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Items: 1 to 20 of 27


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. 2017 Jun 30;292(26):10950-10960. doi: 10.1074/jbc.M116.765966. Epub 2017 May 15.


Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran.

Asgharzade S, Reiisi S, Tabatabaiefar MA, Chaleshtori MH.

Iran J Public Health. 2017 Jan;46(1):76-82.


Clonal Expansion of Lgr5-Positive Cells from Mammalian Cochlea and High-Purity Generation of Sensory Hair Cells.

McLean WJ, Yin X, Lu L, Lenz DR, McLean D, Langer R, Karp JM, Edge ASB.

Cell Rep. 2017 Feb 21;18(8):1917-1929. doi: 10.1016/j.celrep.2017.01.066.


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. 2016 Aug 15;5. pii: e18312. doi: 10.7554/eLife.18312.


Biology and therapy of inherited retinal degenerative disease: insights from mouse models.

Veleri S, Lazar CH, Chang B, Sieving PA, Banin E, Swaroop A.

Dis Model Mech. 2015 Feb;8(2):109-29. doi: 10.1242/dmm.017913. Review.


Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A.

Lopes VS, Williams DS.

Cold Spring Harb Perspect Med. 2015 Jan 20;5(6). pii: a017319. doi: 10.1101/cshperspect.a017319. Review.


Dual adeno-associated virus vectors result in efficient in vitro and in vivo expression of an oversized gene, MYO7A.

Dyka FM, Boye SL, Chiodo VA, Hauswirth WW, Boye SE.

Hum Gene Ther Methods. 2014 Apr;25(2):166-77. doi: 10.1089/hgtb.2013.212.


Mitochondrial DNA variants mediate energy production and expression levels for CFH, C3 and EFEMP1 genes: implications for age-related macular degeneration.

Kenney MC, Chwa M, Atilano SR, Pavlis JM, Falatoonzadeh P, Ramirez C, Malik D, Hsu T, Woo G, Soe K, Nesburn AB, Boyer DS, Kuppermann BD, Jazwinski SM, Miceli MV, Wallace DC, Udar N.

PLoS One. 2013;8(1):e54339. doi: 10.1371/journal.pone.0054339. Epub 2013 Jan 24.


A comprehensive review of retinal gene therapy.

Boye SE, Boye SL, Lewin AS, Hauswirth WW.

Mol Ther. 2013 Mar;21(3):509-19. doi: 10.1038/mt.2012.280. Epub 2013 Jan 29. Review. Erratum in: Mol Ther. 2013 Nov;21(11):2130.


Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus.

Lopes VS, Boye SE, Louie CM, Boye S, Dyka F, Chiodo V, Fofo H, Hauswirth WW, Williams DS.

Gene Ther. 2013 Aug;20(8):824-33. doi: 10.1038/gt.2013.3. Epub 2013 Jan 24.


Autosomal recessive nonsyndromic deafness genes: a review.

Duman D, Tekin M.

Front Biosci (Landmark Ed). 2012 Jun 1;17:2213-36. Review.


Molecular biology of hearing.

Stöver T, Diensthuber M.

GMS Curr Top Otorhinolaryngol Head Neck Surg. 2011;10:Doc06. doi: 10.3205/cto000079. Epub 2012 Apr 26.


Ubiquitin ligase activity of Cul3-KLHL7 protein is attenuated by autosomal dominant retinitis pigmentosa causative mutation.

Kigoshi Y, Tsuruta F, Chiba T.

J Biol Chem. 2011 Sep 23;286(38):33613-21. doi: 10.1074/jbc.M111.245126. Epub 2011 Aug 2.


Functional characterization of the human myosin-7a motor domain.

Heissler SM, Manstein DJ.

Cell Mol Life Sci. 2012 Jan;69(2):299-311. doi: 10.1007/s00018-011-0749-8. Epub 2011 Jun 18.


Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.

Kopplin LJ, Igo RP Jr, Wang Y, Sivakumaran TA, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, SanGiovanni JP, Chew EY, Pauer GJ, Sturgill GM, Joshi T, Tian L, Xi Q, Henning AK, Lee KE, Klein R, Klein BE, Iyengar SK.

Genes Immun. 2010 Dec;11(8):609-21. doi: 10.1038/gene.2010.39. Epub 2010 Sep 23.


A FERM domain autoregulates Drosophila myosin 7a activity.

Yang Y, Baboolal TG, Siththanandan V, Chen M, Walker ML, Knight PJ, Peckham M, Sellers JR.

Proc Natl Acad Sci U S A. 2009 Mar 17;106(11):4189-94. doi: 10.1073/pnas.0808682106. Epub 2009 Mar 2.


Primary cilia in planar cell polarity regulation of the inner ear.

Jones C, Chen P.

Curr Top Dev Biol. 2008;85:197-224. doi: 10.1016/S0070-2153(08)00808-9. Review.


Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.

Roux AF, Faugère V, Le Guédard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M; French Usher Syndrome Collaboration.

J Med Genet. 2006 Sep;43(9):763-8. Epub 2006 May 5.


Drosophila crinkled, mutations of which disrupt morphogenesis and cause lethality, encodes fly myosin VIIA.

Kiehart DP, Franke JD, Chee MK, Montague RA, Chen TL, Roote J, Ashburner M.

Genetics. 2004 Nov;168(3):1337-52.

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