S. Lu

发表

'Fly-ing' from rare to common neurodegenerative disease mechanisms.

H. Bellen, M. Moulton, Mengqi Ma, 2022, Trends in genetics : TIG.

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability.

H. Bellen, K. Boycott, K. Kernohan, 2022, American journal of human genetics.

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.

Michael F. Wangler, Q. K. Tan, R. Pfundt, 2021, American journal of human genetics.

De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement.

Michael F. Wangler, J. Rosenfeld, K. Prescott, 2022, American journal of human genetics.

Recurrent chromosome changes in 62 primary gastric carcinomas detected by comparative genomic hybridization.

J. Trent, X. Guan, J. Sham, 2000, Cancer genetics and cytogenetics.

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures.

W. Chung, Tracy S. Gertler, H. Bellen, 2022, American journal of human genetics.

Sphingolipids in neurodegenerative diseases

H. Bellen, Debdeep Dutta, Xueyang Pan, 2023, Frontiers in Neuroscience.

Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation.

S. G. Tattikota, H. Bellen, Oguz Kanca, 2023, Cell metabolism.

A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins

Michael F. Wangler, S. Celniker, K. Wan, 2023, Cell Reports.