Tachibana Masayoshi - Search Results

Year	Number of Results
2002	4
2003	5
2004	1
2005	3
2006	3
2008	1
2009	1
2018	2
2022	0

1

Mouse models for four types of Waardenburg syndrome.

Tachibana M, Kobayashi Y, Matsushima Y. Tachibana M, et al. Pigment Cell Res. 2003 Oct;16(5):448-54. doi: 10.1034/j.1600-0749.2003.00066.x. Pigment Cell Res. 2003. PMID: 12950719 Review.

2

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. Uehara S, et al. Among authors: tachibana m. Pigment Cell Melanoma Res. 2009 Feb;22(1):111-9. doi: 10.1111/j.1755-148X.2008.00513.x. Epub 2008 Oct 28. Pigment Cell Melanoma Res. 2009. PMID: 18983533

3

Androgen-dependent hereditary mouse keratoconus: linkage to an MHC region.

Tachibana M, Adachi W, Kinoshita S, Kobayashi Y, Honma Y, Hiai H, Matsushima Y. Tachibana M, et al. Invest Ophthalmol Vis Sci. 2002 Jan;43(1):51-7. Invest Ophthalmol Vis Sci. 2002. PMID: 11773012

4

A deletion in the endothelin-B receptor gene is responsible for the Waardenburg syndrome-like phenotypes of WS4 mice.

Ohtani S, Shinkai Y, Horibe A, Katayama K, Tsuji T, Matsushima Y, Tachibana M, Kunieda T. Ohtani S, et al. Among authors: tachibana m. Exp Anim. 2006 Oct;55(5):491-5. doi: 10.1538/expanim.55.491. Exp Anim. 2006. PMID: 17090968 Free article.

5

A new mouse model for infantile neuroaxonal dystrophy, inad mouse, maps to mouse chromosome 1.

Matsushima Y, Kikuchi T, Kikuchi H, Ichihara N, Ishikawa A, Ishijima Y, Tachibana M. Matsushima Y, et al. Among authors: tachibana m. Mamm Genome. 2005 Feb;16(2):73-8. doi: 10.1007/s00335-004-3017-5. Mamm Genome. 2005. PMID: 15859351

6

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. Watanabe K, et al. Among authors: tachibana m. Pigment Cell Res. 2002 Jun;15(3):201-11. doi: 10.1034/j.1600-0749.2002.01080.x. Pigment Cell Res. 2002. PMID: 12028584

7

Annulus of collagen fibrils in mouse cornea and structural matrix alterations in a murine-specific keratopathy.

Quantock AJ, Dennis S, Adachi W, Kinoshita S, Boote C, Meek KM, Matsushima Y, Tachibana M. Quantock AJ, et al. Among authors: tachibana m. Invest Ophthalmol Vis Sci. 2003 May;44(5):1906-11. doi: 10.1167/iovs.02-0884. Invest Ophthalmol Vis Sci. 2003. PMID: 12714622 Free article.

8

Effects of taurine on serum cholesterol levels and development of atherosclerosis in spontaneously hyperlipidaemic mice.

Matsushima Y, Sekine T, Kondo Y, Sakurai T, Kameo K, Tachibana M, Murakami S. Matsushima Y, et al. Among authors: tachibana m. Clin Exp Pharmacol Physiol. 2003 Apr;30(4):295-9. doi: 10.1046/j.1440-1681.2003.03828.x. Clin Exp Pharmacol Physiol. 2003. PMID: 12680850

9

Quantitative trait loci determining weight reduction of testes and pituitary by diethylstilbesterol in LEXF and FXLE recombinant inbred strain rats.

Tachibana M, Lu L, Hiai H, Tamura A, Matsushima Y, Shisa H. Tachibana M, et al. Exp Anim. 2006 Apr;55(2):91-5. doi: 10.1538/expanim.55.91. Exp Anim. 2006. PMID: 16651691 Free article.

10

Hereditary keratoconus-like keratopathy in Japanese wild mice mapped to mouse Chromosome 13.

Tachibana M, Okamoto M, Sakamoto M, Matsushima Y. Tachibana M, et al. Mamm Genome. 2002 Dec;13(12):692-5. doi: 10.1007/s00335-002-3031-4. Mamm Genome. 2002. PMID: 12514747

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