about
Successful treatment of disseminated superficial actinic porokeratosis with Q-switched ruby laser.Generation of keratinocytes from normal and recessive dystrophic epidermolysis bullosa-induced pluripotent stem cells.Generation of 3D skin equivalents fully reconstituted from human induced pluripotent stem cells (iPSCs).Melanin Transfer in Human 3D Skin Equivalents Generated Exclusively from Induced Pluripotent Stem Cells.Bone marrow stem cell therapy for recessive dystrophic epidermolysis bullosa.Building a microphysiological skin model from induced pluripotent stem cells.A Case of Advanced Extramammary Paget's Disease Successfully Controlled by Monthly but Not Weekly Docetaxel Chemotherapy.Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a patient with recessive dystrophic epidermolysis bullosa (RDEB) carrying two compound heterozygous mutations in the COL7A1 gene.Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a healthy individual: WT-iPSC1.Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a healthy individual: WT-iPSC4.Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a healthy individual: WT-iPSC2.Integration-free T cell-derived human induced pluripotent stem cells (iPSCs) from a patient with lymphedema-distichiasis syndrome (LDS) carrying an insertion-deletion complex mutation in the FOXC2 gene.Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa.Acquired hemophilia A and fulminant diabetes mellitus possibly caused by adalimumab in a patient with psoriatic arthritis.Human cord blood-derived unrestricted somatic stem cells promote wound healing and have therapeutic potential for patients with recessive dystrophic epidermolysis bullosa.Synergistic effect of PDGF and FGF2 for cell proliferation and hair inductive activity in murine vibrissal dermal papilla in vitro.Reprogramming of human hair follicle dermal papilla cells into induced pluripotent stem cellsJapanese sporadic case of erythrokeratodermia variabilis caused by the connexin-30.3 (GJB4) mutation: Is Glycine 12 a mutational hotspot in the connexin family?Reduction of interleukin-10 production by B cells in intractable toxic epidermal necrolysisCase of metachronous and multifocal extramammary Paget's diseaseA pediatric case of multiple palisaded encapsulated neuromas of the palms and solesNovel mutation c.263A>G in the ACVRL1 gene in a Japanese patient with hereditary hemorrhagic telangiectasia 2Case of ultraviolet B-mediated photosensitivity during the administration of voriconazoleA novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndromeRituximab-induced vasculitis: Does the immune complex of rituximab play a key role in developing paradoxical adverse events?
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Munenari Itoh
@en
Munenari Itoh
@nl
type
label
Munenari Itoh
@en
Munenari Itoh
@nl
prefLabel
Munenari Itoh
@en
Munenari Itoh
@nl
P31
P496
0000-0003-3640-6355