Multiplex genetic fate mapping reveals a novel route of neocortical neurogenesis, which is altered in the Ts65Dn mouse model of down syndrome

Annals of Internal Medicine

Volumn 158, Issue 6, 2013, Pages 5106-5119

  Tyler, William A ^a   Haydar, Tarik F ^a  

^a BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL COUNT; CONFOCAL MICROSCOPY; DOWN SYNDROME; EMBRYO; FEMALE; GENE MAPPING; GLIA CELL; IMMUNOHISTOCHEMISTRY; MICROCEPHALY; MOUSE; NEOCORTEX; NERVE CELL GROWTH; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SUBVENTRICULAR ZONE; TIME LAPSE IMAGING;

ANIMALS; CELL DIVISION; CELL LINEAGE; DISEASE MODELS, ANIMAL; DOWN SYNDROME; EXCITATORY AMINO ACID TRANSPORTER 1; FATTY ACID-BINDING PROTEINS; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENES, REPORTER; INTEGRASES; MALE; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, MUTANT STRAINS; MICROCEPHALY; MICROSCOPY, VIDEO; NEOCORTEX; NERVE TISSUE PROTEINS; NEURAL STEM CELLS; NEUROGENESIS; ORGAN CULTURE TECHNIQUES; PREGNANCY; RECEPTORS, ANTIGEN, T-CELL, ALPHA-BETA;

EID: 84875161879     PISSN: 00034819     EISSN: 15393704     Source Type: Journal    
DOI: 10.1523/JNEUROSCI.5380-12.2013     Document Type: Article

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