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FGD1
The Atypical Guanine-Nucleotide Exchange Factor, Dock7, Negatively Regulates Schwann Cell Differentiation and Myelination
Cldn19 Clic2 Clmp Cln3
Genome-Wide Alterations in Gene Methylation by the BRAF V600E Mutation in Papillary Thyroid Cancer Cells
Genetic Testing Policy Number: PG0041 ADVANTAGE | ELITE | HMO Last Review: 04/11/2021
Supplementary Table 1: List of the 316 Genes Regulated During Hyperglycemic Euinsulinemic Clamp in Skeletal Muscle
Rho Guanine Nucleotide Exchange Factors: Regulators of Rho Gtpase Activity in Development and Disease
Blueprint Genetics Noonan Syndrome Panel
Two Novel Mutations Confirm FGD1 Is Responsible for the Aarskog Syndrome
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Gen Genetic Test Genetic Test Subjectkey (NDAR GUID)
Rho Gtpase Signalling Pathways in the Morphological Changes Associated with Apoptosis
Rho Activation at a Glance Rho Activation at a Glance
Epilepsy Next-Generation Sequencing Guide
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Rhoa Effector Activity Modulation of HIV-1 Replication by a Novel
Guanine Nucleotide Exchange Factors for Rho Gtpases: Turning on the Switch
Supplementary Data
After a Review of the Current Available Literature, CGS Administrators Has Determined That Testing for the Following Genes/Gene
Top View
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Connective Tissue Disorders
Table S1: Gene Symbol Full Gene Name Entrez Gene ID Refseq A2M
Regulation of Dbl Family Guanine Nucleotide Exchange Factors
Neuronal Cytoskeleton in Intellectual Disability: from Systems Biology and Modeling to Therapeutic Opportunities
Table S-1 Mpkccd Transcriptome
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
FGD1 As a Central Regulator of Extracellular Matrix Remodelling
Genomic Unity® Prenatal Analysis
MLK3 Regulates Bone Development Downstream of the Faciogenital Dysplasia Protein FGD1 in Mice
Rho Family Proteins and Ras Transformation: the Rhoad Less Traveled Gets Congested
Noonan Spectrum Disorders and Rasopathies Precision Panel
A Possible Cause of Autism Spectrum Disorder
Drhogef2 Encodes a Member of the Dbl Family of Oncogenes and Controls Cell Shape Changes During Gastrulation in Drosophila
Faciogenital Dysplasia Protein (FGD1) and Vav, Two Related Proteins Required for Normal Embryonic Development, Are Upstream Regulators of Rho Gtpases Michael F
Spatial Organization of Rho Gtpase Signaling by Rhogef/Rhogap Proteins
Supplementary Table 1. List of Biological Candidate Genes and Their Functional Roles for Genetic Variant Analysis 2 (N=153)
IL-13 System by Β Regulation of the Monocyte IL-1 Transcriptional
Targeted Genes and Methodology Details for Epilepsy/Seizure Genetic Panels
Molecular and Comparative Genetics of Mental Retardation
List of Gene Panels Used for Epilepsy Diagnosis in Different Companies
Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease
Rho Gtpases and Signaling Networks
A Dissertation Entitled the Regulation of Mixed Lineage Kinase 3 By
Supplementary Material
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
Juul Et Al. – Supplementary Material Explanation of Data Presented In
A Novel Frameshift Mutation in the FGD1 Gene Causing Aarskog-Scott Syndrome Patient with Hypogonadism: a Case Report
CENTOGENE's Severe and Early Onset Disorder Gene List
Comprehensive Genetic Test Menu
Frabin and Other Related Cdc42-Specific Guanine Nucleotide Exchange Factors Couple the Actin Cytoskeleton with the Plasma Membrane
A Novel FGD1 Mutation in a Family with Aarskog-Scott Syndrome and Predominant Features of Congenital Joint Contractures
Cellular and Molecular Studies of ALSIN
1 Knock Down of Plakophillin 2 Dysregulates Adhesion Pathway
Multiple Genetic Rare Variants in Autism Spectrum Disorders: a Single-Center Targeted NGS Study
The Rasopathies Molecular Genetics and Genotype-Phenotype Correlations
Regulation of A2 Chimaerin and Associated Phosphorylation Pathways in Neuronal Signalling and Morphogenesis
Structure of Small G Proteins and Their Regulators
FGD1 Gene FYVE, Rhogef and PH Domain Containing 1
Diethylphthalate, Possible Interactions in Fetal Brain Development
M2145: General Genetic Testing, Germline Disorders
Mutant Plasticity Related Gene 1 (PRG1) Acts As a Potential Modifier in SCN1A Related Epilepsy
Crystal Structure of the Dbl and Pleckstrin Homology Domains from the Human Son of Sevenless Protein
Genomic Unity® Neurology Analysis
Use of Pharmacogenetics for Predicting Cancer Prognosis and Treatment Exposure, Response and Toxicity
The Role of Rho Gtpases in Breast Cancer Progression