28 results on '"Lu, Shenzhao"'
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2. A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins.
3. Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma
4. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
5. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development
6. Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation
7. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
8. Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays
9. Author Response: Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays
10. Sphingolipids in neurodegenerative diseases
11. The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability
12. The fly homolog ofSUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival
13. De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement
14. 'Fly-ing' from rare to common neurodegenerative disease mechanisms
15. Finding the ‘Guilty’ Gene Variant of Sporadic Parkinson’s Disease Via CRISPR/Cas9
16. Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
17. The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival.
18. Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
19. Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms
20. Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development
21. Very Long-Chain Fatty Acids Induce Glial-Derived Sphingosine-1-Phosphate Synthesis, Secretion, and Neuroinflammation
22. TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila
23. TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila
24. Homozygous missense variants in YKT6result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma
25. Finding the ‘Guilty’ Gene Variant of Sporadic Parkinson’s Disease Via CRISPR/Cas9
26. A comprehensive Drosophilaresource to identify key functional interactions between SARS-CoV-2 factors and host proteins
27. De novo variants in PLCG1 are associated with hearing impairment, ocular pathology, and cardiac defects.
28. Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays.
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