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1دورية أكاديمية
المؤلفون: Light, Nicholas, Layeghifard, Mehdi, Attery, Ayush, Subasri, Vallijah, Zatzman, Matthew, Anderson, Nathaniel D, Hatkar, Rupal, Blay, Sasha, Chen, David, Novokmet, Ana, Fuligni, Fabio, Tran, James, de Borja, Richard, Agarwal, Himanshi, Waldman, Larissa, Abegglen, Lisa M, Albertson, Daniel, Finlay, Jonathan L, Hansford, Jordan R, Behjati, Sam, Villani, Anita, Gerstung, Moritz, Alexandrov, Ludmil B, Somers, Gino R, Schiffman, Joshua D, Rotter, Varda, Malkin, David, Shlien, Adam
المصدر: nlmid: 101528555 ; essn: 2041-1723
مصطلحات موضوعية: Humans, Tumor Suppressor Protein p53, Genetic Predisposition to Disease, DNA Copy Number Variations, Phosphatidylinositol 3-Kinases, Phylogeny, Li-Fraumeni Syndrome, Germ-Line Mutation, Mutation, Neoplastic Syndromes, Hereditary
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.17863/CAM.93707Test
https://www.repository.cam.ac.uk/handle/1810/346286Test -
2دورية أكاديمية
المؤلفون: Šarac Sanja, Krsmanović Željko, Milić Rade, Radević Tatjana, Lazović-Popović Biljana, Vasiljević Mira, Šarac Momir
المصدر: Vojnosanitetski Pregled, Vol 80, Iss 4, Pp 362-367 (2023)
مصطلحات موضوعية: diagnosis, family, genetic diseases, inborn, li-fraumeni syndrome, mutation, serbia, Medicine (General), R5-920
العلاقة: https://doaj.org/toc/0042-8450Test; https://doaj.org/toc/2406-0720Test; https://doaj.org/article/fa17a636a04e4ed1b0faf05c284cbfc1Test
الإتاحة: https://doi.org/10.2298/VSP211102036STest
https://doaj.org/article/fa17a636a04e4ed1b0faf05c284cbfc1Test -
3دورية أكاديمية
المؤلفون: H. Sahli, Rym Meddeb, M. Chérif, Chiraz Nasr, Aouatef Riahi, Samia Hannachi, Neïla Belguith, Ridha Mrad
مصطلحات موضوعية: The p53 Signaling Network in Cancer Research, Oncology, Medicine, Health Sciences, Hedgehog Signaling in Development and Cancer, Molecular Biology, Biochemistry, Genetics and Molecular Biology, Life Sciences, Engineering Bacteria for Cancer Treatment, Biotechnology, Tumor Regression, Li–Fraumeni syndrome, Germline, Phenotype, Breast cancer, Germline mutation, Sanger sequencing, Biology, Genotype, Pathology, Genotype-phenotype distinction, Male breast cancer, Genetics, FOS Biological sciences, Cancer, Cancer research, Mutation, Gene
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4دورية أكاديمية
المؤلفون: H. Sahli, Rym Meddeb, M. Chérif, Chiraz Nasr, Aouatef Riahi, Samia Hannachi, Neïla Belguith, Ridha Mrad
مصطلحات موضوعية: The p53 Signaling Network in Cancer Research, Oncology, Medicine, Health Sciences, Hedgehog Signaling in Development and Cancer, Molecular Biology, Biochemistry, Genetics and Molecular Biology, Life Sciences, Engineering Bacteria for Cancer Treatment, Biotechnology, Tumor Regression, Li–Fraumeni syndrome, Germline, Phenotype, Breast cancer, Germline mutation, Sanger sequencing, Biology, Genotype, Pathology, Genotype-phenotype distinction, Male breast cancer, Genetics, FOS Biological sciences, Cancer, Cancer research, Mutation, Gene
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5دورية أكاديميةA mouse model for Li-Fraumeni-Like Syndrome with cardiac angiosarcomas associated to POT1 mutations.
المؤلفون: Martínez, Paula, Sánchez-Vázquez, Raúl, Ferrara-Romeo, Iole, Serrano, Rosa, Flores, Juana M, Blasco, MA
المساهمون: Agencia Estatal de Investigación (España), Comunidad de Madrid (España), Ministerio de Ciencia e Innovación (España), Unión Europea. Comisión Europea. European Research Council (ERC), Fundación Banco Santander
مصطلحات موضوعية: Hemangiosarcoma, Telomerase, Animals, Endothelial Cells, Fibroblasts, Humans, Li-Fraumeni Syndrome, Mice, Mutation, Shelterin Complex, Telomere, Telomere-Binding Proteins
العلاقة: https://doi.org/10.1371/journal.pgen.1010260Test.; info:eu-repo/grantAgreement/EC/H2020/882385/EU; info:eu-repo/grantAgreement/ES/SAF2017-82623-R; info:eu-repo/grantAgreement/ES/SAF201572455-EXP; PLoS Genet . 2022 ;18(6):e1010260; http://hdl.handle.net/20.500.12105/18980Test; PLoS genetics
الإتاحة: https://doi.org/20.500.12105/18980Test
https://doi.org/10.1371/journal.pgen.1010260Test
https://hdl.handle.net/20.500.12105/18980Test -
6دورية أكاديمية
المؤلفون: Natalia Parisi Severino, Jaques Waisberg, Maria Candida Barisson Villares Fragoso, Luiz Guilherme Cernaglia Aureliano de Lima, Flavia Balsamo, Alexandre Cruz Henriques, Bianca Bianco, Flávia de Sousa Gehrke
المصدر: Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-7 (2022)
مصطلحات موضوعية: Leiomyosarcoma, Li–Fraumeni syndrome, TP53 gene, Mutation, Case report, Medicine
العلاقة: https://doi.org/10.1186/s13256-022-03671-6Test; https://doaj.org/toc/1752-1947Test; https://doaj.org/article/87c1691d8acd4801b512a2ea87707174Test
الإتاحة: https://doi.org/10.1186/s13256-022-03671-6Test
https://doaj.org/article/87c1691d8acd4801b512a2ea87707174Test -
7دورية أكاديمية
المؤلفون: Capaci V., Bascetta L., Fantuz M., Beznoussenko G. V., Sommaggio R., Cancila V., Bisso A., Campaner E., Mironov A. A., Wisniewski J. R., Ulloa Severino L., Scaini D., Bossi F., Lees J., Alon N., Brunga L., Malkin D., Piazza S., Collavin L., Rosato A., Bicciato S., Tripodo C., Mantovani F., Del Sal G.
المساهمون: Capaci, V., Bascetta, L., Fantuz, M., Beznoussenko, G. V., Sommaggio, R., Cancila, V., Bisso, A., Campaner, E., Mironov, A. A., Wisniewski, J. R., Ulloa Severino, L., Scaini, D., Bossi, F., Lees, J., Alon, N., Brunga, L., Malkin, D., Piazza, S., Collavin, L., Rosato, A., Bicciato, S., Tripodo, C., Mantovani, F., Del Sal, G.
مصطلحات موضوعية: Animal, Biopsy, Breast Neoplasm, Cell Line, Tumor, Cell Transformation, Neoplastic, Female, Fibroblast, Gene Expression Regulation, Golgi Apparatu, Human, Hypoxia-Inducible Factor 1, alpha Subunit, Li-Fraumeni Syndrome, Mice, MicroRNA, Microtubule, Mutation, Primary Cell Culture, Secretory Vesicle, Signal Transduction, Skin, Tumor Microenvironment, Tumor Suppressor Protein p53, Xenograft Model Antitumor Assays
وصف الملف: ELETTRONICO
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32770028; info:eu-repo/semantics/altIdentifier/wos/WOS:000561093500007; volume:11; issue:1; firstpage:-; lastpage:-; numberofpages:19; journal:NATURE COMMUNICATIONS; http://hdl.handle.net/11368/2974198Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089281192; https://www.nature.com/articles/s41467-020-17596-5Test
الإتاحة: https://doi.org/10.1038/s41467-020-17596-5Test
http://hdl.handle.net/11368/2974198Test
https://www.nature.com/articles/s41467-020-17596-5Test -
8دورية أكاديمية
المؤلفون: Capaci V., Bascetta L., Fantuz M., Beznoussenko G. V., Sommaggio R., Cancila V., Bisso A., Campaner E., Mironov A. A., Wisniewski J. R., Ulloa Severino L., Scaini D., Bossi F., Lees J., Alon N., Brunga L., Malkin D., Piazza S., Collavin L., Rosato A., Bicciato S., Tripodo C., Mantovani F., Del Sal G.
المساهمون: Capaci V., Bascetta L., Fantuz M., Beznoussenko G.V., Sommaggio R., Cancila V., Bisso A., Campaner E., Mironov A.A., Wisniewski J.R., Ulloa Severino L., Scaini D., Bossi F., Lees J., Alon N., Brunga L., Malkin D., Piazza S., Collavin L., Rosato A., Bicciato S., Tripodo C., Mantovani F., Del Sal G.
مصطلحات موضوعية: Animals, Biopsy, Breast Neoplasms, Cell Line, Tumor, Cell Transformation, Neoplastic, Female, Fibroblasts, Gene Expression Regulation, Golgi Apparatus, Humans, Hypoxia-Inducible Factor 1, alpha Subunit, Li-Fraumeni Syndrome, Mice, MicroRNAs, Microtubules, Mutation, Primary Cell Culture, Secretory Vesicles, Signal Transduction,Skin, Tumor Microenvironment, Tumor Suppressor Protein p53, Xenograft Model Antitumor Assays, Settore MED/08 - Anatomia Patologica, Settore MED/05 - Patologia Clinica
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32770028; info:eu-repo/semantics/altIdentifier/wos/WOS:000561093500007; volume:11; issue:1; firstpage:3945; numberofpages:19; journal:NATURE COMMUNICATIONS; http://hdl.handle.net/10447/510028Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089281192
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9دورية أكاديمية
المؤلفون: Felipe Batalini, Ellie G. Peacock, Lindsey Stobie, Alison Robertson, Judy Garber, Jeffrey N. Weitzel, Nadine M. Tung
المصدر: Breast Cancer Research, Vol 21, Iss 1, Pp 1-10 (2019)
مصطلحات موضوعية: Mutation, Pathogenic variant, TP53, Li-Fraumeni syndrome, Hereditary breast cancer, Clonal hematopoiesis, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
العلاقة: http://link.springer.com/article/10.1186/s13058-019-1193-1Test; https://doaj.org/toc/1465-542XTest; https://doaj.org/article/ec32db004ab8481dbdebc4950356163fTest
الإتاحة: https://doi.org/10.1186/s13058-019-1193-1Test
https://doaj.org/article/ec32db004ab8481dbdebc4950356163fTest -
10دورية أكاديمية
المؤلفون: Dommering, Charlotte J., Henneman, Lidewij, van der Hout, Annemarie H., Jonker, Marianne A., Tops, Carli M. J., van den Ouweland, Ans M. W., van der Luijt, Rob B., Mensenkamp, Arjen R., Hogervorst, Frans B. L., Redeker, Egbert J. W., de Die-Smulders, Christine E. M., Moll, Annette C., Meijers-Heijboer, Hanne
المصدر: Dommering , C J , Henneman , L , van der Hout , A H , Jonker , M A , Tops , C M J , van den Ouweland , A M W , van der Luijt , R B , Mensenkamp , A R , Hogervorst , F B L , Redeker , E J W , de Die-Smulders , C E M , Moll , A C & Meijers-Heijboer , H 2017 , ' Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands ' , Familial Cancer , vol. ....
مصطلحات موضوعية: Retinoblastoma, Prenatal diagnosis, Von Hippel-Lindau disease, Li-Fraumeni syndrome, Familial adenomatous polyposis, Hereditary breast ovarian cancer, PREIMPLANTATION GENETIC DIAGNOSIS, ASSISTED REPRODUCTION, INCREASED RISK, BREAST-CANCER, SUSCEPTIBILITY, IDENTIFICATION, ATTITUDES, PREDISPOSITION, MUTATION, ISSUES
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1007/s10689-016-9943-zTest
https://hdl.handle.net/11370/e6a4a720-be89-4c96-9bfb-795679a81844Test
https://research.rug.nl/en/publications/e6a4a720-be89-4c96-9bfb-795679a81844Test