Yanagawa Y - Search Results

1

The transcriptional regulation of human aldehyde dehydrogenase I gene. The structural and functional analysis of the promoter.

Yanagawa Y, Chen JC, Hsu LC, Yoshida A. Yanagawa Y, et al. J Biol Chem. 1995 Jul 21;270(29):17521-7. doi: 10.1074/jbc.270.29.17521. J Biol Chem. 1995. PMID: 7615557 Free article.

2

Biological role of human cytosolic aldehyde dehydrogenase 1: hormonal response, retinal oxidation and implication in testicular feminization.

Yoshida A, Hsu LC, Yanagawa Y. Yoshida A, et al. Among authors: yanagawa y. Adv Exp Med Biol. 1993;328:37-44. doi: 10.1007/978-1-4615-2904-0_5. Adv Exp Med Biol. 1993. PMID: 8493914 No abstract available.

3

Molecular mechanism of null expression of aldehyde dehydrogenase-1 in rat liver.

Chen J, Yanagawa Y, Yoshida A. Chen J, et al. Among authors: yanagawa y. Biochem Genet. 1996 Apr;34(3-4):109-16. doi: 10.1007/BF02396244. Biochem Genet. 1996. PMID: 8734411

4

Structure of the human deoxyribonuclease I (DNase I) gene: identification of the nucleotide substitution that generates its classical genetic polymorphism.

Yasuda T, Kishi K, Yanagawa Y, Yoshida A. Yasuda T, et al. Among authors: yanagawa y. Ann Hum Genet. 1995 Jan;59(1):1-15. doi: 10.1111/j.1469-1809.1995.tb01601.x. Ann Hum Genet. 1995. PMID: 7762978

5

Molecular defect of a phosphoglycerate kinase variant associated with haemolytic anaemia and neurological disorders in a large kindred.

Turner G, Fletcher J, Elber J, Yanagawa Y, Davé V, Yoshida A. Turner G, et al. Among authors: yanagawa y. Br J Haematol. 1995 Sep;91(1):60-5. doi: 10.1111/j.1365-2141.1995.tb05245.x. Br J Haematol. 1995. PMID: 7577653

6

Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.

Motegi T, Nakamura K, Terakawa T, Oohira A, Minoda K, Kishi K, Yanagawa Y, Hayakawa H. Motegi T, et al. Among authors: yanagawa y. J Med Genet. 1988 Sep;25(9):628-30. doi: 10.1136/jmg.25.9.628. J Med Genet. 1988. PMID: 3184142 Free PMC article.

7

Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.

Motegi T, Ikeda K, Watanabe K, Yanagawa Y, Minoda K. Motegi T, et al. Among authors: yanagawa y. J Med Genet. 1987 Nov;24(11):696-7. doi: 10.1136/jmg.24.11.696. J Med Genet. 1987. PMID: 3430545 Free PMC article.

8

A recognizable pattern of the midface of retinoblastoma patients with interstitial deletion of 13q.

Motegi T, Kaga M, Yanagawa Y, Kadowaki H, Watanabe K, Inoue A, Komatsu M, Minoda K. Motegi T, et al. Among authors: yanagawa y. Hum Genet. 1983;64(2):160-2. doi: 10.1007/BF00327116. Hum Genet. 1983. PMID: 6885051

9

De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells.

Motegi T, Watanabe K, Nakamura N, Hasegawa T, Yanagawa Y. Motegi T, et al. Among authors: yanagawa y. J Med Genet. 1985 Feb;22(1):64-6. doi: 10.1136/jmg.22.1.64. J Med Genet. 1985. PMID: 2984424 Free PMC article.

10

[Clinical application of rokitamycin in pediatrics].

Yanagawa Y, Fujita M, Hayakawa H. Yanagawa Y, et al. Jpn J Antibiot. 1988 Jul;41(7):871-4. Jpn J Antibiot. 1988. PMID: 3172460 Japanese.

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