PMC Links for Gene (Select 83990) - PMC

Cassandra L. Moyer, Jennifer Ivanovich, Jessica L. Gillespie, Rachel Doberstein, Marc R. Radke, Marcy E. Richardson, Scott H. Kaufmann, Elizabeth M. Swisher, Paul J. Goodfellow

Cancer Res. Author manuscript; available in PMC 2022 Jan 3.

Published in final edited form as: Cancer Res. 2020 Feb 15; 80(4): 857–867. Published online 2019 Dec 10. doi: 10.1158/0008-5472.CAN-19-1991

PMCID:: PMC8722358

Abstract Article PDF–491K

Select item 80771234.

Two tSNPs in BRIP1 are associated with breast cancer during TDT analysis

Xuefei Li, Zhuo Li, Miao Yang, Yan Luo, Li Hu, Zhi Xiao, Aji Huang, Juan Huang

Mol Genet Genomic Med. 2021 Feb; 9(2): e1578. Published online 2021 Jan 5. doi: 10.1002/mgg3.1578

PMCID:: PMC8077123

Abstract Article PDF–837K

Select item 79135795.

Spindle Cell Hemangioma and Atypically Localized Juxtaglomerular Cell Tumor in a Patient with Hereditary BRIP1 Mutation: A Case Report

Jan Papez, Jiri Starha, Pavel Zerhau, Denisa Pavlovska, Marta Jezova, Tomas Jurencak, Katerina Slaba, Martin Sterba, Arpad Kerekes, Tomas Merta, Terezia Haluskova, Hana Palova, Ondrej Slaby, Jaroslav Sterba, Petr Jabandziev

Genes (Basel) 2021 Feb; 12(2): 220. Published online 2021 Feb 3. doi: 10.3390/genes12020220

PMCID:: PMC7913579

Abstract Article PDF–19M

Select item 75763046.

Novel role of BRCA1 interacting C‐terminal helicase 1 (BRIP1) in breast tumour cell invasion

Balsam Rizeq, Saïd Sif, Gheyath K. Nasrallah, Allal Ouhtit

J Cell Mol Med. 2020 Oct; 24(19): 11477–11488. Published online 2020 Sep 5. doi: 10.1111/jcmm.15761

PMCID:: PMC7576304

Abstract Article PDF–1.3M

Select item 75529327.

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

Lara Kamal, Sarah B. Pierce, Christina Canavati, Amal Abu Rayyan, Tamara Jaraysa, Orit Lobel, Suhair Lolas, Barbara M. Norquist, Grace Rabie, Fouad Zahdeh, Ephrat Levy-Lahad, Mary-Claire King, Moien N. Kanaan

Cold Spring Harb Mol Case Stud. 2020 Oct; 6(5): a005652. doi: 10.1101/mcs.a005652

PMCID:: PMC7552932

Abstract Article PDF–4.2M

Select item 73163518.

Cancer-associated mutations in the iron-sulfur domain of FANCJ affect G-quadruplex metabolism

Diana C. Odermatt, Wei Ting C. Lee, Sebastian Wild, Stanislaw K. Jozwiakowski, Eli Rothenberg, Kerstin Gari

PLoS Genet. 2020 Jun; 16(6): e1008740. Published online 2020 Jun 15. doi: 10.1371/journal.pgen.1008740

PMCID:: PMC7316351

Abstract Article PDF–2.0M

Select item 71625379.

FANCJ helicase promotes DNA end resection by facilitating CtIP recruitment to DNA double-strand breaks

Sarmi Nath, Ganesh Nagaraju

PLoS Genet. 2020 Apr; 16(4): e1008701. Published online 2020 Apr 6. doi: 10.1371/journal.pgen.1008701

PMCID:: PMC7162537

Abstract Article PDF–5.4M

Select item 709331010.

Landscape of BRIP1 molecular lesions in gastrointestinal cancers from published genomic studies

Ioannis A Voutsadakis

World J Gastroenterol. 2020 Mar 21; 26(11): 1197–1207. Published online 2020 Mar 21. doi: 10.3748/wjg.v26.i11.1197

PMCID:: PMC7093310

Abstract Article PDF–1.9M

Select item 701715311.

Assembly of a G-Quadruplex Repair Complex by the FANCJ DNA Helicase and the REV1 Polymerase

Kaitlin Lowran, Laura Campbell, Phillip Popp, Colin G. Wu

Genes (Basel) 2020 Jan; 11(1): 5. Published online 2019 Dec 19. doi: 10.3390/genes11010005

PMCID:: PMC7017153

Abstract Article PDF–2.3M

Select item 650521212.

BRIP-1 germline mutation and its role in colon cancer: presentation of two case reports and review of literature

Mir Ali, Celia Dawn Delozier, Uzair Chaudhary

BMC Med Genet. 2019; 20: 75. Published online 2019 May 7. doi: 10.1186/s12881-019-0812-0

PMCID:: PMC6505212

Abstract Article PDF–817K

Select item 615951613.

A minimal threshold of FANCJ helicase activity is required for its response to replication stress or double-strand break repair

Sanjay Kumar Bharti, Joshua A Sommers, Sanket Awate, Marina A Bellani, Irfan Khan, Lynda Bradley, Graeme A King, Yeonee Seol, Venkatasubramanian Vidhyasagar, Yuliang Wu, Takuye Abe, Koji Kobayashi, Kazuo Shin-ya, Hiroyuki Kitao, Marc S Wold, Dana Branzei, Keir C Neuman, Robert M Brosh, Jr

Nucleic Acids Res. 2018 Jul 6; 46(12): 6238–6256. Published online 2018 May 21. doi: 10.1093/nar/gky403

PMCID:: PMC6159516

Abstract Article PDF–7.2M

Select item 584285314.

Four common polymorphisms of BRIP1 (rs2048718, rs4988344, rs4986764, and rs6504074) and cancer risk: evidence from 13,716 cancer patients and 15,590 cancer-free controls

Di Liu, Yi Zheng, Meng Wang, Yujiao Deng, Shuai Lin, Linghui Zhou, Pengtao Yang, Cong Dai, Peng Xu, Qian Hao, Dingli Song, Huafeng Kang, Zhijun Dai

Aging (Albany NY) 2018 Feb; 10(2): 266–277. Published online 2018 Feb 16. doi: 10.18632/aging.101388

PMCID:: PMC5842853

Abstract Article PDF–2.8M

Select item 578471715.

BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer

Nana Weber-Lassalle, Jan Hauke, Juliane Ramser, Lisa Richters, Eva Groß, Britta Blümcke, Andrea Gehrig, Anne-Karin Kahlert, Clemens R. Müller, Karl Hackmann, Ellen Honisch, Konstantin Weber-Lassalle, Dieter Niederacher, Julika Borde, Holger Thiele, Corinna Ernst, Janine Altmüller, Guido Neidhardt, Peter Nürnberg, Kristina Klaschik, Christopher Schroeder, Konrad Platzer, Alexander E. Volk, Shan Wang-Gohrke, Walter Just, Bernd Auber, Christian Kubisch, Gunnar Schmidt, Judit Horvath, Barbara Wappenschmidt, Christoph Engel, Norbert Arnold, Bernd Dworniczak, Kerstin Rhiem, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen

Breast Cancer Res. 2018; 20: 7. Published online 2018 Jan 24. doi: 10.1186/s13058-018-0935-9

PMCID:: PMC5784717

Abstract Article PDF–327K

Select item 540261916.

FANCJ Localization by Mismatch Repair Is Vital to Maintain Genomic Integrity after UV Irradiation

Shawna Guillemette, Amy Branagan, Min Peng, Aashana Dhruva, Orlando D. Schärer, Sharon B. Cantor

Cancer Res. Author manuscript; available in PMC 2017 Apr 24.

Published in final edited form as: Cancer Res. 2014 Feb 1; 74(3): 932–944. Published online 2013 Dec 18. doi: 10.1158/0008-5472.CAN-13-2474

PMCID:: PMC5402619

Abstract Article PDF–961K

Select item 500159617.

FANCJ is essential to maintain microsatellite structure genome-wide during replication stress

Joanna Barthelemy, Helmut Hanenberg, Michael Leffak

Nucleic Acids Res. 2016 Aug 19; 44(14): 6803–6816. Published online 2016 May 13. doi: 10.1093/nar/gkw433

Correction in:: Nucleic Acids Res. 2017 Jan 9; 45(1): 509–511.

PMCID:: PMC5001596

Abstract Article PDF–16M

Select item 495839118.

A variant at a potentially functional microRNA-binding site in BRIP1 was associated with risk of squamous cell carcinoma of the head and neck

Hongliang Liu, Fengqin Gao, Kristina R. Dahlstrom, Guojun Li, Erich M. Sturgis, Jose P. Zevallos, Qingyi Wei, Zhensheng Liu

Tumour Biol. Author manuscript; available in PMC 2016 Jul 24.

Published in final edited form as: Tumour Biol. 2016 Jun; 37(6): 8057–8066. Published online 2015 Dec 28. doi: 10.1007/s13277-015-4682-6

PMCID:: PMC4958391

Abstract Article PDF–396K

Select item 494636619.

Analysis of BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer

Haeyoung Kim, Dae-Yeon Cho, Doo Ho Choi, Gee Hue Jung, Inkyung Shin, Won Park, Seung Jae Huh, Seok Jin Nam, Jeong Eon Lee, Won Ho Gil, Seok Won Kim

Cancer Res Treat. 2016 Jul; 48(3): 955–961. Published online 2016 Jan 19. doi: 10.4143/crt.2015.191

PMCID:: PMC4946366

Abstract Article PDF–686K

Select item 493880220.

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

Douglas F Easton, Fabienne Lesueur, Brennan Decker, Kyriaki Michailidou, Jun Li, Jamie Allen, Craig Luccarini, Karen A Pooley, Mitul Shah, Manjeet K Bolla, Qin Wang, Joe Dennis, Jamil Ahmad, Ella R Thompson, Francesca Damiola, Maroulio Pertesi, Catherine Voegele, Noura Mebirouk, Nivonirina Robinot, Geoffroy Durand, Nathalie Forey, Robert N Luben, Shahana Ahmed, Kristiina Aittomäki, Hoda Anton-Culver, Volker Arndt, Australian Ovarian Cancer Study Group, Caroline Baynes, Matthias W Beckman, Javier Benitez, David Van Den Berg, William J Blot, Natalia V Bogdanova, Stig E Bojesen, Hermann Brenner, Jenny Chang-Claude, Kee Seng Chia, Ji-Yeob Choi, Don M Conroy, Angela Cox, Simon S Cross, Kamila Czene, Hatef Darabi, Peter Devilee, Mikael Eriksson, Peter A Fasching, Jonine Figueroa, Henrik Flyger, Florentia Fostira, Montserrat García-Closas, Graham G Giles, Gord Glendon, Anna González-Neira, Pascal Guénel, Christopher A Haiman, Per Hall, Steven N Hart, Mikael Hartman, Maartje J Hooning, Chia-Ni Hsiung, Hidemi Ito, Anna Jakubowska, Paul A James, Esther M John, Nichola Johnson, Michael Jones, Maria Kabisch, Daehee Kang, kConFab Investigators, Veli-Matti Kosma, Vessela Kristensen, Diether Lambrechts, Na Li, Lifepool Investigators, Annika Lindblom, Jirong Long, Artitaya Lophatananon, Jan Lubinski, Arto Mannermaa, Siranoush Manoukian, Sara Margolin, Keitaro Matsuo, Alfons Meindl, Gillian Mitchell, Kenneth Muir, NBCS Investigators, Ines Nevelsteen, Ans van den Ouweland, Paolo Peterlongo, Sze Yee Phuah, Katri Pylkäs, Simone M Rowley, Suleeporn Sangrajrang, Rita K Schmutzler, Chen-Yang Shen, Xiao-Ou Shu, Melissa C Southey, Harald Surowy, Anthony Swerdlow, Soo H Teo, Rob A E M Tollenaar, Ian Tomlinson, Diana Torres, Thérèse Truong, Celine Vachon, Senno Verhoef, Michelle Wong-Brown, Wei Zheng, Ying Zheng, Heli Nevanlinna, Rodney J Scott, Irene L Andrulis, Anna H Wu, John L Hopper, Fergus J Couch, Robert Winqvist, Barbara Burwinkel, Elinor J Sawyer, Marjanka K Schmidt, Anja Rudolph, Thilo Dörk, Hiltrud Brauch, Ute Hamann, Susan L Neuhausen, Roger L Milne, Olivia Fletcher, Paul D P Pharoah, Ian G Campbell, Alison M Dunning, Florence Le Calvez-Kelm, David E Goldgar, Sean V Tavtigian, Georgia Chenevix-Trench

J Med Genet. Author manuscript; available in PMC 2016 Nov 1.

Published in final edited form as: J Med Genet. 2016 May; 53(5): 298–309. Published online 2016 Feb 26. doi: 10.1136/jmedgenet-2015-103529

PMCID:: PMC4938802

Abstract Article PDF–590K

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