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Results: 1-25 | 26-50
Results: 1-25/50
THE MOLECULAR-GENETIC APPROACH TO BARTTERS-SYNDROME
Authors: KAROLYI L KOCH MC GRZESCHIK KH SEYBERTH HW
Citation: L. Karolyi et al., THE MOLECULAR-GENETIC APPROACH TO BARTTERS-SYNDROME, Journal of molecular medicine, 76(5), 1998, pp. 317-325
LOCALIZATION OF THE PROSTACYCLIN RECEPTOR IN HUMAN KIDNEY
Authors: KOMHOFF M LESENER B NAKAO K SEYBERTH HW NUSING RM
Citation: M. Komhoff et al., LOCALIZATION OF THE PROSTACYCLIN RECEPTOR IN HUMAN KIDNEY, Kidney international, 54(6), 1998, pp. 1899-1908
NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN
Authors: LEMMINK HH KNOERS NVAM KAROLYI L VANDIJK H NIAUDET P ANTIGNAC C GUAYWOODFORD LM GOODYER PR CAREL JC HERMES A SEYBERTH HW MONNENS LAH VANDENHEUVEL LPWJ
Citation: Hh. Lemmink et al., NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN, Kidney international, 54(3), 1998, pp. 720-730
EXPRESSION OF PROSTACYCLIN RECEPTOR PROTEIN AND MESSENGER-RNA IN HUMAN KIDNEY
Authors: LESENER B KOMHOFF M SEYBERTH HW NUSING RM
Citation: B. Lesener et al., EXPRESSION OF PROSTACYCLIN RECEPTOR PROTEIN AND MESSENGER-RNA IN HUMAN KIDNEY, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 1737-1737
EXPRESSION OF THE PROSTAGLANDIN E-2 RECEPTORS EP1, EP2, EP3 AND EP4 IN HUMAN KIDNEY
Authors: MORATH R KLEIN T SEYBERTH HW NUSING RM
Citation: R. Morath et al., EXPRESSION OF THE PROSTAGLANDIN E-2 RECEPTORS EP1, EP2, EP3 AND EP4 IN HUMAN KIDNEY, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 1738-1738
USE OF A CYCLOOXYGENASE-2 SPECIFIC INHIBITOR FOR TREATMENT OF HYPERPROSTAGLANDINE SYNDROME
Authors: NUSING RM REINALTER S KLEIN T SEYBERTH HW
Citation: Rm. Nusing et al., USE OF A CYCLOOXYGENASE-2 SPECIFIC INHIBITOR FOR TREATMENT OF HYPERPROSTAGLANDINE SYNDROME, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 4126-4126
MUTATIONS IN CLCKB-CHANNEL CAUSE BARTTER-SYNDROME
Authors: JECK N KONRAD M WEBER S REINALTER S SEYBERTH HW
Citation: N. Jeck et al., MUTATIONS IN CLCKB-CHANNEL CAUSE BARTTER-SYNDROME, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 4127-4127
A HYPERPROSTAGLANDIN-E SYNDROME MUTATION IN KIR1.1 (RENAL OUTER MEDULLARY POTASSIUM) CHANNELS REVEALS A CRUCIAL RESIDUE FOR CHANNEL FUNCTION IN KIR1.3 CHANNELS
Authors: DERST C WISCHMEYER E PREISIGMULLER R SPAUSCHUS A KONRAD M HENSEN P JECK N SEYBERTH HW DAUT J KARSCHIN A
Citation: C. Derst et al., A HYPERPROSTAGLANDIN-E SYNDROME MUTATION IN KIR1.1 (RENAL OUTER MEDULLARY POTASSIUM) CHANNELS REVEALS A CRUCIAL RESIDUE FOR CHANNEL FUNCTION IN KIR1.3 CHANNELS, The Journal of biological chemistry, 273(37), 1998, pp. 23884-23891
NOVEL MOLECULAR VARIANTS OF THE NA-K-2CL COTRANSPORTER GENE ARE RESPONSIBLE FOR ANTENATAL BARTTER-SYNDROME
Authors: VARGASPOUSSOU R FELDMANN D VOLLMER M KONRAD M KELLY L VANDENHEUVEL LPWJ TEBOURBI L BRANDIS M KAROLYI L HEBERT SC LEMMINK HH DESCHENES G HILDEBRANDT F SEYBERTH HW GUAYWOODFORD LM KNOERS NVAM ANTIGNAC C
Citation: R. Vargaspoussou et al., NOVEL MOLECULAR VARIANTS OF THE NA-K-2CL COTRANSPORTER GENE ARE RESPONSIBLE FOR ANTENATAL BARTTER-SYNDROME, American journal of human genetics, 62(6), 1998, pp. 1332-1340
IMPROVED QUANTIFICATION OF 8-EPI-PROSTAGLANDIN F2-ALPHA AND F-2-ISOPROSTANES BY GAS-CHROMATOGRAPHY TRIPLE-STAGE QUADRUPOLE MASS-SPECTROMETRY - PARTIAL CYCLOOXYGENASE-DEPENDENT FORMATION OF 8-EPI-PROSTAGLANDIN F2-ALPHA IN HUMANS
Authors: SCHWEER H WATZER B SEYBERTH HW NUSING RM
Citation: H. Schweer et al., IMPROVED QUANTIFICATION OF 8-EPI-PROSTAGLANDIN F2-ALPHA AND F-2-ISOPROSTANES BY GAS-CHROMATOGRAPHY TRIPLE-STAGE QUADRUPOLE MASS-SPECTROMETRY - PARTIAL CYCLOOXYGENASE-DEPENDENT FORMATION OF 8-EPI-PROSTAGLANDIN F2-ALPHA IN HUMANS, Journal of mass spectrometry., 32(12), 1997, pp. 1362-1370
PRE-NATAL AND POSTNATAL MANAGEMENT OF HYPERPROSTAGLANDIN-E SYNDROME (HPS) FOLLOWING MOLECULAR-GENETIC DIAGNOSIS FROM AMNIOCYTES
Authors: KONRAD M KOCKERLING A LEONHARDT A KAROLYI L SEYBERTH HW
Citation: M. Konrad et al., PRE-NATAL AND POSTNATAL MANAGEMENT OF HYPERPROSTAGLANDIN-E SYNDROME (HPS) FOLLOWING MOLECULAR-GENETIC DIAGNOSIS FROM AMNIOCYTES, Journal of the American Society of Nephrology, 8, 1997, pp. 433-433
NOVEL ROMK (KCNJ1) MUTATIONS IN 2 SPORADIC CASES WITH HYPERPROSTAGLANDIN-E SYNDROME (ANTENATAL BARTTER-SYNDROME)
Authors: KONRAD M HENSEN P KAROLYI L SEYBERTH HW
Citation: M. Konrad et al., NOVEL ROMK (KCNJ1) MUTATIONS IN 2 SPORADIC CASES WITH HYPERPROSTAGLANDIN-E SYNDROME (ANTENATAL BARTTER-SYNDROME), Journal of the American Society of Nephrology, 8, 1997, pp. 1808-1808
A COMMON NKCC2 MUTATION IN COSTA-RICAN BARTTERS-SYNDROME PATIENTS - EVIDENCE FOR A FOUNDER EFFECT
Authors: KURTZ CL KAROLYI L SEYBERTH HW KOCH MC VARGAS R FELDMANN D VOLLMER M KNOERS NVAM MADRIGAL G GUAYWOODFORD LM
Citation: Cl. Kurtz et al., A COMMON NKCC2 MUTATION IN COSTA-RICAN BARTTERS-SYNDROME PATIENTS - EVIDENCE FOR A FOUNDER EFFECT, Journal of the American Society of Nephrology, 8(11), 1997, pp. 1706-1711
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997)
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650
MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26
LOCALIZATION OF CYCLOOXYGENASE-1 AND CYCLOOXYGENASE-2 IN ADULT AND FETAL HUMAN KIDNEY - IMPLICATION FOR RENAL-FUNCTION
Authors: KOMHOFF M GRONE HJ KLEIN T SEYBERTH HW NUSING RM
Citation: M. Komhoff et al., LOCALIZATION OF CYCLOOXYGENASE-1 AND CYCLOOXYGENASE-2 IN ADULT AND FETAL HUMAN KIDNEY - IMPLICATION FOR RENAL-FUNCTION, American journal of physiology. Renal, fluid and electrolyte physiology, 41(4), 1997, pp. 460-468
DIHYDROPYRIDMIDINASE DEFICIENCY AND CONGENITAL MICROVILLOUS ATROPHY -COINCIDENCE OR GENETIC RELATION
Authors: ASSMANN B HOFFMANN GF WAGNER L BRAUTIGAM C SEYBERTH HW DURAN M VANKUILENBURG ABP WEVERS R VANGENNIP AH
Citation: B. Assmann et al., DIHYDROPYRIDMIDINASE DEFICIENCY AND CONGENITAL MICROVILLOUS ATROPHY -COINCIDENCE OR GENETIC RELATION, Journal of inherited metabolic disease, 20(5), 1997, pp. 681-688
MEASUREMENTS OF URINARY PROSTAGLANDINS IN YOUNG OVULATORY WOMEN DURING THE MENSTRUAL-CYCLE AND IN POSTMENOPAUSAL WOMEN
Authors: FARKER K SCHWEER H VOLLANDT R NASSR N NAGEL U SEYBERTH HW HOFFMANN A OETTEL M
Citation: K. Farker et al., MEASUREMENTS OF URINARY PROSTAGLANDINS IN YOUNG OVULATORY WOMEN DURING THE MENSTRUAL-CYCLE AND IN POSTMENOPAUSAL WOMEN, Prostaglandins, 54(3), 1997, pp. 655-664
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
PROTHROMBIN MARBURG - A DYSFUNCTIONAL COAGULATION PROTEIN
Authors: BECK KH KRAUS M MAGSAAM J KRETSCHMER V LEONHARD A SEYBERTH HW
Citation: Kh. Beck et al., PROTHROMBIN MARBURG - A DYSFUNCTIONAL COAGULATION PROTEIN, Thrombosis research, 88(3), 1997, pp. 337-342
PROSTANOID FORMATION DURING FEEDING OF A PRETERM FORMULA WITH LONG-CHAIN POLYUNSATURATED FATTY-ACIDS IN HEALTHY PRETERM INFANTS DURING THE FIRST WEEKS OF LIFE
Authors: STIER C HESS M WATZER B SCHWEER H SEYBERTH HW LEONHARDT A
Citation: C. Stier et al., PROSTANOID FORMATION DURING FEEDING OF A PRETERM FORMULA WITH LONG-CHAIN POLYUNSATURATED FATTY-ACIDS IN HEALTHY PRETERM INFANTS DURING THE FIRST WEEKS OF LIFE, Pediatric research, 42(4), 1997, pp. 509-513
PROSTANOID BIOSYNTHESIS BY BLOOD MONOCYTES OF CHILDREN WITH HYPERPROSTAGLANDIN-E SYNDROME
Authors: NUSING RM SCHAUB TP KLEIN T SCHWEER H SEYBERTH HW
Citation: Rm. Nusing et al., PROSTANOID BIOSYNTHESIS BY BLOOD MONOCYTES OF CHILDREN WITH HYPERPROSTAGLANDIN-E SYNDROME, Pediatric research, 42(2), 1997, pp. 241-246
PHARMACOKINETICS OF PROSTAGLANDIN-E1 AND ITS MAIN METABOLITES AFTER INTRACAVERNOUS INJECTION AND SHORT-TERM INFUSION OF PROSTAGLANDIN-E1 INPATIENTS WITH ERECTILE DYSFUNCTION
Authors: CAWELLO W SCHWEER H DIETRICH B SEYBERTH HW ALBRECHT D FOX A HOHMUTH H
Citation: W. Cawello et al., PHARMACOKINETICS OF PROSTAGLANDIN-E1 AND ITS MAIN METABOLITES AFTER INTRACAVERNOUS INJECTION AND SHORT-TERM INFUSION OF PROSTAGLANDIN-E1 INPATIENTS WITH ERECTILE DYSFUNCTION, The Journal of urology, 158(4), 1997, pp. 1403-1407
GENERATION OF THE ISOPROSTANE 8-EPI-PROSTAGLANDIN F2-ALPHA IN-VITRO AND IN-VIVO VIA THE CYCLOOXYGENASES
Authors: KLEIN T REUTTER F SCHWEER H SEYBERTH HW NUSING RM
Citation: T. Klein et al., GENERATION OF THE ISOPROSTANE 8-EPI-PROSTAGLANDIN F2-ALPHA IN-VITRO AND IN-VIVO VIA THE CYCLOOXYGENASES, The Journal of pharmacology and experimental therapeutics, 282(3), 1997, pp. 1658-1665
IN-VIVO FORMATION OF PROSTAGLANDIN E(1) AND PROSTAGLANDIN E(2) IN ATOPIC-DERMATITIS
Authors: LEONHARDT A KRAUS M GIELER U SCHWEER H HAPPLE R SEYBERTH HW
Citation: A. Leonhardt et al., IN-VIVO FORMATION OF PROSTAGLANDIN E(1) AND PROSTAGLANDIN E(2) IN ATOPIC-DERMATITIS, British journal of dermatology, 136(3), 1997, pp. 337-340
Risultati: 1-25 | 26-50