Articoli di riviste sul tema "Chromoplexie"
Cita una fonte nei formati APA, MLA, Chicago, Harvard e in molti altri stili
Vedi i top-50 articoli di riviste per l'attività di ricerca sul tema "Chromoplexie".
Accanto a ogni fonte nell'elenco di riferimenti c'è un pulsante "Aggiungi alla bibliografia". Premilo e genereremo automaticamente la citazione bibliografica dell'opera scelta nello stile citazionale di cui hai bisogno: APA, MLA, Harvard, Chicago, Vancouver ecc.
Puoi anche scaricare il testo completo della pubblicazione scientifica nel formato .pdf e leggere online l'abstract (il sommario) dell'opera se è presente nei metadati.
Vedi gli articoli di riviste di molte aree scientifiche e compila una bibliografia corretta.
Serbyn, Nataliia, Myrthe M. Smit, Vimathi S. Gummalla, Gregory J. Brunette e David S. Pellman. "Abstract 6105: Unravelling the mechanistic basis of chromoplexy, a mutational process driving early cancer genome evolution". Cancer Research 83, n. 7_Supplement (4 aprile 2023): 6105. http://dx.doi.org/10.1158/1538-7445.am2023-6105.
Testo completoBallas, Leslie K., Brian R. Hu e David I. Quinn. "Chromoplexy and hypoxic microenvironment drives prostate cancer". Lancet Oncology 15, n. 13 (dicembre 2014): 1419–21. http://dx.doi.org/10.1016/s1470-2045(14)71114-3.
Testo completoAshby, Cody, Michael A. Bauer, Yan Wang, Christopher P. Wardell, Ruslana G. Tytarenko, Purvi Patel, Erin Flynt et al. "Chromothripsis and Chromoplexy Are Associated with DNA Instability and Adverse Clinical Outcome in Multiple Myeloma". Blood 132, Supplement 1 (29 novembre 2018): 408. http://dx.doi.org/10.1182/blood-2018-99-117359.
Testo completoWang, Kendric, Yuzhuo Wang e Colin C. Collins. "Chromoplexy: a new paradigm in genome remodeling and evolution". Asian Journal of Andrology 15, n. 6 (26 agosto 2013): 711–12. http://dx.doi.org/10.1038/aja.2013.109.
Testo completoAshby, Cody, Eileen M. Boyle, Brian A. Walker, Michael A. Bauer, Katie Rose Ryan, Judith Dent, Anjan Thakurta, Erin Flynt, Faith E. Davies e Gareth Morgan. "Chromoplexy and Chromothripsis Are Important Prognostically in Myeloma and Deregulate Gene Function By a Range of Mechanisms". Blood 134, Supplement_1 (13 novembre 2019): 3767. http://dx.doi.org/10.1182/blood-2019-130335.
Testo completoPham, Minh-Tam N., Michael C. Haffner, Heather C. Wick, Jonathan B. Coulter, Anuj Gupta, Roshan V. Chikarmane, Harshath Gupta, Sarah Wheelan, William G. Nelson e Srinivasan Yegnasubramanian. "Abstract 680: Topoisomerase 2 beta facilitates chromatin reorganization during Androgen Receptor induced transcription and contributes to chromoplexy in prostate cancer". Cancer Research 82, n. 12_Supplement (15 giugno 2022): 680. http://dx.doi.org/10.1158/1538-7445.am2022-680.
Testo completoAnderson, Nathaniel D., Richard de Borja, Matthew D. Young, Fabio Fuligni, Andrej Rosic, Nicola D. Roberts, Simon Hajjar et al. "Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors". Science 361, n. 6405 (30 agosto 2018): eaam8419. http://dx.doi.org/10.1126/science.aam8419.
Testo completoShen, Michael M. "Chromoplexy: A New Category of Complex Rearrangements in the Cancer Genome". Cancer Cell 23, n. 5 (maggio 2013): 567–69. http://dx.doi.org/10.1016/j.ccr.2013.04.025.
Testo completoZhang, Cheng-Zhong, e David Pellman. "Cancer Genomic Rearrangements and Copy Number Alterations from Errors in Cell Division". Annual Review of Cancer Biology 6, n. 1 (11 aprile 2022): 245–68. http://dx.doi.org/10.1146/annurev-cancerbio-070620-094029.
Testo completoMustafin, R. N. "Participation of retroelements in chromoanagenesis in cancer development". Siberian journal of oncology 23, n. 5 (15 novembre 2024): 146–56. http://dx.doi.org/10.21294/1814-4861-2024-23-5-146-156.
Testo completoPararajalingam, Prasath, Laura K. Hilton, Krysta M. Coyle, Kostiantyn Dreval, Barbara Meissner, Ari Melnick, Marco A. Marra, David W. Scott e Ryan D. Morin. "Complex Structural Variation Associated with Enhancer Hijacking and Loss of Tumor Suppressors in Mantle Cell Lymphoma". Blood 138, Supplement 1 (5 novembre 2021): 675. http://dx.doi.org/10.1182/blood-2021-153162.
Testo completoSweet-Cordero, E. Alejandro, e Jaclyn A. Biegel. "The genomic landscape of pediatric cancers: Implications for diagnosis and treatment". Science 363, n. 6432 (14 marzo 2019): 1170–75. http://dx.doi.org/10.1126/science.aaw3535.
Testo completoMenghi, Francesca, Koichiro Inaki, XingYi Woo, Pooja A. Kumar, Krzysztof R. Grzeda, Ankit Malhotra, Vinod Yadav et al. "The tandem duplicator phenotype as a distinct genomic configuration in cancer". Proceedings of the National Academy of Sciences 113, n. 17 (7 aprile 2016): E2373—E2382. http://dx.doi.org/10.1073/pnas.1520010113.
Testo completoHattori, Atsushi, e Maki Fukami. "Established and Novel Mechanisms Leading to de novo Genomic Rearrangements in the Human Germline". Cytogenetic and Genome Research 160, n. 4 (2020): 167–76. http://dx.doi.org/10.1159/000507837.
Testo completoBakloushinskaya, Irina. "Chromosome Changes in Soma and Germ Line: Heritability and Evolutionary Outcome". Genes 13, n. 4 (28 marzo 2022): 602. http://dx.doi.org/10.3390/genes13040602.
Testo completoPitel, Beth A., Neeraj Sharma, Cinthya Zepeda-Mendoza, James B. Smadbeck, Kathryn E. Pearce, Stephanie A. Smoley, Joselle Cook et al. "Clinical Value of Next Generation Sequencing in the Detection of Recurring Structural Rearrangements and Copy Number Abnormalities in Acute Myeloid Leukemia". Blood 136, Supplement 1 (5 novembre 2020): 21–22. http://dx.doi.org/10.1182/blood-2020-139691.
Testo completoLiu, Enze, Nathan Becker, Parvathi Sudha, Aneta Mikulasova, Mohammad Abu Zaid, Attaya Suvannasankha, Kelvin P. Lee, Rafat Abonour e Brian A. Walker. "Unraveling Diverse Mechanisms of Complex Structural Variant Interactions through Multiomic Data in Multiple Myeloma". Blood 142, Supplement 1 (28 novembre 2023): 641. http://dx.doi.org/10.1182/blood-2023-186262.
Testo completoAksenova, Anna Y., Anna S. Zhuk, Artem G. Lada, Irina V. Zotova, Elena I. Stepchenkova, Ivan I. Kostroma, Sergey V. Gritsaev e Youri I. Pavlov. "Genome Instability in Multiple Myeloma: Facts and Factors". Cancers 13, n. 23 (26 novembre 2021): 5949. http://dx.doi.org/10.3390/cancers13235949.
Testo completoYin, Xia, Rui Bi, Pengfei Ma, Shengzhe Zhang, Yang Zhang, Yunheng Sun, Yi Zhang et al. "Multiregion whole-genome sequencing depicts intratumour heterogeneity and punctuated evolution in ovarian clear cell carcinoma". Journal of Medical Genetics 57, n. 9 (20 dicembre 2019): 605–9. http://dx.doi.org/10.1136/jmedgenet-2019-106418.
Testo completoKeskus, Ayse, Tanveer Ahmad, Ataberk Donmez, Yi Xie, Isabel Rodriguez, Rose Milano, Nicole Rossi et al. "Abstract 4289: Long-read, assembly-based characterization of rearranged cancer karyotypes". Cancer Research 83, n. 7_Supplement (4 aprile 2023): 4289. http://dx.doi.org/10.1158/1538-7445.am2023-4289.
Testo completoArya, Priyanka, Jennelle C. Hodge, Peggy A. Matlock, Gail H. Vance e Amy M. Breman. "Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis". Cytogenetic and Genome Research 160, n. 11-12 (2020): 671–79. http://dx.doi.org/10.1159/000512898.
Testo completoBraunstein, Marc, Patrick Blaney e Gareth J. Morgan. "Whole-Genome Sequencing Identifies Structural Variation As a Key Driver of Disease Relapse and Aggressive Clinical Behavior in Multiple Myeloma". Blood 142, Supplement 1 (28 novembre 2023): 2773. http://dx.doi.org/10.1182/blood-2023-191008.
Testo completoRustad, Even H., Venkata Yellapantula, Dominik Glodzik, Gunes Gundem, Daniel A. Leongamornlert, Peter J. Campbell, Elli Papaemmanuil, Ola Landgren e Francesco Maura. "Revealing the Impact of Recurrent and Rare Structural Variations in Multiple Myeloma". Blood 134, Supplement_1 (13 novembre 2019): 576. http://dx.doi.org/10.1182/blood-2019-126392.
Testo completoMustafin, R. N. "Relationship of TP53 gene with retroelements in urogenital organs carcinogenesis". Cancer Urology 18, n. 1 (6 maggio 2022): 136–42. http://dx.doi.org/10.17650/1726-9776-2022-18-1-136-142.
Testo completoOey, Harald, Marissa Daniels, Vandana Relan, Tian Mun Chee, Morgan R. Davidson, Ian A. Yang, Jonathan J. Ellis, Kwun M. Fong, Lutz Krause e Rayleen V. Bowman. "Whole-genome sequencing of human malignant mesothelioma tumours and cell lines". Carcinogenesis 40, n. 6 (25 aprile 2019): 724–34. http://dx.doi.org/10.1093/carcin/bgz066.
Testo completoCyrta, Joanna, Joel Rosiene, Rohan Bareja, Sarah Kudman, Wael Al Zoughbi, Samaneh Motanagh, David C. Wilkes et al. "Whole-genome characterization of myoepithelial carcinomas of the soft tissue". Molecular Case Studies 8, n. 7 (dicembre 2022): a006227. http://dx.doi.org/10.1101/mcs.a006227.
Testo completoChoi, Jungmin, Aranzazu Manzano, Weilai Dong, Stefania Bellone, Elena Bonazzoli, Luca Zammataro, Xiaotong Yao et al. "Integrated mutational landscape analysis of uterine leiomyosarcomas". Proceedings of the National Academy of Sciences 118, n. 15 (5 aprile 2021): e2025182118. http://dx.doi.org/10.1073/pnas.2025182118.
Testo completoTakahashi, Katsuhito, Ayako Motoki, Jun Yashima, Noriyuki Masaki, Hiroko Sano, Hiromasa Yamamoto, Junichi Sou et al. "Frequent mutations of genes predisposing to Rho GTPase signal activation and autophagy inhibition in metastatic soft tissue sarcoma unveiled by paired somatic and germline genomic analyses." Journal of Clinical Oncology 37, n. 15_suppl (20 maggio 2019): 11071. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.11071.
Testo completoHovens, Christopher, Matthew Hong, Geoff Macintyre, David Wedge, Peter Van Loo, Sebastian LunkePhD, Ludmil Alexandrov et al. "Tracking clonal diversity in metastatic prostate cancer progression." Journal of Clinical Oncology 33, n. 7_suppl (1 marzo 2015): 193. http://dx.doi.org/10.1200/jco.2015.33.7_suppl.193.
Testo completoOlsen, André, Francesco Favero, Yilong Li, Etsehiwot Girma, Breon Feran, Tony Papenfuss, Kristian Helin, Jüri Reimand e Joachim Weischenfeldt. "Abstract A047: Panorama of complex structural variants in primary localized prostate cancer". Cancer Research 83, n. 11_Supplement (2 giugno 2023): A047. http://dx.doi.org/10.1158/1538-7445.prca2023-a047.
Testo completoSong, Dong, Yang Zhao, Quanhua Mu, Zhuangzhuang Liang, Jiajia Wang, Liangliang Cao, Luonan Chen, jie ma e Jiguang Wang. "EPCO-31. GERMLINE AND SOMATIC MUTATIONS IN PEDIATRIC GERM CELL TUMORS". Neuro-Oncology 23, Supplement_6 (2 novembre 2021): vi8—vi9. http://dx.doi.org/10.1093/neuonc/noab196.030.
Testo completoKim, Sheehyun, Hyundong Yoon, Youngil Koh e Sung-Soo Yoon. "Abstract 6073: Distinct subtype of multiple myeloma revealed by whole genome and transcriptome sequencing". Cancer Research 83, n. 7_Supplement (4 aprile 2023): 6073. http://dx.doi.org/10.1158/1538-7445.am2023-6073.
Testo completoKaltenbach, Sophie, Yannick LE Bris, Bruno Tesson, Aurore Touzart, Guillaume Charbonnier, Vincent Ribrag, Remy Gressin et al. "Optical Genome Mapping Provides New Molecular Insights in High-Risk Mantle Cell Lymphoma: A Lysa Study". Blood 142, Supplement 1 (28 novembre 2023): 6107. http://dx.doi.org/10.1182/blood-2023-173815.
Testo completoMaura, Francesco, Daniel Leongamornlert, Nicos Angelopoulos, Kevin J. Dawson, Mehmet Kemal Samur, Raphael Szalat, Yu-Tzu Tai et al. "The Landscape of Structural Variant Signatures in Multiple Myeloma Identifies Distinct Disease Subgroups with Implications for Pathogenesis". Blood 132, Supplement 1 (29 novembre 2018): 109. http://dx.doi.org/10.1182/blood-2018-99-112420.
Testo completoMimura, Kaito, Norio Shiba, Ai Okada, Kenichi Chiba, Kentaro Watanabe, Takao Deguchi, Kentaro Ohki et al. "Whole-Genome Sequencing of 95 Japanese Patients with Pediatric Acute Myeloid Leukemia". Blood 144, Supplement 1 (5 novembre 2024): 5720. https://doi.org/10.1182/blood-2024-200476.
Testo completoKinnaman, Michael David, Simone Zaccaria, Alvin Makohon-Moore, Gunes Gundem, Juan E. Arango Ossa, Filemon S. Dela Cruz, Paul A. Meyers et al. "Abstract 3556: Assessing patterns of genomic instability in recurrent osteosarcoma". Cancer Research 83, n. 7_Supplement (4 aprile 2023): 3556. http://dx.doi.org/10.1158/1538-7445.am2023-3556.
Testo completoNadeu, Ferran, Romina Royo, Ramon Massoni-Badosa, Beatriz Garcia-Torre, Martí Duran-Ferrer, Kevin J. Dawson, Marta Kulis et al. "Abstract 3795: Early seeding of Richter transformation in chronic lymphocytic leukemia". Cancer Research 82, n. 12_Supplement (15 giugno 2022): 3795. http://dx.doi.org/10.1158/1538-7445.am2022-3795.
Testo completoTytgat, Godelieve, Lieke van Zogchel, Nathalie Lak, Nina Gelineau, Julia Sprokkerieft, Alexandra Letunovska, Marry van den Heuvel et al. "Abstract PR005: A toolbox for the use of cfDNA in pediatric cancer patients". Cancer Research 84, n. 17_Supplement (5 settembre 2024): PR005. http://dx.doi.org/10.1158/1538-7445.pediatric24-pr005.
Testo completoLiu, Enze, Nathan Becker, Parvathi Sudha, Aneta Mikulasova, Rafat Abonour e Brian A. Walker. "Reconstructing Catastrophic Chromothripsis Events Using Multiomic Data Reveals Their Functional Impact in Multiple Myeloma". Blood 144, Supplement 1 (5 novembre 2024): 4644. https://doi.org/10.1182/blood-2024-205167.
Testo completoNacheva, Elisabeth P., Temenuzhka Boneva, Jenny O'Nions, Andrew J. Wilson, Ke Xu, Robert Baker e Rajeev Gupta. "Chromoanagenesis in Haematological Malignancy: Review of Samples from Patients with Acute Leukemia and MDS". Blood 142, Supplement 1 (28 novembre 2023): 1564. http://dx.doi.org/10.1182/blood-2023-186105.
Testo completoYang, Hui, Guillermo Garcia-Manero, Guillermo Montalban-Bravo, Kelly S. Chien, Awdesh Kalia, Zhenya Tang, Yue Wei et al. "High-Throughput Characterization of Cytogenomic Heterogeneity of MDS Using High-Resolution Optical Genome Mapping". Blood 138, Supplement 1 (5 novembre 2021): 105. http://dx.doi.org/10.1182/blood-2021-154005.
Testo completoYellapantula, Venkata D., Even H. Rustad, Dominik Glozdik, Gunes Gundem, Jun Fan, Juan Medina, Akshar Patel et al. "Whole Genome Sequencing of Extramedullary Myeloma Autopsy Tumors Reveals a Genomic Portrait at Culmination of Clonal Convergence". Blood 132, Supplement 1 (29 novembre 2018): 3169. http://dx.doi.org/10.1182/blood-2018-99-118740.
Testo completoMaclachlan, Kylee H., Tina Bagratuni, Efstathios Kastritis, Bachisio Ziccheddu, Sydney X. Lu, Venkata D. Yellapantula, Christopher Famulare et al. "The Genomic Landscape of Waldenström Macroglobulinemia Reveals Sustained Germinal Center Activity and Late-Developing Copy Number Aberrations". Blood 138, Supplement 1 (5 novembre 2021): 2394. http://dx.doi.org/10.1182/blood-2021-148095.
Testo completoSamur, Mehmet K., Marco Roncador, Anil Aktas-Samur, Mariateresa Fulciniti, Abdul Hamid Bazarbachi, Raphael Szalat, Masood A. Shammas et al. "High-Dose Melphalan Significantly Increases Mutational Burden in Multiple Myeloma Cells at Relapse: Results from a Randomized Study in Multiple Myeloma". Blood 136, Supplement 1 (5 novembre 2020): 4–5. http://dx.doi.org/10.1182/blood-2020-139014.
Testo completoBlaney, Patrick, Eileen M. Boyle, Yubao Wang, Hussein Ghamlouch, Jinyoung Choi, Louis Williams, Stoeckle James et al. "Multiomic Mapping of Copy Number and Structural Variation on Chromosome 1 (Chr1) Highlights Multiple Recurrent Disease Drivers". Blood 138, Supplement 1 (5 novembre 2021): 721. http://dx.doi.org/10.1182/blood-2021-148439.
Testo completoDiamond, Benjamin, Bachisio Ziccheddu, Eileen M. Boyle, Kylee H. Maclachlan, Juan Arango Ossa, Justin Taylor, Justin Watts et al. "Chemotherapy-Related Mutational Signatures Reveal the Origins of Therapy-Related Myeloid Neoplasms". Blood 138, Supplement 1 (5 novembre 2021): 3271. http://dx.doi.org/10.1182/blood-2021-145927.
Testo completoDermawan, Josephine K., Emily Slotkin, William D. Tap, Paul Meyers, Leonard Wexler, John Healey, Fabio Vanoli, Chad M. Vanderbilt e Cristina R. Antonescu. "Chromoplexy is a frequent early clonal event in EWSR1-rearranged round cell sarcomas that can be detected using clinically validated targeted sequencing panels". Cancer Research, 9 febbraio 2024. http://dx.doi.org/10.1158/0008-5472.can-23-2573.
Testo completo"Ewing Sarcoma Gene Fusions Can Be Generated via Chromoplexy". Cancer Discovery 8, n. 10 (7 settembre 2018): 1208.1–1208. http://dx.doi.org/10.1158/2159-8290.cd-rw2018-153.
Testo completoLopez, Gonzalo, Laura E. Egolf, Federico M. Giorgi, Sharon J. Diskin e Adam A. Margolin. "svpluscnv: analysis and visualization of complex structural variation data". Bioinformatics, 14 ottobre 2020. http://dx.doi.org/10.1093/bioinformatics/btaa878.
Testo completoLi, Dong, Alanna Strong, Cuiping Hou, Helen Downes, Amanda Barone Pritchard, Pamela Mazzeo, Elaine H. Zackai, Laura K. Conlin e Hakon Hakonarson. "Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism". Molecular Cytogenetics 15, n. 1 (5 agosto 2022). http://dx.doi.org/10.1186/s13039-022-00610-4.
Testo completo