「Pustular psoriasis as an autoinflammatory keratinization disease (AiKD): Genetic predisposing factors and promising therapeutic targets」の関連論文
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Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
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Indoleamine 2,3-Dioxygenase 2 Deficiency Exacerbates Imiquimod-Induced Psoriasis-Like Skin Inflammation
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Generalized Pustular Psoriasis: Clinical Management and Update on Autoinflammatory Aspects
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Myelodysplastic syndrome with trisomy 8 presenting periodic fever and multiple MEFV gene variants outside exon 10: a case report
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Usefulness of interleukin-18 as a diagnostic biomarker to differentiate adult-onset Still’s disease with/without macrophage activation syndrome from other secondary hemophagocytic lymphohistiocytosis in adults
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Cholinergic Urticaria: Subtype Classification and Clinical Approach
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The Role of Gut Microbiome in Psoriasis:Oral Administration of Staphylococcus aureus and Streptococcus danieliae Exacerbates Skin Inflammation of Imiquimod-Induced Psoriasis-Like Dermatitis
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Nationwide survey of refractory asthma with bronchiectasis by inflammatory subtypes
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Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
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A clinical and genetic study of SPG31 in Japan
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Morphea in a Crohn's disease patient undergoing ustekinumab treatment
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FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
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Studies on the molecular pathogenesis and the novel disease-associated genes in dogs with inflammatory colorectal polyps [an abstract of entire text]
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Diagnosis and Characterization of Endoscopic Findings in XIAP Deficiency
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Development of Remote Inflammation through Interneuron Network in the Spinal Cord
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Suppression of Neuropeptide by Botulinum Toxin Improve Imiquimod-induced Psoriasis-like Dermatitis via the Regulation of Neuroimmune System
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Trapping of CDC42 C-terminal variants in the Golgi drives pyrin inflammasome hyperactivation
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Activation of the pentose phosphate pathway in macrophages is crucial for granuloma formation in sarcoidosis
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Dupilumab suppresses relapsing chronic eosinophilic pneumonia with severe asthma
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Analysis of immunologic comorbidities in ulcerative colitis patients: a tool to prevent exacerbations in ulcerative colitis cases
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Genetic and Epigenetic Pathogenesis of Acromegaly
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Labyrinthine calcification in ears with otitis media and antineutrophil cytoplasmic antibody-associated vasculitis (OMAAV): A report of two cases
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Paraproteinemia and neuropathy
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Implications of interleukin-17 in psoriatic lesions as Koebner phenomenon caused by recurrent occupational burns
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Simultaneous Occurrence of Lichen Nitidus and Morphea
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The role of inflammatory biomarkers in predicting primary acquired nasolacrimal duct obstruction and postoperative recurrence
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Case report: Late middle-aged features of FAM111A variant, Kenny–Caffey syndrome type 2-suggestive symptoms during a long follow-up
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Failure of internal fixation for ankle joint Charcot neuroarthropathy with beta(2)-microglobulin amyloidosis: a case report
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The Influence of Atopic Dermatitis on Health-Related Quality of Life in Bangladesh
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The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
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Reduced stratum corneum acylceramides in autosomal recessive congenital ichthyosis with a NIPAL4 mutation
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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
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The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
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Suppression of Systemic Lupus Erythematosus in NZBWF1 mice infected with Hymenolepis microstoma
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
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The Analysis of the Action Mechanisms of Novel Steroid Compounds for the Induction of TSLP Production
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Temporal arteritis with focal pachymeningitis: a deceptive association
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Senescence-associated secretory phenotype promotes chronic ocular graft-vs-host disease in mice and humans (本文)
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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Genomic analysis for the prediction of prognosis in small-bowel cancer
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Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody
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Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
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Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
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CCL2-CCR2 signaling in the skin drives surfactant-induced irritant contact dermatitis via IL-1β-mediated neutrophil accumulation
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Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Inflammatory Skin-Derived Cytokines Accelerate Osteoporosis in Mice with Persistent Skin Inflammation
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Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism
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Studies on the pathological mechanism of alopecia areata in C3H/HeJ mouse model