165 related articles for article (PubMed ID: 8884267)
1. Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.
Chen ZY; Hasson T; Kelley PM; Schwender BJ; Schwartz MF; Ramakrishnan M; Kimberling WJ; Mooseker MS; Corey DP
Genomics; 1996 Sep; 36(3):440-8. PubMed ID: 8884267
[TBL] [Abstract][Full Text] [Related]
2. Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.
Hasson T; Walsh J; Cable J; Mooseker MS; Brown SD; Steel KP
Cell Motil Cytoskeleton; 1997; 37(2):127-38. PubMed ID: 9186010
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D; Blanchard S; Kaplan J; Guilford P; Gibson F; Walsh J; Mburu P; Varela A; Levilliers J; Weston MD
Nature; 1995 Mar; 374(6517):60-1. PubMed ID: 7870171
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.
Weil D; Levy G; Sahly I; Levi-Acobas F; Blanchard S; El-Amraoui A; Crozet F; Philippe H; Abitbol M; Petit C
Proc Natl Acad Sci U S A; 1996 Apr; 93(8):3232-7. PubMed ID: 8622919
[TBL] [Abstract][Full Text] [Related]
7. Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells.
Liu X; Vansant G; Udovichenko IP; Wolfrum U; Williams DS
Cell Motil Cytoskeleton; 1997; 37(3):240-52. PubMed ID: 9227854
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.
Libby RT; Steel KP
Invest Ophthalmol Vis Sci; 2001 Mar; 42(3):770-8. PubMed ID: 11222540
[TBL] [Abstract][Full Text] [Related]
10. Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.
Hasson T; Heintzelman MB; Santos-Sacchi J; Corey DP; Mooseker MS
Proc Natl Acad Sci U S A; 1995 Oct; 92(21):9815-9. PubMed ID: 7568224
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.
el-Amraoui A; Sahly I; Picaud S; Sahel J; Abitbol M; Petit C
Hum Mol Genet; 1996 Aug; 5(8):1171-8. PubMed ID: 8842737
[TBL] [Abstract][Full Text] [Related]
13. Novel myosin VI isoform is abundantly expressed in retina.
Breckler J; Au K; Cheng J; Hasson T; Burnside B
Exp Eye Res; 2000 Jan; 70(1):121-34. PubMed ID: 10644428
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U
Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
[TBL] [Abstract][Full Text] [Related]
15. The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
Kelley PM; Weston MD; Chen ZY; Orten DJ; Hasson T; Overbeck LD; Pinnt J; Talmadge CB; Ing P; Mooseker MS; Corey D; Sumegi J; Kimberling WJ
Genomics; 1997 Feb; 40(1):73-9. PubMed ID: 9070921
[TBL] [Abstract][Full Text] [Related]
16. Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex.
Küssel-Andermann P; El-Amraoui A; Safieddine S; Nouaille S; Perfettini I; Lecuit M; Cossart P; Wolfrum U; Petit C
EMBO J; 2000 Nov; 19(22):6020-9. PubMed ID: 11080149
[TBL] [Abstract][Full Text] [Related]
17. Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.
Ernest S; Rauch GJ; Haffter P; Geisler R; Petit C; Nicolson T
Hum Mol Genet; 2000 Sep; 9(14):2189-96. PubMed ID: 10958658
[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. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Verpy E; Leibovici M; Zwaenepoel I; Liu XZ; Gal A; Salem N; Mansour A; Blanchard S; Kobayashi I; Keats BJ; Slim R; Petit C
Nat Genet; 2000 Sep; 26(1):51-5. PubMed ID: 10973247
[TBL] [Abstract][Full Text] [Related]
20. Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
Orten DJ; Weston MD; Kelley PM; Cremers CW; Wagenaar M; Jacobson SG; Kimberling WJ
Hum Mutat; 2000 Jan; 15(1):114-5. PubMed ID: 10612833
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
