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Articles: Basic Science/Genetics |
Prior Articles
Array comparative genomic hybridization of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage-sensitive loci also associated with schizophrenia, autism, and developmental delay
Journal of Medical Genetics, 09/25/09
Small-molecule signal transduction inhibitors: targeted therapeutic agents for single gene disorders
Journal of Medical Genetics, 09/25/09 Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families
Journal of Medical Genetics, 09/25/09 Do genetic predictors of pain sensitivity associate with persistent widespread pain?
Molecular Pain, 09/24/09
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Fragile X prenatal analyses show full mutation females at high risk for mosaic Turner syndrome: Fragile X leads to chromosome loss
American Journal of Medical Genetics, 09/24/09 Chimeric IgG4 PR3-ANCA induces selective inflammatory responses from neutrophils through engagement of Fcgamma receptors
Immunology, 09/24/09 Suppression of ongoing experimental autoimmune myasthenia gravis by transfer of RelB-silenced bone marrow dentritic cells is associated with a change from a T helper Th17/Th1 to a Th2 and FoxP3+ regulatory T-cell profile
Inflammation Research, 09/24/09 Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair
Human Molecular Genetics, 09/24/09 Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15
Human Molecular Genetics, 09/24/09 Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brain
Human Molecular Genetics, 09/24/09 Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways
Human Molecular Genetics, 09/24/09 Ahi1, whose human ortholog is mutated in Joubert syndrome, is required for Rab8a localization, ciliogenesis and vesicle trafficking
Human Molecular Genetics, 09/24/09 Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis
Human Molecular Genetics, 09/24/09 Mutant huntingtin interacts with beta-tubulin and disrupts vesicular transport and insulin secretion
Human Molecular Genetics, 09/24/09 Pathogenic human L1-CAM mutations reduce the adhesion-dependent activation of EGFR
Human Molecular Genetics, 09/24/09 DNA methylation and gene expression differences in children conceived in vitro or in vivo
Human Molecular Genetics, 09/24/09 Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate -secretase activity
Human Molecular Genetics, 09/24/09 Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression
Human Molecular Genetics, 09/24/09 Dysbindin-1 in dorsolateral prefrontal cortex of schizophrenia cases is reduced in an isoform-specific manner unrelated to dysbindin-1 mRNA expression
Human Molecular Genetics, 09/24/09 Metabolic Control in Type 2 Diabetes Is Associated with Sulfonylurea Receptor-1 (SUR-1) but Not with KCNJ11 Polymorphisms
Archives of Medical Research, 09/24/09
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Indexed Journals: New England Journal of Medicine, The Lancet, Archives of Internal Medicine
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250 Available Pages
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