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101. Which QTc interval estimate is better for predicting sudden death?

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

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

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

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

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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