Cdk5 and its substrates, Dcx and p27kip1, regulate cytoplasmic dilation formation and nuclear elongation in migrating neurons

Development (Cambridge)

Volumn 141, Issue 18, 2014, Pages 3540-3550

  Nishimura, Yoshiaki V ^a,b,c   Shikanai, Mima ^a   Hoshino, Mikio ^d   Ohshima, Toshio ^e   Nabeshima, Yo Ichi ^f   Mizutani, Ken Ichi ^b   Nagata, Koh Ichi ^c   Nakajima, Kazunori ^a   Kawauchi, Takeshi ^a,g  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b DOSHISHA UNIVERSITY   (Japan)

^c INSTITUTE FOR DEVELOPMENTAL RESEARCH   (Japan)

^d NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^e WASEDA UNIVERSITY   (Japan)

^f FOUNDATION FOR BIOMEDICAL RESEARCH AND INNOVATION   (Japan)

^g JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

C jun N terminal kinase; Cdkn1b; Cell migration; Cytoskeleton; Doublecortin; Endocytosis; Mouse; Rab5

Indexed keywords

C-JUN N-TERMINAL KINASE; CDKN1B; CELL MIGRATION; CYTOSKELETON; DOUBLECORTIN; ENDOCYTOSIS; MOUSE; RAB5;

ANIMALS; CELL MOVEMENT; CELL NUCLEUS; CYCLIN-DEPENDENT KINASE 5; CYCLIN-DEPENDENT KINASE INHIBITOR P27; CYTOPLASM; CYTOSKELETON; DNA PRIMERS; ELECTROPORATION; IMMUNOHISTOCHEMISTRY; MICE; MICROTUBULE-ASSOCIATED PROTEINS; NEURONS; NEUROPEPTIDES; PLASMIDS;

EID: 84906875114     PISSN: 09501991     EISSN: 14779129     Source Type: Journal    
DOI: 10.1242/dev.111294     Document Type: Article

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