Artigos de revistas sobre o tema "CNOT3"
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Mittal, Saloni, Akhmed Aslam, Rachel Doidge, Rachel Medica e G. Sebastiaan Winkler. "The Ccr4a (CNOT6) and Ccr4b (CNOT6L) deadenylase subunits of the human Ccr4–Not complex contribute to the prevention of cell death and senescence". Molecular Biology of the Cell 22, n.º 6 (15 de março de 2011): 748–58. http://dx.doi.org/10.1091/mbc.e10-11-0898.
Texto completo da fonteElmén, Lisa, Claudia B. Volpato, Anaïs Kervadec, Santiago Pineda, Sreehari Kalvakuri, Nakissa N. Alayari, Luisa Foco et al. "Silencing of CCR4-NOT complex subunits affects heart structure and function". Disease Models & Mechanisms 13, n.º 7 (29 de maio de 2020): dmm044727. http://dx.doi.org/10.1242/dmm.044727.
Texto completo da fonteZheng, Xiaofeng, Raluca Dumitru, Brad L. Lackford, Johannes M. Freudenberg, Ajeet P. Singh, Trevor K. Archer, Raja Jothi e Guang Hu. "Cnot1, Cnot2, and Cnot3 Maintain Mouse and Human ESC Identity and Inhibit Extraembryonic Differentiation". STEM CELLS 30, n.º 5 (9 de abril de 2012): 910–22. http://dx.doi.org/10.1002/stem.1070.
Texto completo da fonteMcLenachan, Samuel, Dan Zhang, Janya Grainok, Xiao Zhang, Zhiqin Huang, Shang-Chih Chen, Khine Zaw et al. "Determinants of Disease Penetrance in PRPF31-Associated Retinopathy". Genes 12, n.º 10 (28 de setembro de 2021): 1542. http://dx.doi.org/10.3390/genes12101542.
Texto completo da fonteBanowska, Lidia. "Ironia, cnota i „strach śmieszności”. (Herbert – Norwid)". Studia Norwidiana 40 (13 de setembro de 2022): 37–56. http://dx.doi.org/10.18290/sn2240.2.
Texto completo da fonteDíaz-Peña, Roberto, Ana M. Aransay, Beatriz Suárez-Álvarez, Jacome Bruges-Armas, Naiara Rodríguez-Ezpeleta, María Regueiro, Fernando M. Pimentel-Santos et al. "A high density SNP genotyping approach within the 19q13 chromosome region identifies an association of a CNOT3 polymorphism with ankylosing spondylitis". Annals of the Rheumatic Diseases 71, n.º 5 (31 de janeiro de 2012): 714–17. http://dx.doi.org/10.1136/annrheumdis-2011-200661.
Texto completo da fonteSzram, Mariusz. "Can humility exist without poverty? A response by Cappadocian Fathers and John Chrysostom". Vox Patrum 62 (4 de setembro de 2014): 505–10. http://dx.doi.org/10.31743/vp.3599.
Texto completo da fonteInoue, Takeshi, Masahiro Morita, Atsushi Hijikata, Yoko Fukuda-Yuzawa, Shungo Adachi, Kyoichi Isono, Tomokatsu Ikawa et al. "CNOT3 contributes to early B cell development by controlling Igh rearrangement and p53 mRNA stability". Journal of Experimental Medicine 212, n.º 9 (3 de agosto de 2015): 1465–79. http://dx.doi.org/10.1084/jem.20150384.
Texto completo da fonteRodriguez-Gil, Alfonso, Olesja Ritter, Juliane Hornung, Hilda Stekman, Marcus Krüger, Thomas Braun, Elisabeth Kremmer, Michael Kracht e M. Lienhard Schmitz. "HIPK family kinases bind and regulate the function of the CCR4-NOT complex". Molecular Biology of the Cell 27, n.º 12 (15 de junho de 2016): 1969–80. http://dx.doi.org/10.1091/mbc.e15-09-0629.
Texto completo da fonteGłąb, Anna. "Cnota, charakter, dobroć. W nawiązaniu do powieści autobiograficznej Raimonda Gaity Mój ojciec Romulus". Roczniki Filozoficzne 68, n.º 1 (30 de março de 2020): 49–75. http://dx.doi.org/10.18290/rf20681-3.
Texto completo da fonteKaur, Ishwinder, Gopal P. Jadhav, Peter M. Fischer e Gerlof Sebastiaan Winkler. "The Discovery of Substituted 5-(2-Hydroxybenzoyl)-2-Pyridone Analogues as Inhibitors of the Human Caf1/CNOT7 Ribonuclease". Molecules 29, n.º 18 (13 de setembro de 2024): 4351. http://dx.doi.org/10.3390/molecules29184351.
Texto completo da fonteZheng, Xiaofeng, Pengyi Yang, Brad Lackford, Brian D. Bennett, Li Wang, Hui Li, Yu Wang et al. "CNOT3-Dependent mRNA Deadenylation Safeguards the Pluripotent State". Stem Cell Reports 7, n.º 5 (novembro de 2016): 897–910. http://dx.doi.org/10.1016/j.stemcr.2016.09.007.
Texto completo da fonteAbui, Abui Abraham. "The Vices against the Virtue of Temperance among the Atyap Cultural Heritage of Africa: A Philosophical Approach". Roczniki Kulturoznawcze 10, n.º 4 (23 de junho de 2020): 161–77. http://dx.doi.org/10.18290/rkult.2019.10.4-8.
Texto completo da fonteManuela, Priolo, Radio Francesca Clementina, Pizzi Simone, Pintomalli Letizia, Pantaleoni Francesca, Mancini Cecilia, Cordeddu Viviana et al. "Co-Occurring Heterozygous CNOT3 and SMAD6 Truncating Variants: Unusual Presentation and Refinement of the IDDSADF Phenotype". Genes 12, n.º 7 (30 de junho de 2021): 1009. http://dx.doi.org/10.3390/genes12071009.
Texto completo da fonteCejas, Paloma, Alessia Cavazza, C. N. Yandava, Victor Moreno, David Horst, Juan Moreno-Rubio, Emilio Burgos et al. "Transcriptional Regulator CNOT3 Defines an Aggressive Colorectal Cancer Subtype". Cancer Research 77, n.º 3 (29 de novembro de 2016): 766–79. http://dx.doi.org/10.1158/0008-5472.can-16-1346.
Texto completo da fonteWatanabe, C., M. Morita, T. Hayata, T. Nakamoto, C. Kikuguchi, X. Li, Y. Kobayashi et al. "Stability of mRNA influences osteoporotic bone mass via CNOT3". Proceedings of the National Academy of Sciences 111, n.º 7 (3 de fevereiro de 2014): 2692–97. http://dx.doi.org/10.1073/pnas.1316932111.
Texto completo da fonteKieliszek, Zdzisław. "Męstwo a świętość". Studia Warmińskie 49 (31 de dezembro de 2012): 9–22. http://dx.doi.org/10.31648/sw.250.
Texto completo da fonteEskandarian, Samira, Roger J. Grand, Shiva Irani, Mohsen Saeedi e Reza Mirfakhraie. "Depletion of CNOT4 modulates the DNA damage responses following ionizing radiation (IR)". Journal of Cancer Research and Therapeutics 20, n.º 1 (8 de abril de 2023): 126–32. http://dx.doi.org/10.4103/jcrt.jcrt_1723_22.
Texto completo da fonteChang, Nai-Wen, e Yi-Ping Huang. "The RNA degradation pathway is involved in PPARα-modulated anti-oral tumorigenesis". BioMedicine 9, n.º 4 (14 de novembro de 2019): 27. http://dx.doi.org/10.1051/bmdcn/2019090427.
Texto completo da fonteMartin, R., M. Splitt, D. Genevieve, E. Aten, A. Collins, C. I. de Bie, L. Faivre et al. "De novo variants in CNOT3 cause a variable neurodevelopmental disorder". European Journal of Human Genetics 27, n.º 11 (14 de junho de 2019): 1677–82. http://dx.doi.org/10.1038/s41431-019-0413-6.
Texto completo da fonteDoidge, Rachel, Saloni Mittal, Akhmed Aslam e G. Sebastiaan Winkler. "Deadenylation of cytoplasmic mRNA by the mammalian Ccr4–Not complex". Biochemical Society Transactions 40, n.º 4 (20 de julho de 2012): 896–901. http://dx.doi.org/10.1042/bst20120074.
Texto completo da fonteSeki, Masafumi, Kenichi Yoshida, Yusuke Sato, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Motohiro Kato et al. "Genetic Landscapes Of Childhood T-Cell Acute Lymphoblastic Leukemia". Blood 122, n.º 21 (15 de novembro de 2013): 3786. http://dx.doi.org/10.1182/blood.v122.21.3786.3786.
Texto completo da fonteSmółka, Lucyna. "O potrzebie umiaru w kulturze nadmiaru". Horyzonty Wychowania 19, n.º 52 (20 de outubro de 2020): 35–44. http://dx.doi.org/10.35765/hw.1858.
Texto completo da fonteVattathil, Selina M., Yue Liu, Nadia V. Harerimana, Adriana Lori, Ekaterina S. Gerasimov, Thomas G. Beach, Eric M. Reiman et al. "A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3". Genes 12, n.º 6 (26 de maio de 2021): 815. http://dx.doi.org/10.3390/genes12060815.
Texto completo da fonteDelacruz, Richard Glenn C., Imelda T. Sandoval, Kyle Chang, Braden N. Miller, Laura Reyes-Uribe, Ester Borras, Patrick M. Lynch et al. "Functional characterization of CNOT3 variants identified in familial adenomatous polyposis adenomas". Oncotarget 10, n.º 39 (11 de junho de 2019): 3939–51. http://dx.doi.org/10.18632/oncotarget.27003.
Texto completo da fonteTakahashi, Akinori, Chisato Kikuguchi, Masahiro Morita, Tetsuhiro Shimodaira, Noriko Tokai-Nishizumi, Kazumasa Yokoyama, Miho Ohsugi, Toru Suzuki e Tadashi Yamamoto. "Involvement of CNOT3 in mitotic progression through inhibition of MAD1 expression". Biochemical and Biophysical Research Communications 419, n.º 2 (março de 2012): 268–73. http://dx.doi.org/10.1016/j.bbrc.2012.02.007.
Texto completo da fonteLv, Jin, Wen-Jie Ming, Yang Zheng, Sha Xu, Gao-Li Fang, Qing Zhang, Yao Ding e Mei-Ping Ding. "A novel pathogenic variant in CNOT3 causing neurodevelopmental delay and epilepsy". Seizure 107 (abril de 2023): 104–6. http://dx.doi.org/10.1016/j.seizure.2023.03.022.
Texto completo da fonteLisbjerg, Kristian, Karen Grønskov, Mette Bertelsen, Lisbeth Birk Møller e Line Kessel. "Genetic Modifiers of Non-Penetrance and RNA Expression Levels in PRPF31-Associated Retinitis Pigmentosa in a Danish Cohort". Genes 14, n.º 2 (8 de fevereiro de 2023): 435. http://dx.doi.org/10.3390/genes14020435.
Texto completo da fonteSeki, Masafumi, Kenichi Yoshida, Shiraishi Yuichi, Kenichi Chiba, Hiroko Tanaka, Motohiro Kato, Ryoji Hanada et al. "Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia". Blood 124, n.º 21 (6 de dezembro de 2014): 3527. http://dx.doi.org/10.1182/blood.v124.21.3527.3527.
Texto completo da fonteJing, Lin, Meng-En Zhai, Jian Cui, Xin-Yu Fan, Yuan-Yuan Cheng, Jian-Li Jiang e Zhi-Nan Chen. "CNOT3 contributes to cisplatin resistance in lung cancer through inhibiting RIPK3 expression". Apoptosis 24, n.º 7-8 (8 de junho de 2019): 673–85. http://dx.doi.org/10.1007/s10495-019-01550-y.
Texto completo da fontePavanello, Lorenzo, Benjamin Hall, Blessing Airhihen e Gerlof Sebastiaan Winkler. "The central region of CNOT1 and CNOT9 stimulates deadenylation by the Ccr4–Not nuclease module". Biochemical Journal 475, n.º 21 (9 de novembro de 2018): 3437–50. http://dx.doi.org/10.1042/bcj20180456.
Texto completo da fonteAslam, Akhmed, Saloni Mittal, Frederic Koch, Jean-Christophe Andrau e G. Sebastiaan Winkler. "The Ccr4–Not Deadenylase Subunits CNOT7 and CNOT8 Have Overlapping Roles and Modulate Cell Proliferation". Molecular Biology of the Cell 20, n.º 17 (setembro de 2009): 3840–50. http://dx.doi.org/10.1091/mbc.e09-02-0146.
Texto completo da fonteShirai, Yo-Taro, Anna Mizutani, Saori Nishijima, Masafumi Horie, Chisato Kikuguchi, Olga Elisseeva e Tadashi Yamamoto. "CNOT3 targets negative cell cycle regulators in non-small cell lung cancer development". Oncogene 38, n.º 14 (10 de dezembro de 2018): 2580–94. http://dx.doi.org/10.1038/s41388-018-0603-7.
Texto completo da fonteVenturini, Giulia, Anna M. Rose, Amna Z. Shah, Shomi S. Bhattacharya e Carlo Rivolta. "CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance". PLoS Genetics 8, n.º 11 (8 de novembro de 2012): e1003040. http://dx.doi.org/10.1371/journal.pgen.1003040.
Texto completo da fonteGhashghaei, Maryam, Marty Yue, Aaremish Arsalan, Giuseppe Bombaci, Sandra Spencer Miko, Haya Shaalan, Glenn Edin, Gregg Morin, Fabiana Perna e Ly P. Vu. "RNA Deadenylation Subunit CNOT3 Promotes Myeloid Leukemia By Driving Translation of Oncogenic Targets". Blood 140, Supplement 1 (15 de novembro de 2022): 2962–63. http://dx.doi.org/10.1182/blood-2022-163026.
Texto completo da fonteKoszkało, Martyna. "Arystoteles, Tomasz z Akwinu, Jan Duns Szkot: Kilka uwag o różnicy między starożytnym i średniowiecznym pojmowaniem cnoty". Roczniki Filozoficzne 72, n.º 2 (28 de junho de 2024): 489–510. http://dx.doi.org/10.18290/rf24722.24.
Texto completo da fonteVu, Ly, Aaremish Arsalan, Guiseppe Bombaci, Glenn Edin, Lina Garawany, Maryam Ghashghaei, Sandi Miko, Gregg Morin, Fabiana Perna e Marty Yue. "3219 – RNA DEADENYLATION SUBUNIT CNOT3 PROMOTES MYELOID LEUKEMIA BY DRIVING TRANSLATION OF ONCOGENIC TARGETS". Experimental Hematology 111 (2022): S154. http://dx.doi.org/10.1016/j.exphem.2022.07.275.
Texto completo da fonteMeyer, Robert, Matthias Begemann, Stephanie Demuth, Florian Kraft, Daniela Dey, Herdit Schüler, Sabine Busse et al. "Inherited cases of CNOT3 ‐associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies". Clinical Genetics 98, n.º 4 (19 de agosto de 2020): 408–12. http://dx.doi.org/10.1111/cge.13819.
Texto completo da fonteCelary, Ireneusz. "Pastoraltheologische Vorschläge von Papst Franziskus für Ältere Priester und Ordensleute". Warszawskie Studia Pastoralne 1, n.º 34 (1 de janeiro de 2018): 169. http://dx.doi.org/10.21697/wsp.2017.12.1.34.09.
Texto completo da fonteŁojek, Stanisław. "Kim jest megalopsychos?" Etyka 40 (1 de dezembro de 2007): 115–29. http://dx.doi.org/10.14394/etyka.435.
Texto completo da fontePinard, Amélie, Stéphanie Guey, Dongchuan Guo, Alana C. Cecchi, Natasha Kharas, Stephanie Wallace, Ellen S. Regalado et al. "The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy". Genetics in Medicine 22, n.º 2 (2 de setembro de 2019): 427–31. http://dx.doi.org/10.1038/s41436-019-0639-2.
Texto completo da fonteBraun, Rachel M., Max Ferretti, Jesse Miller, Lauren Castellana, Jae Seung Lee, Kristen W. Lynch e Sara Cherry. "Host mRNA deadenylation machinery selectively targets interferon mRNAs, regulating antiviral immunity". Journal of Immunology 210, n.º 1_Supplement (1 de maio de 2023): 236.08. http://dx.doi.org/10.4049/jimmunol.210.supp.236.08.
Texto completo da fonteJung, Ji Hoon, Duckgue Lee, Hyun Min Ko e Hyeung-Jin Jang. "Inhibition of CNOT2 Induces Apoptosis via MID1IP1 in Colorectal Cancer Cells by Activating p53". Biomolecules 11, n.º 10 (10 de outubro de 2021): 1492. http://dx.doi.org/10.3390/biom11101492.
Texto completo da fonteDe Keersmaecker, Kim, Zeynep Kalender Atak, Ning Li, Carmen Vicente, Stephanie Patchett, Tiziana Girardi, Valentina Gianfelici et al. "Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia". Nature Genetics 45, n.º 2 (23 de dezembro de 2012): 186–90. http://dx.doi.org/10.1038/ng.2508.
Texto completo da fonteRaszewska-Żurek, Beata. "Kobieca cnota. Próba zrozumienia ewolucji znaczenia cnoty na przestrzeni wieków". Studia z Filologii Polskiej i Słowiańskiej 46 (25 de setembro de 2015): 83–102. http://dx.doi.org/10.11649/sfps.2011.006.
Texto completo da fonteMao, Qingyan, Qianfeng Zhuang, Jie Shen, Zhen Chen, Dong Xue, Tao Ding e Xiaozhou He. "MiRNA-124 regulates the sensitivity of renal cancer cells to cisplatin-induced necroptosis by targeting the CAPN4-CNOT3 axis". Translational Andrology and Urology 10, n.º 9 (setembro de 2021): 3669–83. http://dx.doi.org/10.21037/tau-21-777.
Texto completo da fonteMeijer, Hedda A., Tobias Schmidt, Sarah L. Gillen, Claudia Langlais, Rebekah Jukes-Jones, Cornelia H. de Moor, Kelvin Cain, Ania Wilczynska e Martin Bushell. "DEAD-box helicase eIF4A2 inhibits CNOT7 deadenylation activity". Nucleic Acids Research 47, n.º 15 (10 de junho de 2019): 8224–38. http://dx.doi.org/10.1093/nar/gkz509.
Texto completo da fonteYamaguchi, Tomokazu, Ryo Ozawa, Takafumi Minato, Midori Hoshizaki, Yutaro Kammura, Kazuma Okawara, Yousef Khalil et al. "Haploinsufficiency of Cnot3 Aggravates Acid-Induced Acute Lung Injury Likely Through Transcriptional and Post-Transcriptional Upregulation of Pro-Inflammatory Genes". Journal of Inflammation Research Volume 17 (agosto de 2024): 5415–25. http://dx.doi.org/10.2147/jir.s468612.
Texto completo da fonteGliniecki, Wojciech. "„DOBRZE DZIAŁAĆ” I „DOBRZE ŻYĆ” – CNOTY JAKO TRWAŁY FUNDAMENT LUDZKIEGO DZIAŁANIA". Studia Pelplińskie 57 (31 de dezembro de 2023): 83–98. http://dx.doi.org/10.12775/splp.2023.006.
Texto completo da fonteStoney, Patrick N., Akiko Yanagiya, Saori Nishijima e Tadashi Yamamoto. "CNOT7 Outcompetes Its Paralog CNOT8 for Integration into The CCR4-NOT Complex". Journal of Molecular Biology 434, n.º 9 (maio de 2022): 167523. http://dx.doi.org/10.1016/j.jmb.2022.167523.
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