المؤلفون: Helena B. Madsen, Louise I. Pease, Rebekah-Louise Scanlan, Mansour Akbari, Lene J. Rasmussen, Daryl P. Shanley, Vilhelm A. Bohr

المصدر: Frontiers in Aging Neuroscience, Vol 15 (2023)

مصطلحات موضوعية: APTX, innate immunity, DNA repair, ataxia, microglia, DNA- and RNA-sensing pathways, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fnagi.2023.1290681/full; https://doaj.org/toc/1663-4365

URL الوصول: https://doaj.org/article/a6596f6c18f54f9cb2dd3ab9d8bb0b99

المؤلفون: Wasserman, Theodore^Aff4, Wasserman, Lori Drucker^Aff4

المساهمون: Wasserman, Theodore, Series Editor^{Aff1, Aff2}, Wasserman, Lori Drucker^Aff3

المصدر: Apraxia: The Neural Network Model. :25-34

المؤلفون: Aguillon, David, Vasquez, Daniel, Madrigal, Lucia, Moreno, Sonia, Hernández, Dora, Isaza-Ruget, Mario, Lopez, Juan Javier, Landires, Iván, Nuñez-Samudio, Virginia, Restrepo, Carlos M., Vidal, Oscar M., Vélez, Jorge I., Arcos-Holzinger, Mauricio, Lopera, Francisco, Arcos-Burgos, Mauricio^{Aff7, IDs12035022028217_cor15}

المصدر: Molecular Neurobiology. 59(6):3845-3858

المؤلفون: Xuan Wu, Nan Dong, Zhensheng Liu, Tieyu Tang, Meirong Liu

المصدر: Frontiers in Neurology, Vol 13 (2022)

مصطلحات موضوعية: ataxia with oculomotor apraxia type 1, oculomotor apraxia, APTX, novel mutation, case report, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fneur.2022.873826/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/78498275e14b45aba444f0074f74c67f

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

URL الوصول: https://escholarship.org/uc/item/33c5w49n

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المؤلفون: David Aguillon, Iván Landires, Sonia Moreno, Virginia Núñez-Samudio, Daniel Vasquez, Mario A. Isaza-Ruget, Oscar M. Vidal, Francisco Lopera, Lucia Madrigal, Mauricio Arcos-Holzinger, Juan Javier Lopez, Mauricio Arcos-Burgos, Jorge I. Vélez, Dora Hernández, Carlos Martín Restrepo

المصدر: Molecular Neurobiology. 59:3845-3858

مصطلحات موضوعية: Ataxia, Cerebellar Ataxia, Apraxias, aptX, Neuroscience (miscellaneous), Colombia, Apraxia, Cellular and Molecular Neuroscience, medicine, Humans, Spinocerebellar Degenerations, Genetics, business.industry, Dysarthria, Siblings, Neuropsychology, Nuclear Proteins, DNA, medicine.disease, Phenotype, DNA-Binding Proteins, Neurology, Mutation, Mutation (genetic algorithm), medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54fd37d6c0d4967b16c8a79b3757d018
https://doi.org/10.1007/s12035-022-02821-7

المؤلفون: Qiang Fu, Fan Yang, Minxue Liao, Noel J. Feeney, Kevin Deng, Nikolaos Serifis, Liang Wei, Hongji Yang, Kai Chen, Shaoping Deng, James F. Markmann

المصدر: Frontiers in Oncology, Vol 9 (2019)

مصطلحات موضوعية: RADIL, APTX, CD8+ T cells, kidney transplantation, kidney cancer, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fonc.2019.00737/full; https://doaj.org/toc/2234-943X

URL الوصول: https://doaj.org/article/0056390a6e26450d811d8e164333d72d

المؤلفون: Johansson, Gustav, Adevåg, Mattias, Milton, Jacob

مصطلحات موضوعية: aptX, BLE, perceived audio quality, LC3, Bluetooth Low Energy, audio codec, real-time, interactive context, Systemvetenskap, informationssystem och informatik, latency, Information Systems

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1481::245d681fdac8f8820b2fca08cbd5ea25
http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-22711