Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits
Journal Article
Overview
publication date
- December 1, 2020
has subject area
- Biochemical Phenomena - Enhancer Elements, Genetic
- Biochemical Phenomena - Transcription, Genetic
- Carrier Proteins - Smad1 Protein
- Cells - Erythrocytes
- DNA-Binding Proteins
- DNA-Binding Proteins - Smad1 Protein
- Disease Attributes - Genetic Predisposition to Disease
- Environment and Public Health - Genome-Wide Association Study
- Environment and Public Health - Genome-Wide Association Study
- Erythroid Cells - Erythrocytes
- Gene Expression - Transcription, Genetic
- Gene Expression Regulation
- Genetic Association Studies - Genome-Wide Association Study
- Genetic Structures - Enhancer Elements, Genetic
- Genetic Techniques - Genome-Wide Association Study
- Genotype - Genetic Predisposition to Disease
- Hemic and Immune Systems - Erythrocytes
- Humans
- Investigative Techniques - Genome-Wide Association Study
- Investigative Techniques - Genome-Wide Association Study
- Peptides - Smad1 Protein
- Phenotype
- Phosphoproteins - Smad1 Protein
- Polymorphism, Single Nucleotide
- Proteins - Smad1 Protein
- Quantitative Trait Loci
- Regulatory Elements, Transcriptional - Enhancer Elements, Genetic
- Sequence Analysis - Genome-Wide Association Study
- Transcription Factors
- Transcription Factors - Smad1 Protein
has restriction
- green
Date in CU Experts
- December 17, 2020 10:15 AM
Full Author List
- Choudhuri A; Trompouki E; Abraham BJ; Colli LM; Kock KH; Mallard W; Yang M-L; Vinjamur DS; Ghamari A; Sporrij A
author count
- 33
citation count
- 21
published in
- Nature Genetics Journal
Other Profiles
International Standard Serial Number (ISSN)
- 1061-4036
Electronic International Standard Serial Number (EISSN)
- 1546-1718
Digital Object Identifier (DOI)
Additional Document Info
start page
- 1333
end page
- 1345
volume
- 52
issue
- 12