about
Chromosomal loci of 50 human keratinocyte cDNAs assigned by fluorescence in situ hybridizationNox1 is involved in angiotensin II-mediated hypertension: a study in Nox1-deficient miceApoptosis signal-regulating kinase 1 (ASK1) is an intracellular inducer of keratinocyte differentiation.Identification of preferred substrate sequences for transglutaminase 1--development of a novel peptide that can efficiently detect cross-linking enzyme activity in the skin.Contribution of IL-18 to atopic-dermatitis-like skin inflammation induced by Staphylococcus aureus product in miceAge-related morphometric changes of inner structures of the skin assessed by in vivo reflectance confocal microscopy.Defective stratum corneum and early neonatal death in mice lacking the gene for transglutaminase 1 (keratinocyte transglutaminase)Cataloging of the genes expressed in human keratinocytes: analysis of 607 randomly isolated cDNA sequences.Variations in both TG1 and TG2 isozyme-specific in situ activities and protein expressions during mouse embryonic developmentSerum cytokines correlated with the disease severity of generalized pustular psoriasisPediatric case report: clinical profile of a patient with PCWH with p.Q377X nonsense mutation in the SOX10 gene.Localised Dominant Dystrophic Epidermolysis Bullosa with a Novel de Novo Mutation in COL7A1 Diagnosed by Next-generation Sequencing.Activation of Molecular Signatures for Antimicrobial and Innate Defense Responses in Skin with Transglutaminase 1 Deficiency.In situ detection of active transglutaminases for keratinocyte type (TGase 1) and tissue type (TGase 2) using fluorescence-labeled highly reactive substrate peptides.A Case of Old Age-Onset Generalized Pustular Psoriasis with a Deficiency of IL-36RN (DITRA) Treated by Granulocyte and Monocyte Apheresis.[Cutaneous necrotizing vasculitis in a patient with Behcet's disease; mimicking polyarteritis nodosa].Analysis of epidermal-type transglutaminase (TGase 3) expression in mouse tissues and cell lines.Gene analysis of human skin and skin diseases.Expression of IL-33 in ocular surface epithelium induces atopic keratoconjunctivitis with activation of group 2 innate lymphoid cells in mice.Growth advantage by overexpression of normal Harvey ras proto-oncogene in cultured rat epidermal keratinocytes.Tetracyclines modulate protease-activated receptor 2-mediated proinflammatory reactions in epidermal keratinocytes.Effects of vanadate on intracellular Ca2+ redistribution and hexose transport across plasma membrane in cultured mouse fibroblasts.Erratum to "Neutrophil-dominant psoriasis-like skin inflammation induced by epidermal-specific expression of Raf in mice" [J. Dermatol. Sci. 58 (2010) 28-35].Varicella-zoster virus-specific cell-mediated immunity in subjects with herpes zoster.YKL-40 is a serum biomarker reflecting the severity of cutaneous lesions in psoriatic arthritis.Case of subepidermal bullous dermatosis with immunoglobulin G autoantibodies against various basement membrane zone proteins.Adult cutaneous alveolar rhabdomyosarcoma on the face diagnosed by the expression of PAX3-FKHR gene fusion transcripts.Staphylococcal enterotoxin B enhances a flare-up reaction of murine contact hypersensitivity through up-regulation of interferon-gamma.The two functional keratin 6 genes of mouse are differentially regulated and evolved independently from their human orthologs.Case of harlequin ichthyosis with a favorable outcome: Early treatment and novel, differentially expressed, alternatively spliced transcripts of the ATP-binding cassette subfamily A member 12 gene.Therapeutic depletion of myeloid lineage leukocytes by adsorptive apheresis for psoriatic arthritis: Efficacy of a non-drug intervention for patients refractory to pharmacologics.Mild case of congenital ichthyosiform erythroderma with periodic exacerbation: Novel mutations in ABCA12 and upregulation of calprotectin in the epidermis.Knocking-in the R142C mutation in transglutaminase 1 disrupts the stratum corneum barrier and postnatal survival of mice.ABCA12-deficient Congenital Ichthyosiform Erythroderma in a Boy with an Intellectual Developmental Delay.Epithelial keratin and filaggrin expression in seborrheic keratosis: evaluation based on histopathological classification.A Japanese Case of Ichthyosiform Erythroderma with a Novel Mutation in NIPAL4/Ichthyin.Characterization of TG2 and TG1-TG2 double knock-out mouse epidermis.Penile pseudomyogenic hemangioendothelioma/epithelioid sarcoma-like hemangioendothelioma with a novel pattern of SERPINE1-FOSB fusion detected by RT-PCR--report of a case.A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb.Neutrophil-dominant psoriasis-like skin inflammation induced by epidermal-specific expression of Raf in mice.
P50
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P50
description
researcher ORCID ID = 0000-0003-0484-2320
@en
wetenschapper
@nl
name
Kiyofumi Yamanishi
@ast
Kiyofumi Yamanishi
@en
Kiyofumi Yamanishi
@es
Kiyofumi Yamanishi
@nl
type
label
Kiyofumi Yamanishi
@ast
Kiyofumi Yamanishi
@en
Kiyofumi Yamanishi
@es
Kiyofumi Yamanishi
@nl
prefLabel
Kiyofumi Yamanishi
@ast
Kiyofumi Yamanishi
@en
Kiyofumi Yamanishi
@es
Kiyofumi Yamanishi
@nl
P106
P1153
7103276042
P31
P496
0000-0003-0484-2320