PMC Links for Gene (Select 2074) - PMC

Khouloud Zayoud, Ichraf Kraoua, Asma Chikhaoui, Nadège Calmels, Sami Bouchoucha, Cathy Obringer, Clément Crochemore, Dorra Najjar, Sinda Zarrouk, Najoua Miladi, Vincent Laugel, Miria Ricchetti, Ilhem Turki, Houda Yacoub-Youssef

Genes (Basel) 2021 Dec; 12(12): 1922. Published online 2021 Nov 29. doi: 10.3390/genes12121922

PMCID:: PMC8701866

Article PDF–2.1M

Select item 86366214.

Mechanism of Rad26-assisted rescue of stalled RNA polymerase II in transcription-coupled repair

Chunli Yan, Thomas Dodd, Jina Yu, Bernice Leung, Jun Xu, Juntaek Oh, Dong Wang, Ivaylo Ivanov

Nat Commun. 2021; 12: 7001. Published online 2021 Dec 1. doi: 10.1038/s41467-021-27295-4

PMCID:: PMC8636621

Article PDF–5.8M

Select item 84655475.

Neuroblastoma Cells Depend on CSB for Faithful Execution of Cytokinesis and Survival

Elena Paccosi, Michele Costantino, Alessio Balzerano, Silvia Filippi, Stefano Brancorsini, Luca Proietti-De-Santis

Int J Mol Sci. 2021 Sep; 22(18): 10070. Published online 2021 Sep 17. doi: 10.3390/ijms221810070

PMCID:: PMC8465547

Article PDF–9.0M

Select item 82952286.

Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries

Iain S. Forrest, Kumardeep Chaudhary, Ha My T. Vy, Shantanu Bafna, Soyeon Kim, Hong-Hee Won, Ruth J.F. Loos, Judy Cho, Louis R. Pasquale, Girish N. Nadkarni, Ghislain Rocheleau, Ron Do

Hum Mutat. Author manuscript; available in PMC 2022 Aug 1.

Published in final edited form as: Hum Mutat. 2021 Aug; 42(8): 969–977. Published online 2021 May 31. doi: 10.1002/humu.24220

PMCID:: PMC8295228

Article PDF–988K

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A role for the Cockayne Syndrome B (CSB)-Elongin ubiquitin ligase complex in signal-dependent RNA polymerase II transcription

Juston C. Weems, Brian D. Slaughter, Jay R. Unruh, Kyle J. Weaver, Brandon D. Miller, Kym M. Delventhal, Joan W. Conaway, Ronald C. Conaway

J Biol Chem. 2021 Jul; 297(1): 100862. Published online 2021 Jun 9. doi: 10.1016/j.jbc.2021.100862

PMCID:: PMC8294581

Article PDF–1.0M

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Cockayne Syndrome Group B (CSB): The Regulatory Framework Governing the Multifunctional Protein and Its Plausible Role in Cancer

Zoi Spyropoulou, Angelos Papaspyropoulos, Nefeli Lagopati, Vassilios Myrianthopoulos, Alexandros G. Georgakilas, Maria Fousteri, Athanassios Kotsinas, Vassilis G. Gorgoulis

Cells. 2021 Apr; 10(4): 866. Published online 2021 Apr 10. doi: 10.3390/cells10040866

PMCID:: PMC8068816

Article PDF–1.2M

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The Winged Helix Domain of CSB Regulates RNAPII Occupancy at Promoter Proximal Pause Sites

Nicole L. Batenburg, Shixin Cui, John R. Walker, Herb E. Schellhorn, Xu-Dong Zhu

Int J Mol Sci. 2021 Apr; 22(7): 3379. Published online 2021 Mar 25. doi: 10.3390/ijms22073379

PMCID:: PMC8037043

Article PDF–4.0M

Select item 796899510.

Current and emerging roles of Cockayne syndrome group B (CSB) protein

Vinod Tiwari, Beverly A Baptiste, Mustafa N Okur, Vilhelm A Bohr

Nucleic Acids Res. 2021 Mar 18; 49(5): 2418–2434. Published online 2021 Feb 15. doi: 10.1093/nar/gkab085

PMCID:: PMC7968995

Article PDF–2.4M

Select item 617587811.

ROS-induced R loops trigger a transcription-coupled but BRCA1/2-independent homologous recombination pathway through CSB

Yaqun Teng, Tribhuwan Yadav, Meihan Duan, Jun Tan, Yufei Xiang, Boya Gao, Jianquan Xu, Zhuobin Liang, Yang Liu, Satoshi Nakajima, Yi Shi, Arthur S. Levine, Lee Zou, Li Lan

Nat Commun. 2018; 9: 4115. Published online 2018 Oct 8. doi: 10.1038/s41467-018-06586-3

PMCID:: PMC6175878

Article PDF–2.8M

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Two novel mutations in ERCC6 cause Cockayne syndrome B in a Chinese family

Chunxia He, Mao Sun, Guoxia Wang, Ying Yang, Libo Yao, Yuanming Wu

Mol Med Rep. 2017 Jun; 15(6): 3957–3962. Published online 2017 Apr 20. doi: 10.3892/mmr.2017.6487

PMCID:: PMC5436194

Article PDF–1.1M

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CSB ablation induced apoptosis is mediated by increased endoplasmic reticulum stress response

Manuela Caputo, Alessio Balzerano, Ivan Arisi, Mara D’Onofrio, Rossella Brandi, Silvia Bongiorni, Stefano Brancorsini, Mattia Frontini, Luca Proietti-De-Santis

PLoS One. 2017; 12(3): e0172399. Published online 2017 Mar 2. doi: 10.1371/journal.pone.0172399

PMCID:: PMC5333825

Article PDF–3.2M

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Ultraviolet-B induces ERCC6 repression in lens epithelium cells of age-related nuclear cataract through coordinated DNA hypermethylation and histone deacetylation

Yong Wang, Fei Li, Guowei Zhang, Lihua Kang, Huaijin Guan

Clin Epigenetics. 2016; 8: 62. Published online 2016 May 26. doi: 10.1186/s13148-016-0229-y

PMCID:: PMC4880862

Article PDF–2.7M

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Pharmacological Bypass of Cockayne Syndrome B Function in Neuronal Differentiation

Yuming Wang, Jace Jones-Tabah, Probir Chakravarty, Aengus Stewart, Alysson Muotri, Rebecca R. Laposa, Jesper Q. Svejstrup

Cell Rep. 2016 Mar 22; 14(11): 2554–2561. Published online 2016 Mar 10. doi: 10.1016/j.celrep.2016.02.051

PMCID:: PMC4806223

Article

Select item 478790216.

Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony

Alexandre T. Vessoni, Roberto H. Herai, Jerome V. Karpiak, Angelica M. S. Leal, Cleber A. Trujillo, Annabel Quinet, Lucymara F. Agnez Lima, Carlos F. M. Menck, Alysson R. Muotri

Hum Mol Genet. 2016 Apr 1; 25(7): 1271–1280. Published online 2016 Jan 10. doi: 10.1093/hmg/ddw008

PMCID:: PMC4787902

Article PDF–1.1M

Select item 461578717.

Regulation of active genome integrity and expression by Rad26p

Shivani Malik, Sukesh R Bhaumik

Nucleus. 2014; 5(6): 520–526. Published online 2014 Oct 31. doi: 10.4161/nucl.36230

PMCID:: PMC4615787

Article PDF–355K

Select item 458625018.

Cockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenal

Leena Maddukuri, Elżbieta Speina, Mette Christiansen, Dominika Dudzińska, Jolanta Zaim, Tomasz Obtułowicz, Sylwia Kabaczyk, Marek Komisarski, Zuzanna Bukowy, Jadwiga Szczegielniak, Andrzej Wójcik, Jaroslaw T. Kuśmierek, Tinna Stevnsner, Vilhelm A. Bohr, Barbara Tudek

Mutat Res. Author manuscript; available in PMC 2015 Sep 29.

Published in final edited form as: Mutat Res. 2009 Jun 18; 666(0): 23–31. Published online 2009 Mar 31. doi: 10.1016/j.mrfmmm.2009.03.007

PMCID:: PMC4586250

Article PDF–2.9M

Select item 432977619.

A Novel ERCC6 Splicing Variant Associated with a Mild Cockayne Syndrome Phenotype

Jonathan M Swartz, Aysehan Akinci, Shayne F. Andrew, Ahmet Siğirci, Joel N Hirschhorn, Ron G Rosenfeld, Andrew Dauber, Vivian Hwa

Horm Res Paediatr. Author manuscript; available in PMC 2015 Nov 1.

Published in final edited form as: Horm Res Paediatr. 2014; 82(5): 344–352. Published online 2014 Nov 1. doi: 10.1159/000368192

PMCID:: PMC4329776

Article PDF–413K

Select item 420516420.

ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination

Laila Shehata, Dimitre R. Simeonov, Anja Raams, Lynne Wolfe, Adeline Vanderver, Xueli Li, Yan Huang, Shannon Garner, Cornelius F. Boerkoel, Audrey Thurm, Gail E. Herman, Cynthia J. Tifft, Miao He, Nicolaas G.J. Jaspers, William A. Gahl

Am J Med Genet A. Author manuscript; available in PMC 2015 Nov 1.

Published in final edited form as: Am J Med Genet A. 2014 Nov; 164(11): 2892–2900. Published online 2014 Sep 22. doi: 10.1002/ajmg.a.36709

PMCID:: PMC4205164

Article PDF–992K

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