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Primary atopic disorders.
scientific article published on 16 March 2018
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
review article
1 reference
PubMed ID
29549114
title
Primary atopic disorders
(English)
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
main subject
atopic dermatitis
1 reference
stated in
PubMed
retrieved
17 June 2019
hypersensitivity
1 reference
stated in
PubMed
retrieved
17 June 2019
author
Jonathan J. Lyons
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
Joshua D Milner
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
author name string
Jonathan J Lyons
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
29549114
retrieved
5 May 2018
reference URL
http://europepmc.org/abstract/MED/29549114
Joshua D Milner
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
29549114
retrieved
5 May 2018
reference URL
http://europepmc.org/abstract/MED/29549114
language of work or name
English
0 references
publication date
16 March 2018
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
published in
Journal of Experimental Medicine
2 references
stated in
PubMed Central
retrieved
17 June 2019
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
volume
215
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
issue
4
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
page(s)
1009-1022
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
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Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment
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2 November 2018
Mitochondrial STAT3 plays a major role in IgE-antigen-mediated mast cell exocytosis
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2 November 2018
Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities
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2 November 2018
Critical role for mast cell Stat5 activity in skin inflammation
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2 November 2018
Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire development
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2 November 2018
Combined immunodeficiency associated with homozygous MALT1 mutations
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2 November 2018
Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience
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2 November 2018
Serum basal tryptase may be a good marker for predicting the risk of anaphylaxis in children with food allergy.
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2 November 2018
Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cells.
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2 November 2018
Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation
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2 November 2018
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting
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2 November 2018
Elevated IgE and atopy in patients treated for early-onset ADA-SCID.
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2 November 2018
TGFβ receptor mutations impose a strong predisposition for human allergic disease
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2 November 2018
The lymphoid lineage-specific actin-uncapping protein Rltpr is essential for costimulation via CD28 and the development of regulatory T cells
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2 November 2018
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency
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2 November 2018
Peptide library-based evaluation of T-cell receptor breadth detects defects in global and regulatory activation in human immunologic diseases
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2 November 2018
High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.
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2 November 2018
Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia
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2 November 2018
Whole-exome sequencing links caspase recruitment domain 11 (CARD11) inactivation to severe combined immunodeficiency
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2 November 2018
Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome
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2 November 2018
Early signaling events that underlie fate decisions of naive CD4(+) T cells toward distinct T-helper cell subsets
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2 November 2018
Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects
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2 November 2018
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population
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2 November 2018
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections
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2 November 2018
The STAT5b Pathway Defect and Autoimmunity
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2 November 2018
Prevalence of atopic disorders and immunodeficiency in patients with ectodermal dysplasia syndromes
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2 November 2018
Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency.
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2 November 2018
Extrathymically generated regulatory T cells control mucosal TH2 inflammation
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2 November 2018
Activation of myeloid cell-specific adhesion class G protein-coupled receptor EMR2 via ligation-induced translocation and interaction of receptor subunits in lipid raft microdomains
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2 November 2018
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions
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2 November 2018
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP
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2 November 2018
Immature B cells preferentially switch to IgE with increased direct Sμ to Sε recombination.
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2 November 2018
Increased risk of asthma and atopic dermatitis in perinatally HIV-infected children and adolescents
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2 November 2018
Filaggrin mutations associated with skin and allergic diseases.
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2 November 2018
Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening.
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2 November 2018
A requisite role for induced regulatory T cells in tolerance based on expanding antigen receptor diversity
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2 November 2018
Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses.
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2 November 2018
STAT5b deficiency: an unsuspected cause of growth failure, immunodeficiency, and severe pulmonary disease
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2 November 2018
The kinase mTOR regulates the differentiation of helper T cells through the selective activation of signaling by mTORC1 and mTORC2.
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2 November 2018
Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5
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2 November 2018
Effect of filaggrin breakdown products on growth of and protein expression by Staphylococcus aureus
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2 November 2018
Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease
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2 November 2018
Mast cells in allergy and infection: versatile effector and regulatory cells in innate and adaptive immunity
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2 November 2018
Cutting edge: lack of high affinity competition for peptide in polyclonal CD4+ responses unmasks IL-4 production
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2 November 2018
WASP: a key immunological multitasker
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2 November 2018
Factors influencing serum total tryptase concentrations in a general adult population
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2 November 2018
Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema.
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2 November 2018
Familial atypical cold urticaria: description of a new hereditary disease
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2 November 2018
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor
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2 November 2018
Combined immunodeficiency associated with DOCK8 mutations
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2 November 2018
Loss of the LAT adaptor converts antigen-responsive T cells into pathogenic effectors that function independently of the T cell receptor
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2 November 2018
Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity.
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2 November 2018
Filaggrin in the frontline: role in skin barrier function and disease
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2 November 2018
Mutations of the Wiskott-Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes
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2 November 2018
In vivo switch to IL-10-secreting T regulatory cells in high dose allergen exposure
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2 November 2018
Omenn syndrome: inflammation in leaky severe combined immunodeficiency
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2 November 2018
Glutamine-enriched enteral nutrition in very low-birth-weight infants: effect on the incidence of allergic and infectious diseases in the first year of life
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2 November 2018
STAT3 mutations in the hyper-IgE syndrome
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2 November 2018
Novel mouse mutants with primary cellular immunodeficiencies generated by genome-wide mutagenesis.
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2 November 2018
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
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2 November 2018
Cytokine modulation of atopic dermatitis filaggrin skin expression
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2 November 2018
Basal serum tryptase level correlates with severity of hymenoptera sting and age.
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2 November 2018
Asthma and airways collapse in two heritable disorders of connective tissue
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2 November 2018
The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model
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2 November 2018
The Wiskott-Aldrich syndrome protein is required for the function of CD4(+)CD25(+)Foxp3(+) regulatory T cells
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2 November 2018
WASP regulates suppressor activity of human and murine CD4(+)CD25(+)FOXP3(+) natural regulatory T cells
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2 November 2018
Wiskott-Aldrich syndrome protein is required for regulatory T cell homeostasis
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2 November 2018
Lymphopenic mice reconstituted with limited repertoire T cells develop severe, multiorgan, Th2-associated inflammatory disease
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2 November 2018
CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes
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2 November 2018
Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity
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2 November 2018
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2 November 2018
The desmosome: cell science lessons from human diseases
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2 November 2018
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.
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2 November 2018
Potent pruritogenic action of tryptase mediated by PAR-2 receptor and its involvement in anti-pruritic effect of nafamostat mesilate in mice
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2 November 2018
Analysis of T-cell repertoire diversity in Wiskott-Aldrich syndrome
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2 November 2018
LEKTI is localized in lamellar granules, separated from KLK5 and KLK7, and is secreted in the extracellular spaces of the superficial stratum granulosum
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2 November 2018
Increased TGF-beta2 in severe asthma with eosinophilia
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2 November 2018
Allergen immunotherapy induces a suppressive memory response mediated by IL-10 in a mouse asthma model
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2 November 2018
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2 November 2018
Complete DiGeorge syndrome: development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases
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2 November 2018
Impaired signaling via the high-affinity IgE receptor in Wiskott-Aldrich syndrome protein-deficient mast cells
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2 November 2018
Identifying the MAGUK protein Carma-1 as a central regulator of humoral immune responses and atopy by genome-wide mouse mutagenesis.
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2 November 2018
Role of TCR-induced extracellular signal-regulated kinase activation in the regulation of early IL-4 expression in naive CD4+ T cells
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2 November 2018
Mast cell tryptases and airway remodeling
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2 November 2018
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2 November 2018
Role of IL-10 in allergen-specific immunotherapy and normal response to allergens
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retrieved
2 November 2018
CARD11 and CARD14 are novel caspase recruitment domain (CARD)/membrane-associated guanylate kinase (MAGUK) family members that interact with BCL10 and activate NF-kappa B
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=5881472
retrieved
2 November 2018
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
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=5881472
retrieved
2 November 2018
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
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=5881472
retrieved
2 November 2018
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
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=5881472
retrieved
2 November 2018
JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation 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=5881472
retrieved
2 November 2018
How WASP regulates actin polymerization
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=5881472
retrieved
2 November 2018
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton 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=5881472
retrieved
2 November 2018
A direct estimate of the human alphabeta T cell receptor diversity
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=5881472
retrieved
2 November 2018
Familial gastrointestinal stromal tumours with germline mutation of the KIT gene
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=5881472
retrieved
2 November 2018
The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor
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=5881472
retrieved
2 November 2018
Induction of Th1 and Th2 CD4+ T cell responses: the alternative approaches
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=5881472
retrieved
2 November 2018
ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency
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=5881472
retrieved
2 November 2018
Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
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=5881472
retrieved
2 November 2018
Defective T cell receptor signaling and CD8+ thymic selection in humans lacking zap-70 kinase
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=5881472
retrieved
2 November 2018
The effect of antigen dose on CD4+ T helper cell phenotype development in a T cell receptor-alpha beta-transgenic model
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=5881472
retrieved
2 November 2018
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
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=5881472
retrieved
2 November 2018
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
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=5881472
retrieved
30 November 2018
Atopy reconsidered
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Decreased expression of filaggrin in atopic skin
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Induction of IL-4-producing CD4+ T cells by antigenic peptides altered for TCR binding
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
IL-25 in atopic dermatitis: a possible link between inflammation and skin barrier dysfunction?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Infant colitis—it's in the genes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neonatal-onset T(-)B(-)NK(+) severe combined immunodeficiency and neutropenia caused by mutated phosphoglucomutase 3
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/29549114
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1084/JEM.20172306
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
PMCID
5881472
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
PubMed ID
29549114
1 reference
stated in
Europe PubMed Central
PMCID
5881472
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29549114%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 March 2020
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