An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference50 articles.
1. Genetic mapping of a cone and rod dysfunction (Aland Island Eye Disease) to the proximal short arm of the human X chromosome;Glass;J. Med. Genet.,1993
2. A gene for X-linked optic atrophy is closely linked to the Xp11.4–Xp11.2 region of the X chromosome;Assinck;Am. J. Hum. Genet.,1997
3. A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4–Xp11.3;Cabot;Am. J. Hum. Genet.,1999
4. Positional cloning of the gene for X-linked retinitis pigmentosa 2;Schwahn;Nat. Genet.,1998
5. A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3–Xq11.2;Koyabashi;Hum. Mol. Genet.,1995
Cited by 78 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. Regucalcin Is a Potential Regulator in Human Cancer: Aiming to Expand into Cancer Therapy;Cancers;2023-11-20
2. Regulation of secretory pathway kinase or kinase-like proteins in human cancers;Frontiers in Immunology;2023-02-07
3. The overexpressed regucalcin represses the growth via regulating diverse pathways linked to EGF signaling in human ovarian cancer SK-OV-3 cells: Involvement of extracellular regucalcin;Life Sciences;2023-02
4. Long Non-coding RNA INE1 Induced Autophagy Promotes Sensitivity of Prostate Cancer Cells to Cisplatin;annals of urologic oncology;2022-11-29
5. Identification of UBA1 as the causative gene of an X‐linked non‐Kennedy spinal–bulbar muscular atrophy;European Journal of Neurology;2022-09-13
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