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Journal Abstract Search

11476 related items for PubMed ID: 10536982

  • 1. Implications of isoform multiplicity of microphthalmia-associated transcription factor in the pathogenesis of auditory-pigmentary syndromes.
    Shibahara S, Yasumoto K, Amae S, Fuse N, Udono T, Takahashi K.
    J Investig Dermatol Symp Proc; 1999 Sep; 4(2):101-4. PubMed ID: 10536982
    [Abstract] [Full Text] [Related]

  • 2. Molecular cloning of cDNA encoding a novel microphthalmia-associated transcription factor isoform with a distinct amino-terminus.
    Fuse N, Yasumoto Ki, Takeda K, Amae S, Yoshizawa M, Udono T, Takahashi K, Tamai M, Tomita Y, Tachibana M, Shibahara S.
    J Biochem; 1999 Dec; 126(6):1043-51. PubMed ID: 10578055
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  • 3. A big gene linked to small eyes encodes multiple Mitf isoforms: many promoters make light work.
    Yasumoto K, Amae S, Udono T, Fuse N, Takeda K, Shibahara S.
    Pigment Cell Res; 1998 Dec; 11(6):329-36. PubMed ID: 9870544
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  • 5. An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness.
    Yajima I, Sato S, Kimura T, Yasumoto K, Shibahara S, Goding CR, Yamamoto H.
    Hum Mol Genet; 1999 Aug; 8(8):1431-41. PubMed ID: 10400990
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  • 7. Genomic analysis of the Microphthalmia locus and identification of the MITF-J/Mitf-J isoform.
    Hershey CL, Fisher DE.
    Gene; 2005 Feb 28; 347(1):73-82. PubMed ID: 15715979
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  • 9. Evidence to suggest that expression of MITF induces melanocyte differentiation and haploinsufficiency of MITF causes Waardenburg syndrome type 2A.
    Tachibana M.
    Pigment Cell Res; 1997 Feb 28; 10(1-2):25-33. PubMed ID: 9170159
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  • 10. Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.
    Steingrímsson E, Moore KJ, Lamoreux ML, Ferré-D'Amaré AR, Burley SK, Zimring DC, Skow LC, Hodgkinson CA, Arnheiter H, Copeland NG.
    Nat Genet; 1994 Nov 28; 8(3):256-63. PubMed ID: 7874168
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  • 11. Microphthalmia-associated transcription factor (MITF): multiplicity in structure, function, and regulation.
    Shibahara S, Takeda K, Yasumoto K, Udono T, Watanabe K, Saito H, Takahashi K.
    J Investig Dermatol Symp Proc; 2001 Nov 28; 6(1):99-104. PubMed ID: 11764295
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  • 12. MITF: a stream flowing for pigment cells.
    Tachibana M.
    Pigment Cell Res; 2000 Aug 28; 13(4):230-40. PubMed ID: 10952390
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  • 14. The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerization.
    Steingrímsson E, Nii A, Fisher DE, Ferré-D'Amaré AR, McCormick RJ, Russell LB, Burley SK, Ward JM, Jenkins NA, Copeland NG.
    EMBO J; 1996 Nov 15; 15(22):6280-9. PubMed ID: 8947051
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  • 15. Transcriptional activation of the melanocyte-specific genes by the human homolog of the mouse Microphthalmia protein.
    Yasumoto K, Mahalingam H, Suzuki H, Yoshizawa M, Yokoyama K.
    J Biochem; 1995 Nov 15; 118(5):874-81. PubMed ID: 8749302
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  • 16. Melanocytes and the microphthalmia transcription factor network.
    Steingrímsson E, Copeland NG, Jenkins NA.
    Annu Rev Genet; 2004 Nov 15; 38():365-411. PubMed ID: 15568981
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  • 17. Identification of a novel isoform of microphthalmia-associated transcription factor that is enriched in retinal pigment epithelium.
    Amae S, Fuse N, Yasumoto K, Sato S, Yajima I, Yamamoto H, Udono T, Durlu YK, Tamai M, Takahashi K, Shibahara S.
    Biochem Biophys Res Commun; 1998 Jun 29; 247(3):710-5. PubMed ID: 9647758
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  • 18. Mitf and Tfe3: members of a b-HLH-ZIP transcription factor family essential for osteoclast development and function.
    Hershey CL, Fisher DE.
    Bone; 2004 Apr 29; 34(4):689-96. PubMed ID: 15050900
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  • 19. Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene.
    Watanabe K, Takeda K, Yasumoto K, Udono T, Saito H, Ikeda K, Takasaka T, Takahashi K, Kobayashi T, Tachibana M, Shibahara S.
    Pigment Cell Res; 2002 Jun 29; 15(3):201-11. PubMed ID: 12028584
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  • 20. Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.
    Tachibana M, Perez-Jurado LA, Nakayama A, Hodgkinson CA, Li X, Schneider M, Miki T, Fex J, Francke U, Arnheiter H.
    Hum Mol Genet; 1994 Apr 29; 3(4):553-7. PubMed ID: 8069297
    [Abstract] [Full Text] [Related]

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