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Nature|April 21, 1994

Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase IIR Drapkin, J T Reardon, A Ansari, et al.

The Journal of Biological Chemistry|October 5, 1993

Comparative analysis of binding of human damaged DNA-binding protein (XPE) and Escherichia coli damage recognition protein (UvrA) to the major ultraviolet photoproducts: T[c,s]T, T[t,s]T, T[6-4]T, and T[Dewar]TJ T Reardon, A F Nichols, S Keeney, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996

Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adductD R Duckett, J T Drummond, A I Murchie, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994

Molecular cloning of the human nucleotide-excision-repair gene ERCC4L H Thompson, K W Brookman, C A Weber, et al.

Nanoscale Advances|September 22, 2022

Enhanced efficacy in drug-resistant cancer cells through synergistic nanoparticle mediated delivery of cisplatin and decitabineM Parhizkar, P J T Reardon, A H Harker, et al.

Nanomedicine : Nanotechnology, Biology, and Medicine|May 18, 2016

Electrohydrodynamic encapsulation of cisplatin in poly (lactic-co-glycolic acid) nanoparticles for controlled drug deliveryMaryam Parhizkar, Philip J T Reardon, Jonathan C Knowles, et al.

The Journal of Investigative Dermatology|November 6, 1998

Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemiaS G Khan, H L Levy, R Legerski, et al.

Molecular and Cellular Biology|November 1, 1996

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologsK W Brookman, J E Lamerdin, M P Thelen, et al.

Molecular and Cellular Biology|October 5, 2001

Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutationJ W George, E P Salazar, M P Vreeswijk, et al.

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Showing results (21-30 of 29) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 29 results.

Nature|April 21, 1994

Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase IIR Drapkin, J T Reardon, A Ansari, et al.

The Journal of Biological Chemistry|October 5, 1993

Comparative analysis of binding of human damaged DNA-binding protein (XPE) and Escherichia coli damage recognition protein (UvrA) to the major ultraviolet photoproducts: T[c,s]T, T[t,s]T, T[6-4]T, and T[Dewar]TJ T Reardon, A F Nichols, S Keeney, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 25, 1996

Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adductD R Duckett, J T Drummond, A I Murchie, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994

Molecular cloning of the human nucleotide-excision-repair gene ERCC4L H Thompson, K W Brookman, C A Weber, et al.

Nanoscale Advances|September 22, 2022

Enhanced efficacy in drug-resistant cancer cells through synergistic nanoparticle mediated delivery of cisplatin and decitabineM Parhizkar, P J T Reardon, A H Harker, et al.

Nanomedicine : Nanotechnology, Biology, and Medicine|May 18, 2016

Electrohydrodynamic encapsulation of cisplatin in poly (lactic-co-glycolic acid) nanoparticles for controlled drug deliveryMaryam Parhizkar, Philip J T Reardon, Jonathan C Knowles, et al.

The Journal of Investigative Dermatology|November 6, 1998

Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemiaS G Khan, H L Levy, R Legerski, et al.

Molecular and Cellular Biology|November 1, 1996

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologsK W Brookman, J E Lamerdin, M P Thelen, et al.

Molecular and Cellular Biology|October 5, 2001

Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutationJ W George, E P Salazar, M P Vreeswijk, et al.

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