SALL1 mutations in Townes-Brocks syndrome and related disorders
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference33 articles.
1. Three novel SALL1 mutations extend the mutational spectrum in Townes-Brocks syndrome
2. Molecular cloning, chromosomal localization, and expression of the murine SALL1 ortholog Sall1
3. RNA surveillance: unforeseen consequences for gene expression, inherited genetic disorders and cancer
4. A gene complex acting downstream of dpp in Drosophila wing morphogenesis
5. A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype
Cited by 59 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. Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype–Phenotype Correlation;Global Medical Genetics;2023-12
2. A function of Spalt major as a sequence-specific DNA binding transcription factor mediates repression ofknirpsin theDrosophilawing imaginal disc;2023-09-05
3. SALL1 enforces microglia-specific DNA binding and function of SMADs to establish microglia identity;Nature Immunology;2023-06-15
4. Disorders of Kidney Formation;Pediatric Kidney Disease;2023
5. A Genotyped Case of Townes–Brocks Syndrome with Absent Pulmonary Valve Syndrome from Turkey;Journal of Pediatric Genetics;2021-12-10
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