O. Swensson

发表

Inflammatory properties of neutrophil-activating protein-1/interleukin 8 (NAP-1/IL-8) in human skin: a light- and electronmicroscopic study.

J. Schröder, E. Christophers, C. Schubert, 1991, The Journal of investigative dermatology.

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

E. Lane, T. Strachan, I. Leigh, 1995, Nature Genetics.

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

T. Meitinger, S. Schuffenhauer, A. Meindl, 1993, Journal of medical genetics.

Morphology of the keratin filament network in palm and sole skin: Evidence for site-dependent features based on stereological analysis

R. Eady, O. Swensson, 1996, Archives of Dermatological Research.

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Jonathan E. Moore, J. Uitto, D. Frazer, 1997, Nature Genetics.

Association of lymphocytic colitis with linear IgA dermatosis.

M. Sticherling, E. Christophers, U. Fölsch, 1999, Zeitschrift fur Gastroenterologie.

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

G. Dölken, W. Krüger, T. Kiefer, 2006, Bone Marrow Transplantation.

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

J. Uitto, W. McLean, F. Smith, 2000, Experimental eye research.

Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.

J. R. McMillan, J. McGrath, R. Eady, 1999, The Journal of investigative dermatology.

Generalized atrophic benign epidermolysis bullosa in 2 siblings complicated by multiple squamous cell carcinomas.

E. Christophers, O. Swensson, 1998, Archives of dermatology.

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

D. Melton, R. Eady, T. Magin, 1996, The Journal of cell biology.

Positive patch tests with a dermatophagoides mix relate to an increased responsiveness to standard patch test allergens

W. Uter, E. Stockfleth, E. Christophers, 2002, Contact dermatitis.

A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

W. McLean, H. Thiel, R. Rochels, 2000, The British journal of ophthalmology.

Microscopic Findings and Clinical Course

S. Ugurel, K. Ruprecht, W. Tilgen, 2016 .

A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy

A. Irvine, W. McLean, J. Moore, 2002, The British journal of ophthalmology.

Transendothelial cell diapedesis of neutrophils in inflamed human skin

E. Christophers, C. Schubert, O. Swensson, 2004, Archives of Dermatological Research.

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.

E. Lane, I. Leigh, M. Shamsher, 1995, The Journal of investigative dermatology.