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J Christof M Gebhardt

Showing results (31-40 of 35) with videos related to

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Nature Communications|April 16, 2026
Discovery of an Endonuclease G-inhibitory Ku80-peptide protecting against leukemogenic rearrangements at the MLL breakpoint clusterJulia Eberle, Ahmed Salem, Mara Hofmann, et al.
Nature Communications|March 16, 2022
Myosin VI regulates the spatial organisation of mammalian transcription initiationYukti Hari-Gupta, Natalia Fili, Ália Dos Santos, et al.
Genes & Development|April 16, 2026
The microprotein SMIM26 connects metabolite transporters of the outer and inner mitochondrial membranes and is essential for respiratory chain functionKevin Heizler, Anastasia Chugunova, Mara Hofmann, et al.
Nature Communications|November 7, 2023
Transcriptional reprogramming by mutated IRF4 in lymphomaNikolai Schleussner, Pierre Cauchy, Vedran Franke, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Nature Communications|April 16, 2026
Discovery of an Endonuclease G-inhibitory Ku80-peptide protecting against leukemogenic rearrangements at the MLL breakpoint clusterJulia Eberle, Ahmed Salem, Mara Hofmann, et al.
Nature Communications|March 16, 2022
Myosin VI regulates the spatial organisation of mammalian transcription initiationYukti Hari-Gupta, Natalia Fili, Ália Dos Santos, et al.
Genes & Development|April 16, 2026
The microprotein SMIM26 connects metabolite transporters of the outer and inner mitochondrial membranes and is essential for respiratory chain functionKevin Heizler, Anastasia Chugunova, Mara Hofmann, et al.
Nature Communications|November 7, 2023
Transcriptional reprogramming by mutated IRF4 in lymphomaNikolai Schleussner, Pierre Cauchy, Vedran Franke, et al.
Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.
Pageof 4