Location of gracile axonal dystrophy(gad) on chromosome 5 of the mouse.
Author:
Affiliation:
1. Laboratory of Animal Genetics, Faculty of Agriculture, Nagoya University
2. Division of Degenerative Neurological Disease National Institute of Neuroscience
3. Division of Animal Models for Human Disease, National Institute of Neuroscience
Publisher
Genetics Society of Japan
Subject
Genetics,General Medicine
Link
http://www.jstage.jst.go.jp/article/ggs1921/62/6/62_6_479/_pdf
Cited by 14 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. Circular breakdown of neural networks due to loss of deubiquitinating enzyme (UCH-L1) in gracile axonal dystrophy (gad) mouse;AIMS Molecular Science;2021
2. A new mouse model for infantile neuroaxonal dystrophy,inad mouse, maps to mouse Chromosome 1;Mammalian Genome;2005-02
3. Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice;Nature Genetics;1999-09
4. Mouse Extracellular Superoxide Dismutase: Primary Structure, Tissue-specific Gene Expression, Chromosomal Localization, and LungIn SituHybridization;American Journal of Respiratory Cell and Molecular Biology;1997-10
5. Axonal degeneration promotes abnormal accumulation of amyloid β-protein in ascending gracile tract of gracile axonal dystrophy (GAD) mouse;Brain Research;1995-10
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