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Marcel F Jonkman

Showing results (71-80 of 124) with videos related to

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Archives of Dermatology|October 19, 2011
Natural gene therapy in dystrophic epidermolysis bullosaPeter C van den Akker, Miranda Nijenhuis, Gonnie Meijer, et al.
Human Mutation|March 26, 2003
Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutationsPetra H L Schuilenga-Hut, Pieter v d Vlies, Marcel F Jonkman, et al.
BMC Dermatology|August 31, 2004
Enhanced diagnostic immunofluorescence using biopsies transported in salineRobert M Vodegel, Marcelus C J M de Jong, Hillegonda J Meijer, et al.
Arthritis and Rheumatism|March 2, 2006
Abundance of the long pentraxin PTX3 at sites of leukocytoclastic lesions in patients with small-vessel vasculitisAndre P van Rossum, Hendri H Pas, Fausto Fazzini, et al.
Plos One|February 23, 2018
A "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosaPeter C van den Akker, Anna M G Pasmooij, Hans Joenje, et al.
International Journal of Medical Informatics|January 10, 2019
Detection of u-serrated patterns in direct immunofluorescence images of autoimmune bullous diseases by inhibition-augmented COSFIRE filtersChenyu Shi, Joost M Meijer, Jiapan Guo, et al.
The Journal of Investigative Dermatology|January 8, 2004
Clouston syndrome can mimic pachyonychia congenitaMaurice A M van Steensel, Marcel F Jonkman, Michel van Geel, et al.
Molecular Therapy. Nucleic Acids|October 19, 2016
Antisense Oligonucleotide-mediated Exon Skipping as a Systemic Therapeutic Approach for Recessive Dystrophic Epidermolysis BullosaJeroen Bremer, Olivier Bornert, Alexander Nyström, et al.
Arthritis Research & Therapy|October 4, 2006
Is disturbed clearance of apoptotic keratinocytes responsible for UVB-induced inflammatory skin lesions in systemic lupus erythematosus?Esther Reefman, Marcelus C J M de Jong, Hilde Kuiper, et al.
JAMA Dermatology|January 29, 2016
Heterozygosity for a Novel Missense Mutation in the ITGB4 Gene Associated With Autosomal Dominant Epidermolysis BullosaIana Turcan, Anna M G Pasmooij, Peter C van den Akker, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Archives of Dermatology|October 19, 2011
Natural gene therapy in dystrophic epidermolysis bullosaPeter C van den Akker, Miranda Nijenhuis, Gonnie Meijer, et al.
Human Mutation|March 26, 2003
Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutationsPetra H L Schuilenga-Hut, Pieter v d Vlies, Marcel F Jonkman, et al.
BMC Dermatology|August 31, 2004
Enhanced diagnostic immunofluorescence using biopsies transported in salineRobert M Vodegel, Marcelus C J M de Jong, Hillegonda J Meijer, et al.
Arthritis and Rheumatism|March 2, 2006
Abundance of the long pentraxin PTX3 at sites of leukocytoclastic lesions in patients with small-vessel vasculitisAndre P van Rossum, Hendri H Pas, Fausto Fazzini, et al.
Plos One|February 23, 2018
A "late-but-fitter revertant cell" explains the high frequency of revertant mosaicism in epidermolysis bullosaPeter C van den Akker, Anna M G Pasmooij, Hans Joenje, et al.
International Journal of Medical Informatics|January 10, 2019
Detection of u-serrated patterns in direct immunofluorescence images of autoimmune bullous diseases by inhibition-augmented COSFIRE filtersChenyu Shi, Joost M Meijer, Jiapan Guo, et al.
The Journal of Investigative Dermatology|January 8, 2004
Clouston syndrome can mimic pachyonychia congenitaMaurice A M van Steensel, Marcel F Jonkman, Michel van Geel, et al.
Molecular Therapy. Nucleic Acids|October 19, 2016
Antisense Oligonucleotide-mediated Exon Skipping as a Systemic Therapeutic Approach for Recessive Dystrophic Epidermolysis BullosaJeroen Bremer, Olivier Bornert, Alexander Nyström, et al.
Arthritis Research & Therapy|October 4, 2006
Is disturbed clearance of apoptotic keratinocytes responsible for UVB-induced inflammatory skin lesions in systemic lupus erythematosus?Esther Reefman, Marcelus C J M de Jong, Hilde Kuiper, et al.
JAMA Dermatology|January 29, 2016
Heterozygosity for a Novel Missense Mutation in the ITGB4 Gene Associated With Autosomal Dominant Epidermolysis BullosaIana Turcan, Anna M G Pasmooij, Peter C van den Akker, et al.
Pageof 13