A. Hata

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Novel mutations of the LDL Receptor Gene in Familial Hypercholesterolemia Pedigrees in Hokkaido

M. Emi, A. Hata, M. Tsuji, 2000 .

Mutations in exon 3 of the lipoprotein lipase gene segregating in a family with hypertriglyceridemia, pancreatitis, and non-insulin-dependent diabetes.

J. Lalouel, A. Hata, L. Kwong, 1993, The Journal of clinical investigation.

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation.

M. Emi, J. Lalouel, A. Hata, 1990, The Journal of clinical investigation.

Ethnic Difference in Contribution of Sp1 Site Variation of COLIA1 Gene in Genetic Predisposition to Osteoporosis

T. Nakajima, M. Emi, A. Hata, 1999, Calcified Tissue International.

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene.

M. Emi, J. Lalouel, M. Robertson, 1990, Nucleic acids research.

Template-switching during DNA synthesis by Thermus aquaticus DNA polymerase I.

S. Odelberg, R. White, R White, 1995, Nucleic acids research.

Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism.

T. Nabeshima, K. Yamamura, Y. Oike, 1999, Human molecular genetics.

Angiotensin converting enzyme as a genetic risk factor for coronary artery spasm. Implication in the pathogenesis of myocardial infarction.

A. Hata, Y. Oike, Y. Ogata, 1995, The Journal of clinical investigation.

Haplotypes of angiotensinogen in essential hypertension.

J. Lalouel, X. Jeunemaître, J. Tichet, 1997, American journal of human genetics.

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

M. Sasaki, H. Inagaki, H. Inagaki, 1995, American journal of clinical pathology.

Multivariate analysis of genetic and acquired factors; T235 variant of the angiotensinogen gene is a potent independent risk factor for preeclampsia.

M. Kanamori, A. Hata, S. Fujimoto, 2001, Seminars in thrombosis and hemostasis.

Association of a variant of the angiotensinogen gene with pure type of hypertension in pregnancy in the Japanese: implication of a racial difference and significance of an age factor.

A. Hata, R. Kishi, S. Fujimoto, 1999, American journal of medical genetics.

Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women.

A. Hata, R. Kishi, T. Asano, 2000, American journal of medical genetics.