Citations for
1MYO3A, PCDH15
MYO3A Causes Human Dominant Deafness and Interacts with Protocadherin 15-CD2 Isoform.
Grati M, Yan D, Raval MH, Walsh T, Ma Q, Chakchouk I, Kannan-Sundhari A, Mittal R, Masmoudi S, Blanton SH, Tekin M, King MC, Yengo CM, Liu XZ.
Hum Mutat 37(5):481-7. doi: 10.1002/humu.22961. Epub 2016 Feb 16. 2016
2MYO3A
Phosphorylation of the kinase domain regulates autophosphorylation of myosin IIIA and its translocation in microvilli.
An BC, Sakai T, Komaba S, Kishi H, Kobayashi S, Kim JY, Ikebe R, Ikebe M.
Biochemistry 53(49):7835-45. doi: 10.1021/bi501247z. Epub 2014 Dec 3. 2014
3MYO3A
Myosin 3A kinase activity is regulated by phosphorylation of the kinase domain activation loop.
Quintero OA, Unrath WC, Stevens SM Jr, Manor U, Kachar B, Yengo CM.
J Biol Chem 288(52):37126-37. doi: 10.1074/jbc.M113.511014. Epub 2013 Nov 10. 2013
4DFNB30, MYO3A
Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss.
Choi BY, Park G, Gim J, Kim AR, Kim BJ, Kim HS, Park JH, Park T, Oh SH, Han KH, Park WY.
PLoS One 8(8):e68692. doi: 10.1371/journal.pone.0068692. eCollection 2013. 2013
5ESPN, MYO3A, MYO3B
Myosin IIIB uses an actin-binding motif in its espin-1 cargo to reach the tips of actin protrusions.
Merritt RC, Manor U, Salles FT, Grati M, Dose AC, Unrath WC, Quintero OA, Yengo CM, Kachar B.
Curr Biol 22(4):320-5. doi: 10.1016/j.cub.2011.12.053. Epub 2012 Jan 19. 2012
6DFNB30, MYO3A
A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA.
Walsh VL, Raviv D, Dror AA, Shahin H, Walsh T, Kanaan MN, Avraham KB, King MC.
Mamm Genome 22(3-4):170-7. doi: 10.1007/s00335-010-9310-6. Epub 2010 Dec 17. 2011
7MYO3A
Intermolecular autophosphorylation regulates myosin IIIa activity and localization in parallel actin bundles.
Quintero OA, Moore JE, Unrath WC, Manor U, Salles FT, Grati M, Kachar B, Yengo CM.
J Biol Chem 285(46):35770-82. doi: 10.1074/jbc.M110.144360. Epub 2010 Sep 7. 2010
8MYO3A
Effect of phosphorylation in the motor domain of human myosin IIIA on its ATP hydrolysis cycle.
Komaba S, Watanabe S, Umeki N, Sato O, Ikebe M.
Biochemistry 49(17):3695-702. doi: 10.1021/bi902211w. 2010
9ESPN, MYO3A
Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments.
Salles FT, Merritt RC Jr, Manor U, Dougherty GW, Sousa AD, Moore JE, Yengo CM, Dosé AC, Kachar B.
Nat Cell Biol 11(4):443-50. doi: 10.1038/ncb1851. Epub 2009 Mar 15. 2009
10MYO3A, MYO3B
Cloning and distribution of myosin 3B in the mouse retina: differential distribution in cone outer segments.
Katti C, Dalal JS, Dosé AC, Burnside B, Battelle BA.
Exp Eye Res 89(2):224-37. doi: 10.1016/j.exer.2009.03.011. Epub 2009 Mar 28. 2009
11MYO3A
The kinase domain alters the kinetic properties of the myosin IIIA motor.
Dosé AC, Ananthanarayanan S, Moore JE, Corsa AC, Burnside B, Yengo CM.
Biochemistry 47(8):2485-96. doi: 10.1021/bi7021574. Epub 2008 Jan 30. 2008
12DFNB11, DFNB30, DFNB32, DFNB43, MYO3A
Non-syndromic, autosomal-recessive deafness.
Petersen MB, Willems PJ.
Clin Genet 69(5):371-92. Review. 2006
13MYO3A, MYO3B
Determination of human myosin III as a motor protein having a protein kinase activity.
Komaba S, Inoue A, Maruta S, Hosoya H, Ikebe M.
J Biol Chem 278(24):21352-60. Epub 2003 Apr 02. 2003
14MYO3A, MYO3B
A class III myosin expressed in the retina is a potential candidate for Bardet-Biedl syndrome.
Dose AC, Burnside B.
Genomics 79(5):621-4. 2002
15DFNB3, DFNB30, MYO3A, DFNB34
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.
Walsh T, Walsh V, Vreugde S, Hertzano R, Shahin H, Haika S, Lee MK, Kanaan M, King MC, Avraham KB.
Proc Natl Acad Sci U S A 99(11):7518-23. 2002
16MYO3A
Cloning and chromosomal localization of a human class III myosin.
Dose AC, Burnside B.
Genomics 67(3):333-42. 2000