344 related articles for article (PubMed ID: 31103816)
1. A humanized mouse model, demonstrating progressive hearing loss caused by MYO6 p.C442Y, is inherited in a semi-dominant pattern.
Wang J; Shen J; Guo L; Cheng C; Chai R; Shu Y; Li H
Hear Res; 2019 Aug; 379():79-88. PubMed ID: 31103816
[TBL] [Abstract][Full Text] [Related]
2. Rescue of autosomal dominant hearing loss by in vivo delivery of mini dCas13X-derived RNA base editor.
Xiao Q; Xu Z; Xue Y; Xu C; Han L; Liu Y; Wang F; Zhang R; Han S; Wang X; Li GL; Li H; Yang H; Shu Y
Sci Transl Med; 2022 Jul; 14(654):eabn0449. PubMed ID: 35857824
[TBL] [Abstract][Full Text] [Related]
3. Clinical Characteristics and In Vitro Analysis of
Oka SI; Day TF; Nishio SY; Moteki H; Miyagawa M; Morita S; Izumi S; Ikezono T; Abe S; Nakayama J; Hyogo M; Okamoto N; Uehara N; Oshikawa C; Kitajiri SI; Usami SI
Genes (Basel); 2020 Mar; 11(3):. PubMed ID: 32143290
[No Abstract] [Full Text] [Related]
4. A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family.
Sanggaard KM; Kjaer KW; Eiberg H; Nürnberg G; Nürnberg P; Hoffman K; Jensen H; Sørum C; Rendtorff ND; Tranebjaerg L
Am J Med Genet A; 2008 Apr; 146A(8):1017-25. PubMed ID: 18348273
[TBL] [Abstract][Full Text] [Related]
5. Gene editing in a Myo6 semi-dominant mouse model rescues auditory function.
Xue Y; Hu X; Wang D; Li D; Li Y; Wang F; Huang M; Gu X; Xu Z; Zhou J; Wang J; Chai R; Shen J; Chen ZY; Li GL; Yang H; Li H; Zuo E; Shu Y
Mol Ther; 2022 Jan; 30(1):105-118. PubMed ID: 34174443
[TBL] [Abstract][Full Text] [Related]
6. Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.
Williams LH; Miller KA; Dahl HH; Manji SS
Hear Res; 2013 May; 299():53-62. PubMed ID: 23485424
[TBL] [Abstract][Full Text] [Related]
7. A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness.
Wong EY; Xu CY; Brahmachary M; Xu PX
PLoS One; 2016; 11(5):e0154984. PubMed ID: 27171474
[TBL] [Abstract][Full Text] [Related]
8. A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells.
Seki Y; Miyasaka Y; Suzuki S; Wada K; Yasuda SP; Matsuoka K; Ohshiba Y; Endo K; Ishii R; Shitara H; Kitajiri SI; Nakagata N; Takebayashi H; Kikkawa Y
PLoS One; 2017; 12(8):e0183477. PubMed ID: 28832620
[TBL] [Abstract][Full Text] [Related]
9. Progressive hearing loss and degeneration of hair cell stereocilia in taperin gene knockout mice.
Chen M; Wang Q; Zhu GH; Hu P; Zhou Y; Wang T; Lai RS; Xiao ZA; Xie DH
Biochem Biophys Res Commun; 2016 Oct; 479(4):703-707. PubMed ID: 27693694
[TBL] [Abstract][Full Text] [Related]
10. Myosin VI Haploinsufficiency Reduced Hearing Ability in Mice.
Seki Y; Shitara H; Ishii R; Ouchi T; Yasuda SP; Kikkawa Y
Neuroscience; 2021 Dec; 478():100-111. PubMed ID: 34619316
[TBL] [Abstract][Full Text] [Related]
11. MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.
Melchionda S; Ahituv N; Bisceglia L; Sobe T; Glaser F; Rabionet R; Arbones ML; Notarangelo A; Di Iorio E; Carella M; Zelante L; Estivill X; Avraham KB; Gasparini P
Am J Hum Genet; 2001 Sep; 69(3):635-40. PubMed ID: 11468689
[TBL] [Abstract][Full Text] [Related]
12. A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study.
Kim BJ; Han JH; Park HR; Kim MY; Kim AR; Oh SH; Park WY; Oh DY; Lee S; Choi BY
J Gene Med; 2018 Jun; 20(6):e3019. PubMed ID: 29607572
[TBL] [Abstract][Full Text] [Related]
13. Knock-In Mice with Myo3a Y137C Mutation Displayed Progressive Hearing Loss and Hair Cell Degeneration in the Inner Ear.
Li P; Wen Z; Zhang G; Zhang A; Fu X; Gao J
Neural Plast; 2018; 2018():4372913. PubMed ID: 30123247
[TBL] [Abstract][Full Text] [Related]
14. A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family.
Doll J; Hofrichter MAH; Bahena P; Heihoff A; Segebarth D; Müller T; Dittrich M; Haaf T; Vona B
Mol Genet Genomic Med; 2020 Aug; 8(8):e1343. PubMed ID: 32519820
[TBL] [Abstract][Full Text] [Related]
15. A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells.
Hertzano R; Shalit E; Rzadzinska AK; Dror AA; Song L; Ron U; Tan JT; Shitrit AS; Fuchs H; Hasson T; Ben-Tal N; Sweeney HL; de Angelis MH; Steel KP; Avraham KB
PLoS Genet; 2008 Oct; 4(10):e1000207. PubMed ID: 18833301
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse.
Mochizuki E; Okumura K; Ishikawa M; Yoshimoto S; Yamaguchi J; Seki Y; Wada K; Yokohama M; Ushiki T; Tokano H; Ishii R; Shitara H; Taya C; Kitamura K; Yonekawa H; Kikkawa Y
Exp Anim; 2010; 59(1):57-71. PubMed ID: 20224170
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
Nakanishi H; Kurima K; Pan B; Wangemann P; Fitzgerald TS; Géléoc GS; Holt JR; Griffith AJ
Sci Rep; 2018 Aug; 8(1):12125. PubMed ID: 30108230
[TBL] [Abstract][Full Text] [Related]
19. Human deafness mutation of myosin VI (C442Y) accelerates the ADP dissociation rate.
Sato O; White HD; Inoue A; Belknap B; Ikebe R; Ikebe M
J Biol Chem; 2004 Jul; 279(28):28844-54. PubMed ID: 15123708
[TBL] [Abstract][Full Text] [Related]
20. A novel MYO6 splice site mutation causes autosomal dominant sensorineural hearing loss type DFNA22 with a favourable outcome after cochlear implantation.
Volk AE; Lang-Roth R; Yigit G; Borck G; Nuernberg G; Rosenkranz S; Nuernberg P; Kubisch C; Beutner D
Audiol Neurootol; 2013; 18(3):192-9. PubMed ID: 23635807
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
