about
Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnessesMutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosisCentriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesisClaudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient miceA 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 dermatitisSentan: a novel specific component of the apical structure of vertebrate motile cilia.External antigen uptake by Langerhans cells with reorganization of epidermal tight junction barriersFlaky tail mouse denotes human atopic dermatitis in the steady state and by topical application with Dermatophagoides pteronyssinus extract.A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.Stress-induced production of chemokines by hair follicles regulates the trafficking of dendritic cells in skin.Odf2-deficient mother centrioles lack distal/subdistal appendages and the ability to generate primary cilia.Nagashima-type palmoplantar keratosis: a common Asian type caused by SERPINB7 protease inhibitor deficiency.Functional involvement of TMF/ARA160 in Rab6-dependent retrograde membrane traffic.SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processing.Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skinEpidermal cell turnover across tight junctions based on Kelvin's tetrakaidecahedron cell shape.Epidermal barrier dysfunction and cutaneous sensitization in atopic diseases.Roles of Wnt Signaling in the Neurogenic Niche of the Adult Mouse Ventricular-Subventricular Zone.Hereditary palmoplantar keratoderma "clinical and genetic differential diagnosis".Langerhans cell antigen capture through tight junctions confers preemptive immunity in experimental staphylococcal scalded skin syndrome.A peculiar internalization of claudins, tight junction-specific adhesion molecules, during the intercellular movement of epithelial cells.Functional tight junction barrier localizes in the second layer of the stratum granulosum of human epidermis.Identification and Characterization of a Recessive Missense Mutation p.P277L in SERPINB7 in Nagashima-Type Palmoplantar Keratosis.3D visualization of epidermal Langerhans cells.Infiltration of mast cells in pachydermia of pachydermoperiostosis.Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosis.Novel KRT9 missense mutation in a Japanese case of epidermolytic palmoplantar keratoderma.Familial acanthosis nigricans with p.K650T FGFR3 mutation.Novel nonsense mutation in SERPINB7 and the treatment of foot odor in a patient with Nagashima-type palmoplantar keratosis.Three cases of Nagashima-type palmoplantar keratosis associated with atopic dermatitis: A diagnostic pitfall.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.Histamine-induced cyclic AMP accumulation in type-1 and type-2 astrocytes in primary culture.Gene knockout analysis of two gamma-tubulin isoforms in mice.Splice site mutation in COL7A1 resulting in aberrant in-frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial.Methotrexate-associated Intravascular Large B-cell Lymphoma in a Patient with Rheumatoid Arthritis.Case of lymphoplasmacytic plaque in children: Analysis of the distribution of infiltrating immune cells.Epidermal tight junction barrier function is altered by skin inflammation, but not by filaggrin-deficient stratum corneum.Case of non-Herlitz junctional epidermolysis bullosa with COL17A1 mutation.Novel frame-shift mutation in SERPINB7 in a Japanese patient with Nagashima-type palmoplantar keratosis.Effective treatment by glycolic acid peeling for cutaneous manifestation of familial generalized acanthosis nigricans caused by FGFR3 mutation.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Akiharu Kubo
@ast
Akiharu Kubo
@en
Akiharu Kubo
@es
Akiharu Kubo
@nl
type
label
Akiharu Kubo
@ast
Akiharu Kubo
@en
Akiharu Kubo
@es
Akiharu Kubo
@nl
prefLabel
Akiharu Kubo
@ast
Akiharu Kubo
@en
Akiharu Kubo
@es
Akiharu Kubo
@nl
P1053
I-2711-2014
P106
P1153
55628552341
P31
P3829
P496
0000-0003-0902-3586
P569
2000-01-01T00:00:00Z