Abnormal renal phenotype in L1 knockout mice: A novel cause of CAKUT

Nephrology Dialysis Transplantation

Volumn 17, Issue SUPPL. 9, 2002, Pages 42-44

  Debiec, Hanna ^a,c   Kutsche, Michael ^b   Schachner, Melitta ^b   Ronco, Pierre ^a  

^a INSERM   (France)

^b UNIVERSITY OF HAMBURG   (Germany)

^c HÔPITAL TENON   (France)

Author keywords

Knockout mice; L1 cell adhesion molecule; Urinary malformations

Indexed keywords

CELL ADHESION MOLECULE; IMMUNOGLOBULIN; L1 PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRANCHING MORPHOGENESIS; CELL BUDDING; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; DISEASE SEVERITY; EMBRYONIC STRUCTURES; GENE DELETION; GENE TARGETING; HEREDITY; HYDRONEPHROSIS; KIDNEY COLLECTING TUBULE; KIDNEY DEVELOPMENT; KIDNEY DUPLICATION; KIDNEY FAILURE; KIDNEY MALFORMATION; KIDNEY MEDULLA; KNOCKOUT MOUSE; MOUSE; NEPHRON; NONHUMAN; PENETRANCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FAMILY; SIGNAL TRANSDUCTION; URETER DUPLICATION; URETER MALFORMATION; URINARY TRACT MALFORMATION;

EID: 0036378926     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/17.suppl_9.42     Document Type: Article

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