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Results: 1-25 | 26-45
Results: 1-25/45
HDL3-MEDIATED INHIBITION OF THROMBIN-INDUCED PLATELET-AGGREGATION ANDFIBRINOGEN BINDING OCCURS VIA DECREASED PRODUCTION OF PHOSPHOINOSITIDE-DERIVED 2ND-MESSENGERS 1,2-DIACYLGLYCEROL AND INOSITOL 1,4,5-TRIS-PHOSPHATE
Authors: NOFER JR WALTER M KEHREL B WIERWILLE S TEPEL M SEEDORF U ASSMANN G
Citation: Jr. Nofer et al., HDL3-MEDIATED INHIBITION OF THROMBIN-INDUCED PLATELET-AGGREGATION ANDFIBRINOGEN BINDING OCCURS VIA DECREASED PRODUCTION OF PHOSPHOINOSITIDE-DERIVED 2ND-MESSENGERS 1,2-DIACYLGLYCEROL AND INOSITOL 1,4,5-TRIS-PHOSPHATE, Arteriosclerosis, thrombosis, and vascular biology, 18(6), 1998, pp. 861-869
DEFECTIVE PEROXISOMAL CATABOLISM OF BRANCHED FATTY ACYL-COENZYME-A INMICE LACKING THE STEROL CARRIER PROTEIN-2 STEROL CARRIER PROTEIN-X GENE-FUNCTION
Authors: SEEDORF U RAABE M ELLINGHAUS P KANNENBERG F FOBKER M ENGEL T DENIS S WOUTERS F WIRTZ KWA WANDERS RJA MAEDA N ASSMANN G
Citation: U. Seedorf et al., DEFECTIVE PEROXISOMAL CATABOLISM OF BRANCHED FATTY ACYL-COENZYME-A INMICE LACKING THE STEROL CARRIER PROTEIN-2 STEROL CARRIER PROTEIN-X GENE-FUNCTION, Genes & development, 12(8), 1998, pp. 1189-1201
THE NONSPECIFIC LIPID TRANSFER PROTEIN (STEROL CARRIER PROTEIN-2) ACTS AS A PEROXISOMAL FATTY ACYL-COA-BINDING PROTEIN
Authors: WIRTZ KWA WOUTERS FS BASTIAENS PH WANDERS RJA SEEDORF U JOVIN TM
Citation: Kwa. Wirtz et al., THE NONSPECIFIC LIPID TRANSFER PROTEIN (STEROL CARRIER PROTEIN-2) ACTS AS A PEROXISOMAL FATTY ACYL-COA-BINDING PROTEIN, Biochemical Society transactions, 26(3), 1998, pp. 374-378
CLONING AND SEQUENCING OF A NOVEL MURINE LIVER CARBOXYLESTERASE CDNA
Authors: ELLINGHAUS P SEEDORF U ASSMANN G
Citation: P. Ellinghaus et al., CLONING AND SEQUENCING OF A NOVEL MURINE LIVER CARBOXYLESTERASE CDNA, Biochimica et biophysica acta, N. Gene structure and expression, 1397(2), 1998, pp. 175-179
IDENTIFICATION OF THE NEWLY DISCOVERED 58 KDA PEROXISOMAL THIOLASE SCPX AS THE MAIN THIOLASE INVOLVED IN BOTH PRISTANIC ACID AND TRIHYDROXYCHOLESTANOIC ACID OXIDATION - IMPLICATIONS FOR PEROXISOMAL BETA-OXIDATION DISORDERS
Authors: WANDERS RJA DENIS S VANBERKEL E WOUTERS F WIRTZ KWA SEEDORF U
Citation: Rja. Wanders et al., IDENTIFICATION OF THE NEWLY DISCOVERED 58 KDA PEROXISOMAL THIOLASE SCPX AS THE MAIN THIOLASE INVOLVED IN BOTH PRISTANIC ACID AND TRIHYDROXYCHOLESTANOIC ACID OXIDATION - IMPLICATIONS FOR PEROXISOMAL BETA-OXIDATION DISORDERS, Journal of inherited metabolic disease, 21(3), 1998, pp. 302-305
ARRHYTHMOGENIC EFFECTS OF PHYTANIC ACID IN STEROL CARRIER PROTEIN-2 KNOCK OUT MICE AND IMPLICATION FOR SUDDEN CARDIAC DEATH
Authors: MOENNIG G SEEDORF U HAVERKAMP W KIRCHHOF P ECKARDT L PULAWSKI P ASSMANN G BREITHARDT G
Citation: G. Moennig et al., ARRHYTHMOGENIC EFFECTS OF PHYTANIC ACID IN STEROL CARRIER PROTEIN-2 KNOCK OUT MICE AND IMPLICATION FOR SUDDEN CARDIAC DEATH, Circulation, 98(17), 1998, pp. 3907-3907
EFFECTS OF GENOTYPE AND DIET ON CHOLESTEROL EFFLUX INTO PLASMA AND LIPOPROTEINS OF NORMAL, APOLIPOPROTEIN A-I-DEFICIENT, AND APOLIPOPROTEINE-DEFICIENT MICE
Authors: HUANG YD ZHU YH LANGER C RAABE M WU SL WIESENHUTTER B SEEDORF U MAEDA N ASSMANN G VONECKARDSTEIN A
Citation: Yd. Huang et al., EFFECTS OF GENOTYPE AND DIET ON CHOLESTEROL EFFLUX INTO PLASMA AND LIPOPROTEINS OF NORMAL, APOLIPOPROTEIN A-I-DEFICIENT, AND APOLIPOPROTEINE-DEFICIENT MICE, Arteriosclerosis, thrombosis, and vascular biology, 17(10), 1997, pp. 2010-2019
A NEW HERITABLE LIPID ABNORMALITY IN CHILDREN WITH PARTIAL SMITH-LEMLI-OPITZ SYNDROME PHENOTYPE
Authors: MESCHEDE D",SEEDORF,"SEEDORF U FOBKER M MINY P FLOTMANN U KOCH HG ULLRICH K ASSMANN G HORST J
Citation: U. Meschede D",seedorf,"seedorf et al., A NEW HERITABLE LIPID ABNORMALITY IN CHILDREN WITH PARTIAL SMITH-LEMLI-OPITZ SYNDROME PHENOTYPE, American journal of medical genetics, 68(3), 1997, pp. 5-5
STEROIDS, FATTY ACYL-COA, AND STEROLS ARE SUBSTRATES OF 80-KDA MULTIFUNCTIONAL PROTEIN
Authors: ADAMSKI J LEENDERS F CARSTENSEN JF KAUFMANN M MARKUS MM HUSEN B TESDORPF JG SEEDORF U DELAUNOIT Y JAKOB F
Citation: J. Adamski et al., STEROIDS, FATTY ACYL-COA, AND STEROLS ARE SUBSTRATES OF 80-KDA MULTIFUNCTIONAL PROTEIN, Steroids, 62(1), 1997, pp. 159-163
PREVALENCE OF CHOLESTEROL ESTER STORAGE DISEASE IN GERMANY AND SARDINIA
Authors: MUNTONI S WIEBUSCH H JANSEN M RUST S LU F SEEDORF U FUNKE H ASSMANN G
Citation: S. Muntoni et al., PREVALENCE OF CHOLESTEROL ESTER STORAGE DISEASE IN GERMANY AND SARDINIA, Atherosclerosis, 134(1-2), 1997, pp. 80-80
THE MUTATION COMMONLY ASSOCIATED WITH THE CHOLESTEROL ESTER STORAGE DISEASE SEEMS TO BE ABSENT IN THE SARDINIAN POPULATION
Authors: MUNTONI S WIEBUSCH H JANSEN M RUST S LU F SEEDORF U MUNTONI S FUNKE H ASSMANN G
Citation: S. Muntoni et al., THE MUTATION COMMONLY ASSOCIATED WITH THE CHOLESTEROL ESTER STORAGE DISEASE SEEMS TO BE ABSENT IN THE SARDINIAN POPULATION, Atherosclerosis, 133(2), 1997, pp. 41-41
REGULATION OF PPAR-ALPHA FUNCTION BY DIETARY PHYTANIC ACID IN NORMAL AND SEP ALPHA-DEFICIENT MICE
Authors: SEEDORF U ELLINGHAUS P GLASS B ASSMANN G
Citation: U. Seedorf et al., REGULATION OF PPAR-ALPHA FUNCTION BY DIETARY PHYTANIC ACID IN NORMAL AND SEP ALPHA-DEFICIENT MICE, Circulation, 96(8), 1997, pp. 3700-3700
ACQUIRED HDL-DEFICIENCY WITH TANGIER-LIKE PHENOTYPE INDUCED BY A SOLUBLE SERUM FACTOR
Authors: WALTER M SEEDORF U ASSMANN G
Citation: M. Walter et al., ACQUIRED HDL-DEFICIENCY WITH TANGIER-LIKE PHENOTYPE INDUCED BY A SOLUBLE SERUM FACTOR, Circulation, 96(8), 1997, pp. 4054-4054
LOW-DENSITY LIPOPROTEINS INHIBIT THE NA+ H+ ANTIPORT IN HUMAN PLATELETS - A NOVEL MECHANISM ENHANCING PLATELET ACTIVITY IN HYPERCHOLESTEROLEMIA/
Authors: NOFER JR TEPEL M KEHREL B WIERWILLE S WALTER M SEEDORF U ZIDEK W ASSMANN G
Citation: Jr. Nofer et al., LOW-DENSITY LIPOPROTEINS INHIBIT THE NA+ H+ ANTIPORT IN HUMAN PLATELETS - A NOVEL MECHANISM ENHANCING PLATELET ACTIVITY IN HYPERCHOLESTEROLEMIA/, Circulation, 95(6), 1997, pp. 1370-1377
STEROL CARRIER PROTEIN-X (SCPX) IS A PEROXISOMAL BRANCHED-CHAIN BETA-KETOTHIOLASE SPECIFICALLY REACTING WITH 3-OXO-PRISTANOYL-COA - A NEW, UNIQUE ROLE FOR SCPX IN BRANCHED-CHAIN FATTY-ACID METABOLISM IN PEROXISOMES
Authors: WANDERS RJA DENIS S WOUTERS F WIRTZ KWA SEEDORF U
Citation: Rja. Wanders et al., STEROL CARRIER PROTEIN-X (SCPX) IS A PEROXISOMAL BRANCHED-CHAIN BETA-KETOTHIOLASE SPECIFICALLY REACTING WITH 3-OXO-PRISTANOYL-COA - A NEW, UNIQUE ROLE FOR SCPX IN BRANCHED-CHAIN FATTY-ACID METABOLISM IN PEROXISOMES, Biochemical and biophysical research communications, 236(3), 1997, pp. 565-569
KNOCKOUT OF MURINE STEROL CARRIER PROTEIN-2 GENE CAUSES A REFSUM-DISEASE LIKE PHENOTYPE
Authors: RAABE M WANDERS RWA ENGEL T BRYSCH P FOBKER M KANNENBERG F ASSMANN G SEEDORF U
Citation: M. Raabe et al., KNOCKOUT OF MURINE STEROL CARRIER PROTEIN-2 GENE CAUSES A REFSUM-DISEASE LIKE PHENOTYPE, Molecular biology of the cell, 7, 1996, pp. 2886-2886
CARBON DISULFIDE-INDUCED MODIFICATION AND CYTOTOXICITY OF LOW-DENSITYLIPOPROTEINS
Authors: WRONSKANOFER T LAURMAN W NOFER JR SEEDORF U WALTER M
Citation: T. Wronskanofer et al., CARBON DISULFIDE-INDUCED MODIFICATION AND CYTOTOXICITY OF LOW-DENSITYLIPOPROTEINS, Toxicology in vitro, 10(4), 1996, pp. 423-429
A MISSENSE MUTATION (THR-6PRO) IN THE LYSOSOMAL ACID LIPASE (LAL) GENE IS PRESENT WITH A HIGH-FREQUENCY IN 3 DIFFERENT ETHNIC POPULATIONS -IMPACT ON SERUM-LIPOPROTEIN CONCENTRATIONS
Authors: MUNTONI S WIEBUSCH H FUNKE H SEEDORF U ROSKOS M SCHULTE H SAKU K ARAKAWA K BALESTRIERI A ASSMANN G
Citation: S. Muntoni et al., A MISSENSE MUTATION (THR-6PRO) IN THE LYSOSOMAL ACID LIPASE (LAL) GENE IS PRESENT WITH A HIGH-FREQUENCY IN 3 DIFFERENT ETHNIC POPULATIONS -IMPACT ON SERUM-LIPOPROTEIN CONCENTRATIONS, Human genetics, 97(2), 1996, pp. 265-267
HIGH-DENSITY-LIPOPROTEINS ENHANCE THE NA+ H+ ANTIPORT IN HUMAN PLATELETS/
Authors: NOFER JR TEPEL M KEHREL B WALTER M SEEDORF U ASSMANN G ZIDEK W
Citation: Jr. Nofer et al., HIGH-DENSITY-LIPOPROTEINS ENHANCE THE NA+ H+ ANTIPORT IN HUMAN PLATELETS/, Thrombosis and haemostasis, 75(4), 1996, pp. 635-641
STRUCTURE AND CHROMOSOMAL ASSIGNMENT OF THE MURINE STEROL CARRIER PROTEIN-2 GENE (SCP2) AND 2 RELATED PSEUDOGENES BY IN-SITU HYBRIDIZATION
Authors: RAABE M SEEDORF U HAMEISTER H ELLINGHAUS P ASSMANN G
Citation: M. Raabe et al., STRUCTURE AND CHROMOSOMAL ASSIGNMENT OF THE MURINE STEROL CARRIER PROTEIN-2 GENE (SCP2) AND 2 RELATED PSEUDOGENES BY IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 73(4), 1996, pp. 279-281
SMITH-LEMLI-OPITZ SYNDROME - TREATMENT WITH CHOLESTEROL AND BILE-ACIDS
Authors: ULLRICH K KOCK HG MESCHEDE D FLOTMANN U SEEDORF U
Citation: K. Ullrich et al., SMITH-LEMLI-OPITZ SYNDROME - TREATMENT WITH CHOLESTEROL AND BILE-ACIDS, Neuropediatrics, 27(2), 1996, pp. 111-112
DEFECTIVE REGULATION OF PHOSPHATIDYLCHOLINE-SPECIFIC PHOSPHOLIPASE-C AND PHOSPHOLIPASE-D IN A KINDRED WITH TANGIER DISEASE - EVIDENCE FOR THE INVOLVEMENT OF PHOSPHATIDYLCHOLINE BREAKDOWN IN HDL-MEDIATED CHOLESTEROL EFFLUX MECHANISMS
Authors: WALTER M REINECKE H GERDES U NOFER JR HOBBEL G SEEDORF U ASSMANN G
Citation: M. Walter et al., DEFECTIVE REGULATION OF PHOSPHATIDYLCHOLINE-SPECIFIC PHOSPHOLIPASE-C AND PHOSPHOLIPASE-D IN A KINDRED WITH TANGIER DISEASE - EVIDENCE FOR THE INVOLVEMENT OF PHOSPHATIDYLCHOLINE BREAKDOWN IN HDL-MEDIATED CHOLESTEROL EFFLUX MECHANISMS, The Journal of clinical investigation, 98(10), 1996, pp. 2315-2323
PORCINE 80-KDA PROTEIN REVEALS INTRINSIC 17-BETA-HYDROXYSTEROID DEHYDROGENASE, FATTY ACYL-COA-HYDRATASE DEHYDROGENASE, AND STEROL TRANSFER ACTIVITIES/
Authors: LEENDERS F TESDORPF JG MARKUS M ENGEL T SEEDORF U ADAMSKI J
Citation: F. Leenders et al., PORCINE 80-KDA PROTEIN REVEALS INTRINSIC 17-BETA-HYDROXYSTEROID DEHYDROGENASE, FATTY ACYL-COA-HYDRATASE DEHYDROGENASE, AND STEROL TRANSFER ACTIVITIES/, The Journal of biological chemistry, 271(10), 1996, pp. 5438-5442
A NOVEL MISSENSE MUTATION (GLY2ARG) IN THE HUMAN LYSOSOMAL ACID LIPASE GENE IS FOUND IN INDIVIDUALS WITH AND WITHOUT CHOLESTEROL ESTER STORAGE DISEASE (CESD)
Authors: WIEBUSCH H MUNTONI S FUNKE H LU F SEEDORF U OBERLE S SCHWARZER U ASSMANN G
Citation: H. Wiebusch et al., A NOVEL MISSENSE MUTATION (GLY2ARG) IN THE HUMAN LYSOSOMAL ACID LIPASE GENE IS FOUND IN INDIVIDUALS WITH AND WITHOUT CHOLESTEROL ESTER STORAGE DISEASE (CESD), Clinical genetics, 50(2), 1996, pp. 106-107
WOLMAN-DISEASE DUE TO HOMOZYGOSITY FOR A NOVEL TRUNCATED VARIANT OF LYSOSOMAL ACID LIPASE (351INSA) ASSOCIATED WITH COMPLETE IN-SITU ACID LIPASE DEFICIENCY
Authors: SEEDORF U HEIKO W SANDRO M ERTAN M HARALD F GERD A
Citation: U. Seedorf et al., WOLMAN-DISEASE DUE TO HOMOZYGOSITY FOR A NOVEL TRUNCATED VARIANT OF LYSOSOMAL ACID LIPASE (351INSA) ASSOCIATED WITH COMPLETE IN-SITU ACID LIPASE DEFICIENCY, Circulation, 94(8), 1996, pp. 196-196
Risultati: 1-25 | 26-45