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Shenzhao Lu

Showing results (1-10 of 19) with videos related to

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Neuroscience Bulletin|October 16, 2016
Finding the 'Guilty' Gene Variant of Sporadic Parkinson's Disease Via CRISPR/Cas9Shenzhao Lu, Jiawei Zhou
Frontiers in Neuroscience|March 6, 2023
Sphingolipids in neurodegenerative diseasesXueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Trends in Genetics : TIG|April 28, 2022
'Fly-ing' from rare to common neurodegenerative disease mechanismsMengqi Ma, Matthew J Moulton, Shenzhao Lu, et al.
Human Molecular Genetics|October 18, 2022
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survivalMengqi Ma, Xi Zhang, Yiming Zheng, et al.
Cell Metabolism|April 21, 2023
Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammationHyung-Lok Chung, Qi Ye, Ye-Jin Park, et al.
Human Molecular Genetics|March 29, 2022
Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanismsYan Huang, Mengqi Ma, Xiao Mao, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Elife|December 11, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between in vivo and in vitro assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Nature Neuroscience|August 26, 2024
Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stressLindsey D Goodman, Isha Ralhan, Xin Li, et al.
American Journal of Human Genetics|September 6, 2022
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disabilityYan Huang, Gabrielle Lemire, Lauren C Briere, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Neuroscience Bulletin|October 16, 2016
Finding the 'Guilty' Gene Variant of Sporadic Parkinson's Disease Via CRISPR/Cas9Shenzhao Lu, Jiawei Zhou
Frontiers in Neuroscience|March 6, 2023
Sphingolipids in neurodegenerative diseasesXueyang Pan, Debdeep Dutta, Shenzhao Lu, et al.
Trends in Genetics : TIG|April 28, 2022
'Fly-ing' from rare to common neurodegenerative disease mechanismsMengqi Ma, Matthew J Moulton, Shenzhao Lu, et al.
Human Molecular Genetics|October 18, 2022
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survivalMengqi Ma, Xi Zhang, Yiming Zheng, et al.
Cell Metabolism|April 21, 2023
Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammationHyung-Lok Chung, Qi Ye, Ye-Jin Park, et al.
Human Molecular Genetics|March 29, 2022
Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanismsYan Huang, Mengqi Ma, Xiao Mao, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Elife|December 11, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between in vivo and in vitro assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Nature Neuroscience|August 26, 2024
Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stressLindsey D Goodman, Isha Ralhan, Xin Li, et al.
American Journal of Human Genetics|September 6, 2022
The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disabilityYan Huang, Gabrielle Lemire, Lauren C Briere, et al.
Pageof 2