Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
about
Development of a blood-based gene expression algorithm for assessment of obstructive coronary artery disease in non-diabetic patientsFunctional SNP of ARHGEF10 confers risk of atherothrombotic strokeThe Guanine nucleotide exchange factor kalirin-7 is a novel synphilin-1 interacting protein and modifies synphilin-1 aggregate transport and formationValidation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smokingAbnormal kalirin signaling in neuropsychiatric disorders.Rho GAPs and GEFs: controling switches in endothelial cell adhesionSmall G proteins in the cardiovascular system: physiological and pathological aspectsKalrn plays key roles within and outside of the nervous systemKalirin promotes neointimal hyperplasia by activating Rac in smooth muscle cellsGene Expression Profiles Link Respiratory Viral Infection, Platelet Response to Aspirin, and Acute Myocardial InfarctionElimination of Kalrn expression in POMC cells reduces anxiety-like behavior and contextual fear learning.Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reportsGenetic and functional association of FAM5C with myocardial infarctionNeuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosisUsing Kalirin conditional knockout mice to distinguish its role in dopamine receptor mediated behaviorsKalrn promoter usage and isoform expression respond to chronic cocaine exposureGenetic Variant of Kalirin Gene Is Associated with Ischemic Stroke in a Chinese Han Population.Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5Genetic analysis of polymorphisms in the kalirin gene for association with age-at-onset in European Huntington disease patients.Identification of kalirin-7 as a potential post-synaptic density signaling hubResequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility.Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.Transcriptional Profiling of Cultured, Embryonic Epicardial Cells Identifies Novel Genes and Signaling Pathways Regulated by TGFβR3 In Vitro.Association of Roadway Proximity with Fasting Plasma Glucose and Metabolic Risk Factors for Cardiovascular Disease in a Cross-Sectional Study of Cardiac Catheterization Patients.Genetic and genomic insights into the molecular basis of atherosclerosis.A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience.The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variablesAn LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.CdGAP/ARHGAP31, a Cdc42/Rac1 GTPase regulator, is critical for vascular development and VEGF-mediated angiogenesis.Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.The genetic basis for survivorship in coronary artery disease.Aspirin exposure reveals novel genes associated with platelet function and cardiovascular events.Molecular signatures of cardiovascular disease risk: potential for test development and clinical application.Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.Neuronal Rho GEFs in synaptic physiology and behavior.Nonenzymatic domains of Kalirin7 contribute to spine morphogenesis through interactions with phosphoinositides and AblKalirin signaling: implications for synaptic pathology.Kalirin, a key player in synapse formation, is implicated in human diseases.
P2860
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P2860
Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Peakwide mapping on chromosome ...... e for coronary artery disease.
@ast
Peakwide mapping on chromosome ...... e for coronary artery disease.
@en
type
label
Peakwide mapping on chromosome ...... e for coronary artery disease.
@ast
Peakwide mapping on chromosome ...... e for coronary artery disease.
@en
prefLabel
Peakwide mapping on chromosome ...... e for coronary artery disease.
@ast
Peakwide mapping on chromosome ...... e for coronary artery disease.
@en
P2093
P2860
P50
P356
P1476
Peakwide mapping on chromosome ...... e for coronary artery disease.
@en
P2093
A Brent Hale
Carol Haynes
Christopher J H Jones
David Crosslin
David Crossman
Elizabeth R Hauser
Liyong Wang
Marco Harris
Pascal J Goldschmidt-Clermont
P2860
P304
P356
10.1086/512981
P407
P50
P577
2007-02-08T00:00:00Z