Zeitschriftenartikel zum Thema „Rfc1“
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Amin, Neelam S., K. Michelle Tuffo und Connie Holm. „Dominant Mutations in Three Different Subunits of Replication Factor C Suppress Replication Defects in Yeast PCNA Mutants“. Genetics 153, Nr. 4 (01.12.1999): 1617–28. http://dx.doi.org/10.1093/genetics/153.4.1617.
Der volle Inhalt der QuelleCullmann, G., K. Fien, R. Kobayashi und B. Stillman. „Characterization of the five replication factor C genes of Saccharomyces cerevisiae.“ Molecular and Cellular Biology 15, Nr. 9 (September 1995): 4661–71. http://dx.doi.org/10.1128/mcb.15.9.4661.
Der volle Inhalt der QuelleCui, Kan, Lei Qin, Xianyu Tang, Jieying Nong, Jin Chen, Nan Wu, Xin Gong, Lixiong Yi, Chenghuizi Yang und 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 (09.06.2022): 1037. http://dx.doi.org/10.3390/genes13061037.
Der volle Inhalt der QuelleGong, Maokai, James Yess, Tatiana Connolly, S. Percy Ivy, Takao Ohnuma, Kenneth H. Cowan und Jeffrey A. Moscow. „Molecular Mechanism of Antifolate Transport-Deficiency in a Methotrexate-Resistant MOLT-3 Human Leukemia Cell Line“. Blood 89, Nr. 7 (01.04.1997): 2494–99. http://dx.doi.org/10.1182/blood.v89.7.2494.
Der volle Inhalt der QuelleNaiki, Takahiro, Tae Kondo, Daisuke Nakada, Kunihiro Matsumoto und 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 (01.09.2001): 5838–45. http://dx.doi.org/10.1128/mcb.21.17.5838-5845.2001.
Der volle Inhalt der QuellePanda, Debasis, Daniel J. Fernandez, Madhu Lal, Eugen Buehler und 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.
Der volle Inhalt der QuelleKai, Mihoko, Hiroyuki Tanaka und 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.
Der volle Inhalt der QuelleMa, David W. L., Richard H. Finnell, Laurie A. Davidson, Evelyn S. Callaway, Ofer Spiegelstein, Jorge A. Piedrahita, J. Michael Salbaum et al. „Folate Transport Gene Inactivation in Mice Increases Sensitivity to Colon Carcinogenesis“. Cancer Research 65, Nr. 3 (01.02.2005): 887–97. http://dx.doi.org/10.1158/0008-5472.887.65.3.
Der volle Inhalt der QuelleXie, Yali, Chris Counter und 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 (01.02.1999): 499–509. http://dx.doi.org/10.1093/genetics/151.2.499.
Der volle Inhalt der QuelleZhao, Rongbao, Feng Gao und 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 (01.06.2002): C1512—C1517. http://dx.doi.org/10.1152/ajpcell.00547.2001.
Der volle Inhalt der QuelleKim, Hee-Sook, und 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 (01.06.2001): 3725–37. http://dx.doi.org/10.1128/mcb.21.11.3725-3737.2001.
Der volle Inhalt der QuelleTraschütz, Andreas, Andrea Cortese, Selina Reich, Natalia Dominik, Jennifer Faber, Heike Jacobi, Annette M. Hartmann et al. „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.
Der volle Inhalt der QuelleBeckwith, W., und 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 (November 2000): 378–91. http://dx.doi.org/10.1007/s004380000339.
Der volle Inhalt der QuelleThieme, Andreas, Christel Depienne und Dagmar Timmann. „Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): from clinical diagnosis towards genetic testing“. Medizinische Genetik 33, Nr. 4 (01.12.2021): 301–10. http://dx.doi.org/10.1515/medgen-2021-2098.
Der volle Inhalt der QuelleDavies, Kayli, David J. Szmulewicz, Louise A. Corben, Martin Delatycki und Paul J. Lockhart. „RFC1-Related Disease“. Neurology Genetics 8, Nr. 5 (29.08.2022): e200016. http://dx.doi.org/10.1212/nxg.0000000000200016.
Der volle Inhalt der QuelleCurrò, Riccardo, Alessandro Salvalaggio, Stefano Tozza, Chiara Gemelli, Natalia Dominik, Valentina Galassi Deforie, Francesca Magrinelli et al. „RFC1 expansions are a common cause of idiopathic sensory neuropathy“. Brain 144, Nr. 5 (01.05.2021): 1542–50. http://dx.doi.org/10.1093/brain/awab072.
Der volle Inhalt der Quellede Jonge, Robert, Wim J. E. Tissing, Jan Hendrik Hooijberg, Gerrit Jansen, Gertjan J. L. Kaspers, Jan Lindemans, Godefridus J. Peters und Rob Pieters. „Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia“. Blood 113, Nr. 10 (05.03.2009): 2284–89. http://dx.doi.org/10.1182/blood-2008-07-165928.
Der volle Inhalt der QuelleAboud Syriani, Dona, Darice Wong, Sameer Andani, Claudio M. De Gusmao, Yuanming Mao, May Sanyoura, Giacomo Glotzer et al. „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.
Der volle Inhalt der QuelleTanaka, Hiroyuki, Koichi Tanaka, Hiroshi Murakami und 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 (01.02.1999): 1038–48. http://dx.doi.org/10.1128/mcb.19.2.1038.
Der volle Inhalt der QuelleNaiki, Takahiro, Toshiyasu Shimomura, Tae Kondo, Kunihiro Matsumoto und 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.
Der volle Inhalt der QuelleReilly, Mary M. „RFC1 CANVAS: the expanding phenotype“. Journal of Neurology, Neurosurgery & Psychiatry 92, Nr. 4 (09.02.2021): 345. http://dx.doi.org/10.1136/jnnp-2020-325504.
Der volle Inhalt der QuelleScriba, Carolin K., Sarah J. Beecroft, Joshua S. Clayton, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Natalia Dominik et al. „A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families“. Brain 143, Nr. 10 (01.10.2020): 2904–10. http://dx.doi.org/10.1093/brain/awaa263.
Der volle Inhalt der QuelleBiselli, Joice Matos, Daniela Brumati, Vivian Fernanda Frigeri, Bruna Lancia Zampieri, Eny Maria Goloni-Bertollo und 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 (November 2008): 329–32. http://dx.doi.org/10.1590/s1516-31802008000600007.
Der volle Inhalt der QuelleMalaquias, Maria João, Luis Braz, Cláudia Santos Silva, Joana Damásio, André Jorge, João M. Lemos, Catarina F. Campos et al. „MultisystemicRFC1-Related Disorder“. Neurology: Clinical Practice 13, Nr. 5 (05.09.2023): e200190. http://dx.doi.org/10.1212/cpj.0000000000200190.
Der volle Inhalt der QuelleGisatulin, Maria, Valerija Dobricic, Christine Zühlke, Yorck Hellenbroich, Vera Tadic, Alexander Münchau, Klaus Isenhardt et al. „Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes“. Neurology 95, Nr. 21 (01.09.2020): e2912-e2923. http://dx.doi.org/10.1212/wnl.0000000000010744.
Der volle Inhalt der QuelleRajgopal, Arun, Esteban E. Sierra, Rongbao Zhao und 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 (01.11.2001): C1579—C1586. http://dx.doi.org/10.1152/ajpcell.2001.281.5.c1579.
Der volle Inhalt der QuelleRoberts, Rhys C. „Removing the idiopathic from the chronic sensory neuropathies“. Brain 144, Nr. 5 (01.05.2021): 1291–92. http://dx.doi.org/10.1093/brain/awab150.
Der volle Inhalt der QuellePaisán-Ruiz, Coro, und Joanna C. Jen. „CANVAS with cerebellar/sensory/vestibular dysfunction from RFC1 intronic pentanucleotide expansion“. Brain 143, Nr. 2 (01.02.2020): 386–90. http://dx.doi.org/10.1093/brain/awaa015.
Der volle Inhalt der QuelleStewart, D. J., M. I. Nunez, J. Jelinek, Z. Guo, D. Hong, S. Gupta, Y. Oki, J. Issa, R. Kurzrock und 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.
Der volle Inhalt der QuelleNoskov, Vladimir N., Hiroyuki Araki und 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 (01.08.1998): 4914–23. http://dx.doi.org/10.1128/mcb.18.8.4914.
Der volle Inhalt der QuelleDeng, Jianxiong, Fangyan Zhong, Weiguo Gu und Feng Qiu. „Exploration of Prognostic Biomarkers among Replication Factor C Family in the Hepatocellular Carcinoma“. Evolutionary Bioinformatics 17 (Januar 2021): 117693432199410. http://dx.doi.org/10.1177/1176934321994109.
Der volle Inhalt der QuelleНужный, Е. П., Н. Ю. Абрамычева, Е. Г. Воробьева, Е. О. Иванова, Ю. А. Шпилюкова, А. И. Белякова-Бодина, Д. В. И et al. „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.
Der volle Inhalt der QuelleCortese, Andrea, Stefano Tozza, Wai Yan Yau, Salvatore Rossi, Sarah J. Beecroft, Zane Jaunmuktane, Zoe Dyer et al. „Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion“. Brain 143, Nr. 2 (01.02.2020): 480–90. http://dx.doi.org/10.1093/brain/awz418.
Der volle Inhalt der QuelleAbramzon, Yevgenya, Ramita Dewan, Andrea Cortese, Susan Resnick, Luigi Ferrucci, Henry Houlden und Bryan J. Traynor. „Investigating RFC1 expansions in sporadic amyotrophic lateral sclerosis“. Journal of the Neurological Sciences 430 (November 2021): 118061. http://dx.doi.org/10.1016/j.jns.2021.118061.
Der volle Inhalt der QuelleDevald, I. V., E. A. Hodus, D. Yu Nokhrin, E. B. Khromova, G. L. Ignatova, D. S. Stashkevich, A. M. Lila und 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.
Der volle Inhalt der QuelleHerrmann, Laura, Mathias Gelderblom, Maxim Bester, Natalie Deininger, Thorsten Schütze, Ute Hidding, Caspar Gross et al. „Multisystemic neurodegeneration caused by biallelic pentanucleotide expansions in RFC1“. Parkinsonism & Related Disorders 95 (Februar 2022): 54–56. http://dx.doi.org/10.1016/j.parkreldis.2022.01.001.
Der volle Inhalt der QuelleTerryn, Joke, Amélie Van Eesbeeck, Sascha Vermeer und 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.
Der volle Inhalt der QuelleZheng, Fengwei, Roxana E. Georgescu, Nina Y. Yao, Michael E. O’Donnell und 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.
Der volle Inhalt der QuelleFacchini, Stefano, Natalia Dominik, Arianna Manini, Stephanie Efthymiou, Riccardo Currò, Bianca Rugginini, Elisa Vegezzi et al. „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.
Der volle Inhalt der QuelleMerrill, Bradley J., und 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 (01.02.1998): 611–24. http://dx.doi.org/10.1093/genetics/148.2.611.
Der volle Inhalt der QuelleWatanabe, Kazuki, Mitsuko Nakashima, Rie Wakatsuki, Tomoyasu Bunai, Yasuomi Ouchi, Tomohiko Nakamura, Hiroaki Miyajima und 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.
Der volle Inhalt der QuellePark, Jeong A., Hyoung Jin Kang, Ho Joon Im, Hee Young Shin und 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.
Der volle Inhalt der QuelleHalmágyi, Gábor M., und 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.
Der volle Inhalt der QuelleSilva Schmitt, Gabriel, Alberto R. M. Martinez, Felipe F. Graça, Fabrício Diniz Lima, Luciana C. Bonadia, Bárbara Juarez Amorim, Anamarli Nucci und Marcondes Cavalcante França. „Dopa‐Responsive Parkinsonism in a Patient With Homozygous RFC1 Expansions“. Movement Disorders 35, Nr. 10 (Oktober 2020): 1889–90. http://dx.doi.org/10.1002/mds.28286.
Der volle Inhalt der QuelleGuerra-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 und 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.
Der volle Inhalt der QuelleAndo, Masahiro, Yujiro Higuchi, Junhui Yuan, Akiko Yoshimura, Takaki Taniguchi, Fumikazu Kojima, Yutaka Noguchi et al. „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.
Der volle Inhalt der QuelleGiovannini, Sara, Marie-Christine Weller, Hana Hanzlíková, Tetsuya Shiota, Shunichi Takeda und 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.
Der volle Inhalt der QuelleTurner, Richard D., Barnaby Hirons, Andrea Cortese und 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.
Der volle Inhalt der QuelleSullivan, Roisin, Wai Yan Yau, Viorica Chelban, Salvatore Rossi, Natalia Dominik, Emer O'Connor, John Hardy, Nicholas Wood, Andrea Cortese und Henry Houlden. „RFC1-related ataxia is a mimic of early multiple system atrophy“. Journal of Neurology, Neurosurgery & Psychiatry 92, Nr. 4 (09.02.2021): 444–46. http://dx.doi.org/10.1136/jnnp-2020-325092.
Der volle Inhalt der QuelleMisbah, Md, Manoj Kumar, Abul Kalam Najmi und 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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