000 01714 a2200493 4500
005 20250518002046.0
264 0 _c20190417
008 201904s 0 0 eng d
022 _a1083-351X
024 7 _a10.1074/jbc.RA118.004462
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aYap, Chan Choo
245 0 0 _aA dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect.
_h[electronic resource]
260 _bThe Journal of biological chemistry
_c12 2018
300 _a18890-18902 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aAdaptor Protein Complex 2
_xmetabolism
650 0 4 _aAnimals
650 0 4 _aBinding Sites
650 0 4 _aCOS Cells
650 0 4 _aCell Adhesion Molecules
_xmetabolism
650 0 4 _aChlorocebus aethiops
650 0 4 _aDendrites
_xgenetics
650 0 4 _aDoublecortin Domain Proteins
650 0 4 _aDoublecortin Protein
650 0 4 _aEndocytosis
_xgenetics
650 0 4 _aHEK293 Cells
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aMicrotubule-Associated Proteins
_xgenetics
650 0 4 _aMutation
650 0 4 _aNerve Growth Factors
_xmetabolism
650 0 4 _aNeurons
_xcytology
650 0 4 _aNeuropeptides
_xgenetics
650 0 4 _aRats
700 1 _aDigilio, Laura
700 1 _aKruczek, Kamil
700 1 _aRoszkowska, Matylda
700 1 _aFu, Xiao-Qin
700 1 _aLiu, Judy S
700 1 _aWinckler, Bettina
773 0 _tThe Journal of biological chemistry
_gvol. 293
_gno. 49
_gp. 18890-18902
856 4 0 _uhttps://doi.org/10.1074/jbc.RA118.004462
_zAvailable from publisher's website
999 _c28909670
_d28909670