المؤلفون: WANG Hui, WANG Xia, GAO Yi, XU Jing, YU Xiaojuan, FAN Fangqin, DING Yan, KANG Yu

المصدر: Zhongguo aizheng zazhi, Vol 33, Iss 5, Pp 499-505 (2023)

مصطلحات موضوعية: hereditary breast-ovarian cancer syndrome, brca1/2 genes, first-degree relatives, gene screening, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: http://www.china-oncology.com/fileup/1007-3639/PDF/1686896453103-452331817.pdfTest; https://doaj.org/toc/1007-3639Test

الوصول الحر: https://doaj.org/article/5791475a68a54235b48dd68dce936b20Test

المؤلفون: Laura Caleca, Paolo Radice

المصدر: Frontiers in Oncology, Vol 13 (2023)

مصطلحات موضوعية: hereditary breast/ovarian cancer (HBOC), BRCA1, VUS, functional analyses, protein-protein interactions (PPIs), ACMG/AMP guidelines, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fonc.2023.1146604/fullTest; https://doaj.org/toc/2234-943XTest

الوصول الحر: https://doaj.org/article/3461b0b8ab7744309c2bc983b609eb65Test

المؤلفون: Tadeusz Kałużewski, Izabela Kubiak, Michał Bednarek, Jordan Sałamunia, Dorota Kucharska, Łukasz Kępczyński, Marek Stempień, Tobiasz Kubicki, Radzisław Trzciński, Zofia Gordon-Sönmez, Anna Bartosińska-Dyc, Agnieszka Gach, Bogdan Kałużewski

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 17, p 13178 (2023)

مصطلحات موضوعية: hereditary breast ovarian cancer, breast cancer, ovarian cancer, hereditary colorectal cancer, colorectal cancer, hereditary endometrial cancer, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1422-0067/24/17/13178Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test

الوصول الحر: https://doaj.org/article/bfcf268b99444af8af6f5b28fe330cc0Test

المؤلفون: Sessa, C, Balmaña, J, Bober, SL, Cardoso, MJ, Colombo, N, Curigliano, G, Domchek, SM, Evans, DG, Fischerova, D, Harbeck, N, Kuhl, C, Lemley, B, Levy-Lahad, E, Lambertini, M, Ledermann, JA, Loibl, S, Phillips, K-A, Shimon, Paluch, ESMO, Guidelines Committee

المصدر: Annals of Oncology , 34 (1) pp. 33-47. (2023)

مصطلحات موضوعية: Risk-reduction, hereditary breast & ovarian cancer syndromes, BRCA, ESMO Clinical Practice Guideline

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10158399/2/Ledermann_Risk%20reduction%20and%20screening%20of%20cancer%20in%20hereditary%20breastTest-ovarian%20cancer%20syndromes_Pre-proof.pdf; https://discovery.ucl.ac.uk/id/eprint/10158399Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10158399/2/Ledermann_Risk%20reduction%20and%20screening%20of%20cancer%20in%20hereditary%20breastTest-ovarian%20cancer%20syndromes_Pre-proof.pdf
https://discovery.ucl.ac.uk/id/eprint/10158399Test/

المؤلفون: Faria, João Paulo, Assumpção, Juliana Godoy, de Oliveira Matos, Lorena, Soardi, Fernanda Caroline, Bretz, Gabriel Pissolati Mattos, Friedman, Eitan, De Marco, Luiz

المصدر: Breast Cancer Res Treat ; ISSN:1573-7217

مصطلحات موضوعية: BRCA1, BRCA2, Germline pathogenic variants, Hereditary breast/ovarian cancer, High-risk individuals genotyping, Multigene panel testing

العلاقة: https://doi.org/10.1007/s10549-024-07383-xTest; https://pubmed.ncbi.nlm.nih.gov/38874686Test

الإتاحة: https://doi.org/10.1007/s10549-024-07383-xTest
https://pubmed.ncbi.nlm.nih.gov/38874686Test

المؤلفون: Dorra BenAyed-Guerfali, Chamseddine Kifagi, Wala BenKridis-Rejeb, Nihel Ammous-Boukhris, Wajdi Ayedi, Afef Khanfir, Jamel Daoud, Raja Mokdad-Gargouri

المصدر: Genes; Volume 13; Issue 8; Pages: 1296

مصطلحات موضوعية: BRCA1/BRCA2 genes, hereditary breast/ovarian cancer, exome sequencing, germline variants, candidate genes, pathogenic variants

جغرافية الموضوع: agris

وصف الملف: application/pdf

العلاقة: Bioinformatics; https://dx.doi.org/10.3390/genes13081296Test

الإتاحة: https://doi.org/10.3390/genes13081296Test

المؤلفون: Laura Cortesi, Bruna Baldassarri, Stefano Ferretti, Elisabetta Razzaboni, Mariangela Bella, Lauro Bucchi, Debora Canuti, Pierandrea De Iaco, Giorgio De Santis, Fabio Falcini, Vania Galli, Lea Godino, Maurizio Leoni, Anna Myriam Perrone, Marco Pignatti, Gianni Saguatti, Donatella Santini, Priscilla Sassoli de'Bianchi, Federica Sebastiani, Mario Taffurelli, Giovanni Tazzioli, Daniela Turchetti, Claudio Zamagni, Carlo Naldoni

المصدر: Cancer Medicine, Vol 9, Iss 7, Pp 2579-2589 (2020)

مصطلحات موضوعية: hereditary breast ovarian cancer, population‐based screening, Tyrer‐Cuzick model, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2045-7634Test

الوصول الحر: https://doaj.org/article/af5aedd27bb04bc5a29867b466c7c92fTest

المؤلفون: Alejandro Moles-Fernández, Joanna Domènech-Vivó, Anna Tenés, Judith Balmaña, Orland Diez, Sara Gutiérrez-Enríquez

المصدر: Cancers; Volume 13; Issue 13; Pages: 3341

مصطلحات موضوعية: spliceogenic deep intronic variants, pseudoexons, cryptic splice sites, splicing regulatory elements, hereditary breast ovarian cancer, in silico prediction tools

وصف الملف: application/pdf

العلاقة: Cancer Informatics and Big Data; https://dx.doi.org/10.3390/cancers13133341Test

الإتاحة: https://doi.org/10.3390/cancers13133341Test

المؤلفون: Arianna Nicolussi, Francesca Belardinilli, Laura Ottini, Marialaura Petroni, Carlo Capalbo, Giuseppe Giannini, Anna Coppa

المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)

مصطلحات موضوعية: BRCA2, hereditary breast/ovarian cancer, splice variant, VUS, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2324-9269Test

الوصول الحر: https://doaj.org/article/e4ea74c0396e45ec882710d7a06ef8dbTest

المؤلفون: Nicolussi A., Belardinilli F., Ottini L., Petroni M., Capalbo C., Giannini G., Coppa A.

المساهمون: Nicolussi, A., Belardinilli, F., Ottini, L., Petroni, M., Capalbo, C., Giannini, G., Coppa, A.

مصطلحات موضوعية: BRCA2, hereditary breast/ovarian cancer, splice variant, VUS

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33159495; info:eu-repo/semantics/altIdentifier/wos/WOS:000586867200001; volume:8; issue:12; numberofpages:6; journal:MOLECULAR GENETICS & GENOMIC MEDICINE; http://hdl.handle.net/11573/1525053Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85096683819

الإتاحة: https://doi.org/10.1002/mgg3.1513Test
http://hdl.handle.net/11573/1525053Test