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Items: 10

1.
MYO5A Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1
Matthias Christen, Madeleine de le Roi, Vidhya Jagannathan, Kathrin Becker, Tosso Leeb
Genes (Basel) 2021 Oct; 12(10): 1479. Published online 2021 Sep 23. doi: 10.3390/genes12101479
PMCID:
PMC8535926
AbstractArticlePDF–1.2M
2.
The cargo-binding domain regulates structure and activity of myosin 5
Kavitha Thirumurugan, Takeshi Sakamoto, John A Hammer, III, James R. Sellers, Peter J. Knight
Nature. Author manuscript; available in PMC 2007 Apr 18.
Published in final edited form as: Nature. 2006 Jul 13; 442(7099): 212–215. doi: 10.1038/nature04865
PMCID:
PMC1852638
ArticlePDF–795K
3.
The Effects of Genotype and Cell Environment on Melanoblast Differentiation in the House Mouse
Clement L. Markert, Willys K. Silvers
Genetics. 1956 May; 41(3): 429–450. doi: 10.1093/genetics/41.3.429
PMCID:
PMC1209793
SummaryPDF–2.6M
4.
A Quantitative Histological Study of the Pigment Found in the Coat-Color Mutants of the House Mouse. IV. the Nature of the Effects of Genic Substitution in Five Major Allelic Series
Elizabeth S. Russell
Genetics. 1949 Mar; 34(2): 146–166. doi: 10.1093/genetics/34.2.146
PMCID:
PMC1209439
SummaryPDF–1.2M
5.
Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5A
Yair Anikster, Marjan Huizing, Paul D. Anderson, Diana L. Fitzpatrick, Aharon Klar, Eva Gross-Kieselstein, Yackov Berkun, Gila Shazberg, William A. Gahl, Haggit Hurvitz
Am J Hum Genet. 2002 Aug; 71(2): 407–414. Published online 2002 Jun 7. doi: 10.1086/341606
Correction in:
Am J Hum Genet. 2002 Oct; 71(4): 1007.
PMCID:
PMC379173
AbstractArticlePDF–395K
6.
Molecular analysis of two mouse dilute locus deletion mutations: spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles.
M C Strobel, P K Seperack, N G Copeland, N A Jenkins
Mol Cell Biol. 1990 Feb; 10(2): 501–509. doi: 10.1128/mcb.10.2.501
PMCID:
PMC360824
SummaryPage BrowsePDF–2.0M
7.
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)
Gaël Ménasché, Chen Hsuan Ho, Ozden Sanal, Jérôme Feldmann, Ilhan Tezcan, Fügen Ersoy, Anne Houdusse, Alain Fischer, Geneviève de Saint Basile
J Clin Invest. 2003 Aug 1; 112(3): 450–456. doi: 10.1172/JCI18264
Correction in:
J Clin Invest. 2005 Apr 1; 115(4): 1100.
PMCID:
PMC166299
AbstractArticlePDF–1.0M
8.
A large step for myosin
Toshio Yanagida, Atsuko H. Iwane
Proc Natl Acad Sci U S A. 2000 Aug 15; 97(17): 9357–9359. doi: 10.1073/pnas.97.17.9357
PMCID:
PMC34028
ArticlePDF–284K
9.
Localization of myosin-V in the centrosome
Enilza M. Espreafico, Donald E. Coling, Vasiliki Tsakraklides, Karin Krogh, Joseph S. Wolenski, Gilda Kalinec, Bechara Kachar
Proc Natl Acad Sci U S A. 1998 Jul 21; 95(15): 8636–8641. doi: 10.1073/pnas.95.15.8636
PMCID:
PMC21128
AbstractArticlePDF–326K
10.
Myosin-V stepping kinetics: A molecular model for processivity
Matthias Rief, Ronald S. Rock, Amit D. Mehta, Mark S. Mooseker, Richard E. Cheney, James A. Spudich
Proc Natl Acad Sci U S A. 2000 Aug 15; 97(17): 9482–9486. doi: 10.1073/pnas.97.17.9482
PMCID:
PMC16890
AbstractArticlePDF–230K

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