Cargando…

Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits

Detalles Bibliográficos
Autores principales:	Paul, Dirk S., Nisbet, James P., Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R., Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D., Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2011
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144961/ http://dx.doi.org/10.1371/annotation/5d0c3be4-6f34-420a-960f-0a880bbf6128

Ejemplares similares

Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits
por: Paul, Dirk S., et al.
Publicado: (2011)

Monocyte Gene Expression Signature of Patients with Early Onset Coronary Artery Disease
por: Sivapalaratnam, Suthesh, et al.
Publicado: (2012)

Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci
por: Paul, Dirk S., et al.
Publicado: (2013)

Identification of candidate genes linking systemic inflammation to atherosclerosis; results of a human in vivo LPS infusion study
por: Sivapalaratnam, Suthesh, et al.
Publicado: (2011)

Increased bleeding and thrombosis in myeloproliferative neoplasms mediated through altered expression of inherited platelet disorder genes
por: Mitchell, Alan, et al.
Publicado: (2023)

Genome-wide Analysis of Simultaneous GATA1/2, RUNX1, FLI1, and SCL Binding in Megakaryocytes Identifies Hematopoietic Regulators
por: Tijssen, Marloes R., et al.
Publicado: (2011)

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome
por: Albers, Cornelis A, et al.
Publicado: (2011)

Platelets in Patients with Premature Coronary Artery Disease Exhibit Upregulation of miRNA340* and miRNA624*
por: Sondermeijer, Brigitte M., et al.
Publicado: (2011)

Mutation in KERA Identified by Linkage Analysis and Targeted Resequencing in a Pedigree with Premature Atherosclerosis
por: Maiwald, Stephanie, et al.
Publicado: (2014)

Single site-specific integration targeting coupled with embryonic stem cell differentiation provides a high-throughput alternative to in vivo enhancer analyses
por: Wilkinson, Adam C., et al.
Publicado: (2013)

Genome-Scale Technology Driven Advances to Research into Normal and Malignant Haematopoiesis
por: Göttgens, Berthold
Publicado: (2012)

Protocol: Precision engineering of plant gene loci by homologous recombination cloning in Escherichia coli
por: Roden, Laura C, et al.
Publicado: (2005)

Genome-Wide Association Studies in Atherosclerosis
por: Sivapalaratnam, S., et al.
Publicado: (2011)

Transcriptional mechanisms of cell fate decisions revealed by single cell expression profiling
por: Moignard, Victoria, et al.
Publicado: (2014)

Concerted bioinformatic analysis of the genome-scale blood transcription factor compendium reveals new control mechanisms
por: Joshi, Anagha, et al.
Publicado: (2014)

Dysregulation of haematopoietic stem cell regulatory programs in acute myeloid leukaemia
por: Basilico, Silvia, et al.
Publicado: (2017)

Lupus Anticoagulant and Abnormal Coagulation Tests in Patients with Covid-19
por: Bowles, Louise, et al.
Publicado: (2020)

Evolution of candidate transcriptional regulatory motifs since the human-chimpanzee divergence
por: Donaldson, Ian J, et al.
Publicado: (2006)

CoMoDis: composite motif discovery in mammalian genomes
por: Donaldson, Ian J., et al.
Publicado: (2007)

TFBScluster web server for the identification of mammalian composite regulatory elements
por: Donaldson, Ian J., et al.
Publicado: (2006)

Transcriptional network control of normal and leukaemic haematopoiesis
por: Sive, Jonathan I., et al.
Publicado: (2014)

Machine learning predicts putative hematopoietic stem cells within large single-cell transcriptomics data sets
por: Hamey, Fiona K., et al.
Publicado: (2019)

Single-Cell Sequencing in Normal and Malignant Hematopoiesis
por: Wilson, Nicola K., et al.
Publicado: (2018)

DNA sequence and structural properties as predictors of human and mouse promoters
por: Akan, Pelin, et al.
Publicado: (2008)

Mipomersen, an apolipoprotein B synthesis inhibitor, lowers low-density lipoprotein cholesterol in high-risk statin-intolerant patients: a randomized, double-blind, placebo-controlled trial
por: Visser, Maartje E., et al.
Publicado: (2012)

Transcription factor co-localization patterns affect human cell type-specific gene expression
por: Wang, Dennis, et al.
Publicado: (2012)

A new RNASeq-based reference transcriptome for sugar beet and its application in transcriptome-scale analysis of vernalization and gibberellin responses
por: Mutasa-Göttgens, Effie S, et al.
Publicado: (2012)

Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations
por: Pöyhönen, Pauli, et al.
Publicado: (2015)

Single Nucleotide Polymorphisms with Cis-Regulatory Effects on Long Non-Coding Transcripts in Human Primary Monocytes
por: Carlsson Almlöf, Jonas, et al.
Publicado: (2014)

Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies
por: Yang, Tsun-Po, et al.
Publicado: (2010)

Single-cell analyses of regulatory network perturbations using enhancer-targeting TALEs suggest novel roles for PU.1 during haematopoietic specification
por: Wilkinson, Adam C., et al.
Publicado: (2014)

Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing
por: Vattulainen, Sanna, et al.
Publicado: (2015)

Compendio de historia universal
por: Basart y Dalmasas, Valentín
Publicado: (1879)

Gene set control analysis predicts hematopoietic control mechanisms from genome-wide transcription factor binding data
por: Joshi, Anagha, et al.
Publicado: (2013)

The LMO2 -25 Region Harbours GATA2-Dependent Myeloid Enhancer and RUNX-Dependent T-Lymphoid Repressor Activity
por: Bonadies, Nicolas, et al.
Publicado: (2015)

Determining Physical Mechanisms of Gene Expression Regulation from Single Cell Gene Expression Data
por: Ezer, Daphne, et al.
Publicado: (2016)

Prognostic value of myocardial perfusion scintigraphy in type 2 diabetic patients with mild, stable angina pectoris
por: Wiersma, Jacobijne J., et al.
Publicado: (2009)

High-throughput elucidation of thrombus formation reveals sources of platelet function variability
por: van Geffen, Johanna P., et al.
Publicado: (2019)

Comparison of Methods for Competitive Tests of Pathway Analysis
por: Evangelou, Marina, et al.
Publicado: (2012)

A HaemAtlas: characterizing gene expression in differentiated human blood cells
por: Watkins, Nicholas A., et al.
Publicado: (2009)

Cannot write session to /tmp/vufind_sessions/sess_sml9lfm1ajrnthguv26ctgt3fe