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T Nardo

Showing results (1-10 of 23) with videos related to

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Oncogene|June 13, 2000
Proneness to UV-induced apoptosis in human fibroblasts defective in transcription coupled repair is associated with the lack of Mdm2 transactivationG Conforti, T Nardo, M D'Incalci, et al.
Nanotechnology|October 1, 2015
Layer-by-layer assembly for biomedical applications in the last decadeP Gentile, I Carmagnola, T Nardo, et al.
Experimental Cell Research|November 21, 1997
Chromosomal instability and telomere length variations during the life span of human fibroblast clonesC Mondello, R Riboni, A Casati, et al.
Human Molecular Genetics|April 18, 2000
Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosumS Colella, T Nardo, E Botta, et al.
Human Genetics|April 1, 1996
Genetic analysis of twenty-two patients with Cockayne syndromeM Stefanini, H Fawcett, E Botta, et al.
Applied Neuropsychology. Adult|May 23, 2026
Comprehensive neuropsychological assessment in complex homelessness: Incorporating performance validity testing and ipsative benchmarksJ Berry, E A Shores, K L Wallace, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
American Journal of Human Genetics|October 3, 1998
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.
Cancer Genetics and Cytogenetics|June 1, 1997
Telomeric fusions in cultured human fibroblasts as a source of genomic instabilityR Riboni, A Casati, T Nardo, et al.
Il Giornale Di Chirurgia|September 17, 2010
[Comparison of plasma matrix metalloproteases 2, 3, 9 in breast carcinomas and fibroadenomas]F Solai, T Nardo, G Patrizi, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Oncogene|June 13, 2000
Proneness to UV-induced apoptosis in human fibroblasts defective in transcription coupled repair is associated with the lack of Mdm2 transactivationG Conforti, T Nardo, M D'Incalci, et al.
Nanotechnology|October 1, 2015
Layer-by-layer assembly for biomedical applications in the last decadeP Gentile, I Carmagnola, T Nardo, et al.
Experimental Cell Research|November 21, 1997
Chromosomal instability and telomere length variations during the life span of human fibroblast clonesC Mondello, R Riboni, A Casati, et al.
Human Molecular Genetics|April 18, 2000
Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosumS Colella, T Nardo, E Botta, et al.
Human Genetics|April 1, 1996
Genetic analysis of twenty-two patients with Cockayne syndromeM Stefanini, H Fawcett, E Botta, et al.
Applied Neuropsychology. Adult|May 23, 2026
Comprehensive neuropsychological assessment in complex homelessness: Incorporating performance validity testing and ipsative benchmarksJ Berry, E A Shores, K L Wallace, et al.
Mutation Research|March 1, 1992
DNA repair investigations in nine Italian patients affected by trichothiodystrophyM Stefanini, S Giliani, T Nardo, et al.
American Journal of Human Genetics|October 3, 1998
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severityE Botta, T Nardo, B C Broughton, et al.
Cancer Genetics and Cytogenetics|June 1, 1997
Telomeric fusions in cultured human fibroblasts as a source of genomic instabilityR Riboni, A Casati, T Nardo, et al.
Il Giornale Di Chirurgia|September 17, 2010
[Comparison of plasma matrix metalloproteases 2, 3, 9 in breast carcinomas and fibroadenomas]F Solai, T Nardo, G Patrizi, et al.
Pageof 3