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Dedicator of cytokinesis 8 (DOCK8) deficiency
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
title
Dedicator of cytokinesis 8 (DOCK8) deficiency
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
author name string
Helen C Su
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
publication date
1 December 2010
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
published in
Current Opinion in Allergy and Clinical Immunology
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
volume
10
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
page(s)
515-520
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
cites work
Selective control of type I IFN induction by the Rac activator DOCK2 during TLR-mediated plasmacytoid dendritic cell activation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
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5 July 2018
Structural variation in the human genome and its role in disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Cellular signaling of Dock family proteins in neural function
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Combined immunodeficiency associated with DOCK8 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Activation of Rho GTPases by DOCK exchange factors is mediated by a nucleotide sensor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Sequential regulation of DOCK2 dynamics by two phospholipids during neutrophil chemotaxis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Primary immune deficiencies with aberrant IgE production
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
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5 July 2018
Genomic changes in progression of low-grade gliomas
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Dock10, a novel CZH protein selectively induced by interleukin-4 in human B lymphocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
The hyper-IgE syndromes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Differential requirement for DOCK2 in migration of plasmacytoid dendritic cells versus myeloid dendritic cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Construction of an open-access database that integrates cross-reference information from the transcriptome and proteome of immune cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
STAT3 mutations in the hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
GEF what? Dock180 and related proteins help Rac to polarize cells in new ways
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
A central role for DOCK2 during interstitial lymphocyte motility and sphingosine-1-phosphate-mediated egress
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
DOCK2 is a Rac activator that regulates motility and polarity during neutrophil chemotaxis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Homozygous deletion and reduced expression of the DOCK8 gene in human lung cancer.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
CZH proteins: a new family of Rho-GEFs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Zizimin2: a novel, DOCK180-related Cdc42 guanine nucleotide exchange factor expressed predominantly in lymphocytes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
DOCK2 is essential for antigen-induced translocation of TCR and lipid rafts, but not PKC-theta and LFA-1, in T cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Haematopoietic cell-specific CDM family protein DOCK2 is essential for lymphocyte migration
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Microcystic adnexal carcinoma associated with primary immunodeficiency, recurrent diffuse herpes simplex virus infection, and cutaneous T-cell lymphoma
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
5 July 2018
Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
28 October 2018
T helper type 2 differentiation and intracellular trafficking of the interleukin 4 receptor-alpha subunit controlled by the Rac activator Dock2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
28 October 2018
Association of deletion 9p, 46,XY gonadal dysgenesis and autistic spectrum disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
28 October 2018
Genomic loss and epigenetic silencing of very-low-density lipoprotein receptor involved in gastric carcinogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
28 October 2018
Differential requirements for DOCK2 and phosphoinositide-3-kinase gamma during T and B lymphocyte homing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3096565
retrieved
28 October 2018
Curative treatment of autosomal-recessive hyper-IgE syndrome by hematopoietic cell transplantation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20864884
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The hyper IgE syndrome and mutations in TYK2
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20864884
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1097/ACI.0B013E32833FD718
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
PMCID
3096565
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
PubMed ID
20864884
1 reference
stated in
Europe PubMed Central
PubMed ID
20864884
retrieved
31 July 2017
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