Podocyte proteins in Galloway-Mowat syndrome

Pediatric Nephrology

Volumn 16, Issue 12, 2001, Pages 1022-1029

  Srivastava, T ^a   Whiting, J M ^a   Garola, R E ^a   Dasouki, M J ^a   Ruotsalainen, V ^b   Tryggvason, K ^c   Hamed, R ^d   Alon, U S ^a  

^a UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

^b UNIVERSITY OF OULU   (Finland)

^c KAROLINSKA INSTITUTE   (Sweden)

^d UNIVERSITY OF JORDAN   (Jordan)

Author keywords

Galloway Mowat syndrome; GLEPP1; Immunohistochemistry; Nephrin; Synaptopodin

Indexed keywords

ALPHA ACTININ; CELL PROTEIN; GLOMERULAR EPITHELIAL PROTEIN 1; MEMBRANE PROTEIN; NEPHRIN; PODOCIN; PODOCYTE PROTEIN; SYNAPTOPODIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CHILD; DISEASE CLASSIFICATION; FEMALE; GALLOWAY MOWAT SYNDROME; GENE MUTATION; GENETIC DISORDER; GLOMERULOSCLEROSIS; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFANT; KIDNEY PARENCHYMA; MALE; MINIMAL CHANGE GLOMERULONEPHRITIS; NEPHROTIC SYNDROME; NERVE CELL; PODOCYTE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEINURIA;

CENTRAL NERVOUS SYSTEM; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; INFANT; INFANT, NEWBORN; KIDNEY GLOMERULUS; MALE; MEMBRANE PROTEINS; MICROFILAMENT PROTEINS; NEPHROTIC SYNDROME; PROTEIN-TYROSINE-PHOSPHATASE; PROTEINS; SYNDROME;

EID: 0035664227     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670100018     Document Type: Article

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