Hata A - Search Results

1

Identification of a Gly862 to Ser substitution in the type I collagen gene from a single spermatozoon.

Iida T, Suzumori K, Ikuta K, Tanemura M, Yagami Y, Okamoto T, Hata A. Iida T, et al. Among authors: hata a. Mol Hum Reprod. 1996 Feb;2(2):131-4. doi: 10.1093/molehr/2.2.131. Mol Hum Reprod. 1996. PMID: 9238670

2

Recurrence of osteogenesis imperfecta because of paternal mosaicism: Gly862-->Ser substitution in a type I collagen gene (COL1A1).

Namikawa C, Suzumori K, Fukushima Y, Sasaki M, Hata A. Namikawa C, et al. Among authors: hata a. Hum Genet. 1995 Jun;95(6):666-70. doi: 10.1007/BF00209484. Hum Genet. 1995. PMID: 7789952

3

A molecular variant of angiotensinogen associated with preeclampsia.

Ward K, Hata A, Jeunemaitre X, Helin C, Nelson L, Namikawa C, Farrington PF, Ogasawara M, Suzumori K, Tomoda S, et al. Ward K, et al. Among authors: hata a. Nat Genet. 1993 May;4(1):59-61. doi: 10.1038/ng0593-59. Nat Genet. 1993. PMID: 8513325

4

Seroprevalence of hepatitis C virus infection and its genotype in Lanzhou, western China.

Wu RR, Mizokami M, Lau JY, Ohno T, Fang ZX, Ohba K, Wu XS, Hata A, Sasaki M, Iino S. Wu RR, et al. Among authors: hata a. J Med Virol. 1995 Feb;45(2):174-8. doi: 10.1002/jmv.1890450211. J Med Virol. 1995. PMID: 7775935

5

Five familial hypercholesterolemic kindreds in Japan with novel mutations of the LDL receptor gene.

Hirayama T, Yamaki E, Hata A, Tsuji M, Hashimoto K, Yamamoto M, Emi M. Hirayama T, et al. Among authors: hata a. J Hum Genet. 1998;43(4):250-4. doi: 10.1007/s100380050083. J Hum Genet. 1998. PMID: 9852677

6

p53 protein expression and p53 gene mutation in thymic epithelial tumors. An immunohistochemical and DNA sequencing study.

Tateyama H, Eimoto T, Tada T, Mizuno T, Inagaki H, Hata A, Sasaki M, Masaoka A. Tateyama H, et al. Among authors: hata a. Am J Clin Pathol. 1995 Oct;104(4):375-81. doi: 10.1093/ajcp/104.4.375. Am J Clin Pathol. 1995. PMID: 7572785

7

Angiotensinogen gene polymorphism in Japanese patients with hypertrophic cardiomyopathy.

Ishanov A, Okamoto H, Yoneya K, Watanabe M, Nakagawa I, Machida M, Onozuka H, Mikami T, Kawaguchi H, Hata A, Kondo K, Kitabatake A. Ishanov A, et al. Among authors: hata a. Am Heart J. 1997 Feb;133(2):184-9. doi: 10.1016/s0002-8703(97)70207-2. Am Heart J. 1997. PMID: 9023164

8

Ornithine transcarbamylase deficiency resulting from a C-to-T substitution in exon 5 of the ornithine transcarbamylase gene.

Hata A, Setoyama C, Shimada K, Takeda E, Kuroda Y, Akaboshi I, Matsuda I. Hata A, et al. Am J Hum Genet. 1989 Jul;45(1):123-7. Am J Hum Genet. 1989. PMID: 2741942 Free PMC article.

9

A novel missense mutation in exon 8 of the ornithine transcarbamylase gene in two unrelated male patients with mild ornithine transcarbamylase deficiency.

Hata A, Matsuura T, Setoyama C, Shimada K, Yokoi T, Akaboshi I, Matsuda I. Hata A, et al. Hum Genet. 1991 May;87(1):28-32. doi: 10.1007/BF01213087. Hum Genet. 1991. PMID: 2037279

10

Compound heterozygote for lipoprotein lipase deficiency: Ser----Thr244 and transition in 3' splice site of intron 2 (AG----AA) in the lipoprotein lipase gene.

Hata A, Emi M, Luc G, Basdevant A, Gambert P, Iverius PH, Lalouel JM. Hata A, et al. Am J Hum Genet. 1990 Oct;47(4):721-6. Am J Hum Genet. 1990. PMID: 2121025 Free PMC article.

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