276 related articles for article (PubMed ID: 10400990)
1. 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
[TBL] [Abstract][Full Text] [Related]
2. Impaired development of melanoblasts in the black-eyed white Mitf(mi-bw) mouse, a model for auditory-pigmentary disorders.
Hozumi H; Takeda K; Yoshida-Amano Y; Takemoto Y; Kusumi R; Fukuzaki-Dohi U; Higashitani A; Yamamoto H; Shibahara S
Genes Cells; 2012 Jun; 17(6):494-508. PubMed ID: 22563733
[TBL] [Abstract][Full Text] [Related]
3. Regulation of pigment cell-specific gene expression by MITF.
Shibahara S; Yasumoto K; Amae S; Udono T; Watanabe K; Saito H; Takeda K
Pigment Cell Res; 2000; 13 Suppl 8():98-102. PubMed ID: 11041365
[TBL] [Abstract][Full Text] [Related]
4. 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; 15(3):201-11. PubMed ID: 12028584
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Insertion of long interspersed element-1 in the Mitf gene is associated with altered neurobehavior of the black-eyed white Mitf(mi-bw) mouse.
Takeda K; Hozumi H; Nakai K; Yoshizawa M; Satoh H; Yamamoto H; Shibahara S
Genes Cells; 2014 Feb; 19(2):126-40. PubMed ID: 24304702
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Altered expression of the iron transporter Nramp1 (Slc11a1) during fetal development of the retinal pigment epithelium in microphthalmia-associated transcription factor Mitf(mi) and Mitf(vitiligo) mouse mutants.
Gelineau-van Waes J; Smith L; van Waes M; Wilberding J; Eudy JD; Bauer LK; Maddox J
Exp Eye Res; 2008 Feb; 86(2):419-33. PubMed ID: 18191835
[TBL] [Abstract][Full Text] [Related]
9. Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2.
Lee M; Goodall J; Verastegui C; Ballotti R; Goding CR
J Biol Chem; 2000 Dec; 275(48):37978-83. PubMed ID: 10973953
[TBL] [Abstract][Full Text] [Related]
10. Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus.
Hallsson JH; Favor J; Hodgkinson C; Glaser T; Lamoreux ML; Magnúsdóttir R; Gunnarsson GJ; Sweet HO; Copeland NG; Jenkins NA; Steingrímsson E
Genetics; 2000 May; 155(1):291-300. PubMed ID: 10790403
[TBL] [Abstract][Full Text] [Related]
11. Effects of mutations at the W locus (c-kit) on inner ear pigmentation and function in the mouse.
Cable J; Huszar D; Jaenisch R; Steel KP
Pigment Cell Res; 1994 Feb; 7(1):17-32. PubMed ID: 7521050
[TBL] [Abstract][Full Text] [Related]
12. Specific expression of Gsta4 in mouse cochlear melanocytes: a novel role for hearing and melanocyte differentiation.
Uehara S; Izumi Y; Kubo Y; Wang CC; Mineta K; Ikeo K; Gojobori T; Tachibana M; Kikuchi T; Kobayashi T; Shibahara S; Taya C; Yonekawa H; Shiroishi T; Yamamoto H
Pigment Cell Melanoma Res; 2009 Feb; 22(1):111-9. PubMed ID: 18983533
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3.
Potterf SB; Furumura M; Dunn KJ; Arnheiter H; Pavan WJ
Hum Genet; 2000 Jul; 107(1):1-6. PubMed ID: 10982026
[TBL] [Abstract][Full Text] [Related]
15. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3.
Watanabe A; Takeda K; Ploplis B; Tachibana M
Nat Genet; 1998 Mar; 18(3):283-6. PubMed ID: 9500554
[TBL] [Abstract][Full Text] [Related]
16. Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently.
Nakayama A; Nguyen MT; Chen CC; Opdecamp K; Hodgkinson CA; Arnheiter H
Mech Dev; 1998 Jan; 70(1-2):155-66. PubMed ID: 9510032
[TBL] [Abstract][Full Text] [Related]
17. Melanocyte-specific microphthalmia-associated transcription factor isoform activates its own gene promoter through physical interaction with lymphoid-enhancing factor 1.
Saito H; Yasumoto K; Takeda K; Takahashi K; Fukuzaki A; Orikasa S; Shibahara S
J Biol Chem; 2002 Aug; 277(32):28787-94. PubMed ID: 12048204
[TBL] [Abstract][Full Text] [Related]
18. Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA).
Morell R; Spritz RA; Ho L; Pierpont J; Guo W; Friedman TB; Asher JH
Hum Mol Genet; 1997 May; 6(5):659-64. PubMed ID: 9158138
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Regional Fluctuation in the Functional Consequence of LINE-1 Insertion in the Mitf Gene: The Black Spotting Phenotype Arisen from the Mitfmi-bw Mouse Lacking Melanocytes.
Takeda K; Hozumi H; Ohba K; Yamamoto H; Shibahara S
PLoS One; 2016; 11(3):e0150228. PubMed ID: 26930598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
