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 *

48 related articles for article (PubMed ID: 9630069)

  • 1. Defects in the human homolog of Drosophila diaphanous in non-syndromic deafness.
    Clin Genet; 1998 Mar; 53(3):174-5. PubMed ID: 9630069
    [No Abstract]   [Full Text] [Related]  

  • 2. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
    Lynch ED; Lee MK; Morrow JE; Welcsh PL; León PE; King MC
    Science; 1997 Nov; 278(5341):1315-8. PubMed ID: 9360932
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Making sense of nonsyndromic deafness.
    Smith RJ; Huygen PL
    Arch Otolaryngol Head Neck Surg; 2003 Apr; 129(4):405-6. PubMed ID: 12707186
    [No Abstract]   [Full Text] [Related]  

  • 4. Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
    Ouyang XM; Xia XJ; Verpy E; Du LL; Pandya A; Petit C; Balkany T; Nance WE; Liu XZ
    Hum Genet; 2002 Jul; 111(1):26-30. PubMed ID: 12136232
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.
    Schoen CJ; Emery SB; Thorne MC; Ammana HR; Sliwerska E; Arnett J; Hortsch M; Hannan F; Burmeister M; Lesperance MM
    Proc Natl Acad Sci U S A; 2010 Jul; 107(30):13396-401. PubMed ID: 20624953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.
    Shaukat S; Fatima Z; Zehra U; Waqar AB
    J Ayub Med Coll Abbottabad; 2003; 15(3):59-64. PubMed ID: 14727345
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evaluation of ESPN, MYO3A, SLC26A5 and USH1C as candidates for hereditary non-syndromic deafness (congenital sensorineural deafness) in Dalmatian dogs.
    Mieskes K; Distl O
    Anim Genet; 2007 Oct; 38(5):533-4. PubMed ID: 17614983
    [No Abstract]   [Full Text] [Related]  

  • 8. Drosophila abelson interacting protein (dAbi) is a positive regulator of abelson tyrosine kinase activity.
    Juang JL; Hoffmann FM
    Oncogene; 1999 Sep; 18(37):5138-47. PubMed ID: 10498863
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Non-syndromic dominant DFNA1.
    Lynch ED; León PE
    Adv Otorhinolaryngol; 2000; 56():60-7. PubMed ID: 10868215
    [No Abstract]   [Full Text] [Related]  

  • 10. Hair hear!
    Phimister B
    Nat Genet; 1998 May; 19(1):8. PubMed ID: 9590277
    [No Abstract]   [Full Text] [Related]  

  • 11. Diaphanous regulates myosin and adherens junctions to control cell contractility and protrusive behavior during morphogenesis.
    Homem CC; Peifer M
    Development; 2008 Mar; 135(6):1005-18. PubMed ID: 18256194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular study on decoding of memory].
    Tsukada A
    Nihon Seirigaku Zasshi; 2004; 66(3):77-8. PubMed ID: 15218888
    [No Abstract]   [Full Text] [Related]  

  • 13. Syndromic choroideremia: sublocalization of phenotypes associated with Martin-Probst deafness mental retardation syndrome.
    Poloschek CM; Kloeckener-Gruissem B; Hansen LL; Bach M; Berger W
    Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):4096-104. PubMed ID: 18487380
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparative mapping of the canine diaphanous homologue 1 (Drosophila) gene (DIAPH1 ) to CFA2q23-q24.2.
    Rak SG; Drögemüller C; Kuiper H; Leeb T; Quignon P; André C; Distl O
    Anim Genet; 2002 Oct; 33(5):389-90. PubMed ID: 12354155
    [No Abstract]   [Full Text] [Related]  

  • 15. Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3.
    Bykhovskaya Y; Mengesha E; Wang D; Yang H; Estivill X; Shohat M; Fischel-Ghodsian N
    Mol Genet Metab; 2004 Nov; 83(3):199-206. PubMed ID: 15542390
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deafness. Sounds from the cochlea.
    Avraham KB
    Nature; 1997 Dec; 390(6660):559-60. PubMed ID: 9403680
    [No Abstract]   [Full Text] [Related]  

  • 17. Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss.
    Chiereghin C; Robusto M; Massa V; Castorina P; Ambrosetti U; Asselta R; Soldà G
    Cells; 2022 May; 11(11):. PubMed ID: 35681420
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Suppression of the ecdysteroid-triggered growth arrest by a novel Drosophila membrane steroid binding protein.
    Fujii-Taira I; Yamaguchi S; Iijima R; Natori S; Homma KJ
    FEBS Lett; 2009 Feb; 583(4):655-60. PubMed ID: 19162019
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetics. Selfish genes could help disease-free mosquitoes spread.
    Enserink M
    Science; 2007 Mar; 315(5820):1777-8. PubMed ID: 17395798
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification and characterization of TRIP8 gene in silico.
    Katoh M; Katoh M
    Int J Mol Med; 2003 Nov; 12(5):817-21. PubMed ID: 14533015
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.