Mian Cao

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Topics

Genome Wide Association

Top Venues

Neural regeneration research

NPJ Parkinson's disease

Proceedings of the National Academy of Sciences of the United States of America

This page only lists publications with an associated author ORCID identifier.

Publications

Xin Yi Ng, Mian Cao
Dysfunction of synaptic endocytic trafficking in Parkinson's disease. Neural regeneration research 19 (12) (2024)
Xin Yi Ng, Mian Cao
Dysfunction of synaptic endocytic trafficking in Parkinson's disease. Neural regeneration research 19 (12) (2024)
Xin Yi Ng, Mian Cao
Dysfunction of synaptic endocytic trafficking in Parkinson's disease. Neural regeneration research 19 (12) (2024)
Xin Yi Ng, Mian Cao
Dysfunction of synaptic endocytic trafficking in Parkinson's disease. Neural regeneration research 19 (12) (2024)
Xin Yi Ng, Yumei Wu, Youneng Lin, Sidra Mohamed Yaqoob, Lois E Greene, Pietro De Camilli, Mian Cao
Mutations in Parkinsonism-linked endocytic proteins synaptojanin1 and auxilin have synergistic effects on dopaminergic axonal pathology. NPJ Parkinson's disease 9 (1) (2023)
Xin Yi Ng, Yumei Wu, Youneng Lin, Sidra Mohamed Yaqoob, Lois E Greene, Pietro De Camilli, Mian Cao
Mutations in Parkinsonism-linked endocytic proteins synaptojanin1 and auxilin have synergistic effects on dopaminergic axonal pathology. NPJ Parkinson's disease 9 (1) (2023)
Xin Yi Ng, Yumei Wu, Youneng Lin, Sidra Mohamed Yaqoob, Lois E Greene, Pietro De Camilli, Mian Cao
Mutations in Parkinsonism-linked endocytic proteins synaptojanin1 and auxilin have synergistic effects on dopaminergic axonal pathology. NPJ Parkinson's disease 9 (1) (2023)
Xin Yi Ng, Yumei Wu, Youneng Lin, Sidra Mohamed Yaqoob, Lois E Greene, Pietro De Camilli, Mian Cao
Mutations in Parkinsonism-linked endocytic proteins synaptojanin1 and auxilin have synergistic effects on dopaminergic axonal pathology. NPJ Parkinson's disease 9 (1) (2023)
Mian Cao, Daehun Park, Yumei Wu, Pietro De Camilli
Absence of Sac2/INPP5F enhances the phenotype of a Parkinson's disease mutation of synaptojanin 1. Proceedings of the National Academy of Sciences of the United States of America 117 (22) (2020)