Search

Your search keyword '"Base Sequence"' showing total 868,134 results

Search Constraints

Start Over You searched for: Descriptor "Base Sequence" Remove constraint Descriptor: "Base Sequence"
868,134 results on '"Base Sequence"'

Search Results

101. A machine learning approach to optimizing cell-free DNA sequencing panels: with an application to prostate cancer

102. Insights into the Structure and Energy of DNA Nanoassemblies.

103. Complex DNA sequence readout mechanisms of the DNMT3B DNA methyltransferase

104. Guidelines for Sanger sequencing and molecular assay monitoring

105. Optimized design of single-cell RNA sequencing experiments for cell-type-specific eQTL analysis.

106. Genomic diversity generated by a transposable element burst in a rice recombinant inbred population

107. Distinct RNA N-demethylation pathways catalyzed by nonheme iron ALKBH5 and FTO enzymes enable regulation of formaldehyde release rates

108. Integrated Single-Cell Transcriptomics and Chromatin Accessibility Analysis Reveals Regulators of Mammary Epithelial Cell Identity

109. Identification of the human DPR core promoter element using machine learning

110. Interplay of Effective Surface Area, Mass Transport, and Electrochemical Features in Nanoporous Nucleic Acid Sensors

111. A scoutRNA Is Required for Some Type V CRISPR-Cas Systems

112. lentiMPRA and MPRAflow for high-throughput functional characterization of gene regulatory elements.

113. A molecular map of murine lymph node blood vascular endothelium at single cell resolution.

114. A large-scale binding and functional map of human RNA-binding proteins

115. A comparison of proteomic, genomic, and osteological methods of archaeological sex estimation.

116. MAGGIE: leveraging genetic variation to identify DNA sequence motifs mediating transcription factor binding and function

117. Structural disruption of exonic stem–loops immediately upstream of the intron regulates mammalian splicing

118. DNA methylation profiling demonstrates superior diagnostic classification to RNA-sequencing in a case of metastatic meningioma.

119. Synergy between the anthocyanin and RDR6/SGS3/DCL4 siRNA pathways expose hidden features of Arabidopsis carbon metabolism.

120. Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract.

121. Genome-wide DNA sampling by Ago nuclease from the cyanobacterium Synechococcus elongatus

122. Statistical inference of differential RNA-editing sites from RNA-sequencing data by hierarchical modeling

123. Bacterial alginate regulators and phage homologs repress CRISPR–Cas immunity

124. LSD1-mediated enhancer silencing attenuates retinoic acid signalling during pancreatic endocrine cell development.

125. Multiexon deletion alleles of ATF6 linked to achromatopsia

126. Whole genome sequencing for mutation discovery in a single case of lysosomal storage disease (MPS type 1) in the dog.

127. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex

128. Full-length transcript characterization of SF3B1 mutation in chronic lymphocytic leukemia reveals downregulation of retained introns.

129. The DNA repair enzyme MUTYH potentiates cytotoxicity of the alkylating agent MNNG by interacting with abasic sites

130. A Bayesian framework for inferring the influence of sequence context on point mutations

131. The repertoire of mutational signatures in human cancer

132. Cutting antiparallel DNA strands in a single active site.

133. Perspectives of US private payers on insurance coverage for pediatric and prenatal exome sequencing: Results of a study from the Program in Prenatal and Pediatric Genomic Sequencing (P3EGS)

134. Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico

135. Genomic and phenotypic analyses of six offspring of a genome-edited hornless bull

136. Dissecting the Regulatory Strategies of NF-κB RelA Target Genes in the Inflammatory Response Reveals Differential Transactivation Logics

137. Vortex fluidics-mediated DNA rescue from formalin-fixed museum specimens.

138. A transcomplementing gene drive provides a flexible platform for laboratory investigation and potential field deployment.

139. The Driver of Extreme Human-Specific Olduvai Repeat Expansion Remains Highly Active in the Human Genome

140. Acoustofluidic Salivary Exosome Isolation A Liquid Biopsy Compatible Approach for Human Papillomavirus–Associated Oropharyngeal Cancer Detection

141. Rapture facilitates inexpensive and high-throughput parent-based tagging in salmonids

142. Estrogen Reverses HDAC Inhibitor-Mediated Repression of Aicda and Class-Switching in Antibody and Autoantibody Responses by Downregulation of miR-26a.

143. Distinctiveness of genes contributing to growth of Pseudomonas syringae in diverse host plant species.

144. Asthma and its relationship to mitochondrial copy number: Results from the Asthma Translational Genomics Collaborative (ATGC) of the Trans-Omics for Precision Medicine (TOPMed) program.

145. STAT3 decoy oligonucleotide-carrying microbubbles with pulsed ultrasound for enhanced therapeutic effect in head and neck tumors.

146. In Vitro Selection of an ATP-Binding TNA Aptamer

147. DNA sequence-dependent activity and base flipping mechanisms of DNMT1 regulate genome-wide DNA methylation

148. At the nexus of three kingdoms: the genome of the mycorrhizal fungus Gigaspora margarita provides insights into plant, endobacterial and fungal interactions

149. Comparative Transcriptomics Analyses across Species, Organs, and Developmental Stages Reveal Functionally Constrained lncRNAs

150. West Nile virus in California, 2003–2018: A persistent threat

Catalog

Books, media, physical & digital resources