PubMed for id: 355302

Year	Number of Results
1999	1
2001	1
2005	1
2007	1
2008	1
2009	1
2011	1
2012	1
2013	4
2014	1
2016	2
2017	1
2019	2
2021	3
2022	2
2023	1
2024	0

1

A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.

Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Khusnutdinova EK, Poliakov A, Metspalu M, Posukh OL, Barashkov NA, Fedorova SA. Solovyev AV, et al. Hum Genet. 2022 Apr;141(3-4):697-707. doi: 10.1007/s00439-021-02405-w. Epub 2021 Nov 27. Hum Genet. 2022. PMID: 34839402

2

[Application value of high-throughput gene copy number variation detection in the diagnosis of enlarged vestibular aqueduct].

Liu YL, Wang LL, Wen J, Mei LY, He CF, Jiang L, Feng Y. Liu YL, et al. Zhonghua Yi Xue Za Zhi. 2021 Jan 12;101(2):103-107. doi: 10.3760/cma.j.cn112137-20201010-02794. Zhonghua Yi Xue Za Zhi. 2021. PMID: 33455124 Chinese.

3

[Analysis of MYO7A gene mutation in a family with non-syndromic autosomal recessive deafness].

Wang S, Qin L, Ding K, Hao B, Bian S, Wang Z, Wang Q, Wang X, Zhang W, Liao S. Wang S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):965-969. doi: 10.3760/cma.j.issn.1003-9406.2019.10.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31598937 Chinese.

4

Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.

Čada Z, Šafka Brožková D, Balatková Z, Plevová P, Rašková D, Laštůvková J, Černý R, Bandúrová V, Koucký V, Hrubá S, Komarc M, Jenčík J, Poisson Marková S, Plzák J, Kluh J, Seeman P. Čada Z, et al. Eur Arch Otorhinolaryngol. 2019 Dec;276(12):3353-3358. doi: 10.1007/s00405-019-05649-5. Epub 2019 Sep 24. Eur Arch Otorhinolaryngol. 2019. PMID: 31552524

5

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.

Liu Y, Wang L, Feng Y, He C, Liu D, Cai X, Jiang L, Chen H, Liu C, Wu H, Mei L. Liu Y, et al. PLoS One. 2016 Dec 20;11(12):e0168508. doi: 10.1371/journal.pone.0168508. eCollection 2016. PLoS One. 2016. PMID: 27997596 Free PMC article. Clinical Trial.

6

Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patients.

Marková S, Šafka Brožková D, Mészárosová A, Neupauerová J, Groh D, Křečková G, Laššuthová P, Seeman P. Marková S, et al. Int J Pediatr Otorhinolaryngol. 2016 Jul;86:27-33. doi: 10.1016/j.ijporl.2016.04.005. Epub 2016 Apr 7. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27260575

7

Prevalence of the 35delG mutation in the GJB2 gene in two samples of non-syndromic deaf subjects from Chile.

Cifuentes L, Arancibia M, Torrente M, Acuña M, Farfán C, Ríos C. Cifuentes L, et al. Biol Res. 2013;46(3):239-42. doi: 10.4067/S0716-97602013000300003. Biol Res. 2013. PMID: 24346070 Free article.

8

Significance of unilateral enlarged vestibular aqueduct.

Greinwald J, DeAlarcon A, Cohen A, Uwiera T, Zhang K, Benton C, Halstead M, Meinzen-Derr J. Greinwald J, et al. Laryngoscope. 2013 Jun;123(6):1537-46. doi: 10.1002/lary.23889. Epub 2013 Feb 9. Laryngoscope. 2013. PMID: 23401162

9

Otoprotective effects of erythropoietin on Cdh23erl/erl mice.

Han F, Yu H, Zheng T, Ma X, Zhao X, Li P, Le L, Su Y, Zheng QY. Han F, et al. Neuroscience. 2013 May 1;237:1-6. doi: 10.1016/j.neuroscience.2013.01.052. Epub 2013 Feb 4. Neuroscience. 2013. PMID: 23384607 Free PMC article.

10

The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia).

Pshennikova VG, Teryutin FM, Cherdonova AM, Borisova TV, Solovyev AV, Romanov GP, Morozov IV, Bondar AA, Posukh OL, Fedorova SA, Barashkov NA. Pshennikova VG, et al. Genes (Basel). 2023 Apr 28;14(5):1001. doi: 10.3390/genes14051001. Genes (Basel). 2023. PMID: 37239361 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

22 results

Results by year