Bestimmung der Zwischenschichtaustauschkopplung in ferromagnetischen Fe- und Co-Schichtsystemen = Determination of the interlayer exchange coupling in ferromagnetic Fe- and Co-double layersVOHL, M.Berichte der Kernforschungsanlage Jülich. 1991, Num 2434, issn 0366-0885, 110 p.Serial Issue

Layered magnetic structures : antiferromagnetic-type interlayer coupling and magnetoresistance due to antiparallel alignmentGRUÊNBERG, P; DEMOKRITOV, S; FUS, A et al.Journal of applied physics. 1991, Vol 69, Num 8, pp 4789-4791, issn 0021-8979, 3 p., p.2AConference Paper

Layered magnetic structures : antiferromagnetic type interlayer coupling and magnetoresistance due to antiparallel alignmentGRUÊNBERG, P; BARNAS, J; SAURENBACH, F et al.Journal of magnetism and magnetic materials. 1991, Vol 93, pp 58-66, issn 0304-8853, 9 p.Conference Paper

Exchange coupling of ferromagnetic layers across nonmagnetic interlayersVOHL, M; WOLF, J. A; GRUÊNBERG, P et al.Journal of magnetism and magnetic materials. 1991, Vol 93, pp 403-406, issn 0304-8853, 4 p.Conference Paper

Molecular size and solvation of low molecular weight poly(ethylene oxide) and phenol-formaldehyde resols in different solventsRIEDI, B; VOHL, M.-J; CALVE, L et al.Journal of applied polymer science. 1990, Vol 39, Num 2, pp 341-353, issn 0021-8995Article

Associations between dietary patterns and obesity phenotypesPARADIS, A.-M; GODIN, G; PERUSSE, L et al.International journal of obesity. 2009, Vol 33, Num 12, pp 1419-1426, issn 0307-0565, 8 p.Article

Features of the metabolic syndrome are modulated by an interaction between the peroxisome proliferator-activated receptor-delta -87T>C polymorphism and dietary fat in French-CanadiansROBITAILLE, J; GAUDET, D; PERUSSE, L et al.International journal of obesity. 2007, Vol 31, Num 3, pp 411-417, issn 0307-0565, 7 p.Article

The PPAR-gamma P12A polymorphism modulates the relationship between dietary fat intake and components of the metabolic syndrome: results from the Québec Family StudyROBITAILLE, J; DESPRES, J.-P; PERUSSE, L et al.Clinical genetics. 2003, Vol 63, Num 2, pp 109-116, issn 0009-9163, 8 p.Article

Haplotypes in the phospholipid transfer protein gene are associated with obesity-related phenotypes : the Québec Family StudyBOSSE, Y; BOUCHARD, L; DESPRES, J.-P et al.International journal of obesity. 2005, Vol 29, Num 11, pp 1338-1345, issn 0307-0565, 8 p.Article

The effect of silyl substituted methotrexate in the treatment of experimental allergic encephalomyelitis in rats mediated by T-line cellsPRZUNTEK, H; WESTARP, M. E; VOHL, M. L et al.Neuropharmacology. 1987, Vol 26, Num 2-3, pp 255-260, issn 0028-3908Article

Associations between USF1 gene variants and cardiovascular risk factors in the Quebec Family StudyCHOQUETTE, A. C; BOUCHARD, L; HOUDE, A et al.Clinical genetics. 2007, Vol 71, Num 3, pp 245-253, issn 0009-9163, 9 p.Article

Detection of a MspI restriction fragment length polymorphism for the human sex hormone-binding globulin (SHBH) geneVOHL, M.-C; DIONNE, F. T; DERIAZ, O et al.Human genetics. 1994, Vol 93, Num 1, issn 0340-6717, p. 84Article

Mercaptopurin und silyliertes Mercaptopurin in der Behandlung der experimentell allergischen Enzephalomyelitis = Mercaptopurine et mercaptopurine silyl dans le traitement de l'encéphalomyélite allergique expérimentale = Mercaptopurine and silylated mercaptopurine in the treatment of the experimental allergic encephalomyelitisVOHL, M. L; WESTARP, M. E; WEKERLE, H et al.Arzneimittel-Forschung. 1990, Vol 40, Num 1, pp 80-84, issn 0004-4172Article

Relationships of abdominal obesity and hyperinsulinemia to angiographically assessed coronary artery disease in men with known mutations in the LDL receptor geneGAUDET, D; VOHL, M.-C; PERRON, P et al.Circulation (New York, N.Y.). 1998, Vol 97, Num 9, pp 871-877, issn 0009-7322Article

Evidence for Interaction between PPARG Pro12Ala and PPARGC1A Gly482Ser Polymorphisms in Determining Type 2 Diabetes Intermediate Phenotypes in Overweight SubjectsRUCHAT, S.-M; WEISNAGEL, S. J; VOHL, M.-C et al.Experimental and clinical endocrinology & diabetes. 2009, Vol 117, Num 9, pp 455-459, issn 0947-7349, 5 p.Article

Contribution of the cholesteryl ester transfer protein gene TaqlB polymorphism to the reduced plasma HDL-cholesterol levels found in abdominal obese men with the features of the insulin resistance syndromeVOHL, M.-C; LAMARCHE, B; PASCOT, A et al.International journal of obesity. 1999, Vol 23, Num 9, pp 918-925, issn 0307-0565Article

Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutationsCOUTURE, P; MORISSETTE, J; GAUDET, D et al.Atherosclerosis. 1999, Vol 143, Num 1, pp 145-151, issn 0021-9150Article

CYR61 polymorphisms are associated with plasma HDL-cholesterol levels in obese individualsBOUCHARD, L; TCHERNOF, A; DESHAIES, Y et al.Clinical genetics. 2007, Vol 72, Num 3, pp 224-229, issn 0009-9163, 6 p.Article

Genetic epistasis in the VLDL catabolic pathway is associated with deleterious variations on triglyceridemia in obese subjectsBRISSON, D; ST-PIERRE, J; SANTURE, M et al.International journal of obesity. 2007, Vol 31, Num 8, pp 1325-1333, issn 0307-0565, 9 p.Article

Influences of the phosphatidylcholine transfer protein gene variants on the LDL peak particle sizeDOLLEY, G; BERTHIER, M. T; LAMARCHE, B et al.Atherosclerosis. 2007, Vol 195, Num 2, pp 297-302, issn 0021-9150, 6 p.Article

T lymphocyte line-mediated experimental allergic encephalomyelitis: a pharmnacologic model for testing of immunosuppressive agents for the treatment of autoimmune central nervous system diseaseWESTARP, M. E; WEKERLE, H; BEN-NUN, A et al.The Journal of pharmacology and experimental therapeutics. 1987, Vol 242, Num 2, pp 614-620, issn 0022-3565Article

Influence of the angiotensin-converting enzyme gene insertion/deletion polymorphism on lipoprotein/lipid response to gemfibrozilBOSSE, Y; VOHL, M-C; DUMONT, M et al.Clinical genetics. 2002, Vol 62, Num 1, pp 45-52, issn 0009-9163Article

Contribution of receptor negative versus receptor defective mutations in the LDL-receptor gene to angiographically assessed coronary artery disease among young (25-49 years) versus middle-aged (50-64 years) menGAUDET, D; VOHL, M.-C; COUTURE, P et al.Atherosclerosis. 1999, Vol 143, Num 1, pp 153-161, issn 0021-9150Article

Relative contribution of low-density lipoprotein receptor and lipoprotein lipase gene mutations to angiographically assessed coronary artery disease among French CanadiansGAUDET, D; VOHL, M.-C; JULIEN, P et al.The American journal of cardiology. 1998, Vol 82, Num 3, pp 299-305, issn 0002-9149Article

HDL cholesterol and TaqIB cholesteryl ester transfer protein gene polymorphism in renal transplant recipientsRADEAU, T; VOHL, M. C; HOUDE, I et al.Nephron. 2000, Vol 84, Num 4, pp 333-341, issn 0028-2766Article