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T Nardo

Showing results (11-20 of 23) with videos related to

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Cancer Research|April 15, 2000
Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levelsF Chavanne, B C Broughton, D Pietra, et al.
Human Molecular Genetics|April 10, 1999
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivityS Colella, T Nardo, D Mallery, et al.
Journal of Medical Genetics|March 1, 1997
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivityR Tupler, G L Marseglia, M Stefanini, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
Nucleic Acids Research|May 9, 2001
Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutantL Queimado, M Rao, R A Schultz, et al.
Molecular and Cellular Biology|June 20, 1998
Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein AV Rapić Otrin, I Kuraoka, T Nardo, et al.
Carcinogenesis|June 1, 1993
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophyM Stefanini, P Lagomarsini, S Giliani, et al.
Oncogene|February 3, 2000
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patientsM D'Errico, A Calcagnile, F Canzona, et al.
American Journal of Human Genetics|October 1, 1993
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophyM Stefanini, W Vermeulen, G Weeda, et al.
Applied Neuropsychology. Adult|April 8, 2021
Brief executive-function assessment tool: A new cognitive impairment screening tool for alcohol and other drug servicesJ Berry, E A Shores, T Nardo, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Cancer Research|April 15, 2000
Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levelsF Chavanne, B C Broughton, D Pietra, et al.
Human Molecular Genetics|April 10, 1999
Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivityS Colella, T Nardo, D Mallery, et al.
Journal of Medical Genetics|March 1, 1997
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivityR Tupler, G L Marseglia, M Stefanini, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
Nucleic Acids Research|May 9, 2001
Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutantL Queimado, M Rao, R A Schultz, et al.
Molecular and Cellular Biology|June 20, 1998
Relationship of the xeroderma pigmentosum group E DNA repair defect to the chromatin and DNA binding proteins UV-DDB and replication protein AV Rapić Otrin, I Kuraoka, T Nardo, et al.
Carcinogenesis|June 1, 1993
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophyM Stefanini, P Lagomarsini, S Giliani, et al.
Oncogene|February 3, 2000
UV mutation signature in tumor suppressor genes involved in skin carcinogenesis in xeroderma pigmentosum patientsM D'Errico, A Calcagnile, F Canzona, et al.
American Journal of Human Genetics|October 1, 1993
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophyM Stefanini, W Vermeulen, G Weeda, et al.
Applied Neuropsychology. Adult|April 8, 2021
Brief executive-function assessment tool: A new cognitive impairment screening tool for alcohol and other drug servicesJ Berry, E A Shores, T Nardo, et al.
Pageof 3