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Items: 1 to 20 of 33

1.
Generalization of fear of movement-related pain and avoidance behavior as predictors of work resumption after back surgery: a study protocol for a prospective study (WABS)
Rini Masuy, Lotte Bamelis, Katleen Bogaerts, Bart Depreitere, Kris De Smedt, Jeroen Ceuppens, Bert Lenaert, Sarah Lonneville, Dieter Peuskens, Johan Van Lerbeirghe, Patrick Van Schaeybroeck, Peter Vorlat, Steefka Zijlstra, Ann Meulders, Johan W. S. Vlaeyen
BMC Psychol. 2022; 10: 39. Published online 2022 Feb 22. doi: 10.1186/s40359-022-00736-5
PMCID:
PMC8862001
ArticlePubReaderPDF–1.0MCite
2.
Role of the DDX11 DNA Helicase in Warsaw Breakage Syndrome Etiology
Diana Santos, Mohammad Mahtab, Ana Boavida, Francesca M. Pisani
Int J Mol Sci. 2021 Mar; 22(5): 2308. Published online 2021 Feb 25. doi: 10.3390/ijms22052308
PMCID:
PMC7956524
ArticlePubReaderPDF–1.7MCite
3.
Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion
Janne J. M. van Schie, Atiq Faramarz, Jesper A. Balk, Grant S. Stewart, Erika Cantelli, Anneke B. Oostra, Martin A. Rooimans, Joanna L. Parish, Cynthia de Almeida Estéves, Katja Dumic, Ingeborg Barisic, Karin E. M. Diderich, Marjon A. van Slegtenhorst, Mohammad Mahtab, Francesca M. Pisani, Hein te Riele, Najim Ameziane, Rob M. F. Wolthuis, Job de Lange
Nat Commun. 2020; 11: 4287. Published online 2020 Aug 27. doi: 10.1038/s41467-020-18066-8
PMCID:
PMC7452896
ArticlePubReaderPDF–4.0MCite
4.
Spotlight on Warsaw Breakage Syndrome
Francesca M Pisani
Appl Clin Genet. 2019; 12: 239–248. Published online 2019 Dec 5. doi: 10.2147/TACG.S186476
PMCID:
PMC6901054
ArticlePubReaderPDF–692KCite
5.
Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?
Roberta Bottega, Luisa M. R. Napolitano, Anna Carbone, Enrico Cappelli, Fabio Corsolini, Silvia Onesti, Anna Savoia, Paolo Gasparini, Flavio Faletra
Mol Genet Genomic Med. 2019 May; 7(5): e639. Published online 2019 Mar 28. doi: 10.1002/mgg3.639
PMCID:
PMC6503064
ArticlePubReaderPDF–622KCite
6.
Warsaw Breakage Syndrome: Further Clinical and Genetic Delineation
Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ann M. Joseph-George, Karen Chong, Ghada M H Abdel-Salam, Mohammed Alowain, Susan I Blaser, Blake C Papsin, Mohammed Butt, Mais Hashem, Nicole Martin, Ruth Godoy, Robert M. Brosh, Jr., Fowzan S Alkuraya, David Chitayat
Am J Med Genet A. Author manuscript; available in PMC 2019 Nov 1.
Published in final edited form as: Am J Med Genet A. 2018 Nov; 176(11): 2404–2418. Published online 2018 Sep 14. doi: 10.1002/ajmg.a.40482
PMCID:
PMC6289708
ArticlePubReaderPDF–1.2MCite
7.
Molecular and Cellular Functions of the Warsaw Breakage Syndrome DNA Helicase DDX11
Francesca M. Pisani, Ettore Napolitano, Luisa M. R. Napolitano, Silvia Onesti
Genes (Basel) 2018 Nov; 9(11): 564. Published online 2018 Nov 21. doi: 10.3390/genes9110564
PMCID:
PMC6266566
ArticlePubReaderPDF–2.3MCite
8.
Interaction of the Warsaw breakage syndrome DNA helicase DDX11 with the replication fork-protection factor Timeless promotes sister chromatid cohesion
Giuseppe Cortone, Ge Zheng, Pasquale Pensieri, Viviana Chiappetta, Rosarita Tatè, Eva Malacaria, Pietro Pichierri, Hongtao Yu, Francesca M. Pisani
PLoS Genet. 2018 Oct; 14(10): e1007622. Published online 2018 Oct 10. doi: 10.1371/journal.pgen.1007622
PMCID:
PMC6179184
ArticlePubReaderPDF–5.6MCite
9.
Warsaw breakage syndrome DDX11 helicase acts jointly with RAD17 in the repair of bulky lesions and replication through abasic sites
Takuya Abe, Masato Ooka, Ryotaro Kawasumi, Keiji Miyata, Minoru Takata, Kouji Hirota, Dana Branzei
Proc Natl Acad Sci U S A. 2018 Aug 14; 115(33): 8412–8417. Published online 2018 Jul 30. doi: 10.1073/pnas.1803110115
PMCID:
PMC6099846
ArticlePubReaderPDF–1.4MCite
10.
Tim/Timeless, a member of the replication fork protection complex, operates with the Warsaw breakage syndrome DNA helicase DDX11 in the same fork recovery pathway
Federica Calì, Sanjay Kumar Bharti, Roberta Di Perna, Robert M. Brosh, Jr, Francesca M. Pisani
Nucleic Acids Res. 2016 Jan 29; 44(2): 705–717. Published online 2015 Oct 25. doi: 10.1093/nar/gkv1112
PMCID:
PMC4737141
ArticlePubReaderPDF–3.0MCite
11.
Identification and Biochemical Characterization of a Novel Mutation in DDX11 Causing Warsaw Breakage Syndrome
José-Mario Capo-Chichi, Sanjay Kumar Bharti, Joshua A. Sommers, Tony Yammine, Eliane Chouery, Lysanne Patry, Guy A. Rouleau, Mark E. Samuels, Fadi F. Hamdan, Jacques L. Michaud, Robert M. Brosh, Jr, André Mégarbane, Zoha Kibar
Hum Mutat. Author manuscript; available in PMC 2015 Oct 9.
Published in final edited form as: Hum Mutat. 2013 Jan; 34(1): 103–107. Published online 2012 Oct 17. doi: 10.1002/humu.22226
PMCID:
PMC4599780
ArticlePubReaderPDF–282KCite
12.
Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome
Sanjay Kumar Bharti, Irfan Khan, Taraswi Banerjee, Joshua A. Sommers, Yuliang Wu, Robert M. Brosh, Jr.
Cell Mol Life Sci. Author manuscript; available in PMC 2015 Aug 14.
Published in final edited form as: Cell Mol Life Sci. 2014 Jul; 71(14): 2625–2639. Published online 2014 Feb 1. doi: 10.1007/s00018-014-1569-4
PMCID:
PMC4537069
ArticlePubReaderPDF–804KCite
13.
Biochemical Characterization of Warsaw Breakage Syndrome Helicase
Yuliang Wu, Joshua A. Sommers, Irfan Khan, Johan P. de Winter, Robert M. Brosh, Jr.
J Biol Chem. 2012 Jan 6; 287(2): 1007–1021. Published online 2011 Nov 18. doi: 10.1074/jbc.M111.276022
PMCID:
PMC3256869
ArticlePubReaderPDF–2.4MCite
14.
Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome
Petra van der Lelij, Anneke B. Oostra, Martin A. Rooimans, Hans Joenje, Johan P. de Winter
Anemia. 2010; 2010: 565268. Published online 2010 Jul 18. doi: 10.1155/2010/565268
PMCID:
PMC3065841
ArticlePubReaderPDF–1.4MCite
15.
Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1
Petra van der Lelij, Krystyna H. Chrzanowska, Barbara C. Godthelp, Martin A. Rooimans, Anneke B. Oostra, Markus Stumm, Małgorzata Z. Zdzienicka, Hans Joenje, Johan P. de Winter
Am J Hum Genet. 2010 Feb 12; 86(2): 262–266. doi: 10.1016/j.ajhg.2010.01.008
PMCID:
PMC2820174
ArticlePubReaderPDF–846KCite
16.
Vertebrate CTF18 and DDX11 essential function in cohesion is bypassed by preventing WAPL-mediated cohesin release
Ryotaro Kawasumi, Takuya Abe, Ivan Psakhye, Keiji Miyata, Kouji Hirota, Dana Branzei
Genes Dev. 2021 Oct 1; 35(19-20): 1368–1382. doi: 10.1101/gad.348581.121
PMCID:
PMC8494208
ArticlePubReaderPDF–4.6MCite
17.
The Genome Stability Maintenance DNA Helicase DDX11 and Its Role in Cancer
Mohammad Mahtab, Ana Boavida, Diana Santos, Francesca M. Pisani
Genes (Basel) 2021 Mar; 12(3): 395. Published online 2021 Mar 10. doi: 10.3390/genes12030395
PMCID:
PMC8000936
ArticlePubReaderPDF–2.6MCite
18.
SARS-CoV-2 detection in setting of viral swabs scarcity: Are MRSA swabs and viral swabs equivalent?
Daniel G. Federman, Shaili Gupta, Gary Stack, Sheldon M. Campbell, David R. Peaper, Louise M. Dembry, Ann Fisher, Asim F. Tarabar, Michael Kozal, Christopher B. Ruser
PLoS One. 2020; 15(8): e0237127. Published online 2020 Aug 5. doi: 10.1371/journal.pone.0237127
PMCID:
PMC7406068
ArticlePubReaderPDF–394KCite
19.
The iron–sulfur helicase DDX11 promotes the generation of single-stranded DNA for CHK1 activation
Anna K Simon, Sandra Kummer, Sebastian Wild, Aleksandra Lezaja, Federico Teloni, Stanislaw K Jozwiakowski, Matthias Altmeyer, Kerstin Gari
Life Sci Alliance. 2020 Mar; 3(3): e201900547. Published online 2020 Feb 18. doi: 10.26508/lsa.201900547
PMCID:
PMC7032568
ArticlePubReaderPDF–2.2MCite
20.
Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2
Atiq Faramarz, Jesper A. Balk, Janne J. M. van Schie, Anneke B. Oostra, Cherien A. Ghandour, Martin A. Rooimans, Rob M. F. Wolthuis, Job de Lange
PLoS One. 2020; 15(1): e0220348. Published online 2020 Jan 14. doi: 10.1371/journal.pone.0220348
PMCID:
PMC6959578
ArticlePubReaderPDF–2.9MCite

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