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Lena Ho

Showing results (41-50 of 46) with videos related to

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Human Genetics|November 2, 2013
C5orf42 is the major gene responsible for OFD syndrome type VIEstelle Lopez, Christel Thauvin-Robinet, Bruno Reversade, et al.
Oncogene|March 3, 2022
PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP productionUpadhyayula S Srinivas, Norbert S C Tay, Patrick Jaynes, et al.
Oncogene|May 6, 2022
Correction: PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP productionUpadhyayula S Srinivas, Norbert S C Tay, Patrick Jaynes, et al.
The Journal of Clinical Investigation|August 5, 2020
Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiencyEnrica Ek Tan, Richard A Hopkins, Chrissie K Lim, et al.
American Journal of Human Genetics|July 2, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathyHui Hui Wong, Sze Hwee Seet, Michael Maier, et al.
American Journal of Human Genetics|May 26, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathyHui Hui Wong, Sze Hwee Seet, Michael Maier, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Human Genetics|November 2, 2013
C5orf42 is the major gene responsible for OFD syndrome type VIEstelle Lopez, Christel Thauvin-Robinet, Bruno Reversade, et al.
Oncogene|March 3, 2022
PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP productionUpadhyayula S Srinivas, Norbert S C Tay, Patrick Jaynes, et al.
Oncogene|May 6, 2022
Correction: PLK1 inhibition selectively induces apoptosis in ARID1A deficient cells through uncoupling of oxygen consumption from ATP productionUpadhyayula S Srinivas, Norbert S C Tay, Patrick Jaynes, et al.
The Journal of Clinical Investigation|August 5, 2020
Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiencyEnrica Ek Tan, Richard A Hopkins, Chrissie K Lim, et al.
American Journal of Human Genetics|July 2, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathyHui Hui Wong, Sze Hwee Seet, Michael Maier, et al.
American Journal of Human Genetics|May 26, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathyHui Hui Wong, Sze Hwee Seet, Michael Maier, et al.
Pageof 5