A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect.

Yap, Chan Choo

A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect. [electronic resource] - The Journal of biological chemistry 12 2018 - 18890-18902 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural

1083-351X

10.1074/jbc.RA118.004462 doi


Adaptor Protein Complex 2--metabolism
Animals
Binding Sites
COS Cells
Cell Adhesion Molecules--metabolism
Chlorocebus aethiops
Dendrites--genetics
Doublecortin Domain Proteins
Doublecortin Protein
Endocytosis--genetics
HEK293 Cells
Humans
Mice
Microtubule-Associated Proteins--genetics
Mutation
Nerve Growth Factors--metabolism
Neurons--cytology
Neuropeptides--genetics
Rats