Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 22
Results: 19
Association of the tumour necrosis factor-308 variant with differential response to anti-TNF agents in the treatment of rheumatoid arthritis.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3532
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- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. NP, doi. 10.1093/hmg/ddn349
- Publication type:
- Article
The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3509, doi. 10.1093/hmg/ddn243
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- Article
A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3539, doi. 10.1093/hmg/ddn247
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- Article
Scrib regulates PAK activity during the cell migration process.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3552, doi. 10.1093/hmg/ddn248
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- Article
The common obesity variant near MC4R gene is associated with higher intakes of total energy and dietary fat, weight change and diabetes risk in women.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3502, doi. 10.1093/hmg/ddn242
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- Article
The in vivo mitochondrial two-step maturation of human frataxin.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3521, doi. 10.1093/hmg/ddn244
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- Article
A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3446, doi. 10.1093/hmg/ddn238
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- Article
Protective role of Engrailed in a Drosophila model of Huntington's disease.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3601, doi. 10.1093/hmg/ddn255
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- Article
Expression of p21waf1/Cip1 in stromal fibroblasts of primary breast tumors.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3596, doi. 10.1093/hmg/ddn252
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- Article
A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3577, doi. 10.1093/hmg/ddn251
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. NP, doi. 10.1093/hmg/ddn346
- Publication type:
- Article
Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in α-mannosidosis mice.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3437, doi. 10.1093/hmg/ddn237
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- Article
Endoplasmic reticulum quality control: a new mechanism of E-cadherin regulation and its implication in cancer.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3566, doi. 10.1093/hmg/ddn249
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- Publication type:
- Article
Functional and structural basis of the nuclear localization signal in the ZIC3 zinc finger domain.
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- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3459, doi. 10.1093/hmg/ddn239
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- Article
The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3487, doi. 10.1093/hmg/ddn241
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. NP, doi. 10.1093/hmg/ddn347
- Publication type:
- Article
Amyloid precursor protein-induced axonopathies are independent of amyloid-β peptides.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. 3474, doi. 10.1093/hmg/ddn240
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 22, p. NP, doi. 10.1093/hmg/ddn348
- Publication type:
- Article