Zeitschriftenartikel zum Thema „Microhomology mediated recombination“
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Jiang, Yuning. „Contribution of Microhomology to Genome Instability: Connection between DNA Repair and Replication Stress“. International Journal of Molecular Sciences 23, Nr. 21 (26.10.2022): 12937. http://dx.doi.org/10.3390/ijms232112937.
Der volle Inhalt der QuelleXu, Yijiang, Hang Zhou, Ginell Post, Hong Zan und Paolo Casali. „Rad52 mediates class-switch DNA recombination to IgD“. Journal of Immunology 208, Nr. 1_Supplement (01.05.2022): 112.17. http://dx.doi.org/10.4049/jimmunol.208.supp.112.17.
Der volle Inhalt der QuelleLee-Theilen, Mieun, Allysia J. Matthews, Dierdre Kelly, Simin Zheng und Jayanta Chaudhuri. „CtIP promotes microhomology-mediated alternative end joining during class-switch recombination“. Nature Structural & Molecular Biology 18, Nr. 1 (05.12.2010): 75–79. http://dx.doi.org/10.1038/nsmb.1942.
Der volle Inhalt der QuelleFrancis, Nigel J., Bairbre McNicholas, Atif Awan, Mary Waldron, Donal Reddan, Denise Sadlier, David Kavanagh et al. „A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome“. Blood 119, Nr. 2 (12.01.2012): 591–601. http://dx.doi.org/10.1182/blood-2011-03-339903.
Der volle Inhalt der QuelleAhrabi, Sara, Sovan Sarkar, Sophia X. Pfister, Giacomo Pirovano, Geoff S. Higgins, Andrew C. G. Porter und Timothy C. Humphrey. „A role for human homologous recombination factors in suppressing microhomology-mediated end joining“. Nucleic Acids Research 44, Nr. 12 (29.04.2016): 5743–57. http://dx.doi.org/10.1093/nar/gkw326.
Der volle Inhalt der QuelleChan, C. Y., M. Kiechle, P. Manivasakam und R. H. Schiestl. „Ionizing radiation and restriction enzymes induce microhomology-mediated illegitimate recombination in Saccharomyces cerevisiae“. Nucleic Acids Research 35, Nr. 15 (11.07.2007): 5051–59. http://dx.doi.org/10.1093/nar/gkm442.
Der volle Inhalt der QuelleLing, Alexanda K., Clare C. So, Michael X. Le, Audrey Y. Chen, Lisa Hung und Alberto Martin. „Double-stranded DNA break polarity skews repair pathway choice during intrachromosomal and interchromosomal recombination“. Proceedings of the National Academy of Sciences 115, Nr. 11 (22.02.2018): 2800–2805. http://dx.doi.org/10.1073/pnas.1720962115.
Der volle Inhalt der QuelleChan, Cecilia Y., und Robert H. Schiestl. „Rad1, rad10 and rad52 Mutations Reduce the Increase of Microhomology Length during Radiation-Induced Microhomology-Mediated Illegitimate Recombination in Saccharomyces cerevisiae“. Radiation Research 172, Nr. 2 (01.08.2009): 141. http://dx.doi.org/10.1667/rr1675.1.
Der volle Inhalt der QuelleNagai, Koki, Hirohito Shima, Miki Kamimura, Junko Kanno, Erina Suzuki, Akira Ishiguro, Satoshi Narumi, Shigeo Kure, Ikuma Fujiwara und Maki Fukami. „Xp22.31 Microdeletion due to Microhomology-Mediated Break-Induced Replication in a Boy with Contiguous Gene Deletion Syndrome“. Cytogenetic and Genome Research 151, Nr. 1 (2017): 1–4. http://dx.doi.org/10.1159/000458469.
Der volle Inhalt der QuelleMeyer, Damon, Becky Xu Hua Fu und Wolf-Dietrich Heyer. „DNA polymerases δ and λ cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiae“. Proceedings of the National Academy of Sciences 112, Nr. 50 (25.11.2015): E6907—E6916. http://dx.doi.org/10.1073/pnas.1507833112.
Der volle Inhalt der QuelleXu, Ran, Ziyi Pan und Takuro Nakagawa. „Gross Chromosomal Rearrangement at Centromeres“. Biomolecules 14, Nr. 1 (24.12.2023): 28. http://dx.doi.org/10.3390/biom14010028.
Der volle Inhalt der QuelleRobert, Isabelle, Françoise Dantzer und Bernardo Reina-San-Martin. „Parp1 facilitates alternative NHEJ, whereas Parp2 suppresses IgH/c-myc translocations during immunoglobulin class switch recombination“. Journal of Experimental Medicine 206, Nr. 5 (13.04.2009): 1047–56. http://dx.doi.org/10.1084/jem.20082468.
Der volle Inhalt der QuelleWang, Xiaobin S., Junfei Zhao, Foon Wu-Baer, Zhengping Shao, Brian J. Lee, Olivia M. Cupo, Raul Rabadan, Jean Gautier, Richard Baer und Shan Zha. „CtIP-mediated DNA resection is dispensable for IgH class switch recombination by alternative end-joining“. Proceedings of the National Academy of Sciences 117, Nr. 41 (28.09.2020): 25700–25711. http://dx.doi.org/10.1073/pnas.2010972117.
Der volle Inhalt der QuelleChen, Changming, Xiaoling Xie, Xi Wu, Yeling Lu, Xuefeng Wang, Wenman Wu, Yiqun Hu und Qiulan Ding. „Complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis“. Thrombosis and Haemostasis 117, Nr. 08 (2017): 1478–85. http://dx.doi.org/10.1160/th17-01-0046.
Der volle Inhalt der QuelleSaribasak, Huseyin, Robert W. Maul, Zheng Cao, Rhonda L. McClure, William Yang, Daniel R. McNeill, David M. Wilson und Patricia J. Gearhart. „XRCC1 suppresses somatic hypermutation and promotes alternative nonhomologous end joining in Igh genes“. Journal of Experimental Medicine 208, Nr. 11 (03.10.2011): 2209–16. http://dx.doi.org/10.1084/jem.20111135.
Der volle Inhalt der QuelleEhrenstein, M. R., C. Rada, A. M. Jones, C. Milstein und M. S. Neuberger. „Switch junction sequences in PMS2-deficient mice reveal a microhomology-mediated mechanism of Ig class switch recombination“. Proceedings of the National Academy of Sciences 98, Nr. 25 (20.11.2001): 14553–58. http://dx.doi.org/10.1073/pnas.241525998.
Der volle Inhalt der QuelleChen, Xiaojiang S., und Richard T. Pomerantz. „DNA Polymerase θ: A Cancer Drug Target with Reverse Transcriptase Activity“. Genes 12, Nr. 8 (27.07.2021): 1146. http://dx.doi.org/10.3390/genes12081146.
Der volle Inhalt der QuelleBothmer, Anne, Davide F. Robbiani, Niklas Feldhahn, Anna Gazumyan, Andre Nussenzweig und Michel C. Nussenzweig. „53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination“. Journal of Experimental Medicine 207, Nr. 4 (05.04.2010): 855–65. http://dx.doi.org/10.1084/jem.20100244.
Der volle Inhalt der QuelleDecottignies, Anabelle. „Microhomology-Mediated End Joining in Fission Yeast Is Repressed by Pku70 and Relies on Genes Involved in Homologous Recombination“. Genetics 176, Nr. 3 (04.05.2007): 1403–15. http://dx.doi.org/10.1534/genetics.107.071621.
Der volle Inhalt der QuelleDing, Qiulan, Guoling You, Jing Dai, Xiaodong Xi, Hongli Wang, Xi Wu, Yeling Lu und Xuefeng Wang. „Characterisation of large F9 deletions in seven unrelated patients with severe haemophilia B“. Thrombosis and Haemostasis 112, Nr. 09 (2014): 459–65. http://dx.doi.org/10.1160/th13-12-1060.
Der volle Inhalt der QuelleYou, Guoling, Kun Chi, Yeling Lu, Qiulan Ding, Jing Dai, Xiaodong Xi, Hongli Wang und Xuefeng Wang. „Identification and characterisation of a novel aberrant pattern of intron 1 inversion with concomitant large insertion and deletion within the F8 gene“. Thrombosis and Haemostasis 112, Nr. 08 (2014): 264–70. http://dx.doi.org/10.1160/th13-10-0892.
Der volle Inhalt der QuelleKohli, Ajay, Simon Griffiths, Natalia Palacios, Richard M Twyman, Philippe Vain, David A. Laurie und Paul Christou. „Molecular characterization of transforming plasmid rearrangements in transgenic rice reveals a recombination hotspot in the CaMV 35S promoter and confirms the predominance of microhomology mediated recombination“. Plant Journal 17, Nr. 6 (März 1999): 591–601. http://dx.doi.org/10.1046/j.1365-313x.1999.00399.x.
Der volle Inhalt der QuelleFiori, Mariangela Stefania, Luca Ferretti, Antonello Di Nardo, Lele Zhao, Susanna Zinellu, Pier Paolo Angioi, Matteo Floris et al. „A Naturally Occurring Microhomology-Mediated Deletion of Three Genes in African Swine Fever Virus Isolated from Two Sardinian Wild Boars“. Viruses 14, Nr. 11 (14.11.2022): 2524. http://dx.doi.org/10.3390/v14112524.
Der volle Inhalt der QuelleFeng, Wanjuan, Dennis A. Simpson, Jang-Eun Cho, Juan Carvajal-Garcia, Chelsea M. Smith, Kathryn M. Headley, Nate Hathaway, Dale A. Ramsden und Gaorav P. Gupta. „Marker-free quantification of repair pathway utilization at Cas9-induced double-strand breaks“. Nucleic Acids Research 49, Nr. 9 (08.05.2021): 5095–105. http://dx.doi.org/10.1093/nar/gkab299.
Der volle Inhalt der QuelleStachler, Aris-Edda, Julia Wörtz, Omer S. Alkhnbashi, Israela Turgeman-Grott, Rachel Smith, Thorsten Allers, Rolf Backofen, Uri Gophna und Anita Marchfelder. „Adaptation induced by self-targeting in a type I-B CRISPR-Cas system“. Journal of Biological Chemistry 295, Nr. 39 (28.07.2020): 13502–15. http://dx.doi.org/10.1074/jbc.ra120.014030.
Der volle Inhalt der QuelleDahal, Sumedha, und Sathees C. Raghavan. „Mitochondrial genome stability in human: understanding the role of DNA repair pathways“. Biochemical Journal 478, Nr. 6 (19.03.2021): 1179–97. http://dx.doi.org/10.1042/bcj20200920.
Der volle Inhalt der QuelleWang, Wenjie, Kuan Li, Zhuo Yang, Quancan Hou, Wei W. Zhao und Qianwen Sun. „RNase H1C collaborates with ssDNA binding proteins WHY1/3 and recombinase RecA1 to fulfill the DNA damage repair in Arabidopsis chloroplasts“. Nucleic Acids Research 49, Nr. 12 (16.06.2021): 6771–87. http://dx.doi.org/10.1093/nar/gkab479.
Der volle Inhalt der QuelleÖz, Robin, Sean M. Howard, Rajhans Sharma, Hanna Törnkvist, Ilaria Ceppi, Sriram KK, Erik Kristiansson, Petr Cejka und Fredrik Westerlund. „Phosphorylated CtIP bridges DNA to promote annealing of broken ends“. Proceedings of the National Academy of Sciences 117, Nr. 35 (19.08.2020): 21403–12. http://dx.doi.org/10.1073/pnas.2008645117.
Der volle Inhalt der QuelleZhao, Yuqin, Kaiping Hou, Yu Liu, Yinan Na, Chao Li, Haoyuan Luo und Hailong Wang. „Helicase HELQ: Molecular Characters Fit for DSB Repair Function“. International Journal of Molecular Sciences 25, Nr. 16 (08.08.2024): 8634. http://dx.doi.org/10.3390/ijms25168634.
Der volle Inhalt der QuelleDohrn, Lisa, Daniela Salles, Simone Y. Siehler, Julia Kaufmann und Lisa Wiesmüller. „BRCA1-mediated repression of mutagenic end-joining of DNA double-strand breaks requires complex formation with BACH1“. Biochemical Journal 441, Nr. 3 (16.01.2012): 919–28. http://dx.doi.org/10.1042/bj20110314.
Der volle Inhalt der QuelleTruong, L. N., Y. Li, L. Z. Shi, P. Y. H. Hwang, J. He, H. Wang, N. Razavian, M. W. Berns und X. Wu. „Microhomology-mediated End Joining and Homologous Recombination share the initial end resection step to repair DNA double-strand breaks in mammalian cells“. Proceedings of the National Academy of Sciences 110, Nr. 19 (22.04.2013): 7720–25. http://dx.doi.org/10.1073/pnas.1213431110.
Der volle Inhalt der QuelleElert-Dobkowska, Ewelina, Iwona Stepniak, Wiktoria Radziwonik-Fraczyk, Amir Jahic, Christian Beetz und Anna Sulek. „SPAST Intragenic CNVs Lead to Hereditary Spastic Paraplegia via a Haploinsufficiency Mechanism“. International Journal of Molecular Sciences 25, Nr. 9 (03.05.2024): 5008. http://dx.doi.org/10.3390/ijms25095008.
Der volle Inhalt der QuelleTomasini, Paula Pellenz, Temenouga Nikolova Guecheva, Natalia Motta Leguisamo, Sarah Péricart, Anne-Cécile Brunac, Jean Sébastien Hoffmann und Jenifer Saffi. „Analyzing the Opportunities to Target DNA Double-Strand Breaks Repair and Replicative Stress Responses to Improve Therapeutic Index of Colorectal Cancer“. Cancers 13, Nr. 13 (23.06.2021): 3130. http://dx.doi.org/10.3390/cancers13133130.
Der volle Inhalt der QuelleLi, Zhichao, und Ralph Bock. „Rapid functional activation of a horizontally transferred eukaryotic gene in a bacterial genome in the absence of selection“. Nucleic Acids Research 47, Nr. 12 (20.05.2019): 6351–59. http://dx.doi.org/10.1093/nar/gkz370.
Der volle Inhalt der QuelleLukashchuk, Natalia, Joshua Armenia, Luis Tobalina, Thomas Hedley Carr, Tsveta Milenkova, Ying L. Liu, Richard T. Penson, Mark E. Robson und Elizabeth Harrington. „BRCA reversion mutations mediated by microhomology-mediated end joining (MMEJ) as a mechanism of resistance to PARP inhibitors in ovarian and breast cancer.“ Journal of Clinical Oncology 40, Nr. 16_suppl (01.06.2022): 5559. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.5559.
Der volle Inhalt der QuelleLukashchuk, Natalia, Joshua Armenia, Luis Tobalina, Thomas Hedley Carr, Tsveta Milenkova, Ying L. Liu, Richard T. Penson, Mark E. Robson und Elizabeth Harrington. „BRCA reversion mutations mediated by microhomology-mediated end joining (MMEJ) as a mechanism of resistance to PARP inhibitors in ovarian and breast cancer.“ Journal of Clinical Oncology 40, Nr. 16_suppl (01.06.2022): 5559. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.5559.
Der volle Inhalt der QuelleHays, Michelle, Katja Schwartz, Danica T. Schmidtke, Dimitra Aggeli und Gavin Sherlock. „Paths to adaptation under fluctuating nitrogen starvation: The spectrum of adaptive mutations in Saccharomyces cerevisiae is shaped by retrotransposons and microhomology-mediated recombination“. PLOS Genetics 19, Nr. 5 (16.05.2023): e1010747. http://dx.doi.org/10.1371/journal.pgen.1010747.
Der volle Inhalt der QuelleProvasek, Vincent E., Joy Mitra, Vikas H. Malojirao und Muralidhar L. Hegde. „DNA Double-Strand Breaks as Pathogenic Lesions in Neurological Disorders“. International Journal of Molecular Sciences 23, Nr. 9 (22.04.2022): 4653. http://dx.doi.org/10.3390/ijms23094653.
Der volle Inhalt der QuelleZhao, Zhihua, Hanshuo Zhang, Tuanlin Xiong, Junyi Wang, Di Yang, Dan Zhu, Juan Li et al. „Suppression of SHROOM1 Improves In Vitro and In Vivo Gene Integration by Promoting Homology-Directed Repair“. International Journal of Molecular Sciences 21, Nr. 16 (13.08.2020): 5821. http://dx.doi.org/10.3390/ijms21165821.
Der volle Inhalt der QuelleLiu, Yu-Chang, Chih-Hao Huang und Ching-Chun Chang. „A Transcriptomic Analysis of Tobacco Leaf with the Functional Loss of the Plastid rpoB Operon Caused by TALEN-Mediated Double-Strand Breakage“. Plants 11, Nr. 21 (26.10.2022): 2860. http://dx.doi.org/10.3390/plants11212860.
Der volle Inhalt der QuelleAnand, Roopesh, Erika Buechelmaier, Ondrej Belan, Matthew Newton, Aleksandra Vancevska, Artur Kaczmarczyk, Tohru Takaki, David S. Rueda, Simon N. Powell und Simon J. Boulton. „HELQ is a dual-function DSB repair enzyme modulated by RPA and RAD51“. Nature 601, Nr. 7892 (22.12.2021): 268–73. http://dx.doi.org/10.1038/s41586-021-04261-0.
Der volle Inhalt der QuelleAlexander, Jessica L., Kelly Beagan, Terry L. Orr-Weaver und Mitch McVey. „Multiple mechanisms contribute to double-strand break repair at rereplication forks inDrosophilafollicle cells“. Proceedings of the National Academy of Sciences 113, Nr. 48 (14.11.2016): 13809–14. http://dx.doi.org/10.1073/pnas.1617110113.
Der volle Inhalt der QuelleTsuji, Hideo, Hiroko Ishii-Ohba, Takanori Katsube, Hideki Ukai, Shiro Aizawa, Masahiro Doi, Kyoji Hioki und Toshiaki Ogiu. „Involvement of Illegitimate V(D)J Recombination or Microhomology-Mediated Nonhomologous End-Joining in the Formation of Intragenic Deletions of the Notch1 Gene in Mouse Thymic Lymphomas“. Cancer Research 64, Nr. 24 (15.12.2004): 8882–90. http://dx.doi.org/10.1158/0008-5472.can-03-1163.
Der volle Inhalt der QuelleHaberland, Vivien M. M., Simon Magin, George Iliakis und Andrea Hartwig. „Impact of Manganese and Chromate on Specific DNA Double-Strand Break Repair Pathways“. International Journal of Molecular Sciences 24, Nr. 12 (20.06.2023): 10392. http://dx.doi.org/10.3390/ijms241210392.
Der volle Inhalt der QuelleJiang, Yuning, und Tarek Abbas. „Abstract 6107: Novel roles for AMBRA1 in regulating DNA double-strand breaks“. Cancer Research 83, Nr. 7_Supplement (04.04.2023): 6107. http://dx.doi.org/10.1158/1538-7445.am2023-6107.
Der volle Inhalt der QuelleYan, Dan, Yao Zhang, Yan Zhang, Jingxi Zhang, Bin Wang, Huixian Chen, Jingxue Shi, Xiaoling Lin, Jincong Zhuo und Kevin Zhou. „Abstract 4532: Discovery of DAT-1000A, a potent Polθ inhibitor that significantly enhances anti-tumor efficacy in combination with PARP inhibitor in homologous-recombination-deficient tumors“. Cancer Research 84, Nr. 6_Supplement (22.03.2024): 4532. http://dx.doi.org/10.1158/1538-7445.am2024-4532.
Der volle Inhalt der QuellePatterson-Fortin, Jeffrey, Heta Jadhav, Constantia Pantelidou, Tin Phan, Carter Grochala, Anita K. Mehta, Jennifer L. Guerriero et al. „Abstract 6190: Polymerase theta inhibition activates the cGAS-STING pathway and cooperates with immune checkpoint blockade in BRCA-deficient cancers“. Cancer Research 83, Nr. 7_Supplement (04.04.2023): 6190. http://dx.doi.org/10.1158/1538-7445.am2023-6190.
Der volle Inhalt der QuelleLe, Bac Viet, Umeshkumar Vekariya, Monika Toma, Margaret Nieborowska-Skorska, Marie-Christine Caron, George Vassiliou, Malgorzata Gozdecka et al. „Inactivation of DNA Polymerase Theta (PolΘ) Is Synthetic Lethal in DNMT3A Mutated Myeloid Malignancies - Potential Clinical Applications“. Blood 142, Supplement 1 (28.11.2023): 580. http://dx.doi.org/10.1182/blood-2023-174333.
Der volle Inhalt der QuelleSamnotra, Vivek, Veronica Moroz, Luda Shtessel, Mita Kuchimanchi, Patrick Hanafin, Malar Pannirselvam, Aishwarya Bhaskar et al. „First-in-human, phase 1/2 study of GSK4524101, an oral DNApolymerase theta inhibitor (POLQi), alone or combined with the poly(ADP-ribose) polymerase (PARP) inhibitor (PARPi) niraparib in adults with solid tumors.“ Journal of Clinical Oncology 42, Nr. 16_suppl (01.06.2024): TPS3174. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.tps3174.
Der volle Inhalt der QuelleToma, Monika, Margaret Nieborowska-Skorska, Adam Karami, Monika Pepek, Tomasz Stoklosa und Tomasz Skorski. „Clonal Targeting of DNA Damage Response Pathways Eradicates Myeloproliferative Neoplasms“. Blood 142, Supplement 1 (28.11.2023): 120. http://dx.doi.org/10.1182/blood-2023-174280.
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