Excess podocyte semaphorin-3A leads to glomerular disease involving plexinA1-nephrin interaction

American Journal of Pathology

Volumn 183, Issue 4, 2013, Pages 1156-1168

  Reidy, Kimberly J ^a   Aggarwal, Pardeep K ^a   Jimenez, Juan J ^a   Thomas, David B ^b   Veron, Delma ^a   Tufro, Alda ^a,b  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 4; GELATINASE B; LAMININ; MESSENGER RNA; NEPHRIN; PLEXIN; PLEXIN A1; SEMAPHORIN 3A; UNCLASSIFIED DRUG; VITRONECTIN RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL SHAPE; CONTROLLED STUDY; CREATININE CLEARANCE; GENE EXPRESSION; GLOMERULOPATHY; GLOMERULUS FILTRATION; IMMUNOHISTOCHEMISTRY; IN VIVO STUDY; KIDNEY CORTEX; KIDNEY HYPERTROPHY; MOUSE; NONHUMAN; PHENOTYPE; PODOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; TRANSGENE;

ANIMALS; CELL SHAPE; DOWN-REGULATION; GLOMERULAR BASEMENT MEMBRANE; INTEGRIN ALPHAVBETA3; KIDNEY DISEASES; KIDNEY GLOMERULUS; MEMBRANE PROTEINS; MICE; NERVE TISSUE PROTEINS; PODOCYTES; PROTEIN BINDING; PROTEINURIA; RECEPTORS, CELL SURFACE; SEMAPHORIN-3A; SIGNAL TRANSDUCTION;

EID: 84884549522     PISSN: 00029440     EISSN: 15252191     Source Type: Journal    
DOI: 10.1016/j.ajpath.2013.06.022     Document Type: Article

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