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 *

146 related articles for article (PubMed ID: 15829536)

  • 41. A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
    Ben-Yosef T; Ness SL; Madeo AC; Bar-Lev A; Wolfman JH; Ahmed ZM; Desnick RJ; Willner JP; Avraham KB; Ostrer H; Oddoux C; Griffith AJ; Friedman TB
    N Engl J Med; 2003 Apr; 348(17):1664-70. PubMed ID: 12711741
    [No Abstract]   [Full Text] [Related]  

  • 42. A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.
    Kitajiri S; Makishima T; Friedman TB; Griffith AJ
    Clin Genet; 2007 Feb; 71(2):148-52. PubMed ID: 17250663
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Two novel LHX3 mutations in patients with combined pituitary hormone deficiency including cervical rigidity and sensorineural hearing loss.
    Ramzan K; Bin-Abbas B; Al-Jomaa L; Allam R; Al-Owain M; Imtiaz F
    BMC Endocr Disord; 2017 Mar; 17(1):17. PubMed ID: 28302169
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genetic modifiers of hereditary hearing loss.
    Riazuddin S; Ahmed ZM; Friedman TB; Griffith AJ; Riazuddin S; Wilcox ER
    Adv Otorhinolaryngol; 2002; 61():224-9. PubMed ID: 12408088
    [No Abstract]   [Full Text] [Related]  

  • 45. A CDH23 missense variant in Beauceron dogs with non-syndromic deafness.
    Abitbol M; Jagannathan V; Lopez M; Courtin A; Dufaure de Citres C; Gache V; Leeb T
    Anim Genet; 2023 Feb; 54(1):73-77. PubMed ID: 36308003
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Two ENU-induced alleles of Atp2b2 cause deafness in mice.
    Carpinelli MR; Manning MG; Kile BT; Burt RA
    PLoS One; 2013; 8(6):e67479. PubMed ID: 23826306
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Changes in cochlear PMCA2 expression correlate with the maturation of auditory sensitivity.
    Watson CJ; Lies SM; Minich RR; Tempel BL
    J Assoc Res Otolaryngol; 2014 Aug; 15(4):543-54. PubMed ID: 24799196
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
    Ficarella R; Di Leva F; Bortolozzi M; Ortolano S; Donaudy F; Petrillo M; Melchionda S; Lelli A; Domi T; Fedrizzi L; Lim D; Shull GE; Gasparini P; Brini M; Mammano F; Carafoli E
    Proc Natl Acad Sci U S A; 2007 Jan; 104(5):1516-21. PubMed ID: 17234811
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect.
    Giacomello M; De Mario A; Lopreiato R; Primerano S; Campeol M; Brini M; Carafoli E
    Cell Calcium; 2011 Dec; 50(6):569-76. PubMed ID: 22047666
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Hair cells, plasma membrane Ca²⁺ ATPase and deafness.
    Giacomello M; De Mario A; Primerano S; Brini M; Carafoli E
    Int J Biochem Cell Biol; 2012 May; 44(5):679-83. PubMed ID: 22349217
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Atp2b2, encoding plasma membrane Ca2+-ATPase type 2, (PMCA2) exhibits tissue-specific first exon usage in hair cells, neurons, and mammary glands of mice.
    Silverstein RS; Tempel BL
    Neuroscience; 2006 Aug; 141(1):245-57. PubMed ID: 16675132
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2.
    Kozel PJ; Friedman RA; Erway LC; Yamoah EN; Liu LH; Riddle T; Duffy JJ; Doetschman T; Miller ML; Cardell EL; Shull GE
    J Biol Chem; 1998 Jul; 273(30):18693-6. PubMed ID: 9668038
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice.
    Street VA; McKee-Johnson JW; Fonseca RC; Tempel BL; Noben-Trauth K
    Nat Genet; 1998 Aug; 19(4):390-4. PubMed ID: 9697703
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Relationship research among CDH23 gene and the risk of noise-induced hearing loss].
    Jiao J; Gu GZ; Chen GS; Zhang HL; Wu H; Li YH; Zhou WH; Yu SF
    Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi; 2020 Feb; 38(2):84-90. PubMed ID: 32306668
    [No Abstract]   [Full Text] [Related]  

  • 55. De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment.
    Smits JJ; Oostrik J; Beynon AJ; Kant SG; de Koning Gans PAM; Rotteveel LJC; Klein Wassink-Ruiter JS; Free RH; Maas SM; van de Kamp J; Merkus P; ; Koole W; Feenstra I; Admiraal RJC; Lanting CP; Schraders M; Yntema HG; Pennings RJE; Kremer H
    Hum Genet; 2019 Jan; 138(1):61-72. PubMed ID: 30535804
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Bioinformatic analysis predicts the regulatory function of noncoding SNPs associated with Long COVID-19 syndrome.
    Maiti AK
    Immunogenetics; 2024 Jul; ():. PubMed ID: 39042286
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Deafness causing neuroplastin missense variants fail to promote plasma membrane Ca
    Liang Y; Ormazabal-Toledo R; Yao S; Shi YS; Herrera-Molina R; Montag D; Lin X
    J Biol Chem; 2024 Jul; 300(7):107474. PubMed ID: 38879011
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Treatment of monogenic and digenic dominant genetic hearing loss by CRISPR-Cas9 ribonucleoprotein delivery in vivo.
    Tao Y; Lamas V; Du W; Zhu W; Li Y; Whittaker MN; Zuris JA; Thompson DB; Rameshbabu AP; Shu Y; Gao X; Hu JH; Pei C; Kong WJ; Liu X; Wu H; Kleinstiver BP; Liu DR; Chen ZY
    Nat Commun; 2023 Aug; 14(1):4928. PubMed ID: 37582836
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Peroxisome Deficiency in Cochlear Hair Cells Causes Hearing Loss by Deregulating BK Channels.
    Fu X; Wan P; Lu L; Wan Y; Liu Z; Hong G; Cao S; Bi X; Zhou J; Qiao R; Guo S; Xiao Y; Wang B; Chang M; Li W; Li P; Zhang A; Sun J; Chai R; Gao J
    Adv Sci (Weinh); 2023 Jul; 10(20):e2300402. PubMed ID: 37171794
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
    Clabout T; Maes L; Acke F; Wuyts W; Van Schil K; Coucke P; Janssens S; De Leenheer E
    Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672845
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.