A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity

Published:2014-06-03 Issue:2 Volume:39 Page:295-302
ISSN:0307-0565
Container-title:International Journal of Obesity
language:en
Short-container-title:Int J Obes

Author:

Philippe J,Stijnen P,Meyre D,De Graeve F,Thuillier D,Delplanque J,Gyapay G,Sand O,Creemers J W,Froguel P,Bonnefond A

Publisher

Springer Science and Business Media LLC

Subject

Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)

Link

http://www.nature.com/articles/ijo201496.pdf

Reference46 articles.

1. El-Sayed Moustafa JS, Froguel P From obesity genetics to the future of personalized obesity therapy. Nat Rev Endocrinol 2013; 9: 402–413.

2. Ramachandrappa S, Farooqi IS Genetic approaches to understanding human obesity. J Clin Investig 2011; 121: 2080–2086.

3. Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF et al. Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet 2013; 45: 501–512.

4. Bonnefond A, Clément N, Fawcett K, Yengo L, Vaillant E, Guillaume J-L et al. Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes. Nat Genet 2012; 44: 297–301.

5. Helgason H, Sulem P, Duvvari MR, Luo H, Thorleifsson G, Stefansson H et al. A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. Nat Genet 2013; 45: 1371–1374.

Cited by 57 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sequencing methods, functional characterization, prevalence, and penetrance of rare coding mutations in panels of monogenic obesity genes from the leptin‐melanocortin pathway: A systematic review;Obesity Reviews;2024-05-23

2. Deciphering the complex interplay of obesity, epithelial barrier dysfunction, and tight junction remodeling: Unraveling potential therapeutic avenues;Obesity Reviews;2024-05-14

3. Hallmarks of the metabolic secretome;Trends in Endocrinology & Metabolism;2024-01

4. Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use;Genetics in Medicine;2023-07

5. Single-cell transcriptomic profiling of human pancreatic islets reveals genes responsive to glucose exposure over 24 hours;2023-06-08

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3