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Results: 1-16 |
Results: 16
ADVANCES IN THE CELL BIOLOGY AND GENETICS OF HUMAN KIDNEY MALFORMATIONS
Authors: WOOLF AS WINYARD PJD
Citation: As. Woolf et Pjd. Winyard, ADVANCES IN THE CELL BIOLOGY AND GENETICS OF HUMAN KIDNEY MALFORMATIONS, Journal of the American Society of Nephrology, 9(6), 1998, pp. 1114-1125
SHORT-TERM URINARY FLOW IMPAIRMENT DEREGULATES PAX2 AND PCNA EXPRESSION AND CELL-SURVIVAL IN FETAL SHEEP KIDNEYS
Authors: ATTAR R QUINN F WINYARD PJD MOURIQUAND PDE FOXALL P HANSON MA WOOLF AS
Citation: R. Attar et al., SHORT-TERM URINARY FLOW IMPAIRMENT DEREGULATES PAX2 AND PCNA EXPRESSION AND CELL-SURVIVAL IN FETAL SHEEP KIDNEYS, The American journal of pathology, 152(5), 1998, pp. 1225-1235
EPITHELIAL GALECTIN-3 DURING HUMAN NEPHROGENESIS AND CHILDHOOD CYSTICDISEASES
Authors: WINYARD PJD BAO Q HUGHES RC WOOLF AS
Citation: Pjd. Winyard et al., EPITHELIAL GALECTIN-3 DURING HUMAN NEPHROGENESIS AND CHILDHOOD CYSTICDISEASES, Journal of the American Society of Nephrology, 8(11), 1997, pp. 1647-1657
ORAL-FACIAL-DIGITAL SYNDROME TYPE-1 IS ANOTHER DOMINANT POLYCYSTIC KIDNEY-DISEASE - CLINICAL, RADIOLOGICAL AND HISTOPATHOLOGICAL FEATURES OF A NEW KINDRED
Authors: FEATHER SA WINYARD PJD DODD S WOOLF AS
Citation: Sa. Feather et al., ORAL-FACIAL-DIGITAL SYNDROME TYPE-1 IS ANOTHER DOMINANT POLYCYSTIC KIDNEY-DISEASE - CLINICAL, RADIOLOGICAL AND HISTOPATHOLOGICAL FEATURES OF A NEW KINDRED, Nephrology, dialysis, transplantation, 12(7), 1997, pp. 1354-1361
ORAL-FACIAL-DIGITAL SYNDROME TYPE-I IS ANOTHER DOMINANT POLYCYSTIC KIDNEY-DISEASE
Authors: FEATHER SA WINYARD PJD DODD S WOOLF AS
Citation: Sa. Feather et al., ORAL-FACIAL-DIGITAL SYNDROME TYPE-I IS ANOTHER DOMINANT POLYCYSTIC KIDNEY-DISEASE, Kidney international, 52(4), 1997, pp. 1131-1131
EXPRESSION OF HEPATOCYTE GROWTH-FACTOR SCATTER FACTOR AND ITS RECEPTOR, MET, SUGGESTS ROLES IN HUMAN EMBRYONIC ORGANOGENESIS
Authors: KOLATSIJOANNOU M MOORE R WINYARD PJD WOOLF AS
Citation: M. Kolatsijoannou et al., EXPRESSION OF HEPATOCYTE GROWTH-FACTOR SCATTER FACTOR AND ITS RECEPTOR, MET, SUGGESTS ROLES IN HUMAN EMBRYONIC ORGANOGENESIS, Pediatric research, 41(5), 1997, pp. 657-665
GALECTIN-3 IN NORMAL POLYCYSTIC AND DYSPLASTIC NEPHROGENESIS
Authors: WOOLF AS BAO Q HUGHES RC WINYARD PJD
Citation: As. Woolf et al., GALECTIN-3 IN NORMAL POLYCYSTIC AND DYSPLASTIC NEPHROGENESIS, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1886-1886
CONGENITAL ENTEROCYTE HEPARAN-SULFATE DEFICIENCY WITH MASSIVE ALBUMINLOSS, SECRETORY DIARRHEA, AND MALNUTRITION
Authors: MURCH SH WINYARD PJD KOLETZKO S WEHNER B CHEEMA HA RISDON RA PHILLIPS AD MEADOWS N KLEIN NJ WALKERSMITH JA
Citation: Sh. Murch et al., CONGENITAL ENTEROCYTE HEPARAN-SULFATE DEFICIENCY WITH MASSIVE ALBUMINLOSS, SECRETORY DIARRHEA, AND MALNUTRITION, Lancet, 347(9011), 1996, pp. 1299-1301
DEREGULATION OF CELL-SURVIVAL IN CYSTIC AND DYSPLASTIC RENAL DEVELOPMENT
Authors: WINYARD PJD NAUTA J LIRENMAN DS HARDMAN P SAMS VR RISDON RA WOOLF AS
Citation: Pjd. Winyard et al., DEREGULATION OF CELL-SURVIVAL IN CYSTIC AND DYSPLASTIC RENAL DEVELOPMENT, Kidney international, 49(1), 1996, pp. 135-146
THE PAX2 TRANSCRIPTION FACTOR IS EXPRESSED IN CYSTIC AND HYPERPROLIFERATIVE DYSPLASTIC EPITHELIA IN HUMAN KIDNEY MALFORMATIONS
Authors: WINYARD PJD RISDON RA SAMS VR DRESSLER GR WOOLF AS
Citation: Pjd. Winyard et al., THE PAX2 TRANSCRIPTION FACTOR IS EXPRESSED IN CYSTIC AND HYPERPROLIFERATIVE DYSPLASTIC EPITHELIA IN HUMAN KIDNEY MALFORMATIONS, The Journal of clinical investigation, 98(2), 1996, pp. 451-459
WT1 EXPRESSION IN THE ABSENCE OF BCL2 MAY EXPLAIN EXCESSIVE APOPTOSISWHICH OCCURS IN HUMAN KIDNEY MALFORMATIONS
Authors: WINYARD PJD RISDON RA WOOLF AS
Citation: Pjd. Winyard et al., WT1 EXPRESSION IN THE ABSENCE OF BCL2 MAY EXPLAIN EXCESSIVE APOPTOSISWHICH OCCURS IN HUMAN KIDNEY MALFORMATIONS, Journal of the American Society of Nephrology, 6(3), 1995, pp. 729-729
KAL, A GENE MUTATED IN KALLMANNS-SYNDROME, IS EXPRESSED IN THE FIRST TRIMESTER OF HUMAN-DEVELOPMENT
Authors: DUKE VM WINYARD PJD THOROGOOD P SOOTHILL P BOULOUX PMG WOOLF AS
Citation: Vm. Duke et al., KAL, A GENE MUTATED IN KALLMANNS-SYNDROME, IS EXPRESSED IN THE FIRST TRIMESTER OF HUMAN-DEVELOPMENT, Molecular and cellular endocrinology, 110(1-2), 1995, pp. 73-79
UNRAVELING THE PATHOGENESIS OF CYSTIC KIDNEY-DISEASES
Authors: WOOLF AS WINYARD PJD
Citation: As. Woolf et Pjd. Winyard, UNRAVELING THE PATHOGENESIS OF CYSTIC KIDNEY-DISEASES, Archives of Disease in Childhood, 72(2), 1995, pp. 103-105
RENAL APLASIA (RA) IN KALLMANNS-SYNDROME (KS) MAY BE EXPLAINED BY KALGENE-EXPRESSION DURING NEPHROGENESIS
Authors: WINYARD PJD DUKE VM THOROGOOD PV NORMAN JT BOULOUX PMG WOOLF AS
Citation: Pjd. Winyard et al., RENAL APLASIA (RA) IN KALLMANNS-SYNDROME (KS) MAY BE EXPLAINED BY KALGENE-EXPRESSION DURING NEPHROGENESIS, Journal of the American Society of Nephrology, 5(3), 1994, pp. 640-640
WIDESPREAD APOPTOSIS OCCURS IN HUMAN RENAL MALFORMATIONS AND CHILDHOOD POLYCYSTIC KIDNEY-DISEASE (P K D)
Authors: WINYARD PJD LIRENMAN DS RISDON RA SAMS VR WOOLF AS
Citation: Pjd. Winyard et al., WIDESPREAD APOPTOSIS OCCURS IN HUMAN RENAL MALFORMATIONS AND CHILDHOOD POLYCYSTIC KIDNEY-DISEASE (P K D), Journal of the American Society of Nephrology, 5(3), 1994, pp. 641-641
BRANCHING OUT WITH THE URETERAL BUD
Authors: HARDMAN P KOLATSI M WINYARD PJD TOWERS PR WOOLF AS
Citation: P. Hardman et al., BRANCHING OUT WITH THE URETERAL BUD, Experimental nephrology, 2(4), 1994, pp. 211-219
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