Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Lunkes

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Nature Medicine|November 14, 1997
Polyglutamines, nuclear inclusions and neurodegenerationA Lunkes, J L Mandel
Human Molecular Genetics|August 13, 1998
A cellular model that recapitulates major pathogenic steps of Huntington's diseaseA Lunkes, J L Mandel
Essays in Biochemistry|September 17, 1999
Pathological mechanisms in Huntington's disease and other polyglutamine expansion diseasesA Lunkes, Y Trottier, J L Mandel
Human 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.
Molecular and Cellular Biology|December 1, 1993
Gal80 proteins of Kluyveromyces lactis and Saccharomyces cerevisiae are highly conserved but contribute differently to glucose repression of the galactose regulonF T Zenke, W Zachariae, A Lunkes, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Philosophical 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.
Experimental Neurology|April 1, 1994
Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locusA Lunkes, L G Goldfarb, F A Platonov, et al.
Genomics|January 20, 1995
Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1A Hernández, C Magariño, S Gispert, et al.
American Journal of Human Genetics|October 1, 1995
Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type KjerA Lunkes, U Hartung, C Magariño, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Nature Medicine|November 14, 1997
Polyglutamines, nuclear inclusions and neurodegenerationA Lunkes, J L Mandel
Human Molecular Genetics|August 13, 1998
A cellular model that recapitulates major pathogenic steps of Huntington's diseaseA Lunkes, J L Mandel
Essays in Biochemistry|September 17, 1999
Pathological mechanisms in Huntington's disease and other polyglutamine expansion diseasesA Lunkes, Y Trottier, J L Mandel
Human 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.
Molecular and Cellular Biology|December 1, 1993
Gal80 proteins of Kluyveromyces lactis and Saccharomyces cerevisiae are highly conserved but contribute differently to glucose repression of the galactose regulonF T Zenke, W Zachariae, A Lunkes, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Philosophical 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.
Experimental Neurology|April 1, 1994
Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locusA Lunkes, L G Goldfarb, F A Platonov, et al.
Genomics|January 20, 1995
Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1A Hernández, C Magariño, S Gispert, et al.
American Journal of Human Genetics|October 1, 1995
Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type KjerA Lunkes, U Hartung, C Magariño, et al.
Pageof 2