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C Jodice

Showing results (1-10 of 24) with videos related to

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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different lociM Frontali, A Novelletto, G Annesi, et al.
Brain Research Bulletin|November 24, 2001
Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitroV Calabresi, S Guida, A Servadio, et al.
Human Biology|December 1, 1995
Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populationsG Pepe, O Rickards, C Jodice, et al.
Cytogenetic and Genome Research|October 4, 2003
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disordersE Mantuano, L Veneziano, C Jodice, et al.
Annals of Human Genetics|February 12, 1998
Population variation analysis at nine loci containing expressed trinucleotide repeatsC Jodice, B Giovannone, V Calabresi, et al.
Gene|July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1E Mantuano, F Trettel, A S Olsen, et al.
Annals of Human Genetics|October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosomeF Persichetti, P Blasi, M Hammer, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
FEBS Letters|September 11, 2003
The AXH module: an independently folded domain common to ataxin-1 and HBP1C de Chiara, C Giannini, S Adinolfi, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

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Pageof 3
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
CAG repeat instability, cryptic sequence variation and pathogeneticity: evidence from different lociM Frontali, A Novelletto, G Annesi, et al.
Brain Research Bulletin|November 24, 2001
Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitroV Calabresi, S Guida, A Servadio, et al.
Human Biology|December 1, 1995
Allele and haplotype frequency distribution of the EcoRI, RsaI, and MspI COL1A2 RFLPs among various human populationsG Pepe, O Rickards, C Jodice, et al.
Cytogenetic and Genome Research|October 4, 2003
Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disordersE Mantuano, L Veneziano, C Jodice, et al.
Annals of Human Genetics|February 12, 1998
Population variation analysis at nine loci containing expressed trinucleotide repeatsC Jodice, B Giovannone, V Calabresi, et al.
Gene|July 17, 1998
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1E Mantuano, F Trettel, A S Olsen, et al.
Annals of Human Genetics|October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosomeF Persichetti, P Blasi, M Hammer, et al.
Brain : a Journal of Neurology|August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxiasP Giunti, M G Sweeney, M Spadaro, et al.
Genomics|September 15, 1996
Construction of a YAC contig covering human chromosome 6p22P Malaspina, A Roetto, F Trettel, et al.
FEBS Letters|September 11, 2003
The AXH module: an independently folded domain common to ataxin-1 and HBP1C de Chiara, C Giannini, S Adinolfi, et al.
Pageof 3