Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Traupe

Showing results (141-150 of 166) with videos related to

Pageof 17
Sort By:
Tissue Antigens|September 15, 2001
Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German familiesM Schmitt-Egenolf, C Windemuth, H C Hennies, et al.
Acta Neurologica Scandinavica|April 10, 2002
Serum cytokine levels do not correlate with disease activity and severity assessed by brain MRI in multiple sclerosisJ Kraus, B S Kuehne, J Tofighi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 10, 2013
Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profileA M Perusquía-Ortiz, V Oji, M C Sauerland, et al.
American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.
European Neurology|November 27, 2001
Prognostic value of soluble tumor necrosis factor receptors 1 and 2 in multiple sclerosis patients treated with interferon beta-1bC Laske, P Oschmann, J Tofighi, et al.
American Journal of Medical Genetics|June 28, 2001
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paragangliomaS Niemann, J Becker-Follmann, G Nürnberg, et al.
Acta Neurologica Scandinavica|March 3, 2001
Induction of sTNF-R1 and sTNF-R2 by interferon beta-1b in correlation with clinical and MRI activityC Laske, P Oschmann, J Tofighi, et al.
The British Journal of Dermatology|December 1, 2015
Association of Cole disease with novel heterozygous mutations in the somatomedin-B domains of the ENPP1 gene: necessary, but not always sufficientN A Schlipf, H Traupe, Y Gilaberte, et al.
Experimental Dermatology|August 22, 2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective lociP Hensen, C Windemuth, U Hüffmeier, et al.
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
Pageof 17

Showing results (141-150 of 166) with videos related to

Sort By:
Pageof 17
Tissue Antigens|September 15, 2001
Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German familiesM Schmitt-Egenolf, C Windemuth, H C Hennies, et al.
Acta Neurologica Scandinavica|April 10, 2002
Serum cytokine levels do not correlate with disease activity and severity assessed by brain MRI in multiple sclerosisJ Kraus, B S Kuehne, J Tofighi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 10, 2013
Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profileA M Perusquía-Ortiz, V Oji, M C Sauerland, et al.
American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.
European Neurology|November 27, 2001
Prognostic value of soluble tumor necrosis factor receptors 1 and 2 in multiple sclerosis patients treated with interferon beta-1bC Laske, P Oschmann, J Tofighi, et al.
American Journal of Medical Genetics|June 28, 2001
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paragangliomaS Niemann, J Becker-Follmann, G Nürnberg, et al.
Acta Neurologica Scandinavica|March 3, 2001
Induction of sTNF-R1 and sTNF-R2 by interferon beta-1b in correlation with clinical and MRI activityC Laske, P Oschmann, J Tofighi, et al.
The British Journal of Dermatology|December 1, 2015
Association of Cole disease with novel heterozygous mutations in the somatomedin-B domains of the ENPP1 gene: necessary, but not always sufficientN A Schlipf, H Traupe, Y Gilaberte, et al.
Experimental Dermatology|August 22, 2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective lociP Hensen, C Windemuth, U Hüffmeier, et al.
Genomics|June 1, 1992
Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panelH Traupe, A M van den Ouweland, B A van Oost, et al.
Pageof 17