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PLXND1
The Extracellular Matrix Phenome Across Species
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis
Different Species Common Arthritis
Functional Specialization of Human Salivary Glands and Origins of Proteins Intrinsic to Human Saliva
Short Article Semaphorin-Plexin Signaling Guides Patterning of The
A Supplemental Fig S1| PLXND1 Genomic Locus. A, Image from the UCSC Genome Browser (Grch37/Hg19). PLXND1 Gene Is Shown in Dark B
GIPC Proteins Negatively Modulate Plexind1 Signaling During Vascular Development
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
HHS Public Access Author Manuscript
PDF-Document
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Identification of Key Proteins Involved in Axon Guidance Related Disorders: a Systems Biology Approach
Peripheral Nerve Single Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
De Novo Mutations in PLXND1 and REV3L Cause MÖBius Syndrome
Multigenic Truncation of the Semaphorin-Plexin Pathway by a Germline Chromothriptic Rearrangement Associated with Moebius Syndrome
Glycoprotein Pathways Altered in Frontotemporal Dementia with Autoimmune Disease
How Can an Interactive Visual Analytics Tool Help Biomedical Scientists Investigate Genotype-Phenotype Relationships?
Top View
Data-Driven and Knowledge-Driven Computational Models of Angiogenesis in Application to Peripheral Arterial Disease
Profilin2 Regulates Actin Rod Assembly in Neuronal Cells
1 Supplementary Material Figure S1. Volcano Plot of Differentially
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Exome Sequencing in Families with Severe Mental Illness Identifies Novel and Rare
Identification of Key Proteins Involved in Axon Guidance Related Disorders: a Systems Biology Approach
Unraveling the Molecular Mechanism Underlying ALS-Linked Astrocyte
A Novel Association of Campomelic Dysplasia with Hydrocephalus Due to an Unbalanced Chromosomal Translocation Upstream of SOX9
Systems Genetic Analysis of Binge-Like Eating in a C57BL/6J X DBA/2J-F2 Cross
Dysfunctional SEMA3E Signaling Underlies Gonadotropin- Releasing Hormone Neuron Deficiency in Kallmann Syndrome
Transcriptional Dynamics During Human Adipogenesis and Its Link to Adipose Morphology and Distribution
Linagliptin and Telmisartan Induced Effects on Renal and Urinary
Protein Interaction Disruption in Cancer Matthew Ruffalo1 and Ziv Bar-Joseph1,2*