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Marcel F Jonkman

Showing results (81-90 of 124) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 2015
Bullous Pemphigoid With a Dual Pattern of Glomerular Immune Complex DiseaseEwout J Hoorn, Noor E Taams, Tiina Hurskainen, et al.
The Journal of Investigative Dermatology|June 25, 2010
Revertant mosaicism due to a second-site mutation in COL7A1 in a patient with recessive dystrophic epidermolysis bullosaAnna M G Pasmooij, Marta Garcia, Maria J Escamez, et al.
Virulence|December 14, 2017
From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteriaAndrea N García-Pérez, Anne de Jong, Sabryna Junker, et al.
European Journal of Dermatology : EJD|August 23, 2011
Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newbornEsteve Darwich, Asunción Vicente, Maria C Bolling, et al.
Experimental Dermatology|July 19, 2018
Murine type VII collagen distorts outcome in human skin graft mouse model for dystrophic epidermolysis bullosaJeroen Bremer, Duco Kramer, Daryll S Eichhorn, et al.
Human Molecular Genetics|February 26, 2015
Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplexKatarzyna B Gostyńska, Miranda Nijenhuis, Henny Lemmink, et al.
The Journal of Investigative Dermatology|July 9, 2016
PDE4 Inhibition as Potential Treatment of Epidermolysis Bullosa AcquisitaHiroshi Koga, Andreas Recke, Gestur Vidarsson, et al.
Journal of the American Academy of Dermatology|November 21, 2017
Serration pattern analysis for differentiating epidermolysis bullosa acquisita from other pemphigoid diseasesJoost M Meijer, Ingeborg Atefi, Gilles F H Diercks, et al.
American Journal of Human Genetics|September 22, 2005
Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosaMarcel F Jonkman, Anna M G Pasmooij, Suzanne G M A Pasmans, et al.
The Journal of Biological Chemistry|December 30, 2004
Deficiency of ATP2C1, a Golgi ion pump, induces secretory pathway defects in endoplasmic reticulum (ER)-associated degradation and sensitivity to ER stressJose Ramos-Castañeda, Young-nam Park, Ming Liu, et al.
Pageof 13

Showing results (81-90 of 124) with videos related to

Sort By:
Pageof 13
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 2015
Bullous Pemphigoid With a Dual Pattern of Glomerular Immune Complex DiseaseEwout J Hoorn, Noor E Taams, Tiina Hurskainen, et al.
The Journal of Investigative Dermatology|June 25, 2010
Revertant mosaicism due to a second-site mutation in COL7A1 in a patient with recessive dystrophic epidermolysis bullosaAnna M G Pasmooij, Marta Garcia, Maria J Escamez, et al.
Virulence|December 14, 2017
From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteriaAndrea N García-Pérez, Anne de Jong, Sabryna Junker, et al.
European Journal of Dermatology : EJD|August 23, 2011
Extensive acantholysis as the major histological feature of a severe case of Dowling Meara-epidermolysis bullosa simplex: a reappraisal of acantholysis in the newbornEsteve Darwich, Asunción Vicente, Maria C Bolling, et al.
Experimental Dermatology|July 19, 2018
Murine type VII collagen distorts outcome in human skin graft mouse model for dystrophic epidermolysis bullosaJeroen Bremer, Duco Kramer, Daryll S Eichhorn, et al.
Human Molecular Genetics|February 26, 2015
Mutation in exon 1a of PLEC, leading to disruption of plectin isoform 1a, causes autosomal-recessive skin-only epidermolysis bullosa simplexKatarzyna B Gostyńska, Miranda Nijenhuis, Henny Lemmink, et al.
The Journal of Investigative Dermatology|July 9, 2016
PDE4 Inhibition as Potential Treatment of Epidermolysis Bullosa AcquisitaHiroshi Koga, Andreas Recke, Gestur Vidarsson, et al.
Journal of the American Academy of Dermatology|November 21, 2017
Serration pattern analysis for differentiating epidermolysis bullosa acquisita from other pemphigoid diseasesJoost M Meijer, Ingeborg Atefi, Gilles F H Diercks, et al.
American Journal of Human Genetics|September 22, 2005
Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosaMarcel F Jonkman, Anna M G Pasmooij, Suzanne G M A Pasmans, et al.
The Journal of Biological Chemistry|December 30, 2004
Deficiency of ATP2C1, a Golgi ion pump, induces secretory pathway defects in endoplasmic reticulum (ER)-associated degradation and sensitivity to ER stressJose Ramos-Castañeda, Young-nam Park, Ming Liu, et al.
Pageof 13