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Min Ae Lee-Kirsch

Showing results (11-20 of 86) with videos related to

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Pediatric Rheumatology Online Journal|January 4, 2024
A rare manifestation of STING-associated vasculopathy with onset in infancy: a case reportSophia Weidler, Sarah Koss, Christine Wolf, et al.
Nature Immunology|September 28, 2010
The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1Nan Yan, Ashton D Regalado-Magdos, Bart Stiggelbout, et al.
Journal of Child Neurology|March 5, 2009
Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 geneGeorgia Ramantani, Pascal Niggemann, Gabriele Hahn, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic RibonucleotidesBarbara Kind, Christine Wolf, Kerstin Engel, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|April 16, 2021
[How Often is Rare Really Rare? A Survey on the Frequency of Rare Diseases at a University Hospital]Tanita Kretschmer, Adrian Danker, Olaf Müller, et al.
Stem Cell Research|August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Stem Cell Research|September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Frontiers in Immunology|October 9, 2023
Case Report: Response of cutaneous lupus lesions in SLE to interferon receptor blockade parallels reduction of interferon score in bloodClaudia Günther, Christine Wolf, Louisa Fennen, et al.
Pediatric Rheumatology Online Journal|September 19, 2023
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositisTimmy Strauss, Claudia Günther, Anja Schnabel, et al.
Pediatric Rheumatology Online Journal|April 12, 2022
Precision treatment of Singleton Merten syndrome with ruxolitinib: a case reportPhilip Broser, Ursula von Mengershausen, Katrin Heldt, et al.
Pageof 9

Showing results (11-20 of 86) with videos related to

Sort By:
Pageof 9
Pediatric Rheumatology Online Journal|January 4, 2024
A rare manifestation of STING-associated vasculopathy with onset in infancy: a case reportSophia Weidler, Sarah Koss, Christine Wolf, et al.
Nature Immunology|September 28, 2010
The cytosolic exonuclease TREX1 inhibits the innate immune response to human immunodeficiency virus type 1Nan Yan, Ashton D Regalado-Magdos, Bart Stiggelbout, et al.
Journal of Child Neurology|March 5, 2009
Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 geneGeorgia Ramantani, Pascal Niggemann, Gabriele Hahn, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic RibonucleotidesBarbara Kind, Christine Wolf, Kerstin Engel, et al.
Gesundheitswesen (Bundesverband Der Arzte Des Offentlichen Gesundheitsdienstes (Germany))|April 16, 2021
[How Often is Rare Really Rare? A Survey on the Frequency of Rare Diseases at a University Hospital]Tanita Kretschmer, Adrian Danker, Olaf Müller, et al.
Stem Cell Research|August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Stem Cell Research|September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Frontiers in Immunology|October 9, 2023
Case Report: Response of cutaneous lupus lesions in SLE to interferon receptor blockade parallels reduction of interferon score in bloodClaudia Günther, Christine Wolf, Louisa Fennen, et al.
Pediatric Rheumatology Online Journal|September 19, 2023
Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositisTimmy Strauss, Claudia Günther, Anja Schnabel, et al.
Pediatric Rheumatology Online Journal|April 12, 2022
Precision treatment of Singleton Merten syndrome with ruxolitinib: a case reportPhilip Broser, Ursula von Mengershausen, Katrin Heldt, et al.
Pageof 9