Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism

Published:2017-03 Issue:3 Volume:6 Page:295-305
ISSN:2212-8778
Container-title:Molecular Metabolism
language:en
Short-container-title:Molecular Metabolism

Author:

Löffler Dennis,Behrendt Susanne,Creemers John W.M.,Klammt Jürgen,Aust Gabriela,Stanik Juraj,Kiess Wieland,Kovacs Peter,Körner Antje^ORCID

Funder

German Research Foundation

European Community's Seventh Framework Programme

European Regional Development Fund

Federal Ministry of Education and Research

IFB AdiposityDiseases

German Diabetes Association

European Society for Pediatric Endocrinology

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference55 articles.

1. Common nonsynonymous variants in PCSK1 confer risk of obesity;Benzinou;Nature Genetics,2008

2. Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals;Nead;Human Molecular Genetics,2015

3. The association of common variants in PCSK1 with obesity: a HuGE review and meta-analysis;Stijnen;American Journal of Epidemiology,2014

4. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes;Strawbridge;Diabetes,2011

5. Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region);Seidah;Genomics,1991

Cited by 27 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. Cardiometabolic Risk Markers in Children With Obesity and Variants in MC4R Pathway-related Genes;Journal of the Endocrine Society;2024-07-25

2. Medical semiology of patients with monogenic obesity: A systematic review;Obesity Reviews;2024-07-02

3. Differential sex‐association between PCSK1 polymorphisms and obesity risk in Portuguese children;American Journal of Human Biology;2023-11-27

4. Metabolic syndrome: Nutri-epigenetic cause or consequence?;Heliyon;2023-11

5. The N221D variant in PCSK1 is highly prevalent in childhood obesity and can influence the metabolic profile;Journal of Pediatric Endocrinology and Metabolism;2023-10-26

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