Modèles in vitro et in vivo de la maladie de Huntington: Enseignements pour les pathologies liées à des expansions de polyglutamine : La génétique des pathologies complexes: Des modèles expérimentaux à l'homme = In vitro and in vivo models for Huntington disease : lessons for the polyglutamine expansion disorders : Genetic dissection of complex diseases: From experimental models to humansHAYDEN, M. R.Pathologie et biologie. 1998, Vol 46, Num 9, pp 695-696, issn 0369-8114Conference Paper

On planting alfalfa and growing orchids : the cloning of the gene causing Huntington diseaseHAYDEN, M. R.Clinical genetics. 1993, Vol 43, Num 5, pp 217-222, issn 0009-9163Article

Predictive testing for Huntington disease : are we ready for widespread community implementation ?HAYDEN, M. R.American journal of medical genetics. 1991, Vol 40, Num 4, pp 515-517, issn 0148-7299Article

Opinion: predictive testing fot Huntington disease in childhood: challenges and implicationsBLOCH, M; HAYDEN, M. R.American journal of human genetics. 1990, Vol 46, Num 1, pp 1-4, issn 0002-9297Article

Molecular genetics of human lipoprotein lipase deficiency : Molecular biolgoy in diagnosis of dyslipidemiasHAYDEN, M. R; MA, Y.Molecular and cellular biochemistry. 1992, Vol 113, Num 2, pp 171-176, issn 0300-8177Article

Patients' rights to laboratory data : Trinucleotide repeat length in Huntington diseaseBURGESS, M. M; HAYDEN, M. R.American journal of medical genetics. 1996, Vol 62, Num 1, pp 6-9, issn 0148-7299Article

Monoamines and their metabolites in Huntington's disease brain : evidence for decreased catechol-O-methyltransferase activityMCGEER, E. G; KREMER, B; HAYDEN, M. R et al.Biological psychiatry (1969). 1993, Vol 33, Num 7, pp 551-553, issn 0006-3223Article

The prediction of exons through an analysis of spliceable open reading framesHUTCHINSON, G. B; HAYDEN, M. R.Nucleic acids research. 1992, Vol 20, Num 13, pp 3453-3462, issn 0305-1048Article

The genomic organization of a novel regulatory myosin light chain gene (MYL5) that maps to chromosome 4p16.3 and shows different patterns of expression between primatesCOLLINS, C; SCHAPPERT, K; HAYDEN, M. R et al.Human molecular genetics (Print). 1992, Vol 1, Num 9, pp 727-733, issn 0964-6906Article

A polymorphic DNA marker at the D10S106 locusWEBER, B; RIESS, O; HAYDEN, M. R et al.Nucleic acids research. 1991, Vol 19, Num 7, issn 0305-1048, p. 1725Article

What monozygotic twins discordant for phenotype illustrate about mechanisms influencing genetic forms of neurodegeneration : EPIGENETICS AND MEDICAL GENETICS - UNITED BY PURPOSEKETELAAR, M. E; HOFSTRA, Rmw; HAYDEN, M. R et al.Clinical genetics. 2012, Vol 81, Num 4, pp 325-333, issn 0009-9163, 9 p.Article

Huntington disease : new insights into the relationship between CAG expansion and diseaseNASIR, J; GOLDBERG, Y. P; HAYDEN, M. R et al.Human molecular genetics (Print). 1996, Vol 5, pp 1431-1435, issn 0964-6906, REVIEWArticle

Mismatch PCR : a rapid method to screen for the Pro²⁰⁷→Leu mutation in the lipoprotein lipase (LPL) geneBIJVOET, S. M; HAYDEN, M. R.Human molecular genetics (Print). 1992, Vol 1, Num 7, issn 0964-6906, p. 541Article

Molecular genetic approaches to the study of the nervous systemHAYDEN, M. R; NICHOLS, J. L.Developmental neuroscience. 1983, Vol 6, Num 4-5, pp 189-214, issn 0378-5866Article

Adoption and the communication of genetic risk: experiences in Huntington diseaseBOMBARD, Y; SEMAKA, A; HAYDEN, M. R et al.Clinical genetics. 2012, Vol 81, Num 1, pp 64-69, issn 0009-9163, 6 p.Article

Remodeling of the endocrine pancreas : The central role of amylin and insulin resistanceHAYDEN, M. R; TYAGI, S. C.Southern medical journal (Birmingham). 2000, Vol 93, Num 1, pp 24-28, issn 0038-4348Article

Brief clinical report: bilateral renal agenesis in twinsDOUGLAS WILSON, R; HAYDEN, M. R.American journal of medical genetics. 1985, Vol 21, Num 1, pp 147-152, issn 0148-7299Article

Unstable Familial Transmissions of Huntington Disease Alleles With 27―35 CAG Repeats (Intermediate Alleles)SEMAKA, A; COLLINS, J. A; HAYDEN, M. R et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 1, pp 314-320, issn 1552-4841, 7 p.Article

Auxiliary-directed dioxygenation : stereoselective synthesis of a diene hydroperoxideDUSSAULT, P. H; HAYDEN, M. R.Tetrahedron letters. 1992, Vol 33, Num 4, pp 443-446, issn 0040-4039Article

(CA)_n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16RIESS, O; WEBER, B; HAYDEN, M. R et al.Human molecular genetics (Print). 1992, Vol 1, Num 6, issn 0964-6906, p. 452Article

Caspases and neurodegeneration: on the cutting edge of new therapeutic approachesWELLINGTON, C. L; HAYDEN, M. R.Clinical genetics. 2000, Vol 57, Num 1, pp 1-10, issn 0009-9163Article

Cholesterol toxicity in pancreatic islets from LDL receptor-deficient mice. Reply to: de Souza JC, de Oliveira CAM, Carneiro EM et al. [letter]KRUIT, J. K; BRUNHAM, L. R; VERCHERE, C. B et al.Diabetologia (Berlin). 2010, Vol 53, Num 11, pp 2463-2464, issn 0012-186X, 2 p.Article

Enhanced susceptibility to pancreatitis in severe hypertriglyceridaemic lipoprotein lipase-deficient mice and agonist-like function of pancreatic lipase in pancreatic cellsWANG, Y; STERNFELD, L; YANG, F et al.Gut. 2009, Vol 58, Num 3, pp 422-430, issn 0017-5749, 9 p.Article

Heterozygosity fat ABCA1 gene mutations: effects on enzymes, apolipoproteins and lipoprotein particle sizeKUIVENHOVEN, J. A; HOVINGH, G. K; ZWINDERMAN, A. H et al.Atherosclerosis. 2003, Vol 171, Num 2, pp 311-319, issn 0021-9150, 9 p.Article

The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery diseaseCLEE, S. M; LOUBSER, O; COLLINS, J et al.Clinical genetics. 2001, Vol 60, Num 4, pp 293-300, issn 0009-9163Article