Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 13
Results: 16
Dynamin-binding protein gene on chromosome 10q is associated with late-onset Alzheimer's disease.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2170, doi. 10.1093/hmg/ddl142
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- Article
Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2157, doi. 10.1093/hmg/ddl141
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- Article
From genome to proteome: developing expression clone resources for the human genome.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2184, doi. 10.1093/hmg/ddl140
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- Article
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2183, doi. 10.1093/hmg/ddl139
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- Article
Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2146, doi. 10.1093/hmg/ddl138
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- Article
MBNL1 and CUGBP1 modify expanded CUG-induced toxicity in a Drosophila model of myotonic dystrophy type 1.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2138, doi. 10.1093/hmg/ddl137
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- Article
Fusion between CIC and DUX4 up-regulates PEA3 family genes in Ewing-like sarcomas with t(4;19)(q35;q13) translocation.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2125, doi. 10.1093/hmg/ddl136
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- Article
Biologically active molecules that reduce polyglutamine aggregation and toxicity.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2114, doi. 10.1093/hmg/ddl135
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- Article
TRPV6 exhibits unusual patterns of polymorphism and divergence in worldwide populations.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2106, doi. 10.1093/hmg/ddl134
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Distant conserved sequences flanking endothelial-specific promoters contain tissue-specific DNase-hypersensitive sites and over-represented motifs.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2098, doi. 10.1093/hmg/ddl133
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- Article
Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2087, doi. 10.1093/hmg/ddl132
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- Article
Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin–protein ligase with monoubiquitylation capacity.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2059, doi. 10.1093/hmg/ddl131
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- Article
Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2076, doi. 10.1093/hmg/ddl130
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- Article
Suppression of Parkin enhances nigrostriatal and motor neuron lesion in mice over-expressing human-mutated tau protein.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2045
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- Article
Frequent genetic and epigenetic abnormalities contribute to the deregulation of cytoglobin in non-small cell lung cancer.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2038, doi. 10.1093/hmg/ddl128
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- Article
Sonic Hedgehog, a key development gene, experienced intensified molecular evolution in primates.
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- Human Molecular Genetics, 2006, v. 15, n. 13, p. 2031, doi. 10.1093/hmg/ddl123
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- Article