Literature DB >> 5980120

Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse.

M S Deol, M C Green.   

Abstract

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Year:  1966        PMID： 5980120     DOI： 10.1017/s0016672300010193

Source DB:  PubMed          Journal:  Genet Res        ISSN： 0016-6723            Impact factor:   1.588


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  18 in total

Review 1.  Mouse chromosome 9.

Authors:  D M Kingsley
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide.

Authors:  Sarath Vijayakumar; Frederic F Depreux; Francine M Jodelka; Jennifer J Lentz; Frank Rigo; Timothy A Jones; Michelle L Hastings
Journal:  Hum Mol Genet       Date:  2017-09-15       Impact factor: 6.150

3.  Altered renal proximal tubular endocytosis and histology in mice lacking myosin-VI.

Authors:  Nanami Gotoh; Qingshang Yan; Zhaopeng Du; Daniel Biemesderfer; Michael Kashgarian; Mark S Mooseker; Tong Wang
Journal:  Cytoskeleton (Hoboken)       Date:  2010-03

Review 4.  Mouse chromosome 9.

Authors:  D M Kingsley
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

5.  Molecular genetic analysis of the dilute-short ear (d-se) region of the mouse.

Authors:  E M Rinchik; L B Russell; N G Copeland; N A Jenkins
Journal:  Genetics       Date:  1986-02       Impact factor: 4.562

Review 6.  Myosin motors at neuronal synapses: drivers of membrane transport and actin dynamics.

Authors:  Matthias Kneussel; Wolfgang Wagner
Journal:  Nat Rev Neurosci       Date:  2013-03-13       Impact factor: 34.870

7.  Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.

Authors:  H O Sweet; R T Bronson; K R Johnson; S A Cook; M T Davisson
Journal:  Mamm Genome       Date:  1996-11       Impact factor: 2.957

Review 8.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

Review 9.  Human hereditary hearing impairment: mouse models can help to solve the puzzle.

Authors:  Karen Vrijens; Lut Van Laer; Guy Van Camp
Journal:  Hum Genet       Date:  2008-09-11       Impact factor: 4.132

10.  Loss of myosin VI no insert isoform (NoI) induces a defect in clathrin-mediated endocytosis and leads to caveolar endocytosis of transferrin receptor.

Authors:  Claudia Puri
Journal:  J Biol Chem       Date:  2009-10-18       Impact factor: 5.157
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