Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Embryology
Reference16 articles.
1. Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27;Craig;Hum. Mol. Genet.,1998
2. A gene responsible for cavernous malformations of the brain maps to chromosome 7q;Dubovsky;Hum. Mol. Genet.,1995
3. KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation;Eerola;Hum. Mol. Genet.,2000
4. Bodenin: a novel murine gene expressed in restricted areas of the brain;Faisst;Dev. Dyn.,1998
5. The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients J;Joutel;Clin. Invest.,2000
Cited by 47 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. Transcriptomic analysis of ipsilateral spinal cord in rats after bone fracture;2023-05-11
2. Heterozygous Loss of KRIT1 in Mice Affects Metabolic Functions of the Liver, Promoting Hepatic Oxidative and Glycative Stress;International Journal of Molecular Sciences;2022-09-22
3. Genetics and Vascular Biology of Brain Vascular Malformations;Stroke;2022
4. Molecular Genetic Features of Cerebral Cavernous Malformations (CCM) Patients: An Overall View from Genes to Endothelial Cells;Cells;2021-03-22
5. KRIT1 as a possible new player in melanoma aggressiveness;Archives of Biochemistry and Biophysics;2020-09
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