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Select item 105658761.

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

Abstract Article PDF–3.7M

Select item 97284972.

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

Abstract Article PDF–2.5M

Select item 95643193.

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

Abstract Article PDF–2.2M

Select item 91197364.

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

Abstract Article PDF–3.3M

Select item 88907695.

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

Abstract Article PDF–7.4M

Select item 85653526.

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

Abstract Article PDF–7.2M

Select item 85143387.

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

Abstract Article PDF–17M

Select item 83064228.

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

Abstract Article PDF–2.1M

Select item 81650309.

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

Abstract Article PDF–2.2M

Select item 774495510.

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

Abstract Article PDF–1.8M

Select item 771887511.

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

Abstract Article PDF–2.4M

Select item 721680912.

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

Abstract Article PDF–859K

Select item 719291013.

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

Abstract Article PDF–4.5M

Select item 714552014.

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

Abstract Article PDF–7.6M

Select item 704971115.

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

Abstract Article PDF–2.8M

Select item 628464516.

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

Abstract Article PDF–133K

Select item 624557017.

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

Abstract Article PDF–2.1M

Select item 613190518.

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

Abstract Article PDF–1.1M

Select item 589149219.

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

Abstract Article PDF–1.2M

Select item 584754120.

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

Abstract Article PDF–4.7M

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