Author

C. G. Burd

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cell Biology· 5

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell signaling & trafficking· 4 Approach:experimental assay· 4 Research Focus:cell type annotation· 3 Organism:human· 2 Assay:proteomics· 2 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Organism:Drosophila· 1

Frequent Co-Authors

A. Hilderink· 2 shared J. C. M. Holthuis· 2 shared J. Parolek· 2 shared T. Sokoya· 2 shared Y. Kim· 2 shared A. S. Klymchenko· 1 shared B. Sarkar· 1 shared C. Chitraju· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersCell Biology

A. Hilderink

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

Bridge-like lipid transfer protein family member 2 suppresses ciliogenesis

J. Parolek, C. G. Burd

This study identifies BLTP2 as a negative regulator of ciliogenesis, functioning as a lipid transfer protein between ER and tubular endosomes.

bioRxiv · Dec 7, 2023Cell Biology

Pathogenic variants of sphingomyelin synthase SMS2 disrupt lipid landscapes in the secretory pathway

T. Sokoya, J. Parolek, M. M. Foged, D. I. Danylchuk, M. Bozan, B. Sarkar, A. Hilderink, M. Philippi, L. D. Botto, P. A. Terhal, O. Maekitie, J. Piehler, Y. Kim, C. G. Burd, A. S. Klymchenko, , J. C. M. Holthuis

The paper shows pathogenic SMS2 variants disrupt lipid landscapes in the secretory pathway by trapping sphingomyelin in the ER and altering cholesterol and glycerophospholipid distributions.

bioRxiv · Apr 2, 2022Cell Biology

Ca2+-activated sphingomyelin scrambling and turnover mediate ESCRT-independent lysosomal repair

P. Niekamp, T. Sokoya, L. Vittadello, Y. Deng, Y. Kim, A. Hilderink, M. Imlau, C. J. Clarke, C. G. Burd, J. C. M. Holthuis

The paper identifies a Ca2+-activated sphingomyelin scrambling pathway that mediates ESCRT-independent lysosomal repair by converting sphingomyelin into repair intermediates.

bioRxiv · Mar 12, 2021Cell Biology

Conditional targeting of phosphatidylserine decarboxylase to lipid droplets

S. Kumar, C. Chitraju, R. V. Farese, T. C. Walther, C. G. Burd

This study identifies a second form of phosphatidylserine decarboxylase, PISD-LD, which localizes to lipid droplets and is regulated by nutritional state, revealing its role in neutral lipid storage.

bioRxiv · Oct 22, 2020Cell Biology

Retromer forms low order oligomers on supported lipid bilayers

C. L. Deatherage, J. Nikolaus, E. Karatekin, C. G. Burd

This study examines Retromer oligomerization on supported lipid bilayers and finds that it forms low-order oligomers without requiring cargo or accessory factors.

bioRxiv · Mar 31, 2020Cell Biology