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CRELD1
Twelve-Year Changes in Protein Profiles in Patients with and Without Gastric Bypass Surgery
Genetics of Atrioventricular Canal Defects Flaminia Pugnaloni1, Maria Cristina Digilio2, Carolina Putotto1, Enrica De Luca1, Bruno Marino1 and Paolo Versacci1*
Contribution of Copy-Number Variation to Down Syndrome–Associated Atrioventricular Septal Defects
Identification of Prognostic and Metastasis-Related Alternative
Rodent Models in Down Syndrome Research: Impact and Future Opportunities Yann Herault1,2,3,4,5,*, Jean M
The Transcription Factor Sox7 Modulates Endocardiac Cushion
Mouse Creld1 Conditional Knockout Project (CRISPR/Cas9)
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
Anti-CRELD1 (Human) Mab O Code No
CRELD1 ELISA Kit (Human) (OKCD01997) Lot# KD2122
Molecular Genetic Analysis of CRELD1 in Patients with Heterotaxy Disorder
CRELD1 Is an Evolutionarily-Conserved Maturational Enhancer of Ionotropic Acetylcholine Receptors
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Co-Expression Networks Reveal the Tissue-Specific Regulation of Transcription and Splicing
Using the Ts65dn Mouse Model of Down Syndrome to Understand the Genetics of Congenital Heart Defects
Plasma Protein Expression Profiles, Cardiovascular Disease, And
Report Missense Mutations in CRELD1 Are Associated With
Overview of the Matrisome—An Inventory of Extracellular Matrix Constituents and Functions
Top View
Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio Rerio
Assessing Conservation of Alternative Splicing with Evolutionary Splicing Graphs
Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier
Basic Composition and Alterations in Chronic Lung Disease
3P25 Deletions
Identifying Patients with Atrioventricular Septal Defect in Down Syndrome Populations by Using Self-Normalizing Neural Networks and Feature Selection
An Investigation of Gene Networks Influenced by Low Dose Ionizing Radiation Using Statistical and Graph Theoretical Algorithms
Genetic Modifiers Predisposing to Congenital Heart Disease in the Sensitized Down Syndrome Population
A Novel Gene Complementing Resistance to Bordetella
CRELD1 (NM 001031717) Human Recombinant Protein Product Data
Genetic Modifiers Predisposing to Congenital
A Novel CRELD1/VEGF Genetic Interaction in Heart Disease and Development
Hsf1base: a Comprehensive Database of HSF1 (Heat Shock Factor 1) Target Genes
Sericin-Induced Melanogenesis in Cultured Retinal Pigment Epithelial Cells Is Associated with Elevated Levels of Hydrogen Peroxide and Inflammatory Proteins
Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier
Exome Sequencing Reveals Novel IRXI Mutation in Congenital Heart Disease
Allelic Interaction Between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects
Novel Copy-Number Variants in a Population-Based Investigation of Classic Heterotaxy
Integrated Analyses of Early Responses to Radiation In
Science Day 2013
CRELD1 Is an Evolutionarily-Conserved