Works matching IS 14345161 AND DT 1998 AND VI 43 AND IP 1

Results: 16

-6A Promoter variant of angiotensinogen and blood pressure variation in Canadian Oji-Cree.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 37, doi. 10.1007/s100380050034

By:

Hegele, R. A.;
Harris, Stewart B.;
Hanley, Anthony J. G.;
Sun, Fang;
Connelly, Philip W.;
Zinman, Bernard

Publication type:

Article

An HLA-binding-motif-aided peptide epitope library: A novel library design for the screening of HLA-DR4-restricted antigenic peptides recognized by CD4[sup +] T cells.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 14, doi. 10.1007/s100380050031

By:

Tana, Takeshi;
Kamikawaji, Nobuhiro;
Savoie, Christopher J.;
Sudo, Tohru;
Kinoshita, Yurika;
Sasazuki, T.

Publication type:

Article

The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 32, doi. 10.1007/s100380050033

By:

Fujimoto, M.;
Kantaputra, Piranit Nik;
Ikegawa, Shiro;
Fukushima, Yoshimitsu;
Sonta, Shin-ichi;
Matsuo, Masafumi;
Ishida, Takafumi;
Matsumoto, Tadashi;
Kondo, Shinji;
Tomita, Hiroaki;
Deng, Han-Xiang;
D'urso, Michele;
Rinaldi, Maria Michela;
Ventruto, Valerio;
Takagi, Toshihisa;
Nakamura, Yusuke;
Niikawa, Norio

Publication type:

Article

Human autoimmune lymphoproliferative syndrome, a defect in the apoptosis-inducing Fas receptor: A lesson from the mouse model.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 2, doi. 10.1007/s100380050029

By:

Nagata, S.

Publication type:

Article

Identification by differential display of eight known genes induced during in vivo intimal hyperplasia.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 9, doi. 10.1007/s100380050030

By:

Itoh, Makoto;
Tsukada, Shuichi;
Orita, Takuya;
Nishiu, J.;
Tomoike, Hitonobu;
Nakamura, Y.;
Tanaka, Toshihiro

Publication type:

Article

Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 22, doi. 10.1007/s100380050032

By:

Saito, Masaaki;
Matsumine, Hiroto;
Tanaka, Hajime;
Ishikawa, Atsushi;
Shimoda-Matsubayashi, Satoe;
Schäffer, Alejandro A.;
Mizuno, Yoshikuni;
Tsuji, S.

Publication type:

Article

High proportion of missense mutations of the BRCA1 and BRCA2 genes in Japanese breast cancer families.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 42, doi. 10.1007/s100380050035

By:

Katagiri, Toyomasa;
Kasumi, Fujio;
Yoshimoto, Masataka;
Nomizu, Tadashi;
Asaishi, Kazuaki;
Abe, Rikiya;
Tsuchiya, Atsuo;
Sugano, Masahiko;
Takai, Shin-ichiro;
Yoneda, Mitsusato;
Fukutomi, Takashi;
Nanba, Kiyoshi;
Makita, Masujiro;
Okazaki, Hiroshi;
Hirata, Kouichi;
Okazaki, Minoru;
Furutsuma, Yoshikazu;
Morishita, Yasuo;
Iino, Yuuichi;
Karino, Takayuki

Publication type:

Article

In situ detection of insulin-like growth factor II (IGF2) and H19 gene expression in hepatocellular carcinoma.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 49, doi. 10.1007/s100380050036

By:

Sohda, T.;
Iwata, Kaoru;
Soejima, Hidenobu;
Kamimura, Seiichiro;
Shijo, Hiroshi;
Yun, Kankatsu

Publication type:

Article

Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cells.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 54, doi. 10.1007/s100380050037

By:

Kogo, Toshiaki;
Satoh, Yoshinori;
Kanazawa, Masaki;
Yamamoto, S.;
Takayanagi, Masaki;
Ohtake, Akira;
Mori, Masataka;
Niimi, Hiroo

Publication type:

Article

New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 59, doi. 10.1007/s100380050038

By:

Kondoh, Tatsuro;
Matsumoto, Tadashi;
Ochi, Makoto;
Sukegawa, Kazuko;
Tsuji, Y.

Publication type:

Article

A severe case of Moebius syndrome with calcification on the fourth ventricular floor.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 62, doi. 10.1007/s100380050039

By:

Matsunaga, Y.;
Amamoto, Nagisa;
Kondoh, Tatsuro;
Ohtsuka, Yuichi;
Miyazoe, Hatsuji;
Kamimura, Naohisa;
Matsumoto, Tadashi;
Tsuji, Yoshiro

Publication type:

Article

A case of craniofacial dysmorphism, congenital heart defects, coccygeal skin folds, generalized skeletal alterations, and hemihypertrophy with linear skin hypopigmentation: A new syndrome?

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 65, doi. 10.1007/s100380050040

By:

Nishimura, G.;
Nagai, Toshiro

Publication type:

Article

A SacII polymorphism in the human ASCL2 (HASH2) gene region.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 69, doi. 10.1007/s100380050041

By:

Miyamoto, T.;
Jinno, Yoshihiro;
Miura, Kiyonori;
Sengoku, Kazuo;
Soejima, Hidenobu;
Yun, Kankatsu;
Yaginuma, Yuji;
Niikawa, Norio;
Ishikawa, Mutsuo

Publication type:

Article

Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 71, doi. 10.1007/s100380050042

By:

Tsukamoto, Kazuhiro;
Haruta, K.;
Shiba, Tadayoshi;
Emi, M.

Publication type:

Article

Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor β locus.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 73, doi. 10.1007/s100380050043

By:

Tsukamoto, Kazuhiro;
Inoue, Satoshi;
Hosoi, Takayuki;
Orimo, Hajime;
Emi, M.

Publication type:

Article

Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus.

Published in:

Journal of Human Genetics, 1998, v. 43, n. 1, p. 75, doi. 10.1007/s100380050044

By:

Watanabe, Ikuyo;
Tsukamoto, Kazuhiro;
Shiba, Tadayoshi;
Emi, M.

Publication type:

Article