about
Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris.MiR-155 is overexpressed in patients with atopic dermatitis and modulates T-cell proliferative responses by targeting cytotoxic T lymphocyte-associated antigen 4.Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitisElevated expression and genetic association links the SOCS3 gene to atopic dermatitisMaternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritanceClinical and genetic studies of Birt-Hogg-Dubé syndrome.A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.Clinical Effectiveness of Moisturizers in Atopic Dermatitis and Related Disorders: A Systematic Review.Characterization of EGFR and ErbB2 expression in atopic dermatitis patients.No association between Birt-Hogg-Dubé syndrome skin fibrofolliculomas and the first 10 described human polyomaviruses or human papillomaviruses.Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis.Topical tacrolimus is a useful adjunctive therapy for bullous pemphigoid.Novel filaggrin mutation but no other loss-of-function variants found in Ethiopian patients with atopic dermatitis.Lack of association between filaggrin gene mutations and onset of psoriasis in childhood.Whole-exome sequencing of Ethiopian patients with ichthyosis vulgaris and atopic dermatitis.[Long-term treatment with interferon-alpha can induce sarcoidosis. The connection can be stronger than earlier believed].Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations.X-linked recessive ichthyosis: an impaired barrier function evokes limited gene responses before and after moisturizing treatments.Moisturizing treatment of patients with atopic dermatitis and ichthyosis vulgaris improves dry skin, but has a modest effect on gene expression regardless of FLG genotype.Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.Cornulin, a marker of late epidermal differentiation, is down-regulated in eczemaLoss-of-function Variants of the Filaggrin Gene are Associated with Atopic Eczema and Associated Phenotypes in Swedish FamiliesAre BIC (miR-155) Polymorphisms Associated with Eczema Susceptibility?[Acute cutaneous symptom complex with subsequent cataract. The internet drug MT-45 may be the cause]Impaired wound healing and cheilitis in a Pachyonychia Congenita K6a familyGenetic Variation in the Inflammasome and Atopic Dermatitis Susceptibility[Birth-Hogg-Dube syndrome--a neglected condition that increases the risk of kidney cancer and pneumothorax]Attitudes and opinions among Swedish dermatologists concerning eczema (atopic dermatitis): results from a keypad sessionGenome-wide linkage analysis of allergic rhinoconjunctivitis in a Swedish populationSusceptibility loci for atopic dermatitis on chromosome 21 in a Swedish populationAnalysis of association and linkage for the interleukin-4 and interleukin-4 receptor b;alpha; regions in Swedish atopic dermatitis familiesSusceptibility loci for atopic dermatitis on chromosomes 3, 13, 15, 17 and 18 in a Swedish populationLinkage and association to candidate regions in Swedish atopic dermatitis familiesThe Wiskott-Aldrich syndrome gene as a candidate gene for atopic dermatitisCharacterization by phenotype of families with atopic dermatitis[A case report. Contact allergy caused by tea tree oil]Exposure-based cognitive behavior therapy for atopic dermatitis: an open trial
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
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հետազոտող
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name
Maria Bradley
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Maria Bradley
@en
Maria Bradley
@es
Maria Bradley
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Maria Bradley
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type
label
Maria Bradley
@ast
Maria Bradley
@en
Maria Bradley
@es
Maria Bradley
@nl
Maria Bradley
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prefLabel
Maria Bradley
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Maria Bradley
@en
Maria Bradley
@es
Maria Bradley
@nl
Maria Bradley
@sl
P106
P21
P31
P496
0000-0001-7192-5041