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Items: 1 to 20 of 31

1.
Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype
Rajalakshmi S. Asur, Danielle C. Kimble, Francis P. Lach, Moonjung Jung, Frank X. Donovan, Aparna Kamat, Raymond J. Noonan, James W. Thomas, Morgan Park, Peter Chines, Adrianna Vlachos, Arleen D. Auerbach, Agata Smogorzewska, Settara C. Chandrasekharappa
Mol Genet Genomic Med. 2018 Jan; 6(1): 77–91. Published online 2017 Nov 30. doi: 10.1002/mgg3.350
PMCID:
PMC5823675
AbstractArticlePDF–3.1M
2.
Bony metastases from breast cancer - a study of foetal antigen 2 as a blood tumour marker
Kwok-Leung Cheung, Ray K Iles, John FR Robertson
World J Surg Oncol. 2010; 8: 38. Published online 2010 May 13. doi: 10.1186/1477-7819-8-38
PMCID:
PMC2879255
AbstractArticlePDF–372K
3.
Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome
S T Holden, J J Cox, I Kesterton, N S Thomas, C Carr, C G Woods
J Med Genet. 2006 Sep; 43(9): 750–754. Published online 2006 May 5. doi: 10.1136/jmg.2006.041673
PMCID:
PMC2564576
AbstractArticlePDF–487K
4.
CDH1、FANCB和APC基因多态性与中国人群肺癌易感性的关系
苏 联椿, 黄 华, 高 敏, 李 永文, 施 睿峰, 陈 琛, 李 宣广, 朱 光胜, 刘 红雨, 陈 军
Zhongguo Fei Ai Za Zhi. 2022 Sep 20; 25(9): 658–664. Chinese. doi: 10.3779/j.issn.1009-3419.2022.102.21
PMCID:
PMC9549421
AbstractArticlePDF–1.9M
5.
Inactivation of the Tumor Suppressor Genes Causing the Hereditary Syndromes Predisposing to Head and Neck Cancer via Promoter Hypermethylation in Sporadic Head and Neck Cancers
Ian M. Smith, Suhail K. Mithani, Wojciech K. Mydlarz, Steven S. Chang, Joseph A. Califano
ORL J Otorhinolaryngol Relat Spec. 2010 May; 72(1): 44–50. Published online 2010 Mar 24. doi: 10.1159/000292104
PMCID:
PMC2881891
AbstractArticlePDF–149K
6.
Evidence for at least eight Fanconi anemia genes.
H Joenje, A B Oostra, M Wijker, F M di Summa, C G van Berkel, M A Rooimans, W Ebell, M van Weel, J C Pronk, M Buchwald, F Arwert
Am J Hum Genet. 1997 Oct; 61(4): 940–944. doi: 10.1086/514881
PMCID:
PMC1715980
SummaryPage BrowsePDF–881K
7.
The interplay of UBE2T and Mule in regulating Wnt/β-catenin activation to promote hepatocellular carcinoma progression
Nicole Pui Yu Ho, Carmen Oi Ning Leung, Tin Lok Wong, Eunice Yuen Ting Lau, Martina Mang Leng Lei, Etienne Ho Kit Mok, Hoi Wing Leung, Man Tong, Irene Oi Lin Ng, Jing Ping Yun, Stephanie Ma, Terence Kin Wah Lee
Cell Death Dis. 2021 Feb; 12(2): 148. Published online 2021 Feb 1. doi: 10.1038/s41419-021-03403-6
PMCID:
PMC7862307
AbstractArticlePDF–4.0M
8.
Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant
Haya H. Al-Balool, David Weber, Yilei Liu, Mark Wade, Kamlesh Guleria, Pitsien Lang Ping Nam, Jake Clayton, William Rowe, Jonathan Coxhead, Julie Irving, David J. Elliott, Andrew G. Hall, Mauro Santibanez-Koref, Michael S. Jackson
Genome Res. 2011 Nov; 21(11): 1788–1799. doi: 10.1101/gr.116442.110
PMCID:
PMC3205564
AbstractArticlePDF–770K
9.
Evidence for subcomplexes in the Fanconi anemia pathway
Annette L. Medhurst, El Houari Laghmani, Jurgen Steltenpool, Miriam Ferrer, Chantal Fontaine, Jan de Groot, Martin A. Rooimans, Rik J. Scheper, Amom Ruhikanta Meetei, Weidong Wang, Hans Joenje, Johan P. de Winter
Blood. 2006 Sep 15; 108(6): 2072–2080. Prepublished online 2006 May 23. doi: 10.1182/blood-2005-11-008151
PMCID:
PMC1895538
AbstractArticle
10.
Modularized Functions of the Fanconi Anemia Core Complex
Yaling Huang, Justin WC Leung, Megan Lowery, Nobuko Matsushita, Yucai Wang, Xi Shen, Do Huong, Minoru Takata, Junjie Chen, Lei Li
Cell Rep. Author manuscript; available in PMC 2015 Jun 26.
Published in final edited form as: Cell Rep. 2014 Jun 26; 7(6): 1849–1857. Published online 2014 Jun 5. doi: 10.1016/j.celrep.2014.04.029
PMCID:
PMC4157997
AbstractArticlePDF–1.4M
11.
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway
Chen Ling, Masamichi Ishiai, Abdullah Mahmood Ali, Annette L Medhurst, Kornelia Neveling, Reinhard Kalb, Zhijiang Yan, Yutong Xue, Anneke B Oostra, Arleen D Auerbach, Maureen E Hoatlin, Detlev Schindler, Hans Joenje, Johan P de Winter, Minoru Takata, Amom Ruhikanta Meetei, Weidong Wang
EMBO J. 2007 Apr 18; 26(8): 2104–2114. Published online 2007 Mar 29. doi: 10.1038/sj.emboj.7601666
PMCID:
PMC1852792
AbstractArticlePDF–378K
12.
The Fanconi anemia pathway promotes replication-dependent DNA interstrand crosslink repair
Puck Knipscheer, Markus Räschle, Agata Smogorzewska, Milica Enoiu, The Vinh Ho, Orlando D. Schärer, Stephen J. Elledge, Johannes C. Walter
Science. Author manuscript; available in PMC 2010 Jul 26.
Published in final edited form as: Science. 2009 Dec 18; 326(5960): 1698–1701. Published online 2009 Nov 12. doi: 10.1126/science.1182372
PMCID:
PMC2909596
AbstractArticlePDF–1.9M
13.
A Human Orthologue of Archaeal DNA Repair Protein Hef is Defective in Fanconi Anemia Complementation Group M
Amom Ruhikanta Meetei, Annette L. Medhurst, Chen Ling, Yutong Xue, Thiyam Ramsing Singh, Patrick Bier, Jurgen Steltenpool, Stacie Stone, Inderjeet Dokal, Christopher G. Mathew, Maureen Hoatlin, Hans Joenje, Johan P. de Winter, Weidong Wang
Nat Genet. Author manuscript; available in PMC 2009 Jul 1.
Published in final edited form as: Nat Genet. 2005 Sep; 37(9): 958–963. Published online 2005 Aug 21. doi: 10.1038/ng1626
PMCID:
PMC2704909
AbstractArticlePDF–2.2M
14.
MHF1-MHF2, a Histone-Fold-Containing Protein Complex, Participates in the Fanconi Anemia Pathway via FANCM
Thiyam Ramsing Singh, Dorina Saro, Abdullah Mahmood Ali, Xiao-feng Zheng, Chang-hu Du, Michael W. Killen, Aristidis Sachpatzidis, Kebola Wahengbam, Andrew J. Pierce, Yong Xiong, Patrick Sung, Amom Ruhikanta Meetei
Mol Cell. Author manuscript; available in PMC 2011 Mar 26.
Published in final edited form as: Mol Cell. 2010 Mar 26; 37(6): 879–886. doi: 10.1016/j.molcel.2010.01.036
PMCID:
PMC2848122
AbstractArticlePDF–1.9M
15.
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway
Abdullah Mahmood Ali, Arun Pradhan, Thiyam Ramsingh Singh, Changhu Du, Jie Li, Kebola Wahengbam, Elke Grassman, Arleen D. Auerbach, Qishen Pang, Amom Ruhikanta Meetei
Blood. 2012 Apr 5; 119(14): 3285–3294. Prepublished online 2012 Feb 17. doi: 10.1182/blood-2011-10-385963
PMCID:
PMC3321854
AbstractArticle
16.
A ubiquitin-binding protein FAAP20 links RNF8-mediated ubiquitination to the Fanconi anemia DNA Repair network
Zhijiang Yan, Rong Guo, Manikandan Paramasivam, Weiping Shen, Chen Ling, David Fox, III, Yucai Wang, Anneke B. Oostra, Julia Kuehl, Duck-Yeon Lee, Minoru Takata, Maureen E. Hoatlin, Detlev Schindler, Hans Joenje, Johan P. de Winter, Lei Li, Michael M. Seidman, Weidong Wang
Mol Cell. Author manuscript; available in PMC 2013 Jul 13.
Published in final edited form as: Mol Cell. 2012 Jul 13; 47(1): 61–75. Published online 2012 Jun 14. doi: 10.1016/j.molcel.2012.05.026
PMCID:
PMC3398238
AbstractArticlePDF–4.8M
17.
A histone-fold complex and FANCM form a conserved DNA remodeling complex to maintain genome stability
Zhijiang Yan, Mathieu Delannoy, Chen Ling, Danielle Daee, Fekret Osman, Parameswary A. Muniandy, Xi Shen, Anneke B. Oostra, Hansen Du, Jurgen Steltenpool, Ti Lin, Beatrice Schuster, Chantal Decaillet, Andrzej Stasiak, Alicja Z. Stasiak, Stacie Stone, Maureen E. Hoatlin, Detlev Schindler, Chris Woodcock, Hans Joenje, Ranjan Sen, Johan P. de Winter, Lei Li, Michael M. Seidman, Matthew C. Whitby, Kyungjae Myung, Angelos Constantinou, Weidong Wang
Mol Cell. Author manuscript; available in PMC 2011 Mar 26.
Published in final edited form as: Mol Cell. 2010 Mar 26; 37(6): 865–878. doi: 10.1016/j.molcel.2010.01.039
PMCID:
PMC2847587
AbstractArticlePDF–1.9M
18.
CFTR interactome mapping using the mammalian membrane two‐hybrid high‐throughput screening system
Sang Hyun Lim, Jamie Snider, Liron Birimberg‐Schwartz, Wan Ip, Joana C Serralha, Hugo M Botelho, Miquéias Lopes‐Pacheco, Madalena C Pinto, Mohamed Taha Moutaoufik, Mara Zilocchi, Onofrio Laselva, Mohsen Esmaeili, Max Kotlyar, Anna Lyakisheva, Priscilla Tang, Lucía López Vázquez, Indira Akula, Farzaneh Aboualizadeh, Victoria Wong, Ingrid Grozavu, Teuta Opacak‐Bernardi, Zhong Yao, Meg Mendoza, Mohan Babu, Igor Jurisica, Tanja Gonska, Christine E Bear, Margarida D Amaral, Igor Stagljar
Mol Syst Biol. 2022 Feb; 18(2): e10629. Published online 2022 Feb 14. doi: 10.15252/msb.202110629
PMCID:
PMC8842165
AbstractArticlePDF–3.0M
19.
DNA Repair Network Analysis Reveals Shieldin as a Key Regulator of NHEJ and PARP Inhibitor Sensitivity
Rajat Gupta, Kumar Somyajit, Takeo Narita, Elina Maskey, Andre Stanlie, Magdalena Kremer, Dimitris Typas, Michael Lammers, Niels Mailand, Andre Nussenzweig, Jiri Lukas, Chunaram Choudhary
Cell. Author manuscript; available in PMC 2021 May 10.
Published in final edited form as: Cell. 2018 May 3; 173(4): 972–988.e23. Published online 2018 Apr 12. doi: 10.1016/j.cell.2018.03.050
PMCID:
PMC8108093
AbstractArticlePDF–3.5M
20.
Proteomic characterization of chromosomal common fragile site (CFS)-associated proteins uncovers ATRX as a regulator of CFS stability
David Pladevall-Morera, Stephanie Munk, Andreas Ingham, Lorenza Garribba, Eliene Albers, Ying Liu, Jesper V Olsen, Andres J Lopez-Contreras
Nucleic Acids Res. 2019 Sep 5; 47(15): 8004–8018. Published online 2019 Jun 10. doi: 10.1093/nar/gkz510
Correction in:
Nucleic Acids Res. 2019 Sep 5; 47(15): 8332.
PMCID:
PMC6735892
AbstractArticlePDF–5.4M

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