PubMed (OMIM) for id: 419894

Year	Number of Results
1994	1
1995	1
1996	1
1997	1
1999	1
2000	1
2001	2
2002	1
2003	2
2004	3
2005	1
2024	0

1

The structure of the myosin VI motor reveals the mechanism of directionality reversal.

Ménétrey J, Bahloul A, Wells AL, Yengo CM, Morris CA, Sweeney HL, Houdusse A. Ménétrey J, et al. Nature. 2005 Jun 9;435(7043):779-85. doi: 10.1038/nature03592. Nature. 2005. PMID: 15944696 Free PMC article.

2

Human deafness mutation of myosin VI (C442Y) accelerates the ADP dissociation rate.

Sato O, White HD, Inoue A, Belknap B, Ikebe R, Ikebe M. Sato O, et al. J Biol Chem. 2004 Jul 9;279(28):28844-54. doi: 10.1074/jbc.M314332200. Epub 2004 Apr 29. J Biol Chem. 2004. PMID: 15123708 Free article.

3

Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).

Mohiddin SA, Ahmed ZM, Griffith AJ, Tripodi D, Friedman TB, Fananapazir L, Morell RJ. Mohiddin SA, et al. J Med Genet. 2004 Apr;41(4):309-14. doi: 10.1136/jmg.2003.011973. J Med Genet. 2004. PMID: 15060111 Free PMC article. No abstract available.

4

The mechanism of myosin VI translocation and its load-induced anchoring.

Altman D, Sweeney HL, Spudich JA. Altman D, et al. Cell. 2004 Mar 5;116(5):737-49. doi: 10.1016/s0092-8674(04)00211-9. Cell. 2004. PMID: 15006355 Free article.

5

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Karolyi IJ, et al. Hum Mol Genet. 2003 Nov 1;12(21):2797-805. doi: 10.1093/hmg/ddg308. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966030

6

Mutations of MYO6 are associated with recessive deafness, DFNB37.

Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. Ahmed ZM, et al. Am J Hum Genet. 2003 May;72(5):1315-22. doi: 10.1086/375122. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687499 Free PMC article.

7

Myosin VI is required for E-cadherin-mediated border cell migration.

Geisbrecht ER, Montell DJ. Geisbrecht ER, et al. Nat Cell Biol. 2002 Aug;4(8):616-20. doi: 10.1038/ncb830. Nat Cell Biol. 2002. PMID: 12134162

8

Myosin VI is a processive motor with a large step size.

Rock RS, Rice SE, Wells AL, Purcell TJ, Spudich JA, Sweeney HL. Rock RS, et al. Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13655-9. doi: 10.1073/pnas.191512398. Epub 2001 Nov 13. Proc Natl Acad Sci U S A. 2001. PMID: 11707568 Free PMC article.

9

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.

Melchionda S, Ahituv N, Bisceglia L, Sobe T, Glaser F, Rabionet R, Arbones ML, Notarangelo A, Di Iorio E, Carella M, Zelante L, Estivill X, Avraham KB, Gasparini P. Melchionda S, et al. Am J Hum Genet. 2001 Sep;69(3):635-40. doi: 10.1086/323156. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468689 Free PMC article.

10

Genomic structure of the human unconventional myosin VI gene.

Ahituv N, Sobe T, Robertson NG, Morton CC, Taggart RT, Avraham KB. Ahituv N, et al. Gene. 2000 Dec 31;261(2):269-75. doi: 10.1016/s0378-1119(00)00535-7. Gene. 2000. PMID: 11167014

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

15 results

Results by year