Artykuły w czasopismach na temat „Rfc1”
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Amin, Neelam S., K. Michelle Tuffo i Connie Holm. "Dominant Mutations in Three Different Subunits of Replication Factor C Suppress Replication Defects in Yeast PCNA Mutants". Genetics 153, nr 4 (1.12.1999): 1617–28. http://dx.doi.org/10.1093/genetics/153.4.1617.
Pełny tekst źródłaCullmann, G., K. Fien, R. Kobayashi i B. Stillman. "Characterization of the five replication factor C genes of Saccharomyces cerevisiae." Molecular and Cellular Biology 15, nr 9 (wrzesień 1995): 4661–71. http://dx.doi.org/10.1128/mcb.15.9.4661.
Pełny tekst źródłaCui, Kan, Lei Qin, Xianyu Tang, Jieying Nong, Jin Chen, Nan Wu, Xin Gong, Lixiong Yi, Chenghuizi Yang i Shitou Xia. "A Single Amino Acid Substitution in RFC4 Leads to Endoduplication and Compromised Resistance to DNA Damage in Arabidopsis thaliana". Genes 13, nr 6 (9.06.2022): 1037. http://dx.doi.org/10.3390/genes13061037.
Pełny tekst źródłaGong, Maokai, James Yess, Tatiana Connolly, S. Percy Ivy, Takao Ohnuma, Kenneth H. Cowan i Jeffrey A. Moscow. "Molecular Mechanism of Antifolate Transport-Deficiency in a Methotrexate-Resistant MOLT-3 Human Leukemia Cell Line". Blood 89, nr 7 (1.04.1997): 2494–99. http://dx.doi.org/10.1182/blood.v89.7.2494.
Pełny tekst źródłaNaiki, Takahiro, Tae Kondo, Daisuke Nakada, Kunihiro Matsumoto i Katsunori Sugimoto. "Chl12 (Ctf18) Forms a Novel Replication Factor C-Related Complex and Functions Redundantly with Rad24 in the DNA Replication Checkpoint Pathway". Molecular and Cellular Biology 21, nr 17 (1.09.2001): 5838–45. http://dx.doi.org/10.1128/mcb.21.17.5838-5845.2001.
Pełny tekst źródłaPanda, Debasis, Daniel J. Fernandez, Madhu Lal, Eugen Buehler i Bernard Moss. "Triad of human cellular proteins, IRF2, FAM111A, and RFC3, restrict replication of orthopoxvirus SPI-1 host-range mutants". Proceedings of the National Academy of Sciences 114, nr 14 (20.03.2017): 3720–25. http://dx.doi.org/10.1073/pnas.1700678114.
Pełny tekst źródłaKai, Mihoko, Hiroyuki Tanaka i Teresa S. F. Wang. "Fission Yeast Rad17 Associates with Chromatin in Response to Aberrant Genomic Structures". Molecular and Cellular Biology 21, nr 10 (15.05.2001): 3289–301. http://dx.doi.org/10.1128/mcb.21.10.3289-3301.2001.
Pełny tekst źródłaMa, David W. L., Richard H. Finnell, Laurie A. Davidson, Evelyn S. Callaway, Ofer Spiegelstein, Jorge A. Piedrahita, J. Michael Salbaum i in. "Folate Transport Gene Inactivation in Mice Increases Sensitivity to Colon Carcinogenesis". Cancer Research 65, nr 3 (1.02.2005): 887–97. http://dx.doi.org/10.1158/0008-5472.887.65.3.
Pełny tekst źródłaXie, Yali, Chris Counter i Eric Alani. "Characterization of the Repeat-Tract Instability and Mutator Phenotypes Conferred by a Tn3 Insertion in RFC1, the Large Subunit of the Yeast Clamp Loader". Genetics 151, nr 2 (1.02.1999): 499–509. http://dx.doi.org/10.1093/genetics/151.2.499.
Pełny tekst źródłaZhao, Rongbao, Feng Gao i I. David Goldman. "Reduced folate carrier transports thiamine monophosphate: an alternative route for thiamine delivery into mammalian cells". American Journal of Physiology-Cell Physiology 282, nr 6 (1.06.2002): C1512—C1517. http://dx.doi.org/10.1152/ajpcell.00547.2001.
Pełny tekst źródłaKim, Hee-Sook, i Steven J. Brill. "Rfc4 Interacts with Rpa1 and Is Required for Both DNA Replication and DNA Damage Checkpoints in Saccharomyces cerevisiae". Molecular and Cellular Biology 21, nr 11 (1.06.2001): 3725–37. http://dx.doi.org/10.1128/mcb.21.11.3725-3737.2001.
Pełny tekst źródłaTraschütz, Andreas, Andrea Cortese, Selina Reich, Natalia Dominik, Jennifer Faber, Heike Jacobi, Annette M. Hartmann i in. "Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease". Neurology 96, nr 9 (25.01.2021): e1369-e1382. http://dx.doi.org/10.1212/wnl.0000000000011528.
Pełny tekst źródłaBeckwith, W., i M. A. McAlear. "Allele-specific interactions between the yeast RFC1 and RFC5 genes suggest a basis for RFC subunit-subunit interactions". Molecular Genetics and Genomics 264, nr 4 (listopad 2000): 378–91. http://dx.doi.org/10.1007/s004380000339.
Pełny tekst źródłaThieme, Andreas, Christel Depienne i Dagmar Timmann. "Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): from clinical diagnosis towards genetic testing". Medizinische Genetik 33, nr 4 (1.12.2021): 301–10. http://dx.doi.org/10.1515/medgen-2021-2098.
Pełny tekst źródłaDavies, Kayli, David J. Szmulewicz, Louise A. Corben, Martin Delatycki i Paul J. Lockhart. "RFC1-Related Disease". Neurology Genetics 8, nr 5 (29.08.2022): e200016. http://dx.doi.org/10.1212/nxg.0000000000200016.
Pełny tekst źródłaCurrò, Riccardo, Alessandro Salvalaggio, Stefano Tozza, Chiara Gemelli, Natalia Dominik, Valentina Galassi Deforie, Francesca Magrinelli i in. "RFC1 expansions are a common cause of idiopathic sensory neuropathy". Brain 144, nr 5 (1.05.2021): 1542–50. http://dx.doi.org/10.1093/brain/awab072.
Pełny tekst źródłade Jonge, Robert, Wim J. E. Tissing, Jan Hendrik Hooijberg, Gerrit Jansen, Gertjan J. L. Kaspers, Jan Lindemans, Godefridus J. Peters i Rob Pieters. "Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia". Blood 113, nr 10 (5.03.2009): 2284–89. http://dx.doi.org/10.1182/blood-2008-07-165928.
Pełny tekst źródłaAboud Syriani, Dona, Darice Wong, Sameer Andani, Claudio M. De Gusmao, Yuanming Mao, May Sanyoura, Giacomo Glotzer i in. "Prevalence of RFC1-mediated spinocerebellar ataxia in a North American ataxia cohort". Neurology Genetics 6, nr 3 (20.05.2020): e440. http://dx.doi.org/10.1212/nxg.0000000000000440.
Pełny tekst źródłaTanaka, Hiroyuki, Koichi Tanaka, Hiroshi Murakami i Hiroto Okayama. "Fission Yeast Cdc24 Is a Replication Factor C- and Proliferating Cell Nuclear Antigen-Interacting Factor Essential for S-Phase Completion". Molecular and Cellular Biology 19, nr 2 (1.02.1999): 1038–48. http://dx.doi.org/10.1128/mcb.19.2.1038.
Pełny tekst źródłaNaiki, Takahiro, Toshiyasu Shimomura, Tae Kondo, Kunihiro Matsumoto i Katsunori Sugimoto. "Rfc5, in Cooperation with Rad24, Controls DNA Damage Checkpoints throughout the Cell Cycle inSaccharomyces cerevisiae". Molecular and Cellular Biology 20, nr 16 (15.08.2000): 5888–96. http://dx.doi.org/10.1128/mcb.20.16.5888-5896.2000.
Pełny tekst źródłaReilly, Mary M. "RFC1 CANVAS: the expanding phenotype". Journal of Neurology, Neurosurgery & Psychiatry 92, nr 4 (9.02.2021): 345. http://dx.doi.org/10.1136/jnnp-2020-325504.
Pełny tekst źródłaScriba, Carolin K., Sarah J. Beecroft, Joshua S. Clayton, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Natalia Dominik i in. "A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families". Brain 143, nr 10 (1.10.2020): 2904–10. http://dx.doi.org/10.1093/brain/awaa263.
Pełny tekst źródłaBiselli, Joice Matos, Daniela Brumati, Vivian Fernanda Frigeri, Bruna Lancia Zampieri, Eny Maria Goloni-Bertollo i Érika Cristina Pavarino-Bertelli. "A80G polymorphism of reduced folate carrier 1 (RFC1) and C776G polymorphism of transcobalamin 2 (TC2) genes in Down's syndrome etiology". Sao Paulo Medical Journal 126, nr 6 (listopad 2008): 329–32. http://dx.doi.org/10.1590/s1516-31802008000600007.
Pełny tekst źródłaMalaquias, Maria João, Luis Braz, Cláudia Santos Silva, Joana Damásio, André Jorge, João M. Lemos, Catarina F. Campos i in. "MultisystemicRFC1-Related Disorder". Neurology: Clinical Practice 13, nr 5 (5.09.2023): e200190. http://dx.doi.org/10.1212/cpj.0000000000200190.
Pełny tekst źródłaGisatulin, Maria, Valerija Dobricic, Christine Zühlke, Yorck Hellenbroich, Vera Tadic, Alexander Münchau, Klaus Isenhardt i in. "Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes". Neurology 95, nr 21 (1.09.2020): e2912-e2923. http://dx.doi.org/10.1212/wnl.0000000000010744.
Pełny tekst źródłaRajgopal, Arun, Esteban E. Sierra, Rongbao Zhao i I. David Goldman. "Expression of the reduced folate carrier SLC19A1 in IEC-6 cells results in two distinct transport activities". American Journal of Physiology-Cell Physiology 281, nr 5 (1.11.2001): C1579—C1586. http://dx.doi.org/10.1152/ajpcell.2001.281.5.c1579.
Pełny tekst źródłaRoberts, Rhys C. "Removing the idiopathic from the chronic sensory neuropathies". Brain 144, nr 5 (1.05.2021): 1291–92. http://dx.doi.org/10.1093/brain/awab150.
Pełny tekst źródłaPaisán-Ruiz, Coro, i Joanna C. Jen. "CANVAS with cerebellar/sensory/vestibular dysfunction from RFC1 intronic pentanucleotide expansion". Brain 143, nr 2 (1.02.2020): 386–90. http://dx.doi.org/10.1093/brain/awaa015.
Pełny tekst źródłaStewart, D. J., M. I. Nunez, J. Jelinek, Z. Guo, D. Hong, S. Gupta, Y. Oki, J. Issa, R. Kurzrock i I. I. Wistuba. "Decitabine effect on human tumor expression of various transporters". Journal of Clinical Oncology 27, nr 15_suppl (20.05.2009): 2540. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.2540.
Pełny tekst źródłaNoskov, Vladimir N., Hiroyuki Araki i Akio Sugino. "The RFC2 Gene, Encoding the Third-Largest Subunit of the Replication Factor C Complex, Is Required for an S-Phase Checkpoint in Saccharomyces cerevisiae". Molecular and Cellular Biology 18, nr 8 (1.08.1998): 4914–23. http://dx.doi.org/10.1128/mcb.18.8.4914.
Pełny tekst źródłaDeng, Jianxiong, Fangyan Zhong, Weiguo Gu i Feng Qiu. "Exploration of Prognostic Biomarkers among Replication Factor C Family in the Hepatocellular Carcinoma". Evolutionary Bioinformatics 17 (styczeń 2021): 117693432199410. http://dx.doi.org/10.1177/1176934321994109.
Pełny tekst źródłaНужный, Е. П., Н. Ю. Абрамычева, Е. Г. Воробьева, Е. О. Иванова, Ю. А. Шпилюкова, А. И. Белякова-Бодина, Д. В. И i in. "CANVAS is a common form of late-onset hereditary ataxia". Nauchno-prakticheskii zhurnal «Medicinskaia genetika», nr 4(213) (30.04.2020): 51–52. http://dx.doi.org/10.25557/2073-7998.2020.04.51-52.
Pełny tekst źródłaCortese, Andrea, Stefano Tozza, Wai Yan Yau, Salvatore Rossi, Sarah J. Beecroft, Zane Jaunmuktane, Zoe Dyer i in. "Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion". Brain 143, nr 2 (1.02.2020): 480–90. http://dx.doi.org/10.1093/brain/awz418.
Pełny tekst źródłaAbramzon, Yevgenya, Ramita Dewan, Andrea Cortese, Susan Resnick, Luigi Ferrucci, Henry Houlden i Bryan J. Traynor. "Investigating RFC1 expansions in sporadic amyotrophic lateral sclerosis". Journal of the Neurological Sciences 430 (listopad 2021): 118061. http://dx.doi.org/10.1016/j.jns.2021.118061.
Pełny tekst źródłaDevald, I. V., E. A. Hodus, D. Yu Nokhrin, E. B. Khromova, G. L. Ignatova, D. S. Stashkevich, A. M. Lila i A. L. Burmistrova. "Evaluation of the influence of polymorphisms of the transporter genes (<i>RFC1</i>, <i>MDR1</i>) and <i>GGH</i> on the efficacy of methotrexate in rheumatoid arthritis". Modern Rheumatology Journal 17, nr 4 (20.08.2023): 28–34. http://dx.doi.org/10.14412/1996-7012-2023-4-28-34.
Pełny tekst źródłaHerrmann, Laura, Mathias Gelderblom, Maxim Bester, Natalie Deininger, Thorsten Schütze, Ute Hidding, Caspar Gross i in. "Multisystemic neurodegeneration caused by biallelic pentanucleotide expansions in RFC1". Parkinsonism & Related Disorders 95 (luty 2022): 54–56. http://dx.doi.org/10.1016/j.parkreldis.2022.01.001.
Pełny tekst źródłaTerryn, Joke, Amélie Van Eesbeeck, Sascha Vermeer i Wim Vandenberghe. "The Characteristic Eye Movement Disorder of RFC1 ‐Linked CANVAS". Movement Disorders Clinical Practice 7, nr 2 (24.01.2020): 230–31. http://dx.doi.org/10.1002/mdc3.12896.
Pełny tekst źródłaZheng, Fengwei, Roxana E. Georgescu, Nina Y. Yao, Michael E. O’Donnell i Huilin Li. "DNA is loaded through the 9-1-1 DNA checkpoint clamp in the opposite direction of the PCNA clamp". Nature Structural & Molecular Biology 29, nr 4 (21.03.2022): 376–85. http://dx.doi.org/10.1038/s41594-022-00742-6.
Pełny tekst źródłaFacchini, Stefano, Natalia Dominik, Arianna Manini, Stephanie Efthymiou, Riccardo Currò, Bianca Rugginini, Elisa Vegezzi i in. "Optical Genome Mapping Enables Detection and Accurate Sizing of RFC1 Repeat Expansions". Biomolecules 13, nr 10 (19.10.2023): 1546. http://dx.doi.org/10.3390/biom13101546.
Pełny tekst źródłaMerrill, Bradley J., i Connie Holm. "The RAD52 Recombinational Repair Pathway is Essential in pol30 (PCNA) Mutants That Accumulate Small Single-Stranded DNA Fragments During DNA Synthesis". Genetics 148, nr 2 (1.02.1998): 611–24. http://dx.doi.org/10.1093/genetics/148.2.611.
Pełny tekst źródłaWatanabe, Kazuki, Mitsuko Nakashima, Rie Wakatsuki, Tomoyasu Bunai, Yasuomi Ouchi, Tomohiko Nakamura, Hiroaki Miyajima i Hirotomo Saitsu. "Cognitive Impairment in a Complex Family With AAGGG and ACAGG Repeat Expansions in RFC1 Detected by ExpansionHunter Denovo". Neurology Genetics 8, nr 3 (16.05.2022): e682. http://dx.doi.org/10.1212/nxg.0000000000000682.
Pełny tekst źródłaPark, Jeong A., Hyoung Jin Kang, Ho Joon Im, Hee Young Shin i Hyo Seop Ahn. "Association of genetic polymorphisms in the folate pathway with efficacy and toxicity of methotrexate in pediatric osteosarcoma." Journal of Clinical Oncology 31, nr 15_suppl (20.05.2013): 10051. http://dx.doi.org/10.1200/jco.2013.31.15_suppl.10051.
Pełny tekst źródłaHalmágyi, Gábor M., i David J. Szmulewicz. "Correction to: Vestibular function testing in patients with RFC1 mutations". Journal of Neurology 269, nr 4 (10.03.2022): 2264. http://dx.doi.org/10.1007/s00415-022-10975-6.
Pełny tekst źródłaSilva Schmitt, Gabriel, Alberto R. M. Martinez, Felipe F. Graça, Fabrício Diniz Lima, Luciana C. Bonadia, Bárbara Juarez Amorim, Anamarli Nucci i Marcondes Cavalcante França. "Dopa‐Responsive Parkinsonism in a Patient With Homozygous RFC1 Expansions". Movement Disorders 35, nr 10 (październik 2020): 1889–90. http://dx.doi.org/10.1002/mds.28286.
Pełny tekst źródłaGuerra-Shinohara, Elvira Maria, Kelma Cordeiro da Silva Giusti, Nathalia Sierra Monteiro, Robson José Lazaro, Fernanda Midori Seino, Carolina Tosin Bueno, Mário Henrique Burlacchini Carvalho, Antônio Amorim Filho, Carlos Chiattone i Marcelo Zugaib. "Effect of Genetic Polymorphisms Related to Folate and Homocysteine Metabolism In the Etiology of Recurrent Miscarriages". Blood 116, nr 21 (19.11.2010): 5136. http://dx.doi.org/10.1182/blood.v116.21.5136.5136.
Pełny tekst źródłaAndo, Masahiro, Yujiro Higuchi, Junhui Yuan, Akiko Yoshimura, Takaki Taniguchi, Fumikazu Kojima, Yutaka Noguchi i in. "Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible". Biomedicines 10, nr 7 (29.06.2022): 1546. http://dx.doi.org/10.3390/biomedicines10071546.
Pełny tekst źródłaGiovannini, Sara, Marie-Christine Weller, Hana Hanzlíková, Tetsuya Shiota, Shunichi Takeda i Josef Jiricny. "ATAD5 deficiency alters DNA damage metabolism and sensitizes cells to PARP inhibition". Nucleic Acids Research 48, nr 9 (16.04.2020): 4928–39. http://dx.doi.org/10.1093/nar/gkaa255.
Pełny tekst źródłaTurner, Richard D., Barnaby Hirons, Andrea Cortese i Surinder S. Birring. "Chronic Cough as a Genetic Neurological Disorder? Insights from Cerebellar Ataxia with Neuropathy and Vestibular Areflexia Syndrome (CANVAS)". Lung 201, nr 6 (18.11.2023): 511–19. http://dx.doi.org/10.1007/s00408-023-00660-4.
Pełny tekst źródłaSullivan, Roisin, Wai Yan Yau, Viorica Chelban, Salvatore Rossi, Natalia Dominik, Emer O'Connor, John Hardy, Nicholas Wood, Andrea Cortese i Henry Houlden. "RFC1-related ataxia is a mimic of early multiple system atrophy". Journal of Neurology, Neurosurgery & Psychiatry 92, nr 4 (9.02.2021): 444–46. http://dx.doi.org/10.1136/jnnp-2020-325092.
Pełny tekst źródłaMisbah, Md, Manoj Kumar, Abul Kalam Najmi i Mymoona Akhtar. "Identification of expression profiles and prognostic value of RFCs in colorectal cancer". Scientific Reports 14, nr 1 (19.03.2024). http://dx.doi.org/10.1038/s41598-024-56361-2.
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