208 related articles for article (PubMed ID: 12545186)
1. Myosins and pathology: genetics and biology.
Redowicz MJ
Acta Biochim Pol; 2002; 49(4):789-804. PubMed ID: 12545186
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Myosin mutations in hypertrophic cardiomyopathy and functional implications.
Vosberg HP
Herz; 1994 Apr; 19(2):75-83. PubMed ID: 8194835
[TBL] [Abstract][Full Text] [Related]
4. [Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].
Ramírez CD; Padrón R
Invest Clin; 2004 Mar; 45(1):69-99. PubMed ID: 15058760
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Molecular genetics of familial hypertrophic cardiomyopathy.
Hengstenberg C; Schwartz K
J Mol Cell Cardiol; 1994 Jan; 26(1):3-10. PubMed ID: 8196066
[TBL] [Abstract][Full Text] [Related]
8. The molecular genetics of hypertrophic cardiomyopathy: prognostic implications.
Sorajja P; Elliott PM; McKenna WJ
Europace; 2000 Jan; 2(1):4-14. PubMed ID: 11225594
[No Abstract] [Full Text] [Related]
9. Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. Molecular force level of mutant myosins may have a prognostic implication.
Fujita H; Sugiura S; Momomura S; Omata M; Sugi H; Sutoh K
J Clin Invest; 1997 Mar; 99(5):1010-5. PubMed ID: 9062359
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Myosins and deafness.
Redowicz MJ
J Muscle Res Cell Motil; 1999 Apr; 20(3):241-8. PubMed ID: 10471988
[TBL] [Abstract][Full Text] [Related]
12. An alternative domain near the nucleotide-binding site of Drosophila muscle myosin affects ATPase kinetics.
Miller BM; Zhang S; Suggs JA; Swank DM; Littlefield KP; Knowles AF; Bernstein SI
J Mol Biol; 2005 Oct; 353(1):14-25. PubMed ID: 16154586
[TBL] [Abstract][Full Text] [Related]
13. Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.
Roopnarine O; Leinwand LA
Biophys J; 1998 Dec; 75(6):3023-30. PubMed ID: 9826622
[TBL] [Abstract][Full Text] [Related]
14. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.
Delprat B; Michel V; Goodyear R; Yamasaki Y; Michalski N; El-Amraoui A; Perfettini I; Legrain P; Richardson G; Hardelin JP; Petit C
Hum Mol Genet; 2005 Feb; 14(3):401-10. PubMed ID: 15590698
[TBL] [Abstract][Full Text] [Related]
15. Hypertrophic cardiomyopathy.
Capek P; Brdicka R
Cas Lek Cesk; 2006; 145(2):93-6; discussion 96-7. PubMed ID: 16521396
[TBL] [Abstract][Full Text] [Related]
16. Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish.
Seiler C; Ben-David O; Sidi S; Hendrich O; Rusch A; Burnside B; Avraham KB; Nicolson T
Dev Biol; 2004 Aug; 272(2):328-38. PubMed ID: 15282151
[TBL] [Abstract][Full Text] [Related]
17. Myosin VI and VIIa distribution among inner ear epithelia in diverse fishes.
Coffin AB; Dabdoub A; Kelley MW; Popper AN
Hear Res; 2007 Feb; 224(1-2):15-26. PubMed ID: 17204383
[TBL] [Abstract][Full Text] [Related]
18. Lack of evidence of exon 13 mutations in the beta cardiac myosin heavy chain gene with familial hypertrophic cardiomyopathy in Japan.
Ashizawa N; Yamashita S; Usa T; Hayashi I; Kapuku GH; Oku Y; Tokunaga Y; Urano T; Yano K
J Intern Med; 1993 Sep; 234(3):341-3. PubMed ID: 8354989
[No Abstract] [Full Text] [Related]
19. Unconventional myosins in inner-ear sensory epithelia.
Hasson T; Gillespie PG; Garcia JA; MacDonald RB; Zhao Y; Yee AG; Mooseker MS; Corey DP
J Cell Biol; 1997 Jun; 137(6):1287-307. PubMed ID: 9182663
[TBL] [Abstract][Full Text] [Related]
20. Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.
Belyantseva IA; Boger ET; Naz S; Frolenkov GI; Sellers JR; Ahmed ZM; Griffith AJ; Friedman TB
Nat Cell Biol; 2005 Feb; 7(2):148-56. PubMed ID: 15654330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
