BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 9480987)

  • 1. 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]  

  • 2. 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; 34(4):689-96. PubMed ID: 15050900
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitf and Tfe3, two members of the Mitf-Tfe family of bHLH-Zip transcription factors, have important but functionally redundant roles in osteoclast development.
    Steingrimsson E; Tessarollo L; Pathak B; Hou L; Arnheiter H; Copeland NG; Jenkins NA
    Proc Natl Acad Sci U S A; 2002 Apr; 99(7):4477-82. PubMed ID: 11930005
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linking osteopetrosis and pycnodysostosis: regulation of cathepsin K expression by the microphthalmia transcription factor family.
    Motyckova G; Weilbaecher KN; Horstmann M; Rieman DJ; Fisher DZ; Fisher DE
    Proc Natl Acad Sci U S A; 2001 May; 98(10):5798-803. PubMed ID: 11331755
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage of M-CSF signaling to Mitf, TFE3, and the osteoclast defect in Mitf(mi/mi) mice.
    Weilbaecher KN; Motyckova G; Huber WE; Takemoto CM; Hemesath TJ; Xu Y; Hershey CL; Dowland NR; Wells AG; Fisher DE
    Mol Cell; 2001 Oct; 8(4):749-58. PubMed ID: 11684011
    [TBL] [Abstract][Full Text] [Related]  

  • 6. TFE3, a transcription factor homologous to microphthalmia, is a potential transcriptional activator of tyrosinase and TyrpI genes.
    Verastegui C; Bertolotto C; Bille K; Abbe P; Ortonne JP; Ballotti R
    Mol Endocrinol; 2000 Mar; 14(3):449-56. PubMed ID: 10707962
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mitf is expressed in osteoclast progenitors in vitro.
    Kawaguchi N; Noda M
    Exp Cell Res; 2000 Nov; 260(2):284-91. PubMed ID: 11035923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Involvement of transcription factor encoded by the mi locus in the expression of c-kit receptor tyrosine kinase in cultured mast cells of mice.
    Tsujimura T; Morii E; Nozaki M; Hashimoto K; Moriyama Y; Takebayashi K; Kondo T; Kanakura Y; Kitamura Y
    Blood; 1996 Aug; 88(4):1225-33. PubMed ID: 8695840
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recent developments in the understanding of the pathophysiology of osteopetrosis.
    Felix R; Hofstetter W; Cecchini MG
    Eur J Endocrinol; 1996 Feb; 134(2):143-56. PubMed ID: 8630510
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular cause of the severe functional deficiency in osteoclasts by an arginine deletion in the basic domain of Mi transcription factor.
    Nomura S; Sakuma T; Higashibata Y; Oboki K; Sato M
    J Bone Miner Metab; 2001; 19(3):183-7. PubMed ID: 11368304
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Different effect of various mutant MITF encoded by mi, Mior, or Miwh allele on phenotype of murine mast cells.
    Kim DK; Morii E; Ogihara H; Lee YM; Jippo T; Adachi S; Maeyama K; Kim HM; Kitamura Y
    Blood; 1999 Jun; 93(12):4179-86. PubMed ID: 10361115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. The microphthalmia transcription factor regulates expression of the tartrate-resistant acid phosphatase gene during terminal differentiation of osteoclasts.
    Luchin A; Purdom G; Murphy K; Clark MY; Angel N; Cassady AI; Hume DA; Ostrowski MC
    J Bone Miner Res; 2000 Mar; 15(3):451-60. PubMed ID: 10750559
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The leucine zipper of TFE3 dictates helix-loop-helix dimerization specificity.
    Beckmann H; Kadesch T
    Genes Dev; 1991 Jun; 5(6):1057-66. PubMed ID: 2044953
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Abnormal expression of mouse mast cell protease 5 gene in cultured mast cells derived from mutant mi/mi mice.
    Morii E; Jippo T; Tsujimura T; Hashimoto K; Kim DK; Lee YM; Ogihara H; Tsujino K; Kim HM; Kitamura Y
    Blood; 1997 Oct; 90(8):3057-66. PubMed ID: 9376586
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.