Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma

Published:2022-01 Issue:1 Volume:24 Page:157-169
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Yang Muyi,Johnsson Per,Bräutigam Lars,Yang Xiaohong R.,Thrane Kim,Gao Jiwei,Tobin Nicholas P.,Zhou Yitian,Yu Rong,Nagy Noemi,Engström Pär G.,Tuominen Rainer,Eriksson Hanna,Lundeberg Joakim,Tucker Margaret A.,Goldstein Alisa M.,Egyhazi-Brage Suzanne,Zhao Jian,Cao Yihai,Höiom Veronica

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference35 articles.

1. Melanoma genetics;Read;J Med Genet,2016

2. Pigmentary characteristics and moles in relation to melanoma risk;Titus-Ernstoff;Int J Cancer,2005

3. Genetic determinants of hair, eye and skin pigmentation in Europeans;Sulem;Nat Genet,2007

4. Genetic epidemiology of cutaneous melanoma: a global perspective;Goldstein;Arch Dermatol,2001

5. Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study;Davies;Pigment Cell Melanoma Res,2012

Cited by 1 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. Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy;Nature Communications;2024-08-22

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