Developmental interneuron subtype deficits after targeted loss of Arx

BMC Neuroscience

Volumn 17, Issue 1, 2016, Pages

  Marsh, Eric D ^a,b   Nasrallah, MacLean Pancoast ^a,b   Walsh, Caroline ^a   Murray, Kaitlin A ^a   Nicole Sunnen, C ^a   McCoy, Almedia ^a   Golden, Jeffrey A ^a,b,c  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

Development; Interneuron; Migration

Indexed keywords

ADULT; ANIMAL EXPERIMENT; ANIMAL TISSUE; BRAIN CORTEX; CELL COUNT; DORSAL REGION; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; INTERNEURON; NEURAL STEM CELL; NONHUMAN; PRECURSOR; STOCHASTIC MODEL; X CHROMOSOME INACTIVATION; ANIMAL; C57BL MOUSE; CELL MOTION; CYTOLOGY; DEFICIENCY; GENETICS; GROWTH, DEVELOPMENT AND AGING; METABOLISM; NEOCORTEX; PATHOLOGY; PHYSIOLOGY; TRANSGENIC MOUSE;

ARX PROTEIN, MOUSE; CALB2 PROTEIN, MOUSE; CALBINDIN; CALRETININ; HOMEODOMAIN PROTEIN; NEUROPEPTIDE Y; PARVALBUMIN; TRANSCRIPTION FACTOR;

ANIMALS; CALBINDIN 2; CALBINDINS; CELL COUNT; CELL MOVEMENT; HIPPOCAMPUS; HOMEODOMAIN PROTEINS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; INTERNEURONS; MICE, INBRED C57BL; MICE, TRANSGENIC; NEOCORTEX; NEURAL STEM CELLS; NEUROPEPTIDE Y; PARVALBUMINS; TRANSCRIPTION FACTORS;

EID: 84977109228     PISSN: None     EISSN: 14712202     Source Type: Journal    
DOI: 10.1186/s12868-016-0265-8     Document Type: Article

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