The Genetic Determination of Skin Pigmentation: KITLG and the KITLG/c-Kit Pathway as Key Players in the Onset of Human Familial Pigmentary Diseases
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference26 articles.
1. Ethnic variation in tyrosinase and TYRP1 expression in photoexposed and photoprotected human skin;Alaluf;Pigment Cell Res,2003
2. KITLG mutations cause familial progressive hyper- and hypopigmentation;Amyere;J Invest Dermatol,2011
3. Gene expression profiling analysis of solar lentigo in relation to immunohistochemical characteristics;Aoki;Br J Dermatol,2007
4. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype;Brems;Nat Genet,2007
5. Dyschromatosis universalis hereditaria as an autosomal recessive disease in five members of one family;Bukhari;J Eur Acad Dermatol Venereol,2006
Cited by 48 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. Mapping and annotating genomic loci to prioritize genes and implicate distinct polygenic adaptations for skin color;Nature Communications;2024-06-07
2. Therapeutic modulation of KIT ligand in melanocytic disorders with implications for mast cell diseases;Experimental Dermatology;2024-05
3. Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses;BMC Genomics;2023-08-01
4. A pigmentary manifestation associated with PPP2R5D-related neurodevelopmental disorder: a case report and review of literature;Bulletin of the National Research Centre;2023-07-10
5. Familial Gastrointestinal Stromal Tumor Associated with Zebra-like Pigmentation;Biomedicines;2023-05-30
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