Shenzhao Lu
Shenzhao Lu
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Extracellular αB-crystallin modulates the inflammatory responses
Y Guo, P Liang, S Lu, R Chen, Y Yin, J Zhou
Biochemical and biophysical research communications 508 (1), 282-288, 2019
Suppression of astrocytic autophagy by αB-crystallin contributes to α-synuclein inclusion formation
S Lu, Y Guo, P Liang, S Zhang, S Yin, Y Yin, X Wang, F Ding, X Gu, ...
Translational neurodegeneration 8, 1-14, 2019
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila
LD Goodman, H Cope, Z Nil, TA Ravenscroft, WL Charng, S Lu, AC Tien, ...
The American Journal of Human Genetics 108 (9), 1669-1691, 2021
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
S Lu, R Hernan, PC Marcogliese, Y Huang, TS Gertler, M Akcaboy, S Liu, ...
The American Journal of Human Genetics 109 (4), 571-586, 2022
'Fly-ing'from rare to common neurodegenerative disease mechanisms
M Ma, MJ Moulton, S Lu, HJ Bellen
Trends in Genetics, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement
S Lu, M Ma, X Mao, CA Bacino, J Jankovic, VR Sutton, JA Bartley, X Wang, ...
The American Journal of Human Genetics 109 (10), 1932-1943, 2022
The recurrent de novo c. 2011C> T missense variant in MTSS2 causes syndromic intellectual disability
Y Huang, G Lemire, LC Briere, F Liu, MW Wessels, X Wang, M Osmond, ...
The American Journal of Human Genetics 109 (10), 1923-1931, 2022
Inhibition of astrocytic DRD2 suppresses CNS inflammation in an animal model of multiple sclerosis
S Lu, Y Wu, Y Guo, P Liang, S Yin, Y Yin, X Zhang, YF Liu, H Wang, ...
Journal of Experimental Medicine 219 (9), e20210998, 2022
Finding the ‘Guilty’ Gene Variant of Sporadic Parkinson’s Disease Via CRISPR/Cas9
S Lu, J Zhou
Neuroscience bulletin 33, 115-117, 2017
Sphingolipids in neurodegenerative diseases
X Pan, D Dutta, S Lu, HJ Bellen
Frontiers in Neuroscience 17, 1137893, 2023
Very Long-Chain Fatty Acids Induce Glial-Derived Sphingosine-1-Phosphate Synthesis, Secretion, and Neuroinflammation
H Chung, Q Ye, YJ Park, Z Zuo, O Kanca, JW Mok, SG Tattikota, S Lu, ...
Cell Metabolism 35 (5), 855-874, 2023
向骊羽, 赵浩宇, 黄孟飞, 鹿伸朝, 范婕妤, 耿宇聪, 陶科, 侯太平
四川大学学报: 自然科学版 49 (4), 914-918, 2012
Loss of neuron navigator 2 impairs brain and cerebellar development
A Accogli, S Lu, I Musante, P Scudieri, JA Rosenfeld, M Severino, ...
The Cerebellum 22 (2), 206-222, 2023
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival
M Ma, X Zhang, Y Zheng, S Lu, X Pan, X Mao, H Pan, H Chung, H Wang, ...
Human Molecular Genetics 32 (6), 984-997, 2023
Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms
Y Huang, M Ma, X Mao, D Pehlivan, O Kanca, F Un-Candan, L Shu, ...
Human Molecular Genetics 31 (16), 2751-2765, 2022
A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins
A Guichard, S Lu, O Kanca, D Bressan, Y Huang, M Ma, SS Juste, ...
Cell Reports 42 (8), 2023
Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays
X Pan, AN Alvarez, M Ma, S Lu, MW Crawford, LC Briere, O Kanca, ...
medRxiv, 2023
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