The Dwarf Phenotype in GH240B Mice, Haploinsufficient for the Autism Candidate Gene Neurobeachin, Is Caused by Ectopic Expression of Recombinant Human Growth Hormone
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference41 articles.
1. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE;PB Celestino-Soper;Hum Mol Genet,2011
2. An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities;EB Kaminsky;Genet Med,2011
3. A discovery resource of rare copy number variations in individuals with autism spectrum disorder;A Prasad;G3 (Bethesda),2012
4. Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder;K Reddy;BMC Med Genet,2005
5. Association of autism, retinoblastoma, and reduced esterase D activity;E Ritvo;Arch Gen Psychiatry,1988
Cited by 10 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. NMJ-related diseases beyond the congenital myasthenic syndromes;Frontiers in Cell and Developmental Biology;2023-08-04
2. Genome-Wide Estimates of Runs of Homozygosity, Heterozygosity, and Genetic Load in Two Chinese Indigenous Goat Breeds;Frontiers in Genetics;2022-04-26
3. Spectrum of social alterations in the Neurobeachin haploinsufficiency mouse model of autism;Brain Research Bulletin;2021-02
4. MITOL dysfunction causes dwarfism with anterior pituitary hypoplasia;The Journal of Biochemistry;2020-06-26
5. Regulation of murine skeletal muscle growth by STAT5B is age- and sex-specific;Skeletal Muscle;2019-06-24
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