Nucleotide Excision Repair

Biochemical Analysis of the Damage Recognition Process in Nucleotide Excision Repair

You, J., Wang, M., & Lee, S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210603200 · Cited by 108

The Escherichia coli 3-Methyladenine DNA Glycosylase AlkA Has a Remarkably Versatile Active Site

O’Brien, P., & Ellenberger, T. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m403860200 · Cited by 108

Model for XPC-independent Transcription-coupled Repair of Pyrimidine Dimers in Humans

Mu, D., & Sancar, A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.12.7570 · Cited by 107

DNase I footprint of ABC excinuclease.

Houten, B. V., Gamper, H., Sancar, A., & Hearst, J. E. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45185-x · Cited by 106

Dimerization of Escherichia coli UvrA and its binding to undamaged and ultraviolet light damaged DNA

Mazur, S. J., & Grossman, L. I. (1991) · Biochemistry · doi:10.1021/bi00232a009 · Cited by 106

Identification of a damaged-DNA binding domain of the XPA protein

Kuraoka, I., Morita, E. H., Saijo, M., Matsuda, T., Morikawa, K., Shirakawa, M., & Tanaka, K. (1996) · Mutation Research/DNA Repair · doi:10.1016/0921-8777(95)00038-0 · Cited by 106

Nucleotide Excision Repair from Site-Specifically Platinum-Modified Nucleosomes

Wang, D., Hara, R., Singh, G., Sancar, A., & Lippard, S. J. (2003) · Biochemistry · doi:10.1021/bi034264k · Cited by 104

Crystal structure of the DNA nucleotide excision repair enzyme UvrB from Thermus thermophilus

Machius, M., Henry, L., Palnitkar, M., & Deisenhofer, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.11717 · Cited by 104

DNA Repair Excision Nuclease Attacks Undamaged DNA

Branum, M. E., Reardon, J. T., & Sancar, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101032200 · Cited by 103

The β-Hairpin Motif of UvrB Is Essential for DNA Binding, Damage Processing, and UvrC-mediated Incisions

Škorvaga, M., Theis, K. W., Mandavilli, B. S., Kisker, C., & Houten, B. V. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m108847200 · Cited by 103

Requirement of Yeast RAD2, a Homolog of Human XPG Gene, for Efficient RNA Polymerase II Transcription

Lee, S.-K., Yu, S., Prakash, L., & Prakash, S. (2002) · Cell · doi:10.1016/s0092-8674(02)00795-x · Cited by 103

hMutSβ Is Required for the Recognition and Uncoupling of Psoralen Interstrand Cross-Links In Vitro

Zhang, N., Lu, X., Zhang, X., Peterson, C. A., & Legerski, R. J. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.7.2388-2397.2002 · Cited by 103

Active site of (A)BC excinuclease. II. Binding, bending, and catalysis mutants of UvrB reveal a direct role in 3‘ and an indirect role in 5‘ incision.

Lin, J., Phillips, A. M., Hearst, J. E., & Sancar, A. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)37098-x · Cited by 102

Incision of DNA–protein crosslinks by UvrABC nuclease suggests a potential repair pathway involving nucleotide excision repair

Minko, I. G., Zou, Y., & Lloyd, R. S. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.042700399 · Cited by 101

Identification and Characterization of XPC-Binding Domain of hHR23B

Masutani, C., Araki, M., Sugasawa, K., van der Spek, P. J., Yamada, A., Uchida, A., Maekawa, T., Bootsma, D., Hoeijmakers, J. H. J., & Hanaoka, F. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.12.6915 · Cited by 100

Characterization of the Helicase Activity of the Escherichia coli UvrAB Protein Complex

Oh, E. Y., & Grossman, L. I. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)85091-3 · Cited by 100

Replication Protein A (RPA) Binding to Duplex Cisplatin-damaged DNA Is Mediated through the Generation of Single-stranded DNA

Patrick, S. M., & Turchi, J. J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.21.14972 · Cited by 99

Strand opening by the UvrA2B complex allows dynamic recognition of DNA damage

Zou, Y., & Houten, B. V. (1999) · The EMBO Journal · doi:10.1093/emboj/18.17.4889 · Cited by 98

Sequential binding of DNA repair proteins RPA and ERCC1 to XPA in vitro

Saijo, M. (1996) · Nucleic Acids Research · doi:10.1093/nar/24.23.4719 · Cited by 98

Construction of DNA substrates modified with psoralen at a unique site and study of the action mechanism of ABC excinuclease on these uniformly modified substrates.

Houten, B. V., Gamper, H., Hearst, J. E., & Sancar, A. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)66993-5 · Cited by 97

Electron Crystal Structure of the Transcription Factor and DNA Repair Complex, Core TFIIH

Chang, W., & Kornberg, R. D. (2000) · Cell · doi:10.1016/s0092-8674(00)00083-0 · Cited by 97

DDB, a Putative DNA Repair Protein, Can Function as a Transcriptional Partner of E2F1

Hayes, S. A., Shiyanov, P. A., Chen, X., & Raychaudhuri, P. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.1.240 · Cited by 96

Damaged DNA-binding Protein DDB Stimulates the Excision of Cyclobutane Pyrimidine Dimers in Vitro in Concert with XPA and Replication Protein A

Wakasugi, M., Shimizu, M., Morioka, H., Linn, S., Nikaido, O., & Matsunaga, T. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m011177200 · Cited by 95

Use of psoralen-modified oligonucleotides to trap three-stranded RecA-DNA complexes and repair of these cross-linked complexes by ABC excinuclease.

Cheng, S., Houten, B. V., Gamper, H., Sancar, A., & Hearst, J. E. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)68152-9 · Cited by 92

Partial Reconstitution of Human DNA Mismatch Repair In Vitro: Characterization of the Role of Human Replication Protein A

Ramilo, C. A., Gu, L., Guo, S., Zhang, X., Patrick, S. M., Turchi, J. J., & Li, G. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.7.2037-2046.2002 · Cited by 91

Binding of human single-stranded DNA binding protein to DNA damaged by the anticancer drug cis-diamminedichloroplatinum (II).

Clugston, C. K., McLaughlin, K., Kenny, M. K., & Brown, R. E. (1992) · PubMed · Cited by 90

Nucleotide excision repair, a tracking mechanism in search of damage

Grossman, L. I., & Thiagalingam, S. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)85273-0 · Cited by 89

Beat the clock: paradigms for NTPases in the maintenance of biological fidelity

Burgess, S. M., & Guthrie, C. (1993) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(93)90094-4 · Cited by 88

Replication Protein A Interactions with DNA. III. Molecular Basis of Recognition of Damaged DNA

Lao, Y., Gomes, X. V., Ren, Y., Taylor, J., & Wold, M. S. (2000) · Biochemistry · doi:10.1021/bi991704s · Cited by 85

Structure and Function of the UvrB Protein

Hsu, D. S., Kim, S., Sun, Q. H., & Sancar, A. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.14.8319 · Cited by 84

Functional Analysis of Human Replication Protein A in Nucleotide Excision Repair

Stigger, E., Drissi, R., & Lee, S. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.15.9337 · Cited by 84

The carboxy-terminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH

Uchida, A., Sugasawa, K., Masutani, C., Dohmae, N., Araki, M., Yokoi, M., Ohkuma, Y., & Hanaoka, F. (2002) · DNA repair · doi:10.1016/s1568-7864(02)00031-9 · Cited by 84

Induction of DNA Replication-mediated Double Strand Breaks by Psoralen DNA Interstrand Cross-links

Bessho, T. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212323200 · Cited by 84

Repair of DNA Covalently Linked to Protein

Connelly, J. C., & Leach, D. R. F. (2004) · Molecular Cell · doi:10.1016/s1097-2765(04)00056-5 · Cited by 82

Cho, a second endonuclease involved in Escherichia coli nucleotide excision repair

Moolenaar, G. F., van Rossum-Fikkert, S. E., van Kesteren, M., & Goosen, N. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.032584099 · Cited by 81

Electron microscopic study of (A)BC excinuclease

Shi, Q., Thresher, R., Sancar, A., & Griffith, J. D. (1992) · Journal of Molecular Biology · doi:10.1016/0022-2836(92)90957-l · Cited by 78

The nucleotide excision repair protein UvrB, a helicase-like enzyme with a catch

Theis, K. W., Škorvaga, M., Machius, M., Nakagawa, N., Houten, B. V., & Kisker, C. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(00)00032-x · Cited by 78

Structural Determinants for Substrate Binding and Catalysis by the Structure-specific Endonuclease XPG

Hohl, M., Thorel, F., Clarkson, S. G., & Schärer, O. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m213155200 · Cited by 77

Impaired Regulation of Tumor Suppressor p53 Caused by Mutations in the Xeroderma Pigmentosum DDB2 Gene: Mutual Regulatory Interactions between p48 DDB2 and p53

Itoh, T., O’Shea, C. E., & Linn, S. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.21.7540-7553.2003 · Cited by 77

Crystal Structure of Thermus thermophilus HB8 UvrB Protein, a Key Enzyme of Nucleotide Excision Repair

Nakagawa, N., Sugahara, M., Masui, R., Kato, R., Fukuyama, K., & Kuramitsu, S. (1999) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a022566 · Cited by 75

Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH

Marinoni, J., Roy, R., Vermeulen, W., Miniou, P., Lutz, Y., Weeda, G., Seroz, T., Gomez, D. M., Hoeijmakers, J. H. J., & Egly, J. (1997) · The EMBO Journal · doi:10.1093/emboj/16.5.1093 · Cited by 75

Architecture of nucleotide excision repair complexes: DNA is wrapped by UvrB before and after damage recognition

Verhoeven, E. E. A., Wyman, C., Moolenaar, G. F., Hoeijmakers, J. H. J., & Goosen, N. (2001) · The EMBO Journal · doi:10.1093/emboj/20.3.601 · Cited by 74

A Yeast Four-hybrid System Identifies Cdk-activating Kinase as a Regulator of the XPD Helicase, a Subunit of Transcription Factor IIH

Sandrock, B., & Egly, J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105570200 · Cited by 71

Cell-free repair of UV-damaged simian virus 40 chromosomes in human cell extracts. I. Development of a cell-free system detecting excision repair of UV-irradiated SV40 chromosomes.

Sugasawa, K., Masutani, C., & Hanaoka, F. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)52982-3 · Cited by 70

Evidence from Extended X-ray Absorption Fine Structure and Site-specific Mutagenesis for Zinc Fingers in UvrA Protein of Escherichia coli

Navaratnam, S., Myles, G. M., Strange, R. W., & Sancar, A. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)71588-3 · Cited by 70

Structural features of the minimal DNA binding domain (M98-F219) of human nucleotide excision repair protein XPA

Buchko, G. W. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.11.2779 · Cited by 70

Site-specific mutagenesis of conserved residues within Walker A and B sequences of Escherichia coli UvrA protein

Myles, G. M., Hearst, J. E., & Sancar, A. (1991) · Biochemistry · doi:10.1021/bi00230a004 · Cited by 69

Excision Repair in Man and the Molecular Basis of Xeroderma Pigmentosum SyndromePreprint

Reardon, J. T., Thompson, L. H., & Sancar, A. (1993) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1993.058.01.067 · Cited by 67

Identification of the different intermediates in the interaction of (A)BC excinuclease with its substrates by DNase I footprinting on two uniquely modified oligonucleotides

Bertrand-Burggraf, E., Selby, C. P., Hearst, J. E., & Sancar, A. (1991) · Journal of Molecular Biology · doi:10.1016/0022-2836(91)90854-y · Cited by 66

Effect of Damage Type on Stimulation of Human Excision Nuclease by SWI/SNF Chromatin Remodeling Factor

Hara, R., & Sancar, A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.12.4121-4125.2003 · Cited by 65

Endogenous lesions, S-phase-independent spontaneous mutations, and evolutionary strategies for base excision repair

Holmquist, G. P. (1998) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/s0027-5107(98)00051-7 · Cited by 64

Enhancement of Damage-Specific DNA Binding of XPA by Interaction with the ERCC1 DNA Repair Protein

Nagai, A., Saijo, M., Kuraoka, I., Matsuda, T., Kodo, N., Nakatsu, Y., Mimaki, T., Mino, M., Biggerstaff, M., Wood, R. D., et al. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1905 · Cited by 61

Binding of XPA and RPA to Damaged DNA Investigated by Fluorescence Anisotropy

Hey, T., Lipps, G., & Krauss, G. (2001) · Biochemistry · doi:10.1021/bi002166i · Cited by 59

Stopped-flow Kinetic Analysis of Replication Protein A-binding DNA

Patrick, S. M., & Turchi, J. J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010314200 · Cited by 58

RPA Stabilizes the XPA-Damaged DNA Complex through Protein−Protein Interaction

Wang, M., Mahrenholz, A. M., & Lee, S. (2000) · Biochemistry · doi:10.1021/bi000472q · Cited by 56

p52 Mediates XPB Function within the Transcription/Repair Factor TFIIH

Jawhari, A., Lainé, J., Dubaele, S., Lamour, V., Poterszman, A., Coin, F., Moras, D., & Egly, J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m203792200 · Cited by 56

Role of E.coli Transcription-Repair Coupling Factor Mfd in Nun-mediated Transcription Termination

Washburn, R. S., Wang, Y., & Gottesman, M. E. (2003) · Journal of Molecular Biology · doi:10.1016/s0022-2836(03)00465-0 · Cited by 55

The function of zinc in gene 32 protein from T4

Giedroc, D. P., Keating, K. M., Williams, K. R., et al. (1987) · Biochemistry · doi:10.1021/bi00391a007 · Cited by 55

Database of mouse strains carrying targeted mutations in genes affecting biological responses to DNA damage Version 5

Friedberg, E. C. (2003) · DNA repair · doi:10.1016/s1568-7864(03)00005-3 · Cited by 54

Nucleotide Excision Repair in the Third Kingdom

Öğrünç, M., Becker, D., Ragsdale, S. W., et al. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.21.5796-5798.1998 · Cited by 54

XPC interacts with both HHR23B and HHR23A in vivo

Li, L., Lu, X., Peterson, C. A., & Legerski, R. J. (1997) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(97)00002-5 · Cited by 53

Thermodynamic Cooperativity and Kinetic Proofreading in DNA Damage Recognition and Repair

Reardon, J. T., & Sancar, A. (2004) · Cell Cycle · doi:10.4161/cc.3.2.645 · Cited by 51

Human Transcription Release Factor 2 Dissociates RNA Polymerases I and II Stalled at a Cyclobutane Thymine Dimer

Hara, R., Selby, C. P., Liu, M., Price, D. H., & Sancar, A. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.35.24779 · Cited by 50

REX1, a Novel Gene Required for DNA Repair

Cenkci, B., Petersen, J. L., & Small, G. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303249200 · Cited by 50

Identification of the XPG Region That Causes the Onset of Cockayne Syndrome by Using Xpg Mutant Mice Generated by the cDNA-Mediated Knock-In Method

Shiomi, N., Kito, S., Oyama, M., Matsunaga, T., Harada, Y., Ikawa, M., Okabe, M., & Shiomi, T. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.9.3712-3719.2004 · Cited by 49

Roots: Mutation frequency decline revisited

Witkin, E. M. (1994) · BioEssays · doi:10.1002/bies.950160613 · Cited by 46

Peptide-N-glycanases and DNA repair proteins, Xp-C/Rad4, are, respectively, active and inactivated enzymes sharing a common transglutaminase fold

Anantharaman, V. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.16.1627 · Cited by 45

The Role of ATP Binding and Hydrolysis by UvrB during Nucleotide Excision Repair

Moolenaar, G. F., Herron, M. F. P., Monaco, V., van der MAREL, G. A., van Boom, J. H., Visse, R., & Goosen, N. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.11.8044 · Cited by 44

A cut above: Discovery of an alternative excision repair pathway in bacteria

Van Houten, B., Eisen, J. A., & Hanawalt, P. C. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.062062599 · Cited by 44

Deficiency in the Nuclease Activity of Xeroderma Pigmentosum G in Mice Leads to Hypersensitivity to UV Irradiation

Tian, M., Jones, D. A., Smith, M., Shinkura, R., & Alt, F. W. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.6.2237-2242.2004 · Cited by 43

Deletion mutagenesis of the Escherichia coli UvrA protein localizes domains for DNA binding, damage recognition, and protein-protein interactions

Claassen, L. A., & Grossman, L. I. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)99175-1 · Cited by 42

The limited strand‐separating activity of the UvrAB protein complex and its role in the recognition of DNA damage

Gordienko, I., & Rupp, W. D. (1997) · The EMBO Journal · doi:10.1093/emboj/16.4.889 · Cited by 42

Adaptive enhancement and kinetics of nucleotide excision repair in humans

Ye, N., de Bianchi, M. S. A., Bianchi, N. O., & Holmquist, G. P. (1999) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(99)00022-1 · Cited by 40

The C-terminal region of Escherichia coli UvrC contributes to the flexibility of the UvrABC nucleotide excision repair system

Verhoeven, E. E. A. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.11.2492 · Cited by 39

The repair patch ofE.coli(A)BC excinuclease

Sibghat-Ullah, Sancar, A., & Hearst, J. E. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.17.5051 · Cited by 39

Isolation and characterization of functional domains of UvrA

Myles, G. M., & Sancar, A. (1991) · Biochemistry · doi:10.1021/bi00230a005 · Cited by 38

Rodent UV-Sensitive Mutant Cell Lines in Complementation Groups 6-10 Have Normal General Excision Repair Activity

Reardon, J. T., Thompson, L. H., & Sancar, A. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.5.1015 · Cited by 37

Human andE.coliexcinucleases are affected differently by the sequence context of acetylaminofluorene–guanine adduct

Mu, D., Bertrand-Burggraf, E., Huang, J.-C., Fuchs, B. P. P., & Sancar, A. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.23.4869 · Cited by 36

Reconstitution of damage DNA excision reaction from SV40 minichromosomes with purified nucleotide excision repair proteins

Araki, M., Masutani, C., Maekawa, T., Watanabe, Y., Yamada, A., Kusumoto, R., Sakai, D., Sugasawa, K., Ohkuma, Y., & Hanaoka, F. (2000) · Mutation Research/DNA Repair · doi:10.1016/s0921-8777(99)00067-1 · Cited by 35

Structural Characterization of the Cysteine-rich Domain of TFIIH p44 Subunit

Fribourg, S., Kellenberger, E., Rogniaux, H., Poterszman, A., DORSSELAER, A. V., Thierry, J., Egly, J., Moras, D., & Kieffer, B. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m004960200 · Cited by 31

Isolation of human complexes proficient in nucleotide excision repair

He, Z. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.6.1136 · Cited by 31

Sequence-dependent modulation of nucleotide excision repair: the efficiency of the incision reaction is inversely correlated with the stability of the pre-incision UvrB-DNA complex

Delagoutte, E., Bertrand-Burggraf, E., Dunand, J., et al. (1997) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0830 · Cited by 26

Two Forms of UvrC Protein with Different Double-stranded DNA Binding Affinities

Tang, M.-S., Nazimiec, M. E., Ye, X., Iyer, G. H., Eveleigh, J., Zheng, Y., Zhou, W., & Tang, Y.-Y. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m008538200 · Cited by 23

The C-terminal half of UvrC protein is sufficient to reconstitute (A)BC excinuclease.

Lin, J., & Sancar, A. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.15.6824 · Cited by 22

Reconstitution of recombinant TFIIH that can mediate activator‐dependent transcription

Fukuda, A., Yamauchi, J., Wu, S.-Y., Chiang, C., Muramatsu, M., & Hisatake, K. (2001) · Genes to Cells · doi:10.1046/j.1365-2443.2001.00456.x · Cited by 20

Functional Domains of the E. coli UvrABC Proteins in Nucleotide Excision Repair

Goosen, N., Moolenaar, G. F., Visse, R., & van de Putte, P. (1998) · Nucleic acids and molecular biology · doi:10.1007/978-3-642-48770-5_5 · Cited by 19

Double-strand Break Repair in Human CellsPreprint

West, S. C., Chappell, C., Hanakahi, L. A., Masson, J., McIlwraith, M. J., & Dyck, E. V. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.315 · Cited by 18

Domain Mapping of the DNA Binding, Endonuclease, and ERCC1 Binding Properties of the Human DNA Repair Protein XPF

McCutchen‐Maloney, S. L., Giannecchini, C. A., Hwang, M. H., et al. (1999) · Biochemistry · doi:10.1021/bi990591+ · Cited by 17

The Isomerization of the UvrB–DNA Preincision Complex Couples the UvrB and UvrC Activities

Delagoutte, E., Fuchs, R. P., & Bertrand-Burggraf, E. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)00401-1 · Cited by 16

Understanding the Complexity of an Organism's Responses to DNA DamagePreprint

Walker, G. C. (2000) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2000.65.1 · Cited by 16

Xeroderma pigmentosum

Constant, E. (1989) · Plastic & Reconstructive Surgery · doi:10.1097/00006534-198908000-00093 · Cited by 12

Characterization of Transcription-Repair Coupling Factors in E. Coli and Humans

Selby, C. P., & Sancar, A. (2003) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(03)71023-4 · Cited by 8

Signaling cascades: Escape from kinetic proofreading

MacGlashan, D. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.131215498 · Cited by 6

Conserved genetic programs in insect and mammalian brain development

(1999) · doi:10.1002/(sici)1521-1878(199908)21:8

Untitled work

(1999) · doi:10.1002/(sici)1098-1004(1999)14:1

Untitled work

Richardson, M. (1999) · doi:10.1002/(sici)1521-1878(199907)21:7

Microbial shifts in the aging mouse gut

Langille, M. G., Meehan, C. J., Koenig, J. E., Dhanani, A. S., Rose, R. A., Howlett, S. E., & Beiko, R. G. (2014) · Microbiome · doi:10.1186/s40168-014-0050-9 · Cited by 437

Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase

Kang, T.-H., Lindsey-Boltz, L. A., Reardon, J. T., & Sancar, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0915085107 · Cited by 250

Focus on UV-Induced DNA Damage and Repair—Disease Relevance and Protective Strategies

Kciuk, M., Marciniak, B., Mojzych, M., & Kontek, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197264 · Cited by 168

Roles of UVA radiation and DNA damage responses in melanoma pathogenesis

Khan, A. Q., Travers, J. B., & Kemp, M. G. (2018) · Environmental and Molecular Mutagenesis · doi:10.1002/em.22176 · Cited by 152

Phylogenomic analysis of the GIY-YIG nuclease superfamily

Dunin-Horkawicz, S., Feder, M., & Bujnicki, J. M. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-98 · Cited by 133

Base excision repair and nucleotide excision repair

Izumi, T., & Mellon, I. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85679-9.00017-9 · Cited by 6

Base Excision Repair and Nucleotide Excision Repair

Izumi, T., & Mellon, I. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803309-8.00017-3 · Cited by 22

Direct involvement of p53 in the base excision repair pathway of the DNA repair machinery

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