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Results: 1-25 | 26-50 | 51-57
Results: 1-25/57
MOLECULAR-GENETIC STUDY OF FINNS WITH HYPOALPHALIPOPROTEINEMIA AND HYPERALPHALIPOPROTEINEMIA - A NOVEL GLY(230)ARG MUTATION (LCAT(FIN)) OF LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) ACCOUNTS FOR 5-PERCENT OF CASES WITH VERY-LOW SERUM HDL CHOLESTEROL LEVELS
Authors: MIETTINEN HE GYLLING H TENHUNEN J VIRTAMO J JAUHIAINEN M HUTTUNEN JL KANTOLA I MIETTINEN TA KONTULA K
Citation: He. Miettinen et al., MOLECULAR-GENETIC STUDY OF FINNS WITH HYPOALPHALIPOPROTEINEMIA AND HYPERALPHALIPOPROTEINEMIA - A NOVEL GLY(230)ARG MUTATION (LCAT(FIN)) OF LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) ACCOUNTS FOR 5-PERCENT OF CASES WITH VERY-LOW SERUM HDL CHOLESTEROL LEVELS, Arteriosclerosis, thrombosis, and vascular biology, 18(4), 1998, pp. 591-598
MOLECULAR-GENETICS OF THE LONG QT SYNDROME - 2 NOVEL MUTATIONS OF THEKVLQT1 GENE AND PHENOTYPIC-EXPRESSION OF THE MUTANT-GENE IN A LARGE KINDRED
Authors: SAARINEN K SWAN H KAINULAINEN K TOIVONEN L VIITASALO M KONTULA K
Citation: K. Saarinen et al., MOLECULAR-GENETICS OF THE LONG QT SYNDROME - 2 NOVEL MUTATIONS OF THEKVLQT1 GENE AND PHENOTYPIC-EXPRESSION OF THE MUTANT-GENE IN A LARGE KINDRED, Human mutation, 11(2), 1998, pp. 158-165
GENETIC RISK-FACTORS AND ISCHEMIC CEREBROVASCULAR-DISEASE - ROLE OF COMMON VARIATION OF THE GENES ENCODING APOLIPOPROTEINS AND ANGIOTENSIN-CONVERTING ENZYME
Authors: AALTOSETALA K PALOMAKI H MIETTINEN H VUORIO A KUUSI T RAININKO R SALONEN O KASTE M KONTULA K
Citation: K. Aaltosetala et al., GENETIC RISK-FACTORS AND ISCHEMIC CEREBROVASCULAR-DISEASE - ROLE OF COMMON VARIATION OF THE GENES ENCODING APOLIPOPROTEINS AND ANGIOTENSIN-CONVERTING ENZYME, Annals of medicine, 30(2), 1998, pp. 224-233
EVALUATION OF QT INTERVAL DURATION AND DISPERSION AND PROPOSED CLINICAL-CRITERIA IN DIAGNOSIS OF LONG QT SYNDROME IN PATIENTS WITH A GENETICALLY UNIFORM TYPE OF LQT1
Authors: SWAN H SAARINEN K KONTULA K TOIVONEN L VIITASALO M
Citation: H. Swan et al., EVALUATION OF QT INTERVAL DURATION AND DISPERSION AND PROPOSED CLINICAL-CRITERIA IN DIAGNOSIS OF LONG QT SYNDROME IN PATIENTS WITH A GENETICALLY UNIFORM TYPE OF LQT1, Journal of the American College of Cardiology, 32(2), 1998, pp. 486-491
A MUTATION IN KVLQT1 CAUSES DECREASED SINUS RATE WITHOUT EVIDENCE OF AUTONOMIC NERVOUS ABNORMALITIES
Authors: SWAN H VIITASALO M SAARINEN K KONTULA K TOIVONEN L
Citation: H. Swan et al., A MUTATION IN KVLQT1 CAUSES DECREASED SINUS RATE WITHOUT EVIDENCE OF AUTONOMIC NERVOUS ABNORMALITIES, Journal of the American College of Cardiology, 31(2), 1998, pp. 193-193
A COMMON PENTANUCLEOTIDE POLYMORPHISM OF THE 3'-UNTRANSLATED PART OF THE LEPTIN RECEPTOR GENE GENERATES A PUTATIVE STEM-LOOP MOTIF IN THE MESSENGER-RNA AND IS ASSOCIATED WITH SERUM-INSULIN LEVELS IN OBESE INDIVIDUALS
Authors: OKSANEN L KAPRIO J MUSTAJOKI P KONTULA K
Citation: L. Oksanen et al., A COMMON PENTANUCLEOTIDE POLYMORPHISM OF THE 3'-UNTRANSLATED PART OF THE LEPTIN RECEPTOR GENE GENERATES A PUTATIVE STEM-LOOP MOTIF IN THE MESSENGER-RNA AND IS ASSOCIATED WITH SERUM-INSULIN LEVELS IN OBESE INDIVIDUALS, International journal of obesity, 22(7), 1998, pp. 634-640
QT INTERVAL DYNAMICS AND SINUS NODE FUNCTION DURING EXERCISE TEST PATIENTS WITH A C-TERMINAL MUTATION OF KVLQT1 CAUSING LONG QT SYNDROME
Authors: SWAN H SAARINEN K VLITASALO M KONTULA K TOLVONEN L
Citation: H. Swan et al., QT INTERVAL DYNAMICS AND SINUS NODE FUNCTION DURING EXERCISE TEST PATIENTS WITH A C-TERMINAL MUTATION OF KVLQT1 CAUSING LONG QT SYNDROME, Circulation, 98(17), 1998, pp. 807-807
A FOUNDER MUTATION OF THE POTASSIUM CHANNEL KVLQT1 ACCOUNTS FOR ONE-THIRD OF CASES WITH LONG QT SYNDROME IN FINNS
Authors: SAARINEN K SWAN H TOIVONEN L VIITASALO M PASTERNACK M HIRVELA E SAARMA M KONTULA K
Citation: K. Saarinen et al., A FOUNDER MUTATION OF THE POTASSIUM CHANNEL KVLQT1 ACCOUNTS FOR ONE-THIRD OF CASES WITH LONG QT SYNDROME IN FINNS, Circulation, 98(17), 1998, pp. 2401-2401
HEMOCHROMATOSIS GENE HFE CYS282TYR POLYMORPHISM IS ASSOCIATED WITH 2-FOLD INCREASED RISK OF ACUTE MYOCARDIAL-INFARCTION IN MEN
Authors: TUOMAINEN TP KONTULA K NYYSSONEN K LAKKA TA SALONEN JT
Citation: Tp. Tuomainen et al., HEMOCHROMATOSIS GENE HFE CYS282TYR POLYMORPHISM IS ASSOCIATED WITH 2-FOLD INCREASED RISK OF ACUTE MYOCARDIAL-INFARCTION IN MEN, Circulation, 98(17), 1998, pp. 2417-2417
SITOSTANOL ESTER MARGARINE WITHOUT AND WITH SIMVASTATIN IN DIETARY-TREATMENT OR FAMILIES HETEROZYGOUS OF FAMILIAL HYPERCHOLESTEROLEMIA NORTH-KARELIA DELETION
Authors: VUORIO AF GYLLING H TURTOLA H KONTULA K MIETTINEN TA
Citation: Af. Vuorio et al., SITOSTANOL ESTER MARGARINE WITHOUT AND WITH SIMVASTATIN IN DIETARY-TREATMENT OR FAMILIES HETEROZYGOUS OF FAMILIAL HYPERCHOLESTEROLEMIA NORTH-KARELIA DELETION, Circulation, 98(17), 1998, pp. 2804-2804
FAMILIAL MODERATE HYPERCHOLESTEROLEMIA CAUSED BY ASP235-]GLU MUTATIONOF THE LDL RECEPTOR GENE AND COOCCURRENCE OF A DE-NOVO DELETION OF THE LDL RECEPTOR GENE IN THE SAME FAMILY
Authors: KOIVISTO UM GYLLING H MIETTINEN TA KONTULA K
Citation: Um. Koivisto et al., FAMILIAL MODERATE HYPERCHOLESTEROLEMIA CAUSED BY ASP235-]GLU MUTATIONOF THE LDL RECEPTOR GENE AND COOCCURRENCE OF A DE-NOVO DELETION OF THE LDL RECEPTOR GENE IN THE SAME FAMILY, Arteriosclerosis, thrombosis, and vascular biology, 17(7), 1997, pp. 1392-1399
APOLIPOPROTEIN A-I-FIN (LEU159-]ARG) MUTATION AFFECTS LECITHIN - CHOLESTEROL ACYLTRANSFERASE ACTIVATION AND SUBCLASS DISTRIBUTION OF HDL BUT NOT CHOLESTEROL EFFLUX FROM FIBROBLASTS
Authors: MIETTINEN HE JAUHIAINEN M GYLLING H EHNHOLM S PALOMAKI A MIETTINEN TA KONTULA K
Citation: He. Miettinen et al., APOLIPOPROTEIN A-I-FIN (LEU159-]ARG) MUTATION AFFECTS LECITHIN - CHOLESTEROL ACYLTRANSFERASE ACTIVATION AND SUBCLASS DISTRIBUTION OF HDL BUT NOT CHOLESTEROL EFFLUX FROM FIBROBLASTS, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 3021-3032
FAMILIAL HYPERCHOLESTEROLEMIA IN THE FINNISH NORTH KARELIA - A MOLECULAR, CLINICAL, AND GENEALOGICAL STUDY
Authors: VUORIO AF TURTOLA H PIILAHTI KM REPO P KANNINEN T KONTULA K
Citation: Af. Vuorio et al., FAMILIAL HYPERCHOLESTEROLEMIA IN THE FINNISH NORTH KARELIA - A MOLECULAR, CLINICAL, AND GENEALOGICAL STUDY, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 3127-3138
NEONATAL DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN NEWBORNS BORN TO A PARENT WITH A MOLECULARLY DEFINED HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Authors: VUORIO AF TURTOLA H KONTULA K
Citation: Af. Vuorio et al., NEONATAL DIAGNOSIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN NEWBORNS BORN TO A PARENT WITH A MOLECULARLY DEFINED HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 3332-3337
POLYMORPHISMS OF THE GENES ENCODING APOPROTEIN-A-I, APOPROTEIN-B, APOPROTEIN-C-III, AND APOPROTEIN-E AND LDL-RECEPTOR, AND CHOLESTEROL AND LDL METABOLISM DURING INCREASED CHOLESTEROL INTAKE - COMMON ALLELES OFTHE APOPROTEIN-E GENE SHOW THE GREATEST REGULATORY IMPACT
Authors: GYLLING H KONTULA K KOIVISTO UM MIETTINEN HE MIETTINEN TA
Citation: H. Gylling et al., POLYMORPHISMS OF THE GENES ENCODING APOPROTEIN-A-I, APOPROTEIN-B, APOPROTEIN-C-III, AND APOPROTEIN-E AND LDL-RECEPTOR, AND CHOLESTEROL AND LDL METABOLISM DURING INCREASED CHOLESTEROL INTAKE - COMMON ALLELES OFTHE APOPROTEIN-E GENE SHOW THE GREATEST REGULATORY IMPACT, Arteriosclerosis, thrombosis, and vascular biology, 17(1), 1997, pp. 38-44
APOLIPOPROTEIN A-I-FIN - DOMINANTLY INHERITED HYPOALPHALIPOPROTEINEMIA DUE TO A SINGLE-BASE SUBSTITUTION IN THE APOLIPOPROTEIN-A-I GENE
Authors: MIETTINEN HE GYLLING H MIETTINEN TA VIIKARI J PAULIN L KONTULA K
Citation: He. Miettinen et al., APOLIPOPROTEIN A-I-FIN - DOMINANTLY INHERITED HYPOALPHALIPOPROTEINEMIA DUE TO A SINGLE-BASE SUBSTITUTION IN THE APOLIPOPROTEIN-A-I GENE, Arteriosclerosis, thrombosis, and vascular biology, 17(1), 1997, pp. 83-90
DELETIONS OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE UNDERLYING FAMILIAL HYPERCHOLESTEROLEMIA - SCREENING BY POLYMERASE CHAIN-REACTION USING POOLED DNA AND BLOOD-SAMPLES
Authors: VUORIO AF PAULIN L TURTOLA H KONTULA K
Citation: Af. Vuorio et al., DELETIONS OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE UNDERLYING FAMILIAL HYPERCHOLESTEROLEMIA - SCREENING BY POLYMERASE CHAIN-REACTION USING POOLED DNA AND BLOOD-SAMPLES, Molecular and cellular probes, 11(1), 1997, pp. 65-70
MARKERS FOR THE GENE OB AND SERUM LEPTIN LEVELS IN HUMAN MORBID-OBESITY
Authors: OKSANEN L OHMAN M HEIMAN M KAINULAINEN K KAPRIO J MUSTAJOKI P KOIVISTO V KOSKENVUO M JANNE OA PELTONEN L KONTULA K
Citation: L. Oksanen et al., MARKERS FOR THE GENE OB AND SERUM LEPTIN LEVELS IN HUMAN MORBID-OBESITY, Human genetics, 99(5), 1997, pp. 559-564
PLATELET FIBRINOGEN RECEPTOR POLYMORPHISM HPA-1 IN ACUTE MYOCARDIAL-INFARCTION AND ACUTE ISCHEMIC STROKE
Authors: KEKOMAKI S HAMALAINEN I KASTE M KAUPPINENMAKELIN R MIETTINEN H PALOMAKI H KONTULA K
Citation: S. Kekomaki et al., PLATELET FIBRINOGEN RECEPTOR POLYMORPHISM HPA-1 IN ACUTE MYOCARDIAL-INFARCTION AND ACUTE ISCHEMIC STROKE, Thrombosis and haemostasis, 1997, pp. 1041-1041
PREVALENCE OF FACTOR-V LEIDEN IN YOUNG-ADULTS WITH RETINAL VEIN OCCLUSION
Authors: LINNA T YLIKORKALA A KONTULA K PUSKA P TERVO T
Citation: T. Linna et al., PREVALENCE OF FACTOR-V LEIDEN IN YOUNG-ADULTS WITH RETINAL VEIN OCCLUSION, Thrombosis and haemostasis, 77(1), 1997, pp. 214-216
NOVEL POLYMORPHISM OF THE HUMAN OB GENE PROMOTER IN LEAN AND MORBIDLYOBESE SUBJECTS
Authors: OKSANEN L KAINULAINEN K HEIMAN M MUSTAJOKI P KAUPPINENMAKELIN R KONTULA K
Citation: L. Oksanen et al., NOVEL POLYMORPHISM OF THE HUMAN OB GENE PROMOTER IN LEAN AND MORBIDLYOBESE SUBJECTS, International journal of obesity, 21(6), 1997, pp. 489-494
AUTOSOMAL-DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MULTIPLEDELETIONS OF MTDNA - CLINICAL, BIOCHEMICAL, AND MOLECULAR-GENETIC FEATURES OF THE 10Q-LINKED DISEASE
Authors: SUOMALAINEN A MAJANDER A WALLIN M SETALA K KONTULA K LEINONEN H SALMI T PAETAU A HALTIA M VALANNE L LONNQVIST J PELTONEN L SOMER H
Citation: A. Suomalainen et al., AUTOSOMAL-DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MULTIPLEDELETIONS OF MTDNA - CLINICAL, BIOCHEMICAL, AND MOLECULAR-GENETIC FEATURES OF THE 10Q-LINKED DISEASE, Neurology, 48(5), 1997, pp. 1244-1253
LEPTIN CONCENTRATION IN CORD-BLOOD CORRELATES WITH INTRAUTERINE GROWTH
Authors: KOISTINEN HA KOIVISTO VA ANDERSSON S KARONEN SL KONTULA K OKSANEN L TERAMO KA
Citation: Ha. Koistinen et al., LEPTIN CONCENTRATION IN CORD-BLOOD CORRELATES WITH INTRAUTERINE GROWTH, The Journal of clinical endocrinology and metabolism, 82(10), 1997, pp. 3328-3330
LCAT DEFICIENCY CAUSED BY A NOVEL LCATFIN (GLY230ARG) AND LCAT ARG399CYS MUTATIONS - INCREASED FREQUENCY OF LCATFIN AMONG SUBJECTS WITH LOWHDL-C LEVELS
Authors: MIETTINEN HE GYLLING H VIRTAMO J TENHUNEN J JAUHIAINEN M KANTOLA I HUTTUNEN J KONTULA K
Citation: He. Miettinen et al., LCAT DEFICIENCY CAUSED BY A NOVEL LCATFIN (GLY230ARG) AND LCAT ARG399CYS MUTATIONS - INCREASED FREQUENCY OF LCATFIN AMONG SUBJECTS WITH LOWHDL-C LEVELS, Atherosclerosis, 134(1-2), 1997, pp. 70-70
FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN THE FINNISH NORTH KARELIA - A GENEALOGICAL, MOLECULAR AND CLINICAL-STUDY
Authors: VUORIO AF TURTOLA H PIILAHTI KM REPO P KANNINEN T KONTULA K
Citation: Af. Vuorio et al., FAMILIAL HYPERCHOLESTEROLEMIA (FH) IN THE FINNISH NORTH KARELIA - A GENEALOGICAL, MOLECULAR AND CLINICAL-STUDY, Atherosclerosis, 134(1-2), 1997, pp. 84-84
Risultati: 1-25 | 26-50 | 51-57