Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 1
Results: 27
Natural competence of mammalian mitochondria allows the molecular investigation of mitochondrial gene expression.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 143, doi. 10.1093/hmg/ddi435
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- Article
Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in mice.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 113, doi. 10.1093/hmg/ddi433
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Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 65, doi. 10.1093/hmg/ddi427
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Polymorphisms in the PON gene cluster are associated with Alzheimer disease.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 77, doi. 10.1093/hmg/ddi428
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- Article
Distinct expression profile in fumarate-hydratase-deficient uterine fibroids.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 97, doi. 10.1093/hmg/ddi431
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IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 1, doi. 10.1093/hmg/ddi398
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- Article
Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear poly(A)-binding protein with a single-domain intracellular antibody.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 105, doi. 10.1093/hmg/ddi432
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Aberrant dysferlin trafficking in cells lacking caveolin or expressing dystrophy mutants of caveolin-3.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 129, doi. 10.1093/hmg/ddi434
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- Article
Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 23, doi. 10.1093/hmg/ddi422
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- Article
Proteasome impairment does not contribute to pathogenesis in R6/2 Huntington’s disease mice: exclusion of proteasome activator REGγ as a therapeutic target.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 33, doi. 10.1093/hmg/ddi423
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Telomere instability in the male germline.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 45, doi. 10.1093/hmg/ddi424
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- Article
Intracerebral adeno-associated virus-mediated gene transfer in rapidly progressive forms of metachromatic leukodystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 53, doi. 10.1093/hmg/ddi425
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- Article
Identification and characterization of the methyl arginines in the fragile X mental retardation protein Fmrp.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 87, doi. 10.1093/hmg/ddi429
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- Article
Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 155, doi. 10.1093/hmg/ddi436
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- Article
Loss of polycystin-1 or polycystin-2 results in dysregulated apolipoprotein expression in murine tissues via alterations in nuclear hormone receptors.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. 11, doi. 10.1093/hmg/ddi421
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- Article
The emerging science of epigenomics.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r95, doi. 10.1093/hmg/ddl095
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Pharmacogenomics: from bedside to clinical practice.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r89, doi. 10.1093/hmg/ddl087
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Integrating biological data through the genome.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r81, doi. 10.1093/hmg/ddl086
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- Article
Sleeping beauty: a novel cancer gene discovery tool.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r75, doi. 10.1093/hmg/ddl061
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Lessons from studying monogenic disease for common disease.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r67, doi. 10.1093/hmg/ddl060
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Structural variants: changing the landscape of chromosomes and design of disease studies.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r57, doi. 10.1093/hmg/ddl057
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Evolution at the nucleotide level: the problem of multiple whole-genome alignment.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r51, doi. 10.1093/hmg/ddl056
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Ethical issues in medical-sequencing research: implications of genotype–phenotype studies for individuals and populations.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r45, doi. 10.1093/hmg/ddl049
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From genome to proteome: developing expression clone resources for the human genome.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r31, doi. 10.1093/hmg/ddl048
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Non-coding RNA.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r17, doi. 10.1093/hmg/ddl046
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Influence of human genome polymorphism on gene expression.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r9, doi. 10.1093/hmg/ddl044
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Genome-wide location analysis: insights on transcriptional regulation.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r1, doi. 10.1093/hmg/ddl043
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- Article