Pages that link to "Q40422474"
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The following pages link to Filaggrin mutations, atopic eczema, hay fever, and asthma in children (Q40422474):
Displaying 50 items.
- Skin-derived TSLP triggers progression from epidermal-barrier defects to asthma (Q21145827) (← links)
- Atopic dermatitis: a candidate for disease‐modifying strategy (Q26828477) (← links)
- Mutations in the filaggrin gene and food allergy (Q26999482) (← links)
- Eosinophil-dependent skin innervation and itching following contact toxicant exposure in mice. (Q27310396) (← links)
- Consensus Conference on Clinical Management of pediatric Atopic Dermatitis (Q28071974) (← links)
- Filaggrin in the frontline: role in skin barrier function and disease (Q28242202) (← links)
- Eczema in early childhood is strongly associated with the development of asthma and rhinitis in a prospective cohort (Q31077487) (← links)
- Alterations in epithelial barrier function and host defense responses in chronic rhinosinusitis (Q33573943) (← links)
- The link between allergies and eosinophilic esophagitis: implications for management strategies (Q33649482) (← links)
- Filaggrin gene mutation c.3321delA is associated with various clinical features of atopic dermatitis in the Chinese Han population (Q33655186) (← links)
- Filaggrin gene defects are independent risk factors for atopic asthma in a Polish population: a study in ECAP cohort (Q33834147) (← links)
- A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming. (Q33858072) (← links)
- An update on the genetics of atopic dermatitis: scratching the surface in 2009. (Q33868032) (← links)
- Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children. (Q33903373) (← links)
- Application of genetic/genomic approaches to allergic disorders (Q34107682) (← links)
- Multi-locus stepwise regression: a haplotype-based algorithm for finding genetic associations applied to atopic dermatitis (Q34143324) (← links)
- Interplay of filaggrin loss-of-function variants, allergic sensitization, and eczema in a longitudinal study covering infancy to 18 years of age. (Q34189662) (← links)
- Context-Specific Protein Network Miner – An Online System for Exploring Context-Specific Protein Interaction Networks from the Literature (Q34228405) (← links)
- Epistasis between serine protease inhibitor Kazal-type 5 (SPINK5) and thymic stromal lymphopoietin (TSLP) genes contributes to childhood asthma (Q34294586) (← links)
- Filaggrin loss-of-function mutations are associated with food allergy in childhood and adolescence (Q34294641) (← links)
- Peanut allergy: effect of environmental peanut exposure in children with filaggrin loss-of-function mutations (Q34303315) (← links)
- Epicutaneous exposure to staphylococcal superantigen enterotoxin B enhances allergic lung inflammation via an IL-17A dependent mechanism. (Q34357756) (← links)
- New insights into the epidemiology of childhood atopic dermatitis (Q34397465) (← links)
- Association of filaggrin variants with asthma and rhinitis: is eczema or allergic sensitization status an effect modifier? (Q34796072) (← links)
- A polymorphism affecting MYB binding within the promoter of the PDCD4 gene is associated with severe asthma in children. (Q34974977) (← links)
- Role of macrophage migration inhibitory factor (MIF) in pollen-induced allergic conjunctivitis and pollen dermatitis in mice. (Q35043911) (← links)
- Atopic dermatitis: a disease of altered skin barrier and immune dysregulation (Q35065037) (← links)
- Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance (Q35165436) (← links)
- Genetics of allergic diseases (Q35556785) (← links)
- Association of common filaggrin null mutations with atopy but not chronic rhinosinusitis. (Q35588826) (← links)
- Skin Barrier Disruption: A Requirement for Allergen Sensitization? (Q35757285) (← links)
- Cutaneous exposure to agglomerates of silica nanoparticles and allergen results in IgE-biased immune response and increased sensitivity to anaphylaxis in mice (Q35786805) (← links)
- Allergy as an epithelial barrier disease (Q35805327) (← links)
- Increased risk of pertussis in patients with asthma (Q35875902) (← links)
- Influence of Asthma Epidemiology on the Risk for Other Diseases (Q35895182) (← links)
- One Remarkable Molecule: Filaggrin (Q36043328) (← links)
- Do Early Skin Care Practices Alter the Risk of Atopic Dermatitis? A Case‐Control Study (Q36095749) (← links)
- The persistence of atopic dermatitis and filaggrin (FLG) mutations in a US longitudinal cohort (Q36291414) (← links)
- Assessment of the association between atopic conditions and tympanostomy tube placement in children. (Q36375783) (← links)
- The frequency of polymorphic variants of filaggrin gene and clinical atopic dermatitis (Q36690488) (← links)
- Raman profiles of the stratum corneum define 3 filaggrin genotype-determined atopic dermatitis endophenotypes (Q36770783) (← links)
- Management of itch in atopic dermatitis (Q36991444) (← links)
- Reliability and validity of genotyping filaggrin null mutations. (Q37009417) (← links)
- Asthma and risk of selective IgA deficiency or common variable immunodeficiency: a population-based case-control study (Q37122237) (← links)
- Different risk factor patterns for adult asthma, rhinitis and eczema: results from West Sweden Asthma Study (Q37150859) (← links)
- Advances in mechanisms of asthma, allergy, and immunology in 2008. (Q37163582) (← links)
- Pediatric asthma: a different disease (Q37180205) (← links)
- A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis (Q37286978) (← links)
- Eczema genetics: current state of knowledge and future goals (Q37390367) (← links)
- Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum. (Q37406747) (← links)