These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 29400105)

  • 21. Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.
    Akita J; Abe S; Shinkawa H; Kimberling WJ; Usami S
    J Hum Genet; 2001; 46(7):355-61. PubMed ID: 11450843
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation of EYA4 in a large Chinese family with autosomal dominant middle-frequency sensorineural hearing loss by targeted exome sequencing.
    Sun Y; Zhang Z; Cheng J; Lu Y; Yang CL; Luo YY; Yang G; Yang H; Zhu L; Zhou J; Yao HQ
    J Hum Genet; 2015 Jun; 60(6):299-304. PubMed ID: 25809937
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A DNA variant within the MYO7A promoter regulates YY1 transcription factor binding and gene expression serving as a potential dominant DFNA11 auditory genetic modifier.
    Street VA; Li J; Robbins CA; Kallman JC
    J Biol Chem; 2011 Apr; 286(17):15278-86. PubMed ID: 21378158
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Gene mapping for autosomal dominant nonsyndromic hearing loss DFNA11].
    Yuan H; Han DY; Wang QJ; Zong L; Zhao YL
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Jun; 42(6):422-7. PubMed ID: 17702415
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A.
    Ben-Salem S; Rehm HL; Willems PJ; Tamimi ZA; Ayadi H; Ali BR; Al-Gazali L
    Mol Biol Rep; 2014 Jan; 41(1):193-200. PubMed ID: 24194196
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.
    He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Lin J; Lu X
    Int J Pediatr Otorhinolaryngol; 2017 Aug; 99():40-43. PubMed ID: 28688563
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.
    Tang ZH; Chen JR; Zheng J; Shi HS; Ding J; Qian XD; Zhang C; Chen JL; Wang CC; Li L; Chen JZ; Yin SK; Huang TS; Chen P; Guan MX; Wang JF
    Stem Cells Transl Med; 2016 May; 5(5):561-71. PubMed ID: 27013738
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS.
    Kim YR; Kim HM; Lee B; Baek JI; Lee KY; Park HJ; Kim UK
    Genes Genomics; 2023 Feb; 45(2):225-230. PubMed ID: 36630074
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [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
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):965-969. PubMed ID: 31598937
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family.
    Sanggaard KM; Kjaer KW; Eiberg H; Nürnberg G; Nürnberg P; Hoffman K; Jensen H; Sørum C; Rendtorff ND; Tranebjaerg L
    Am J Med Genet A; 2008 Apr; 146A(8):1017-25. PubMed ID: 18348273
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sensorineural hearing impairment non-syndromic, dominant DFNA11.
    Tamagawa Y; Kitamura K; Ishida T; Nishizawa M; Liu XZ; Walsh J; Steel KP; Brown SD
    Adv Otorhinolaryngol; 2000; 56():103-6. PubMed ID: 10868221
    [No Abstract]   [Full Text] [Related]  

  • 32. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
    Riazuddin S; Nazli S; Ahmed ZM; Yang Y; Zulfiqar F; Shaikh RS; Zafar AU; Khan SN; Sabar F; Javid FT; Wilcox ER; Tsilou E; Boger ET; Sellers JR; Belyantseva IA; Riazuddin S; Friedman TB
    Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
    Bakhchane A; Charif M; Bousfiha A; Boulouiz R; Nahili H; Rouba H; Charoute H; Lenaers G; Barakat A
    PLoS One; 2017; 12(5):e0176516. PubMed ID: 28472130
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.
    Payne M; Yang Z; Katz BJ; Warner JE; Weight CJ; Zhao Y; Pearson ED; Treft RL; Hillman T; Kennedy RJ; Meire FM; Zhang K
    Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Natural history and retinal structure in patients with Usher syndrome type 1 owing to MYO7A mutation.
    Lenassi E; Saihan Z; Cipriani V; Le Quesne Stabej P; Moore AT; Luxon LM; Bitner-Glindzicz M; Webster AR
    Ophthalmology; 2014 Feb; 121(2):580-7. PubMed ID: 24199935
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness.
    Huang A; Yuan Y; Liu Y; Zhu Q; Dai P
    J Transl Med; 2015 May; 13():154. PubMed ID: 25963406
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).
    Luijendijk MW; Van Wijk E; Bischoff AM; Krieger E; Huygen PL; Pennings RJ; Brunner HG; Cremers CW; Cremers FP; Kremer H
    Hum Genet; 2004 Jul; 115(2):149-56. PubMed ID: 15221449
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Spectrum of
    Kabahuma RI; Schubert WD; Labuschagne C; Yan D; Blanton SH; Pepper MS; Liu XZ
    Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33671976
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetic counseling in Usher syndrome: linkage and mutational analysis of 10 Colombian families.
    Tamayo ML; Lopez G; Gelvez N; Medina D; Kimberling WJ; Rodríguez V; Tamayo GE; Bernal JE
    Genet Couns; 2008; 19(1):15-27. PubMed ID: 18564497
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].
    Jin Z; Cheng J; Lu Y; Li J; Sun Y; Yuan H; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.