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Items: 1 to 20 of 56

1.
Pulse-SILAC and Interactomics Reveal Distinct DDB1-CUL4–Associated Factors, Cellular Functions, and Protein Substrates
Jennifer Raisch, Marie-Line Dubois, Marika Groleau, Dominique Lévesque, Thomas Burger, Carla-Marie Jurkovic, Romain Brailly, Gwendoline Marbach, Alyson McKenna, Catherine Barrette, Pierre-Étienne Jacques, François-Michel Boisvert
Mol Cell Proteomics. 2023 Oct; 22(10): 100644. Published online 2023 Sep 7. doi: 10.1016/j.mcpro.2023.100644
PMCID:
PMC10565876
AbstractArticlePDF–3.7M
2.
Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts
Xiao-Dan Hao, Yi-Zhi Yao, Kai-Ge Xu, Bin Dong, Wen-Hua Xu, Jing-Jing Zhang
Invest Ophthalmol Vis Sci. 2022 Dec; 63(13): 1. Published online 2022 Dec 1. doi: 10.1167/iovs.63.13.1
PMCID:
PMC9728497
AbstractArticlePDF–2.5M
3.
A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family
Zeeshan Gauhar, Leon Tejwani, Uzma Abdullah, Sadia Saeed, Shagufta Shafique, Mazhar Badshah, Jungmin Choi, Weilai Dong, Carol Nelson-Williams, Richard P. Lifton, Janghoo Lim, Ghazala K. Raja
Cells. 2022 Oct; 11(19): 3090. Published online 2022 Sep 30. doi: 10.3390/cells11193090
PMCID:
PMC9564319
AbstractArticlePDF–2.2M
4.
OpenCell: proteome-scale endogenous tagging enables the cartography of human cellular organization
Nathan H. Cho, Keith C. Cheveralls, Andreas-David Brunner, Kibeom Kim, André C. Michaelis, Preethi Raghavan, Hirofumi Kobayashi, Laura Savy, Jason Y. Li, Hera Canaj, James Y.S. Kim, Edna M. Stewart, Christian Gnann, Frank McCarthy, Joana P. Cabrera, Rachel M. Brunetti, Bryant B. Chhun, Greg Dingle, Marco Y. Hein, Bo Huang, Shalin B. Mehta, Jonathan S. Weissman, Rafael Gómez-Sjöberg, Daniel N. Itzhak, Loic A. Royer, Matthias Mann, Manuel D. Leonetti
Science. Author manuscript; available in PMC 2022 Sep 11.
Published in final edited form as: Science. 2022 Mar 11; 375(6585): eabi6983. Published online 2022 Mar 11. doi: 10.1126/science.abi6983
PMCID:
PMC9119736
AbstractArticlePDF–3.3M
5.
ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylation
Yana van der Weegen, Klaas de Lint, Diana van den Heuvel, Yuka Nakazawa, Tycho E.T. Mevissen, Janne J.M. van Schie, Marta San Martin Alonso, Daphne E.C. Boer, Román González-Prieto, Ishwarya V. Narayanan, Noud H.M. Klaassen, Annelotte P. Wondergem, Khashayar Roohollahi, Josephine C. Dorsman, Yuichiro Hara, Alfred C.O. Vertegaal, Job de Lange, Johannes C. Walter, Sylvie M. Noordermeer, Mats Ljungman, Tomoo Ogi, Rob M.F. Wolthuis, Martijn S. Luijsterburg
Nat Cell Biol. Author manuscript; available in PMC 2022 Jun 9.
Published in final edited form as: Nat Cell Biol. 2021 Jun; 23(6): 595–607. Published online 2021 Jun 9. doi: 10.1038/s41556-021-00688-9
PMCID:
PMC8890769
AbstractArticlePDF–7.4M
6.
Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation
Manuela Lanzafame, Giulia Branca, Claudia Landi, Mingyue Qiang, Bruno Vaz, Tiziana Nardo, Debora Ferri, Manuela Mura, Sebastian Iben, Miria Stefanini, Fiorenzo A Peverali, Luca Bini, Donata Orioli
Nucleic Acids Res. 2021 Nov 8; 49(19): 10911–10930. Published online 2021 Sep 28. doi: 10.1093/nar/gkab819
PMCID:
PMC8565352
AbstractArticlePDF–7.2M
7.
Structural basis of human transcription–DNA repair coupling
Goran Kokic, Felix R. Wagner, Aleksandar Chernev, Henning Urlaub, Patrick Cramer
Nature. 2021; 598(7880): 368–372. Published online 2021 Sep 15. doi: 10.1038/s41586-021-03906-4
PMCID:
PMC8514338
AbstractArticlePDF–17M
8.
Cockayne Syndrome-Associated CSA and CSB Mutations Impair Ribosome Biogenesis, Ribosomal Protein Stability, and Global Protein Folding
Mingyue Qiang, Fatima Khalid, Tamara Phan, Christina Ludwig, Karin Scharffetter-Kochanek, Sebastian Iben
Cells. 2021 Jul; 10(7): 1616. Published online 2021 Jun 28. doi: 10.3390/cells10071616
PMCID:
PMC8306422
AbstractArticlePDF–2.1M
9.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
10.
Cockayne syndrome proteins CSA and CSB maintain mitochondrial homeostasis through NAD+ signaling
Mustafa N. Okur, Evandro F. Fang, Elayne M. Fivenson, Vinod Tiwari, Deborah L. Croteau, Vilhelm A. Bohr
Aging Cell. 2020 Dec; 19(12): e13268. Published online 2020 Nov 9. doi: 10.1111/acel.13268
PMCID:
PMC7744955
AbstractArticlePDF–1.8M
11.
Integrative genomic analysis implicates ERCC6 and its interaction with ERCC8 in susceptibility to breast cancer
Roxana Moslehi, Hui-Shien Tsao, Nur Zeinomar, Cristy Stagnar, Sean Fitzpatrick, Amiran Dzutsev
Sci Rep. 2020; 10: 21276. Published online 2020 Dec 4. doi: 10.1038/s41598-020-77037-7
PMCID:
PMC7718875
AbstractArticlePDF–2.4M
12.
Atypical features and de novo heterozygous mutations in two siblings with Cockayne syndrome
Shuiyan Wu, Ying Liu, Qian Zhang, Xiangying Meng, Linlin Huang, Zhong Xu, Chunxu Zhang, Ying Li, Ting Chen, Zhenjiang Bai
Mol Genet Genomic Med. 2020 May; 8(5): e1204. Published online 2020 Mar 11. doi: 10.1002/mgg3.1204
PMCID:
PMC7216809
AbstractArticlePDF–859K
13.
The cooperative action of CSB, CSA, and UVSSA target TFIIH to DNA damage-stalled RNA polymerase II
Yana van der Weegen, Hadar Golan-Berman, Tycho E. T. Mevissen, Katja Apelt, Román González-Prieto, Joachim Goedhart, Elisheva E. Heilbrun, Alfred C. O. Vertegaal, Diana van den Heuvel, Johannes C. Walter, Sheera Adar, Martijn S. Luijsterburg
Nat Commun. 2020; 11: 2104. Published online 2020 Apr 30. doi: 10.1038/s41467-020-15903-8
Correction in:
Nat Commun. 2020; 11: 5734.
PMCID:
PMC7192910
AbstractArticlePDF–4.5M
14.
Transcription-coupled nucleotide excision repair is coordinated by ubiquitin and SUMO in response to ultraviolet irradiation
Frauke Liebelt, Joost Schimmel, Matty Verlaan – de Vries, Esra Klemann, Martin E van Royen, Yana van der Weegen, Martijn S Luijsterburg, Leon H Mullenders, Alex Pines, Wim Vermeulen, Alfred C O Vertegaal
Nucleic Acids Res. 2020 Jan 10; 48(1): 231–248. Published online 2019 Nov 13. doi: 10.1093/nar/gkz977
PMCID:
PMC7145520
AbstractArticlePDF–7.6M
15.
Cockayne syndrome group A and B proteins function in rRNA transcription through nucleolin regulation
Mustafa N Okur, Jong-Hyuk Lee, Wasif Osmani, Risako Kimura, Tyler G Demarest, Deborah L Croteau, Vilhelm A Bohr
Nucleic Acids Res. 2020 Mar 18; 48(5): 2473–2485. Published online 2020 Jan 23. doi: 10.1093/nar/gkz1242
PMCID:
PMC7049711
AbstractArticlePDF–2.8M
16.
Detection and clinical significance of DNA repair gene ERCC8 tag SNPs in gastric cancer
Xingre Lu, Fengyu Chen, Xiaowen Liu, Diao Yuan, Yunju Zi, Xiang He, Deyong Zhu
Turk J Gastroenterol. 2018 Jul; 29(4): 392–396. Published online 2018 May 30. doi: 10.5152/tjg.2018.17662
PMCID:
PMC6284645
AbstractArticlePDF–133K
17.
CSA and CSB proteins interact with p53 and regulate its Mdm2-dependent ubiquitination
Paolo Latini, Mattia Frontini, Manuela Caputo, Juraj Gregan, Lubos Cipak, Silvia Filippi, Vivek Kumar, Renier Vélez-Cruz, Miria Stefanini, Fabrizio Palitti, Luca Proietti-De-Santis
Cell Cycle. Author manuscript; available in PMC 2018 Nov 20.
Published in final edited form as: Cell Cycle. 2011 Nov 1; 10(21): 3719–3730. Published online 2011 Nov 1. doi: 10.4161/cc.10.21.17905
PMCID:
PMC6245570
AbstractArticlePDF–2.1M
18.
First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene
Alain Chebly, Sandra Corbani, Joelle Abou Ghoch, Cybel Mehawej, André Megarbane, Eliane Chouery
BMC Med Genet. 2018; 19: 161. Published online 2018 Sep 10. doi: 10.1186/s12881-018-0677-7
PMCID:
PMC6131905
AbstractArticlePDF–1.1M
19.
Deep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome
Audrey Schalk, Géraldine Greff, Nathalie Drouot, Cathy Obringer, Hélène Dollfus, Vincent Laugel, Jamel Chelly, Nadège Calmels
Eur J Hum Genet. 2018 Apr; 26(4): 527–536. Published online 2018 Feb 8. doi: 10.1038/s41431-017-0009-y
PMCID:
PMC5891492
AbstractArticlePDF–1.2M
20.
TRiC controls transcription resumption after UV damage by regulating Cockayne syndrome protein A
Alex Pines, Madelon Dijk, Matthew Makowski, Elisabeth M. Meulenbroek, Mischa G. Vrouwe, Yana van der Weegen, Marijke Baltissen, Pim J. French, Martin E. van Royen, Martijn S. Luijsterburg, Leon H. Mullenders, Michiel Vermeulen, Wim Vermeulen, Navraj S. Pannu, Haico van Attikum
Nat Commun. 2018; 9: 1040. Published online 2018 Mar 12. doi: 10.1038/s41467-018-03484-6
PMCID:
PMC5847541
AbstractArticlePDF–4.7M

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