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Alan R Lehmann

Showing results (61-70 of 90) with videos related to

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Molecular Biology of the Cell|April 28, 2006
Postreplication repair and PCNA modification in Schizosaccharomyces pombeJonathan Frampton, Anja Irmisch, Catherine M Green, et al.
Molecular Cell|February 18, 2010
Regulation of translesion synthesis DNA polymerase eta by monoubiquitinationMarzena Bienko, Catherine M Green, Simone Sabbioneda, et al.
Plos One|March 3, 2011
Interactions between the Nse3 and Nse4 components of the SMC5-6 complex identify evolutionarily conserved interactions between MAGE and EID FamiliesJessica J R Hudson, Katerina Bednarova, Lucie Kozakova, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2015
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skinLavinia Arseni, Manuela Lanzafame, Emmanuel Compe, et al.
Science (New York, N.Y.)|December 17, 2005
Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesisMarzena Bienko, Catherine M Green, Nicola Crosetto, et al.
The Journal of Investigative Dermatology|September 26, 2025
A Splicing Variant in XPA Results in Delayed Onset of Clinical Features of Xeroderma PigmentosumAnita van den Heuvel, Annelotte P Wondergem, Mihyun Kim, et al.
The Journal of Clinical Investigation|September 9, 2025
TFIIH-p52ΔC defines a ninth xeroderma pigmentosum complementation-group XP-J and restores TFIIH stability to p8-defective trichothiodystrophyYuka Nakazawa, Lin Ye, Yasuyoshi Oka, et al.
The Journal of Clinical Investigation|September 9, 2025
XP-J, a ninth xeroderma pigmentosum complementation group, results from mutations in GTF2H4, encoding TFIIH-p52 subunitHiva Fassihi, Shehla Mohammed, Yuka Nakazawa, et al.
Frontiers in Neuroscience|April 10, 2025
Clinical and molecular overlap between nucleotide excision repair (NER) disorders and <i>DYRK1A</i> haploinsufficiency syndromeNicolas Le May, Jérémie Courraud, Imène Boujelbène, et al.
Human Mutation|September 16, 2006
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationshipsElena Botta, Judith Offman, Tiziana Nardo, et al.
Pageof 9

Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Molecular Biology of the Cell|April 28, 2006
Postreplication repair and PCNA modification in Schizosaccharomyces pombeJonathan Frampton, Anja Irmisch, Catherine M Green, et al.
Molecular Cell|February 18, 2010
Regulation of translesion synthesis DNA polymerase eta by monoubiquitinationMarzena Bienko, Catherine M Green, Simone Sabbioneda, et al.
Plos One|March 3, 2011
Interactions between the Nse3 and Nse4 components of the SMC5-6 complex identify evolutionarily conserved interactions between MAGE and EID FamiliesJessica J R Hudson, Katerina Bednarova, Lucie Kozakova, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 22, 2015
TFIIH-dependent MMP-1 overexpression in trichothiodystrophy leads to extracellular matrix alterations in patient skinLavinia Arseni, Manuela Lanzafame, Emmanuel Compe, et al.
Science (New York, N.Y.)|December 17, 2005
Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesisMarzena Bienko, Catherine M Green, Nicola Crosetto, et al.
The Journal of Investigative Dermatology|September 26, 2025
A Splicing Variant in XPA Results in Delayed Onset of Clinical Features of Xeroderma PigmentosumAnita van den Heuvel, Annelotte P Wondergem, Mihyun Kim, et al.
The Journal of Clinical Investigation|September 9, 2025
TFIIH-p52ΔC defines a ninth xeroderma pigmentosum complementation-group XP-J and restores TFIIH stability to p8-defective trichothiodystrophyYuka Nakazawa, Lin Ye, Yasuyoshi Oka, et al.
The Journal of Clinical Investigation|September 9, 2025
XP-J, a ninth xeroderma pigmentosum complementation group, results from mutations in GTF2H4, encoding TFIIH-p52 subunitHiva Fassihi, Shehla Mohammed, Yuka Nakazawa, et al.
Frontiers in Neuroscience|April 10, 2025
Clinical and molecular overlap between nucleotide excision repair (NER) disorders and <i>DYRK1A</i> haploinsufficiency syndromeNicolas Le May, Jérémie Courraud, Imène Boujelbène, et al.
Human Mutation|September 16, 2006
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationshipsElena Botta, Judith Offman, Tiziana Nardo, et al.
Pageof 9