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List of works by Akiharu Kubo

3D visualization of epidermal Langerhans cells

scientific article published in January 2013

A Japanese case of Mal de Meleda with SLURP1 mutation

scientific article published on 02 July 2014

A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.

scientific article

A homozygous nonsense mutation in the gene for Tmem79, a component for the lamellar granule secretory system, produces spontaneous eczema in an experimental model of atopic dermatitis

scientific journal article

A peculiar internalization of claudins, tight junction-specific adhesion molecules, during the intercellular movement of epithelial cells

scientific article published on March 2004

Altered stratum corneum barrier and enhanced percutaneous immune responses in filaggrin-null mice

scientific article published on 10 March 2012

Case of Conradi-Hünermann-Happle syndrome due to a nonsense mutation of c.245G>A (p.W82*)

scientific article published on 27 February 2019

Case of autosomal recessive woolly hair/hypotrichosis with a homozygous c.736T>A mutation of LIPH caused by maternal uniparental disomy of chromosome 3

scientific article published on 11 August 2020

Case of dominant dystrophic epidermolysis bullosa with amniotic band syndrome

scientific article published on 30 April 2016

Case of intermediate recessive dystrophic epidermolysis bullosa with negative LH7.2 staining

scientific article published on 12 July 2020

Case of lymphoplasmacytic plaque in children: Analysis of the distribution of infiltrating immune cells.

scientific article published on 14 April 2016

Case of non-Herlitz junctional epidermolysis bullosa with COL17A1 mutation.

scientific article published on 9 January 2015

Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis

scientific article

Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice

scientific journal article

Clonal Expansion of Second-Hit Cells with Somatic Recombinations or C>T Transitions Form Porokeratosis in MVD or MVK Mutant Heterozygotes

scientific article published on 15 June 2019

Distinct behavior of human Langerhans cells and inflammatory dendritic epidermal cells at tight junctions in patients with atopic dermatitis

scientific article published on 01 October 2014

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

scientific article published on 02 November 2016

Effective treatment by glycolic acid peeling for cutaneous manifestation of familial generalized acanthosis nigricans caused by FGFR3 mutation.

scientific article published on 27 January 2016

Effects of glycolic acid peeling on the cutaneous manifestation of generalized acanthosis nigricans caused by FGFR3 mutation: A report of one sporadic and two familial cases

scientific article published on 16 June 2017

Eosinophilic pustular folliculitis with palmoplantar lesions and nail deformity

scientific article published on 16 July 2020

Epidermal barrier dysfunction and cutaneous sensitization in atopic diseases

scientific article published on February 2012

Epidermal cell turnover across tight junctions based on Kelvin's tetrakaidecahedron cell shape

scientific article

Epidermal tight junction barrier function is altered by skin inflammation, but not by filaggrin-deficient stratum corneum.

scientific article published on 22 November 2014

Epidermolysis bullosa acquisita exacerbated by systemic estrogen and progesterone treatment and pregnancy

scientific article published on 01 May 1997

External antigen uptake by Langerhans cells with reorganization of epidermal tight junction barriers

scientific article

Familial acanthosis nigricans with p.K650T FGFR3 mutation

scientific article published on 25 October 2017

Flaky tail mouse denotes human atopic dermatitis in the steady state and by topical application with Dermatophagoides pteronyssinus extract.

scientific article

Functional involvement of TMF/ARA160 in Rab6-dependent retrograde membrane traffic.

scientific article

Functional tight junction barrier localizes in the second layer of the stratum granulosum of human epidermis.

scientific article

Gene knockout analysis of two gamma-tubulin isoforms in mice

scientific article published in June 2005

Hereditary palmoplantar keratoderma "clinical and genetic differential diagnosis".

scientific article published on March 2016

Herpetiform pemphigus showing reactivity with pemphigus vulgaris antigen (desmoglein 3)

scientific article published on 01 July 1997

Histamine-induced cyclic AMP accumulation in type-1 and type-2 astrocytes in primary culture

scientific article published in November 1991

Identification and Characterization of a Recessive Missense Mutation p.P277L in SERPINB7 in Nagashima-Type Palmoplantar Keratosis

scientific article

Identification of a human papillomavirus type 58 lineage in multiple Bowen's disease on the fingers: Case report and published work review

scientific article published on 23 July 2018

Infiltration of mast cells in pachydermia of pachydermoperiostosis

scientific article published on 13 February 2017

Japanese recurrent mutation c.6216+5G>T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa

scientific article published on 09 October 2015

Langerhans cell antigen capture through tight junctions confers preemptive immunity in experimental staphylococcal scalded skin syndrome.

scientific article published on 5 December 2011

Linear keratinocytic epidermal nevi on trunk skin caused by a somatic FGFR2 p.C382R mutation

scientific article published on 27 April 2018

Methotrexate-associated Intravascular Large B-cell Lymphoma in a Patient with Rheumatoid Arthritis.

scientific article published on 15 June 2016

Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis

scientific article

Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin

scientific article

Nagashima-type palmoplantar keratosis caused by biallelic maternal mutation of SERPINB7 with segmental uniparental disomy of chromosome 18q

scientific article published on 06 September 2020

Nagashima-type palmoplantar keratosis: a common Asian type caused by SERPINB7 protease inhibitor deficiency

scientific article

Novel KRT9 missense mutation in a Japanese case of epidermolytic palmoplantar keratoderma.

scientific article published on 25 October 2017

Novel frame-shift mutation in SERPINB7 in a Japanese patient with Nagashima-type palmoplantar keratosis.

scientific article

Novel gene mutations in Chédiak-Higashi syndrome with hyperpigmentation

scientific article published on 27 June 2019

Novel nonsense mutation in SERPINB7 and the treatment of foot odor in a patient with Nagashima-type palmoplantar keratosis

scientific article published on 25 April 2017

Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia

scientific article

Periungual squamous cell carcinoma induced by human papillomavirus type 59 in an immunosuppressed patient

scientific article published on 01 July 2009

Phakomatosis Pigmentokeratotica

scientific article published on 01 October 2019

Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation

scientific article published on 23 October 2020

Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses

scientific article

Recurrent gastrointestinal perforation in a patient with Ehlers-Danlos syndrome due to tenascin-X deficiency

scientific article published on 13 March 2015

Roles of Wnt Signaling in the Neurogenic Niche of the Adult Mouse Ventricular-Subventricular Zone.

scientific article

SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processing

scientific article

Sentan: a novel specific component of the apical structure of vertebrate motile cilia

scientific article

Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosis

scientific article published on 11 March 2017

Splice site mutation in COL7A1 resulting in aberrant in-frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial.

scientific article published on 3 March 2018

Stress-induced production of chemokines by hair follicles regulates the trafficking of dendritic cells in skin.

scientific article

Subclinical hypopigmentation of the skin and hair in a Japanese patient with Hermansky-Pudlak syndrome type 3

scientific article published on 16 October 2019

Successful treatment of widespread chronic gluteal hidradenitis suppurativa with combination of recycled skin graft and negative-pressure wound therapy

scientific article published on 21 September 2016

Successful treatment with secukinumab of three psoriatic patients undergoing dialysis

scientific article published on 27 October 2019

Three cases of Nagashima-type palmoplantar keratosis associated with atopic dermatitis: A diagnostic pitfall.

scientific article published on 23 November 2017

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