Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Patricia Lanzano"'
Autor:
Emily Breidbart, MD, Lauren Golden, MD, Claudia Gonzaga-Jauregui, PhD, Liyong Deng, MD, Patricia Lanzano, BA, Charles LeDuc, PhD, JianCheng Guo, MD, PhD, John D. Overton, PhD, Jeffery Reid, PhD, Alan Shuldiner, MD, Wendy K. Chung, MD, PhD
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 5, Pp e411-e414 (2018)
ABSTRACT: Objective: To present a case of adult-onset familial diabetes mellitus in which a genetic etiology typical for neonatal diabetes was identified.Methods: We conducted whole-exome and Sanger sequencing, assessed clinical presentation and fami
Externí odkaz:
https://doaj.org/article/931e4b2fa6ff491b856e88e674076187
Autor:
Xiao Fan, Wendy K. Chung, Emily Breidbart, Rudolph L. Leibel, Jiancheng Guo, Patricia Lanzano, Charles A. LeDuc, Liyong Deng
Publikováno v:
J Pediatr Endocrinol Metab
Objectives There have been few large-scale studies utilizing exome sequencing for genetically undiagnosed maturity onset diabetes of the young (MODY), a monogenic form of diabetes that is under-recognized. We describe a cohort of 160 individuals with
Autor:
John D. Overton, Jiancheng Guo, Patricia Lanzano, Emily Breidbart, Lauren Golden, Jeffery Reid, Charles A. LeDuc, Alan R. Shuldiner, Claudia Gonzaga-Jauregui, Wendy K. Chung, Liyong Deng
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 5, Pp e411-e414 (2018)
Objective: To present a case of adult-onset familial diabetes mellitus in which a genetic etiology typical for neonatal diabetes was identified.Methods: We conducted whole-exome and Sanger sequencing, assessed clinical presentation and family history
Autor:
Jian-min Liu, Patricia Lanzano, Thomas L. Nickolas, Zhenyan He, Na Luo, Rudolph L. Leibel, Lori M. Zeltser, Kevin W. Williams, Ioanna Mosialou, Liyong Deng, Steven Shikhel, Wendy K. Chung, Stavroula Kousteni, Mishaela R. Rubin, Jeffrey E. Pessin, Richard A. Friedman, Yiru Huang, Jonathan Barasch, Haihong Zong, Antonio Maurizi
Publikováno v:
Nature. 546(7658)
Bone has recently emerged as a pleiotropic endocrine organ that secretes at least two hormones, FGF23 and osteocalcin, which regulate kidney function and glucose homeostasis, respectively. These findings have raised the question of whether other bone
Autor:
Jonathan Barasch, Ioanna Mosialou, Liyong Deng, Steven Shikhel, Haihong Zong, Wendy K. Chung, Thomas Nicholas, Antonio Maurizi, Jeffrey E. Pessin, Lori M. Zeltser, Patricia Lanzano, Stavroula Kousteni, Kevin W. Williams, Mishaela R. Rubin, Na Luo, Rudolph L. Leibel, Jian-min Liu, Yiru Huang, Richard A. Friedman, Zhenyan He
Bone has recently emerged as a pleiotropic endocrine organ that secretes at least two hormones, FGF23 and osteocalcin, which regulate kidney function and glucose homeostasis, respectively. These findings have raised the question of whether other bone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5200dc2407cadcc0364621f928ffcfc
http://hdl.handle.net/11697/180280
http://hdl.handle.net/11697/180280
Autor:
Diana R. O’Day, Jayne F. Martin Carli, Wendy K. Chung, Charles A. LeDuc, Michael Rosenbaum, Rudolph L. Leibel, Liheng Wang, Dieter Egli, George Stratigopoulos, Patricia Lanzano, Dan Doherty
Publikováno v:
Cell Metabolism. 19:767-779
SummaryCommon polymorphisms in the first intron of FTO are associated with increased body weight in adults. Previous studies have suggested that a CUX1-regulatory element within the implicated FTO region controls expression of FTO and the nearby cili
Autor:
Yufeng Shen, Roja Motaghedi, Svetlana Ten, Joan C. Han, Rudolph L. Leibel, Noel K. Maclaren, Wendy K. Chung, Patricia Lanzano, Yee Him Cheung, Richard Gill, Nazrat M. Mirza, Jack A. Yanovski
Publikováno v:
Obesity. 22:576-584
Objective Obesity is a major public health problem that increases risk for a broad spectrum of co-morbid conditions. Despite evidence for a strong genetic contribution to susceptibility to obesity, previous efforts to discover the relevant genes usin
Autor:
Patricia Lanzano, Katrina Celis, Gloria H. Su, Christen J. Lennon, Maria Teresa Guerra Rendon, Sidney B. Eisig, David C. Hoffman, Henry Ostos, Wendy K. Chung, Edwin Guzman, José Arturo Pacheco Nuñez, Andrew C. Birkeland, Joseph Haddad
Publikováno v:
The Laryngoscope. 122:2082-2087
Objectives/Hypothesis: Orofacial clefts are the most common craniofacial birth defects in humans, with the majority of orofacial clefts occurring as nonsyndromic cleft lip with or without cleft palate (NSCLP). We previously demonstrated associations
Publikováno v:
Cardiology in the Young. 22:194-201
BackgroundHeterotaxy syndrome is caused by left–right asymmetry disturbances and is associated with abnormal lateralisation of the abdominal and thoracic organs. The heart is frequently involved and the severity of the abnormality usually determine
Autor:
Megan C. MacDougall, Harry R. Kissileff, Wendy K. Chung, Joo Lee Song, Kathleen L. Keller, Patricia Lanzano, Hope Cassano, Adrienne Reid, Liyong Deng
Publikováno v:
Obesity. 18:1194-1200
Previous studies have shown that inherited taste blindness to bitter compounds like 6-n-propylthiouracil (PROP) may be a risk factor for obesity, but this literature has been highly controversial. The objectives of this study were (i) to confirm find