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

J S Kern

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 2, 2004
[Hereditary blistering disorders]C Has, J S Kern, L Bruckner-Tuderman
The British Journal of Dermatology|October 15, 2021
Ultralow-dose rituximab in pemphigus: a single-centre experienceK Simpson, Z M Low, T Yap, et al.
Clinical and Experimental Dermatology|December 6, 2014
Alitretinoin in the treatment of palmoplantar mycosis fungoides: a new and promising therapeutic approachB Miernik, V Schmidt, K Technau-Hafsi, et al.
Nature|March 14, 2003
Nanosecond radio bursts from strong plasma turbulence in the Crab pulsarT H Hankins, J S Kern, J C Weatherall, et al.
Dermatology (Basel, Switzerland)|June 23, 2012
Acromelanosis albo-punctata: a distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvementA W Arnold, J S Kern, P H Itin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 18, 2009
A familial case of tricho-rhino-phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 geneA Sendi-Naderi, H-J Lüdecke, S Unger, 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|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 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 2, 2004
[Hereditary blistering disorders]C Has, J S Kern, L Bruckner-Tuderman
The British Journal of Dermatology|October 15, 2021
Ultralow-dose rituximab in pemphigus: a single-centre experienceK Simpson, Z M Low, T Yap, et al.
Clinical and Experimental Dermatology|December 6, 2014
Alitretinoin in the treatment of palmoplantar mycosis fungoides: a new and promising therapeutic approachB Miernik, V Schmidt, K Technau-Hafsi, et al.
Nature|March 14, 2003
Nanosecond radio bursts from strong plasma turbulence in the Crab pulsarT H Hankins, J S Kern, J C Weatherall, et al.
Dermatology (Basel, Switzerland)|June 23, 2012
Acromelanosis albo-punctata: a distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvementA W Arnold, J S Kern, P H Itin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 18, 2009
A familial case of tricho-rhino-phalangeal syndrome type III with a novel missense mutation in exon 6 of the TRPS1 geneA Sendi-Naderi, H-J Lüdecke, S Unger, 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|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 2