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87 related items for PubMed ID: 9390817
21. A novel type of myosin encoded by the mouse deafness gene shaker-2. Wakabayashi Y, Takahashi Y, Kikkawa Y, Okano H, Mishima Y, Ushiki T, Yonekawa H, Kominami R. Biochem Biophys Res Commun; 1998 Jul 30; 248(3):655-9. PubMed ID: 9703981 [Abstract] [Full Text] [Related]
23. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C. Development; 2008 Apr 30; 135(8):1427-37. PubMed ID: 18339676 [Abstract] [Full Text] [Related]
26. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction. Robertson NG, Cremers CW, Huygen PL, Ikezono T, Krastins B, Kremer H, Kuo SF, Liberman MC, Merchant SN, Miller CE, Nadol JB, Sarracino DA, Verhagen WI, Morton CC. Hum Mol Genet; 2006 Apr 01; 15(7):1071-85. PubMed ID: 16481359 [Abstract] [Full Text] [Related]
27. Development of the vertebrate ear: insights from knockouts and mutants. Fekete DM. Trends Neurosci; 1999 Jun 01; 22(6):263-9. PubMed ID: 10354604 [Abstract] [Full Text] [Related]
28. 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 01; 30(3):257-8. PubMed ID: 11850623 [Abstract] [Full Text] [Related]
29. Interactions between FGF and Wnt signals and Tbx3 gene expression in mammary gland initiation in mouse embryos. Eblaghie MC, Song SJ, Kim JY, Akita K, Tickle C, Jung HS. J Anat; 2004 Jul 01; 205(1):1-13. PubMed ID: 15255957 [Abstract] [Full Text] [Related]
30. Fibroblast growth factor receptor-1 is essential for in vitro cardiomyocyte development. Dell'Era P, Ronca R, Coco L, Nicoli S, Metra M, Presta M. Circ Res; 2003 Sep 05; 93(5):414-20. PubMed ID: 12893744 [Abstract] [Full Text] [Related]
31. Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype. Murakami S, Balmes G, McKinney S, Zhang Z, Givol D, de Crombrugghe B. Genes Dev; 2004 Feb 01; 18(3):290-305. PubMed ID: 14871928 [Abstract] [Full Text] [Related]
32. Zebrafish as a model for hearing and deafness. Whitfield TT. J Neurobiol; 2002 Nov 05; 53(2):157-71. PubMed ID: 12382273 [Abstract] [Full Text] [Related]
33. Genetic deafness--progress with mouse models. Brown SD, Steel KP. Hum Mol Genet; 1994 Nov 05; 3 Spec No():1453-6. PubMed ID: 7849737 [Abstract] [Full Text] [Related]
34. Deregulated FGFR3 mutants in multiple myeloma cell lines with t(4;14): comparative analysis of Y373C, K650E and the novel G384D mutations. Ronchetti D, Greco A, Compasso S, Colombo G, Dell'Era P, Otsuki T, Lombardi L, Neri A. Oncogene; 2001 Jun 14; 20(27):3553-62. PubMed ID: 11429702 [Abstract] [Full Text] [Related]
35. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, Fridell RA. Genomics; 1999 Nov 01; 61(3):243-58. PubMed ID: 10552926 [Abstract] [Full Text] [Related]
36. The genetics of deafness: a model for genomic and biological complexity. Avraham KB. Ernst Schering Res Found Workshop; 2002 Nov 01; (36):71-93. PubMed ID: 11859565 [No Abstract] [Full Text] [Related]
37. A compendium of mouse knockouts with inner ear defects. Anagnostopoulos AV. Trends Genet; 2002 Oct 01; 18(10):499. PubMed ID: 12350347 [Abstract] [Full Text] [Related]
38. Phenotypic analysis of mice carrying human-type MAFB p.Leu239Pro mutation. Kanai M, Jeon H, Ojima M, Nishino T, Usui T, Yadav MK, Kulathunga K, Morito N, Takahashi S, Hamada M. Biochem Biophys Res Commun; 2020 Mar 05; 523(2):452-457. PubMed ID: 31882119 [Abstract] [Full Text] [Related]
39. Transgenic insertional mutagenesis. Applications to inner-ear genetics. Friedman RA. Arch Otolaryngol Head Neck Surg; 1996 Mar 05; 122(3):252-7. PubMed ID: 8607951 [Abstract] [Full Text] [Related]
40. Complexity and integration in the control of inner-ear development. Swiderski DL, Gong TW, Mustapha M. Genome Biol; 2007 Mar 05; 8(9):315. PubMed ID: 17915040 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]