Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

Published:2000-09-01 Issue:1 Volume:26 Page:93-96
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Hong Susan E.,Shugart Yin Yao,Huang David T.,Shahwan Saad Al,Grant P. Ellen,Hourihane Jonathan O'B.,Martin Neil D.T.,Walsh Christopher A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0900_93.pdf

Reference28 articles.

1. Reiner, O. et al. Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats. Nature 364, 717–721 (1993).

2. Gleeson, J.G. et al. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein . Cell 92, 63–72 (1998).

3. des Portes, V. et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 92, 51–61 ( 1998).

4. Pilz, D.T. et al. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum. Mol. Genet. 7, 2029–2037 (1998).

5. Walsh, C.A. Genetic malformations of the human cerebral cortex. Neuron 23, 19–29 (1999).

Cited by 763 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. Co-activation of LIN28A and CTNNB1 disturbs cortical neuronal migration and pia mater integrity;2024-08-02

2. A homozygous nonsense variant in the alternatively spliced VLDLR exon 4 causes a neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia;Journal of Human Genetics;2024-07-31

3. De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism;Journal of Clinical Investigation;2024-07-09

4. OCRL1 Deficiency Affects the Intracellular Traffic of ApoER2 and Impairs Reelin-Induced Responses;Biomolecules;2024-07-05

5. Exploring causal mechanisms of psychosis risk;Neuroscience & Biobehavioral Reviews;2024-07

同舟云学术

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