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Results: 1-11 |
Results: 11
MUTATIONS IN THE HEPATIC LIPASE, LIPOPROTEIN-LIPASE AND APO-E BUT NOTTHE INSULIN-RECEPTOR ARE SUSCEPTIBILITY ALLELES MODIFYING FAMILIAL COMBINED HYPERLIPIDEMIA
Authors: GEHRISCH S KOSTKA H JULIUS U HANEFELD M SCHROEDER HE JAROSS W
Citation: S. Gehrisch et al., MUTATIONS IN THE HEPATIC LIPASE, LIPOPROTEIN-LIPASE AND APO-E BUT NOTTHE INSULIN-RECEPTOR ARE SUSCEPTIBILITY ALLELES MODIFYING FAMILIAL COMBINED HYPERLIPIDEMIA, Atherosclerosis (Amsterdam), 138, 1998, pp. 18-18
ASSOCIATION OF GENETIC-VARIANTS IN THE B-DOMAIN OF FACTOR-V GENE WITHAPC RESISTANCE
Authors: KOSTKA H SIEGERT G GEHRISCH S KUHLISCH E JAROSS W
Citation: H. Kostka et al., ASSOCIATION OF GENETIC-VARIANTS IN THE B-DOMAIN OF FACTOR-V GENE WITHAPC RESISTANCE, Circulation, 98(17), 1998, pp. 2383-2383
FUNCTIONAL IMPLICATIONS OF A NEW VARIANT OF THE HUMAN HEPATIC LIPASE GENE - INSIGHTS FROM IN-VIVO TURNOVER STUDIES
Authors: PIETZSCH J GEHRISCH S JULIUS U GROMEIER S KOSTKA H JAROSS W HANEFELD M
Citation: J. Pietzsch et al., FUNCTIONAL IMPLICATIONS OF A NEW VARIANT OF THE HUMAN HEPATIC LIPASE GENE - INSIGHTS FROM IN-VIVO TURNOVER STUDIES, The FASEB journal, 11(9), 1997, pp. 3360-3360
DECREASED APC-RESPONSE IN PATIENTS LACKING FACTOR-V-LEIDEN - LABORATORY DIAGNOSTIC AND CLINICAL RELEVANCE
Authors: SIEGERT G GEHRISCH S SCHELLONG S SCHWARZ T RUNGE E LUTHKE K
Citation: G. Siegert et al., DECREASED APC-RESPONSE IN PATIENTS LACKING FACTOR-V-LEIDEN - LABORATORY DIAGNOSTIC AND CLINICAL RELEVANCE, Thrombosis and haemostasis, 1997, pp. 1302-1302
POINT MUTATIONS IN THE GENES OF LIPOPROTEIN-LIPASE, HEPATIC LIPASE, AND INSULIN-RECEPTOR AS POSSIBLE SUSCEPTIBILITY ALLELES IN FAMILIAL COMBINED HYPERLIPIDEMIA
Authors: JAROSS W GEHRISCH S JULIUS U KOSTKA H HANEFELD HM
Citation: W. Jaross et al., POINT MUTATIONS IN THE GENES OF LIPOPROTEIN-LIPASE, HEPATIC LIPASE, AND INSULIN-RECEPTOR AS POSSIBLE SUSCEPTIBILITY ALLELES IN FAMILIAL COMBINED HYPERLIPIDEMIA, Atherosclerosis, 134(1-2), 1997, pp. 25-26
DIRECT EFFECTS OF THE ASN291SER VARIANT OF THE HUMAN LIPOPROTEIN-LIPASE ON THE CATABOLISM OF VLDL1 AND VLDL2 IN-VIVO
Authors: PIETZSCH J JULIUS U NITZSCHE S GEHRISCH S LEONHARDT W JAROSS W HANEFELD M
Citation: J. Pietzsch et al., DIRECT EFFECTS OF THE ASN291SER VARIANT OF THE HUMAN LIPOPROTEIN-LIPASE ON THE CATABOLISM OF VLDL1 AND VLDL2 IN-VIVO, Atherosclerosis, 134(1-2), 1997, pp. 26-27
FUNCTIONAL IMPLICATIONS OF THE HUMAN LIPOPROTEIN-LIPASE ASP9ASN VARIANT - INSIGHTS FROM IN-VIVO KINETIC-STUDIES
Authors: PIETZSCH J JULIUS U NITZSCHE S GEHRISCH S KOSTKA H JAROSS W HANEFELD M
Citation: J. Pietzsch et al., FUNCTIONAL IMPLICATIONS OF THE HUMAN LIPOPROTEIN-LIPASE ASP9ASN VARIANT - INSIGHTS FROM IN-VIVO KINETIC-STUDIES, Atherosclerosis, 134(1-2), 1997, pp. 26-26
THE LDL RECEPTOR GENE MUTATION CINCINNATI-1 IS COMMON IN THE GERMAN POPULATION AND THE PHENOTYPE IS SEVERELY MODIFIED BY DISTINCT APO-E ANDOR THE HEPATIC LIPASE (HL) GENOTYPES/
Authors: GEHRISCH S STEINFELDT F NAEKE A HANEFELD M JAROSS W KOSTKA H BOCHMANN H
Citation: S. Gehrisch et al., THE LDL RECEPTOR GENE MUTATION CINCINNATI-1 IS COMMON IN THE GERMAN POPULATION AND THE PHENOTYPE IS SEVERELY MODIFIED BY DISTINCT APO-E ANDOR THE HEPATIC LIPASE (HL) GENOTYPES/, Circulation, 96(8), 1997, pp. 3706-3706
FAST AMPLIFICATION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE AND DETECTION OF A LARGE DELETION BY MEANS OF LONG POLYMERASE CHAIN-REACTION
Authors: BOCHMANN H GEHRISCH S JAROSS W
Citation: H. Bochmann et al., FAST AMPLIFICATION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE AND DETECTION OF A LARGE DELETION BY MEANS OF LONG POLYMERASE CHAIN-REACTION, European journal of clinical chemistry and clinical biochemistry, 34(12), 1996, pp. 955-959
SUSCEPTIBILITY ALLELES OF THE HEPATIC LIPASE (HL) AND LIPOPROTEIN-LIPASE (LPL) BUT NOT INSULIN-RECEPTOR (INSR) ARE INVOLVED IN FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL)
Authors: GEHRISCH S KOSTKA H JULIUS U SCHROEDER HE JAROSS W
Citation: S. Gehrisch et al., SUSCEPTIBILITY ALLELES OF THE HEPATIC LIPASE (HL) AND LIPOPROTEIN-LIPASE (LPL) BUT NOT INSULIN-RECEPTOR (INSR) ARE INVOLVED IN FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL), Circulation, 94(8), 1996, pp. 1584-1584
POINT MUTATIONS IN THE HEPATIC TRIGLYCERIDE LIPASE (HTGL) GENE IN FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL)
Authors: GEHRISCH S TESCHE R KOSTKA H JULIUS U JAROSS W
Citation: S. Gehrisch et al., POINT MUTATIONS IN THE HEPATIC TRIGLYCERIDE LIPASE (HTGL) GENE IN FAMILIAL COMBINED HYPERLIPIDEMIA (FCHL), Circulation, 92(8), 1995, pp. 2352-2352
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