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Journal Abstract Search

274 related items for PubMed ID: 10400990

  • 21. Effect of the mutant microphthalmia-associated transcription factor found in Tietz syndrome on the in vitro development of mast cells.
    Shigemura T, Shiohara M, Tanaka M, Takeuchi K, Koike K.
    J Pediatr Hematol Oncol; 2010 Aug; 32(6):442-7. PubMed ID: 20485200
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  • 22. 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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  • 25. 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; 6(1):99-104. PubMed ID: 11764295
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  • 26. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome.
    Bondurand N, Pingault V, Goerich DE, Lemort N, Sock E, Le Caignec C, Wegner M, Goossens M.
    Hum Mol Genet; 2000 Aug 12; 9(13):1907-17. PubMed ID: 10942418
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  • 27. Microphthalmia-associated transcription factor in the Wnt signaling pathway.
    Saito H, Yasumoto K, Takeda K, Takahashi K, Yamamoto H, Shibahara S.
    Pigment Cell Res; 2003 Jun 12; 16(3):261-5. PubMed ID: 12753399
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  • 28. Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome).
    Amiel J, Watkin PM, Tassabehji M, Read AP, Winter RM.
    Clin Dysmorphol; 1998 Jan 12; 7(1):17-20. PubMed ID: 9546825
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  • 29. SLUG (SNAI2) deletions in patients with Waardenburg disease.
    Sánchez-Martín M, Rodríguez-García A, Pérez-Losada J, Sagrera A, Read AP, Sánchez-García I.
    Hum Mol Genet; 2002 Dec 01; 11(25):3231-6. PubMed ID: 12444107
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  • 30. Sensorineural deafness and pigmentation genes: melanocytes and the Mitf transcriptional network.
    Price ER, Fisher DE.
    Neuron; 2001 Apr 01; 30(1):15-8. PubMed ID: 11343641
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  • 31. Microphthalmia-associated transcription factor is expressed in projection neurons of the mouse olfactory bulb.
    Ohba K, Takeda K, Yamamoto H, Shibahara S.
    Genes Cells; 2015 Dec 01; 20(12):1088-102. PubMed ID: 26522736
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  • 32. Lipocalin-type prostaglandin D synthase as a melanocyte marker regulated by MITF.
    Takeda K, Yokoyama S, Aburatani H, Masuda T, Han F, Yoshizawa M, Yamaki N, Yamamoto H, Eguchi N, Urade Y, Shibahara S.
    Biochem Biophys Res Commun; 2006 Jan 27; 339(4):1098-106. PubMed ID: 16337607
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  • 33. MITF: a stream flowing for pigment cells.
    Tachibana M.
    Pigment Cell Res; 2000 Aug 27; 13(4):230-40. PubMed ID: 10952390
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  • 36. Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in iPS-derived melanocytes.
    Wen J, Song J, Chen J, Feng Z, Jing Q, Gong W, Kang X, Mei L, He C, Ma L, Feng Y.
    Pigment Cell Melanoma Res; 2024 Jan 27; 37(1):21-35. PubMed ID: 37559350
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  • 37. Mitf-D, a newly identified isoform, expressed in the retinal pigment epithelium and monocyte-lineage cells affected by Mitf mutations.
    Takeda K, Yasumoto Ki, Kawaguchi N, Udono T, Watanabe Ki, Saito H, Takahashi K, Noda M, Shibahara S.
    Biochim Biophys Acta; 2002 Feb 20; 1574(1):15-23. PubMed ID: 11955610
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  • 38. Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10.
    Verastegui C, Bille K, Ortonne JP, Ballotti R.
    J Biol Chem; 2000 Oct 06; 275(40):30757-60. PubMed ID: 10938265
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  • 39. Melanocytes and the microphthalmia transcription factor network.
    Steingrímsson E, Copeland NG, Jenkins NA.
    Annu Rev Genet; 2004 Oct 06; 38():365-411. PubMed ID: 15568981
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  • 40. Microphthalmia-associated transcription factor ensures the elongation of axons and dendrites in the mouse frontal cortex.
    Ohba K, Takeda K, Furuse T, Suzuki T, Wakana S, Suzuki T, Yamamoto H, Shibahara S.
    Genes Cells; 2016 Dec 06; 21(12):1365-1379. PubMed ID: 27859996
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