Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 19
Results: 15
Depletion of type IA regulatory subunit (RIα) of protein kinase A (PKA) in mammalian cells and tissues activates mTOR and causes autophagic deficiency.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2962, doi. 10.1093/hmg/ddl239
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- Article
VEGF polymorphisms are associated with neovascular age-related macular degeneration.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2955, doi. 10.1093/hmg/ddl238
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- Article
CTCF binding sites promote transcription initiation and prevent DNA methylation on the maternal allele at the imprinted H19/Igf2 locus.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2945, doi. 10.1093/hmg/ddl237
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- Article
Identification of gene expression signatures in autoimmune disease without the influence of familial resemblance.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2973, doi. 10.1093/hmg/ddl236
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- Publication type:
- Article
Targeted disruption of the synovial sarcoma-associated SS18 gene causes early embryonic lethality and affects PPARBP expression.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2936, doi. 10.1093/hmg/ddl235
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- Article
Downstream target genes of the neuropeptide S–NPSR1 pathway.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2923, doi. 10.1093/hmg/ddl234
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- Article
Conserved distances between vertebrate highly conserved elements.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2911, doi. 10.1093/hmg/ddl232
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- Publication type:
- Article
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21–q24 from a high-density SNP genome-wide linkage scan.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2903, doi. 10.1093/hmg/ddl231
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- Publication type:
- Article
C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3ε.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2888, doi. 10.1093/hmg/ddl230
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- Article
Variation in MICA and MICB genes and enhanced susceptibility to paucibacillary leprosy in South India.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2880, doi. 10.1093/hmg/ddl229
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- Article
Complementary roles of genes regulated by two paternally methylated imprinted regions on chromosomes 7 and 12 in mouse placentation.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2869, doi. 10.1093/hmg/ddl228
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- Article
Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2972, doi. 10.1093/hmg/ddl226
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- Article
Aberrant cortical synaptic plasticity and dopaminergic dysfunction in a mouse model of huntington's disease.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2856, doi. 10.1093/hmg/ddl224
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- Publication type:
- Article
Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans.
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- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2846, doi. 10.1093/hmg/ddl219
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- Article
Neurofibromin plays a critical role in modulating osteoblast differentiation of mesenchymal stem/progenitor cells.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 19, p. 2837
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- Publication type:
- Article