يعرض 1 - 10 نتائج من 7,343 نتيجة بحث عن '"Transcription factor II A"', وقت الاستعلام: 1.18s تنقيح النتائج
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    رسالة جامعية

    المؤلفون: Borralleras Fumaña, Cristina

    المساهمون: University/Department: Universitat Pompeu Fabra. Departament de Ciències Experimentals i de la Salut

    مرشدي الرسالة: Campuzano Uceda, María Victoria, Pérez Jurado, Luis Alberto

    المصدر: TDX (Tesis Doctorals en Xarxa)

    Time: 616.8

    وصف الملف: application/pdf

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    رسالة جامعية

    المؤلفون: Segura Puimedon, Maria

    المساهمون: University/Department: Universitat Pompeu Fabra. Departament de Ciències Experimentals i de la Salut

    مرشدي الرسالة: Pérez Jurado, Luis Alberto, Campuzano Uceda, María Victoria

    المصدر: TDX (Tesis Doctorals en Xarxa)

    وصف الملف: application/pdf

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    دورية أكاديمية

    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

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