| 1 | MYO7A, MYO7B
|
| Structure of Myo7b/USH1C complex suggests a general PDZ domain binding mode by MyTH4-FERM myosins.
|
| Li J, He Y, Weck ML, Lu Q, Tyska MJ, Zhang M.
|
| Proc Natl Acad Sci U S A 114(19):E3776-E3785. doi: 10.1073/pnas.1702251114. Epub 2017 Apr 24.
2017
|
| 2 | MYO7A
|
| Human myosin VIIa is a very slow processive motor protein on various cellular actin structures.
|
| Sato O, Komatsu S, Sakai T, Tsukasaki Y, Tanaka R, Mizutani T, Watanabe TM, Ikebe R, Ikebe M.
|
| J Biol Chem 292(26):10950-10960. doi: 10.1074/jbc.M116.765966. Epub 2017 May 15.
2017
|
| 3 | DFNB2, MYO7A
|
| Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
|
| Bakhchane A, Charif M, Bousfiha A, Boulouiz R, Nahili H, Rouba H, Charoute H, Lenaers G, Barakat A.
|
| PLoS One 12(5):e0176516. doi: 10.1371/journal.pone.0176516. eCollection 2017.
2017
|
| 4 | MYO5A, MYO7A, MYRIP, RIMBP2
|
| Exophilin-8 assembles secretory granules for exocytosis in the actin cortex via interaction with RIM-BP2 and myosin-VIIa.
|
| Fan F, Matsunaga K, Wang H, Ishizaki R, Kobayashi E, Kiyonari H, Mukumoto Y, Okunishi K, Izumi T.
|
| Elife 6. pii: e26174. doi: 10.7554/eLife.26174.
2017
|
| 5 | MYO7A
|
| The unconventional myosin CRINKLED and its mammalian orthologue MYO7A regulate caspases in their signalling roles.
|
| Orme MH, Liccardi G, Moderau N, Feltham R, Wicky-John S, Tenev T, Aram L, Wilson R, Bianchi K, Morris O, Monteiro Domingues C, Robertson D, Tare M, Wepf A, Williams D, Bergmann A, Gstaiger M, Arama E, Ribeiro PS, Meier P.
|
| Nat Commun 7:10972. doi: 10.1038/ncomms10972.
2016
|
| 6 | MYO7A, PDZD7, WHRN
|
| PDZD7-MYO7A complex identified in enriched stereocilia membranes.
|
| Morgan CP, Krey JF, Grati M, Zhao B, Fallen S, Kannan-Sundhari A, Liu XZ, Choi D, Müller U, Barr-Gillespie PG.
|
| Elife 5. pii: e18312. doi: 10.7554/eLife.18312.
2016
|
| 7 | MYO7A, USH1B
|
| Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations.
|
| Sumaroka A, Matsui R, Cideciyan AV, McGuigan DB 3rd, Sheplock R, Schwartz SB, Jacobson SG.
|
| Invest Ophthalmol Vis Sci 57(9):OCT253-61. doi: 10.1167/iovs.15-18860.
2016
|
| 8 | MYO7A
|
| The unconventional myosin CRINKLED and its mammalian orthologue MYO7A regulate caspases in their signalling roles.
|
| Orme MH, Liccardi G, Moderau N, Feltham R, Wicky-John S, Tenev T, Aram L, Wilson R, Bianchi K, Morris O, Monteiro Domingues C, Robertson D, Tare M, Wepf A, Williams D, Bergmann A, Gstaiger M, Arama E, Ribeiro PS, Meier P.
|
| Nat Commun 7:10972. doi: 10.1038/ncomms10972.
2016
|
| 9 | MYO7A
|
| Structure and Regulation of the Movement of Human Myosin VIIA.
|
| Sakai T, Jung HS, Sato O, Yamada MD, You DJ, Ikebe R, Ikebe M.
|
| J Biol Chem 290(28):17587-98. doi: 10.1074/jbc.M114.599365. Epub 2015 May 22.
2015
|
| 10 | MYO7A
|
| FERM domain-containing unconventional myosin VIIA interacts with integrin β5 subunit and regulates αvβ5-mediated cell adhesion and migration.
|
| Liu Y, Guan L, Zhan J, Lu D, Wan J, Zhang H.
|
| FEBS Lett 588(17):2859-66. doi: 10.1016/j.febslet.2014.06.049. Epub 2014 Jul 2.
2014
|
| 11 | CDH23, CNGA3, MYO7A
|
| Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction.
|
| Selvakumar D, Drescher MJ, Drescher DG.
|
| J Biol Chem 288(10):7215-29. doi: 10.1074/jbc.M112.443226. Epub 2013 Jan 17.
2013
|
| 12 | MYO7A, USH1B
|
| Myosin7a deficiency results in reduced retinal activity which is improved by gene therapy.
|
| Colella P, Sommella A, Marrocco E, Di Vicino U, Polishchuk E, Garcia Garrido M, Seeliger MW, Polishchuk R, Auricchio A.
|
| PLoS One 8(8):e72027. doi: 10.1371/journal.pone.0072027. eCollection 2013.
2013
|
| 13 | CDH23, MYO7A, PCDH15, USH1C, USH1G
|
| Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.
|
| Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, Sahel JA, El-Amraoui A, Petit C.
|
| J Cell Biol 199(2):381-99. doi: 10.1083/jcb.201202012. Epub 2012 Oct 8.
2012
|
| 14 | DFNA11, MYO7A
|
| Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China.
|
| Sun Y, Chen J, Sun H, Cheng J, Li J, Lu Y, Lu Y, Jin Z, Zhu Y, Ouyang X, Yan D, Dai P, Han D, Yang W, Wang R, Liu X, Yuan H.
|
| J Hum Genet 56(1):64-70. Epub 2010 Dec 9.
2011
|
| 15 | MYO7A, USH1B, USH2A
|
| Functional analysis of splicing mutations in MYO7A and USH2A genes.
|
| Jaijo T, Aller E, Aparisi MJ, García-García G, Hernan I, Gamundi MJ, Nájera C, Carballo M, Millán JM.
|
| Clin Genet 79(3):282-8. doi: 10.1111/j.1399-0004.2010.01454.x.
2011
|
| 16 | MYO7A, YY1
|
| A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier.
|
| Street VA, Li J, Robbins CA, Kallman JC.
|
| J Biol Chem 286(17):15278-86. Epub 2011 Mar 4.
2011
|
| 17 | CDH23, DFNB10, DFNB12, DFNB2, DFNB23, DFNB3, DFNB6, DFNB63, DFNB7, DFNB8, DFNB9, DFNB91, LRTOMT, MYO15A, MYO7A, OTOF, PCDH15, SERPINB6, TMC1, TMIE, TMPRSS3
|
| Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey.
|
| Duman D, Sirmaci A, Cengiz FB, Ozdag H, Tekin M.
|
| Genet Test Mol Biomarkers 15(1-2):29-33. Epub 2010 Nov 30. Erratum in: Genet Test Mol Biomarkers. 2011 Sep;15(9):663.
2011
|
| 18 | MYO7A, USH1C, USH1G
|
| Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction.
|
| Grati M, Kachar B.
|
| Proc Natl Acad Sci U S A 108(28):11476-81. Epub 2011 Jun 27.
2011
|
| 19 | MYO7a, RPE65, USH1b
|
| The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65.
|
| Lopes VS, Gibbs D, Libby RT, Aleman TS, Welch DL, Lillo C, Jacobson SG, Radu RA, Steel KP, Williams DS.
|
| Hum Mol Genet 20(13):2560-70. Epub 2011 Apr 14. 2011
|
| 20 | MYO7A
|
| The many different cellular functions of MYO7A in the retina.
|
| Williams DS, Lopes VS.
|
| Biochem Soc Trans 39(5):1207-10. Review.
2011
|
| 21 | MYO7A, USH1B
|
| Retinal disease course in Usher syndrome 1B due to MYO7A mutations.
|
| Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS.
|
| Invest Ophthalmol Vis Sci. 52(11):7924-36. 2011
|
| 22 | CDH23, DFNB84, DFNB85, LHFPL5, MYO15A, MYO7A, PJVK, PTPRQ, TECTA, TMPRSS3
|
| Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
|
| Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M.
|
| Eur J Hum Genet 18(4):407-13. Epub 2009 Nov 4. 2010
|
| 23 | ADGRV1, CDH23, CLRN1, MYO7A, PCDH15, USH1B, USH1C, USH1D, USH1F, USH1G, USH2A, USH2C, USH2D, USH3A, WHRN
|
| Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.
|
| Zallocchi M, Sisson JH, Cosgrove D.
|
| Biochemistry 49(6):1236-47.PMID: 20058854 2010
|
| 24 | MYO7A
|
| Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B.
|
| Gibbs D, Diemer T, Khanobdee K, Hu J, Bok D, Williams DS.
|
| Invest Ophthalmol Vis Sci. 51(2):1130-5. 2010
|
| 25 | DFNB2, MYO7A
|
| Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation.
|
| Hildebrand MS, Thorne NP, Bromhead CJ, Kahrizi K, Webster JA, Fattahi Z, Bataejad M, Kimberling WJ, Stephan D, Najmabadi H, Bahlo M, Smith RJ.
|
| Clin Genet 77(6):563-71. Epub 2010 Feb 4.PMID: 20132242 2010
|
| 26 | CDH23, MYO7A, USH1B, USH1D
|
| Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.
|
| Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Takizawa Y, Hosono K, Mizuta K, Mineta H, Minoshima S.
|
| J Hum Genet 55(12):796-800. Epub 2010 Sep 16.
2010
|
| 27 | MYO7A
|
| Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence.
|
| Gibbs D, Cideciyan AV, Jacobson SG, Williams DS.
|
| Invest Ophthalmol Vis Sci. 50(9):4386-93 2009
|
| 28 | MYO5A, MYO7A, MYRIP
|
| Myrip uses distinct domains in the cellular activation of myosin VA and myosin VIIA in melanosome transport.
|
| Ramalho JS, Lopes VS, Tarafder AK, Seabra MC, Hume AN.
|
| Pigment Cell Melanoma Res 22(4):461-73. Epub 2009 Mar 21.
2009
|
| 29 | ADGRV1, MYO7A, USH1G, VEZT, WHRN
|
| A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells.
|
| Maerker T, van Wijk E, Overlack N, Kersten FF, McGee J, Goldmann T, Sehn E, Roepman R, Walsh EJ, Kremer H, Wolfrum U.
|
| Hum Mol Genet 17(1):71-86. Epub 2007 Sep 28. 2008
|
| 30 | MYO7A, DFNB2
|
| 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 29(4):502-11. 2008
|
| 31 | ADGRV1, MYO7A, PCDH15, USH1B, USH1F, USH2A, USH2C
|
| Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
|
| Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Gardner LM, Prosser HM, Mishra M, Bech-Hansen NT, Herrera W, Schwartz SB, Liu XZ, Kimberling WJ, Steel KP, Williams DS.
|
| Hum Mol Genet 17(15):2405-15. Epub 2008 May 7. 2008
|
| 32 | MYO7A, USH1B
|
| Impacts of Usher syndrome type IB mutations on human myosin VIIa motor function.
|
| Watanabe S, Umeki N, Ikebe R, Ikebe M.
|
| Biochemistry 47(36):9505-13. Epub 2008 Aug 13.
2008
|
| 33 | MYO7A, USH1B
|
| UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes.
|
| Baux D, Faugère V, Larrieu L, Le Guédard-Méreuze S, Hamroun D, Béroud C, Malcolm S, Claustres M, Roux AF.
|
| Hum Mutat 29(8):E76-87.
2008
|
| 34 | MYO7A
|
| MYO7A mutation screening in Usher syndrome type I patients from diverse origins.
|
| Jaijo T, Aller E, Beneyto M, Najera C, Graziano C, Turchetti D, Seri M, Ayuso C, Baiget M, Moreno F, Morera C, Perez-Garrigues H, Millan JM.
|
| J Med Genet 44(3):e71. No abstract available. 2007
|
| 35 | MYO7A, MYRIP
|
| Analysis of the linkage of MYRIP and MYO7A to melanosomes by RAB27A in retinal pigment epithelial cells.
|
| Klomp AE, Teofilo K, Legacki E, Williams DS.
|
| Cell Motil Cytoskeleton 64(6):474-87.
2007
|
| 36 | ADGRV1, CDH23, CLRN1, MYO7A, PCDH15, USH1B, USH1C, USH1D, USH1F, USH2B, USH2C
|
| First evidence for a molecular link between Usher 1 and Usher 2 syndromes.
|
| Stein R.
|
| Clin Genet 69(6):483-485. No abstract available. 2006
|
| 37 | USH1C, USH1G, MYO7A, PCDH15, CDH23
|
| Interactions in the network of Usher syndrome type 1 proteins.
|
| Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C.
|
| Hum Mol Genet 14(3):347-56. Epub 2004 Dec 08. 2005
|
| 38 | LRRC4C, MYO15A, MYO7A, WHRN
|
| 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 14(3):401-10. Epub 2004 Dec 08. 2005
|
| 39 | MYO7A, MYO1C, PLEKHB1
|
| PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa.
|
| Etournay R, El-Amraoui A, Bahloul A, Blanchard S, Roux I, Pezeron G, Michalski N, Daviet L, Hardelin JP, Legrain P, Petit C.
|
| J Cell Sci 118(Pt 13):2891-9. 2005
|
| 40 | MYO7A
|
| The unconventional myosin-VIIa associates with lysosomes.
|
| Soni LE, Warren CM, Bucci C, Orten DJ, Hasson T.
|
| Cell Motil Cytoskeleton. 62(1):13-26. 2005
|
| 41 | MYO7A, DFNA11
|
| Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).
|
| Luijendijk MW, Van Wijk E, Bischoff AM, Krieger E, Huygen PL, Pennings RJ, Brunner HG, Cremers CW, Cremers FP, Kremer H.
|
| Hum Genet 115(2):149-56. Epub 2004 Jun 02. 2004
|
| 42 | MYO7A, DFNA11
|
| Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11).
|
| Bolz H, Bolz SS, Schade G, Kothe C, Mohrmann G, Hess M, Gal A.
|
| Hum Mutat 24(3):274-5. 2004
|
| 43 | MYO7A
|
| Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein.
|
| Gibbs, D.; Kitamoto, J.; Williams, D. S.
|
| Proc Natl Acad Sci U S A. 100: 6481-6486 2003
|
| 44 | MYO7A, MYRIP
|
| Slac2-c (synaptotagmin-like protein homologue lacking C2 domains-c), a novel linker protein that interacts with Rab27, myosin Va/VIIa, and actin.
|
| Fukuda M, Kuroda TS.
|
| J Biol Chem 277(45):43096-103. 2002
|
| 45 | MYO7A, MYRIP
|
| MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes.
|
| El-Amraoui A, Schonn JS, Kussel-Andermann P, Blanchard S, Desnos C, Henry JP, Wolfrum U, Darchen F, Petit C.
|
| EMBO Rep 3(5):463-70. Epub 2002 Apr 18. 2002
|
| 46 | KEAP1, MYO7A
|
| A human homologue of Drosophila kelch associates with myosin-VIIa in specialized adhesion junctions.
|
| Velichkova M, Guttman J, Warren C, Eng L, Kline K, Vogl AW, Hasson T.
|
| Cell Motil Cytoskeleton 51(3):147-64. 2002
|
| 47 | MYO7A, USH1C
|
| Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.
|
| Boeda, B.; El-Amraoui, A.; Bahloul, A.; Goodyear, R.; Daviet, L.; Blanchard, S.; Perfettini, I.; Fath, K. R.; Shorte, S.; Reiners, J.; Houdusse, A.; Legrain, P.; Wolfrum, U.; Richardson, G.; Petit, C.
|
| EMBO J. 21: 6689-6699 2002
|
| 48 | MYO7A, MYRIP, RAB27A
|
| MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes.
|
| El-Amraoui A, Schonn JS, Küssel-Andermann P, Blanchard S, Desnos C, Henry JP, Wolfrum U, Darchen F, Petit C.
|
| EMBO Rep 3(5):463-70. Epub 2002 Apr 18.
2002
|
| 49 | DFNB2, MYO7A, USH1B
|
| From DFNB2 to Usher syndrome: variable expressivity of the same disease.
|
| Zina ZB, Masmoudi S, Ayadi H, Chaker F, Ghorbel AM, Drira M, Petit C.
|
| Am J Med Genet 101(2):181-3. No abstract available. 2001
|
| 50 | CALM1, MAP2, MYO7A
|
| Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B).
|
| Todorov PT, Hardisty RE, Brown SD.
|
| Biochem J. 354(Pt 2):267-74. 2001
|
| 51 | MYO7A
|
| A specific promoter of the sensory cells of the inner ear defined by transgenesis.
|
| Boeda, B.; Weil, D.; Petit, C.
|
| Hum. Molec. Genet. 10: 1581-1589 2001
|
| 52 | MYO7A
|
| 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 9(14):2189-96. 2000
|
| 53 | MYO7A
|
| Unconventional myosin VIIA is a novel A-kinase-anchoring protein.
|
| Kussel-Andermann P, El-Amraoui A, Safieddine S, Hardelin JP, Nouaille S, Camonis J, Petit C.
|
| J Biol Chem 275(38):29654-9. 2000
|
| 54 | CDH23, DFNB12, MYO7A, USH1B, USH1D
|
| Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
|
| Astuto LM, Weston MD, Carney CA, Hoover DM, Cremers CW, Wagenaar M, Moller C, Smith RJ, Pieke-Dahl S, Greenberg J, Ramesar R, Jacobson SG, Ayuso C, Heckenlively JR, Tamayo M, Gorin MB, Reardon W, Kimberling WJ.
|
| Am J Hum Genet 67(6):1569-74. 2000
|
| 55 | VEZT, MYO7A
|
| Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex.
|
| KŸssel-Andermann P, El-Amraoui A, Safieddine S, Nouaille S, Perfettini I, Lecuit M, Cossart P, Wolfrum U, Petit C.
|
| EMBO J 19(22):6020-9. 2000
|
| 56 | MYO7A
|
| Myosin VIIa participates in opsin transport through the photoreceptor cilium.
|
| Liu, X.; Udovichenko, I. P.; Brown, S. D. M.; Steel, K. P.; Williams, D. S.
|
| J. Neurosci. 19: 6267-6274 2000
|
| 57 | MYO7A, USH1B
|
| Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome.
|
| Espinos C, et al.
|
| Hum Genet 102 : 691-694. 1998
|
| 58 | DFNB2, MYO7A, USH1B
|
| Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.
|
| Liu XZ, et al.
|
| Am J Hum Genet 63 : 909-912. 1998
|
| 59 | MYO7A, USH1B
|
| Map refinement of the Usher syndrome type 1B gene, MYO7A, relative to 11q13.5 microsatellite markers.
|
| Mouglabey YB, Nimri S, Sayegh F, El Zir E, Slim R.
|
| Clin Genet 54(2):155-8. 1998
|
| 60 | EPB41, EPB41L2, KRIT1, MSN, MYO15A, MYO7A, NF2, PTPN14, PTPN21, PTPN3, RDX, EZR
|
| The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane.
|
| Chishti AH, Kim AC, Marfatia SM, Lutchman M, Hanspal M, Jindal H, Liu SC, Low PS, Rouleau GA, Mohandas N, Chasis JA, Conboy JG, Gascard P, Takakuwa Y, Huang SC, Benz EJ Jr, Bretscher A, Fehon RG, Gusella JF, Ramesh V, Solomon F, Marchesi VT, Tsukita S, Tsukita S, Hoover KB, et al.
|
| Trends Biochem Sci 23(8):281-2. Review. No abstract available 1998
|
| 61 | MYO7A, USH1B
|
| Myosin VIIA gene : heterogeneity of the mutations responsible for Usher syndrome type IB.
|
| LŽvy G, et al.
|
| Hum Mol Genet 6 : 111-116. 1997
|
| 62 | MYO7A, USH1B
|
| The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
|
| Kelley PM, et al.
|
| Genomics 40 : 73-79. 1997
|
| 63 | DFNB2, MYO7A
|
| 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 16(2):188-90. 1997
|
| 64 | DFNB2, MYO7A
|
| The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
|
| Weil D, Kussel P, Blanchard S, Levy G, Levi-Acobas F, Drira M, Ayadi H, Petit C.
|
| Nat Genet 16(2):191-3. 1997
|
| 65 | MYO7A, USH1B
|
| Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.
|
| Liu XZ, Newton VE, Steel KP, Brown SD.
|
| Hum Mutat 10(2):168-70. 1997
|
| 66 | MYO7A, USH1B
|
| Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
|
| Adato A, Weil D, Kalinski H, Pel-Or Y, Ayadi H, Petit C, Korostishevsky M, Bonne-Tamir B.
|
| Am J Hum Genet 61(4):813-21. 1997
|
| 67 | DFNA11, MYO7A
|
| Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.
|
| Liu XZ, Walsh J, Tamagawa Y, Kitamura K, Nishizawa M, Steel KP, Brown SD.
|
| Nat Genet 17(3):268-9. 1997
|
| 68 | MYO7A, USH1B
|
| 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, et al.
|
| Hum Mol Genet 5 : 1171-1178. 1996
|
| 69 | MYO7A, USH1B
|
| Human myosin VIIA responsible for the Usher 1B syndrome : a predicted membrane-associated motor protein expressed in developing sensory epithelia.
|
| Weil D, et al.
|
| Proc Natl Acad Sci U S A 93 : 3232-3237. 1996
|
| 70 | MYO7A, USH1B
|
| Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.
|
| Chen ZY, et al.
|
| Genomics 36 : 440-448. 1996
|
| 71 | MYO7A, USH1B
|
| Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
|
| Weston MD, et al.
|
| Am J Hum Genet 59 : 1074-1083. 1996
|
| 72 | MYO10, MYO1A, MYO1C, MYO1D, MYO7A, MYO5B, MYO7B, MYO1E, MYO1B, MYO1F
|
| Mapping of unconventional myosins in mouse and human.
|
| Hasson T, Skowron JF, Gilbert DJ, Avraham KB, Perry WL, Bement WM,Anderson BL, Sherr EH, Chen ZY, Greene LA, Ward DC, Corey DP, Mooseker MS,Copeland NG, Jenkins NA.
|
| Genomics 36(3):431-9. 1996
|
| 73 | MYO7A, USH1B
|
| A type VII myosin encoded by the mouse deafness gene shaker-1.
|
| Gibson F, et al.
|
| Nature 374 : 62-64. 1995
|
| 74 | MYO7A, USH1B
|
| Defective myosin VIIA gene responsible for Usher syndrome type 1B.
|
| Weil D, et al.
|
| Nature 374 : 60-61. 1995
|
| 75 | MYO10, MYO1B, MYO1D, MYO5A, MYO7A, MYO7B
|
| Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types.
|
| Bement WM, Hasson T, Wirth JA, Cheney RE, Mooseker MS.
|
| Proc Natl Acad Sci U S A 91(14):6549-53. 1994
|