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Lu, Shenzhao
38
results:
Search for persons
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Format
Online (38)
Mediatypes
Articles (Online) (18)
OpenAccess-fulltext (20)
Sorted by: Relevance
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?
1
De novo variants in FRYL are associated with developmental ..:
Pan, Xueyang
;
Tao, Alice M.
;
Lu, Shenzhao
...
The American Journal of Human Genetics. 111 (2024) 4 - p. 742-760 , 2024
Link:
https://doi.org/10.1016/..
?
2
Homozygous missense variants in YKT6 result in loss of func..:
Ma, Mengqi
;
Ganapathi, Mythily
;
Zheng, Yiming
...
Genetics in Medicine. 26 (2024) 7 - p. 101125 , 2024
Link:
https://doi.org/10.1016/..
?
3
Sphingolipids in neurodegenerative diseases:
Pan, Xueyang
;
Dutta, Debdeep
;
Lu, Shenzhao
.
Frontiers in Neuroscience. 17 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
Allelic strengths of encephalopathy-associated UBA5 variant..:
Pan, Xueyang
;
Alvarez, Albert N
;
Ma, Mengqi
...
eLife. 12 (2023) - p. , 2023
Link:
https://doi.org/10.7554/..
?
5
A comprehensive Drosophila resource to identify key functio..:
Guichard, Annabel
;
Lu, Shenzhao
;
Kanca, Oguz
...
Cell Reports. 42 (2023) 8 - p. 112842 , 2023
Link:
https://doi.org/10.1016/..
?
6
Very-long-chain fatty acids induce glial-derived sphingosin..:
Chung, Hyung-lok
;
Ye, Qi
;
Park, Ye-Jin
...
Cell Metabolism. 35 (2023) 5 - p. 855-874.e5 , 2023
Link:
https://doi.org/10.1016/..
?
7
Allelic strengths of encephalopathy-associated UBA5 variant..:
Pan, Xueyang
;
Alvarez, Albert N
;
Ma, Mengqi
...
eLife. 12 (2023) - p. , 2023
Link:
https://doi.org/10.7554/..
?
8
The recurrent de novo c.2011C>T missense variant in MTSS2 c..:
Huang, Yan
;
Lemire, Gabrielle
;
Briere, Lauren C.
...
The American Journal of Human Genetics. 109 (2022) 10 - p. 1923-1931 , 2022
Link:
https://doi.org/10.1016/..
?
9
'Fly-ing' from rare to common neurodegenerative disease mec..:
Ma, Mengqi
;
Moulton, Matthew J.
;
Lu, Shenzhao
.
Trends in Genetics. 38 (2022) 9 - p. 972-984 , 2022
Link:
https://doi.org/10.1016/..
?
10
De novo variants in FRMD5 are associated with developmental..:
Lu, Shenzhao
;
Ma, Mengqi
;
Mao, Xiao
...
The American Journal of Human Genetics. 109 (2022) 10 - p. 1932-1943 , 2022
Link:
https://doi.org/10.1016/..
?
11
Novel dominant and recessive variants in human ROBO1 cause ..:
Huang, Yan
;
Ma, Mengqi
;
Mao, Xiao
...
Human Molecular Genetics. 31 (2022) 16 - p. 2751-2765 , 2022
Link:
https://doi.org/10.1093/..
?
12
The fly homolog ofSUPT16H, a gene associated with neurodeve..:
Ma, Mengqi
;
Zhang, Xi
;
Zheng, Yiming
...
Human Molecular Genetics. 32 (2022) 6 - p. 984-997 , 2022
Link:
https://doi.org/10.1093/..
?
13
Inhibition of astrocytic DRD2 suppresses CNS inflammation i..:
Lu, Shen-zhao
;
Wu, Yue
;
Guo, Yong-shun
...
Journal of Experimental Medicine. 219 (2022) 9 - p. , 2022
Link:
https://doi.org/10.1084/..
?
14
Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Dev..:
Accogli, Andrea
;
Lu, Shenzhao
;
Musante, Ilaria
...
The Cerebellum. 22 (2022) 2 - p. 206-222 , 2022
Link:
https://doi.org/10.1007/..
?
15
Suppression of astrocytic autophagy by αB-crystallin contri..:
Lu, Shen-zhao
;
Guo, Yong-shun
;
Liang, Pei-zhou
...
Translational Neurodegeneration. 8 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
1-15