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Molecular and Cellular Biology Volume 24, 2004 - Issue 9
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DNA Dynamics and Chromosome Structure

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

Naoko Shiomi1 Research Center for Radiation Safety
,
Seiji Kito1 Research Center for Radiation Safety
,
Masaki Oyama2 Laboratory of Molecular Human Genetics, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa920-0934
,
Tsukasa Matsunaga2 Laboratory of Molecular Human Genetics, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa920-0934
,
Yoshi-Nobu Harada3 Frontier Research Center, National Institute of Radiological Sciences, Inage-ku, Chiba263-8555
,
Masahito Ikawa4 Genome Information Research Center, Osaka University, Suita, Osaka565-0871, Japan
,
Masaru Okabe4 Genome Information Research Center, Osaka University, Suita, Osaka565-0871, Japan
&
Tadahiro Shiomi1 Research Center for Radiation SafetyCorrespondence[email protected]
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Pages 3712-3719 | Received 09 Sep 2003, Accepted 26 Jan 2004, Published online: 27 Mar 2023

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Kelly S. Trego, Sophia B. Chernikova, Albert R. Davalos, J. Jefferson P. Perry, L. David Finger, Cliff Ng, Miaw-Sheue Tsai, Steven M. Yannone, John A. Tainer, Judith Campisi & Priscilla K. Cooper. (2011) The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome. Cell Cycle 10:12, pages 1998-2007.
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Jaan-Olle Andressoo, Geert Weeda, Jan de Wit, James R. Mitchell, Rudolf B. Beems, Harry van Steeg, Gijsbertus T. J. van der Horst & Jan H. Hoeijmakers. (2009) An Xpb Mouse Model for Combined Xeroderma Pigmentosum and Cockayne Syndrome Reveals Progeroid Features upon Further Attenuation of DNA Repair. Molecular and Cellular Biology 29:5, pages 1276-1290.
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Fabrizio Thorel, Angelos Constantinou, Isabelle Dunand-Sauthier, Thierry Nouspikel, Philippe Lalle, Anja Raams, Nicolaas G. J. Jaspers, Wim Vermeulen, Mahmud K. K. Shivji, Richard D. Wood & Stuart G. Clarkson. (2004) Definition of a Short Region of XPG Necessary for TFIIH Interaction and Stable Recruitment to Sites of UV Damage. Molecular and Cellular Biology 24:24, pages 10670-10680.
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Riasha Pal, Nilanjan Paul, Deep Bhattacharya, Sudeshna Rakshit, Geetha Shanmugam & Koustav Sarkar. (2022) XPG in the Nucleotide Excision Repair and Beyond: a study on the different functional aspects of XPG and its associated diseases. Molecular Biology Reports 49:8, pages 7995-8006.
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Alba Muniesa-Vargas, Arjan F. Theil, Cristina Ribeiro-Silva, Wim Vermeulen & Hannes Lans. (2022) XPG: a multitasking genome caretaker. Cellular and Molecular Life Sciences 79:3.
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Lee Mulderrig & Juan I. Garaycoechea. (2020) XPF-ERCC1 protects liver, kidney and blood homeostasis outside the canonical excision repair pathways. PLOS Genetics 16:4, pages e1008555.
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Sofia J. Araújo & Isao Kuraoka. (2019) Nucleotide excision repair genes shaping embryonic development. Open Biology 9:10, pages 190166.
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Mariangela Sabatella, Arjan F Theil, Cristina Ribeiro-Silva, Jana Slyskova, Karen Thijssen, Chantal Voskamp, Hannes Lans & Wim Vermeulen. (2018) Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features. Nucleic Acids Research 46:18, pages 9563-9577.
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Georgia Chatzinikolaou, Zivkos Apostolou, Tamara Aid-Pavlidis, Anna Ioannidou, Ismene Karakasilioti, Giorgio L. Papadopoulos, Michalis Aivaliotis, Maria Tsekrekou, John Strouboulis, Theodore Kosteas & George A. Garinis. (2017) ERCC1–XPF cooperates with CTCF and cohesin to facilitate the developmental silencing of imprinted genes. Nature Cell Biology 19:5, pages 421-432.
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Sung-Lim Yu & Sung-Keun Lee. (2017) Ultraviolet radiation: DNA damage, repair, and human disorders. Molecular & Cellular Toxicology 13:1, pages 21-28.
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Mohsen Hosseini, Khaled Ezzedine, Alain Taieb & Hamid R. Rezvani. (2015) Oxidative and Energy Metabolism as Potential Clues for Clinical Heterogeneity in Nucleotide Excision Repair Disorders. Journal of Investigative Dermatology 135:2, pages 341-351.
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H. Hijazi, M.A. Salih, M.H.A. Hamad, H.H. Hassan, S.B.M. Salih, K.A. Mohamed, M.M. Mukhtar, Z.A. Karrar, S. Ansari, N. Ibrahim & F.S. Alkuraya. (2015) Pellagra-like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit. Clinical Genetics 87:1, pages 56-61.
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Mi-Sun Kang, Sung-Lim Yu, Ho-Yeol Kim, Choco Michael Gorospe, Byung Hyune Choi, Sung Haeng Lee & Sung-Keun Lee. (2014) Yeast RAD2 , a homolog of human XPG , plays a key role in the regulation of the cell cycle and actin dynamics . Biology Open 3:1, pages 29-41.
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Joost P.M. MelisHarry van SteegMirjam Luijten. (2013) Oxidative DNA Damage and Nucleotide Excision Repair. Antioxidants & Redox Signaling 18:18, pages 2409-2419.
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Dick Jaarsma, Ingrid van der Pluijm, Gijsbertus T.J. van der Horst & Jan H.J. Hoeijmakers. (2013) Cockayne syndrome pathogenesis: Lessons from mouse models. Mechanisms of Ageing and Development 134:5-6, pages 180-195.
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