271 related articles for article (PubMed ID: 30199819)
1. Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway.
Fetoni AR; Zorzi V; Paciello F; Ziraldo G; Peres C; Raspa M; Scavizzi F; Salvatore AM; Crispino G; Tognola G; Gentile G; Spampinato AG; Cuccaro D; Guarnaccia M; Morello G; Van Camp G; Fransen E; Brumat M; Girotto G; Paludetti G; Gasparini P; Cavallaro S; Mammano F
Redox Biol; 2018 Oct; 19():301-317. PubMed ID: 30199819
[TBL] [Abstract][Full Text] [Related]
2. Degradation of cochlear Connexin26 accelerate the development of age-related hearing loss.
Xu K; Chen S; Bai X; Xie L; Qiu Y; Liu XZ; Wang XH; Kong WJ; Sun Y
Aging Cell; 2023 Nov; 22(11):e13973. PubMed ID: 37681746
[TBL] [Abstract][Full Text] [Related]
3. Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs.
Lee MY; Takada T; Takada Y; Kappy MD; Beyer LA; Swiderski DL; Godin AL; Brewer S; King WM; Raphael Y
Hear Res; 2015 Oct; 328():102-12. PubMed ID: 26232528
[TBL] [Abstract][Full Text] [Related]
4. Down-regulation of AMPK signaling pathway rescues hearing loss in TFB1 transgenic mice and delays age-related hearing loss.
Zhao J; Li G; Zhao X; Lin X; Gao Y; Raimundo N; Li GL; Shang W; Wu H; Song L
Aging (Albany NY); 2020 Apr; 12(7):5590-5611. PubMed ID: 32240104
[TBL] [Abstract][Full Text] [Related]
5. Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy.
Takada Y; Beyer LA; Swiderski DL; O'Neal AL; Prieskorn DM; Shivatzki S; Avraham KB; Raphael Y
Hear Res; 2014 Mar; 309():124-35. PubMed ID: 24333301
[TBL] [Abstract][Full Text] [Related]
6. Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions.
Santarelli R; Cama E; Scimemi P; Dal Monte E; Genovese E; Arslan E
Eur Arch Otorhinolaryngol; 2008 Jan; 265(1):43-51. PubMed ID: 17701047
[TBL] [Abstract][Full Text] [Related]
7. Codeficiency of Lysosomal Mucolipins 3 and 1 in Cochlear Hair Cells Diminishes Outer Hair Cell Longevity and Accelerates Age-Related Hearing Loss.
Wiwatpanit T; Remis NN; Ahmad A; Zhou Y; Clancy JC; Cheatham MA; García-Añoveros J
J Neurosci; 2018 Mar; 38(13):3177-3189. PubMed ID: 29453205
[TBL] [Abstract][Full Text] [Related]
8. Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the
Maslova EA; Orishchenko KE; Posukh OL
Biomolecules; 2021 Jan; 11(1):. PubMed ID: 33466560
[TBL] [Abstract][Full Text] [Related]
9. Degradation and modification of cochlear gap junction proteins in the early development of age-related hearing loss.
Tajima S; Danzaki K; Ikeda K; Kamiya K
Exp Mol Med; 2020 Jan; 52(1):166-175. PubMed ID: 31988333
[TBL] [Abstract][Full Text] [Related]
10. Connexins 30 and 43 expression changes in relation to age-related hearing loss.
Pineros J; Zhu X; Ding B; Frisina RD
Hear Res; 2024 Mar; 444():108971. PubMed ID: 38359484
[TBL] [Abstract][Full Text] [Related]
11. A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies.
Albuloushi A; Lovgren ML; Steel A; Yeoh Y; Waters A; Zamiri M; Martin PE
Exp Dermatol; 2020 Oct; 29(10):970-979. PubMed ID: 32866991
[TBL] [Abstract][Full Text] [Related]
12. Connexin 30 deletion exacerbates cochlear senescence and age-related hearing loss.
Paciello F; Zorzi V; Raspa M; Scavizzi F; Grassi C; Mammano F; Fetoni AR
Front Cell Dev Biol; 2022; 10():950837. PubMed ID: 36016655
[TBL] [Abstract][Full Text] [Related]
13. Cx26 gene mutations in idiopathic progressive hearing loss.
Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
[TBL] [Abstract][Full Text] [Related]
14. Palmoplantar keratoderma with deafness phenotypic variability in a patient with an inherited GJB2 frameshift variant and novel missense variant.
Bedoukian EC; Rentas S; Skraban C; Shao Q; Treat J; Laird DW; Sullivan KE
Mol Genet Genomic Med; 2021 Feb; 9(2):e1574. PubMed ID: 33443819
[TBL] [Abstract][Full Text] [Related]
15. Hearing function in heterozygous carriers of a pathogenic GJB2 gene mutation.
Groh D; Seeman P; Jilek M; Popelář J; Kabelka Z; Syka J
Physiol Res; 2013; 62(3):323-30. PubMed ID: 23489192
[TBL] [Abstract][Full Text] [Related]
16. α-Synuclein deficiency and efferent nerve degeneration in the mouse cochlea: a possible cause of early-onset presbycusis.
Park SN; Back SA; Choung YH; Kim HL; Akil O; Lustig LR; Park KH; Yeo SW
Neurosci Res; 2011 Nov; 71(3):303-10. PubMed ID: 21840348
[TBL] [Abstract][Full Text] [Related]
17. Age-associated decline in Nrf2 signaling and associated mtDNA damage may be involved in the degeneration of the auditory cortex: Implications for central presbycusis.
Li Y; Zhao X; Hu Y; Sun H; He Z; Yuan J; Cai H; Sun Y; Huang X; Kong W; Kong W
Int J Mol Med; 2018 Dec; 42(6):3371-3385. PubMed ID: 30272261
[TBL] [Abstract][Full Text] [Related]
18. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).
Cohn ES; Kelley PM; Fowler TW; Gorga MP; Lefkowitz DM; Kuehn HJ; Schaefer GB; Gobar LS; Hahn FJ; Harris DJ; Kimberling WJ
Pediatrics; 1999 Mar; 103(3):546-50. PubMed ID: 10049954
[TBL] [Abstract][Full Text] [Related]
19. Otoacoustic emissions and brainstem evoked potentials in compound carriers of connexin 26 mutations.
Engel-Yeger B; Zaaroura S; Zlotogora J; Shalev S; Hujeirat Y; Carrasquillo M; Saleh B; Pratt H
Hear Res; 2003 Jan; 175(1-2):140-51. PubMed ID: 12527132
[TBL] [Abstract][Full Text] [Related]
20. Reduced expression of Connexin26 and its DNA promoter hypermethylation in the inner ear of mimetic aging rats induced by d-galactose.
Wu X; Wang Y; Sun Y; Chen S; Zhang S; Shen L; Huang X; Lin X; Kong W
Biochem Biophys Res Commun; 2014 Sep; 452(3):340-6. PubMed ID: 25159847
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]