Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julie Stöy"'
Autor:
Rochelle N. Naylor, Kashyap A. Patel, Jarno L. T. Kettunen, Jonna M. E. Männistö, Julie Støy, Jacques Beltrand, Michel Polak, ADA/EASD PMDI, Tina Vilsbøll, Siri A. W. Greeley, Andrew T. Hattersley, Tiinamaija Tuomi
Publikováno v:
Communications Medicine, Vol 4, Iss 1, Pp 1-17 (2024)
Abstract Background Beta-cell monogenic forms of diabetes have strong support for precision medicine. We systematically analyzed evidence for precision treatments for GCK-related hyperglycemia, HNF1A-, HNF4A- and HNF1B-diabetes, and mitochondrial dia
Externí odkaz:
https://doaj.org/article/c6131c68651d4205b6f18e53add807da
Autor:
Camila Alvarez-Silva, Alireza Kashani, Tue Haldor Hansen, Nishal Kumar Pinna, Ranjit Mohan Anjana, Anirban Dutta, Shruti Saxena, Julie Støy, Ulla Kampmann, Trine Nielsen, Torben Jørgensen, Visvanathan Gnanaprakash, Rameshkumar Gnanavadivel, Aswath Sukumaran, Coimbatore Subramanian Shanthi Rani, Kristine Færch, Venkatesan Radha, Muthuswamy Balasubramanyam, Gopinath Balakrish Nair, Bhabatosh Das, Henrik Vestergaard, Torben Hansen, Sharmila Shekhar Mande, Viswanathan Mohan, Manimozhiyan Arumugam, Oluf Pedersen
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-13 (2021)
Abstract Background Type 2 diabetes (T2D), a multifactorial disease influenced by host genetics and environmental factors, is the most common endocrine disease. Several studies have shown that the gut microbiota as a close-up environmental mediator i
Externí odkaz:
https://doaj.org/article/aa5d473cc056406e8a1a606b374ea278
Autor:
Julie Støy, Elisa De Franco, Honggang Ye, Soo-Young Park, Graeme I. Bell, Andrew T. Hattersley
Publikováno v:
Molecular Metabolism, Vol 52, Iss , Pp 101280- (2021)
Background: While insulin has been central to the pathophysiology and treatment of patients with diabetes for the last 100 years, it has only been since 2007 that genetic variation in the INS gene has been recognised as a major cause of monogenic dia
Externí odkaz:
https://doaj.org/article/7b6472ca2feb41e7aae6548de0286d87
Autor:
Julie Støy, Niels Grarup, Arne Hørlyck, Liselotte Ibsen, Jørgen Rungby, Per Løgstrup Poulsen, Ivan Brandslund, Cramer Christensen, Torben Hansen, Oluf Pedersen, Niels Møller, Ulla Kampmann
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e109646 (2014)
The genetics of hypertension has been scrutinized in large-scale genome-wide association studies (GWAS) with a large number of common genetic variants identified, each exerting subtle effects on disease susceptibility. An amino acid polymorphism, p.A
Externí odkaz:
https://doaj.org/article/ca19679e82e94baaa4d3544673968e9b
Autor:
Benjamin A. Alman, Valerie A. Arboleda, Andrew Arnold, Graeme I. Bell, Albert M. Beckers, Xavier Y. Bertagna, Jerome Bertherat, Jane H. Christensen, Karine Clément, Shelly A. Cummings, Adrian F. Daly, Manuela Dittmar, Koen M.A. Dreijerink, Beatrice Dubern, Alexandra Dumitrescu, David A. Ehrmann, Sian Ellard, Douglas B. Evans, James A. Fagin, Alice A. Fleming, Helmut Grasberger, Siri A. Greeley, Lionel Groussin, David J. Halsall, Andrew T. Hattersley, Leslie Hoffman, Michael F. Holick, Jo W.M. Höppener, Vivian Hwa, Camilo Jimenez, Loren Joseph, George J. Kahaly, Kelly Lauter, Lawrence C. Layman, Rosella Libe, Cornelius J.M. Lips, Rob B. Van de Luijt, Nicholas Mitsiades, Rinki Murphy, Bernadette P.M. van Nesselrooij, Maria I. New, Saroj Nimkarn, Stephen O’Rahilly, Louis H. Philipson, Joachim Pohlenz, Kenneth S. Polonsky, Kenan Qin, Sally Radovick, Samuel Refetoff, Thereasa A. Rich, Soren Rittig, Christopher J. Romero, Ron G. RosenfeLd, David B. Savage, Robert K. Semple, Julie Stöy, Constantine A. Stratakis, Bernard S. Strauss, Patrick Tounian, Eric Vilain, Guy Van Vliet, Roy E. Weiss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd75a890ff9d567a98f7b5fa90f7e4c6
https://doi.org/10.1016/b978-0-12-374430-2.00032-8
https://doi.org/10.1016/b978-0-12-374430-2.00032-8
