Works matching IS 14345161 AND DT 1999 AND VI 44 AND IP 3

Results: 16

Prenatal diagnosis of peroxisomal d-3-hydroxyacyl-CoA dehydratase / d-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 143, doi. 10.1007/s100380050131

By:

Suzuki, Y.;
Zhang, Zhongyi;
Shimozawa, Nobuyuki;
Muro, Masami;
Shono, Hideaki;
Toda, Shuji;
Miyahara, Shin-ichi;
Hashimoto, Takashi;
Usuda, Nobuteru;
Ito, Masayuki;
Takashima, Sachio;
Kondo, Naomi

Publication type:

Article

Association of radial bone mineral density with CA repeat polymorphism at the interleukin 6 locus in postmenoposal Japanese women.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 148, doi. 10.1007/s100380050132

By:

Tsukamoto, Kazuhiro;
Yoshida, Hideo;
Watanabe, Shuichiro;
Suzuki, Takao;
Miyao, Mariko;
Hosoi, Takayuki;
Orimo, Hajime;
Emi, M.

Publication type:

Article

Position-independent human β-globin gene expression mediated by a recombinant adeno-associated virus vector carrying the chicken β-globin insulator.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 152, doi. 10.1007/s100380050133

By:

Inoue, Takahito;
Yamaza, Haruyoshi;
Sakai, Yasuyoshi;
Mizuno, Shin-ichi;
Ohno, Mizuki;
Hamasaki, Naotaka;
Fukumaki, Y.

Publication type:

Article

Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 163, doi. 10.1007/s100380050134

By:

Imamura, Takuji;
Okano, Y.;
Shintaku, Haruo;
Hase, Yutaka;
Isshiki, Gen

Publication type:

Article

Association of diffuse panbronchiolitis with microsatellite polymorphism of the human interleukin 8 (IL-8) gene.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 169, doi. 10.1007/s100380050135

By:

Emi, M.;
Keicho, Naoto;
Tokunaga, Katsushi;
Katsumata, Harumi;
Souma, Sachi;
Nakata, Koichiro;
Taguchi, Yoshio;
Ohishi, Nobuya;
Azuma, Arata;
Kudoh, Shoji

Publication type:

Article

Significantly elevated expression of PF4 (platelet factor 4) and eotaxin in the NOA mouse, a model for atopic dermatitis.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 173, doi. 10.1007/s100380050136

By:

Watanabe, Otsu;
Natori, Kyoko;
Tamari, Mayumi;
Shiomoto, Yasuhisa;
Kubo, Shuji;
Nakamura, Y.

Publication type:

Article

Germline mutations of E-cadherin gene in Korean familial gastric cancer patients.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 177, doi. 10.1007/s100380050137

By:

Yoon, Kyong-Ah;
Ku, J.-L.;
Yang, Han-Kwang;
Kim, Woo Ho;
Park, Suk Young;
Park, J.-G.

Publication type:

Article

The Fusion Gene at the ABO-Secretor Locus (FUT2): absence in Chinese populations.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 181, doi. 10.1007/s100380050138

By:

Liu, Yu-Hua;
Koda, Yoshiro;
Soejima, Mikiko;
Pang, H.;
Wang, Bao-Jie;
Kim, Doo-Sung;
Oh, Heung-Bum;
Kimura, H.

Publication type:

Article

Cloning, tissue expression, and chromosomal assignment of human MRJ gene for a member of the DNAJ protein family.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 185, doi. 10.1007/s100380050139

By:

Seki, Naohiko;
Hattori, Atsushi;
Hayashi, Akiko;
Kozuma, Sumie;
Miyajima, Nobuyuki;
Saito, T.

Publication type:

Article

Isolation and chromosomal mapping of a novel human gene showing homology to Na[sup +] /PO4 cotransporter.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 190, doi. 10.1007/s100380050140

By:

Shibui, Akiko;
Tsunoda, Takeshi;
Seki, Naohiko;
Suzuki, Yutaka;
Sugane, Kazuo;
Sugano, S.

Publication type:

Article

Isolation and chromosomal assignment of a human gene encoding protein inhibitor of activated STAT3 (PIAS3).

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 193, doi. 10.1007/s100380050141

By:

Ueki, Nobuhide;
Seki, Naohiko;
Yano, Kazuhiro;
Saito, Toshiyuki;
Masuho, Yasuhiko;
Muramatsu, M.

Publication type:

Article

Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes (SMC) family.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 197, doi. 10.1007/s100380050142

By:

Nishiwaki, Tadashi;
Daigo, Yataro;
Kawasoe, Teru;
Nagasawa, Yutaka;
Ishiguro, Hideyuki;
Fujita, Manabu;
Furukawa, Yoichi;
Nakamura, Y.

Publication type:

Article

Genomic organization, mapping, and polymorphisms of the gene encoding human cartilage intermediate layer protein (CILP).

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 203, doi. 10.1007/s100380050143

By:

Nakamura, Isao;
Okawa, Akihiko;
Ikegawa, Shiro;
Takaoka, Kunio;
Nakamura, Y.

Publication type:

Article

Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 206, doi. 10.1007/s100380050144

By:

Ogawa, A.;
Yamamoto, Shigenori;
Takayanagi, Masaki;
Kogo, Toshiaki;
Kanazawa, Masaki;
Kohno, Yoichi

Publication type:

Article

Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 210, doi. 10.1007/s100380050145

By:

Hirata, Keiko;
Nakagawa, M.;
Higuchi, Itsuro;
Hashimoto, Kenichiro;
Hanada, Kouichi;
Takahashi, Kouichi;
Niiyama, Takahito;
Izumi, Koutarou;
Sakoda, Shunichi;
Yamada, Hirohisa;
Osame, Mitsuhiro

Publication type:

Article

A novel nonsense mutation at Glu-631 in a Spanish family with complement component 7 deficiency.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 3, p. 215, doi. 10.1007/s100380050146

By:

Horiuchi, T.;
Ferrer, Joana M.;
Serra, P.;
Matamoros, Núria;
López-Trascasa, Margarita;
Hashimura, Chinami;
Niho, Yoshiyuki

Publication type:

Article