يعرض 1 - 20 نتائج من 245 نتيجة بحث عن '"Single-strand annealing"', وقت الاستعلام: 0.70s تنقيح النتائج
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    المساهمون: Horae Gene Therapy Center, Department of Pediatrics, Department of Neurology

    المصدر: Molecular neurodegeneration ; 15 ; 1 ; 13

    Relation: Link to Article in PubMed; Andrade NS, Ramic M, Esanov R, Liu W, Rybin MJ, Gaidosh G, Abdallah A, Del'Olio S, Huff TC, Chee NT, Anatha S, Gendron TF, Wahlestedt C, Zhang Y, Benatar M, Mueller C, Zeier Z. Dipeptide repeat proteins inhibit homology-directed DNA double strand break repair in C9ORF72 ALS/FTD. Mol Neurodegener. 2020 Feb 24;15(1):13. doi:10.1186/s13024-020-00365-9. PMID: 32093728; PMCID: PMC7041170. Link to article on publisher's site; 1750-1326 (Linking); http://hdl.handle.net/20.500.14038/41384; https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5184&context=oapubs&unstamped=1; https://escholarship.umassmed.edu/oapubs/4165; oapubs/4165

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    المساهمون: Medicine, School of Medicine

    المصدر: PMC

    وصف الملف: application/pdf

    Relation: Frontiers in Oncology; Kelm JM, Samarbakhsh A, Pillai A, et al. Recent Advances in the Development of Non-PIKKs Targeting Small Molecule Inhibitors of DNA Double-Strand Break Repair. Front Oncol. 2022;12:850883. Published 2022 Apr 6. doi:10.3389/fonc.2022.850883; https://hdl.handle.net/1805/33647

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    المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2018 Aug . 115(35), E8286-E8295.

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    المساهمون: Balboni, Beatrice, Marotta, Roberto, Rinaldi, Francesco, Milordini, Giulia, Varignani, Giulia, Girotto, Stefania, Cavalli, Andrea

    مصطلحات موضوعية: RAD52, Single Strand Annealing

    وصف الملف: ELETTRONICO

    Relation: info:eu-repo/semantics/altIdentifier/pmid/39112549; volume:7; issue:1; firstpage:1; lastpage:12; numberofpages:12; journal:COMMUNICATIONS BIOLOGY; https://hdl.handle.net/11585/977234

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    المؤلفون: Iyama, Teruaki, Wilson, David M

    المصدر: DNA Repair. 12(8)

    مصطلحات موضوعية: Genetics, Stem Cell Research, Stem Cell Research - Nonembryonic - Human, Cancer, Neurosciences, 1.1 Normal biological development and functioning, 2.1 Biological and endogenous factors, Aetiology, Underpinning research, Generic health relevance, Neurological, Animals, DNA, DNA Damage, DNA Repair, Disease Models, Animal, Humans, Neurons, O(6)-Methylguanine-DNA Methyltransferase, Pyrimidine Dimers, 6-4PPs, 8-oxoguanine DNA glycosylase, AOA1, AP, AP endonuclease 1, APE1, APTX, ATM, CPDs, CS, CSR, Cockayne syndrome, DAR, DNA double strand break repair, DNA polymerase β, DNA repair, DNA single strand break repair, DNA single strand breaks, DNA-PKcs, DNA-dependent protein kinase catalytic subunit, DSBR, Dividing and non-dividing, ERCC1, Endogenous DNA damage, FEN1, GG-NER, HNPCC, HR, IR, MAP, MCSZ, MGMT, MMR, MPG, MUTYH, MUTYH-associated polyposis, N-methylpurine-DNA glycosylase, NEIL1, NER, NHEJ, NSC, NTH1, Neural cells, Neurological disorder, O(6)-methylguanine-DNA methyltransferase, OGG1, PARP1, PCNA, PG, PNKP, PUA, Pol β, RFC, RNA polymerase, RNAP, RPA, SCAN1, SCID, SDSA, SSA, SSBR, SSBs, TC-NER, TDP1, TFIIH, TOP1, TTD, Top1 cleavage complex, Top1cc, UNG, X-ray repair cross-complementing protein 1, XP, XRCC1, aprataxin, apurinic/apyrimidinic, ataxia telangiectasia mutated, ataxia with ocular motor apraxia 1, class switch recombination, cyclobutane pyrimidine dimers, dRP, deoxyribose-5-phosphate, endonuclease III-like 1, endonuclease VIII-like 1, excision repair cross complementing 1, flap endonuclease 1, global genome-NER, hereditary nonpolyposis colorectal cancer, homologous recombination, human mutY homolog, ionizing radiation, microcephaly with early-onset, intractable seizures and developmental delay, mismatch repair, neural stem cells, nonhomologous end joining, nucleotide excision repair, phospho-α, β-unsaturated aldehyde, phosphoglycolate, poly(ADP-ribose) polymerase-1, polynucleotide kinase 3′-phosphatase, proliferating cellular nuclear antigen, pyrimidine-(6, 4)-pyrimidone photoproducts., replication factor C, replication protein A, severe combined immunodeficient, single-strand annealing, spinocerebellar ataxia with axonal neuropathy-1, synthesis-dependent strand annealing, topoisomerase 1, transcription domains-associated repair, transcription factor II H, transcription-coupled NER, trichothiodystrophy, tyrosyl-DNA phosphodiesterase 1, uracil-DNA glycosylase, xeroderma pigmentosum, Biochemistry and Cell Biology, Developmental Biology

    وصف الملف: application/pdf