207 related articles for article (PubMed ID: 8947051)
1. 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]
2. The novel mouse microphthalmia mutations Mitfmi-enu5 and Mitfmi-bcc2 produce dominant negative Mitf proteins.
Hansdottir AG; Pálsdóttir K; Favor J; Neuhäuser-Klaus A; Fuchs H; de Angelis MH; Steingrímsson E
Genomics; 2004 May; 83(5):932-5. PubMed ID: 15081122
[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. 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]
5. 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]
6. Synergy of PEBP2/CBF with mi transcription factor (MITF) for transactivation of mouse mast cell protease 6 gene.
Ogihara H; Kanno T; Morii E; Kim DK; Lee YM; Sato M; Kim WY; Nomura S; Ito Y; Kitamura Y
Oncogene; 1999 Aug; 18(32):4632-9. PubMed ID: 10467408
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. The NMR solution structure of a mutant of the Max b/HLH/LZ free of DNA: insights into the specific and reversible DNA binding mechanism of dimeric transcription factors.
Sauvé S; Tremblay L; Lavigne P
J Mol Biol; 2004 Sep; 342(3):813-32. PubMed ID: 15342239
[TBL] [Abstract][Full Text] [Related]
10. Dorsal retinal pigment epithelium differentiates as neural retina in the microphthalmia (mi/mi) mouse.
Bumsted KM; Barnstable CJ
Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):903-8. PubMed ID: 10711712
[TBL] [Abstract][Full Text] [Related]
11. Identification of the region of mi transcription factor which is responsible for the synergy with PEBP2/CBF.
Morii E; Ogihara H; Kanno T; Kim DK; Nomura S; Ito Y; Kitamura Y
Biochem Biophys Res Commun; 1999 Jul; 261(1):53-7. PubMed ID: 10405322
[TBL] [Abstract][Full Text] [Related]
12. Involvement of transcription factor encoded by the mouse mi locus (MITF) in apoptosis of cultured mast cells induced by removal of interleukin-3.
Tsujimura T; Hashimoto K; Morii E; Tunio GM; Tsujino K; Kondo T; Kanakura Y; Kitamura Y
Am J Pathol; 1997 Oct; 151(4):1043-51. PubMed ID: 9327738
[TBL] [Abstract][Full Text] [Related]
13. Genomic analysis of the Microphthalmia locus and identification of the MITF-J/Mitf-J isoform.
Hershey CL; Fisher DE
Gene; 2005 Feb; 347(1):73-82. PubMed ID: 15715979
[TBL] [Abstract][Full Text] [Related]
14. The basic helix-loop-helix domain of the E47 transcription factor requires other protein regions for full DNA binding activity.
Lu J; Sloan SR
Biochem Biophys Res Commun; 2002 Feb; 290(5):1521-8. PubMed ID: 11820794
[TBL] [Abstract][Full Text] [Related]
15. Regulation of the MiTF/TFE bHLH-LZ transcription factors through restricted spatial expression and alternative splicing of functional domains.
Kuiper RP; Schepens M; Thijssen J; Schoenmakers EF; van Kessel AG
Nucleic Acids Res; 2004; 32(8):2315-22. PubMed ID: 15118077
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene.
Mochii M; Ono T; Matsubara Y; Eguchi G
Dev Biol; 1998 Apr; 196(2):145-59. PubMed ID: 9576828
[TBL] [Abstract][Full Text] [Related]
19. Electroretinographic assessment of retinal function in microphthalmia mutant mice.
Möller A; Eysteinsson T; Steingrímsson E
Exp Eye Res; 2004 Apr; 78(4):837-48. PubMed ID: 15037118
[TBL] [Abstract][Full Text] [Related]
20. Viral mutations enhance the Max binding properties of the vMyc b-HLH-LZ domain.
Crouch DH; Fisher F; La Rocca SA; Goding CR; Gillespie DA
Nucleic Acids Res; 2005; 33(16):5235-42. PubMed ID: 16166655
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]