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Articles: Basic Science/Genetics |
Prior Articles
Potential late-onset Alzheimer's disease-associated mutations in the ADAM10 gene attenuate -secretase activity
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 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 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 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 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 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 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 Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways
Human Molecular Genetics, 09/24/09 Pro12Ala Polymorphism in PPAR?2 Associated with Depression in Chinese Nonagenarians/Centenarians
Archives of Medical Research, 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 Do genetic predictors of pain sensitivity associate with persistent widespread pain?
Molecular Pain, 09/24/09
Free full text
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 Intrarenal Dopamine Attenuates Deoxycorticosterone Acetate/High Salt–Induced Blood Pressure Elevation in Part Through Activation of a Medullary Cyclooxygenase 2 Pathway
Hypertension, 09/23/09 P53 is dispensable for the induction of apoptosis after inhibition of protein kinase CK2
The Prostate, 09/23/09 SRD5A2 V89L polymorphism and prostate cancer risk: A meta-analysis
The Prostate, 09/23/09 Development and Validation of a Fluorescent Microsphere Immunoassay for Soluble CD30 Testing
Clinical and Vaccine Immunology, 09/23/09
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Indexed Journals: American Family Physician, Archives of Family Med, Annals of Family Med
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