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Nature Cell Biology
|
February 26, 2026
Mitochondria contact lipid droplets through the mitochondrial import complex binding to lipid metabolism enzyme Ayr1
Sandra Heinen, Vitasta Tiku, Alexander Grevel, et al.
Iscience
|
November 9, 2020
c-Abl Inhibition Activates TFEB and Promotes Cellular Clearance in a Lysosomal Disorder
Pablo S Contreras, Pablo J Tapia, Lila González-Hódar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia
Maria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Science (New York, N.Y.)
|
September 8, 2022
The human disease gene LYSET is essential for lysosomal enzyme transport and viral infection
Christopher M Richards, Sabrina Jabs, Wenjie Qiao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2021
Pathogenic variants in GNPTAB and GNPTG encoding distinct subunits of GlcNAc-1-phosphotransferase differentially impact bone resorption in patients with mucolipidosis type II and III
Giorgia Di Lorenzo, Lena M Westermann, Timur A Yorgan, et al.
Nature Cell Biology
|
December 21, 2022
Sphingolipid subtypes differentially control proinsulin processing and systemic glucose homeostasis
Kerstin Griess, Michael Rieck, Nadine Müller, et al.
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Showing results (71-80 of 76) with videos related to
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Page
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You have reached the last page of results.
This site can display upto 76 results.
Nature Cell Biology
|
February 26, 2026
Mitochondria contact lipid droplets through the mitochondrial import complex binding to lipid metabolism enzyme Ayr1
Sandra Heinen, Vitasta Tiku, Alexander Grevel, et al.
Iscience
|
November 9, 2020
c-Abl Inhibition Activates TFEB and Promotes Cellular Clearance in a Lysosomal Disorder
Pablo S Contreras, Pablo J Tapia, Lila González-Hódar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 20, 2024
Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia
Maria Asif, Arwa Ishaq A Khayyat, Salem Alawbathani, et al.
Science (New York, N.Y.)
|
September 8, 2022
The human disease gene LYSET is essential for lysosomal enzyme transport and viral infection
Christopher M Richards, Sabrina Jabs, Wenjie Qiao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2021
Pathogenic variants in GNPTAB and GNPTG encoding distinct subunits of GlcNAc-1-phosphotransferase differentially impact bone resorption in patients with mucolipidosis type II and III
Giorgia Di Lorenzo, Lena M Westermann, Timur A Yorgan, et al.
Nature Cell Biology
|
December 21, 2022
Sphingolipid subtypes differentially control proinsulin processing and systemic glucose homeostasis
Kerstin Griess, Michael Rieck, Nadine Müller, et al.
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