المؤلفون: Andrzej Jasiewicz, Helena Rudnicka, Wojciech Kluźniak, Wojciech Gronwald, Tomasz Kluz, Cezary Cybulski, Anna Jakubowska, Jan Lubiński, Jacek Gronwald

المصدر: Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-5 (2022)

مصطلحات موضوعية: BRCA1 and BRCA2 mutation, Ovarian cancer, Poland, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1897-4287Test

الوصول الحر: https://doaj.org/article/8bb72149f5204bcc8c65fb5e8e223ccdTest

المؤلفون: Hamdi, Yosr, Soucy, Penny, Kuchenbaeker, Karoline B, Pastinen, Tomi, Droit, Arnaud, Lemaçon, Audrey, Adlard, Julian, Aittomäki, Kristiina, Andrulis, Irene L, Arason, Adalgeir, Arnold, Norbert, Arun, Banu K, Azzollini, Jacopo, Bane, Anita, Barjhoux, Laure, Barrowdale, Daniel, Benitez, Javier, Berthet, Pascaline, Blok, Marinus J, Bobolis, Kristie, Bonadona, Valérie, Bonanni, Bernardo, Bradbury, Angela R, Brewer, Carole, Buecher, Bruno, Buys, Saundra S, Caligo, Maria A, Chiquette, Jocelyne, Chung, Wendy K, Claes, Kathleen BM, Daly, Mary B, Damiola, Francesca, Davidson, Rosemarie, De la Hoya, Miguel, De Leeneer, Kim, Diez, Orland, Ding, Yuan Chun, Dolcetti, Riccardo, Domchek, Susan M, Dorfling, Cecilia M, Eccles, Diana, Eeles, Ros, Einbeigi, Zakaria, Ejlertsen, Bent, EMBRACE, Engel, Christoph, Gareth Evans, D, Feliubadalo, Lidia, Foretova, Lenka, Fostira, Florentia, Foulkes, William D, Fountzilas, George, Friedman, Eitan, Frost, Debra, Ganschow, Pamela, Ganz, Patricia A, Garber, Judy, Gayther, Simon A, GEMO Study Collaborators, Gerdes, Anne-Marie, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Greene, Mark H, Gronwald, Jacek, Hahnen, Eric, Hamann, Ute, Hansen, Thomas VO, Hart, Steven, Hays, John L, HEBON, Hogervorst, Frans BL, Hulick, Peter J, Imyanitov, Evgeny N, Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, Jensen, Uffe Birk, John, Esther M, Joseph, Vijai, Just, Walter, Kaczmarek, Katarzyna, Karlan, Beth Y, KConFab Investigators, Kets, Carolien M, Kirk, Judy, Kriege, Mieke, Laitman, Yael, Laurent, Maïté, Lazaro, Conxi, Leslie, Goska, Lester, Jenny, Lesueur, Fabienne, Liljegren, Annelie, Loman, Niklas, Loud, Jennifer T, Manoukian, Siranoush, Mariani, Milena

المصدر: Breast cancer research and treatment. 161(1)

مصطلحات موضوعية: EMBRACE, GEMO Study Collaborators, HEBON, KConFab Investigators, Chromosomes, Human, Pair 11, Humans, Breast Neoplasms, Genetic Predisposition to Disease, Risk, Gene Expression, Heterozygote, Mutation, Alleles, Genes, BRCA1, Genes, BRCA2, Quantitative Trait Loci, Female, Genetic Variation, Biomarkers, Tumor, BRCA1 and BRCA2 mutation carriers, Breast cancer, Cis-regulatory variants, Differential allelic expression, Genetic modifiers, Genetic susceptibility, Chromosomes, Human, Pair 11, Genes, BRCA1, BRCA2, Biomarkers, Tumor, Oncology & Carcinogenesis, Oncology and Carcinogenesis, Clinical Sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/03k1w9cmTest

المؤلفون: Alena Savanevich, Olgierd Ashuryk, Cezary Cybulski, Jan Lubiński, Jacek Gronwald

المصدر: Hereditary Cancer in Clinical Practice, Vol 19, Iss 1, Pp 1-4 (2021)

مصطلحات موضوعية: BRCA1 and BRCA2 mutation, Mutation, Epithelial ovarian cancer, Belarus, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1897-4287Test

الوصول الحر: https://doaj.org/article/405db68e7b2947ca951d7f43cb9f83aeTest

المؤلفون: Lisa Krassuski, Vera Vennedey, Stephanie Stock, Sibylle Kautz-Freimuth

المصدر: BMC Medical Informatics and Decision Making, Vol 19, Iss 1, Pp 1-13 (2019)

مصطلحات موضوعية: BRCA1 and BRCA2, Female BRCA1 and BRCA2 mutation carriers, Familial breast cancer, Familial ovarian cancer, Hereditary breast and ovarian cancer, HBOC, Computer applications to medicine. Medical informatics, R858-859.7

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s12911-019-0872-2Test; https://doaj.org/toc/1472-6947Test

الوصول الحر: https://doaj.org/article/b05c7431a5d2498e89d83d50ee30ad0eTest

المؤلفون: M. Tsyganov M., M. Ibragimova K., A. Pevzner M., N. Litviakov V., М. Цыганов М., М. Ибрагимова К., А. Певзнер М., Н. Литвяков В.

المصدر: Siberian journal of oncology; Том 19, № 3 (2020); 97-101 ; Сибирский онкологический журнал; Том 19, № 3 (2020); 97-101 ; 2312-3168 ; 1814-4861 ; 10.21294/1814-4861-2020-19-3

مصطلحات موضوعية: breast cancer, BRCA1 and BRCA2 mutation in the tumor, loss of heterozygosity, microarray analysis, personalized medicine, рак молочной железы, мутация BRCA1 и BRCA2 в опухоли, потеря гетерозиготности, микроматричный анализ, персонализированная медицина

وصف الملف: application/pdf

العلاقة: https://www.siboncoj.ru/jour/article/view/1492/751Test; Ryland G.L., Doyle M.A., Goode D., Boyle S.E., Choong D.Y., Rowley S.M., Li J., Bowtell D.D., Tothill R.W., Campbell I.G. Loss of heterozygosity: what is it good for? BMC Med Genomics. 2015; 8: 45. doi:10.1186/s12920-015-0123-z.; Knudson A.G. Mutation and cancer: statistical study of retinoblastoma. Proceedings of the National Academy of Sciences. 1971; 68(4): 820–823.; Chen Y., Chen C. DNA copy number variation and loss of heterozygosity in relation to recurrence of and survival from head and neck squamous cell carcinoma: a review. Head Neck. 2008; 30(10): 1361–83. doi:10.1002/hed.20861.; Silva J.M., Silva J., Sanchez A., Garcia J.M., Dominguez G., Provencio M., Sanfrutos L., Jareño E., Colas A., España P., Bonilla F. Tumor DNA in plasma at diagnosis of breast cancer patients is a valuable predictor of disease-free survival. Clinical Cancer Research, 2002; 8(12): 3761–3766.; Okudela K., Tateishi Y., Umeda S., Mitsui H., Suzuki T., Saito Y., Woo T., Tajiri M., Masuda M., Miyagi Y., Ohashi K. Allelic Imbalance in the miR-31 Host Gene Locus in Lung Cancer-Its Potential Role in Carcinogenesis. PLoS One. 2014 Jun 30; 9(6): e100581. doi:10.1371/ journal.pone.0100581.; Fleming J.L., Dworkin A.M., Allain D.C., Fernandez S., Wei L., Peters S.B., Iwenofu O.H., Ridd K., Bastian B.C., Toland A.E. Allele – specific imbalance mapping identifies HDAC9 as a candidate gene for cutaneous squamous cell carcinoma. Int J Cancer. 2014 Jan 1; 134(1): 244–8. doi:10.1002/ijc.28339.; Shikeeva A., Kekeeva T., Zavalishina L., Andreeva I., Frank G. Allelic imbalance in patients with non-small cell lung cancer. Arkh Patol. 2013; 75(2): 3–8.; Saito M., Okamoto A., Kohno T., Takakura S., Shinozaki H., Isonishi S., Yasuhara T., Yoshimura T., Ohtake Y., Ochiai K., Yokota J., Tanaka T. Allelic imbalance and mutations of the PTEN gene in ovarian cancer. Int J Cancer. 2000; 85(2): 160–165.; Beckmann M.W., Picard F., An H.X., van Roeyen C.R., Dominik S.I., Mosny D.S., Schnürch H.G., Bender H.G., Niederacher D. Clinical impact of detection of loss of heterozygosity of BRCA1 and BRCA2 markers in sporadic breast cancer. Br J Cancer. 1996 May; 73(10): 1220–6.; Maxwell K.N., Wubbenhorst B., Wenz B.M., De Sloover D., Pluta J., Emery L., Barrett A., Kraya A.A., Anastopoulos I.N., Yu S., Jiang Y., Chen H., Zhang N.R., Hackman N., D'Andrea K., Daber R., Morrissette J.J.D., Mitra N., Feldman M., Domchek S.M., Nathanson K.L. BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers. Nat Commun. 2017 Aug 22; 8(1): 319. doi:10.1038/s41467-017-00388-9.; Sokolenko A., Savanevich A., Stepuro T., Shulga A., Berlev I., Imyanitov E., Petrov N. Loss of heterozygosity at the BRCA1 locus as a marker of sen-sitivity for adjuvant chemotherapy in hereditary ovarian cancer. Biological Markers in Fundamental and Clinical Medicine. 2017; 1(3): 29–31.; Telli M.L., Hellyer J., Audeh W., Jensen K.C., Bose S., Timms K.M., Gutin A., Abkevich V., Peterson R.N., Neff C., Hughes E., Sangale Z., Jones J., Hartman A.R., Chang P.J., Vinayak S., Wenstrup R., Ford J.M. Homologous recombination deficiency (HRD) status predicts response to standard neoadjuvant chemotherapy in patients with triple-negative or BRCA1/2 mutation-associated breast cancer. Breast Cancer Res Treat. 2018 Apr; 168(3): 625–630. doi:10.1007/s10549-017-4624-7.; Pennington K.P., Walsh T., Harrell M.I., Lee M.K., Pennil C.C., Rendi M.H., Thornton A., Norquist B.M., Casadei S., Nord A.S., Agnew K.J., Pritchard C.C., Scroggins S., Garcia R.L., King M.C., Swisher E.M. Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas. Clin Cancer Res. 2014 Feb 1; 20(3): 764–75. doi:10.1158/1078-0432.CCR-13-2287.; Литвяков Н.В., Чердынцева Н.В., Цыганов М.М., Денисов Е.В., Мерзлякова М.К., Гарбуков Е.Ю., Вторушин С.В., Завьялова М.В., Слонимская Е.М. Ассоциация генетического полиморфизма с изменением экспрессии генов множественной лекарственной устойчивости в опухоли молочной железы в процессе неоадъювантной химиотерапии. Медицинская генетика. 2011; 10(10): 37–43.; Sakr S., Abdulfatah E., Loehr A., Simmons A., Morris R., AliFehmi R. Prognostic impact of loss of heterozygosity in uterine serous carcinoma. Gynecol Oncol. 2018; 149(1): 72.; https://www.siboncoj.ru/jour/article/view/1492Test

الإتاحة: https://doi.org/10.21294/1814-4861-2020-19-3-97-101Test
https://doi.org/10.21294/1814-4861-2020-19-3Test
https://doi.org/10.1002/hed.20861Test
https://doi.org/10.1002/ijc.28339Test
https://doi.org/10.1038/s41467-017-00388-9Test
https://doi.org/10.1007/s10549-017-4624-7Test
https://doi.org/10.1158/1078-0432.CCR-13-2287Test
https://www.siboncoj.ru/jour/article/view/1492Test

المؤلفون: Tomasz Kluz, Andrzej Jasiewicz, Elżbieta Marczyk, Robert Jach, Anna Jakubowska, Jan Lubiński, Steven A. Narod, Jacek Gronwald

المصدر: Hereditary Cancer in Clinical Practice, Vol 16, Iss 1, Pp 1-4 (2018)

مصطلحات موضوعية: BRCA1 and BRCA2 mutation, Ovarian cancer, Poland, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: http://link.springer.com/article/10.1186/s13053-018-0089-xTest; https://doaj.org/toc/1897-4287Test

الوصول الحر: https://doaj.org/article/08e452cec3374d109ae9bce46c958b9cTest

المؤلفون: Kluz, Tomasz, Jasiewicz, Andrzej, Marczyk, Elżbieta, Jach, Robert, Jakubowska, Anna, Lubiński, Jan, Narod, Steven A., Gronwald, Jacek

مصطلحات موضوعية: BRCA1 and BRCA2 mutation, ovarian cancer, Poland

العلاقة: Hereditary Cancer in Clinical Practice, T. 16; https://ruj.uj.edu.pl/xmlui/handle/item/142814Test

الإتاحة: https://doi.org/10.1186/s13053-018-0089-xTest
https://ruj.uj.edu.pl/xmlui/handle/item/142814Test

المصدر: kConFab Investigators , HEBON , GEMO Study Collaborators & EMBRACE 2017 , ' Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression : identification of a modifier of breast cancer risk at locus 11q22.3 ' , Breast Cancer Research and Treatment , vol. 161 , no. 1 , pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2Test

مصطلحات موضوعية: BRCA1 and BRCA2 mutation carriers, Breast cancer, Cis-regulatory variants, Differential allelic expression, Genetic modifiers, Genetic susceptibility

الإتاحة: https://doi.org/10.1007/s10549-016-4018-2Test
https://research.manchester.ac.uk/en/publications/297daadb-b2b0-4813-bce9-9ad9ad394da0Test
http://www.scopus.com/inward/record.url?scp=84992735226&partnerID=8YFLogxKTest

المؤلفون: Hamdi, Yosr, Soucy, Penny, Kuchenbaeker, Karoline B., Pastinen, Tomi, Droit, Arnaud, Lemacon, Audrey, Adlard, Julian, Aittomaki, Kristiina, Andrulis, Irene L., Arason, Adalgeir, Arnold, Norbert, Arun, Banu K., Azzollini, Jacopo, Bane, Anita, Barjhoux, Laure, Barrowdale, Daniel, Benitez, Javier, Berthet, Pascaline, Blok, Marinus J., Bobolis, Kristie, Bonadona, Valerie, Bonanni, Bernardo, Bradbury, Angela R., Brewer, Carole, Buecher, Bruno, Buys, Saundra, Caligo, Maria A., Chiquette, Jocelyne, Chung, Wendy K., Claes, Kathleen B. M., Daly, Mary B., Damiola, Francesca, Davidson, Rosemarie, de la Hoya, Miguel, De Leeneer, Kim, Diez, Orland, Ding, Yuan Chun, Dolcetti, Riccardo, Domchek, Susan M., Dorfling, Cecilia M., Eccles, Diana, Eeles, Ros, Einbeigi, Zakaria, Ejlertsen, Bent, Engel, Christoph, Evans, D. Gareth, Feliubadalo, Lidia, Foretova, Lenka, Fostira, Florentia, Oosterwijk, Jan C.

المصدر: Hamdi , Y , Soucy , P , Kuchenbaeker , K B , Pastinen , T , Droit , A , Lemacon , A , Adlard , J , Aittomaki , K , Andrulis , I L , Arason , A , Arnold , N , Arun , B K , Azzollini , J , Bane , A , Barjhoux , L , Barrowdale , D , Benitez , J , Berthet , P , Blok , M J , Bobolis , K , Bonadona , V , Bonanni , B , Bradbury , A R , Brewer , ....

مصطلحات موضوعية: Breast cancer, Genetic modifiers, Differential allelic expression, Genetic susceptibility, Cis-regulatory variants, BRCA1 and BRCA2 mutation carriers, OVARIAN-CANCER, CYCLIN E-CDK2, HUMAN-CELLS, DISEASE, NPAT, INVESTIGATORS, CONSORTIUM, DNA

وصف الملف: application/pdf

العلاقة: https://research.rug.nl/en/publications/067e10d1-11ed-418a-abe1-fec3def09b30Test

الإتاحة: https://doi.org/10.1007/s10549-016-4018-2Test
https://hdl.handle.net/11370/067e10d1-11ed-418a-abe1-fec3def09b30Test
https://research.rug.nl/en/publications/067e10d1-11ed-418a-abe1-fec3def09b30Test

المؤلفون: Hamdi, Y. (Yosr), Soucy, P. (Penny), Kuchenbaeker, K.B. (Karoline B.), Pastinen, T. (Tomi), Droit, A. (Arnaud), Lemaçon, A. (Audrey), Adlard, J.W. (Julian), Aittomäki, K. (Kristiina), Andrulis, I.L. (Irene), Arason, A. (Adalgeir), Arnold, N. (Norbert), Arun, B.K. (Banu), Azzollini, J., Bane, A.L. (Anita L.), Barjhoux, L. (Laure), Barrowdale, D. (Daniel), Benítez, J. (Javier), Berthet, P. (Pascaline), Blok, M.J. (Marinus), Bobolis, K.A. (Kristie A.), Bonadona, V. (Valérie), Bonnani, B. (Bernardo), Bradbury, A.R. (Angela R.), Brewer, C. (Carole), Buecher, B. (Bruno), Buys, S.S. (Saundra S.), Caligo, M.A. (Maria), Chiquette, J. (Jocelyne), Chung, W. (Wendy), Claes, K.B.M. (Kathleen B.M.), Daly, M.B. (Mary B.), Damiola, F. (Francesca), Davidson, R. (Rosemarie), Hoya, M. (Miguel) de La, De Leeneer, K. (Kim), Díez, O. (Orland), Ding, Y.C. (Yuan), Dolcetti, R. (Riccardo), Domchek, S.M. (Susan), Dorfling, C.M. (Cecilia), Eccles, D. (Diana), Eeles, R. (Ros), Einbeigi, Z. (Zakaria), Ejlertsen, B. (Bent), EMBRACE, Engel, C. (Christoph), Gareth Evans, D., Feliubadaló, L. (L.), Foretova, L. (Lenka), Fostira, F. (Florentia), Foulkes, W.D. (William D.), Fountzilas, G. (George), Friedman, E. (Eitan), Frost, D. (Debra), Ganschow, P. (Pamela), Ganz, P.A. (Patricia A.), Garber, J. (Judy), Gayther, S.A. (Simon), GEMO Study Collaborators, Gerdes, A-M. (Anne-Marie), Glendon, G. (Gord), Godwin, A.K. (Andrew K.), Goldgar, D. (David), Greene, M.H. (Mark H.), Gronwald, J. (Jacek), Hahnen, E. (Eric), Hamann, U. (Ute), Hansen, T.V.O. (Thomas), Hart, S. (Stewart), Hays, J. (John), HEBON, Hogervorst, F.B.L. (Frans), Hulick, P.J. (Peter), Imyanitov, E.N. (Evgeny), Isaacs, C. (Claudine), Izatt, L. (Louise), Jakubowska, A. (Anna), James, M. (Margaret), Janavicius, R. (Ramunas), Jensen, U.B., John, E.M. (Esther), Joseph, V. (Vijai), Just, W. (Walter), Kaczmarek, K. (Katarzyna), Karlan, B.Y. (Beth Y.), KConFab Investigators, Kets, C.M. (Marleen), Kirk, J. (Judy), Kriege, M. (Mieke), Laitman, Y. (Yael), Laurent, M. (Maïté), Lázaro, C. (Conxi), Leslie, G. (Goska), Lester, K.J. (Kathryn), Lesueur, F. (Fabienne), Liljegren, A. (Annelie), Loman, N. (Niklas), Loud, J.T. (Jennifer), Manoukian, S. (Siranoush), Mariani, M. (Milena), Mazoyer, S. (Sylvie), McGuffog, L. (Lesley), Meijers-Heijboer, E.J. (Hanne), Meindl, A. (Alfons), Miller, A. (Austin), Montagna, M. (Marco), Mulligan, A.-M. (Anna-Marie), Nathanson, K.L. (Katherine), Neuhausen, S.L. (Susan), Nevanlinna, H. (Heli), Nussbaum, R.L. (Robert L.), Olah, E. (Edith), Olopade, O.I. (Olufunmilayo I.), Ong, K.-R. (Kai-Ren), Oosterwijk, J.C. (Jan), Osorio, A. (Ana), Papi, L. (Laura), Park, S.K. (Sue K.), Pedersen, I.S. (Inge Sokilde), Peissel, B. (Bernard), Segura, P.P. (Pedro Perez), Peterlongo, P. (Paolo), Phelan, C. (Catherine), Radice, P. (Paolo), Rantala, J. (Johanna), Rappaport-Fuerhauser, C. (Christine), Rennert, G. (Gad), Richardson, A.L. (Andrea), Robson, M. (Mark), Rodriguez, G.C. (Gustavo), Rookus, M.A. (Matti), Schmutzler, R.K. (Rita), Sevenet, N. (Nicolas), Shah, P.D. (Payal D.), Singer, C.F. (Christian), Slavin, T.P. (Thomas P.), Snape, K. (Katie), Sokolowska, J. (Johanna), Sønderstrup, I.M.H. (Ida Marie Heeholm), Southey, M.C. (Melissa), Spurdle, A.B. (Amanda), Stadler, Z. (Zsofia), Stoppa-Lyonnet, D. (Dominique), Sukiennicki, G. (Grzegorz), Sutter, C. (Christian), Tan, Y. (Yen), Tea, M.-K., Teixeira, P.J., Teulé, A. (A.), Teo, S.-H. (Soo-Hwang), Terry, M.B. (Mary Beth), Thomassen, M. (Mads), Tihomirova, L. (Laima), Tischkowitz, M. (Marc), Tognazzo, S. (Silvia), Toland, A.E. (Amanda), Tung, N. (Nadine), Ouweland, A.M.W. (Ans) van den, Luijt, R.B. (Rob) van der, Engelen, K. (Klaartje) van, Rensburg, E.J. (Elizabeth) van, Varon-Mateeva, R. (Raymonda), Wapenschmidt, B. (Barbara), Wijnen, J.T. (Juul), Rebbeck, R. (Timothy), Chenevix-Trench, G. (Georgia), Offit, K. (Kenneth), Couch, F.J. (Fergus J.), Nord, S. (Silje), Easton, D.F. (Douglas F.), Antoniou, A.C. (Antonis), Simard, J. (Jacques)

المصدر: Breast Cancer Research and Treatment, pp. 1-18

مصطلحات موضوعية: BRCA1 and BRCA2 mutation carriers, Breast cancer, Cis-regulatory variants, Differential allelic expression, Genetic modifiers, Genetic susceptibility

وصف الملف: application/pdf

العلاقة: http://repub.eur.nl/pub/93996Test; urn:hdl:1765/93996

الإتاحة: https://doi.org/10.1007/s10549-016-4018-2Test
http://repub.eur.nl/pub/93996Test