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 *

115 related articles for article (PubMed ID: 8069297)

  • 1. 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; 3(4):553-7. PubMed ID: 8069297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.
    Tassabehji M; Newton VE; Read AP
    Nat Genet; 1994 Nov; 8(3):251-5. PubMed ID: 7874167
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 8(3):256-63. PubMed ID: 7874168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein.
    Hodgkinson CA; Moore KJ; Nakayama A; Steingrímsson E; Copeland NG; Jenkins NA; Arnheiter H
    Cell; 1993 Jul; 74(2):395-404. PubMed ID: 8343963
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation.
    Tripathi RK; Flanders DJ; Young TL; Oetting WS; Ramaiah A; King RA; Boissy RE; Nordlund JJ
    Pigment Cell Res; 1999 Jun; 12(3):187-92. PubMed ID: 10385915
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3.
    Weilbaecher KN; Hershey CL; Takemoto CM; Horstmann MA; Hemesath TJ; Tashjian AH; Fisher DE
    J Exp Med; 1998 Mar; 187(5):775-85. PubMed ID: 9480987
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The rat microphthalmia-associated transcription factor gene (Mitf) maps at 4q34-q41 and is mutated in the mib rats.
    Opdecamp K; Vanvooren P; Rivière M; Arnheiter H; Motta R; Szpirer J; Szpirer C
    Mamm Genome; 1998 Aug; 9(8):617-21. PubMed ID: 9680380
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Manifestations of microphthalmia.
    Jackson IJ; Raymond S
    Nat Genet; 1994 Nov; 8(3):209-10. PubMed ID: 7874158
    [No Abstract]   [Full Text] [Related]  

  • 10. Expression of the microphthalmia-associated basic helix-loop-helix leucine zipper transcription factor Mi in avian neuroretina cells induces a pigmented phenotype.
    Planque N; Turque N; Opdecamp K; Bailly M; Martin P; Saule S
    Cell Growth Differ; 1999 Jul; 10(7):525-36. PubMed ID: 10437920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 118(5):874-81. PubMed ID: 8749302
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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(22):6280-9. PubMed ID: 8947051
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cloning and characterization of the murine genes for bHLH-ZIP transcription factors TFEC and TFEB reveal a common gene organization for all MiT subfamily members.
    Rehli M; Den Elzen N; Cassady AI; Ostrowski MC; Hume DA
    Genomics; 1999 Feb; 56(1):111-20. PubMed ID: 10036191
    [TBL] [Abstract][Full Text] [Related]  

  • 15. TFEC is a macrophage-restricted member of the microphthalmia-TFE subfamily of basic helix-loop-helix leucine zipper transcription factors.
    Rehli M; Lichanska A; Cassady AI; Ostrowski MC; Hume DA
    J Immunol; 1999 Feb; 162(3):1559-65. PubMed ID: 9973413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Loss of DNA binding ability of the transcription factor encoded by the mutant mi locus.
    Morii E; Takebayashi K; Motohashi H; Yamamoto M; Nomura S; Kitamura Y
    Biochem Biophys Res Commun; 1994 Dec; 205(2):1299-304. PubMed ID: 7802662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate.
    Lister JA; Robertson CP; Lepage T; Johnson SL; Raible DW
    Development; 1999 Sep; 126(17):3757-67. PubMed ID: 10433906
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cloning of the murine Mist1 gene and assignment to mouse chromosome band 5G2-5G3.
    Pin CL; Lemercier C; Konieczny SF
    Cytogenet Cell Genet; 1999; 86(3-4):219-22. PubMed ID: 10575209
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A helix-loop-helix transcription factor-like gene is located at the mi locus.
    Hughes MJ; Lingrel JB; Krakowsky JM; Anderson KP
    J Biol Chem; 1993 Oct; 268(28):20687-90. PubMed ID: 8407885
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19.
    Edelhoff S; Ayer DE; Zervos AS; Steingrímsson E; Jenkins NA; Copeland NG; Eisenman RN; Brent R; Disteche CM
    Oncogene; 1994 Feb; 9(2):665-8. PubMed ID: 8290278
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.