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

Min Ae Lee-Kirsch

Showing results (41-50 of 86) with videos related to

Pageof 9
Sort By:
The Journal of Investigative Dermatology|August 17, 2021
Photosensitivity and cGAS-Dependent IFN-1 Activation in Patients with Lupus and TREX1 DeficiencyNicole Berndt, Christine Wolf, Kristina Fischer, et al.
Diabetes Care|May 24, 2011
Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotypeJulia Rohayem, Christian Ehlers, Bärbel Wiedemann, et al.
The Journal of Investigative Dermatology|April 15, 2011
Association screening in the Epidermal Differentiation Complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczemaIngo Marenholz, Vladimir A Gimenez Rivera, Jorge Esparza-Gordillo, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 19, 2007
A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupusMin Ae Lee-Kirsch, Dipanjan Chowdhury, Scott Harvey, et al.
Annals of the Rheumatic Diseases|August 28, 2016
Familial chilblain lupus due to a gain-of-function mutation in STINGNadja König, Christoph Fiehn, Christine Wolf, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 25, 2017
Lack of Trex1 Causes Systemic Autoimmunity despite the Presence of Antiretroviral DrugsMartin Achleitner, Martin Kleefisch, Alexander Hennig, et al.
Science Immunology|January 11, 2024
Disrupted degradative sorting of TLR7 is associated with human lupusHarshita Mishra, Claire Schlack-Leigers, Ee Lyn Lim, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2023
Hemophagocytic lymphohistiocytosis-like hyperinflammation due to a de novo mutation in DPP9Christine Wolf, Hannah Fischer, Jörn-Sven Kühl, et al.
Nature Communications|May 28, 2016
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNAChristine Wolf, Alexander Rapp, Nicole Berndt, et al.
Frontiers in Immunology|August 4, 2025
Case Report: Heterozygous <i>ADAR</i> c.3019G>A pathogenic variant associated with variable neurological symptoms and incomplete penetrance in a four-generational familyAnn-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
The Journal of Investigative Dermatology|August 17, 2021
Photosensitivity and cGAS-Dependent IFN-1 Activation in Patients with Lupus and TREX1 DeficiencyNicole Berndt, Christine Wolf, Kristina Fischer, et al.
Diabetes Care|May 24, 2011
Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotypeJulia Rohayem, Christian Ehlers, Bärbel Wiedemann, et al.
The Journal of Investigative Dermatology|April 15, 2011
Association screening in the Epidermal Differentiation Complex (EDC) identifies an SPRR3 repeat number variant as a risk factor for eczemaIngo Marenholz, Vladimir A Gimenez Rivera, Jorge Esparza-Gordillo, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 19, 2007
A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupusMin Ae Lee-Kirsch, Dipanjan Chowdhury, Scott Harvey, et al.
Annals of the Rheumatic Diseases|August 28, 2016
Familial chilblain lupus due to a gain-of-function mutation in STINGNadja König, Christoph Fiehn, Christine Wolf, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 25, 2017
Lack of Trex1 Causes Systemic Autoimmunity despite the Presence of Antiretroviral DrugsMartin Achleitner, Martin Kleefisch, Alexander Hennig, et al.
Science Immunology|January 11, 2024
Disrupted degradative sorting of TLR7 is associated with human lupusHarshita Mishra, Claire Schlack-Leigers, Ee Lyn Lim, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2023
Hemophagocytic lymphohistiocytosis-like hyperinflammation due to a de novo mutation in DPP9Christine Wolf, Hannah Fischer, Jörn-Sven Kühl, et al.
Nature Communications|May 28, 2016
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNAChristine Wolf, Alexander Rapp, Nicole Berndt, et al.
Frontiers in Immunology|August 4, 2025
Case Report: Heterozygous <i>ADAR</i> c.3019G>A pathogenic variant associated with variable neurological symptoms and incomplete penetrance in a four-generational familyAnn-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
Pageof 9