Zobrazeno 1 - 7
of 7
pro vyhledávání: '"STEVEN CHERNAUSEK"'
Autor:
Madhusmita Rout, Gurpreet S. Wander, Sarju Ralhan, Jai Rup Singh, Christopher E. Aston, Piers R. Blackett, Steven Chernausek, Dharambir K. Sanghera
Publikováno v:
Therapeutic Advances in Endocrinology and Metabolism, Vol 14 (2023)
Background: Genome-wide polygenic risk scores (PRS) have shown high specificity and sensitivity in predicting type 2 diabetes (T2D) risk in Europeans. However, the PRS-driven information and its clinical significance in non-Europeans are underreprese
Externí odkaz:
https://doaj.org/article/bce06ec84a3c48589a66921ffcd4117a
Autor:
Jacqueline Alexander, April M Teague, Jing Chen, Christopher E Aston, Yuet-Kin Leung, Steven Chernausek, Rebecca A Simmons, Sara E Pinney
Publikováno v:
PLoS ONE, Vol 13, Iss 2, p e0190698 (2018)
AIMS/HYPOTHESIS:We hypothesized that diabetes during pregnancy (DDP) alters genome-wide DNA methylation in placenta resulting in differentially methylated loci of metabolically relevant genes and downstream changes in RNA and protein expression. METH
Externí odkaz:
https://doaj.org/article/b395292cf3f74da892314d4f49cdcea2
Autor:
JEANIE B. TRYGGESTAD, MEGAN M. KELSEY, SILVA A. ARSLANIAN, STEVEN CHERNAUSEK, KIMBERLY DREWS, ELIA N. ESCANAME, MITCHELL GEFFNER, ELVIRA M. ISGANAITIS
Publikováno v:
Diabetes. 71
This analysis compared microvascular and cardiac outcomes from women in the Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) study, originally diagnosed with youth-onset Type 2 diabetes between the ages of 10-17 yrs, who experie
Autor:
Minu George, Steven Chernausek
Short stature is one of the most common conditions presenting to paediatric endocrinology clinics. After careful history, physical examination, and standard laboratory diagnosis, the majority are classified as having idiopathic short stature. The ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cad828802ac4e632bc1eb042122cdc7b
https://doi.org/10.1093/med/9780198870197.003.0183
https://doi.org/10.1093/med/9780198870197.003.0183
Autor:
Mary Helen Black, Megan M. Kelsey, Steven Chernausek, Jose M. Mercader, Lynne E. Wagenknecht, Jose C. Florez, Rachana Shah, Jennifer Todd, Jason Flannick, Dana Dabelea, Ling Chen, Shylaja Srinivasan, Rose Gubitosi-Klug, Jasmin Divers, Sam Gidding, Alisa Manning
Publikováno v:
Diabetes. 67
The prevalence of type 2 diabetes is increasing in youth, particularly in certain ethnic groups, and studies have highlighted differences between youth- and adult-onset disease. However, its genetic determinants remain largely unexplored. To identify
Autor:
Natalie D Shaw, Harrison Brand, Zachary A Kupchinsky, Hemant Bengani, Lacey Plummer, Takako I Jones, Serkan Erdin, Kathleen A Williamson, Joe Rainger, Alexei Stortchevoi, Kaitlin Samocha, Benjamin B Currall, Donncha S Dunican, Ryan L Collins, Jason R Willer, Angela Lek, Monkol Lek, Malik Nassan, Shahrin Pereira, Tammy Kammin, Diane Lucente, Alexandra Silva, Catarina M Seabra, Colby Chiang, Yu An, Morad Ansari, Jacqueline K Rainger, Shelagh Joss, Jill Clayton Smith, Margaret F Lippincott, Sylvia S Singh, Nirav Patel, Jenny W Jing, Jennifer R Law, Nalton Ferraro, Alain Verloes, Anita Rauch, Katharina Steindl, Markus Zweier, Ianina Scheer, Daisuke Sato, Nobuhiko Okamoto, Christina Jacobsen, Jeanie Tryggestad, Steven Chernausek, Lisa A Schimmenti, Benjamin Brasseur, Claudia Cesaretti, Jose E García-Ortiz, Tatiana Pineda Buitrago, Orlando Perez Silva, Jodi D Hoffman, Wolfgang Mühlbauer, Klaus W Ruprecht, Bart L Loeys, Masato Shino, Angela M Kaindl, Chie-Hee Cho, Cynthia C Morton, Richard R Meehan, Veronica van Heyningen, Eric C Liao, Ravikumar Balasubramanian, Janet E Hall, Stephanie B Seminara, Daniel Macarthur, Steven A Moore, Koh-ichiro Yoshiura, James F Gusella, Joseph A Marsh, John M Graham, Angela E Lin, Nicholas Katsanis, Peter L Jones, William F Crowley, Erica E Davis, David R FitzPatrick, Michael E Talkowski
Publikováno v:
Nature Genetics. 49:969-969
Autor:
Ron G. Rosenfeld, James France, Kenneth M. Attie, Jo Anne Brasel, Stephen Burstein, Jose F. Cara, Steven Chernausek, Ronald W. Gotlin, Joyce Kuntze, Barbara M. Lippe, Patrick C. Mahoney, Wayne V. Moore, Paul Saenger, Ann J. Johanson
Publikováno v:
The Journal of Pediatrics. 121:49-55
Seventy girls with Turner syndrome, verified by karyotype, were randomly assigned to observation or treatment with human growth hormone (hGH), oxandrolone, or a combination of hGH plus oxandrolone for a period of 12 to 24 months, to assess the effect