452 results on '"Pfeufer Arne"'
Search Results
102. Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy
103. Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25
104. Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction
105. Correction: Genetic Structure of Europeans: A View from the North–East
106. Common variants in KCNN3 are associated with lone atrial fibrillation
107. Genome-wide association study of PR interval
108. Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery
109. Drug-Sensitized Zebrafish Screen Identifies Multiple Genes, Including GINS3 , as Regulators of Myocardial Repolarization
110. A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations
111. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
112. Genetic Structure of Europeans: A View from the North–East
113. Common variants at ten loci modulate the QT interval duration in the QTSCD Study
114. Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes
115. Response to comments on 'a common genetic variant is associated with adult and childhood obesity'
116. Long QT Syndrome–Associated Mutations in KCNQ1 and KCNE1 Subunits Disrupt Normal Endosomal Recycling of I Ks Channels
117. Common Genetic Variants in ANK2 Modulate QT Interval
118. SLC2A9 influences uric acid concentrations with pronounced sex-specific effects
119. Variability of intraindividual QT interval estimates corrected for heart rate in a population-based follow-up study
120. Abstract 640: Common Genetic Variation in the Promotor of the Ankyrin-2 Gene Modifies QT Interval
121. Increased long-term QT interval variability in individuals with an abnormal electrocardiogram at baseline results from a population study
122. Association mapping of QT interval in a 500k genome-wide scan: confirmation of NOS1AP and identification of a spectrum of additional QTLS
123. Genetics of the ECG: QT or not QT- A genetic analysis of a complex electrophysiological trait confirms several previously detected associations
124. Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation
125. The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts
126. Regulation of Endocytic Recycling of KCNQ1/KCNE1 Potassium Channels
127. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.
128. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
129. No Replication of Association Between Estrogen Receptor α Gene Polymorphisms and Susceptibility to Myocardial Infarction in a Large Sample of Patients of European Descent
130. Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population
131. The association of a SNP upstream of INSIG2 with Body Mass Index is reproduced in several but not all cohorts
132. Global gene expression in human myocardium?oligonucleotide microarray analysis of regional diversity and transcriptional regulation in heart failure
133. The intron 6 G/T polymorphism of c-myb oncogene and the risk for coronary in-stent restenosis
134. TaqMan Systems for Genotyping of Disease-Related Polymorphisms Present in the Gene Encoding Apolipoprotein E
135. Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
136. 13. Jahrestagung der Sektion Molekulare Diagnostik der DGKL am 15. und 16. Mai 2014 in der Evangelischen Akademie Tutzing Report on the 13th Annual Meeting of the Section of Molecular Diagnostics of the DGKL on 15th/16th May 2014 in Tutzing
137. Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21
138. Chymase gene locus is not associated with myocardial infarction and is not linked to heart size or blood pressure
139. Angiotensin-Converting Enzyme and Heart Chymase gene Polymorphisms in Hypertrophic Cardiomyopathy**This study was supported by a grant-in-aid from the Bundesministerium für Bildung und Forschung and the European commission grant (ERBCHBGCT 940725.
140. SNP Prioritization Using a Bayesian Probability of Association.
141. Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.
142. Lack of replication in polymorphisms reported to be associated with atrial fibrillation.
143. Genome-Wide Association Studies of the PR Interval in African Americans.
144. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
145. Long QT Syndrome—Associated Mutations in KCNQ1 and KCNE1 Subunits Disrupt Normal Endosomal Recycling of I[subKs] Channels.
146. A multimetric approach to analysis of genome-wide association by single markers and composite likelihood.
147. Functional profiling of human atrial and ventricular gene expression.
148. SNiPA: an interactive, genetic variant-centered annotation browser.
149. A Large Candidate Gene Survey Identifies the KCNE1D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
150. Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
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