253 related articles for article (PubMed ID: 12032315)
1. 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; 2002 May; 99(11):7518-23. PubMed ID: 12032315
[TBL] [Abstract][Full Text] [Related]
2. Differential localizations of and requirements for the two Drosophila ninaC kinase/myosins in photoreceptor cells.
Porter JA; Hicks JL; Williams DS; Montell C
J Cell Biol; 1992 Feb; 116(3):683-93. PubMed ID: 1730774
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.
Qu R; Sang Q; Xu Y; Feng R; Jin L; He L; Wang L
Int J Pediatr Otorhinolaryngol; 2016 May; 84():43-7. PubMed ID: 27063751
[TBL] [Abstract][Full Text] [Related]
4. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Riazuddin S; Nazli S; Ahmed ZM; Yang Y; Zulfiqar F; Shaikh RS; Zafar AU; Khan SN; Sabar F; Javid FT; Wilcox ER; Tsilou E; Boger ET; Sellers JR; Belyantseva IA; Riazuddin S; Friedman TB
Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
[TBL] [Abstract][Full Text] [Related]
5. Cloning and chromosomal localization of a human class III myosin.
Dosé AC; Burnside B
Genomics; 2000 Aug; 67(3):333-42. PubMed ID: 10936054
[TBL] [Abstract][Full Text] [Related]
6. Role of the ninaC proteins in photoreceptor cell structure: ultrastructure of ninaC deletion mutants and binding to actin filaments.
Hicks JL; Liu X; Williams DS
Cell Motil Cytoskeleton; 1996; 35(4):367-79. PubMed ID: 8956007
[TBL] [Abstract][Full Text] [Related]
7. 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; 2011 Apr; 22(3-4):170-7. PubMed ID: 21165622
[TBL] [Abstract][Full Text] [Related]
8. Termination of phototransduction requires binding of the NINAC myosin III and the PDZ protein INAD.
Wes PD; Xu XZ; Li HS; Chien F; Doberstein SK; Montell C
Nat Neurosci; 1999 May; 2(5):447-53. PubMed ID: 10321249
[TBL] [Abstract][Full Text] [Related]
9. 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; 2016 May; 37(5):481-7. PubMed ID: 26841241
[TBL] [Abstract][Full Text] [Related]
10. Distinct roles of the Drosophila ninaC kinase and myosin domains revealed by systematic mutagenesis.
Porter JA; Montell C
J Cell Biol; 1993 Aug; 122(3):601-12. PubMed ID: 8335687
[TBL] [Abstract][Full Text] [Related]
11. A class III myosin expressed in the retina is a potential candidate for Bardet-Biedl syndrome.
Dosé AC; Burnside B
Genomics; 2002 May; 79(5):621-4. PubMed ID: 11991710
[TBL] [Abstract][Full Text] [Related]
12. Light-dependent translocation of visual arrestin regulated by the NINAC myosin III.
Lee SJ; Montell C
Neuron; 2004 Jul; 43(1):95-103. PubMed ID: 15233920
[TBL] [Abstract][Full Text] [Related]
13. Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
Nal N; Ahmed ZM; Erkal E; Alper OM; Lüleci G; Dinç O; Waryah AM; Ain Q; Tasneem S; Husnain T; Chattaraj P; Riazuddin S; Boger E; Ghosh M; Kabra M; Riazuddin S; Morell RJ; Friedman TB
Hum Mutat; 2007 Oct; 28(10):1014-9. PubMed ID: 17546645
[TBL] [Abstract][Full Text] [Related]
14. Dependence on a retinophilin/myosin complex for stability of PKC and INAD and termination of phototransduction.
Venkatachalam K; Wasserman D; Wang X; Li R; Mills E; Elsaesser R; Li HS; Montell C
J Neurosci; 2010 Aug; 30(34):11337-45. PubMed ID: 20739554
[TBL] [Abstract][Full Text] [Related]
15. MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.
Chen AH; Stephan DA; Hasson T; Fukushima K; Nelissen CM; Chen AF; Jun AI; Ramesh A; Van Camp G; Smith RJ
Arch Otolaryngol Head Neck Surg; 2001 Aug; 127(8):921-5. PubMed ID: 11493199
[TBL] [Abstract][Full Text] [Related]
16. Knock-In Mice with Myo3a Y137C Mutation Displayed Progressive Hearing Loss and Hair Cell Degeneration in the Inner Ear.
Li P; Wen Z; Zhang G; Zhang A; Fu X; Gao J
Neural Plast; 2018; 2018():4372913. PubMed ID: 30123247
[TBL] [Abstract][Full Text] [Related]
17. A new compartment at stereocilia tips defined by spatial and temporal patterns of myosin IIIa expression.
Schneider ME; Dosé AC; Salles FT; Chang W; Erickson FL; Burnside B; Kachar B
J Neurosci; 2006 Oct; 26(40):10243-52. PubMed ID: 17021180
[TBL] [Abstract][Full Text] [Related]
18. Dependence of calmodulin localization in the retina on the NINAC unconventional myosin.
Porter JA; Yu M; Doberstein SK; Pollard TD; Montell C
Science; 1993 Nov; 262(5136):1038-42. PubMed ID: 8235618
[TBL] [Abstract][Full Text] [Related]
19. Mouse class III myosins: kinase activity and phosphorylation sites.
Dalal JS; Stevens SM; Alvarez S; Munoz N; Kempler KE; Dosé AC; Burnside B; Battelle BA
J Neurochem; 2011 Nov; 119(4):772-84. PubMed ID: 21895655
[TBL] [Abstract][Full Text] [Related]
20. Invertebrate and vertebrate class III myosins interact with MORN repeat-containing adaptor proteins.
Mecklenburg KL; Freed SA; Raval M; Quintero OA; Yengo CM; O'Tousa JE
PLoS One; 2015; 10(3):e0122502. PubMed ID: 25822849
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
