153 related articles for article (PubMed ID: 32388442)
1. Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene.
Huang CY; Tsai YH; Tsai YC; Lu YC; Chan YH; Hsu CJ; Chiou SH; Wu CC; Cheng YF
Stem Cell Res; 2020 May; 45():101795. PubMed ID: 32388442
[TBL] [Abstract][Full Text] [Related]
2. Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene.
Yang X; Liu N; Mu H; Lv Y; Zhang H; Li Y; Guan J; Gai Z; Liu Y
Stem Cell Res; 2021 Mar; 51():102188. PubMed ID: 33517119
[TBL] [Abstract][Full Text] [Related]
3. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
Xiao ZA; Xie DH
Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
[TBL] [Abstract][Full Text] [Related]
4. Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2.
Fukunaga I; Oe Y; Danzaki K; Ohta S; Chen C; Iizumi M; Shiga T; Matsuoka R; Anzai T; Hibiya-Motegi R; Tajima S; Ikeda K; Akamatsu W; Kamiya K
Stem Cell Res; 2021 May; 53():102290. PubMed ID: 33780732
[TBL] [Abstract][Full Text] [Related]
5. Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss.
Fukunaga I; Shirai K; Oe Y; Danzaki K; Ohta S; Shiga T; Chen C; Ikeda K; Akamatsu W; Kawano A; Kamiya K
Stem Cell Res; 2020 Jul; 47():101910. PubMed ID: 32745712
[TBL] [Abstract][Full Text] [Related]
6. Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation.
Fukunaga I; Shiga T; Chen C; Oe Y; Danzaki K; Ohta S; Matsuoka R; Anzai T; Hibiya-Motegi R; Tajima S; Ikeda K; Akamatsu W; Kamiya K
Stem Cell Res; 2020 Mar; 43():101674. PubMed ID: 31926383
[TBL] [Abstract][Full Text] [Related]
7. Generation of induced pluripotent stem cells MMCi001-A from a Taiwanese hearing loss patient carrying GJB2 pV37I mutation.
Lu HE; Tsai CL; Chiu IM; Pan YL; Lin YF; Lin HC; Hsu YC
Stem Cell Res; 2020 Jan; 42():101692. PubMed ID: 31896484
[TBL] [Abstract][Full Text] [Related]
8. Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation.
Chan YH; Cheng YF; Chen YT; Huang CY; Lin CH; Hu CJ; Lu YC; Wu CC; Hsu CJ
Stem Cell Res; 2018 Dec; 33():51-55. PubMed ID: 30316039
[TBL] [Abstract][Full Text] [Related]
9. [A follow-up study of abnormal mutation in neonatal deafness gene screening].
Liu QM; Tian Y; Yu JJ; He QQ; Peng L; Guo XQ; Li DY; Chen T
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Dec; 54(12):881-887. PubMed ID: 31887812
[No Abstract] [Full Text] [Related]
10. Hearing Phenotypes of Patients with Hearing Loss Homozygous for the
Guo C; Huang SS; Yuan YY; Zhou Y; Wang N; Kang DY; Yang SY; Zhang X; Gao X; Dai P
Neural Plast; 2020; 2020():8841522. PubMed ID: 32802038
[TBL] [Abstract][Full Text] [Related]
11. Modeling gap junction beta 2 gene-related deafness with human iPSC.
Fukunaga I; Oe Y; Danzaki K; Ohta S; Chen C; Shirai K; Kawano A; Ikeda K; Kamiya K
Hum Mol Genet; 2021 Jul; 30(15):1429-1442. PubMed ID: 33997905
[TBL] [Abstract][Full Text] [Related]
12. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
[TBL] [Abstract][Full Text] [Related]
13. [Screening of hot-spot deafness gene mutations among 277 cochlear implantation patients in Sichuan province].
Jiang TF; Peng JJ; Zheng H; Chen XL; Kong WL
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Aug; 32(15):1177-1182. PubMed ID: 30282152
[No Abstract] [Full Text] [Related]
14. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
[TBL] [Abstract][Full Text] [Related]
16. Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population.
Kim SY; Kim AR; Han KH; Kim MY; Jeon EH; Koo JW; Oh SH; Choi BY
PLoS One; 2015; 10(6):e0125416. PubMed ID: 26061264
[TBL] [Abstract][Full Text] [Related]
17. [Application of next generation sequencing in congenital sensorineural deafness].
Xu B; Chen Y; Jiang A; Chen C; Wang K; Zheng J; Fu Y
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):811-815. PubMed ID: 29921047
[No Abstract] [Full Text] [Related]
18. GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.
Shi GZ; Gong LX; Xu XH; Nie WY; Lin Q; Qi YS
Hear Res; 2004 Nov; 197(1-2):19-23. PubMed ID: 15504600
[TBL] [Abstract][Full Text] [Related]
19. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
Liu XZ; Xia XJ; Ke XM; Ouyang XM; Du LL; Liu YH; Angeli S; Telischi FF; Nance WE; Balkany T; Xu LR
Hum Genet; 2002 Oct; 111(4-5):394-7. PubMed ID: 12384781
[TBL] [Abstract][Full Text] [Related]
20. In Vitro Models of GJB2-Related Hearing Loss Recapitulate Ca
Fukunaga I; Fujimoto A; Hatakeyama K; Aoki T; Nishikawa A; Noda T; Minowa O; Kurebayashi N; Ikeda K; Kamiya K
Stem Cell Reports; 2016 Dec; 7(6):1023-1036. PubMed ID: 27840044
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
