Works matching IS 14345161 AND DT 2001 AND VI 46 AND IP 1

Results: 11

Gender-specific haplotype association of collagen α2 (XI) gene in ossification of the posterior longitudinal ligament of the spine.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 1, doi. 10.1007/s100380170117

By:

Maeda, S.;
Koga, H.;
Matsunaga, S.;
Numasawa, T.;
Ikari, K.;
Furushima, K.;
Harata, S.;
Takeda, J.;
Sakou, T.;
Komiya, S.;
Inoue, I.

Publication type:

Article

Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 5, doi. 10.1007/s100380170118

By:

Kyo, K.;
Muto, T.;
Nagawa, H.;
Lathrop, G. M.;
Nakamura, Y.

Publication type:

Article

IQGAP1, a negative regulator of cell-cell adhesion, is upregulated by gene amplification at 15q26 in gastric cancer cell lines HSC39 and 40A.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 21, doi. 10.1007/s100380170119

By:

Sugimoto, N.;
Imoto, I.;
Fukuda, Y.;
Kurihara, N.;
Kuroda, S.;
Tanigami, A.;
Kaibuchi, K.;
Kamiyama, R.;
Inazawa, J.

Publication type:

Article

Five novel single-nucleotide polymorphisms of human interferon gamma identified by sequencing the entire gene.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 32, doi. 10.1007/s100380170121

By:

Iwasaki, H.;
Ota, N.;
Nakajima, T.;
Shinohara, Y.;
Kodaira, M.;
Kajita, M.;
Emi, M.

Publication type:

Article

Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene (DRD4) with schizophrenia and personality traits.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 26, doi. 10.1007/s100380170120

By:

Mitsuyasu, H.;
Hirata, N.;
Sakai, Y.;
Shibata, H.;
Takeda, Y.;
Ninomiya, H.;
Kawasaki, H.;
Tashiro, N.;
Fukumaki, Y.

Publication type:

Article

Nine novel single-nucleotide polymorphisms in the integrin β4 (ITGB4) gene in the Japanese population.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 35, doi. 10.1007/s100380170122

By:

Hirano, A.;
Nagai, H.;
Harada, H.;
Terada, Y.;
Haga, S.;
Kajiwara, T.;
Emi, M.

Publication type:

Article

Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 38, doi. 10.1007/s100380170123

By:

Itoh, T.;
Kikuchi, K.;
Odagawa, Y.;
Takata, S.;
Yano, K.;
Okada, S.;
Haneda, N.;
Ogawa, S.;
Nakano, O.;
Kawahara, Y.;
Kasai, H.;
Nakayama, T.;
Fukutomi, T.;
Sakurada, H.;
Shimizu, A.;
Yazaki, Y.;
Nagai, R.;
Nakamura, Y.;
Tanaka, T.

Publication type:

Article

A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 41, doi. 10.1007/s100380170124

By:

Hirai, H.;
Nakajima, S.;
Miyauchi, A.;
Nishimura, K.;
Shimizu, N.;
Shima, M.;
Michigami, T.;
Ozono, K.;
Okada, S.

Publication type:

Article

α-1-Antichymotrypsin gene A1252G variant (ACT Isehara-1) is associated with a lacunar type of ischemic cerebrovascular disease.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 45, doi. 10.1007/s100380170125

By:

Tachikawa, H.;
Tsuda, M.;
Onoe, K.;
Ueno, M.;
Takagi, S.;
Shinohara, Y.

Publication type:

Article

Novel single nucleotide polymorphisms of the human colony-stimulating factor 2 (CSF2) gene identified by sequencing the entire gene.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 48, doi. 10.1007/s100380170126

By:

Kajita, M.;
Iwasaki, H.;
Ota, N.;
Shinohara, Y.;
Kodaira, M.;
Nakajima, T.;
Emi, M.

Publication type:

Article

Novel single nucleotide polymorphisms of the human nuclear factor kappa-B 2 gene identified by sequencing the entire gene.

Published in:

Journal of Human Genetics, 2001, v. 46, n. 1, p. 50, doi. 10.1007/s100380170127

By:

Shinohara, Y.;
Iwasaki, H.;
Ota, N.;
Nakajima, T.;
Kodaira, M.;
Kajita, M.;
Shiba, T.;
Emi, M.

Publication type:

Article