Shenzhao Lu

发表

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.

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.

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

J. Pruneda, Oguz Kanca, D. Sweetser, 2023, eLife.

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

H. Bellen, J. Pruneda, Oguz Kanca, 2023, medRxiv.

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.

Denise G. Lanza, Jason D. Heaney, J. Posey, 2024, American journal of human genetics.

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.

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.

De novo variants in PLCG1 are associated with hearing impairment, ocular pathology, and cardiac defects

Lauren S Blieden, S. Lalani, B. Mandriani, 2024, medRxiv.

Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress.

Oguz Kanca, Julie Jacquemyn, Isha Ralhan, 2024, Nature neuroscience.

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

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