No evidence for AT2R gene derangement in human urinary tract anomalies

Kidney International

Volumn 59, Issue 4, 2001, Pages 1244-1249

  Hiraoka, Masahiro ^a,b,c,d   Taniguchi, Takanobu ^a,b,c,d   Nakai, Hideo ^a,b,c,d   Kino, Minoru ^a,b,c,d   Okada, Yuusaku ^a,b,c,d   Tanizawa, Akihiko ^a,b,c,d   Tsukahara, Hirokazu ^a,b,c,d   Ohshima, Yusei ^a,b,c,d   Muramatsu, Ikunobu ^a,b,c,d   Mayumi, Mitsufumi ^a,b,c,d  

^a UNIVERSITY OF FUKUI   (Japan)

^b Tokyo Metropolitan Kiyose Children's Hospital   (Japan)

^c KANSAI MEDICAL UNIVERSITY   (Japan)

^d SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Angiotensin II; CAKUT; Gene mutation; Japanese population; Multicystic dysplastic kidney; Renal hypoplasia; Ureteropelvic junction stenosis

Indexed keywords

ANGIOTENSIN RECEPTOR;

ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; HUMAN; INTRON; KIDNEY HYPOPLASIA; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; MALE; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEX RATIO; URETEROPELVIC JUNCTION OBSTRUCTION; URINARY TRACT MALFORMATION; VESICOURETERAL REFLUX; X CHROMOSOME;

EID: 0035072796     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2001.0590041244.x     Document Type: Article

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