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Human Molecular Genetics|August 13, 1998
A cellular model that recapitulates major pathogenic steps of Huntington's diseaseA Lunkes, J L MandelEssays in Biochemistry|September 17, 1999
Pathological mechanisms in Huntington's disease and other polyglutamine expansion diseasesA Lunkes, Y Trottier, J L MandelPhilosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's diseaseA Lunkes, Y Trottier, J Fagart, et al.La Revue Du Praticien|January 15, 1997
[Genetic diseases and unstable expansions of trinucleotide repeats]J L MandelAmerican Journal of Medical Genetics|July 15, 1994
Towards identification of X-linked mental retardation genes: a proposalJ L MandelHuman Genetics|May 1, 1993
Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkageA Lunkes, S Gispert, J Enczmann, et al.Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|May 12, 2004
Fragile X mental retardation syndrome: from pathogenesis to diagnostic issuesJ L Mandel, V BiancalanaNucleic Acids Research|December 20, 1979
DNA methylation: organ specific variations in the methylation pattern within and around ovalbumin and other chicken genesJ L Mandel, P ChambonThe EMBO Journal|November 1, 1984
The glyceraldehyde 3 phosphate dehydrogenase gene family: structure of a human cDNA and of an X chromosome linked pseudogene; amazing complexity of the gene family in mouseA Hanauer, J L MandelCurrent Opinion in Neurobiology|February 7, 1998
Deciphering the cause of Friedreich ataxiaM Koenig, J L MandelPageof 20