121 related articles for article (PubMed ID: 10868225)
1. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
Friedman TB; Hinnant JT; Fridell RA; Wilcox ER; Raphael Y; Camper SA
Adv Otorhinolaryngol; 2000; 56():131-44. PubMed ID: 10868225
[No Abstract] [Full Text] [Related]
2. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
Wang A; Liang Y; Fridell RA; Probst FJ; Wilcox ER; Touchman JW; Morton CC; Morell RJ; Noben-Trauth K; Camper SA; Friedman TB
Science; 1998 May; 280(5368):1447-51. PubMed ID: 9603736
[TBL] [Abstract][Full Text] [Related]
3. Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
Fattahi Z; Shearer AE; Babanejad M; Bazazzadegan N; Almadani SN; Nikzat N; Jalalvand K; Arzhangi S; Esteghamat F; Abtahi R; Azadeh B; Smith RJ; Kahrizi K; Najmabadi H
Am J Med Genet A; 2012 Aug; 158A(8):1857-64. PubMed ID: 22736430
[TBL] [Abstract][Full Text] [Related]
4. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.
Probst FJ; Fridell RA; Raphael Y; Saunders TL; Wang A; Liang Y; Morell RJ; Touchman JW; Lyons RH; Noben-Trauth K; Friedman TB; Camper SA
Science; 1998 May; 280(5368):1444-7. PubMed ID: 9603735
[TBL] [Abstract][Full Text] [Related]
5. Unconventional myosins, the basis for deafness in mouse and man.
Hasson T
Am J Hum Genet; 1997 Oct; 61(4):801-5. PubMed ID: 9382088
[No Abstract] [Full Text] [Related]
6. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.
Liang Y; Wang A; Belyantseva IA; Anderson DW; Probst FJ; Barber TD; Miller W; Touchman JW; Jin L; Sullivan SL; Sellers JR; Camper SA; Lloyd RV; Kachar B; Friedman TB; Fridell RA
Genomics; 1999 Nov; 61(3):243-58. PubMed ID: 10552926
[TBL] [Abstract][Full Text] [Related]
7. A novel type of myosin encoded by the mouse deafness gene shaker-2.
Wakabayashi Y; Takahashi Y; Kikkawa Y; Okano H; Mishima Y; Ushiki T; Yonekawa H; Kominami R
Biochem Biophys Res Commun; 1998 Jul; 248(3):655-9. PubMed ID: 9703981
[TBL] [Abstract][Full Text] [Related]
8. Unconventional myosins and the genetics of hearing loss.
Friedman TB; Sellers JR; Avraham KB
Am J Med Genet; 1999 Sep; 89(3):147-57. PubMed ID: 10704189
[TBL] [Abstract][Full Text] [Related]
9. The architecture of hearing.
Pennisi E
Science; 1997 Nov; 278(5341):1223-4. PubMed ID: 9411747
[No Abstract] [Full Text] [Related]
10. 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]
11. Mutation analysis of the mouse myosin VIIA deafness gene.
Mburu P; Liu XZ; Walsh J; Saw D; Cope MJ; Gibson F; Kendrick-Jones J; Steel KP; Brown SD
Genes Funct; 1997 Jun; 1(3):191-203. PubMed ID: 9680294
[TBL] [Abstract][Full Text] [Related]
12. Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.
Liang Y; Wang A; Probst FJ; Arhya IN; Barber TD; Chen KS; Deshmukh D; Dolan DF; Hinnant JT; Carter LE; Jain PK; Lalwani AK; Li XC; Lupski JR; Moeljopawiro S; Morell R; Negrini C; Wilcox ER; Winata S; Camper SA; Friedman TB
Am J Hum Genet; 1998 Apr; 62(4):904-15. PubMed ID: 9529344
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
Liburd N; Ghosh M; Riazuddin S; Naz S; Khan S; Ahmed Z; Riazuddin S; Liang Y; Menon PS; Smith T; Smith AC; Chen KS; Lupski JR; Wilcox ER; Potocki L; Friedman TB
Hum Genet; 2001 Nov; 109(5):535-41. PubMed ID: 11735029
[TBL] [Abstract][Full Text] [Related]
14. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
Friedman TB; Liang Y; Weber JL; Hinnant JT; Barber TD; Winata S; Arhya IN; Asher JH
Nat Genet; 1995 Jan; 9(1):86-91. PubMed ID: 7704031
[TBL] [Abstract][Full Text] [Related]
15. Deaf and dizzy mice with mutated myosin motors.
Gillespie PG
Nat Med; 1996 Jan; 2(1):27-9. PubMed ID: 8564830
[No Abstract] [Full Text] [Related]
16. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
Liu XZ; Walsh J; Mburu P; Kendrick-Jones J; Cope MJ; Steel KP; Brown SD
Nat Genet; 1997 Jun; 16(2):188-90. PubMed ID: 9171832
[TBL] [Abstract][Full Text] [Related]
17. Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
Rehman AU; Bird JE; Faridi R; Shahzad M; Shah S; Lee K; Khan SN; Imtiaz A; Ahmed ZM; Riazuddin S; Santos-Cortez RL; Ahmad W; Leal SM; Riazuddin S; Friedman TB
Hum Mutat; 2016 Oct; 37(10):991-1003. PubMed ID: 27375115
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
Weil D; Küssel P; Blanchard S; Lévy G; Levi-Acobas F; Drira M; Ayadi H; Petit C
Nat Genet; 1997 Jun; 16(2):191-3. PubMed ID: 9171833
[TBL] [Abstract][Full Text] [Related]
20. Molecular motors: sensing a function for myosin-VIIa.
Hasson T
Curr Biol; 1999 Nov; 9(22):R838-41. PubMed ID: 10574757
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
