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Dock8
IDF Patient & Family Handbook
Two Locus Inheritance of Non-Syndromic Midline Craniosynostosis Via Rare SMAD6 and 4 Common BMP2 Alleles 5 6 Andrew T
Type of the Paper (Article
DOCK8 Drives Src-Dependent NK Cell Effector Function Conor J
DOCK8 Regulates Fitness and Function of Regulatory T Cells Through Modulation of IL-2 Signaling
Bioinformatics Analysis of Potential Key Genes and Mechanisms in Type 2 Diabetes Mellitus Basavaraj Vastrad1, Chanabasayya Vastrad*2
Identification of Transcriptional Mechanisms Downstream of Nf1 Gene Defeciency in Malignant Peripheral Nerve Sheath Tumors Daochun Sun Wayne State University
Patient & Family Handbook
Hyper Ige Syndromes and DOCK8 Forms of HIES Table 20:1
Supplemental Figures (1-6) Unhighlighted
DOCK8 Regulates Signal Transduction Events to Control Immunity
270 Genes Genetic Insights Panel
Early-Life Epilepsies and the Emerging Role of Genetic Testing
CD147 Promotes Src-Dependent Activation of Rac1 Signaling Through STAT3/DOCK8 During the Motility of Hepatocellular Carcinoma Cells
DOCK8 Deficiency Without Hyper-Ige in a Child with a Large Deletion
Original Article Two DOCK7 Polymorphisms and Their Haplotypes Are Associated with the Risk of Coronary Artery Disease and Ischemic Stroke
DOCK8 Regulates Protective Immunity by Controlling the Function and Survival of Rorgt Þ Ilcs
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
Top View
Investigating Developmental and Epileptic Encephalopathy Using Drosophila Melanogaster
The Essential Role of DOCK8 in Humoral Immunity
Rho Gtpase Regulators and Effectors in Autism Spectrum Disorders
Hyper Ige Syndrome
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Supporting Table 1. Genes Differentially Expressed in Heparg Cells by the Coculture Condition
Dock8 Interacts with Nck1 in Mediating Schwann Cell Precursor Migration
Determining the Differential Roles of the Dock Family Of
Patient Information Sheet HIES Hyperimmunoglobulin E Syndromes
Rasgrp1 Mutation Increases Naïve T-Cell CD44
Detection of Rare Germline Variants in the Genomes of B Cell Neoplasms
DOCK8 NEJM Presentation
Spatial Organization of Rho Gtpase Signaling by Rhogef/Rhogap Proteins
Diagnostic Genetic Testing Requisition
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Prospective Diagnostic Analysis of Copy Number Variants Using SNP Microarrays in Individuals with Autism Spectrum Disorders
Mechanisms of Impaired Neutrophil Migration by Micrornas in Myelodysplastic Syndromes
Overexpression of Hepatocyte Chemerin-156 Lowers Tumor Burden in a Murine Model of Diethylnitrosamine-Induced Hepatocellular Carcinoma
Growth-Factor Receptor-Bound Protein-2 (Grb2) Signaling in B Cells Controls Lymphoid Follicle Organization and Germinal Center Reaction
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
Supplementary Material For
DOCK8 Immunodeficiency Syndrome?
DOCK8 Immunodeficiency Syndrome
Individual Genome Sequence Gene List (By Disease)
Table of Contents List of Investigators
Next Generation Sequencing Panel for Hereditary Lymphoma
Insights Into the Biological Functions of Dock Family Guanine Nucleotide Exchange Factors
Calorie Restriction Prevents Metabolic Ageing Caused by Abnormal SIRT1 Function in Adipose Tissues Cheng Xu , Yu Cai , Pengchen
I. Supplemental Methods A. Lipid Analysis B. Proteomics C. Gene Reporter (Luciferase) Assays D
Mice with Mutations of Dock7 Have Generalized Hypopigmentation and White-Spotting but Show Normal Neurological Function
Responsive Nuclear Proteins in Collecting Duct Cells
Hyperimmunoglobulin E Syndromes (HIES)
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0800 987 8986 About This Booklet Summary
Identification and Functional Analysis of Novel DOCK8 Mutations
Estimation of the Genetic Substitution Rate of Hanwoo and Holstein Cattle Using Whole Genome Sequencing Data
Genetics of Cerebral Small Vessel Disease
1 Supplementary Table 2B. List of Spliced Oncogenes and Tumor
Genetic, Clinical, and Laboratory Markers for DOCK8 Immunodeficiency Syndrome