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Jessie E Greenslade

Showing results (1-10 of 6) with videos related to

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Biorxiv : the Preprint Server for Biology|March 27, 2026
Single-cell chromatin profiling reveals dynamic regulatory logic and enhancer elements in brain and retina developmentJessie E Greenslade, Hemagowri Veeravenkatasubramanian, Marisa L Reed, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Barcoding Notch signaling in the developing brainAbigail Siniscalco, Roshan Priyarangana Perera, Jessie E Greenslade, et al.
Brain Pathology (Zurich, Switzerland)|March 29, 2021
Serpin neuropathology in the P497S UBQLN2 mouse model of ALS/FTDNicole R Higgins, Jessie E Greenslade, Josephine J Wu, et al.
Development (Cambridge, England)|November 22, 2024
Barcoding Notch signaling in the developing brainAbigail M Siniscalco, Roshan Priyarangana Perera, Jessie E Greenslade, et al.
Human Molecular Genetics|April 23, 2021
ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein importBrian C Lin, Trong H Phung, Nicole R Higgins, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2020
ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of functionJosephine J Wu, Ashley Cai, Jessie E Greenslade, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Biorxiv : the Preprint Server for Biology|March 27, 2026
Single-cell chromatin profiling reveals dynamic regulatory logic and enhancer elements in brain and retina developmentJessie E Greenslade, Hemagowri Veeravenkatasubramanian, Marisa L Reed, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Barcoding Notch signaling in the developing brainAbigail Siniscalco, Roshan Priyarangana Perera, Jessie E Greenslade, et al.
Brain Pathology (Zurich, Switzerland)|March 29, 2021
Serpin neuropathology in the P497S UBQLN2 mouse model of ALS/FTDNicole R Higgins, Jessie E Greenslade, Josephine J Wu, et al.
Development (Cambridge, England)|November 22, 2024
Barcoding Notch signaling in the developing brainAbigail M Siniscalco, Roshan Priyarangana Perera, Jessie E Greenslade, et al.
Human Molecular Genetics|April 23, 2021
ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein importBrian C Lin, Trong H Phung, Nicole R Higgins, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2020
ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of functionJosephine J Wu, Ashley Cai, Jessie E Greenslade, et al.
Pageof 1