Literature DB >> 9795099

Myosin V in the brain: mutations lead to neurological defects.

G M Langford1, B J Molyneaux.   

Abstract

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Keywords:  Non-programmatic

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Year:  1998        PMID： 9795099     DOI： 10.1016/s0165-0173(98)00020-4

Source DB:  PubMed          Journal:  Brain Res Brain Res Rev


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  8 in total

1.  Cytoplasmic dynein LC8 interacts with lyssavirus phosphoprotein.

Authors:  Y Jacob; H Badrane; P E Ceccaldi; N Tordo
Journal:  J Virol       Date:  2000-11       Impact factor: 5.103

2.  Chemical-genetic inhibition of a sensitized mutant myosin Vb demonstrates a role in peripheral-pericentriolar membrane traffic.

Authors:  D William Provance; Christopher R Gourley; Colleen M Silan; L C Cameron; Kevan M Shokat; James R Goldenring; Kavita Shah; Peter G Gillespie; John A Mercer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-06       Impact factor: 11.205

3.  Cargo Transport by Two Coupled Myosin Va Motors on Actin Filaments and Bundles.

Authors:  M Yusuf Ali; Andrej Vilfan; Kathleen M Trybus; David M Warshaw
Journal:  Biophys J       Date:  2016-11-15       Impact factor: 4.033

4.  Myosin Va bound to phagosomes binds to F-actin and delays microtubule-dependent motility.

Authors:  A Al-Haddad; M A Shonn; B Redlich; A Blocker; J K Burkhardt; H Yu; J A Hammer; D G Weiss; W Steffen; G Griffiths; S A Kuznetsov
Journal:  Mol Biol Cell       Date:  2001-09       Impact factor: 4.138

5.  Griscelli syndrome type 2: a novel mutation in RAB27A gene with different clinical features in 2 siblings: a diagnostic conundrum.

Authors:  Kirtisudha Mishra; Shilpy Singla; Suvasini Sharma; Renu Saxena; Vineeta Vijay Batra
Journal:  Korean J Pediatr       Date:  2014-02-24

6.  Localization of myosin II and V isoforms in cultured rat sympathetic neurones and their potential involvement in presynaptic function.

Authors:  Yoshiko Takagishi; Sugiko Futaki; Kanako Itoh; Enilza M Espreafico; Noriko Murakami; Yoshiharu Murata; Sumiko Mochida
Journal:  J Physiol       Date:  2005-09-15       Impact factor: 5.182

7.  Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

Authors:  Gaël Ménasché; Chen Hsuan Ho; Ozden Sanal; Jérôme Feldmann; Ilhan Tezcan; Fügen Ersoy; Anne Houdusse; Alain Fischer; Geneviève de Saint Basile
Journal:  J Clin Invest       Date:  2003-08       Impact factor: 14.808

8.  A single point-mutation within the melanophilin gene causes the lavender plumage colour dilution phenotype in the chicken.

Authors:  Mohsen Vaez; Sarah A Follett; Bertrand Bed'hom; David Gourichon; Michèle Tixier-Boichard; Terry Burke
Journal:  BMC Genet       Date:  2008-01-15       Impact factor: 2.797
  8 in total

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