Akiharu Kubo

Professor

Kobe University Graduate School of Medicine

Japan

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Akiharu Kubo is a Professor at Kobe University Graduate School of Medicine in Japan. His research focuses on dermatological conditions and molecular mechanisms related to skin disorders, as evidenced by his recent articles on tight junction formation, localized scleroderma, and genetic skin diseases. He has contributed significantly to studies on therapeutic approaches for cutaneous vascular anomalies and the genetic basis of skin peeling syndromes.

Articles (21)

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2025

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2021

Collaborators (14)

Yasushi Suga

JAPAN

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Tadashi Terui

JAPAN

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Aki Minoda

Associate Professor

LIRMM

NETHERLANDS

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ANDREW KOWALCZYK

Pennsylvania State University

UNITED STATES

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Koremasa Hayama

Assistant professor

Nihon University

JAPAN

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Tomoko Kawai

National Institute of Child Health and Human Development

JAPAN

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Toshihide Higashino

Chief Dermatologist

Self-Defense Forces Central Hospital

JAPAN

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Masayuki Amagai

JAPAN

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Yuma Cho

Kyushu University

JAPAN

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Kenjiro Kosaki

Professor

Keio University

JAPAN

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Hideki Fujita

Associate professor

Nihon University

JAPAN

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Nobuo Kanazawa

Chief Professor

Hyogo medical university

JAPAN

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Noriko Umegaki-Arao

Tokyo Women's Medical University

JAPAN

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Yuki Saito

National Cancer Center Research Institute

JAPAN

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Akiharu Kubo

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Articles (21)

Rho-ROCK liberates sequestered claudin for rapid de novo tight junction formation

Rho-ROCK liberates sequestered claudin for rapid de novo tight junction formation

A case of localized scleroderma with variable response to excimer light therapy

Topical sirolimus therapy for cutaneous vascular anomalies: A randomized phase II clinical trial

Acute generalized exanthematous pustulosis showing a discrepancy between results of patch test and drug‐induced lymphocyte stimulation test

History and prospects of Nagashima‐type palmoplantar keratosis, the most common palmoplantar keratoderma in east Asian populations

Perspectives and history in genodermatoses

Gene-specific somatic epigenetic mosaicism of FDFT1 underlies a non-hereditary localized form of porokeratosis.

Coincidence of acral peeling skin syndrome and Nagashima‐type palmoplantar keratosis in a Japanese pedigree with acral skin peeling

A case of nodular cutaneous amyloidosis presenting as refractory leg skin ulcers

Case of type 1 segmental Darier's disease with a novel mosaic mutation in the ATP2A2 gene

Cutaneous cryptococcosis due to Cryptococcus neoformans with the formation of a giant subcutaneous nodule

Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism

Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein

Neurofibromatosis type 2 with mild Pierre-Robin sequence showing a heterozygous chromosome 22q12 microdeletion encompassing NF2 and MN1

Palmar whitish change after water exposure in a familial mild case of loricrin keratoderma (loricrin ichthyosis)

Improvement of redness and hyperkeratosis in a case of Nagashima‐type palmoplantar keratosis during Tofacitinib treatment for ulcerative colitis

Differential Pathomechanisms of Desmoglein 1 Transmembrane Domain Mutations in Skin Disease

Frequent FGFR3 and Ras Gene Mutations in Skin Tags or Acrochordons

Japanese guidelines for the management of palmoplantar keratoderma

Autosomal dominant familial acanthosis nigricans caused by a C-terminal nonsense mutation of FGFR3

Collaborators (14)

Yasushi Suga

Tadashi Terui

Aki Minoda

ANDREW KOWALCZYK

Koremasa Hayama

Tomoko Kawai

Toshihide Higashino

Masayuki Amagai

Yuma Cho

Kenjiro Kosaki

Hideki Fujita

Nobuo Kanazawa

Noriko Umegaki-Arao

Yuki Saito

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