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Sabine Fuchs

Showing results (81-90 of 84) with videos related to

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Human Genetics|September 21, 2019
MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathyMelissa H Broeks, Hanan E Shamseldin, Amal Alhashem, et al.
Cell Reports Methods|November 19, 2024
Accelerated production of human epithelial organoids in a miniaturized spinning bioreactorShicheng Ye, Ary Marsee, Gilles S van Tienderen, et al.
Proteomics|May 20, 2025
Meeting Report: The Japanese-German Symposium on the "Advancement and Application of Proteoform-Centric Proteomics" (Kyoto, Japan, 2024)Nobuaki Takemori, Philipp T Kaulich, Jan Hahn, et al.
Human Molecular Genetics|August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5CKlaas Koop, Weimin Yuan, Federico Tessadori, et al.
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Showing results (81-90 of 84) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 84 results.
Human Genetics|September 21, 2019
MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathyMelissa H Broeks, Hanan E Shamseldin, Amal Alhashem, et al.
Cell Reports Methods|November 19, 2024
Accelerated production of human epithelial organoids in a miniaturized spinning bioreactorShicheng Ye, Ary Marsee, Gilles S van Tienderen, et al.
Proteomics|May 20, 2025
Meeting Report: The Japanese-German Symposium on the "Advancement and Application of Proteoform-Centric Proteomics" (Kyoto, Japan, 2024)Nobuaki Takemori, Philipp T Kaulich, Jan Hahn, et al.
Human Molecular Genetics|August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5CKlaas Koop, Weimin Yuan, Federico Tessadori, et al.
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