BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 20106873)

  • 1. Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse.
    Richter CA; Amin S; Linden J; Dixon J; Dixon MJ; Tucker AS
    Hum Mol Genet; 2010 Apr; 19(8):1551-60. PubMed ID: 20106873
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM; Dror AA; Avraham KB
    Int J Dev Biol; 2007; 51(6-7):609-31. PubMed ID: 17891721
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical features, treatment and genetic background of Treacher Collins syndrome.
    Marszałek B; Wójcicki P; Kobus K; Trzeciak WH
    J Appl Genet; 2002; 43(2):223-33. PubMed ID: 12080178
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic background has a major effect on the penetrance and severity of craniofacial defects in mice heterozygous for the gene encoding the nucleolar protein Treacle.
    Dixon J; Dixon MJ
    Dev Dyn; 2004 Apr; 229(4):907-14. PubMed ID: 15042714
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities.
    Dixon J; Jones NC; Sandell LL; Jayasinghe SM; Crane J; Rey JP; Dixon MJ; Trainor PA
    Proc Natl Acad Sci U S A; 2006 Sep; 103(36):13403-8. PubMed ID: 16938878
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A functional SNP in the promoter region of TCOF1 is associated with reduced gene expression and YY1 DNA-protein interaction.
    Masotti C; Armelin-Correa LM; Splendore A; Lin CJ; Barbosa A; Sogayar MC; Passos-Bueno MR
    Gene; 2005 Oct; 359():44-52. PubMed ID: 16102917
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.
    Zhang X; Fan Y; Zhang Y; Xue H; Chen X
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1410-5. PubMed ID: 23838542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mouse models for deafness: lessons for the human inner ear and hearing loss.
    Avraham KB
    Ear Hear; 2003 Aug; 24(4):332-41. PubMed ID: 12923424
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Circling mouse: possible animal model for deafness.
    Lee JW; Lee EJ; Hong SH; Chung WH; Lee HT; Lee TW; Lee JR; Kim HT; Suh JG; Kim TY; Ryoo ZY
    Comp Med; 2001 Dec; 51(6):550-4. PubMed ID: 11924819
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mouse TCOF1 is expressed widely, has motifs conserved in nucleolar phosphoproteins, and maps to chromosome 18.
    Paznekas WA; Zhang N; Gridley T; Jabs EW
    Biochem Biophys Res Commun; 1997 Sep; 238(1):1-6. PubMed ID: 9299440
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
    Vreugde S; Erven A; Kros CJ; Marcotti W; Fuchs H; Kurima K; Wilcox ER; Friedman TB; Griffith AJ; Balling R; Hrabé De Angelis M; Avraham KB; Steel KP
    Nat Genet; 2002 Mar; 30(3):257-8. PubMed ID: 11850623
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hush puppy: a new mouse mutant with pinna, ossicle, and inner ear defects.
    Pau H; Fuchs H; de Angelis MH; Steel KP
    Laryngoscope; 2005 Jan; 115(1):116-24. PubMed ID: 15630379
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.
    Su PH; Chen JY; Chen SJ; Yu JS
    J Formos Med Assoc; 2006 Jun; 105(6):518-21. PubMed ID: 16801042
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources.
    Parker LL; Gao J; Zuo J
    Brain Res; 2006 May; 1091(1):235-42. PubMed ID: 16630581
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons.
    So RB; Gonzales B; Henning D; Dixon J; Dixon MJ; Valdez BC
    Gene; 2004 Mar; 328():49-57. PubMed ID: 15019983
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation.
    Teber OA; Gillessen-Kaesbach G; Fischer S; Böhringer S; Albrecht B; Albert A; Arslan-Kirchner M; Haan E; Hagedorn-Greiwe M; Hammans C; Henn W; Hinkel GK; König R; Kunstmann E; Kunze J; Neumann LM; Prott EC; Rauch A; Rott HD; Seidel H; Spranger S; Sprengel M; Zoll B; Lohmann DR; Wieczorek D
    Eur J Hum Genet; 2004 Nov; 12(11):879-90. PubMed ID: 15340364
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sensorineural hearing loss in insulin-like growth factor I-null mice: a new model of human deafness.
    Cediel R; Riquelme R; Contreras J; Díaz A; Varela-Nieto I
    Eur J Neurosci; 2006 Jan; 23(2):587-90. PubMed ID: 16420467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation.
    Gonzales B; Henning D; So RB; Dixon J; Dixon MJ; Valdez BC
    Hum Mol Genet; 2005 Jul; 14(14):2035-43. PubMed ID: 15930015
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients.
    Zhang C; An L; Xue H; Hao S; Yan Y; Zhang Q; Jin X; Li Q; Zhou B; Feng X; Ma P; Wang X; Chen X; Chen C; Cao Z; Ma X
    J Clin Lab Anal; 2021 Jan; 35(1):e23567. PubMed ID: 32909271
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deafness genes.
    Kitamura K; Takahashi K; Tamagawa Y; Noguchi Y; Kuroishikawa Y; Ishikawa K; Hagiwara H
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.