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Miria Stefanini

Showing results (1-10 of 36) with videos related to

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Orphanet Journal of Rare Diseases|November 3, 2011
Xeroderma pigmentosumAlan R Lehmann, David McGibbon, Miria Stefanini
Mechanisms of Ageing and Development|April 10, 2013
From laboratory tests to functional characterisation of Cockayne syndromeManuela Lanzafame, Bruno Vaz, Tiziana Nardo, et al.
The Journal of Investigative Dermatology|November 13, 2009
Bmi-1 reduction plays a key role in physiological and premature aging of primary human keratinocytesSonia Cordisco, Riccardo Maurelli, Sergio Bondanza, et al.
Experimental Dermatology|February 6, 2015
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytesManuela Lanzafame, Elena Botta, Massimo Teson, et al.
Human Molecular Genetics|October 24, 2002
Reduced level of the repair/transcription factor TFIIH in trichothiodystrophyElena Botta, Tiziana Nardo, Alan R Lehmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2006
DNA nucleotide excision repair-dependent signaling to checkpoint activationFederica Marini, Tiziana Nardo, Michele Giannattasio, et al.
Molecular Biology of the Cell|March 10, 2006
Rac3-induced neuritogenesis requires binding to Neurabin IDonata Orioli, Ivan N Colaluca, Miria Stefanini, et al.
Molecular Cell|January 24, 2006
p8/TTD-A as a repair-specific TFIIH subunitFrédéric Coin, Luca Proietti De Santis, Tiziana Nardo, et al.
Human Mutation|December 17, 2008
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD geneElena Botta, Tiziana Nardo, Donata Orioli, et al.
Molecular and Cellular Biology|August 8, 2007
In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutationGentaro Yasuda, Ryotaro Nishi, Eriko Watanabe, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Orphanet Journal of Rare Diseases|November 3, 2011
Xeroderma pigmentosumAlan R Lehmann, David McGibbon, Miria Stefanini
Mechanisms of Ageing and Development|April 10, 2013
From laboratory tests to functional characterisation of Cockayne syndromeManuela Lanzafame, Bruno Vaz, Tiziana Nardo, et al.
The Journal of Investigative Dermatology|November 13, 2009
Bmi-1 reduction plays a key role in physiological and premature aging of primary human keratinocytesSonia Cordisco, Riccardo Maurelli, Sergio Bondanza, et al.
Experimental Dermatology|February 6, 2015
Reference genes for gene expression analysis in proliferating and differentiating human keratinocytesManuela Lanzafame, Elena Botta, Massimo Teson, et al.
Human Molecular Genetics|October 24, 2002
Reduced level of the repair/transcription factor TFIIH in trichothiodystrophyElena Botta, Tiziana Nardo, Alan R Lehmann, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2006
DNA nucleotide excision repair-dependent signaling to checkpoint activationFederica Marini, Tiziana Nardo, Michele Giannattasio, et al.
Molecular Biology of the Cell|March 10, 2006
Rac3-induced neuritogenesis requires binding to Neurabin IDonata Orioli, Ivan N Colaluca, Miria Stefanini, et al.
Molecular Cell|January 24, 2006
p8/TTD-A as a repair-specific TFIIH subunitFrédéric Coin, Luca Proietti De Santis, Tiziana Nardo, et al.
Human Mutation|December 17, 2008
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD geneElena Botta, Tiziana Nardo, Donata Orioli, et al.
Molecular and Cellular Biology|August 8, 2007
In vivo destabilization and functional defects of the xeroderma pigmentosum C protein caused by a pathogenic missense mutationGentaro Yasuda, Ryotaro Nishi, Eriko Watanabe, et al.
Pageof 4