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Paymaan Jafar-Nejad

Showing results (1-10 of 75) with videos related to

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Bone|September 13, 2023
Antisense oligonucleotides targeting a NOTCH3 mutation in male mice ameliorate the cortical osteopenia of lateral meningocele syndromeErnesto Canalis, Magda Mocarska, Lauren Schilling, et al.
Plos One|January 3, 2025
A NOTCH3 pathogenic variant influences osteogenesis and can be targeted by antisense oligonucleotides in induced pluripotent stem cellsErnesto Canalis, Jungeun Yu, Lauren Schilling, et al.
Frontiers in Neuroscience|October 30, 2023
Reduction of <i>Kcnt1</i> is therapeutic in mouse models of <i>SCN1A</i> and <i>SCN8A</i> epilepsySophie F Hill, Paymaan Jafar-Nejad, Frank Rigo, et al.
Current Genomics|September 2, 2009
Gene clusters, molecular evolution and disease: a speculationLeah I Elizondo, Paymaan Jafar-Nejad, J Marietta Clewing, et al.
Cells|June 25, 2026
Neurodegenerative NMNAT2 Deficiency Promotes APP Processing in a SARM1-Dependent MannerAndrea Enriquez, Sen Yang, Karen Ling, et al.
Biorxiv : the Preprint Server for Biology|May 4, 2026
NMNAT2-SARM1 Axis Drives Redox Failure and Disrupts APP Processing in NeuronsAndrea Enriquez, Sen Yang, Karen Ling, et al.
Medical Education Online|December 28, 2013
Playback Theatre as a tool to enhance communication in medical educationRamiro Salas, Kenya Steele, Amy Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
Regional rescue of spinocerebellar ataxia type 1 phenotypes by 14-3-3epsilon haploinsufficiency in mice underscores complex pathogenicity in neurodegenerationPaymaan Jafar-Nejad, Christopher S Ward, Ronald Richman, et al.
Epilepsia|July 27, 2022
Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2Sophie F Hill, Julie M Ziobro, Paymaan Jafar-Nejad, et al.
Cell Reports|December 15, 2021
Sarm1 haploinsufficiency or low expression levels after antisense oligonucleotides delay programmed axon degenerationStacey Anne Gould, Jonathan Gilley, Karen Ling, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Bone|September 13, 2023
Antisense oligonucleotides targeting a NOTCH3 mutation in male mice ameliorate the cortical osteopenia of lateral meningocele syndromeErnesto Canalis, Magda Mocarska, Lauren Schilling, et al.
Plos One|January 3, 2025
A NOTCH3 pathogenic variant influences osteogenesis and can be targeted by antisense oligonucleotides in induced pluripotent stem cellsErnesto Canalis, Jungeun Yu, Lauren Schilling, et al.
Frontiers in Neuroscience|October 30, 2023
Reduction of <i>Kcnt1</i> is therapeutic in mouse models of <i>SCN1A</i> and <i>SCN8A</i> epilepsySophie F Hill, Paymaan Jafar-Nejad, Frank Rigo, et al.
Current Genomics|September 2, 2009
Gene clusters, molecular evolution and disease: a speculationLeah I Elizondo, Paymaan Jafar-Nejad, J Marietta Clewing, et al.
Cells|June 25, 2026
Neurodegenerative NMNAT2 Deficiency Promotes APP Processing in a SARM1-Dependent MannerAndrea Enriquez, Sen Yang, Karen Ling, et al.
Biorxiv : the Preprint Server for Biology|May 4, 2026
NMNAT2-SARM1 Axis Drives Redox Failure and Disrupts APP Processing in NeuronsAndrea Enriquez, Sen Yang, Karen Ling, et al.
Medical Education Online|December 28, 2013
Playback Theatre as a tool to enhance communication in medical educationRamiro Salas, Kenya Steele, Amy Lin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
Regional rescue of spinocerebellar ataxia type 1 phenotypes by 14-3-3epsilon haploinsufficiency in mice underscores complex pathogenicity in neurodegenerationPaymaan Jafar-Nejad, Christopher S Ward, Ronald Richman, et al.
Epilepsia|July 27, 2022
Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2Sophie F Hill, Julie M Ziobro, Paymaan Jafar-Nejad, et al.
Cell Reports|December 15, 2021
Sarm1 haploinsufficiency or low expression levels after antisense oligonucleotides delay programmed axon degenerationStacey Anne Gould, Jonathan Gilley, Karen Ling, et al.
Pageof 8