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Human Genetics
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September 21, 2019
MDH1 deficiency is a metabolic disorder of the malate-aspartate shuttle associated with early onset severe encephalopathy
Melissa 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 bioreactor
Shicheng 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 RAB5C
Klaas Koop, Weimin Yuan, Federico Tessadori, et al.
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of 9
Search research articles
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Showing results (81-90 of 84) with videos related to
Sort By:
Page
of 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 encephalopathy
Melissa 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 bioreactor
Shicheng 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 RAB5C
Klaas Koop, Weimin Yuan, Federico Tessadori, et al.
Page
of 9