Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 6

Results: 9

The (CA)n polymorphism of the TNFR2 gene is associated with peak bone density in Chinese nuclear families.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 301, doi. 10.1007/s10038-005-0249-5

By:

Hong Xu;
Lan-Juan Zhao;
Shu-Feng Lei;
Miao-Xin Li;
Xiao Sun;
Fei-Yan Deng;
De-Ke Jiang;
Hong-Wen Deng

Publication type:

Article

The relationship between C677T methylenetetrahydrofolate reductase gene polymorphism and retinopathy in type 2 diabetes: a meta-analysis.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 267, doi. 10.1007/s10038-005-0250-z

By:

Zintzaras, Elias;
Chatzoulis, Dimitrios Z.;
Karabatsas, Costas H.;
Stefanidis, Ioannis

Publication type:

Article

A novel (TG) n(GA) m repeat polymorphism 254 bp downstream of the mast cell chymase ( CMA1) gene is associated with atopic asthma and total serum IgE levels.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 276, doi. 10.1007/s10038-005-0252-x

By:

Sharma, Shilpy;
Rajan, U. Mabali;
Kumar, Amrendra;
Soni, Abha;
Ghosh, Balaram

Publication type:

Article

Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 311, doi. 10.1007/s10038-005-0254-8

By:

Byung-Hoon Jeong;
Nam-Ho Kim;
Jae-Il Kim;
Carp, Richard;
Yong-Sun Kim

Publication type:

Article

Paraoxonase 1 status in the Thai population.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 293, doi. 10.1007/s10038-005-0255-7

By:

Phuntuwate, Wimon;
Suthisisang, Chuthamanee;
Koanantakul, Banhan;
Mackness, Michael;
Mackness, Bharti

Publication type:

Article

A novel locus of coralliform cataract mapped to chromosome 2p24-pter.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 305, doi. 10.1007/s10038-005-0251-y

By:

Linghan Gao;
Wei Qin;
Hao Cui;
Guoyin Feng;
Ping Liu;
Weiqi Gao;
Lin Ma;
Pu Li;
Lin He;
Songbin Fu

Publication type:

Article

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 317, doi. 10.1007/s10038-005-0257-5

By:

Zahed, Laila;
Zahreddine, Hala;
Noureddine, Baha';
Rebeiz, Nelly;
Shakar, Nadine;
Zalloua, Pierre;
Haddad, Fadi

Publication type:

Article

Division of linkage disequilibrium between absolute linkage disequilibrium and linkage equilibrium.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 315, doi. 10.1007/s10038-005-0256-6

By:

Kuno, Shin-ichi

Publication type:

Article

Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus.

Published in:

Journal of Human Genetics, 2005, v. 50, n. 6, p. 283, doi. 10.1007/s10038-005-0253-9

By:

Maeda, Shiro;
Tsukada, Shuichi;
Kanazawa, Akio;
Sekine, Akihiro;
Tsunoda, Tatsuhiko;
Koya, Daisuke;
Maegawa, Hiroshi;
Kashiwagi, Atsunori;
Babazono, Tetsuya;
Matsuda, Masafumi;
Tanaka, Yasushi;
Fujioka, Tomoaki;
Hirose, Hiroshi;
Eguchi, Takashi;
Ohno, Yoichi;
Groves, Christopher;
Hattersley, Andrew;
Hitman, Graham;
Walker, Mark;
Kaku, Kohei

Publication type:

Article

Works matching IS 14345161 AND DT 2005 AND VI 50 AND IP 6

The (CA)<sub>n</sub> polymorphism of the TNFR2 gene is associated with peak bone density in Chinese nuclear families.

The relationship between C677T methylenetetrahydrofolate reductase gene polymorphism and retinopathy in type 2 diabetes: a meta-analysis.

A novel (TG)<sub> n</sub>(GA)<sub> m</sub> repeat polymorphism 254 bp downstream of the mast cell chymase ( CMA1) gene is associated with atopic asthma and total serum IgE levels.

Polymorphisms at codons 56 and 174 of the prion-like protein gene (PRND) are not associated with sporadic Creutzfeldt-Jakob disease.

Paraoxonase 1 status in the Thai population.

A novel locus of coralliform cataract mapped to chromosome 2p24-pter.

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.

Division of linkage disequilibrium between absolute linkage disequilibrium and linkage equilibrium.

Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus.