature responses similar to brown adipose was first reported in the neck and trunk of some human adults in 2. Beige adipocytes take on a multilocular appearance (containing several lipid droplets) and increase expression of uncoupling protein 1 (UCP1). Release of catecholamines from sympathetic nerves results in UCP1 activation and usually occurs after extended periods of cold exposure or in response to overfeeding. The drug 2,4- dinitrophenol, which also acts as a chemical uncoupler similarly to UCP1, was used for weight loss in the 1. However, it was quickly discontinued when excessive dosing led to adverse side effects including hyperthermia and death. However, the use of such drugs has proven largely unsuccessful due to several challenges, including varying species receptor specificity and poor oral bioavailability. Browning in response to chronic cold exposure has been well documented and is a reversible process. A study in mice demonstrated that cold- induced browning can be completely reversed in 2. UCP1 seen within a 2. Three regulators of transcription are central to WAT browning and serve as targets for many of the molecules known to influence this process. Among these molecules are irisin and fibroblast growth factor 2. FGF2. 1), which have been well- studied and are believed to be important regulators of browning. Irisin is secreted from muscle in response to exercise and has been shown to increase browning by acting on beige preadipocytes. Studies of WAT browning have greatly benefited from advances in these techniques, as beige fat is rapidly gaining popularity as a therapeutic target for the treatment of obesity and diabetes. DNA microarray is a bioinformatics tool used to quantify expression levels of various genes simultaneously, and has been used extensively in the study of adipose tissue. One such study used microarray analysis in conjunction with Ingenuity IPA software to look at changes in WAT and BAT gene expression when mice were exposed to temperatures of 2. It was discovered that many of the pathways upregulated in WAT after cold exposure are also highly expressed in BAT, such as oxidative phosphorylation, fatty acid metabolism, and pyruvate metabolism. Incorporating RNA- Seq into browning studies is of great value, as it offers better specificity, sensitivity, and a more comprehensive overview of gene expression than other methods. RNA- Seq has been used in both human and mouse studies in an attempt characterize beige adipocytes according to their gene expression profiles and to identify potential therapeutic molecules that may induce the beige phenotype. One such study used RNA- Seq to compare gene expression profiles of WAT from wild- type (WT) mice and those overexpressing Early B- Cell Factor- 2 (EBF2). WAT from the transgenic animals exhibited a brown fat gene program and had decreased WAT specific gene expression compared to the WT mice. This tool has enabled examination of epigenetic regulation of browning and helps elucidate the mechanisms by which protein- DNA interactions stimulate the differentiation of beige adipocytes. Studies observing the chromatin landscapes of beige adipocytes have found that adipogenesis of these cells results from the formation of cell specific chromatin landscapes, which regulate the transcriptional program and, ultimately, control differentiation. ![]() Amazon. com: Garcinia Cambogia Capsules- Pure Extract- Natural Dietary Supplement for Weight Loss- 1. Ct Veggie Diet Pills- CERTIFIED AS 8. HCA (OTHERS AREN'T)- Appetite Suppressant- MADE IN THE USA!: Health & Personal Care. What Did Doctors Say About Garcinia Cambogia? If taken before meals it is excellent for weight loss because of Garcinia's appetite- blocking abilities.. The natural extract from the rind of the small, pumpkin- shaped fruit is called hydroxycitric acid (HCA).. Our product contains 1. Garcinia Cambogia extract with 8. HCA. Garcinia Cambogia blocks the formation of fat cells. Since it also curbs your appetite and your food cravings it can double or triple one's weight loss.. 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For patients who have a donor available, this procedure promises quicker recoveries, better transplant results and reduced waiting times. That expertise means we are among the most experienced in safely removing part of the donor’s liver to help the recipient resume a normal life as quickly as possible. Living liver donation involves an extremely complex surgery that must remove part of a person’s liver and place it in the recipient’s body. The experience of the surgical team should be your first consideration when choosing your living donor center. This skilled team has extra training and expertise in living donor procedures. These nations perform the highest volumes of living donor liver transplants in the world, and our surgeons sought training opportunities that would provide a high volume of experience. Meet our team. Dedicated living donor nurse coordinators: Our dedicated nurse coordinators work with all living liver donors. They are highly familiar with the needs, questions and experiences of living donors and will be there for you throughout the process. Meet the transplant nurse coordinators. Clear operating roles and procedures: We have established a clear procedure for these complex surgeries. The same people handle the same duties in each operation, which leads to a proven record of success. Because liver transplantation is such a successful procedure, doctors are recommending this procedure for more and more patients. ![]() Unfortunately, there are not enough donor organs available, which means that more people are waiting for transplants. To solve this problem, surgeons can remove a portion of a living person’s liver and implant it in the liver recipient. The liver regrows to its full size in both people. In addition to making more liver transplants available, patients who receive living donor transplants experience these advantages: Transplanting patients earlier in the liver disease progression often prevents them from becoming very sick. They also recover faster from the transplant surgery. The graft – the new liver – is more likely to survive when it comes from a living donor. The recipient’s body is less likely to reject the donated organ (graft). Recipients spend less time on the waiting list. Learn more about liver disease and liver transplant. The best candidates for living liver donation are family members or close, personal friends of the recipient. Liver donation is a major abdominal surgery and a serious commitment. Living donors should meet these criteria: Have an important personal relationship with the recipient Come forward to donate willingly. Be between the ages of 1. Have a compatible blood type with the recipient Be in excellent health. Not have uncontrolled high blood pressure, liver disease, diabetes or heart disease. Be about the same physical size as the recipient, or larger We consider living liver donation for all patients. Ultimately, the safety of the recipient and donor determine whether a live donor transplant is an option. In general, the following guidelines make patients most likely to benefit from a living donor liver transplant: Patients must have a relative or close friend who is willing to donate a portion of their liver and who is a compatible donor. Eligible recipients usually have symptoms of liver failure and have MELD scores (Model for End- Stage Liver Disease) that do not let them receive a transplant in a timely manner. The MELD score ranks how sick a patient is and how much they need a transplant. Recipient MELD scores must be greater than 1. In competitive transplant regions like the one UMMC is in (UNOS Region 2), patients with lower MELD scores are likely to be on the waiting list for a long time before a traditional (cadaver) transplant becomes available. Donating a portion of your liver is a generous gift of life. Part of the donor’s liver is resected (removed) in an open abdominal surgery. This surgery involves the following steps: Before the procedure: On the day of the operation, donors and recipients come to our Same Day Surgery unit. ![]() We will do some final tests to make sure you are ready. These might include a physical exam, blood work, X- rays, an EKG or other tests to make sure you do not have an infection or other issue that could cause problems with the transplant. In operating rooms that are next to each other, we gently put the donor and recipient to sleep and prepare for surgery. Donor procedure: We make an incision under the donor’s rib cage and carefully assess the actual size of the liver, which we’ve already seen with a CT (computed tomography) scan during the evaluation. ![]() ![]() ![]() The surgeons remove the donor’s gallbladder and inject dye into the biliary tree (the bile ducts and gallbladder) to make sure it is safe for division. Then they dissect the portal vein and artery where it divides the different sides of the liver. They isolate the vein that drains that part of the liver and divide the liver in half very carefully. The surgeons close the surgical incision. The patient goes into recovery. Recipient procedure: Meanwhile, surgeons immediately implant the resected (surgically removed) liver in the recipient. The liver transplant surgery usually takes 4 to 8 hours as surgeons reattach blood vessels and bile ducts. ![]() After the procedure: We aim to have the donor up and out of bed the night of the surgery. The morning after surgery, they can walk down the hallway to visit their liver recipient. Most donors go home about 5 to 6 days after surgery. Within about 2 months, the liver re- grows to its original size in both the donor and in the recipient. We know that donors have lots of questions. If you are considering donation, we will assign you a donor advocate from our social work department. The donor advocate can help you to figure out your best interests privately, outside of conversations with the surgical team. We want you to feel comfortable asking questions during every step of the process. Weight loss issues related to specific diseases include: As chronic obstructive pulmonary disease (COPD) advances, about 35% of patients experience severe weight loss. What is Flat Tummy Tea? Firstly, Flat Tummy Tea is a drink kit, designed for detoxification, consisting of Activate and Cleanse. The ingredients are senna, taraxacum. Can a Food Diary Help You Lose Weight? Wondering how to keep a food journal? Here are 8 tips for making a food diary work for you. For additional information about living donor liver transplant, please call the Transplant office at 1- 4. If you are interested in becoming a living liver donor, please click below to download our questionnaire. For referring physicians: To refer a patient or get more information, please call 1- 8. A physician service representative from Consultation and Referral Services will direct your call to the appropriate physician or department. For more details, please visit our section for referring physicians. More Information. NEW from the author of Burn the Fat, Feed the Muscle: The Burn the Fat Online Body Transformation System.![]() The country's top Paleo experts share their tips for successful weight loss on a Paleo diet and discuss how you can lose weight today with Paleo. Weight Loss and Diet Essentials WLR's New Habits New Me Challenge. 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Learn the premises of the controversial diet book The China Study, which suggests that eliminating meats and dairy from the U.S. Save yourself from reaching for sugar laden nutritionally bankrupt caffeine-loaded quick fixes when your energy sags by keeping Paleo snacks at the ready! China Study Diet offers over 120 plant-based recipes to help you easily adopt a plant-based diet to improve health and prevent disease. ![]() China has a bold plan to tackle bad bank loans and its first deadline is closer than you think. Chinese authorities continue to get more serious in addressing unproductive debt in the economy and banks’ understatement of bad debts. The recent appointment of Guo Shuqing as the new head of the China Banking Regulatory Commission (CBRC) is a clear sign of Beijing’s intent on accelerating non- performing loan (NPL) resolutions and unwinding excess debt. I used this 30-day reset autoimmune diet plan to help manage my Hashimotos Thyroiditis and get my autoimmune disease into remission. China, officially the People's Republic of China (PRC), is a unitary sovereign state in East Asia and the world's most populous country, with a population of over 1. How to Lose Weight Without Dieting. Losing weight is a common goal for many people. Most try a few diet programs or plans to help reach their healthy or ideal weight. Plan A Visit; Find a Doctor; Patient Story; FAQ; Ask a Question; Make an Appointment; Hospital Charges; Kidney Service China has always thrived on word of mouth.![]() Guo hasn’t wasted any time. In Circular 4. 6 issued last month, the CBRC stepped- up its enforcement of prohibited accounting practises that banks have been employing to understate credit exposures and warehouse problem loans, particularly regarding interbank exposures and wealth management products (WMPs), culminating in what we believe will be an increased flow of NPL sales throughout 2. While these practises have been banned for a while, this Circular stated four key pieces of new information. Details – The notice listed numerous specific examples of prohibited practises in a highly- detailed fashion for the first time. Examinations - The CBRC is requiring banks to conduct internal self- audits, reporting back by June 1. Enforcement- In parallel with internal self- audits, the CBRC is doing extensive on- site examinations, and will require banks to reclassify any misclassifications of credit exposures by November 3. Penalties – The CBRC will continue to institute penalties for non- compliance and disclose these as a matter of public record. As an example, there were 2. March 2. 9 totaling 4. US$6. 3. 3 million). We believe there are five meaningful impacts from this CBRC initiative. Firstly, increased recognition and sales of NPLs. To the extent these prohibited measures have been used to warehouse problem loans, any required re- classifications back as more appropriate loan exposures should result in higher NPLs. In anticipation of this, and on the back of internal audits now underway, we expect banks to be willing sellers of these exposures before the November 3. We are already witnessing increased sales of NPL portfolios. Secondly, another accounting benefit is achieving lower risk weightings on credit exposures for the purposes of calculating regulatory capital ratios, thereby increasing the reported ratios and appearing to have better balance sheet strength. Regulators require minimum capital ratios, which take into account the “riskiness” of their assets. By classifying exposures as “less risky”, banks can show a better regulatory capital ratio, and appear to have better capital strength. Many of these practises are now explicitly prohibited under Circular 4. As an example, by reclassifying a loan (high risk- weight, say 7. RWAs), and therefore report higher capital ratios. In the case of WMPs, many loan exposures were completely removed from balance sheets altogether, completely removing those RWAs. Under Circular 4. NPLs), RWAs will rise causing regulatory capital ratios to decline. Again, this process may prompt banks to consider simply selling these portfolios rather than re- classifying them into higher risk- weighted categories and thereby reporting lower capital ratios – in some cases breaching regulatory minimums. Granted, this may cause them to take increased provision expenses to write- down bad loans, but reporting lower profit is arguably more palatable than reporting lower capital ratios - - especially given that balance sheet strength is more highly valued in the current environment than is profitability. Thirdly, by requiring certain loan exposures be brought back onto balance sheets, or by re- classifying from what was considered a liquid asset (e. Importantly, it is our understanding that many of these structures were used to create liquidity among banks, particularly among the smaller banks which have a higher reliance on the interbank activities that are under scrutiny by the CBRC. By unwinding these structures, these banks are likely to face liquidity pressures and therefore higher funding costs on their deposits. Therefore, in coordination with the CBRC examinations, we expect the PBOC to employ various market intervention activities in coming months to ease funding pressures in the interbank market in order to prevent extreme volatility or even a negative liquidity event. Fourthly,by unwinding these irregular accounting and structuring practises - particularly the opaque disclosures of off- balance sheet WMPs and certain interbank assets – bank balance sheets will be more transparent. And perhaps more importantly, counterparty risk within the banking system will be more able to be properly assessed. The result is a far more transparent banking system where risks will be more measurable and able to be appropriately priced. Fifthly, we believe this Circular is yet another example of the Chinese regulators’ concerted efforts to work collaboratively to reduce system leverage and reign in excessive credit. While this may result in slower credit growth overall (and therefore lower GDP growth), it will also result in better capital allocation toward more sustainable, productive GDP growth in the longer term. While we view reduced system leverage as a necessary and positive development, from a public markets perspective, it is likely to withdraw liquidity and result in a sell- off in both equities and bonds. This is already happening, particularly regarding WMP activities, as banks cut back on issuance of these products during their internal audit phase required by Circular 4. This is likely to accelerate in coming months as internal audits are concluded and banks work toward meeting the CBRC enforcement deadline. Andrew Brown is a partner for macro and strategy at Shore. Vest Capital Partners. Robot Check. Enter the characters you see below. Sorry, we just need to make sure you're not a robot. For best results, please make sure your browser is accepting cookies. Particle Accelerators Are Changing the Way We Look at Ancient Turds. Shit’s wild. No, seriously, there’s so much you can learn about animals, their lifestyles, and the world they interacted with based on what shows up in their poo. Especially if the poo is over 2. Most of the methods used to look at fossilized shit, more commonly called coprolites, are fairly outdated. Scientists mainly use two- dimensional imaging techniques that require cutting literal slices of the sample to look at them up close. Three- dimensional imaging methods in the lab might miss the smallest features like hairs or insect legs. Disclaimer: You are leaving a Gizmodo Media Group, LLC website and going to a third party site, which is subject to its own privacy policy and terms of use. ![]() But a team of Swedish scientists have a better way to reveal the poo’s secrets: particle accelerators. Accelerating particles is for more than just dense particle physics. ![]() A special type of accelerator, called a synchrotron, sends electrons racing around an enormous racetrack, in this case the half- mile- round European Synchrotron Radiation Facility. Every time the electrons change direction, they let out high- powered x- rays that shoot down a beam pipe where the poop awaits its close- up. The new paper marks the first time that researchers have imaged fossilized poo with this specific kind of accelerator imaging, called “propagation phase- contrast synchrotron microtomography.” Once the x- rays actually hit the poop, they’re collected and used to create an image based on what light was and wasn’t absorbed. The phase contrasting part just means that the image can be even further sharpened by comparing how the alignment of the light waves shift. The increased resolution is important. One poop, a part of a several- inch- long coil from a big swimming meateater, contained pieces of an ancient fish and bivalves. Pieces of the fish’s pelvic tract remained intact despite digestion. Another several- inch- long poop (not coiled) clearly contained parts of a beetle, and was maybe made by some sort of dog- sized insectivorous lizard. Other researchers thought this was a cool paper. But this scat story is far from over.“Getting information from coprolites is difficult,” Distinguished Professor of Paleontology Robert Reisz from the University of Toronto Mississauga told Gizmodo in an email. He pointed out that the arguments presented in this “nice piece of work” are reasonable but speculative. A financial advisor venlafaxine online uk Drone strikes should also be recalibrated and used only when necessary. Critical individuals that serve as key communication. ![]() ![]() Portal Looks Great As A Lego Diorama. Look at that orange hole in the wall! Brick. 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This project examines the organizational structures found in William Forsythe's dance. One Flat Thing, reproduced by translating and transforming them into new objects - . Belly dance history and origins. How this dance form originated in Egypt and Turkey and how oriental or raqs sharqi dance spread to the West. The dance, with its giant, dual-dancer costumes and kung. Ballet began in royal courts in the early 1600's, and early forms of this elegant and sophisticated art involved long skirts and. LINKS TO OTHER "MUSICAL" SITES: LIST OF FAMOUS FEMALE SINGERS From Opera to Punk Rockers! LIST OF FAMOUS MALE SINGERS From Opera to Funk! THE NAMES OF. GET TO KNOW US. Charlotte Ballet’s staff is a group of individuals with a common passion: creating artistically excellent programming from beautiful classics to. A healthy weight is the weight your body naturally settles into when you consistently eat a nutritious diet, are physically active, and balance the calories you eat. ![]() The Benefits of Pilates. Just what can Pilates exercises do for you? Original panel cartoon art from The New Yorker. MODERN DANCE HISTORY. I’ll use the expression modern dance history to talk about figures, choreographic productions and related facts occurred in western culture. Letting loose on the dance floor makes you more attractive, reveals study. Don't let embarrassment hold you back. Eu acho que este coment. ![]() ![]() ![]() Formulado com chás e extrato de ervas específicas, Natu Diet não só inibe o apetite como também tira a vontade. Protege o estômago e ajuda na eliminação de.![]() ![]() ![]() Com ervas medicinais, Composto Natu Diet é um suplemento fitoterápico que combate. Natu Diet é contra indicado para. Com ervas medicinais, Composto Natu Diet é um suplemento fitoterápico que pode ajudar combater a obesidade. Ajuda na queima de gordura;. Composto Natu Diet. COMPOSTO NATU DIET MULTI ERVAS. Composto Natu Diet Multi Ervas. Dieta Emagrecedor; Ch. EMAGREÇA DE MANEIRA SAUDAVEL COM O COMPOSTO NATU DIET MULTI ERVAS. INDICADO NO. O produto ajuda na inibição natural do apetite e. Composto Natu Diet, um produto fitoterápico que pode ajudar no combate a obesidade. Elaborado com ervas medicinais que auxiliam na perda de peso. ![]() |