Phenotypic characterization of a Csf1r haploinsufficient mouse model of adult-onset leukodystrophy with axonal spheroids and pigmented glia (ALSP)-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Phenotypic characterization of a Csf1r haploinsufficient mouse model of adult-onset leukodystrophy with axonal spheroids and pigmented glia (ALSP)

Published:2015-02 Issue: Volume:74 Page:219-228
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Chitu Violeta,Gokhan Solen,Gulinello Maria,Branch Craig A.,Patil Madhuvati,Basu Ranu,Stoddart Corrina,Mehler Mark F.,Stanley E. Richard

Funder

National Institutes of Health

Rose F. Kennedy Intellectual Disabilities Research Center

Publisher

Elsevier BV

Subject

Neurology

Reference61 articles.

1. A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids;Ahmed;J. Neurol. Sci.,2013

2. Hereditary diffuse leucoencephalopathy with spheroids;Axelsson;Acta Psychiatr. Scand. Suppl.,1984

3. Identification and characterization of a high-affinity granulocyte–macrophage colony-stimulating factor receptor on primary rat oligodendrocytes;Baldwin;Blood,1993

4. Trans-signaling is a dominant mechanism for the pathogenic actions of interleukin-6 in the brain;Campbell;J. Neurosci.,2014

5. Object recognition and object orientation in Alzheimer's disease;Caterini;Neuropsychology,2002

Cited by 90 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. Heterozygous missense CSF1R variants hamper in vitro CD34+-derived dendritic cell generation but not in vivo dendritic cell development;Molecular Immunology;2024-10

2. Deciphering glial contributions to CSF1R-related disorder via single-nuclear transcriptomic profiling: a case study;Acta Neuropathologica Communications;2024-08-28

3. Microglia protect against age-associated brain pathologies;Neuron;2024-08

4. Therapeutic potential of human microglia transplantation in a chimeric model of CSF1R-related leukoencephalopathy;Neuron;2024-08

5. The effect of a dominant kinase-deadCsf1rmutation associated with adult-onset leukoencephalopathy on brain development and neuropathology;2024-06-13

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