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Results: 1-11 |
Results: 11
FINE MAPPING OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE LOCUS (PKHD1) AND THE GENES MUT, RDS, CSNK2-BETA, AND GSTA1 AT 6P21.1-P12
Authors: MUCHER G BECKER J KNAPP M BUTTNER R MOSER M RUDNIKSCHONEBORN S SOMLO S GERMINO G ONUCHIC L AVNER E GUAYWOODFORD L ZERRES K
Citation: G. Mucher et al., FINE MAPPING OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE LOCUS (PKHD1) AND THE GENES MUT, RDS, CSNK2-BETA, AND GSTA1 AT 6P21.1-P12, Genomics, 48(1), 1998, pp. 40-45
URINARY RETINOL EXCRETION AND KIDNEY-FUNCTION IN CHILDREN WITH SHIGELLOSIS
Authors: MITRA AK ALVAREZ JO GUAYWOODFORD L FUCHS GJ WAHED MA STEPHENSEN CB
Citation: Ak. Mitra et al., URINARY RETINOL EXCRETION AND KIDNEY-FUNCTION IN CHILDREN WITH SHIGELLOSIS, The American journal of clinical nutrition, 68(5), 1998, pp. 1095-1103
RENAL TUBULAR ALKALOSIS WITH CHRONIC HYPERKALEMIA
Authors: SAID M ZAYED A GUAYWOODFORD L WARNOCK DG
Citation: M. Said et al., RENAL TUBULAR ALKALOSIS WITH CHRONIC HYPERKALEMIA, Journal of the American Society of Nephrology, 8, 1997, pp. 509-509
RECESSIVE FIBRO-CYSTIC RENAL-HEPATIC DISEASE - A NEW GENETIC VARIANT
Authors: PARFREY P JONES G CRAMER B HEFFERTON D GUAYWOODFORD L YOUNG TL DAVIDSON W
Citation: P. Parfrey et al., RECESSIVE FIBRO-CYSTIC RENAL-HEPATIC DISEASE - A NEW GENETIC VARIANT, Journal of the American Society of Nephrology, 8, 1997, pp. 1822-1822
URINARY VITAMIN-A LOSS IN CHILDREN WITH ACUTE SHIGELLOSIS
Authors: MITRA AK ALVAREZ JO WAHED MA FUCHS GJ GUAYWOODFORD L STEPHENSEN CB
Citation: Ak. Mitra et al., URINARY VITAMIN-A LOSS IN CHILDREN WITH ACUTE SHIGELLOSIS, The FASEB journal, 11(3), 1997, pp. 822-822
ENHANCED APOPTOTIC CELL-DEATH OF RENAL EPITHELIAL-CELLS IN MICE LACKING TRANSCRIPTION FACTOR AP-2-BETA
Authors: MOSER M PSCHERER A ROTH C BECKER J MUCHER G ZERRES K DIXKENS C WEIS J GUAYWOODFORD L BUETTNER R FASSLER R
Citation: M. Moser et al., ENHANCED APOPTOTIC CELL-DEATH OF RENAL EPITHELIAL-CELLS IN MICE LACKING TRANSCRIPTION FACTOR AP-2-BETA, Genes & development, 11(15), 1997, pp. 1938-1948
AN INTEGRATED GENETIC AND PHYSICAL MAP OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE REGION
Authors: LENS XM ONUCHIC LF WU GQ HAYASHI T DAOUST M MOCHIZUKI T SANTARINA LB STOCKWIN JM MUCHER G BECKER J SWEENY WE AVNER ED GUAYWOODFORD L ZERRES K SOMLO S GERMINO GG
Citation: Xm. Lens et al., AN INTEGRATED GENETIC AND PHYSICAL MAP OF THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE REGION, Genomics, 41(3), 1997, pp. 463-466
MUTATIONS IN THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL (ROMK) CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME
Authors: LEMMINK HH KNOERS NAVM BINDELS RJ NILLESEN WN KANSEN M VANDERKEMP A MONNENS LAH VANDENHEUVEL LPWJ AMIGNAC C FELDMANN D HILDEBRANDT F SEYBERTH HW GUAYWOODFORD L
Citation: Hh. Lemmink et al., MUTATIONS IN THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL (ROMK) CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME, Kidney international, 52(2), 1997, pp. 570-571
MOLECULAR-GENETIC IDENTIFICATION OF FAMILIES WITH JUVENILE NEPHRONOPHTHISIS TYPE-1 - RATE OF PROGRESSION TO RENAL-FAILURE
Authors: HILDEBRANDT F STRAHM B NOTHWANG HG GRETZ N SCHNIEDERS B SINGHSAWHNEY I KUTT R VOLLMER M BRANDIS M BODE U BRODEHL J LATTA K BROUHARD B DIPPEL J FELDHOFF C WINGEN M FILLER G GHIGGERI GM GUAYWOODFORD L HOPPE B KLARE B KUIJTEN RH KUHN K LEUMANN E NEUMANN HPH VOSSMERBAUMER U NEUMAYER HH RASCHER W SCHARER K STOLPE HJ
Citation: F. Hildebrandt et al., MOLECULAR-GENETIC IDENTIFICATION OF FAMILIES WITH JUVENILE NEPHRONOPHTHISIS TYPE-1 - RATE OF PROGRESSION TO RENAL-FAILURE, Kidney international, 51(1), 1997, pp. 261-269
LOCALIZATION OF THE GENE FOR AUTOSOMAL RECESSIVE POLYCYSTIC DISEASE TO AN 1 CM GENETIC INTERVAL BETWEEN NEW FLANKING MARKERS IN 6P21.1-P12 - EXCLUSION AND FINEMAPPING OF THE CANDIDATE GENES MCM, RDS, CKII-BETA, GSTA1
Authors: BECKER J MUCHER G KNAPP M BUETTNER R MOSER M GUAYWOODFORD L SOMLO S GERMINO G AVNER E ZERRES K
Citation: J. Becker et al., LOCALIZATION OF THE GENE FOR AUTOSOMAL RECESSIVE POLYCYSTIC DISEASE TO AN 1 CM GENETIC INTERVAL BETWEEN NEW FLANKING MARKERS IN 6P21.1-P12 - EXCLUSION AND FINEMAPPING OF THE CANDIDATE GENES MCM, RDS, CKII-BETA, GSTA1, American journal of human genetics, 61(4), 1997, pp. 1556-1556
URINARY RETINOL LOSS IN CHILDREN WITH ACUTE SHIGELLOSIS
Authors: MITRA AK ALVAREZ JO WAHED MA FUCHS GJ GUAYWOODFORD L STEPHENSEN CB
Citation: Ak. Mitra et al., URINARY RETINOL LOSS IN CHILDREN WITH ACUTE SHIGELLOSIS, The American journal of clinical nutrition, 66(1), 1997, pp. 27-27
Risultati: 1-11 |