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PLXNA2
Prioritization and Evaluation of Depression Candidate Genes by Combining Multidimensional Data Resources
Supplemental Table 1. Complete Gene Lists and GO Terms from Figure 3C
Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways
Case–Control Association Study of 59 Candidate Genes Reveals the DRD2
Whole Exome Sequencing Reveals NOTCH1 Mutations in Anaplastic Large Cell Lymphoma and Points to Notch Both As a Key Pathway and a Potential Therapeutic Target
Molecular Genetics of Schizophrenia and Related Intermediate
Genome-Wide Association Meta-Analysis for Early Age-Related Macular Degeneration Highlights Novel Loci and Insights for Advanced Disease Thomas W
Potential Impact of Mir-137 and Its Targets in Schizophrenia
NIH Public Access Author Manuscript Schizophr Res
The Tumor Suppressor CIC Directly Regulates MAPK Pathway Genes Via Histone Deacetylation Simon Weissmann1,2, Paul A
Dysregulation of Post-Transcriptional Modification by Copy Number
Genome-Wide Association Meta-Analysis for Early Age-Related
Identification of Novel TMPRSS2:ERG Mechanisms in Prostate Cancer Metastasis: Involvement of MMP9 and PLXNA2
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
GATA6 Mutations Cause Human Cardiac Outflow Tract Defects by Disrupting Semaphorin-Plexin Signaling
Identification of the Semaphorin Receptor PLXNA2 As a Candidate For
Association Between Snps and Gene Expression in Multiple Regions of the Human Brain
Anxiety and Comorbid Measures Associated with PLXNA2
Top View
Sema6a and Plxna2 Mediate Spatially Regulated Repulsion Within the Developing Eye to Promote Eye Vesicle Cohesion Alicia M
Anxiety and Comorbid Measures Associated with PLXNA2
Semaphorin 3A—Glycosaminoglycans Interaction As Therapeutic Target for Axonal Regeneration
Axon Guidance Signaling Modulates Epithelial to Mesenchymal Transition in Stem Cell
A CATH Domain Functional Family Based Approach to Identify
Gene Expression Profile in Similar Tissues Using Transcriptome Sequencing Data of Whole-Body Horse Skeletal Muscle
Systematic Analysis, Comparison, and Integration of Disease Based Human
GATA6 Mutations Cause Human Cardiac Outflow Tract Defects by Disrupting Semaphorin-Plexin Signaling
Unravelling the Genetic Basis of Schizophrenia and Bipolar Disorder with T GWAS: a Systematic Review ∗ Diana P
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Genome-Wide Search Reveals the Existence of a Limited Number of Thyroid Hormone Receptor Alpha Target Genes in Cerebellar Neurons
Extended Methods
PLXNA2 Identified As a Candidate Gene by Genome-Wide Association Analysis for Mandibular Prognathism in Human Chondrocytes
GATA6 Antibody Purified Mouse Monoclonal Antibody (Mab) Catalog # AP52675
Convergent Functional Genomic Studies of Omega-3 Fatty Acids in Stress Reactivity, Bipolar Disorder and Alcoholism
Transcriptomics-Based Phenotypic Screening Supports Drug Discovery in Human Glioblastoma Cells
2014 Luzi Sonija 0538952 Eth
Long Non-Coding RNA Repertoire and Open Chromatin Regions Constitute
Biallelic and Monoallelic Variants in PLXNA1 Are Implicated in a Novel Neurodevelopmental Disorder with Variable Cerebral and Eye Anomalies
Periodic Table of Neurotrophic and Neurotactic Factors
A Novel Function of the Proneural Factor Ascl1 in Progenitor Proliferation Identified by Genome-Wide Characterization of Its Targets
Rethinking Schizophrenia Through the Lens of Evolution: Shedding Light on the Enigma
Mouse Plxna2 Conditional Knockout Project (CRISPR/Cas9)
A Single-Cell Transcriptomic and Anatomic Atlas of Mouse
Identification of TMPRSS2-ERG Mechanisms in Prostate Cancer Invasiveness: Involvement of MMP-9 and Plexin B1
Transcriptional Programs in Transient Embryonic Zones of the Cerebral Cortex Defined by High-Resolution Mrna Sequencing
Chapter 1 General Introduction