260 related articles for article (PubMed ID: 21368133)
1. Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).
Zheng J; Miller KK; Yang T; Hildebrand MS; Shearer AE; DeLuca AP; Scheetz TE; Drummond J; Scherer SE; Legan PK; Goodyear RJ; Richardson GP; Cheatham MA; Smith RJ; Dallos P
Proc Natl Acad Sci U S A; 2011 Mar; 108(10):4218-23. PubMed ID: 21368133
[TBL] [Abstract][Full Text] [Related]
2. Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.
Kammerer R; Rüttiger L; Riesenberg R; Schäuble C; Krupar R; Kamp A; Sunami K; Eisenried A; Hennenberg M; Grunert F; Bress A; Battaglia S; Schrewe H; Knipper M; Schneider MR; Zimmermann W
J Biol Chem; 2012 Jun; 287(26):21584-98. PubMed ID: 22544735
[TBL] [Abstract][Full Text] [Related]
3. Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
Wang H; Wang X; He C; Li H; Qing J; Grati M; Hu Z; Li J; Hu Y; Xia K; Mei L; Wang X; Yu J; Chen H; Jiang L; Liu Y; Men M; Zhang H; Guan L; Xiao J; Zhang J; Liu X; Feng Y
J Hum Genet; 2015 Mar; 60(3):119-126. PubMed ID: 25589040
[TBL] [Abstract][Full Text] [Related]
4. Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.
Cheatham MA; Goodyear RJ; Homma K; Legan PK; Korchagina J; Naskar S; Siegel JH; Dallos P; Zheng J; Richardson GP
J Neurosci; 2014 Jul; 34(31):10325-38. PubMed ID: 25080593
[TBL] [Abstract][Full Text] [Related]
5. Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
Donaudy F; Snoeckx R; Pfister M; Zenner HP; Blin N; Di Stazio M; Ferrara A; Lanzara C; Ficarella R; Declau F; Pusch CM; Nürnberg P; Melchionda S; Zelante L; Ballana E; Estivill X; Van Camp G; Gasparini P; Savoia A
Am J Hum Genet; 2004 Apr; 74(4):770-6. PubMed ID: 15015131
[TBL] [Abstract][Full Text] [Related]
6. Genetic heterogeneity of deafness phenotypes linked to DFNA4.
Yang T; Pfister M; Blin N; Zenner HP; Pusch CM; Smith RJ
Am J Med Genet A; 2005 Nov; 139(1):9-12. PubMed ID: 16222661
[TBL] [Abstract][Full Text] [Related]
7. Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.
Xia A; Gao SS; Yuan T; Osborn A; Bress A; Pfister M; Maricich SM; Pereira FA; Oghalai JS
Dis Model Mech; 2010; 3(3-4):209-23. PubMed ID: 20142329
[TBL] [Abstract][Full Text] [Related]
8. Age-related degradation of tectorial membrane dynamics with loss of CEACAM16.
Mansour A; Sellon JB; Filizzola D; Ghaffari R; Cheatham MA; Freeman DM
Biophys J; 2021 Nov; 120(21):4777-4785. PubMed ID: 34555361
[TBL] [Abstract][Full Text] [Related]
9. A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.
Choi BO; Kang SH; Hyun YS; Kanwal S; Park SW; Koo H; Kim SB; Choi YC; Yoo JH; Kim JW; Park KD; Choi KG; Kim SJ; Züchner S; Chung KW
Hum Mutat; 2011 Jun; 32(6):669-77. PubMed ID: 21480433
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family.
Bai H; Yang X; Temuribagen ; Guilan ; Suyalatu ; Narisu ; Wu H; Chen Y; Liu Y; Wu Q
BMC Med Genet; 2014 Mar; 15():34. PubMed ID: 25008054
[TBL] [Abstract][Full Text] [Related]
12. Thyroid hormone-deficient period prior to the onset of hearing is associated with reduced levels of beta-tectorin protein in the tectorial membrane: implication for hearing loss.
Knipper M; Richardson G; Mack A; Müller M; Goodyear R; Limberger A; Rohbock K; Köpschall I; Zenner HP; Zimmermann U
J Biol Chem; 2001 Oct; 276(42):39046-52. PubMed ID: 11489885
[TBL] [Abstract][Full Text] [Related]
13. TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.
Moteki H; Nishio SY; Hashimoto S; Takumi Y; Iwasaki S; Takeichi N; Fukuda S; Usami S
J Hum Genet; 2012 Sep; 57(9):587-92. PubMed ID: 22718023
[TBL] [Abstract][Full Text] [Related]
14. Genomic structure, cochlear expression, and mutation screening of KCNK6, a candidate gene for DFNA4.
Mhatre AN; Li J; Chen AF; Yost CS; Smith RJ; Kindler CH; Lalwani AK
J Neurosci Res; 2004 Jan; 75(1):25-31. PubMed ID: 14689445
[TBL] [Abstract][Full Text] [Related]
15. Discovery of MYH14 as an important and unique deafness gene causing prelingually severe autosomal dominant nonsyndromic hearing loss.
Kim BJ; Kim AR; Han JH; Lee C; Oh DY; Choi BY
J Gene Med; 2017 Apr; 19(4):. PubMed ID: 28221712
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
Verhoeven K; Van Laer L; Kirschhofer K; Legan PK; Hughes DC; Schatteman I; Verstreken M; Van Hauwe P; Coucke P; Chen A; Smith RJ; Somers T; Offeciers FE; Van de Heyning P; Richardson GP; Wachtler F; Kimberling WJ; Willems PJ; Govaerts PJ; Van Camp G
Nat Genet; 1998 May; 19(1):60-2. PubMed ID: 9590290
[TBL] [Abstract][Full Text] [Related]
17. [c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor].
Yang R; Li H; Zhan CX; Mao HY; Zhan TL; Zhu ZF; Liu P; Yuan WL; Ke T; Wang Q; Liu MG; Tang ZH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Jun; 27(3):259-62. PubMed ID: 20533261
[TBL] [Abstract][Full Text] [Related]
18. Tectorins crosslink type II collagen fibrils and connect the tectorial membrane to the spiral limbus.
Andrade LR; Salles FT; Grati M; Manor U; Kachar B
J Struct Biol; 2016 May; 194(2):139-46. PubMed ID: 26806019
[TBL] [Abstract][Full Text] [Related]
19. A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.
Zhang D; Wu J; Yuan Y; Li X; Gao X; Han M; Gao S; Huang S; Dai P
Ann Hum Genet; 2022 Jul; 86(4):207-217. PubMed ID: 35292975
[TBL] [Abstract][Full Text] [Related]
20. Prevalence and Clinical Characteristics of Hearing Loss Caused by
Hiramatsu K; Nishio SY; Kitajiri SI; Kitano T; Moteki H; Usami SI; On Behalf Of The Deafness Gene Study Consortium
Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681017
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
