171 related articles for article (PubMed ID: 34828318)
1. A
Yen TT; Chen IC; Hua MW; Wei CY; Shih KH; Li JL; Lin CH; Hsiao TH; Chen YM; Jiang RS
Genes (Basel); 2021 Oct; 12(11):. PubMed ID: 34828318
[TBL] [Abstract][Full Text] [Related]
2. A novel
Li Q; Liang P; Wang S; Li W; Wang J; Yang Y; An X; Chen J; Zha D
Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33846771
[TBL] [Abstract][Full Text] [Related]
3. A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2.
Huang B; Liu Y; Gao X; Xu J; Dai P; Zhu Q; Yuan Y
BMC Med Genet; 2017 Mar; 18(1):36. PubMed ID: 28340560
[TBL] [Abstract][Full Text] [Related]
4. Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss.
Wang H; Zhao Y; Yi Y; Gao Y; Liu Q; Wang D; Li Q; Lan L; Li N; Guan J; Yin Z; Han B; Zhao F; Zong L; Xiong W; Yu L; Song L; Yi X; Yang L; Petit C; Wang Q
PLoS One; 2014; 9(8):e103133. PubMed ID: 25116015
[TBL] [Abstract][Full Text] [Related]
5. Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss.
Ramzan M; Idrees H; Mujtaba G; Sobreira N; Witmer PD; Naz S
Gene; 2019 Jul; 705():109-112. PubMed ID: 31028865
[TBL] [Abstract][Full Text] [Related]
6. Absence of KCNQ4 mutation in Bengali families with ADNSHL originated from West Bengal, India.
Adhikary B; Bankura B; Biswas S; Paul S; Das M
Int J Pediatr Otorhinolaryngol; 2017 Sep; 100():35-38. PubMed ID: 28802383
[TBL] [Abstract][Full Text] [Related]
7. AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss.
Thorpe RK; Walls WD; Corrigan R; Schaefer A; Wang K; Huygen P; Casavant TL; Smith RJH
Hum Genet; 2022 Apr; 141(3-4):877-887. PubMed ID: 35038006
[TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 gene.
Arnett J; Emery SB; Kim TB; Boerst AK; Lee K; Leal SM; Lesperance MM
Arch Otolaryngol Head Neck Surg; 2011 Jan; 137(1):54-9. PubMed ID: 21242547
[TBL] [Abstract][Full Text] [Related]
9. Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.
Naito T; Nishio SY; Iwasa Y; Yano T; Kumakawa K; Abe S; Ishikawa K; Kojima H; Namba A; Oshikawa C; Usami S
PLoS One; 2013; 8(5):e63231. PubMed ID: 23717403
[TBL] [Abstract][Full Text] [Related]
10. Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan.
Su CC; Yang JJ; Shieh JC; Su MC; Li SY
Audiol Neurootol; 2007; 12(1):20-6. PubMed ID: 17033161
[TBL] [Abstract][Full Text] [Related]
11. Genetic variation in KCNQ4 gene is associated with susceptibility to noise-induced hearing loss in a Chinese population.
Guo H; Ding E; Sheng R; Cheng J; Cai W; Guo J; Wang N; Zhang H; Zhu B
Environ Toxicol Pharmacol; 2018 Oct; 63():55-59. PubMed ID: 30153627
[TBL] [Abstract][Full Text] [Related]
12. A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators.
Shin DH; Jung J; Koh YI; Rim JH; Lee JS; Choi HJ; Joo SY; Yu S; Cha DH; Lee SY; Lee JH; Lee MG; Choi JY; Gee HY
Hum Mutat; 2019 Mar; 40(3):335-346. PubMed ID: 30556268
[TBL] [Abstract][Full Text] [Related]
13. [The genotype-phenotype correlation analysis and genetic counseling of hearing loss patients with novel
Zhang X; Wang H; Li J; Li D; Wu K; Wu X; Wang Q
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2023 Jan; 37(1):25-30;35. PubMed ID: 36597364
[No Abstract] [Full Text] [Related]
14. Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment.
Jung J; Lin H; Koh YI; Ryu K; Lee JS; Rim JH; Choi HJ; Lee HJ; Kim HY; Yu S; Jin H; Lee JH; Lee MG; Namkung W; Choi JY; Gee HY
Exp Mol Med; 2019 Aug; 51(8):1-12. PubMed ID: 31434872
[TBL] [Abstract][Full Text] [Related]
15. A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype-phenotype correlation.
Kamada F; Kure S; Kudo T; Suzuki Y; Oshima T; Ichinohe A; Kojima K; Niihori T; Kanno J; Narumi Y; Narisawa A; Kato K; Aoki Y; Ikeda K; Kobayashi T; Matsubara Y
J Hum Genet; 2006; 51(5):455-460. PubMed ID: 16596322
[TBL] [Abstract][Full Text] [Related]
16. Overlooked KCNQ4 variants augment the risk of hearing loss.
Oh KS; Roh JW; Joo SY; Ryu K; Kim JA; Kim SJ; Jang SH; Koh YI; Kim DH; Kim HY; Choi M; Jung J; Namkung W; Nam JH; Choi JY; Gee HY
Exp Mol Med; 2023 Apr; 55(4):844-859. PubMed ID: 37009795
[TBL] [Abstract][Full Text] [Related]
17. Valproic Acid Inhibits Progressive Hereditary Hearing Loss in a KCNQ4 Variant Model through HDAC1 Suppression.
Nam YS; Choi YM; Lee S; Cho HH
Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982769
[TBL] [Abstract][Full Text] [Related]
18. Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss.
Lee SY; Choi HB; Park M; Choi IS; An J; Kim A; Kim E; Kim N; Han JH; Kim MY; Lee SM; Oh DY; Kim BJ; Yi N; Kim NKD; Lee C; Park WY; Koh YI; Gee HY; Cho HS; Kang TM; Choi BY
Exp Mol Med; 2021 Jul; 53(7):1192-1204. PubMed ID: 34316018
[TBL] [Abstract][Full Text] [Related]
19. A Japanese family showing high-frequency hearing loss with KCNQ4 and TECTA mutations.
Ishikawa K; Naito T; Nishio SY; Iwasa Y; Nakamura K; Usami S; Ichimura K
Acta Otolaryngol; 2014 Jun; 134(6):557-63. PubMed ID: 24655070
[TBL] [Abstract][Full Text] [Related]
20. Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss.
Jung J; Choi HB; Koh YI; Rim JH; Choi HJ; Kim SH; Lee JH; An J; Kim A; Lee JS; Joo SY; Yu S; Choi JY; Kang TM; Gee HY
Sci Rep; 2018 Nov; 8(1):16659. PubMed ID: 30413759
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]