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The Journal of Investigative Dermatology
|
August 17, 2021
Photosensitivity and cGAS-Dependent IFN-1 Activation in Patients with Lupus and TREX1 Deficiency
Nicole Berndt, Christine Wolf, Kristina Fischer, et al.
Diabetes Care
|
May 24, 2011
Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype
Julia 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 eczema
Ingo 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 lupus
Min 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 STING
Nadja 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 Drugs
Martin Achleitner, Martin Kleefisch, Alexander Hennig, et al.
Science Immunology
|
January 11, 2024
Disrupted degradative sorting of TLR7 is associated with human lupus
Harshita 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 DPP9
Christine 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 DNA
Christine 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 family
Ann-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
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of 9
Search research articles
Search
Showing results (41-50 of 86) with videos related to
Sort By:
Page
of 9
The Journal of Investigative Dermatology
|
August 17, 2021
Photosensitivity and cGAS-Dependent IFN-1 Activation in Patients with Lupus and TREX1 Deficiency
Nicole Berndt, Christine Wolf, Kristina Fischer, et al.
Diabetes Care
|
May 24, 2011
Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype
Julia 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 eczema
Ingo 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 lupus
Min 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 STING
Nadja 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 Drugs
Martin Achleitner, Martin Kleefisch, Alexander Hennig, et al.
Science Immunology
|
January 11, 2024
Disrupted degradative sorting of TLR7 is associated with human lupus
Harshita 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 DPP9
Christine 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 DNA
Christine 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 family
Ann-Kathrin Bauer, Iris Marquardt, Benedikt Sundermann, et al.
Page
of 9