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Alan R Lehmann

Showing results (71-80 of 90) with videos related to

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Nature Communications|January 31, 2017
Specialized interfaces of Smc5/6 control hinge stability and DNA associationAaron Alt, Hung Q Dang, Owen S Wells, et al.
The Journal of Investigative Dermatology|January 9, 2016
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/AfghanistanMieran Sethi, Shaheen Haque, Heather Fawcett, et al.
Molecular Cell|March 16, 2010
Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cellsTomoo Ogi, Siripan Limsirichaikul, René M Overmeer, et al.
The Journal of Investigative Dermatology|June 29, 2005
Two new XPD patients compound heterozygous for the same mutation demonstrate diverse clinical featuresMitsuo Fujimoto, Suzanne N Leech, Therina Theron, et al.
Brain : a Journal of Neurology|June 24, 2008
Neurological symptoms and natural course of xeroderma pigmentosumAnu Anttinen, Leena Koulu, Eeva Nikoskelainen, et al.
Molecular and Cellular Biology|September 2, 2005
Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndromeTherina Theron, Maria I Fousteri, Marcel Volker, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2015
XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiencyChaowan Guo, Yuka Nakazawa, Lisa Woodbine, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patientsBernard C Broughton, Agnes Cordonnier, Wim J Kleijer, et al.
Brain : a Journal of Neurology|December 1, 2023
Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progressionHector Garcia-Moreno, Douglas R Langbehn, Adesoji Abiona, et al.
American Journal of Human Genetics|March 22, 2016
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient TrichothiodystrophyChristiane Kuschal, Elena Botta, Donata Orioli, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Nature Communications|January 31, 2017
Specialized interfaces of Smc5/6 control hinge stability and DNA associationAaron Alt, Hung Q Dang, Owen S Wells, et al.
The Journal of Investigative Dermatology|January 9, 2016
A Distinct Genotype of XP Complementation Group A: Surprisingly Mild Phenotype Highly Prevalent in Northern India/Pakistan/AfghanistanMieran Sethi, Shaheen Haque, Heather Fawcett, et al.
Molecular Cell|March 16, 2010
Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cellsTomoo Ogi, Siripan Limsirichaikul, René M Overmeer, et al.
The Journal of Investigative Dermatology|June 29, 2005
Two new XPD patients compound heterozygous for the same mutation demonstrate diverse clinical featuresMitsuo Fujimoto, Suzanne N Leech, Therina Theron, et al.
Brain : a Journal of Neurology|June 24, 2008
Neurological symptoms and natural course of xeroderma pigmentosumAnu Anttinen, Leena Koulu, Eeva Nikoskelainen, et al.
Molecular and Cellular Biology|September 2, 2005
Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndromeTherina Theron, Maria I Fousteri, Marcel Volker, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2015
XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiencyChaowan Guo, Yuka Nakazawa, Lisa Woodbine, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patientsBernard C Broughton, Agnes Cordonnier, Wim J Kleijer, et al.
Brain : a Journal of Neurology|December 1, 2023
Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progressionHector Garcia-Moreno, Douglas R Langbehn, Adesoji Abiona, et al.
American Journal of Human Genetics|March 22, 2016
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient TrichothiodystrophyChristiane Kuschal, Elena Botta, Donata Orioli, et al.
Pageof 9