Artykuły w czasopismach na temat „BRCA1”
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Friedlander, Michael, Kathleen N. Moore, Nicoletta Colombo, Giovanni Scambia, Byoung-Gie Kim, Ana Oaknin, Alla Sergeevna Lisyanskaya i in. "Efficacy of maintenance olaparib for newly diagnosed, advanced ovarian cancer patients (pts) by BRCA1 or BRCA2 mutation in the phase III SOLO1 trial." Journal of Clinical Oncology 37, nr 15_suppl (20.05.2019): 5551. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.5551.
Pełny tekst źródłaZhang, Yinuo. "BRCA1, BRCA2 and primary ovarian insufficiency". E3S Web of Conferences 165 (2020): 05009. http://dx.doi.org/10.1051/e3sconf/202016505009.
Pełny tekst źródłaShao, Changxia, Michael S. Chang, Fred C. Lam, Andrew R. Marley, Huilin Tang, Yiqing Song, Chelsey Miller i in. "A Systematic Review and Meta-Analysis on the Prognostic Value of BRCA Mutations, Homologous Recombination Gene Mutations, and Homologous Recombination Deficiencies in Cancer". Journal of Oncology 2022 (20.07.2022): 1–12. http://dx.doi.org/10.1155/2022/5830475.
Pełny tekst źródłaRichters, Lisa Katharina, Philip C. Schouten, Stefan Kommoss, Jan Hauke, Alexander Burges, Dimo Dietrich, Ahmed El-Balat i in. "BRCA-like classification in ovarian cancer: Results from the AGO-TR1-trial." Journal of Clinical Oncology 35, nr 15_suppl (20.05.2017): 5546. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.5546.
Pełny tekst źródłaWang, Aifen, Robert W. Holloway, Lijuan Cui, Yan Sun i Zihan Zhao. "Association betweenBRCA1 and BRCA2 mutations and prognosis in women with endometrial carcinoma." Journal of Clinical Oncology 37, nr 15_suppl (20.05.2019): e17115-e17115. http://dx.doi.org/10.1200/jco.2019.37.15_suppl.e17115.
Pełny tekst źródłaLabidi-Galy, Sana Intidhar, Manuel Rodrigues, Jose L. Sandoval, Jean Emmanuel Kurtz, Florian Heitz, Anna Maria Mosconi, Ignacio Romero i in. "Efficacy of maintenance olaparib plus bevacizumab in patients with newly diagnosed advanced ovarian cancer according to BRCA mutation genotype in the phase III PAOLA-1/ENGOT-ov25 trial." Journal of Clinical Oncology 40, nr 16_suppl (1.06.2022): 5571. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.5571.
Pełny tekst źródłaLabidi-Galy, Sana Intidhar, Manuel Rodrigues, Jose L. Sandoval, Jean Emmanuel Kurtz, Florian Heitz, Anna Maria Mosconi, Ignacio Romero i in. "Efficacy of maintenance olaparib plus bevacizumab in patients with newly diagnosed advanced ovarian cancer according to BRCA mutation genotype in the phase III PAOLA-1/ENGOT-ov25 trial." Journal of Clinical Oncology 40, nr 16_suppl (1.06.2022): 5571. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.5571.
Pełny tekst źródłaPonce, Jordi, Sergi Fernandez-Gonzalez, Iris Calvo, Maite Climent, Judith Peñafiel, Lidia Feliubadaló, Alex Teulé i in. "Assessment of ovarian reserve and reproductive outcomes in BRCA1 or BRCA2 mutation carriers". International Journal of Gynecologic Cancer 30, nr 1 (27.11.2019): 83–88. http://dx.doi.org/10.1136/ijgc-2019-000626.
Pełny tekst źródłaSy, Shirley M. H., Michael S. Y. Huen i Junjie Chen. "PALB2 is an integral component of the BRCA complex required for homologous recombination repair". Proceedings of the National Academy of Sciences 106, nr 17 (15.04.2009): 7155–60. http://dx.doi.org/10.1073/pnas.0811159106.
Pełny tekst źródłaArun, Banu, Angelica Gutierrez Barrera, Rachel M. Layman, Stephen K. Gruschkus, Isabelle Bedrosian, Constance T. Albarracin, Carlos Hernando Barcenas, Vicente Valero, Jennifer Keating Litton i Debu Tripathy. "Outcome of patients with breast cancer and a germline BRCA mutation in a prospective cohort." Journal of Clinical Oncology 38, nr 15_suppl (20.05.2020): 1544. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.1544.
Pełny tekst źródłaFoglietta, Jennifer, Vienna Ludovini, Fortunato Bianconi, Lorenza Pistola, Maria Sole Reda, Antonella Al-Refaie, Francesca Romana Tofanetti i in. "Prevalence and Spectrum of BRCA Germline Variants in Central Italian High Risk or Familial Breast/Ovarian Cancer Patients: A Monocentric Study". Genes 11, nr 8 (12.08.2020): 925. http://dx.doi.org/10.3390/genes11080925.
Pełny tekst źródłaShao, Changxia, Andrew Marley, Huilin Tang, Jun Wan, Chelsey Miller, Madeline Brown, Yiqing Song, Jiali Han i Gboyega Adeboyeje. "A comprehensive literature review and meta-analysis on prognostic value of BRCAm, HRRm and HRD+ across tumor types." Journal of Clinical Oncology 39, nr 15_suppl (20.05.2021): 3125. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.3125.
Pełny tekst źródłaRhiem, K., C. Fischer, K. Bosse, B. Wappenschmidt i R. K. Schmutzler. "Increased risk of cervical cancer in high-risk families with and without mutations in the BRCA1 and BRCA2 genes". Journal of Clinical Oncology 25, nr 18_suppl (20.06.2007): 5588. http://dx.doi.org/10.1200/jco.2007.25.18_suppl.5588.
Pełny tekst źródłaKauff, Noah D., Susan M. Domchek, Tara M. Friebel, Mark E. Robson, Johanna Lee, Judy E. Garber, Claudine Isaacs i in. "Risk-Reducing Salpingo-Oophorectomy for the Prevention of BRCA1- and BRCA2-Associated Breast and Gynecologic Cancer: A Multicenter, Prospective Study". Journal of Clinical Oncology 26, nr 8 (10.03.2008): 1331–37. http://dx.doi.org/10.1200/jco.2007.13.9626.
Pełny tekst źródłaBrankovic-Magic, Mirjana, Jelena Dobricic, Radmila Jankovic, Irene Konstantopoulou, Drakoulis Yannoukakos i Sinisa Radulovic. "Identifying and testing for hereditary susceptibility to breast/ovarian cancer in Serbia: Where are we now?" Archive of Oncology 14, nr 3-4 (2006): 131–35. http://dx.doi.org/10.2298/aoo0604131b.
Pełny tekst źródłaTun, N. M., G. M. Villani i K. Ong. "Risk of having BRCA mutations in women with triple-negative breast cancer: A systematic review and meta-analysis." Journal of Clinical Oncology 29, nr 27_suppl (20.09.2011): 160. http://dx.doi.org/10.1200/jco.2011.29.27_suppl.160.
Pełny tekst źródłaMurciano-Goroff, Yonina R., Alison M. Schram, Ezra Rosen, Yelena Y. Janjigian, Michael F. Berger, Mark Donoghue, Chaitanya Bandlamudi i Alexander E. Drilon. "BRCA reversion mutations in a pan-cancer cohort to reveal BRCA-dependence in select noncanonical BRCA-mutant histologies." Journal of Clinical Oncology 39, nr 15_suppl (20.05.2021): 3012. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.3012.
Pełny tekst źródłaReisinger, Raquel, Sergiusz Wesolowski, Umang Swami, Pedro C. Barata, Edgar Javier Hernandez, Roberto Nussenzveig, Gordon Lemmon i in. "Differences in the genomic landscape of advanced prostate cancer (aPC) patients (pts) with BRCA1 versus BRCA2 mutations as detected by machine learning analysis of the comprehensive genomic profile (CGP) of cell-free DNA (cfDNA)." Journal of Clinical Oncology 39, nr 6_suppl (20.02.2021): 162. http://dx.doi.org/10.1200/jco.2021.39.6_suppl.162.
Pełny tekst źródłaBracci, Ciarapica, Zabaleta, Tartaglione, Pirozzi, Giuliani, Piva i in. "BRCA1 and BRCA2 Gene Expression: Diurnal Variability and Influence of Shift Work". Cancers 11, nr 8 (9.08.2019): 1146. http://dx.doi.org/10.3390/cancers11081146.
Pełny tekst źródłaChahla, Elie, Antonio Cheesman, Suzanne M. Mahon, Robert W. Garrett, Ben P. Bradenham, Theresa L. Schwartz, Louay Omran, Jason R. Taylor i Samer Alkaade. "Frequency and Significance of Abnormal Pancreatic Imaging in Patients with BRCA1 and BRCA2 Genetic Mutations". Scientifica 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/5619358.
Pełny tekst źródłaAtchley, Deann P., Constance T. Albarracin, Adriana Lopez, Vicente Valero, Christopher I. Amos, Ana Maria Gonzalez-Angulo, Gabriel N. Hortobagyi i Banu K. Arun. "Clinical and Pathologic Characteristics of Patients With BRCA-Positive and BRCA-Negative Breast Cancer". Journal of Clinical Oncology 26, nr 26 (10.09.2008): 4282–88. http://dx.doi.org/10.1200/jco.2008.16.6231.
Pełny tekst źródłaKiechle, M. "Hereditäres Mammakarzinom: BRCA1, BRCA2 und BRCA3". Senologie - Zeitschrift für Mammadiagnostik und -therapie 8, nr 02 (czerwiec 2011): 103. http://dx.doi.org/10.1055/s-0031-1271518.
Pełny tekst źródłaSokol, Ethan, Smruthy Sivakumar, Brennan Decker, Jeffrey Ross i Priti Hegde. "Abstract P5-13-02: Serially biopsied BRCA1/2 mutant breast tumors frequently acquire alterations in BRCA1, BRCA2, and CREBBP". Cancer Research 82, nr 4_Supplement (15.02.2022): P5–13–02—P5–13–02. http://dx.doi.org/10.1158/1538-7445.sabcs21-p5-13-02.
Pełny tekst źródłaBisgin, Atil, Ibrahim Boga, Ozge Sonmezler, Cem Mujde, Abdullah Hanta i Sevcan Tug Bozdogan. "Meta-analysis and single-center experience on the comprehensive genomic characterization and landscape of BRCA1 and BRCA2 in Turkey." Journal of Clinical Oncology 38, nr 15_suppl (20.05.2020): e13611-e13611. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e13611.
Pełny tekst źródłaSahnane, Nora, Ileana Carnevali, Giorgio Formenti, Jvan Casarin, Sofia Facchi, Raffaella Bombelli, Eleonora Di Lauro i in. "BRCA Methylation Testing Identifies a Subset of Ovarian Carcinomas without Germline Variants That Can Benefit from PARP Inhibitor". International Journal of Molecular Sciences 21, nr 24 (19.12.2020): 9708. http://dx.doi.org/10.3390/ijms21249708.
Pełny tekst źródłaЖурман, В. Н., Н. Г. Плехова i М. Л. Филипенко. "Mutational Status of BRCA Genes in Ovarian Cancer". Евразийский онкологический журнал, nr 2 (16.08.2022): 118–25. http://dx.doi.org/10.34883/pi.2022.10.2.016.
Pełny tekst źródłaZajchowski, Deborah A., Hugh Salamon i Ken D. Yamaguchi. "Proliferation pathway aberration frequencies in BRCA1- and BRCA2-mutated ovarian cancers." Journal of Clinical Oncology 30, nr 15_suppl (20.05.2012): 5074. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.5074.
Pełny tekst źródłaVidra, Radu, Tudor Eliade Ciuleanu, Adina Nemeș, Oana Pascu, Ana Maria Heroiu, Nicoleta Antone, Andreea Iulia Vidrean i in. "Spectrum of BRCA1/2 Mutations in Romanian Breast and Ovarian Cancer Patients". International Journal of Environmental Research and Public Health 19, nr 7 (4.04.2022): 4314. http://dx.doi.org/10.3390/ijerph19074314.
Pełny tekst źródłaKeung, Yi-Kong, Adriana Hu, Annie Yeung, Amy Chan i Eddie Hu. "Higher prevalence of BRCA2 mutations among Chinese breast cancer patients in a community oncology clinic." Journal of Clinical Oncology 30, nr 15_suppl (20.05.2012): e12017-e12017. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.e12017.
Pełny tekst źródłaMitamura, Takashi, Masayuki Sekine, Masami Arai, Yuka Shibata, Momoko Kato, Shiro Yokoyama, Hiroko Yamashita i in. "Risk factors for lymph node metastasis of ovarian, fallopian tube and primary peritoneal cancer in hereditary breast and ovarian cancer syndrome". Japanese Journal of Clinical Oncology 50, nr 12 (17.07.2020): 1380–85. http://dx.doi.org/10.1093/jjco/hyaa124.
Pełny tekst źródłaWen, Lu, Xiuxiu Li, Junping Shi, Shuo Zhang, Rui Wang, Ming Yao i Jun Guo. "Allele-specific expression mediates primary resistance to poly (ADP-ribose) polymerase inhibitor therapy in a case of BRCA1/2 double-germline mutant gastric cancer". Journal of International Medical Research 48, nr 3 (27.11.2019): 030006051988622. http://dx.doi.org/10.1177/0300060519886226.
Pełny tekst źródłaFaermann, Renata, Eitan Friedman, Orit Kaidar-Person, Jonathan Weidenfeld, Malka Brodsky, Anat Shalmon, Osnat Halshtok Neiman i in. "Ductal Carcinoma In Situ (DCIS) Diagnosed by MRI-Guided Biopsy among BRCA1/BRCA2 Mutation Carriers". Breast Journal 2022 (27.10.2022): 1–7. http://dx.doi.org/10.1155/2022/4317693.
Pełny tekst źródłaLattimore, Vanessa, John Pearson, Arthur Morley-Bunker, kConFab Investigators, Amanda Spurdle, Bridget Robinson, Margaret Currie i Logan Walker. "Quantifying BRCA1 and BRCA2 mRNA Isoform Expression Levels in Single Cells". International Journal of Molecular Sciences 20, nr 3 (6.02.2019): 693. http://dx.doi.org/10.3390/ijms20030693.
Pełny tekst źródłaAyoub, Jean-Pierre, Hans Wildiers, Michael Friedlander, Banu K. Arun, Hyo S. Han, Shannon Puhalla, Yaroslav Shparyk i in. "Safety and efficacy of veliparib plus carboplatin/paclitaxel in patients with HER2-negative metastatic or locally advanced breast cancer: subgroup analyses by germline BRCA1/2 mutations and hormone receptor status from the phase-3 BROCADE3 trial". Therapeutic Advances in Medical Oncology 13 (styczeń 2021): 175883592110596. http://dx.doi.org/10.1177/17588359211059601.
Pełny tekst źródłaJung, J., E. Kang, J. M. Gwak, A. N. Seo, S. Y. Park, A. S. Lee, H. Baek, S. Chae, E. K. Kim i S. W. Kim. "Association between basal-like phenotype and BRCA1/2 germline mutations in Korean breast cancer patients". Current Oncology 23, nr 5 (26.10.2016): 298. http://dx.doi.org/10.3747/co.23.3054.
Pełny tekst źródłaLi, Jiaheng, Bojin Zhao, Teng Huang, Zixin Qin i San Ming Wang. "Human BRCA pathogenic variants were originated during recent human history". Life Science Alliance 5, nr 5 (14.02.2022): e202101263. http://dx.doi.org/10.26508/lsa.202101263.
Pełny tekst źródłaWeitzel, Jeffrey N., Jessica Clague, Arelis Martir-Negron, Raquel Ogaz, Josef Herzog, Charité Ricker, Chelsy Jungbluth i in. "Prevalence and Type ofBRCAMutations in Hispanics Undergoing Genetic Cancer Risk Assessment in the Southwestern United States: A Report From the Clinical Cancer Genetics Community Research Network". Journal of Clinical Oncology 31, nr 2 (10.01.2013): 210–16. http://dx.doi.org/10.1200/jco.2011.41.0027.
Pełny tekst źródłaPal, Tuya, Deborah Cragun, Xuefeng Wang, Sean J. Yoder, Tania MESA, Marilin Rosa, Ann Tezak, Anne Weidner, Susan Thomas Vadaparampil i Catherine Phelan. "Characterization of germline and tumor genomic profile in unselected young black breast cancer patients." Journal of Clinical Oncology 35, nr 15_suppl (20.05.2017): e13090-e13090. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.e13090.
Pełny tekst źródłaNovikova, EI, EA Kudinova, VK Bozhenko i VA Solodkiy. "Characteristics of BRCA-associated breast cancer in the population of the Russian Federation". Features of HIV and SARS-CoV-2 coinfection in a pandemic, nr 2021(1) (luty 2021): 24–29. http://dx.doi.org/10.24075/brsmu.2021.006.
Pełny tekst źródłaGasparri, Maria Luisa, Serena Bellaminutti, Ammad Ahmad Farooqi, Ilaria Cuccu, Violante Di Donato i Andrea Papadia. "Endometrial Cancer and BRCA Mutations: A Systematic Review". Journal of Clinical Medicine 11, nr 11 (31.05.2022): 3114. http://dx.doi.org/10.3390/jcm11113114.
Pełny tekst źródłaShatavi, Seerin Viviane, Lindsay Dohany, Mohammad Muhsin Chisti, Ishmael A. Jaiyesimi i Dana Zakalik. "Unique genetic characteristics of BRCA mutation carriers in a cohort of Arab American women." Journal of Clinical Oncology 31, nr 15_suppl (20.05.2013): 1541. http://dx.doi.org/10.1200/jco.2013.31.15_suppl.1541.
Pełny tekst źródłaCaleca, Laura, Mara Colombo, Thomas van Overeem Hansen, Conxi Lázaro, Siranoush Manoukian, Michael T. Parsons, Amanda B. Spurdle i Paolo Radice. "GFP-Fragment Reassembly Screens for the Functional Characterization of Variants of Uncertain Significance in Protein Interaction Domains of the BRCA1 and BRCA2 Genes". Cancers 11, nr 2 (28.01.2019): 151. http://dx.doi.org/10.3390/cancers11020151.
Pełny tekst źródłaChoi, Doo Ho, Min Hyuk Lee, Allen E. Bale, Darryl Carter i Bruce G. Haffty. "Incidence of BRCA1 and BRCA2 Mutations in Young Korean Breast Cancer Patients". Journal of Clinical Oncology 22, nr 9 (1.05.2004): 1638–45. http://dx.doi.org/10.1200/jco.2004.04.179.
Pełny tekst źródłaFerrone, Cristina R., Douglas A. Levine, Laura H. Tang, Peter J. Allen, William Jarnagin, Murray F. Brennan, Kenneth Offit i Mark E. Robson. "BRCA Germline Mutations in Jewish Patients With Pancreatic Adenocarcinoma". Journal of Clinical Oncology 27, nr 3 (20.01.2009): 433–38. http://dx.doi.org/10.1200/jco.2008.18.5546.
Pełny tekst źródłaCastro, Elena, David Olmos, Chee Leng Goh, Ed Saunders, Daniel Leongamornlert, Malgorzata Tymrakiewicz, Elizabeth Bancroft i in. "Effect of germ-line BRCA mutations in biochemical relapse and survival after treatment for localized prostate cancer." Journal of Clinical Oncology 31, nr 6_suppl (20.02.2013): 29. http://dx.doi.org/10.1200/jco.2013.31.6_suppl.29.
Pełny tekst źródłaArun, Banu, Soley Bayraktar, Diane D. Liu, Angelica M. Gutierrez Barrera, Deann Atchley, Lajos Pusztai, Jennifer Keating Litton i in. "Response to Neoadjuvant Systemic Therapy for Breast Cancer in BRCA Mutation Carriers and Noncarriers: A Single-Institution Experience". Journal of Clinical Oncology 29, nr 28 (1.10.2011): 3739–46. http://dx.doi.org/10.1200/jco.2011.35.2682.
Pełny tekst źródłaKwong, A., L. Wong, C. Wong, F. Law, E. Tang, W. Chan, E. S. Ma, J. M. Ford i D. W. West. "Clinical and pathological characteristics of Chinese patients with BRCA related breast cancer". Journal of Clinical Oncology 27, nr 15_suppl (20.05.2009): e22226-e22226. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.e22226.
Pełny tekst źródłaGraeser, Monika K., Christoph Engel, Kerstin Rhiem, Dorothea Gadzicki, Ulrich Bick, Karin Kast, Ursula G. Froster i in. "Contralateral Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers". Journal of Clinical Oncology 27, nr 35 (10.12.2009): 5887–92. http://dx.doi.org/10.1200/jco.2008.19.9430.
Pełny tekst źródłaJoó, József Gábor, Szabolcs Ládi, B. Zsolt Nagy i Zoltán Langmár. "Management of hereditary ovarian cancer". Orvosi Hetilap 152, nr 40 (październik 2011): 1596–608. http://dx.doi.org/10.1556/oh.2011.29218.
Pełny tekst źródłaSafra, Tamar, Wei-Chu V. Lai, Tara Berman, Lucia Borgato, Elsa Reich, Maria Alvear, Franco Muggia i Sharon Pelles-Avraham. "BRCA mutations and outcome in epithelial ovarian cancer (EOC): Experience in ethnically diverse groups." Journal of Clinical Oncology 30, nr 15_suppl (20.05.2012): 5078. http://dx.doi.org/10.1200/jco.2012.30.15_suppl.5078.
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