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S Cocozza

Showing results (31-40 of 81) with videos related to

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Human Molecular Genetics|June 1, 1993
A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1M Pandolfo, M Munaro, S Cocozza, et al.
Molecular and Cellular Biology|March 1, 1990
Extinction and activation of the thyroglobulin promoter in hybrids of differentiated and transformed thyroid cellsI M Bonapace, M Sanchez, S Obici, et al.
Neurology|July 11, 2001
Serum transferrin receptor levels in Friedreich's and other degenerative ataxiasV Scarano, T de Cristofaro, G De Michele, et al.
Nucleic Acids Research|March 25, 1988
Eco RI RFLP in the human IGF II geneS Cocozza, S Garofalo, R Robledo, et al.
American Journal of Human Genetics|February 1, 1997
The effect of parental gender on the GAA dynamic mutation in the FRDA geneL Pianese, F Cavalcanti, G De Michele, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1986
The complete structure of the rat thyroglobulin geneA M Musti, E V Avvedimento, C Polistina, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|September 30, 1987
DNA polymorphisms as potential genetic risk markers for cardiovascular diseasesS Cocozza, A Monticelli, S Garofalo, et al.
Diabetes|April 1, 1992
NIDDM associated with mutation in tyrosine kinase domain of insulin receptor geneS Cocozza, A Porcellini, G Riccardi, et al.
Acta Neurologica|August 1, 1992
Friedreich's disease. A linkage study in southern and central ItalyF Cavalcanti, S Cocozza, A Filla, et al.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patientsA Perretti, L Santoro, B Lanzillo, et al.
Pageof 9

Showing results (31-40 of 81) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|June 1, 1993
A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1M Pandolfo, M Munaro, S Cocozza, et al.
Molecular and Cellular Biology|March 1, 1990
Extinction and activation of the thyroglobulin promoter in hybrids of differentiated and transformed thyroid cellsI M Bonapace, M Sanchez, S Obici, et al.
Neurology|July 11, 2001
Serum transferrin receptor levels in Friedreich's and other degenerative ataxiasV Scarano, T de Cristofaro, G De Michele, et al.
Nucleic Acids Research|March 25, 1988
Eco RI RFLP in the human IGF II geneS Cocozza, S Garofalo, R Robledo, et al.
American Journal of Human Genetics|February 1, 1997
The effect of parental gender on the GAA dynamic mutation in the FRDA geneL Pianese, F Cavalcanti, G De Michele, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1986
The complete structure of the rat thyroglobulin geneA M Musti, E V Avvedimento, C Polistina, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|September 30, 1987
DNA polymorphisms as potential genetic risk markers for cardiovascular diseasesS Cocozza, A Monticelli, S Garofalo, et al.
Diabetes|April 1, 1992
NIDDM associated with mutation in tyrosine kinase domain of insulin receptor geneS Cocozza, A Porcellini, G Riccardi, et al.
Acta Neurologica|August 1, 1992
Friedreich's disease. A linkage study in southern and central ItalyF Cavalcanti, S Cocozza, A Filla, et al.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I: multimodal electrophysiological study and comparison between SCA1 and SCA2 patientsA Perretti, L Santoro, B Lanzillo, et al.
Pageof 9