BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 32476383)

  • 1. [Hearing loss due to mutations or lack of the gene coding protein stereocillin].
    Markova TG; Alekseeva NN; Mironovich OL; Bliznets EA; Lalayants MR; Polyakov AV; Tavartkiladze GA
    Vestn Otorinolaringol; 2020; 85(2):14-20. PubMed ID: 32476383
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian population.
    Markova TG; Alekseeva NN; Mironovich OL; Galeeva NM; Lalayants MR; Bliznetz EA; Chibisova SS; Polyakov AV; Tavartkiladze GA
    Int J Pediatr Otorhinolaryngol; 2020 Nov; 138():110247. PubMed ID: 32705992
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    Eur Arch Otorhinolaryngol; 2019 Dec; 276(12):3353-3358. PubMed ID: 31552524
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Early audiological phenotype in patients with mutations in the USH2A gene.
    Markova TG; Lalayants MR; Alekseeva NN; Ryzhkova OP; Shatokhina OL; Galeeva NM; Bliznetz EA; Weener ME; Belov OA; Chibisova SS; Polyakov AV; Tavartkiladze GA
    Int J Pediatr Otorhinolaryngol; 2022 Jun; 157():111140. PubMed ID: 35452909
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [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]  

  • 7. STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic.
    Plevova P; Paprskarova M; Tvrda P; Turska P; Slavkovsky R; Mrazkova E
    Otol Neurotol; 2017 Dec; 38(10):e393-e400. PubMed ID: 28984810
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spectrum of Genes for Non-
    Shatokhina O; Galeeva N; Stepanova A; Markova T; Lalayants M; Alekseeva N; Tavarkiladze G; Markova T; Bessonova L; Petukhova M; Guseva D; Anisimova I; Polyakov A; Ryzhkova O; Bliznetz E
    Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Genetic characteristic analysis of slight-to-moderate sensorineural hearing loss in children].
    Zhou R; Guan J; Wang Q
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Jan; 38(1):18-22. PubMed ID: 38297844
    [No Abstract]   [Full Text] [Related]  

  • 10. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.
    Francey LJ; Conlin LK; Kadesch HE; Clark D; Berrodin D; Sun Y; Glessner J; Hakonarson H; Jalas C; Landau C; Spinner NB; Kenna M; Sagi M; Rehm HL; Krantz ID
    Am J Med Genet A; 2012 Feb; 158A(2):298-308. PubMed ID: 22147502
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
    Safka Brozkova D; Poisson Marková S; Mészárosová AU; Jenčík J; Čejnová V; Čada Z; Laštůvková J; Rašková D; Seeman P
    Clin Genet; 2020 Dec; 98(6):548-554. PubMed ID: 32860223
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances].
    Lalaiants MR; Markova TG; Bakhshinian VV; Bliznets EA; Poliakov AV; Tavartikiladze GA
    Vestn Otorinolaringol; 2014; (2):37-43. PubMed ID: 24781170
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics.
    Vona B; Hofrichter MA; Neuner C; Schröder J; Gehrig A; Hennermann JB; Kraus F; Shehata-Dieler W; Klopocki E; Nanda I; Haaf T
    Clin Genet; 2015; 87(1):49-55. PubMed ID: 26011646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life].
    Lalaiants MR; Bliznets EA; Markova TG; Poliakov AV; Tavartkiladze GA
    Vestn Otorinolaringol; 2011; (3):31-5. PubMed ID: 21720291
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frequency and clinical features of hearing loss caused by STRC deletions.
    Yokota Y; Moteki H; Nishio SY; Yamaguchi T; Wakui K; Kobayashi Y; Ohyama K; Miyazaki H; Matsuoka R; Abe S; Kumakawa K; Takahashi M; Sakaguchi H; Uehara N; Ishino T; Kosho T; Fukushima Y; Usami SI
    Sci Rep; 2019 Mar; 9(1):4408. PubMed ID: 30867468
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss.
    Markova T; Alekseeva N; Lalayants M; Ryzhkova O; Shatokhina O; Galeeva N; Bliznetz E; Belov O; Chibisova S; Polyakov A; Tavartkiladze G
    J Pers Med; 2022 Nov; 12(11):. PubMed ID: 36579563
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities.
    Wu CC; Chen PJ; Chiu YH; Lu YC; Wu MC; Hsu CJ
    Audiol Neurootol; 2008; 13(3):172-81. PubMed ID: 18075246
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.