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1
المؤلفون: Yuan, Yuan, Ju, Young Seok, Kim, Youngwook, Li, Jun, Wang, Yumeng, Yoon, Christopher J, Yang, Yang, Martincorena, Inigo, Creighton, Chad J, Weinstein, John N, Xu, Yanxun, Han, Leng, Kim, Hyung-Lae, Nakagawa, Hidewaki, Park, Keunchil, Campbell, Peter J, Liang, Han
المساهمون: Borg, Åke, Creator, Ringnér, Markus, Creator, Staaf, Johan, Creator
المصدر: Nature Genetics. 52(3):342-352
مصطلحات موضوعية: Cell Cycle/genetics, DNA Copy Number Variations, DNA Repair/genetics, DNA, Mitochondrial/genetics, Genome, Human/genetics, Humans, Mutation, Neoplasms/genetics, Oxidative Phosphorylation, Sequence Analysis, RNA, Whole Genome Sequencing, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics
الوصول الحر: https://lup.lub.lu.se/record/8f1c62ab-fa08-4872-abf2-d33f162c1225Test
http://dx.doi.org/10.1038/s41588-019-0557-xTest -
2
المؤلفون: Gerstung, Moritz, Jolly, Clemency, Leshchiner, Ignaty, Dentro, Stefan C, Gonzalez, Santiago, Rosebrock, Daniel, Mitchell, Thomas J, Rubanova, Yulia, Anur, Pavana, Yu, Kaixian, Tarabichi, Maxime, Deshwar, Amit, Wintersinger, Jeff, Kleinheinz, Kortine, Vázquez-García, Ignacio, Haase, Kerstin, Jerman, Lara, Sengupta, Subhajit, Macintyre, Geoff, Malikic, Salem, Donmez, Nilgun, Livitz, Dimitri G, Cmero, Marek, Demeulemeester, Jonas, Schumacher, Steven, Fan, Yu, Yao, Xiaotong, Lee, Juhee, Schlesner, Matthias, Boutros, Paul C, Bowtell, David D, Zhu, Hongtu, Getz, Gad, Imielinski, Marcin, Beroukhim, Rameen, Sahinalp, S Cenk, Ji, Yuan, Peifer, Martin, Markowetz, Florian, Mustonen, Ville, Yuan, Ke, Wang, Wenyi, Morris, Quaid D, Spellman, Paul T, Wedge, David C, Van Loo, Peter
المساهمون: Borg, Åke, Creator, Ringnér, Markus, Creator, Staaf, Johan, Creator
المصدر: Nature. 578(7793):122-128
مصطلحات موضوعية: DNA Repair/genetics, Evolution, Molecular, Gene Dosage, Genes, Tumor Suppressor, Genetic Variation, Genome, Human/genetics, Humans, Mutagenesis, Insertional/genetics, Neoplasms/genetics, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics
الوصول الحر: https://lup.lub.lu.se/record/7f8ffa06-e8e9-402f-9107-0b4d690e5da6Test
http://dx.doi.org/10.1038/s41586-019-1907-7Test -
3دورية أكاديمية
المؤلفون: Lautrup, Sofie, Myrup Holst, Camilla, Yde, Anne, Asmussen, Stine, Thinggaard, Vibeke, Larsen, Knud, Laursen, Lisbeth Schmidt, Richner, Mette, Vaegter, Christian B, Prieto, G Aleph, Berchtold, Nicole, Cotman, Carl W, Stevnsner, Tinna
المصدر: Lautrup , S , Myrup Holst , C , Yde , A , Asmussen , S , Thinggaard , V , Larsen , K , Laursen , L S , Richner , M , Vaegter , C B , Prieto , G A , Berchtold , N , Cotman , C W & Stevnsner , T 2023 , ' The role of aging and brain-derived neurotrophic factor signaling in expression of base excision repair genes in the human brain ' , Aging Cell , vol. 22 , no. 9 , e13905 . https://doi.org/10.1111/acel.13905Test
مصطلحات موضوعية: DNA repair, aging, base excision repair, brain, brain-derived neurotrophic factor, cyclic-AMP response element-binding protein, neurons, Aging/genetics, Humans, Signal Transduction/genetics, Brain-Derived Neurotrophic Factor/genetics, DNA Repair/genetics, Animals, Mice, Brain/metabolism
الإتاحة: https://doi.org/10.1111/acel.13905Test
https://pure.au.dk/portal/en/publications/8456f268-b3f3-4f4b-9ec7-6bd2cfd153c8Test
http://www.scopus.com/inward/record.url?scp=85162248395&partnerID=8YFLogxKTest -
4دورية أكاديمية
المؤلفون: Sørensen, Simon Grund, Shrikhande, Amruta, Poulsgaard, Gustav Alexander, Christensen, Mikkel Hovden, Bertl, Johanna, Laursen, Britt Elmedal, Hoffmann, Eva R, Pedersen, Jakob Skou
المصدر: Sørensen , S G , Shrikhande , A , Poulsgaard , G A , Christensen , M H , Bertl , J , Laursen , B E , Hoffmann , E R & Pedersen , J S 2023 , ' Pan-cancer association of DNA repair deficiencies with whole-genome mutational patterns ' , eLife , vol. 12 , e81224 . https://doi.org/10.7554/elife.81224Test
مصطلحات موضوعية: BRCA1 Protein/genetics, BRCA2 Protein/genetics, DNA Helicases/genetics, DNA Repair-Deficiency Disorders, DNA Repair/genetics, Humans, Male, Mutation, Neoplasms/genetics, Nuclear Proteins/genetics, Transcription Factors/genetics, predictive modelling, DNA damage response, mutational signatures, personalised medicine, repair deficiency
العلاقة: https://pure.au.dk/portal/da/publications/pancancer-association-ofTest-dna-repair-deficiencies-with-wholegenome-mutational-patterns(6d841269-ef5f-41e2-a050-6f671e6994dd).html
الإتاحة: https://doi.org/10.7554/elife.81224Test
https://pure.au.dk/portal/da/publications/pancancer-association-ofTest-dna-repair-deficiencies-with-wholegenome-mutational-patterns(6d841269-ef5f-41e2-a050-6f671e6994dd).html -
5دورية أكاديمية
المساهمون: Matthew R Smith, Howard I Scher, Shahneen Sandhu, Eleni Efstathiou, Primo N Lara Jr, Evan Y Yu, Daniel J George, Kim N Chi, Fred Saad, Olof Ståhl, David Olmos, Daniel C Danila, Gary E Mason, Byron M Espina, Xin Zhao, Karen A Urtishak, Peter Francis, Angela Lopez-Gitlitz, Karim Fizazi, GALAHAD investigators, Choi, Young Deuk
مصطلحات موضوعية: Adolescent, Adult, Androgen Antagonists / therapeutic use, Androgens, Antineoplastic Agents* / therapeutic use, Antineoplastic Combined Chemotherapy Protocols / therapeutic use, DNA Repair / genetics, Humans, Indazoles, Male, Piperidines, Prostatic Neoplasms, Castration-Resistant* / drug therapy, Castration-Resistant* / genetics, Castration-Resistant* / pathology, Thrombocytopenia
العلاقة: LANCET ONCOLOGY; J02154; OAK-2022-10336; https://ir.ymlib.yonsei.ac.kr/handle/22282913/194821Test; T202302360; LANCET ONCOLOGY, Vol.23(3) : 362-373, 2022-03
الإتاحة: https://doi.org/10.1016/s1470-2045Test(21)00757-9
https://ir.ymlib.yonsei.ac.kr/handle/22282913/194821Test -
6دورية أكاديمية
المؤلفون: Meijer, Titia G, Nguyen, Luan, Van Hoeck, Arne, Sieuwerts, Anieta M, Verkaik, Nicole S, Ladan, Marjolijn M, Ruigrok-Ritstier, Kirsten, van Deurzen, Carolien H M, van de Werken, Harmen J G, Lips, Esther H, Linn, Sabine C, Memari, Yasin, Davies, Helen, Nik-Zainal, Serena, Kanaar, Roland, Martens, John W M, Cuppen, Edwin, Jager, Agnes, van Gent, Dik C
المساهمون: CMM Groep Cuppen, Cancer, Pathologie
مصطلحات موضوعية: Antineoplastic Agents/therapeutic use, BRCA1 Protein/genetics, BRCA2 Protein/genetics, Breast Neoplasms/diagnosis, DNA, Female, Homologous Recombination/genetics, Humans, Poly(ADP-ribose) Polymerase Inhibitors/pharmacology, Poly(ADP-ribose) Polymerases/genetics, Recombinational DNA Repair/genetics, Genetics, Molecular Biology, Cancer Research, Journal Article
وصف الملف: application/pdf
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7دورية أكاديمية
المؤلفون: Pathak, Gita A., Polimanti, Renato, Silzer, Talisa K., Wendt, Frank R., Chakraborty, Ranajit, Phillips, Nicole R.
المصدر: BMC Cancer
مصطلحات موضوعية: DNA repair, mitochondria, proctitis, radiotherapy, Aged, DNA Copy Number Variations / genetics, DNA Repair / genetics, Europe, Humans, Male, Middle Aged, Mitochondria / metabolism, Proctitis / genetics, Proctitis / radiotherapy, Transcriptome / genetics
وصف الملف: application/pdf
العلاقة: https://doi.org/10.1186/s12885-020-07457-1Test; Pathak, G. A., Polimanti, R., Silzer, T. K., Wendt, F. R., Chakraborty, R., & Phillips, N. R. (2020). Genetically-regulated transcriptomics & copy number variation of proctitis points to altered mitochondrial and DNA repair mechanisms in individuals of European ancestry. BMC cancer, 20(1), 954. https://doi.org/10.1186/s12885-020-07457-1Test; https://hdl.handle.net/20.500.12503/31927Test; 20
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8دورية أكاديمية
المؤلفون: Grange, Laura J, Reynolds, John J, Ullah, Farid, Isidor, Bertrand, Shearer, Robert F, Latypova, Xenia, Baxley, Ryan M, Oliver, Antony W, Ganesh, Anil, Cooke, Sophie L, Jhujh, Satpal S, McNee, Gavin S, Hollingworth, Robert, Higgs, Martin R, Natsume, Toyoaki, Khan, Tahir, Martos-Moreno, Gabriel Á, Chupp, Sharon, Mathew, Christopher G, Parry, David, Simpson, Michael A, Nahavandi, Nahid, Yüksel, Zafer, Drasdo, Mojgan, Kron, Anja, Vogt, Petra, Jonasson, Annemarie, Seth, Saad Ahmed, Gonzaga-Jauregui, Claudia, Brigatti, Karlla W, Stegmann, Alexander P A, Kanemaki, Masato, Josifova, Dragana, Uchiyama, Yuri, Oh, Yukiko, Morimoto, Akira, Osaka, Hitoshi, Ammous, Zineb, Argente, Jesús, Matsumoto, Naomichi, Stumpel, Constance T R M, Taylor, Alexander M R, Jackson, Andrew P, Bielinsky, Anja-Katrin, Mailand, Niels, Le Caignec, Cedric, Davis, Erica E, Stewart, Grant S
المصدر: Grange , L J , Reynolds , J J , Ullah , F , Isidor , B , Shearer , R F , Latypova , X , Baxley , R M , Oliver , A W , Ganesh , A , Cooke , S L , Jhujh , S S , McNee , G S , Hollingworth , R , Higgs , M R , Natsume , T , Khan , T , Martos-Moreno , G Á , Chupp , S , Mathew , C G , Parry , D , Simpson , M A , Nahavandi , N ....
مصطلحات موضوعية: Humans, Cell Cycle Proteins/genetics, Microcephaly/genetics, DNA Repair/genetics, Chromosomes/metabolism, Genomic Instability, DNA-Binding Proteins/metabolism, Ubiquitin-Protein Ligases/metabolism, Chromosomal Proteins, Non-Histone/metabolism
العلاقة: https://cris.maastrichtuniversity.nl/en/publications/d25cbc54-c6a3-46e2-bcc9-fb0afe819ff4Test
الإتاحة: https://doi.org/10.1038/s41467-022-34349-8Test
https://cris.maastrichtuniversity.nl/en/publications/d25cbc54-c6a3-46e2-bcc9-fb0afe819ff4Test -
9دورية أكاديمية
المؤلفون: Constantin, D., Dubuis, G., Conde-Rubio, MDC, Widmann, C.
المصدر: The FEBS journal, vol. 289, no. 3, pp. 808-831
مصطلحات موضوعية: Cell Nucleolus/genetics, Cytidine Deaminase/genetics, DNA Breaks, Double-Stranded/drug effects, DNA Damage/drug effects, DNA Damage/genetics, DNA End-Joining Repair/genetics, DNA Repair/drug effects, DNA Repair/genetics, Etoposide/pharmacology, Gene Expression Regulation/drug effects, Genome, Human/genetics, Homologous Recombination/genetics, Humans, Multigene Family/genetics, Mutagens/pharmacology, Mutation/genetics, Tumor Suppressor Protein p53/genetics, APOBEC3C, DNA repair, cancer biology, nucleolus, p53
وصف الملف: application/pdf
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34528388; info:eu-repo/semantics/altIdentifier/eissn/1742-4658; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_549304C0D4F30; https://serval.unil.ch/notice/serval:BIB_549304C0D4F3Test; urn:issn:1742-464X; https://serval.unil.ch/resource/serval:BIB_549304C0D4F3.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_549304C0D4F30Test
الإتاحة: https://doi.org/10.1111/febs.16202Test
https://serval.unil.ch/notice/serval:BIB_549304C0D4F3Test
https://serval.unil.ch/resource/serval:BIB_549304C0D4F3.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_549304C0D4F30Test -
10دورية أكاديمية
المؤلفون: Cordts, Isabell, Oender, Demet, Tzschach, Andreas, Meiss, Frank, Schmidt, Axel, Kreiß, Martina, Cremer, Kirsten, Mensah, Martin A, Park, Joohyun, Rautenberg, Maren, Deininger, Natalie, Sturm, Marc, Traschuetz, Andreas, Lingor, Paul, Klopstock, Thomas, Weiler, Markus, Marxreiter, Franz, Synofzik, Matthis, Posch, Christian, Sirokay, Judith, Klockgether, Thomas, Haack, Tobias B, Deschauer, Marcus, Kobeleva, Xenia, Karin, Ivan, Minnerop, Martina, Koertvelyessy, Peter, Biskup, Saskia, Forchhammer, Stephan, Binder, Johannes
المصدر: Movement disorders 37(8), 1707-1718 (2022). doi:10.1002/mds.29071
مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adult, Cockayne Syndrome: complications, Cockayne Syndrome: genetics, DNA Repair: genetics, Humans, Skin, Skin Neoplasms: genetics, Xeroderma Pigmentosum: genetics, Xeroderma Pigmentosum: metabolism, Xeroderma Pigmentosum: pathology, Xeroderma Pigmentosum Group D Protein: genetics, Xeroderma Pigmentosum Group D Protein: metabolism, NER, UV sensitivity, ataxia, dementia, xeroderma pigmentosum
جغرافية الموضوع: DE
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:35699229; info:eu-repo/semantics/altIdentifier/issn/1531-8257; info:eu-repo/semantics/altIdentifier/issn/0885-3185; https://pub.dzne.de/record/164860Test; https://pub.dzne.de/search?p=id:%22DZNE-2022-01304%22Test
النص الكامل