Works matching IS 09646906 AND DT 2005 AND VI 14 AND IP 19
Results: 16
Distinct gene expression profiles and reduced JNK signaling in retinitis pigmentosa caused by RP1 mutations.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2945, doi. 10.1093/hmg/ddi325
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- Article
Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasia.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2929, doi. 10.1093/hmg/ddi324
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- Article
Functional SNPs in the distal promoter of the ST2 gene are associated with atopic dermatitis.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2919, doi. 10.1093/hmg/ddi323
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- Article
Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2911, doi. 10.1093/hmg/ddi322
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- Article
Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2893, doi. 10.1093/hmg/ddi321
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- Article
FcγRIIB Ile232Thr transmembrane polymorphism associated with human systemic lupus erythematosus decreases affinity to lipid rafts and attenuates inhibitory effects on B cell receptor signaling.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2881, doi. 10.1093/hmg/ddi320
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- Publication type:
- Article
HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2871, doi. 10.1093/hmg/ddi319
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- Publication type:
- Article
The 'involution' of mannose-binding lectin.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2859, doi. 10.1093/hmg/ddi318
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- Article
Pas1, a G<sub>1</sub> cyclin, regulates amino acid uptake and rescues a delay in G<sub>1</sub> arrest in Tsc1 and Tsc2 mutants in Schizosaccharomyces pombe.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2851, doi. 10.1093/hmg/ddi317
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- Publication type:
- Article
A-type lamins are essential for TGF-β1 induced PP2A to dephosphorylate transcription factors.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2839, doi. 10.1093/hmg/ddi316
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- Publication type:
- Article
The soluble epoxide hydrolase gene harbors sequence variation associated with susceptibility to and protection from incident ischemic stroke.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2829, doi. 10.1093/hmg/ddi315
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- Article
Engineering translocations with delayed replication: evidence for cis control of chromosome replication timing.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2813, doi. 10.1093/hmg/ddi314
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- Publication type:
- Article
Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2801, doi. 10.1093/hmg/ddi313
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- Publication type:
- Article
Endoplasmic reticulum stress compromises the ubiquitin–proteasome system.
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- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2787
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- Publication type:
- Article
Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2779, doi. 10.1093/hmg/ddi311
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- Publication type:
- Article
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 19, p. 2769, doi. 10.1093/hmg/ddi310
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- Publication type:
- Article