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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
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
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
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
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
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
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
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

Found: 9

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

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.

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

Paraoxonase 1 status in the Thai population.

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

Molecular basis of oculocutaneous albinism type 1 in Lebanese patients.

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

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.