The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

Levitus, Marieke, Waisfisz, Quinten, Godthelp, Barbara C, Vries, Yne de, Hussain, Shobbir, Wiegant, Wouter W, Elghalbzouri-Maghrani, Elhaam, Steltenpool, Jûrgen +8 more·2005·Nature Genetics
DOI 10.1038/ng1625

Cited by (432)

Items 101–200 of 432

  1. A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer
    The UKGPCS Collaborators, The British Association of Urological Surgeons' Section of Oncology, Kote-Jarai, Z, Jugurnauth, S, Mulholland, S, Leongamornlert, D A, Guy, M, Edwards, S, Tymrakiewitcz, M, O'Brien, L, Hall, A et al. · 2009 · British Journal of Cancer
  2. UBE2T, the Fanconi Anemia Core Complex, and FANCD2 Are Recruited Independently to Chromatin: a Basis for the Regulation of FANCD2 Monoubiquitination
    Arno F. Alpi, Frédéric Langevin, Georgina Mosedale, Yuichi Machida, Anindya Dutta, Ketan J. Patel · 2007 · Molecular and Cellular Biology
  3. Fanconi Anemia
    Allison M. Green, Gary M. Kupfer · 2009 · Hematology/Oncology Clinics of North America
  4. Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC)
    Courtney Denton Dinardo, Sarah A. Bannon, Mark J. Routbort, Anna R. K. Franklin, Maureen E. Mork, Mary Y. Armanios, Emily Margaret Mace, Jordan Scott Orange, Meselle Jeff‐Eke, Jane E. Churpek et al. · 2016 · Clinical Lymphoma Myeloma & Leukemia
  5. BACH1 is a DNA repair protein supporting BRCA1 damage response
    Peng, M, Litman, R, Jin, Z, Fong, G, Cantor, S B · 2006 · Oncogene
  6. Inherited bone marrow failure in the pediatric patient
    Inderjeet S Dokal, Hemanth Tummala, Tom Vulliamy · 2022 · Blood
  7. Fanconi anemia (FA) binding protein FAAP20 stabilizes FA complementation group A (FANCA) and participates in interstrand cross-link repair
    Justin W. C. Leung, Yucai Wang, Ka-wing Fong, Michael S.Y. Huen, Lei Li, Junjie Chen · 2012 · Proceedings of the National Academy of Sciences
  8. History of DNA Helicases
    Robert M. Brosh, Steven W. Matson · 2020 · Genes
  9. FANCM and FAAP24 Maintain Genome Stability via Cooperative as Well as Unique Functions
    Yucai Wang, Justin W. C. Leung, Yingjun Jiang, Megan G. Lowery, Huong Do, Karen M. Vásquez, Junjie Chen, Weidong Wang, Lei Li · 2013 · Molecular Cell
  10. Fanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults
    M. Schneider, Kate Chandler, Marc D. Tischkowitz, Stefan Meyer · 2014 · Clinical Genetics
  11. ATR-dependent phosphorylation of FANCA on serine 1449 after DNA damage is important for FA pathway function
    Natalie Bucheimer Collins, James B. Wilson, Thomas Bush, Andrei Tomashevski, Kate J. Roberts, Nigel J. Jones, Gary M. Kupfer · 2008 · Blood
  12. The Fanconi anemia/BRCA pathway: A coordinator of cross-link repair
    Kanchan D. Mirchandani, Alan D. D’Andrea · 2006 · Experimental Cell Research
  13. Mechanisms of hexameric helicases
    Amy J. Fernandez, James M. Berger · 2021 · Critical Reviews in Biochemistry and Molecular Biology
  14. Multistep mechanism of G-quadruplex resolution during DNA replication
    Sato, Koichi, Martin-Pintado, Nerea, Post, Harm, Altelaar, Maarten, Knipscheer, Puck · 2021 · Science Advances
  15. Updates on breast cancer genetics: Clinical implications of detecting syndromes of inherited increased susceptibility to breast cancer
    Erin Frances Cobain, Kara J. Milliron, Sofia Diana Merajver · 2016 · Seminars in Oncology
  16. Single-Molecule Analysis Reveals Differential Effect of ssDNA-Binding Proteins on DNA Translocation by XPD Helicase
    Masayoshi Honda, Jeehae Park, Robert A. Pugh, Taekjip Ha, Maria Spies · 2009 · Molecular Cell
  17. BRCA1 tumor suppressor network: focusing on its tail
    Wang, Bin · 2012 · Cell & Bioscience
  18. Germline mutation in the RAD51B gene confers predisposition to breast cancer
    L. Golmard, V. Caux-Moncoutier, Grégoire Davy, Essam Al Ageeli, B. Poirot, C. Tirapo, D. Michaux, C. Barbaroux, C. D. d'Enghien, A. Nicolas et al. · 2013 · BMC Cancer
  19. PALB2: The hub of a network of tumor suppressors involved in DNA damage responses
    Jung‐Young Park, Fan Zhang, Paul R. Andreassen · 2014 · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer
  20. Molecular and cellular functions of the FANCJ DNA helicase defective in cancer and in Fanconi anemia
    Robert M. Brosh, Sharon B. Cantor · 2014 · Frontiers in Genetics
  21. Unraveling the Fanconi anemia–DNA repair connection
    Larry H. Thompson · 2005 · Nature Genetics
  22. Fanconi Anemia Pathway: Mechanisms of Breast Cancer Predisposition Development and Potential Therapeutic Targets
    Can-Bin Fang, Hua-Tao Wu, Manli Zhang, Jing Liu, Guo‐Jun Zhang · 2020 · Frontiers in Cell and Developmental Biology
  23. Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes
    Wu, Yuliang, Sommers, Joshua A., Suhasini, Avvaru N., Leonard, Thomas, Deakyne, Julianna S., Mazin, Alexander V., Shin-ya, Kazuo, Kitao, Hiroyuki, Brosh, Robert M. · 2010 · Blood
  24. Inherited Mutations in Breast Cancer Genes—Risk and Response
    Andrew Y. Shuen, William D. Foulkes · 2011 · Journal of Mammary Gland Biology and Neoplasia
  25. Inflammatory Reactive Oxygen Species-Mediated Hemopoietic Suppression in Fancc-Deficient Mice
    Daniel P. Sejas, Reena Rani, Yuhui Qiu, Xiaoling Zhang, Sara R. Fagerlie, Hiroyasu Nakano, David A. Williams, Qishen Pang · 2007 · The Journal of Immunology
  26. The structure of the catalytic subunit FANCL of the Fanconi anemia core complex
    Ambrose R. Cole, Laurence Lewis, Helen Walden · 2010 · Nature Structural & Molecular Biology
  27. FANCD2, FANCJ and BRCA2 cooperate to promote replication fork recovery independently of the Fanconi Anemia core complex
    Maya Raghunandan, Indrajit Chaudhury, Stephanie L. Kelich, Helmut Hanenberg, Alexandra Sobeck · 2015 · Cell Cycle
  28. Homologous Recombination Is Required for Genome Stability in the Absence of DOG-1 in Caenorhabditis elegans
    Jillian L. Youds, Nigel J. O'Neil, A. Rose · 2006 · Genetics
  29. RecQL5 Promotes Genome Stabilization through Two Parallel Mechanisms—Interacting with RNA Polymerase II and Acting as a Helicase
    M. Nurul Islam, David Fox, Rong Guo, Takemi Enomoto, Weidong Wang · 2010 · Molecular and Cellular Biology
  30. Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome
    Simon T. Holden, James J. Cox, I Kesterton, N S Thomas, C Carr, C G Woods · 2006 · Journal of Medical Genetics
  31. 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, G. Stewart, E. Cantelli, A. Oostra, M. Rooimans, Joanna L. Parish, Cynthia de Almeida Estéves, K. Dumic et al. · 2020 · Nature Communications
  32. Fanconi anemia deficiency stimulates HPV-associated hyperplastic growth in organotypic epithelial raft culture
    Elizabeth E. Hoskins, T A Morris, Jennifer M. Higginbotham, Nicole A. Spardy, Edward Cha, Priscilla N. Kelly, DA Williams, Kathryn A. Wikenheiser‐Brokamp, Stefan M. Duensing, Susanne I. Wells · 2008 · Oncogene
  33. The Fanconi anemia pathway: Repairing the link between DNA damage and squamous cell carcinoma
    Lindsey E. Romick‐Rosendale, Vivian Wai Yan Lui, Jennifer Rubin Grandis, Susanne I. Wells · 2013 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
  34. Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care
    Rossella Graffeo, Luca Livraghi, Olivia Pagani, Aron Goldhirsch, Ann H. Partridge, Judy Ellen Garber · 2016 · Breast Cancer Research and Treatment
  35. C. elegans FANCD2 responds to replication stress and functions in interstrand cross-link repair
    Spencer James Collis, Louise J. Barber, Jordan D. Ward, Julie S. Martin, Simon J. Boulton · 2006 · DNA repair
  36. Dedicated to the core: Understanding the Fanconi anemia complex
    Allan M. Gurtan, Alan D. D’Andrea · 2006 · DNA repair
  37. Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management
    Giovanni Pagano, Annarita Aiello Talamanca, Giuseppe Castello, Federico Vicente Pallardó, Adriana Zatterale, Paolo Degan · 2011 · Biological Chemistry
  38. G-quadruplex resolution: From molecular mechanisms to physiological relevance
    Koichi Sato, Puck Knipscheer · 2023 · DNA repair
  39. Fanconi anemia and breast cancer susceptibility meet again
    Ephrat Levy‐Lahad · 2010 · Nature Genetics
  40. Disease-causing missense mutations in human DNA helicase disorders
    Avvaru N. Suhasini, Robert M. Brosh · 2012 · Mutation Research/Reviews in Mutation Research
  41. 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 · 2014 · Cellular and Molecular Life Sciences
  42. Survival of the fittest: in vivo selection and stem cell gene therapy
    Tobias Neff, Brian C. Beard, Hans‐Peter Kiem · 2005 · Blood
  43. The Fanconi anemia pathway and ubiquitin
    Céline F. Jacquemont, Toshiyasu Taniguchi · 2007 · BMC Biochemistry
  44. Rare BRIP1 Missense Alleles Confer Risk for Ovarian and Breast Cancer
    Cassandra L. Moyer, Jennifer L. Ivanovich, Jessica L. Gillespie, Rachel Doberstein, Marc R. Radke, Marcy E. Richardson, Scott H. Kaufmann, Elizabeth M. Swisher, Paul J. Goodfellow · 2019 · Cancer Research
  45. MRE11–RAD50–NBS1 is a critical regulator of FANCD2 stability and function during DNA double‐strand break repair
    Céline Lopez‐Roques, Yan Coulombe, Mathieu Delannoy, Julien Vignard, Simona Grossi, Isabelle Brodeur, Amélie Rodrigue, Jean Gautier, Alicja Z. Stasiak, Andrzej Stasiak et al. · 2009 · The EMBO Journal
  46. Targeting the FANCJ–BRCA1 interaction promotes a switch from recombination to polη-dependent bypass
    Xie, J, Litman, R, Wang, S, Peng, M, Guillemette, S, Rooney, T, Cantor, S B · 2010 · Oncogene
  47. Recent advances in understanding hematopoiesis in Fanconi Anemia
    Grover C. Bagby · 2018 · F1000Research
  48. HES1 is a novel interactor of the Fanconi anemia core complex
    Cedric Stevens Tremblay, Feng F. Huang, Ouassila Habi, Caroline Huard, Chantal Godin, Georges Lévesque, Madeleine Carreau · 2008 · Blood
  49. Tagging Single Nucleotide Polymorphisms in the BRIP1 Gene and Susceptibility to Breast and Ovarian Cancer
    Honglin Song, Susan J. Ramus, Susanne K. Kjær, Estrid Vilma Solyom Høgdall, Richard A. DiCioccio, Alice S. Whittemore, Valerie M. McGuire, Claus Kim Høgdall, Ian J. Jacobs, Douglas F. Easton et al. · 2007 · PLoS ONE
  50. Ubiquitylation and the Fanconi anemia pathway
    Elizabeth Garner, Agata Smogorzewska · 2011 · FEBS Letters
  51. FANCD2 and DNA Damage
    Manoj K. Nepal, Raymond Che, Chi Ma, Jun Zhang, Peiwen Fei · 2017 · International Journal of Molecular Sciences
  52. Next-Generation Sequencing for Inherited Breast Cancer Risk: Counseling through the Complexity
    Irene R. Rainville, Huma Q. Rana · 2014 · Current Oncology Reports
  53. Hsp90 regulates the Fanconi anemia DNA damage response pathway
    Tsukasa Oda, Toshiya Hayano, Hidenobu Miyaso, Nobuhiro Takahashi, Takayuki Yamashita · 2007 · Blood
  54. FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway
    Kenichiro MATSUZAKI, Valérie Borel, Carrie A. Adelman, Detlev Schindler, Simon J. Boulton · 2015 · Genes & Development
  55. Fanconi Anemia Complementation Group FANCD2 Protein Serine 331 Phosphorylation Is Important for Fanconi Anemia Pathway Function and BRCA2 Interaction
    Gang Zhi, James B. Wilson, Xiaoyong Chen, Diane S. Krause, Yuxuan Xiao, Nigel J. Jones, Gary M. Kupfer · 2009 · Cancer Research
  56. Fanconi anemia and Bloom's syndrome crosstalk through FANCJ–BLM helicase interaction
    Avvaru N. Suhasini, Robert M. Brosh · 2011 · Trends in Genetics
  57. Holding All the Cards—How Fanconi Anemia Proteins Deal with Replication Stress and Preserve Genomic Stability
    Arindam Datta, Robert M. Brosh · 2019 · Genes
  58. A Distinct Triplex DNA Unwinding Activity of ChlR1 Helicase
    Manhong Guo, Kristian Hundseth, Hao Ding, Venkatasubramanian Vidhyasagar, Akira Inoue, Chi-Hung Nguyen, Rula Zain, Jeremy S. Lee, Yuliang Wu · 2015 · Journal of Biological Chemistry
  59. Brief Report: Human Pluripotent Stem Cell Models of Fanconi Anemia Deficiency Reveal an Important Role for Fanconi Anemia Proteins in Cellular Reprogramming and Survival of Hematopoietic Progenitors
    Sun Yung, Katarzyna Tilgner, Maria H. Ledran, Saba Habibollah, Irina E. Neganova, Chatchawan Singhapol, Gabriele Christine Saretzki, Miodrag Stojković, Lyle Armstrong, Stefan Alexander Przyborski et al. · 2012 · Stem Cells
  60. A guanine-flipping and sequestration mechanism for G-quadruplex unwinding by RecQ helicases
    Andrew F. Voter, Yupeng Qiu, Ramreddy Tippana, Sua Myong, James L. Keck · 2018 · Nature Communications
  61. The Role of Fanconi Anemia/BRCA Genes in Zebrafish Sex Determination
    Adriana Rodríguez‐Marí, John H. Postlethwait · 2011 · Methods in cell biology
  62. FANCJ Helicase Uniquely Senses Oxidative Base Damage in Either Strand of Duplex DNA and Is Stimulated by Replication Protein A to Unwind the Damaged DNA Substrate in a Strand-specific Manner
    Avvaru N. Suhasini, Joshua A. Sommers, Aaron C. Mason, Oleg N. Voloshin, R. Daniel Camerini‐Otero, Marc S. Wold, Robert M. Brosh · 2009 · Journal of Biological Chemistry
  63. Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing
    Johan J. P. Gille, Karijn Floor, Lianne Kerkhoven, Najim Ameziane, Hans Joenje, Johan P. de Winter · 2012 · Anemia
  64. The FANC pathway and mitosis: A replication legacy
    Valeria Naim, Filippo Rosselli · 2009 · Cell Cycle
  65. A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network
    José Antonio Casado, Elsa Callén, Ariana Jacome, Paula Rı́o, María Castellà, Stephan Lobitz, Teresa Ferró, Arturo Muñoz, Julián Sevilla, A Cantalejo et al. · 2006 · Journal of Medical Genetics
  66. Mycobacterium tuberculosis DinG Is a Structure-specific Helicase That Unwinds G4 DNA
    R. Thakur, Ambika Desingu, Shivakumar Basavaraju, S. Subramanya, D. Rao, G. Nagaraju · 2014 · Journal of Biological Chemistry
  67. The FANC/BRCA Pathway Releases Replication Blockades by Eliminating DNA Interstrand Cross-Links
    Xavier Renaudin, Filippo Rosselli · 2020 · Genes
  68. Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2
    Shobbir Hussain, James B. Wilson, Eric Blom, Larry H. Thompson, Patrick Sung, Susan M. Gordon, Gary M. Kupfer, Hans Joenje, Christopher George Mathew, Nigel J. Jones · 2006 · DNA repair
  69. Replication stalling and DNA microsatellite instability
    Rujuta Yashodhan Gadgil, Joanna Barthelemy, Todd Lewis, Michael Leffak · 2016 · Biophysical Chemistry
  70. A never-ending story: the steadily growing family of the FA and FA-like genes
    Anna Gueiderikh, Filippo Rosselli, Januario B.C. Neto · 2017 · Genetics and Molecular Biology
  71. DNA repair and neurological disease: From molecular understanding to the development of diagnostics and model organisms
    Arwa A. Abugable, Julia L.M. Morris, Nelma M. Palminha, Ringaile Zaksauskaite, Swagat Ray, Sherif F. El‐Khamisy · 2019 · DNA repair
  72. Dental-craniofacial manifestation and treatment of rare diseases
    En Luo, Hanghang Liu, Qiucheng Zhao, Bing Shi, Qianming Chen · 2019 · International Journal of Oral Science
  73. Cytogenetic Instability in Ovarian Epithelial Cells from Women at Risk of Ovarian Cancer
    Tanja B. Pejovic, Jane E. Yates, Hong Yan Liu, Laura E. Hays, Yassmine M. N. Akkari, Yumi Torimaru, Winifred W. Keeble, R. Keaney Rathbun, William Harry Rodgers, Allen E. Bale et al. · 2006 · Cancer Research
  74. FANCM–FAAP24 and FANCJ: FA proteins that metabolize DNA
    Abdullah Mahmood Ali, Thiyam Ramsing Singh, Amom Ruhikanta Meetei · 2009 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
  75. Strategies for DNA interstrand crosslink repair: Insights from worms, flies, frogs, and slime molds
    Mitch McVey · 2010 · Environmental and Molecular Mutagenesis
  76. Fanconi Anemia Proteins, DNA Interstrand Crosslink Repair Pathways, and Cancer Therapy
    Paul R. Andreassen, Keqin Ren · 2009 · Current Cancer Drug Targets
  77. IOP1 Protein Is an External Component of the Human Cytosolic Iron-Sulfur Cluster Assembly (CIA) Machinery and Functions in the MMS19 Protein-dependent CIA Pathway
    Mineaki Seki, Yukiko Takeda, Kazuhiro Iwaï, Kiyoji Tanaka · 2013 · Journal of Biological Chemistry
  78. Hereditary breast cancer syndromes and genetic testing
    Thereasa A. Rich, Ashley Woodson, Jennifer Keating Litton, Banu K Arun · 2014 · Journal of Surgical Oncology
  79. Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2
    Kyung Jin Eoh, Ji Eun Kim, Hyung Seok Park, Seung‐Tae Lee, Ji Soo Park, Jung Woo Han, Jung‐Yun Lee, Sunghoon Kim, Sang Wun Kim, Jae‐Hoon Kim et al. · 2017 · Cancer Research and Treatment
  80. Delayed diagnosis and complications of Fanconi anaemia at advanced age – a paradigm
    Kirsten Huck, Helmut Hanenberg, Sonja Gudowius, Roland R. Fenk, Reinhard Kalb, Kornelia Neveling, Beate Betz, Dieter Niederacher, Rainer R. Haas, Ulrich Göbel et al. · 2006 · British Journal of Haematology
  81. The Fanconi anemia pathway limits the severity of mutagenesis
    John M. Hinz, Peter B. Nham, Edmund P. Salazar, Larry H. Thompson · 2006 · DNA repair
  82. Contributions of the specialised DNA polymerases to replication of structured DNA
    Caroline M Wickramasinghe, Hayat Arzouk, Alexander Frey, Ahmed Maiter, Julian E. Sale · 2015 · DNA repair
  83. Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2
    Barbara C. Godthelp, Paul P.W. van Buul, Nicolaas G.J. Jaspers, Elhaam Elghalbzouri-Maghrani, Annemarie van Duyn-Goedhart, Fré Arwert, Hans Joenje, Małgorzata Z. Zdzienicka · 2006 · Mutation research. Fundamental and molecular mechanisms of mutagenesis
  84. TheArabidopsis thalianaHomolog of the Helicase RTEL1 Plays Multiple Roles in Preserving Genome Stability
    Julia Recker, Alexander Knoll, Holger Puchta · 2014 · The Plant Cell
  85. Insights into Fanconi Anaemia from the structure of human FANCE
    Ravi K. Nookala, Shobbir Hussain, Luca Pellegrini · 2007 · Nucleic Acids Research
  86. FANCJ/BACH1 Acetylation at Lysine 1249 Regulates the DNA Damage Response
    Jenny Xie, Min Peng, Shawna Guillemette, Steven Quan, Stephanie Maniatis, Yuliang Wu, Aditya Venkatesh, Scott A. Shaffer, Robert M. Brosh, Sharon B. Cantor · 2012 · PLoS Genetics
  87. Continuous in vivo infusion of interferon-gamma (IFN-γ) enhances engraftment of syngeneic wild-type cells in Fanca–/– and Fancg–/– mice
    Yue Cindy Si, Samantha L. M. Ciccone, Feng‐Chun Yang, Jin Yuan, Daisy Zeng, Chen Shi, Henri J. van de Vrugt, John K. Critser, Fré Arwert, Laura S. Haneline et al. · 2006 · Blood
  88. Expression of the BRCA1-interacting protein Brip1/BACH1/FANCJ is driven by E2F and correlates with human breast cancer malignancy
    Eelen, G, Vanden Bempt, I, Verlinden, L, Drijkoningen, M, Smeets, A, Neven, P, Christiaens, M R, Marchal, K, Bouillon, R, Verstuyf, A · 2008 · Oncogene
  89. Inhibition of BACH1 (FANCJ) helicase by backbone discontinuity is overcome by increased motor ATPase or length of loading strand
    Gupta, Rigu, Sharma, Sudha, Doherty, Kevin M., Sommers, Joshua A., Cantor, Sharon B., Brosh, Robert M. · 2006 · Nucleic Acids Research
  90. Helicases FANCJ, RTEL1 and BLM Act on Guanine Quadruplex DNA in Vivo
    Peter M. Lansdorp, Niek van Wietmarschen · 2019 · Genes
  91. Functional Interplay between BRCA2/FancD1 and FancC in DNA Repair
    Hiroyuki Kitao, Kazuhiko Yamamoto, Nobuko Matsushita, Mioko Ohzeki, Masamichi Ishiai, Minoru Takata · 2006 · Journal of Biological Chemistry
  92. Systematic identification of key genes and pathways in the development of invasive cervical cancer
    Guoping Niu, Duping Wang, Yunfeng Pei, Sun Li · 2017 · Gene
  93. DNA helicases and their roles in cancer
    Srijita Dhar, Arindam Datta, Robert M. Brosh · 2020 · DNA repair
  94. AMD3100 synergizes with G-CSF to mobilize repopulating stem cells in Fanconi anemia knockout mice
    Anna C. Pulliam, Michael J. Hobson, Samantha L. M. Ciccone, Yan Li, Chen Shi, Edward F. Srour, Feng‐Chun Yang, Hal E. Broxmeyer, D. Wade Clapp · 2008 · Experimental Hematology
  95. Chl1 DNA Helicase Regulates Scc2 Deposition Specifically during DNA-Replication in Saccharomyces cerevisiae
    Soumya Rudra, Robert V. Skibbens · 2013 · PLoS ONE
  96. FANCJ: Solving problems in DNA replication
    Kevin J. Hiom · 2010 · DNA repair
  97. 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 · 2010 · Anemia
  98. Andrographolide induces DNA damage in prostate cancer cells
    Ingrid Forestier-Román, Andres R. Lopez-Rivas, María M. Sánchez-Vázquez, Krizia Rohena-Rivera, Gretchen Nieves-Burgos, Humberto Ortiz‐Zuazaga, Carlos A. Torres‐Ramos, Magaly Martínez‐Ferrer · 2019 · Oncotarget
  99. DNA Structure-Induced Recruitment and Activation of the Fanconi Anemia Pathway Protein FANCD2
    Alexandra Sobeck, Stacie Stone, Maureen E. Hoatlin · 2007 · Molecular and Cellular Biology
  100. FAVL elevation in human tumors disrupts Fanconi anemia pathway signaling and promotes genomic instability and tumor growth
    Jun Zhang, Deping Zhao, Hwan Ki Park, Hong Wang, Roy B. Dyer, Wanguo Liu, George G. Klee, Mark A. McNiven, Donald J. Tindall, Julian R. Molina et al. · 2010 · Journal of Clinical Investigation