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Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis

Autor: R A Eady, David W. Melton, Thomas M. Magin, Sabine Leitgeb, O Swensson, R M Porter

Publikováno v: The Journal of Cell Biology

Bullous congenital ichthyosiform erythroderma (BCIE) is a dominantly inherited blistering skin disorder caused by point mutations in the suprabasal cytokeratins 1 or 10. Targeting the murine cytokeratin 10 gene in ES cells resulted in mice with diffe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3da825f3204adcff6db978e4ef0c4cc2
http://europepmc.org/articles/PMC2120736

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[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]

Autor: O, Swensson, B, Swensson, B, Nölle, R, Rochels, B, Wannke, H J, Thiel

Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 217(1)

Meesmann's corneal dystrophy (OMIM 122,100) is a rare autosomal dominant disorder of the corneal epithelium. It manifests in early childhood and affects both eyes. The disease is characterized by variable patterned dot-like corneal opacities and intr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::82772245aeb200dfeed90d57c1d523b3
https://pubmed.ncbi.nlm.nih.gov/10949816

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[Pachyonychia congenita. Keratin gene mutations with pleiotropic effect]

Autor: O, Swensson

Publikováno v: Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete. 50(7)

Pachyonychia congenita (PC) comprises a heterogeneous group of autosomal dominantly inherited conditions showing characteristic nail thickening and associated signs such as palmoplantar keratoderma, follicular keratoses, and mucosal leukokeratoses. L

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5cca9988bc3b1465930b3e25759ccc8c
https://pubmed.ncbi.nlm.nih.gov/10464680

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Association of lymphocytic colitis with linear IgA dermatosis

Autor: E, Stüber, O, Swensson, R, Nitsche, T, Nickel, M, Sticherling, E, Christophers, U R, Fölsch

Publikováno v: Zeitschrift fur Gastroenterologie. 37(6)

The case of a 66-year-old female patient is presented, who suffered from chronic watery diarrhea. In addition, she developed linear IgA dermatosis after oral treatment of a presumed yeast infection with nystatin. To evaluate the reason for her diarrh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3fa16407bb30c4586112d3b18c811ed4
https://pubmed.ncbi.nlm.nih.gov/10427659

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Comèl-Netherton syndrome complicated by papillomatous skin lesions containing human papillomaviruses 51 and 52 and plane warts containing human papillomavirus 16

Autor: R, Fölster-Holst, O, Swensson, E, Stockfleth, H, Mönig, U, Mrowietz, E, Christophers

Publikováno v: The British journal of dermatology. 140(6)

We describe a 28-year-old woman with characteristic clinical signs of Comèl-Netherton syndrome (CNS) who showed numerous plane warts on her face and forearms and papillomatous skin tumours affecting her groins and genitoanal skin. Using human papill

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8fa9c7afe2582c31b0a122f6382fdd00
https://pubmed.ncbi.nlm.nih.gov/10354085

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Linear IgA disease associated with lymphocytic colitis

Autor: O, Swensson, E, Stüber, T, Nickel, M, Sticherling, R F, Ghohestani, R, Nitsche, E, Christophers

Publikováno v: The British journal of dermatology. 140(2)

A 66-year-old woman presented with a bullous skin eruption and chronic diarrhoea. Lesional skin showed subepidermal blistering, and direct immunofluorescence of perilesional skin revealed linear deposits of IgA at the dermoepidermal junction, establi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::684aea2dd2546907f52fa00395fe452c
https://pubmed.ncbi.nlm.nih.gov/10233230

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[Progressive disseminated essential telangiectasia with conjunctival involvement]

Autor: B, Swensson, O, Swensson, G, Häring

Publikováno v: Klinische Monatsblatter fur Augenheilkunde. 212(2)

Widespread idiopathic telangiectasia (generalized essential telangiectasia) is a rare skin disorder characterized by the development and gradual spreading of telangiectases. The condition tends to affect women in their midthirties. For no apparent re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fa161f8ad52095ce0c5b129071aa1643
https://pubmed.ncbi.nlm.nih.gov/9577812

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Facial rash mimicking cutaneous acute graft-versus-host disease after allogeneic stem cell transplantation for osteomyelofibrosis – was Demodex the culprit?

Autor: E W Herbst, C Busemann, O Swensson, Gottfried Dölken, Thomas Kiefer, C Lotze, William Krüger, Frank Schüler

Publikováno v: Bone Marrow Transplantation. 37:711-712

Facial rash mimicking cutaneous acute graft-versus-host disease after allogeneic stem cell transplantation for osteomyelofibrosis – was Demodex the culprit?

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::42cf1c86dc4b08b267f09f5b53f867af
https://doi.org/10.1038/sj.bmt.1705296

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