Peng Xu

9PUBLICATIONS
41CO-AUTHORS
Neurology and neuromuscular diseasesHaematological tumoursProteomics and intermolecular interactions (excl. medical proteomics)Infant and child healthPhotochemistry
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Publications (9)

|Jul 10, 2026
Dystrophic changes of nigrostriatal axons harboring a Synj1 Parkinson mutation suggest catastrophic failure of endocytic mechanisms.

|Sep 16, 2025
Impaired hematopoiesis and embryonic lethality at midgestation of mice lacking both lipid transfer proteins VPS13A and VPS13C.

Peng Xu, Rubia Isler Mancuso, Marianna Leonzino

|Sep 03, 2025
Multiple interactions recruit BLTP2 to ER-PM contacts to control plasma membrane dynamics.

Anbang Dai, Peng Xu, Chase Amos

|Jun 04, 2025
Defect in hematopoiesis and embryonic lethality at midgestation of <i>Vps13a/Vps13c</i> double knockout mice.

Peng Xu, Rubia Isler Mancuso, Marianna Leonzino

|Apr 10, 2025
The bridge-like lipid transport protein VPS13C/PARK23 mediates ER-lysosome contacts following lysosome damage.

Xinbo Wang, Peng Xu, Amanda Bentley-DeSousa

|Apr 18, 2024
Parkinsonism Sac domain mutation in Synaptojanin-1 affects ciliary properties in iPSC-derived dopaminergic neurons.

Nisha Mohd Rafiq, Kenshiro Fujise, Martin Shaun Rosenfeld

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Frequent Collaborators

8 joint publications

Pietro De Camilli

2 joint publications

Lin Shao

2 joint publications

Chase Amos

2 joint publications

Shawn M Ferguson