Works matching IS 09646906 AND DT 2003 AND VI 12 AND IP 2
Results: 28
A central role of interferon regulatory factor-1 for the limitation of neointimal hyperplasia.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 177, doi. 10.1093/hmg/ddg018
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Nonsense mediated decay downregulates conserved alternatively spliced ABCC4 transcripts bearing nonsense codons
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 99, doi. 10.1093/hmg/ddg011
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Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 189, doi. 10.1093/hmg/ddg020
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Interaction of αPIX (ARHGEF6) with β-parvin (PARVB) suggests an involvement of αPIX in integrin-mediated signaling.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 155, doi. 10.1093/hmg/ddg019
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Human BOULE gene rescues meiotic defects in infertile flies.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 169, doi. 10.1093/hmg/ddg017
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The potential role of gene duplications in the evolution of imprinting mechanisms.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 215, doi. 10.1093/hmg/ddg296
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Intramembrane-cleaving aspartic proteases and disease: presenilins, signal peptide peptidase and their homologs.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 201, doi. 10.1093/hmg/ddg303
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Recent advances in the genetics of schizophrenia.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 125, doi. 10.1093/hmg/ddg302
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Williams–Beuren syndrome: a challenge for genotype–phenotype correlations.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 229, doi. 10.1093/hmg/ddg299
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A fragile balance: FMR1 expression levels.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 249, doi. 10.1093/hmg/ddg298
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Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 87, doi. 10.1093/hmg/ddg014
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Pathogenesis of polyglutamine disorders: aggregation revisited.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 173, doi. 10.1093/hmg/ddg295
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PTEN: tumour suppressor, multifunctional growth regulator and more.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 239, doi. 10.1093/hmg/ddg288
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Towards integrated clinico-genomic models for personalized medicine: combining gene expression signatures and clinical factors in breast cancer outcomes prediction.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 153, doi. 10.1093/hmg/ddg287
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DNA methylation and Rett syndrome.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 221, doi. 10.1093/hmg/ddg286
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Disorders of mitochondrial protein synthesis.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 293, doi. 10.1093/hmg/ddg285
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The zebrafish as a model for muscular dystrophy and congenital myopathy.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 265, doi. 10.1093/hmg/ddg279
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Proteomics of heart disease.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 135, doi. 10.1093/hmg/ddg278
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Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 195, doi. 10.1093/hmg/ddg276
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Therapeutic gene silencing in the nervous system.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 279, doi. 10.1093/hmg/ddg275
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Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatases.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 285, doi. 10.1093/hmg/ddg273
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Glycosylation defects: a new mechanism for muscular dystrophy?
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 259, doi. 10.1093/hmg/ddg272
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Fly models of Huntington's disease.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 187, doi. 10.1093/hmg/ddg271
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Genomic microarrays in human genetic disease and cancer.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 145, doi. 10.1093/hmg/ddg261
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Perturbations of chromatin structure in human genetic disease: recent advances.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 207, doi. 10.1093/hmg/ddg260
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Exposing the MYtH about base excision repair and human inherited disease.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 159, doi. 10.1093/hmg/ddg259
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Of mice and (wo)men: genotype–phenotype correlations in BRCA1.
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- Human Molecular Genetics, 2003, v. 12, n. 2, p. 271, doi. 10.1093/hmg/ddg258
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The Newfoundland population: a unique resource for genetic investigation of complex diseases†Newfound Genomics is a private genomics company based in Newfoundland. Sylvia Bartlett and Lynette Peddle are laboratory scientists at Newfound Genomics. Dr ...
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 2, p. 167, doi. 10.1093/hmg/ddg257
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