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Items: 1 to 20 of 296

1.
ERCC2 mutations alter the genomic distribution pattern of somatic mutations and are independently prognostic in bladder cancer
Jayne A. Barbour, Tong Ou, Haocheng Yang, Hu Fang, Noel C. Yue, Xiaoqiang Zhu, Michelle W. Wong-Brown, Yuen T. Wong, Nikola A. Bowden, Song Wu, Jason W.H. Wong
Cell Genom. 2024 Aug 14; 4(8): 100627. Published online 2024 Aug 2. doi: 10.1016/j.xgen.2024.100627
PMCID:
PMC11406173
AbstractArticlePDF–5.1M
2.
Antagonistic roles of canonical and alternative-RPA in disease-associated tandem CAG repeat instability
Terence Gall-Duncan, Jennifer Luo, Carla-Marie Jurkovic, Laura A. Fischer, Kyota Fujita, Amit L. Deshmukh, Rachel J. Harding, Stephanie Tran, Mustafa Mehkary, Vanessa Li, David E. Leib, Ran Chen, Hikari Tanaka, Amanda G. Mason, Dominique Lévesque, Mahreen Khan, Mortezaali Razzaghi, Tanya Prasolava, Stella Lanni, Nozomu Sato, Marie-Christine Caron, Gagan B. Panigrahi, Peixiang Wang, Rachel Lau, Arturo López Castel, Jean-Yves Masson, Lynette Tippett, Clinton Turner, Maria Spies, Albert R. La Spada, Eric I. Campos, Maurice A. Curtis, François-Michel Boisvert, Richard L.M. Faull, Beverly L. Davidson, Masayuki Nakamori, Hitoshi Okazawa, Marc S. Wold, Christopher E. Pearson
Cell. Author manuscript; available in PMC 2024 Oct 26.
Published in final edited form as: Cell. 2023 Oct 26; 186(22): 4898–4919.e25. Published online 2023 Oct 11. doi: 10.1016/j.cell.2023.09.008
PMCID:
PMC11209935
AbstractArticlePDF–3.0M
3.
The association between XPD rs13181 and rs1799793 polymorphism and oral cancer risk: evidence from a meta-analysis
Wenli Zeng, Wanting Xu, Wu Long
BMC Cancer. 2024; 24: 738. Published online 2024 Jun 15. doi: 10.1186/s12885-024-12503-3
PMCID:
PMC11180391
AbstractArticlePDF–4.9M
4.
Very low prevalence of XPD K751Q polymorphism and its association with XPD expression and outcomes of FOLFOX‐4 treatment in Asian patients with colorectal carcinoma
Jiun‐I. Lai, Cheng‐Hwai Tzeng, Po‐Min Chen, Jen‐Kou Lin, Tzu‐Chen Lin, Wei‐Shone Chen, Jeng‐Kae Jiang, Huann‐Sheng Wang, Wei‐Shu Wang
Cancer Sci. 2009 Jul; 100(7): 1261–1266. Published online 2009 Apr 20. doi: 10.1111/j.1349-7006.2009.01186.x
PMCID:
PMC11159978
AbstractArticlePDF–1.0M
5.
Comprehensive analysis of DNA repair gene polymorphisms and survival in patients with early stage non‐small‐cell lung cancer
Min Kim, Hyo‐Gyoung Kang, Shin Yup Lee, Hyung Cheol Lee, Eung Bae Lee, Yi Young Choi, Won Kee Lee, Sukki Cho, Guang Jin, Hyo‐Sung Jheon, Ji Woong Son, Myung‐Hoon Lee, Deuk Kju Jung, Seung Ick Cha, Chang Ho Kim, Young Mo Kang, Sin Kam, Tae Hoon Jung, Sanghoon Jheon, Jae Yong Park
Cancer Sci. 2010 Nov; 101(11): 2436–2442. Published online 2010 Jul 31. doi: 10.1111/j.1349-7006.2010.01699.x
PMCID:
PMC11159840
AbstractArticlePDF–209K
6.
Epidermal growth factor receptor intron 1 CA dinucleotide repeat polymorphism and survival of advanced gastric cancer patients treated with cetuximab plus modified FOLFOX6
Sae‐Won Han, Do‐Youn Oh, Seock‐Ah Im, Sook Ryun Park, Keun‐Wook Lee, Hong Suk Song, Nam‐Su Lee, Kyung Hee Lee, In Sil Choi, Moon Hee Lee, Min A Kim, Woo Ho Kim, Yung‐Jue Bang, Tae‐You Kim
Cancer Sci. 2010 Mar; 101(3): 793–799. Published online 2009 Nov 23. doi: 10.1111/j.1349-7006.2009.01447.x
PMCID:
PMC11158883
AbstractArticlePDF–174K
7.
Influence of GSTP1 I105V polymorphism on cumulative neuropathy and outcome of FOLFOX‐4 treatment in Asian patients with colorectal carcinoma
Yen‐Chung Chen, Cheng‐Hwai Tzeng, Po‐Min Chen, Jen‐Kou Lin, Tzu‐Chen Lin, Wei‐Shone Chen, Jeng‐Kae Jiang, Huann‐Sheng Wang, Wei‐Shu Wang
Cancer Sci. 2010 Feb; 101(2): 530–535. Published online 2009 Oct 28. doi: 10.1111/j.1349-7006.2009.01418.x
PMCID:
PMC11158438
AbstractArticlePDF–396K
8.
Genetic Polymorphisms of XPC, XPD, XPG Genes and their Association with Radiotherapy Induced Toxicity among Head and Neck Cancer Patients: A Hospital Based Study from Maharashtra
Anand K. Gudur, Shivani R. Kale, Rashmi A. Gudur, Suresh J. Bhosale, Kailas D. Datkhile
Asian Pac J Cancer Prev. 2024; 25(1): 191–199. doi: 10.31557/APJCP.2024.25.1.191
PMCID:
PMC10911723
AbstractArticlePDF–492K
9.
Differing structures and dynamics of two photolesions portray verification differences by the human XPD helicase
Iwen Fu, Nicholas E Geacintov, Suse Broyde
Nucleic Acids Res. 2023 Dec 11; 51(22): 12261–12274. Published online 2023 Nov 2. doi: 10.1093/nar/gkad974
PMCID:
PMC10711554
AbstractArticlePDF–2.6M
10.
Lesion recognition by XPC, TFIIH and XPA in DNA Excision Repair
Jinseok Kim, Chia-Lung Li, Xuemin Chen, Yanxiang Cui, Filip M. Golebiowski, Huaibin Wang, Fumio Hanaoka, Kaoru Sugasawa, Wei Yang
Nature. Author manuscript; available in PMC 2023 Aug 11.
Published in final edited form as: Nature. 2023 May; 617(7959): 170–175. Published online 2023 Apr 19. doi: 10.1038/s41586-023-05959-z
PMCID:
PMC10416759
AbstractArticlePDF–6.2M
11.
C9orf72 protein quality control by UBR5‐mediated heterotypic ubiquitin chains
Julia Jülg, Dieter Edbauer, Christian Behrends
EMBO Rep. 2023 Aug; 24(8): e55895. Published online 2023 Jun 15. doi: 10.15252/embr.202255895
PMCID:
PMC10398660
AbstractArticlePDF–2.4M
12.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing
Engin Demirdizen, Ruslan Al-Ali, Ashwin Narayanan, Xueyuan Sun, Julianna Patricia Varga, Bianca Steffl, Manuela Brom, Damir Krunic, Claudia Schmidt, Gabriele Schmidt, Felix Bestvater, Julian Taranda, Şevin Turcan
Neuro Oncol. 2023 Jun; 25(6): 1031–1043. Published online 2022 Nov 22. doi: 10.1093/neuonc/noac233
PMCID:
PMC10237422
AbstractArticlePDF–23M
13.
Involvement of ERCC1 (rs3212986) and ERCC2 (rs1799793, rs13181) polymorphisms of DNA repair genes in breast cancer occurrence in Burkina Faso
Marc Donald Wilfried Adico, Abdou Azaque Zouré, Herman Karim Sombié, Touwendpoulimdé Isabelle Kiendrebeogo, Soayebo Dabré, Lanyo Jospin Amegnona, Bélélé Siméon Bakyono, Lassina Traoré, Teega‐Wendé Clarisse Ouedraogo, Rogomenoma Alice Ouedraogo, Théodora M. Zohoncon, Albert Théophane Yonli, Bagora Bayala, Hierrhum Aboubacar Bambara, Florencia W. Djigma, Jacques Simpore
Mol Genet Genomic Med. 2023 Apr; 11(4): e2134. Published online 2023 Jan 3. doi: 10.1002/mgg3.2134
PMCID:
PMC10094077
AbstractArticlePDF–1.1M
14.
A disease-associated XPA allele interferes with TFIIH binding and primarily affects transcription-coupled nucleotide excision repair
Diana van den Heuvel, Mihyun Kim, Annelotte P. Wondergem, Paula J. van der Meer, Myrèse Witkamp, Ferdy Lambregtse, Hyun-Suk Kim, Folkert Kan, Katja Apelt, Angela Kragten, Román González-Prieto, Alfred C. O. Vertegaal, Jung-Eun Yeo, Byung-Gyu Kim, Remco van Doorn, Orlando D. Schärer, Martijn S. Luijsterburg
Proc Natl Acad Sci U S A. 2023 Mar 14; 120(11): e2208860120. Published online 2023 Mar 9. doi: 10.1073/pnas.2208860120
PMCID:
PMC10089173
AbstractArticlePDF–6.2M
15.
Multiplexed kinase interactome profiling quantifies cellular network activity and plasticity
Martin Golkowski, Andrea Lius, Tanmay Sapre, Ho-Tak Lau, Taylor Moreno, Dustin J. Maly, Shao-En Ong
Mol Cell. Author manuscript; available in PMC 2023 Apr 4.
Published in final edited form as: Mol Cell. 2023 Mar 2; 83(5): 803–818.e8. Published online 2023 Feb 2. doi: 10.1016/j.molcel.2023.01.015
PMCID:
PMC10072906
AbstractArticlePDF–4.2M
16.
TFIIH mutations can impact on translational fidelity of the ribosome
Fatima Khalid, Tamara Phan, Mingyue Qiang, Pallab Maity, Theresa Lasser, Sebastian Wiese, Marianna Penzo, Marius Alupei, Donata Orioli, Karin Scharffetter-Kochanek, Sebastian Iben
Hum Mol Genet. 2023 Apr 1; 32(7): 1102–1113. Published online 2022 Oct 29. doi: 10.1093/hmg/ddac268
PMCID:
PMC10026254
AbstractArticlePDF–1.6M
17.
CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopment
Daphne J. Smits, Jordy Dekker, Rachel Schot, Brahim Tabarki, Amal Alhashem, Jeroen A. A. Demmers, Dick H. W. Dekkers, Antonio Romito, Peter J. van der Spek, Tjakko J. van Ham, Aida M. Bertoli-Avella, Grazia M. S. Mancini
Hum Genet. 2023; 142(3): 379–397. Published online 2022 Dec 20. doi: 10.1007/s00439-022-02511-3
PMCID:
PMC9950183
AbstractArticlePDF–2.4M
18.
Debilitating hip degeneration in trichothiodystrophy: Association with ERCC2/XPD mutations, osteosclerosis, osteopenia, coxa valga, contractures, and osteonecrosis
John J. DiGiovanna, Grant Randall, Alexandra Edelman, Rina Allawh, Michael Xiong, Deborah Tamura, Sikandar G. Khan, Elizabeth R. H. Rizza, James C. Reynolds, Scott M. Paul, Suvimol C. Hill, Kenneth H. Kraemer
Am J Med Genet A. Author manuscript; available in PMC 2023 Dec 1.
Published in final edited form as: Am J Med Genet A. 2022 Dec; 188(12): 3448–3462. Published online 2022 Sep 14. doi: 10.1002/ajmg.a.62962
PMCID:
PMC9669218
AbstractArticlePDF–1.6M
19.
Phosphorylation of XPD drives its mitotic role independently of its DNA repair and transcription functions
Emmanuel Compe, Evanthia Pangou, Nicolas Le May, Clémence Elly, Cathy Braun, Ji-Hyun Hwang, Frédéric Coin, Izabela Sumara, Kwang-Wook Choi, Jean-Marc Egly
Sci Adv. 2022 Aug; 8(33): eabp9457. Published online 2022 Aug 17. doi: 10.1126/sciadv.abp9457
PMCID:
PMC9385140
AbstractArticlePDF–1.2M
20.
Combinatorial targeting of a chromatin complex comprising Dot1L, menin and the tyrosine kinase BAZ1B reveals a new therapeutic vulnerability of endocrine therapy-resistant breast cancer
Annamaria Salvati, Viola Melone, Assunta Sellitto, Francesca Rizzo, Roberta Tarallo, Tuula A. Nyman, Giorgio Giurato, Giovanni Nassa, Alessandro Weisz
Breast Cancer Res. 2022; 24: 52. Published online 2022 Jul 18. doi: 10.1186/s13058-022-01547-7
PMCID:
PMC9290241
AbstractArticlePDF–8.2M

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