A Point Mutation in a Plasma Membrane Ca2+-ATPase Gene Causes Deafness in Wriggle Mouse Sagami
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference24 articles.
1. Genes responsible for human hereditary deafness: symphony of a thousand
2. splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
3. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
4. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
5. A type VII myosin encoded by the mouse deafness gene shaker-1
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1. The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca2+-microdomains by tuning PMCA3 activity;Cell Death & Disease;2022-10-07
2. Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme;BMC Biology;2022-03-17
3. Collateral damage: Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme;2021-06-30
4. Crosstalk among Calcium ATPases: PMCA, SERCA and SPCA in Mental Diseases;International Journal of Molecular Sciences;2021-03-10
5. Primary Active Ca2+ Transport Systems in Health and Disease;Cold Spring Harbor Perspectives in Biology;2019-09-09
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