DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» DGCR6
DGCR6
Association of Gene Ontology Categories with Decay Rate for Hepg2 Experiments These Tables Show Details for All Gene Ontology Categories
DGCR6 at the Proximal Part of the Digeorge Critical Region Is Involved in Conotruncal Heart Defects
Network Effects of the Neuropsychiatric 15Q13.3 Microdeletion on the Transcriptome and Epigenome in Human Induced Neurons
Detailed Characterization of Human Induced Pluripotent Stem Cells Manufactured for Therapeutic Applications
Unraveling the Genetic and Developmental Mysteries of 22Q11 Deletion Syndrome
CREB-Dependent Transcription in Astrocytes: Signalling Pathways, Gene Profiles and Neuroprotective Role in Brain Injury
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
REVIEW the 22Q11.2 Deletion Syndrome
Juvenile Rheumatoid Arthritis and Del(22Ql 1) Syndrome: a Non
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Genetic Variation at the 22Q11 PRODH2 DGCR6 Locus Presents an Unusual Pattern and Increases Susceptibility to Schizophrenia
A Chicken Model for DGCR6 As a Modifier Gene in the Digeorge Critical Region
Deleted Genes Associated with Digeorge/22Q11.2 Deletion Syndrome
Supplementary Materials Table of Contents
Connecting Myelin-Related and Synaptic Dysfunction in Schizophrenia with SNP-Rich Gene Expression Hubs
6Cognitive and Behavioral Characteristics of Children With
Dysregulation of DGCR6 and DGCR6L: Psychopathological Outcomes in Chromosome 22Q11.2 Deletion Syndrome
Top View
Genetic Variation at the 22Q11 PRODH2 DGCR6 Locus Presents an Unusual Pattern and Increases Susceptibility to Schizophrenia
A Molecular Analysis of 22Q11.2 Deletion Syndrome
A Compelling Genetic Hypothesis for a Complex Disease: PRODH2 DGCR6 Variation Leads to Schizophrenia Susceptibility
Iv Identification of Novel Imprinted Domains in The
Spatiotemporal 22Q11.21 Protein Network Implicates DGCR8-Dependent Microrna Biogenesis As a Risk for Late Fetal Cortical Development in Psychiatric Diseases
Ohnologs Are Overrepresented in Pathogenic Copy Number Mutations
Atypical Microdeletion 22Q11.2 in a Patient with Tetralogy of Fallot
(12) United States Patent (10) Patent No.: US 7,935,500 B2 Gerber Et Al
Microrna Binding Microrna Binding Probe Set Entrez Gene Gene
Genome Sequencing Analysis of Blood Cells Identifies Germline
Comparative Mapping of the 22Q11. 2 Deletion Region and the Potential of Simple Model Organisms
Dysregulation of DGCR6 and DGCR6L: Psychopathological Outcomes in Chromosome 22Q11.2 Deletion Syndrome
Consequences of 22Q11.2 Microdeletion on the Genome, Individual and Population Levels
The 22Q11 PRODH/DGCR6 Deletion Is Frequent in Hyperprolinemic Subjects but Is Not a Strong Risk Factor for ASD
Comparative Mapping of the Human 22Q11 Chromosomal Region and the Orthologous Region in Mice Reveals Complex Changes in Gene Organization
Recurrent Copy Number Variations As Risk Factors for Autism Spectrum Disorders: Analysis of the Clinical Implications
Chromosomal Microdeletions: Dissecting Del22q11 Syndrome
DGCR6 (NM 005675) Human Untagged Clone Product Data