Yamada Y - Search Results

1

Dyssegmental dysplasia, Silverman-Handmaker type: unexpected role of perlecan in cartilage development.

Arikawa-Hirasawa E, Wilcox WR, Yamada Y. Arikawa-Hirasawa E, et al. Among authors: yamada y. Am J Med Genet. 2001 Winter;106(4):254-7. doi: 10.1002/ajmg.10229. Am J Med Genet. 2001. PMID: 11891676 Review.

2

Perlecan is essential for cartilage and cephalic development.

Arikawa-Hirasawa E, Watanabe H, Takami H, Hassell JR, Yamada Y. Arikawa-Hirasawa E, et al. Among authors: yamada y. Nat Genet. 1999 Nov;23(3):354-8. doi: 10.1038/15537. Nat Genet. 1999. PMID: 10545953

3

Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.

Arikawa-Hirasawa E, Wilcox WR, Le AH, Silverman N, Govindraj P, Hassell JR, Yamada Y. Arikawa-Hirasawa E, et al. Among authors: yamada y. Nat Genet. 2001 Apr;27(4):431-4. doi: 10.1038/86941. Nat Genet. 2001. PMID: 11279527

4

[Roles of perlecan in development and disease: studies in knockout mice and human disorders].

Arikawa-Hirasawa E, Yamada Y. Arikawa-Hirasawa E, et al. Among authors: yamada y. Seikagaku. 2001 Oct;73(10):1257-61. Seikagaku. 2001. PMID: 11725543 Review. Japanese. No abstract available.

5

Role of CDMP-1 in skeletal morphogenesis: promotion of mesenchymal cell recruitment and chondrocyte differentiation.

Tsumaki N, Tanaka K, Arikawa-Hirasawa E, Nakase T, Kimura T, Thomas JT, Ochi T, Luyten FP, Yamada Y. Tsumaki N, et al. Among authors: yamada y. J Cell Biol. 1999 Jan 11;144(1):161-73. doi: 10.1083/jcb.144.1.161. J Cell Biol. 1999. PMID: 9885252 Free PMC article.

6

Differential expression of laminin alpha chains during proliferative and differentiation stages in a model for skin morphogenesis.

Fleischmajer R, Kuroda K, Utani A, Douglas MacDonald E, Perlish JS, Arikawa-Hirasawa E, Sekiguchi K, Sanzen N, Timpl R, Yamada Y. Fleischmajer R, et al. Among authors: yamada y. Matrix Biol. 2000 Dec;19(7):637-47. doi: 10.1016/s0945-053x(00)00092-5. Matrix Biol. 2000. PMID: 11102753

7

Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene.

Watanabe H, Kimata K, Line S, Strong D, Gao LY, Kozak CA, Yamada Y. Watanabe H, et al. Among authors: yamada y. Nat Genet. 1994 Jun;7(2):154-7. doi: 10.1038/ng0694-154. Nat Genet. 1994. PMID: 7920633

8

Mice lacking link protein develop dwarfism and craniofacial abnormalities.

Watanabe H, Yamada Y. Watanabe H, et al. Among authors: yamada y. Nat Genet. 1999 Feb;21(2):225-9. doi: 10.1038/6016. Nat Genet. 1999. PMID: 9988279

9

Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan.

Watanabe H, Nakata K, Kimata K, Nakanishi I, Yamada Y. Watanabe H, et al. Among authors: yamada y. Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6943-7. doi: 10.1073/pnas.94.13.6943. Proc Natl Acad Sci U S A. 1997. PMID: 9192671 Free PMC article.

10

Expression and structure of cartilage proteins.

Yamada Y, Horton W, Miyashita T, Savagner P, Hassell J, Doege K. Yamada Y, et al. J Craniofac Genet Dev Biol. 1991 Oct-Dec;11(4):350-6. J Craniofac Genet Dev Biol. 1991. PMID: 1812134 Review.

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