Works matching IS 14345161 AND DT 2004 AND VI 49 AND IP 9

Results: 8

Comparison between various strategies for the disease-gene mapping using linkage disequilibrium analyses: studies on adenine phosphoribosyltransferase deficiency used as an example.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 463, doi. 10.1007/s10038-004-0175-y

By:

Kuno, Shin-ichi;
Taniguchi, Atsuo;
Saito, Akira;
Tsuchida-Otsuka, Sanae;
Kamatani, Naoyuki

Publication type:

Article

Association of paraoxonase 1 gene polymorphisms with risk of Parkinson’s disease: a meta-analysis.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 474, doi. 10.1007/s10038-004-0176-x

By:

Zintzaras, Elias;
Hadjigeorgiou, Georgios M.

Publication type:

Article

Genetic background of people in the Dominican Republic with or without obese type 2 diabetes revealed by mitochondrial DNA polymorphism.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 495, doi. 10.1007/s10038-004-0179-7

By:

Tajima, Atsushi;
Hamaguchi, Kazuyuki;
Terao, Hideo;
Oribe, Ayako;
Perrotta, Victor M.;
Baez, Carlos Amoros;
Arias, Jose R.;
Yoshimatsu, Hironobu;
Sakata, Toshiie;
Horai, Satoshi

Publication type:

Article

Association between the PPARa-L162V polymorphism and components of the metabolic syndrome.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 482, doi. 10.1007/s10038-004-0177-9

By:

Robitaille, Julie;
Brouillette, Charles;
Houde, Alain;
Lemieux, Simone;
Pérusse, Louis;
Tchernof, André;
Gaudet, Daniel;
Vohl, Marie-Claude

Publication type:

Article

Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 500, doi. 10.1007/s10038-004-0180-1

By:

Lupi, Anna;
De Riso, Antonio;
Della Torre, Sara;
Rossi, Antonio;
Campari, Elena;
Vilarinho, Laura;
Cetta, Giuseppe;
Forlino, Antonella

Publication type:

Article

Identification of a common mutation in mucopolysaccharidosis IVA: correlation among genotype, phenotype, and keratan sulfate.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 490, doi. 10.1007/s10038-004-0178-8

By:

Tomatsu, Shunji;
Dieter, Tatiana;
Schwartz, Ida V.;
Sarmient, Piedad;
Giugliani, Roberto;
Barrera, Luis A.;
Guelbert, Norberto;
Kremer, Raquel;
Repetto, Gabriela M.;
Gutierrez, Monica A.;
Nishioka, Tatsuo;
Peña Serrato, Olga;
Montaño, Adriana Maria;
Yamaguchi, Seiji;
Noguchi, Akihiko

Publication type:

Article

Identification of 108 SNPs inTSC,WNK1, andWNK4and their association with hypertension in a Japanese general population.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 507, doi. 10.1007/s10038-004-0181-0

By:

Kokubo, Yoshihiro;
Kamide, Kei;
Inamoto, Nozomu;
Tanaka, Chihiro;
Banno, Mariko;
Takiuchi, Shin;
Kawano, Yuhei;
Tomoike, Hitonobu;
Miyata, Toshiyuki

Publication type:

Article

High throughput multiple combination extraction from large scale polymorphism data by exact tree method.

Published in:

Journal of Human Genetics, 2004, v. 49, n. 9, p. 455, doi. 10.1007/s10038-004-0174-z

By:

Miyaki, Koichi;
Omae, Kazuyuki;
Murata, Mitsuru;
Tanahashi, Norio;
Saito, Ikuo;
Watanabe, Kiyoaki

Publication type:

Article