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C Has

Showing results (71-80 of 90) with videos related to

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Human Brain Mapping|April 7, 2021
Delayed access to conscious processing in multiple sclerosis: Reduced cortical activation and impaired structural connectivityArzu C Has Silemek, Jean-Philippe Ranjeva, Bertrand Audoin, et al.
The British Journal of Dermatology|October 28, 2017
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutationA Reimer, A Schwieger-Briel, Y He, et al.
Clinical Genetics|August 27, 2014
FERMT1 promoter mutations in patients with Kindler syndromeC Has, N Chmel, L Levati, et al.
The British Journal of Dermatology|April 11, 2016
A unique LAMB3 splice-site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countriesB Mayer, P Silló, M Mazán, et al.
The British Journal of Dermatology|July 26, 2008
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytesC Has, R J Ludwig, C Herz, et al.
The British Journal of Dermatology|March 5, 2010
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotypeM J Arin, G Grimberg, H Schumann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 21, 2021
Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin DiseasesC Has, M El Hachem, H Bučková, et al.
The British Journal of Dermatology|August 18, 2009
Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohortJ S Kern, G Grüninger, R Imsak, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|July 29, 2014
Phased-array of microcoils allows MR microscopy of ex vivo human skin samples at 9.4 TK Göbel, O G Gruschke, J Leupold, et al.
The Journal of Pathology|October 24, 2007
Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoformsJ S Kern, C Herz, E Haan, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Human Brain Mapping|April 7, 2021
Delayed access to conscious processing in multiple sclerosis: Reduced cortical activation and impaired structural connectivityArzu C Has Silemek, Jean-Philippe Ranjeva, Bertrand Audoin, et al.
The British Journal of Dermatology|October 28, 2017
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutationA Reimer, A Schwieger-Briel, Y He, et al.
Clinical Genetics|August 27, 2014
FERMT1 promoter mutations in patients with Kindler syndromeC Has, N Chmel, L Levati, et al.
The British Journal of Dermatology|April 11, 2016
A unique LAMB3 splice-site mutation with founder effect from the Balkans causes lethal epidermolysis bullosa in several European countriesB Mayer, P Silló, M Mazán, et al.
The British Journal of Dermatology|July 26, 2008
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytesC Has, R J Ludwig, C Herz, et al.
The British Journal of Dermatology|March 5, 2010
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotypeM J Arin, G Grimberg, H Schumann, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 21, 2021
Practical management of epidermolysis bullosa: consensus clinical position statement from the European Reference Network for Rare Skin DiseasesC Has, M El Hachem, H Bučková, et al.
The British Journal of Dermatology|August 18, 2009
Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohortJ S Kern, G Grüninger, R Imsak, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|July 29, 2014
Phased-array of microcoils allows MR microscopy of ex vivo human skin samples at 9.4 TK Göbel, O G Gruschke, J Leupold, et al.
The Journal of Pathology|October 24, 2007
Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoformsJ S Kern, C Herz, E Haan, et al.
Pageof 9