Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice

Journal of Neuroscience

Volumn 23, Issue 5, 2003, Pages 1569-1573

  Ren, Jun ^a   Lee, Syann ^a   Pagliardini, Silvia ^a   Gérard, Matthieu ^b   Stewart, Colin L ^c   Greer, John J ^a   Wevrick, Rachel ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b DIF   (France)

^c NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Apnea; Breathing; Medulla; necdin; Newborn; Prader Willi

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL CYCLE; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FEMALE; GENE; GENE DELETION; LACZ GENE; MALE; MOUSE; NDN GENE; NERVE CELL; NERVE CELL DIFFERENTIATION; NEUROMODULATION; NEWBORN; NEWBORN PERIOD; NONHUMAN; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REGULATORY MECHANISM; REPORTER GENE; RESPIRATION CENTER; RESPIRATORY DRIVE; RESPIRATORY FAILURE;

EID: 0037335439     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.23-05-01569.2003     Document Type: Article

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