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

Ingrid Hausser

Showing results (41-50 of 112) with videos related to

Pageof 12
Sort By:
Molecular Therapy. Nucleic Acids|April 6, 2016
Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa KeratinocytesCristina Chamorro, Angeles Mencía, David Almarza, et al.
The Journal of Clinical Investigation|April 21, 2005
Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagenCassian Sitaru, Sidonia Mihai, Christoph Otto, et al.
The Journal of Cell Biology|April 4, 2007
12R-lipoxygenase deficiency disrupts epidermal barrier functionNikolas Epp, Gerhard Fürstenberger, Karsten Müller, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|May 22, 2013
Early venous manifestation of Ehlers-Danlos syndrome Type IV through a novel mutation in COL3A1Heiko Wendorff, Jaroslav Pelisek, Alexander Zimmermann, et al.
Human Molecular Genetics|February 16, 2011
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entityManuela Pigors, Dimitra Kiritsi, Sebastian Krümpelmann, et al.
Cell Communication and Signaling : CCS|April 6, 2017
TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cellsFabia Fricke, Jennifer Lee, Malwina Michalak, et al.
Human Molecular Genetics|March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Stroke|September 7, 2002
Ultrastructural connective tissue aberrations in patients with intracranial aneurysmsCaspar Grond-Ginsbach, Holger Schnippering, Ingrid Hausser, et al.
Skin Health and Disease|February 8, 2023
The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromesNatasha Stembridge, Brent J Doolan, Mark E Lavallee, et al.
Molecular & Cellular Proteomics : MCP|April 12, 2017
Database-augmented Mass Spectrometry Analysis of Exosomes Identifies Claudin 3 as a Putative Prostate Cancer BiomarkerThomas Stefan Worst, Jost von Hardenberg, Julia Christina Gross, et al.
Pageof 12

Showing results (41-50 of 112) with videos related to

Sort By:
Pageof 12
Molecular Therapy. Nucleic Acids|April 6, 2016
Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa KeratinocytesCristina Chamorro, Angeles Mencía, David Almarza, et al.
The Journal of Clinical Investigation|April 21, 2005
Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagenCassian Sitaru, Sidonia Mihai, Christoph Otto, et al.
The Journal of Cell Biology|April 4, 2007
12R-lipoxygenase deficiency disrupts epidermal barrier functionNikolas Epp, Gerhard Fürstenberger, Karsten Müller, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|May 22, 2013
Early venous manifestation of Ehlers-Danlos syndrome Type IV through a novel mutation in COL3A1Heiko Wendorff, Jaroslav Pelisek, Alexander Zimmermann, et al.
Human Molecular Genetics|February 16, 2011
Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entityManuela Pigors, Dimitra Kiritsi, Sebastian Krümpelmann, et al.
Cell Communication and Signaling : CCS|April 6, 2017
TGFBR2-dependent alterations of exosomal cargo and functions in DNA mismatch repair-deficient HCT116 colorectal cancer cellsFabia Fricke, Jennifer Lee, Malwina Michalak, et al.
Human Molecular Genetics|March 1, 2006
A human keratin 10 knockout causes recessive epidermolytic hyperkeratosisFelix B Müller, Marcel Huber, Tamar Kinaciyan, et al.
Stroke|September 7, 2002
Ultrastructural connective tissue aberrations in patients with intracranial aneurysmsCaspar Grond-Ginsbach, Holger Schnippering, Ingrid Hausser, et al.
Skin Health and Disease|February 8, 2023
The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromesNatasha Stembridge, Brent J Doolan, Mark E Lavallee, et al.
Molecular & Cellular Proteomics : MCP|April 12, 2017
Database-augmented Mass Spectrometry Analysis of Exosomes Identifies Claudin 3 as a Putative Prostate Cancer BiomarkerThomas Stefan Worst, Jost von Hardenberg, Julia Christina Gross, et al.
Pageof 12