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List of works by Kazue Yoshida

Application of moisturizer to neonates prevents development of atopic dermatitis

article

Autoreactive CD4(+) T-cell clones to beta2-glycoprotein I in patients with antiphospholipid syndrome: preferential recognition of the major phospholipid-binding site

scientific article published on 01 September 2001

Cutaneous type pemphigus vulgaris: a rare clinical phenotype of pemphigus.

scientific article

Delayed-onset heat intolerance in a Japanese patient with X-linked hypohidrotic ectodermal dysplasia associated with a large deletion involving four genes.

scientific article published on 26 April 2017

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

Ectopic expression of epidermal antigens renders the lung a target organ in paraneoplastic pemphigus.

scientific article published on 31 May 2013

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

scientific article published on 22 November 2014

First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24.

scientific article published on 19 October 2016

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

scientific article

Immune response towards the amino-terminus of desmoglein 1 prevails across different activity stages in nonendemic pemphigus foliaceus

scientific article published on 15 February 2010

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

scientific article published on 27 April 2018

Novel EDA hemizygous frame-shift mutation c. 731delG (p.R244Qfs*36) underlies hypohidrotic ectodermal dysplasia in a Japanese family

scientific article published on 01 December 2014

Novel heterozygous deletion mutation c.821delC in the AAA domain of BCS1L underlies Björnstad syndrome

scientific article published on 20 January 2017

Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family.

scientific article published on 13 April 2017

Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate-ectodermal dysplasia syndrome in an Asian patient.

scientific article published on 24 April 2015

Restricted T-cell receptor beta-chain usage by T cells autoreactive to beta(2)-glycoprotein I in patients with antiphospholipid syndrome

scientific article published on 01 April 2002