Developmental retardation, microcephaly, and peptiduria in mice without aminopeptidase P1

Biochemical and Biophysical Research Communications

Volumn 429, Issue 3-4, 2012, Pages 204-209

  Yoon, Sang Ho ^a   Bae, Young Soo ^b   Mun, Mi Sun ^a   Park, Kyeong Yeol ^a   Ye, Sang Kyu ^a   Kim, Eunjoon ^b   Kim, Myoung Hwan ^a,c  

^a Seoul National University College of Medicine   (South Korea)

^b Korea Advanced Institute of Science and Technology (KAIST)   (South Korea)

^c Seoul National University Bundang Hospital   (South Korea)

Author keywords

Aminopeptidase P1 (APP1); APP1 deficiency; Developmental retardation; Microcephaly; Peptiduria; Xpnpep1 Knockout

Indexed keywords

AMINOPEPTIDASE P; AMINOPEPTIDASE P1; IMINO OLIGOPEPTIDE; OLIGOPEPTIDE; UNCLASSIFIED DRUG;

ABNORMAL URINE COMPOSITION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BODY GROWTH; BRAIN DEVELOPMENT; CONTROLLED STUDY; DISEASE SEVERITY; EMBRYO; ENZYME DEFICIENCY; FEMALE; GENE INACTIVATION; GROWTH RETARDATION; MALE; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; MICROCEPHALY; MOUSE; NEWBORN; NONHUMAN; PEPTIDURIA; PHYSICAL DEVELOPMENT; PRIORITY JOURNAL; PROTEIN METABOLISM; PROTEIN URINE LEVEL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; URINALYSIS; URINE COLOR;

AMINOPEPTIDASES; ANIMALS; GROWTH DISORDERS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; MICROCEPHALY; PEPTIDES;

MAMMALIA; MUS;

EID: 84870702727     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2012.10.104     Document Type: Article

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