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Judy Liu

Showing results (21-30 of 28) with videos related to

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Elife|March 1, 2017
Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cuesJulieta E Lischinsky, Katie Sokolowski, Peijun Li, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
Dynamic Regulation OF The Chromatin Environment By Ash1L Modulates Human Neuronal Structure And FunctionMegha Jhanji, Joseph A Ward, Calvin S Leung, et al.
Epilepsy Currents|March 31, 2021
Proceedings of the Sleep and Epilepsy Workshop: Section 1 Decreasing Seizures-Improving Sleep and Seizures, Themes for Future ResearchMark Quigg, Carl W Bazil, Melanie Boly, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Cancer Research|June 8, 2011
Overcoming hypoxia-induced apoptotic resistance through combinatorial inhibition of GSK-3β and CDK1Patrick A Mayes, Nathan G Dolloff, Colin J Daniel, et al.
Epilepsia|June 12, 2016
Rasmussen encephalitis tissue transfer programCarol A Kruse, Carlos A Pardo, Adam L Hartman, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Elife|March 1, 2017
Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cuesJulieta E Lischinsky, Katie Sokolowski, Peijun Li, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
Dynamic Regulation OF The Chromatin Environment By Ash1L Modulates Human Neuronal Structure And FunctionMegha Jhanji, Joseph A Ward, Calvin S Leung, et al.
Epilepsy Currents|March 31, 2021
Proceedings of the Sleep and Epilepsy Workshop: Section 1 Decreasing Seizures-Improving Sleep and Seizures, Themes for Future ResearchMark Quigg, Carl W Bazil, Melanie Boly, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Human Molecular Genetics|October 4, 2017
TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypesJulian Curiel, Guillermo Rodríguez Bey, Asako Takanohashi, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Cancer Research|June 8, 2011
Overcoming hypoxia-induced apoptotic resistance through combinatorial inhibition of GSK-3β and CDK1Patrick A Mayes, Nathan G Dolloff, Colin J Daniel, et al.
Epilepsia|June 12, 2016
Rasmussen encephalitis tissue transfer programCarol A Kruse, Carlos A Pardo, Adam L Hartman, et al.
Pageof 3