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1 Association between polymorphisms in the fibrinogen α- and β-genes on the post-trauma fibrinogen increase
article 1998    
Author: Ferrer-Antunes, C. · Maat, M.P.M. de · Palmeiro, A. · Pimentel, J. · Fernandes, V.
Keywords: Health · Adult · Aged · Alleles · Craniocerebral Trauma · Female · Fibrinogen · Gene Frequency · Genotype · Humans · Male · Middle Aged · Polymorphism, Genetic · Thoracic Injuries
[Abstract]

2 A polymorphic cluster in the 5' region of the human coagulation factor VII gene: Detection, frequency, and linkage disequilibrium
article 1997    
Author: Acqua, G. Dell · Iacoviello, L. · Orazio, A. D · Bitondo, R. Di · Castelnuovo, A. Di · Donati, M.B.
Keywords: Health · Base Sequence · Factor VII · Gene Frequency · Genotype · Humans · Linkage Disequilibrium · Molecular Sequence Data · Polymerase Chain Reaction · Polymorphism, Genetic · Promoter Regions (Genetics)

3 Bcl I polymorphism in the fibrinogen β-chain gene is associated with the risk of familial myocardial infarction by increasing plasma fibrinogen levels: A case-control study in a sample of GISSI-2 patients
article 1997    
Author: Zito, F. · Castelnuovo, A. di · Amore, C. · D'Orazio, A. · Donati, M.B. · Iacoviello, L.
Keywords: Case-Control Studies · Deoxyribonucleases, Type II Site-Specific · Female · Fibrinogen · Gene Frequency · Genotype · Humans · Italy · Male · Middle Aged · Myocardial Infarction · Polymorphism, Genetic · Polymorphism, Restriction Fragment Length · Risk
[Abstract]

4 Population haplotype analysis and evolutionary relations of the COL2A1 gene
article 1996    
Author: Meulenbelt, I. · Williams, G.J. · Koppele, J.M.T.E. · Giessen, G.C.D.E. van · Slagboom, P.E.
Keywords: Biology · collagen type 11 · allelism · article · evolution · gene assignment · gene frequency · gene linkage disequilibrium · genetic analysis · haplotype · human · human cell · population genetics · priority journal · Collagen · European Continental Ancestry Group · Evolution, Molecular · Gene Frequency · Genetics, Population · Genotype · Haplotypes · Humans · Linkage (Genetics) · Linkage Disequilibrium · Mutation · Netherlands · Osteoarthritis · Polymorphism, Genetic · Polymorphism, Restriction Fragment Length
[Abstract]

5 Deep-vein thrombosis is not associated with the P/S186 polymorphism of histidine-rich glycoprotein
article 1999    
Author: Rattink, A.P. · Hennis, B.C. · Lievers, C.J.A. · Maat, M.P.M. de · Bertina, R. · Mennen, L.I. · Rosendaal, F.R.
Keywords: Health · glycoprotein · histidine · plasma protein · adult · allelism · article · controlled study · deep vein thrombosis · DNA polymorphism · exon · female · gene frequency · gene locus · genetic association · human · immunodiffusion · major clinical study · priority journal
[Abstract]

6 Apolipoprotein A-IV polymorhism and its effect on plasma lipid and apolipoprotein concentrations
article 1988    
Author: Knijff, P. de · Rosseneu, M. · Beisiegel, U. · Keersgieter, W. de · Frants, R.R. · Havekes, L.M.
Keywords: Biology · Triacylglycerol · Apolipoprotein blood level · Heredity · Lipid blood level · Population genetics · Protein polymorphism · Blood · Genetic polymorphism · Genetics · Phenotype · Adult · Alleles · Animal · Apolipoproteins · Apolipoproteins A · Apolipoproteins B · Cholesterol · Gene Frequency · Human · Lipids · Male · Phenotype · Polymorphism (Genetics) · Rabbits · Triglycerides
[PDF] [Abstract]

7 Expression of type III hyperlipoproteinemia in apolipoprotein E2 (Arg158→Cys) homozygotes is associated with hyperinsulinemia
article 2002    
Author: Beer, F. de · Stalenhoef, A.F.H. · Hoogerbrugge, N. · Kastelein, J.J.P. · Leuven, J.A.G. · Duijn, C.M. van · Havekes, L.M. · Smelt, A.H.M.
Keywords: Adult · Age of Onset · Aging · Apolipoprotein E2 · Apolipoproteins E · Comorbidity · Coronary Disease · Estrogens · Female · Gene Expression · Gene Frequency · Homozygote · Humans · Hyperinsulinism · Hyperlipoproteinemia Type III · Male · Menopause · Middle Aged · Netherlands · Peripheral Vascular Diseases · Prevalence · Regression Analysis · Sex Factors
[Abstract]

8 Alcohol consumption and type 2 diabetes: Influence of genetic variation in alcohol dehydrogenase
article 2007    
Author: Beulens, J.W.J. · Rimm, E.B. · Hendriks, H.F.J. · Hu, F.B. · Manson, J.E. · Hunter, D.J. · Mukamal, K.J.
Keywords: Health · Biomedical Research · alcohol dehydrogenase · alcohol dehydrogenase 1C · adult · alcohol consumption · alcohol oxidation · article · controlled study · disease association · female · gene frequency · genetic polymorphism · genotype · heterozygote · homozygote · human · major clinical study · male · morbidity · non insulin dependent diabetes mellitus · priority journal · risk factor · Adult · Alcohol Dehydrogenase · Alcohol Drinking · Case-Control Studies · Diabetes Mellitus, Type 2 · Female · Gene Frequency · Genotype · Humans · Male · Middle Aged · Polymorphism, Genetic · Questionnaires · Reference Values · Smoking · Variation (Genetics)
[Abstract]

9 Plasma apoAV levels are markedly elevated in severe hypertriglyceridemia and positively correlated with the APOA5 S19W polymorphism
article 2007    
Author: Henneman, P. · Schaap, F.G. · Havekes, L.M. · Rensen, P.C.N. · Frants, R.R. · Tol, A. van · Hattori, H. · Smelt, A.H.M. · Dijk, K.W. van
Keywords: Biology · Biomedical Research · apoAV · Hypertriglyceridemia · Lipoprotein lipase · Plasma apoAV concentration · SNP-analysis · apolipoprotein A5 · adult · allele · article · circulation · controlled study · endoplasmic reticulum · female · gene frequency · gene mutation · genetic polymorphism · genetic variability · haplotype · human · hypertriglyceridemia · lipolysis · major clinical study · male · priority journal · protein secretion · single nucleotide polymorphism · Adult · Alleles · Apolipoproteins A · Base Sequence · Case-Control Studies · DNA Primers · Female · Gene Frequency · Haplotypes · Humans · Hypertriglyceridemia · Male · Middle Aged · Polymorphism, Single Nucleotide
[Abstract]

10 The association between IGF-1 polymorphisms, IGF-1 serum levels, and cognitive functions in healthy adults: The amsterdam growth and health longitudinal study
article 2014    
Author: Licht, C.M.M. · Turenhout, L.C. van · Deijen, J.B. · Koppes, L.L.J. · Mechelen, W. van · Twisk, J.W.R. · Drent, M.L.
Keywords: Workplace · Somatomedin C · Adult · Body mass · Caucasian · Clinical assessment · Cognition · Gene frequency · Gene location · Genetic association · Genetic polymorphism · Heterozygote · Homozygote · Human experiment · IGF 1 gene · Intelligence quotient · Mental task · Mental test · Middle aged · Paired associate learning · Promoter region · Protein blood level · Spatial memory · Working memory · Work and Employment · Healthy Living · Resilient Organisations · WHC - Work, Health and Care · ELSS - Earth, Life and Social Sciences
[PDF] [Abstract]

11 The expression of type III hyperlipoproteinemia: Involvement of lipolysis genes
article 2009    
Author: Henneman, P. · Sman-de Beer, F. van der · Moghaddam, P.H. · Huijts, P. · Stalenhoef, A.F.H. · Kastelein, J.J.P. · Duijn, C.M. van · Havekes, L.M. · Frants, R.R. · Dijk, K.W. van · Smelt, A.H.M.
Keywords: Biology · Biomedical Research · adenine · apolipoprotein A5 · apolipoprotein C3 · apolipoprotein E2 · cytosine · guanine · lipoprotein lipase · liver triacylglycerol lipase · thymine · adult · aged · article · controlled study · disease severity · female · gene expression · gene frequency · gene function · gene linkage disequilibrium · genetic association · genetic polymorphism · genetic variability · human · human cell · hyperlipidemia · hyperlipoproteinemia type 3 · hypertriglyceridemia · lipolysis · lipoprotein blood level · major clinical study · male · mutational analysis · Netherlands · priority journal
[Abstract]

12 Identification and genetic analysis of a common molecular variant of histidine-rich glycoprotein with a difference of 2KD in apparent molecular weight
article 1995    
Author: Hennis, B.C. · Boheemen, P.A. van · Wakabayashi, S. · Koide, T. · Hoffmann, J.J.M.L. · Kievit, P. · Dooijewaard, G. · Jansen, J.G. · Klutf, C.
Keywords: Biology · glycoprotein · histidine · proline · serine · allele · article · clinical article · exon · family study · gene amplification · gene frequency · genetic analysis · genetic polymorphism · homozygosity · human · immunoblotting · inheritance · molecular weight · polyacrylamide gel electrophoresis · priority journal · protein variant · sequence analysis · silver staining · Amino Acid Sequence · Base Sequence · Blood Proteins · Case-Control Studies · Exons · Genetic Code · Genotype · Glycoproteins · Humans · Molecular Sequence Data · Molecular Weight · Pedigree · Phenotype · Polymorphism, Genetic · Proteins · Variation (Genetics)
[Abstract]

13 Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels
article 1994    
Author: Knijff, P. de · Maagdenberg, A.M.J.M. van den · Frants, R.R. · Havekes, L.M.
Keywords: Biology · Apolipoprotein (apo) E · Atherosclerosis · Familial Dysbetalipoproteinemia (FD) · Mutations · Polymorphisms · Type III Hyperlipoproteinemia · Cholesterol · Chylomicron · Low density lipoprotein receptor · Triacylglycerol · Very low density lipoprotein · Alzheimer disease · Atherosclerosis · Cholesterol blood level · Coronary artery disease · Creutzfeldt jakob disease · Gene mutation · Genetic heterogeneity · Genetic linkage · Genetic polymorphism · Ligand binding · Lipoprotein metabolism · Alleles · Amino Acid Sequence · Base Sequence · DNA · Female · Gene Frequency · Human · Hyperlipidemia · Hyperlipoproteinemia Type III · Lipids · Lipoproteins · Male · Molecular Sequence Data · Mutation · Variation (Genetics)
[Abstract]

14 Modulating effect of the A-278C promoter polymorphism in the cholesterol 7alpha-hydroxylase gene on serum lipid levels in normolipidaemic and hypertriglyceridaemic individuals
article 2004    
Author: Hofman, M.K. · Groenendijk, M. · Verkuijlen, P.J.J.H. · Jonkers, I.J.A.M. · Mohrschladt, M.F. · Smelt, A.H.M. · Princen, H.M.G.
Keywords: Biology · Biomedical Research · CYP7A1 · Hyperlipidaemia · Modifier gene · Polymorphism · Triglycerides · apolipoprotein E3 · cholesterol · cholesterol 7alpha monooxygenase · isoprotein · lipid · low density lipoprotein · triacylglycerol · very low density lipoprotein · controlled study · DNA polymorphism · familial hypercholesterolemia · gene control · homozygosity · hyperlipidemia · hyperlipoproteinemia type 3 · lipid blood level · major clinical study · promoter region · triacylglycerol blood level · Adult · Aged · Cholesterol 7-alpha-Hydroxylase · Female · Gene Frequency · Genotype · Humans · Hypertriglyceridemia · Male · Middle Aged · Polymorphism, Genetic · Promoter Regions (Genetics) · Triglycerides
[Abstract]

15 Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population
article 2003    
Author: Beekman, M. · Heijmans, B.T. · Martin, N.G. · Whitfield, J.B. · Pedersen, N.L. · Faire, U. de · Snieder, H. · Lakenberg, N. · Suchiman, H.E.D. · Knijff, P. de · Frants, R.R. · Ommen, G.J.B. van · Kluft, C. · Vogler, G.P. · Boomsma, D.I. · Slagboom, P.E.
Keywords: Health · Cardiovascular risk factors · Linkage · Quantitative trait locus (QTL) · Twin pairs · Apolipoprotein · Lipid · Low density lipoprotein cholesterol · Australia · Cardiovascular risk · Caucasian · Cholesterol blood level · Chromosome 19 · Controlled study · Dizygotic twins · Genetic correlation · Genetic linkage · Genetic variability · Lipid blood level · Lipid metabolism · Major clinical study · Netherlands · Phenotype · Population research · Quantitative analysis · Quantitative trait locus · Risk factor · Scoring system · Sweden · Tandem repeat · Adolescent · Adult · Aged · Cardiovascular Diseases · Cholesterol, LDL · Chromosomes, Human, Pair 19 · European Continental Ancestry Group · Female · Gene Frequency · Genetic Markers · Genetics, Population · Humans · Linkage (Genetics) · Lod Score · Male · Middle Aged · Phenotype · Quantitative Trait Loci · Twins, Dizygotic · Variation (Genetics)
[Abstract]

16 The lipoprotein lipase (Asn291 → Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia
article 1996    
Author: Hoffer, M.J.V. · Bredie, S.J.H. · Boomsma, D.I. · Reymer, P.W.A. · Kastelein, J.J.P. · Knijff, P. de · Demacker, P.N.M. · Stalenhoef, A.F.H. · Havekes, L.M. · Frants, R.R.
Keywords: Biology · Cholesterol · Familial combined hyperlipidaemia · Lipoprotein lipase · LPL(Asn291→ Ser) mutation · Triglycerides · cholesterol · high density lipoprotein cholesterol · lipoprotein lipase · low density lipoprotein cholesterol · triacylglycerol · very low density lipoprotein · adult · article · controlled study · coronary artery atherosclerosis · enzyme activity · familial hyperlipemia · gene mutation · genetic predisposition · human · major clinical study · male · pedigree analysis · priority journal · Base Sequence · Cholesterol · Coronary Disease · Female · Gene Frequency · Genetic Predisposition to Disease · Heterozygote · Humans · Hyperlipidemia, Familial Combined · Lipids · Lipoprotein Lipase · Male · Molecular Sequence Data · Netherlands · Pedigree · Point Mutation · Prevalence · Risk Factors · Triglycerides
[Abstract]

Search results also available in MS Excel format.

Showing 1 to 16 of 16 found. | Sort by date