BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 35062939)

  • 1. Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants.
    Ma P; Zhou B; Kang Q; Chen X; Tian X; Hui L; Hao S; Wu H; Zhang C
    Mol Genet Genomic Med; 2024 Jun; 12(6):e2434. PubMed ID: 38860500
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation spectra and founder effect of TMC1 in patients with non-syndromic deafness in Xiamen area, China.
    Jiang Y; Gao S; Wu L; Jin X; Deng T; Wang L; Huang S; Gao X; Chen J; Han D; Gao H; Dai P
    Am J Med Genet B Neuropsychiatr Genet; 2018 Apr; 177(3):301-307. PubMed ID: 29533536
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades.
    Shadab M; Abbasi AA; Ejaz A; Ben-Mahmoud A; Gupta V; Kim HG; Vona B
    J Cell Mol Med; 2024 Apr; 28(8):e18119. PubMed ID: 38534090
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.
    Zhang L; Yang JY; Wang QQ; Gao X; Wang GJ; Han MY; Kang DY; Han DY; Huang SS; Yuan YY
    BMC Med Genomics; 2024 Jan; 17(1):32. PubMed ID: 38254107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
    AitRaise I; Amalou G; Bakhchane A; Bousfiha A; Abdelghaffar H; Majida C; Bonnet C; Petit C; Barakat A
    Biochem Genet; 2024 Jun; 62(3):1914-1924. PubMed ID: 37777971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo variants are a common cause of genetic hearing loss.
    Klimara MJ; Nishimura C; Wang D; Kolbe DL; Schaefer AM; Walls WD; Frees KL; Smith RJH; Azaiez H
    Genet Med; 2022 Dec; 24(12):2555-2567. PubMed ID: 36194208
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Local administration of an AAV-TMPRSS3 vector in aged Tmprss3 mutant mice with progressive deafness restores hearing].
    Richard ÉM; Delprat B
    Med Sci (Paris); 2024 May; 40(5):402-404. PubMed ID: 38819271
    [No Abstract]   [Full Text] [Related]  

  • 8. A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
    Shaikh RS; Ramzan K; Nazli S; Sattar S; Khan SN; Riazuddin S; Ahmed ZM; Friedman TB; Riazuddin S
    Am J Med Genet A; 2005 Nov; 138(4):392-5. PubMed ID: 16158433
    [No Abstract]   [Full Text] [Related]  

  • 9. Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High-Throughput Sequencing in a Unique Cohort from South India.
    Justin Margret J; Jayasankaran C; Amritkumar P; Azaiez H; Srisailapathy CRS
    Adv Genet (Hoboken); 2024 Jun; 5(2):2300206. PubMed ID: 38884051
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetics & Epigenetics of Hereditary Deafness: An Historical Overview.
    Martini A; Sorrentino F; Sorrentino U; Cassina M
    Audiol Res; 2021 Nov; 11(4):629-635. PubMed ID: 34842610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Case report of a novel mutation in the TNC gene in Chinese patients with nonsyndromic hearing loss.
    Li S; Li S; Chen D; Zhao S; Liu C; Zhang R; Chen Y; Guo X; Song X
    Medicine (Baltimore); 2024 Apr; 103(16):e37702. PubMed ID: 38640279
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Considering gene therapy to protect from X-linked deafness DFNX2 and associated neurodevelopmental disorders.
    Defourny J
    Ibrain; 2022; 8(4):431-441. PubMed ID: 37786584
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
    Bernardinelli E; Huber F; Roesch S; Dossena S
    Biomedicines; 2023 Jun; 11(6):. PubMed ID: 37371790
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.
    Ma J; Ma X; Lin K; Huang R; Bi X; Ming C; Li L; Li X; Li G; Zhao L; Yang T; Gao Y; Zhang T
    Hum Genomics; 2023 Jan; 17(1):1. PubMed ID: 36597107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic Analysis of the
    Wang WQ; Gao X; Huang SS; Kang DY; Xu JC; Yang K; Han MY; Zhang X; Yang SY; Yuan YY; Dai P
    Front Genet; 2022; 13():825082. PubMed ID: 35711932
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA
    Yu X; Li S; Ding Y
    J Clin Lab Anal; 2022 Apr; 36(4):e24298. PubMed ID: 35218233
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variant analysis of 92 Chinese Han families with hearing loss.
    Jin X; Huang S; An L; Zhang C; Dai P; Gao H; Ma X
    BMC Med Genomics; 2022 Jan; 15(1):12. PubMed ID: 35062939
    [TBL] [Abstract][Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.