Single nucleotide polymorphisms in theMATP gene are associated with normal human pigmentation variation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference32 articles.
1. 2BY2. 2003. 2BY2 Fishers exact test program. Version 02 July 2003. New York.
2. ASSOCIATE. 2002. Associate linkage disequilibrium program. Version 1.5 March 2002. New York.
3. Characterization of Melanocyte Stimulating Hormone Receptor Variant Alleles in Twins with Red Hair
4. Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4
5. Identification of Aim-1 as the underwhiteMouse Mutant and Its Transcriptional Regulation by MITF
Cited by 195 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. Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans;Translational Vision Science & Technology;2024-09-03
2. Cattle Cell Atlas: a multi-tissue single cell expression repository for advanced bovine genomics and comparative biology;2024-07-03
3. Associations of methylene tetrahydrofolate reductase (MTHFR) polymorphism with hepatocellular carcinoma in Egyptian population;Egyptian Liver Journal;2024-05-19
4. Skin colour: A window into human phenotypic evolution and environmental adaptation;Molecular Ecology;2024-05-07
5. Associations of Methylenetetrahydrofolate reductase (MTHFR) polymorphism with Hepatocellular carcinoma In Egyptian population.;2023-08-25
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