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Artykuły w czasopismach na temat "RUNX"
Chuang, Linda Shyue Huey, Jian Ming Khor, Soak Kuan Lai, Shubham Garg, Vaidehi Krishnan, Cheng-Gee Koh, Sang Hyun Lee i Yoshiaki Ito. "Aurora kinase-induced phosphorylation excludes transcription factor RUNX from the chromatin to facilitate proper mitotic progression". Proceedings of the National Academy of Sciences 113, nr 23 (23.05.2016): 6490–95. http://dx.doi.org/10.1073/pnas.1523157113.
Pełny tekst źródłaShin, Boyoung, Hiroyuki Hosokawa, Maile Romero-Wolf, Wen Zhou, Kaori Masuhara, Victoria R. Tobin, Ditsa Levanon, Yoram Groner i Ellen V. Rothenberg. "Runx1 and Runx3 drive progenitor to T-lineage transcriptome conversion in mouse T cell commitment via dynamic genomic site switching". Proceedings of the National Academy of Sciences 118, nr 4 (21.01.2021): e2019655118. http://dx.doi.org/10.1073/pnas.2019655118.
Pełny tekst źródłaMorita, Ken, Kensho Suzuki, Shintaro Maeda, Yoshihide Mitsuda, Ayaka Yano, Yoshimi Yamada, Hiroki Kiyose i in. "Cluster Regulation of RUNX Family By "Gene Switch" Triggers a Profound Tumor Regression of Diverse Origins". Blood 128, nr 22 (2.12.2016): 443. http://dx.doi.org/10.1182/blood.v128.22.443.443.
Pełny tekst źródłaMasuda, Tatsuya, Hirohito Kubota, Naoya Sakuramoto, Asuka Hada, Ayaka Horiuchi, Asami Sasaki, Kanako Takeda i in. "RUNX-NFAT Axis As a Novel Therapeutic Target for AML and T Cell Immunity". Blood 136, Supplement 1 (5.11.2020): 25–26. http://dx.doi.org/10.1182/blood-2020-143458.
Pełny tekst źródłaChuang, Linda Shyue Huey, Junichi Matsuo, Daisuke Douchi, Nur Astiana Bte Mawan i Yoshiaki Ito. "RUNX3 in Stem Cell and Cancer Biology". Cells 12, nr 3 (25.01.2023): 408. http://dx.doi.org/10.3390/cells12030408.
Pełny tekst źródłade Bruijn, Marella, i Elaine Dzierzak. "Runx transcription factors in the development and function of the definitive hematopoietic system". Blood 129, nr 15 (13.04.2017): 2061–69. http://dx.doi.org/10.1182/blood-2016-12-689109.
Pełny tekst źródłaSuzuki, Kensho, Ken Morita, Shintaro Maeda, Hiroki Kiyose, Souichi Adachi i Yasuhiko Kamikubo. "Paradoxical Enhancement of Leukemogenesis in Acute Myeloid Leukemia Cells with Moderately Attenuated RUNX1 Expressions". Blood 128, nr 22 (2.12.2016): 2710. http://dx.doi.org/10.1182/blood.v128.22.2710.2710.
Pełny tekst źródłaKlunker, Sven, Mark M. W. Chong, Pierre-Yves Mantel, Oscar Palomares, Claudio Bassin, Mario Ziegler, Beate Rückert i in. "Transcription factors RUNX1 and RUNX3 in the induction and suppressive function of Foxp3+ inducible regulatory T cells". Journal of Experimental Medicine 206, nr 12 (16.11.2009): 2701–15. http://dx.doi.org/10.1084/jem.20090596.
Pełny tekst źródłaAndo, Kiyohiro, i Akira Nakagawara. "The RUNX Family Defines Trk Phenotype and Aggressiveness of Human Neuroblastoma through Regulation of p53 and MYCN". Cells 12, nr 4 (8.02.2023): 544. http://dx.doi.org/10.3390/cells12040544.
Pełny tekst źródłaZhao, Ling, Jennifer L. Cannons, Lucio H. Castilla, Pamela L. Schwartzberg i Pu Paul Liu. "The Role of CBFβ in T Cell Development." Blood 104, nr 11 (16.11.2004): 3234. http://dx.doi.org/10.1182/blood.v104.11.3234.3234.
Pełny tekst źródłaRozprawy doktorskie na temat "RUNX"
LeBlanc, Kimberly T. "Runx Expression in Normal and Osteoarthritic Cartilage: Possible Functions of Runx Proteins in Chondrocytes: A Dissertation". eScholarship@UMMS, 2013. https://escholarship.umassmed.edu/gsbs_diss/655.
Pełny tekst źródłaLeBlanc, Kimberly T. "Runx Expression in Normal and Osteoarthritic Cartilage: Possible Functions of Runx Proteins in Chondrocytes: A Dissertation". eScholarship@UMMS, 2002. http://escholarship.umassmed.edu/gsbs_diss/655.
Pełny tekst źródłaWhiteman, Hannah Juliette. "RUNX expression and function in human B cells". Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.422343.
Pełny tekst źródłaChen, Aichun. "Regulation of lozenge transcription factor activity and blood cell development by MLF and its partner DnaJ-1". Thesis, Toulouse 3, 2017. http://www.theses.fr/2017TOU30064/document.
Pełny tekst źródłaHematopoiesis is the process of formation of fully differentiated blood cells from hematopoietic stem cells (HSCs). This process is tightly controlled by the integration of developmental and homeostatic signals to ensure the generation of an appropriate number of each blood cell type. At the molecular level, the regulation of this developmental process is mediated by a number of transcription factors, especially by members of the RUNX family, and mutations affecting these factors are at the origin of numerous hemopathies, including leukemia. Intriguingly, many transcriptional regulators and signaling pathways controlling blood cell development are evolutionarily conserved from humans to Drosophila melanogaster. Hence, the fruit fly has become a potent and simplified model to study the mechanisms underlying the specification of blood cell lineages and the regulation of blood cell homeostasis. Members of the Myeloid Leukemia Factor (MLF) family have been implicated in hematopoiesis and in oncogenic blood cell transformation, but their function and molecular mechanism of action remain elusive. Previous work in Drosophila showed that MLF stabilizes the RUNX transcription factor Lozenge (LZ) and controls the number of LZ+ blood cells. During my PhD, I sought to further decipher the molecular mechanism of action of MLF on Lozenge during blood cell development. Using a proteomic approach in Drosophila Kc167 cells, we identified the Hsp40 co-chaperone family member DnaJ-1 and its chaperone partner Hsc70-4 as two partners of MLF. These interactions were confirmed by co-immunoprecipitations and in vitro pull-down assays. Importantly, we found that knocking down DnaJ-1 or Hsc70-4 expression in Kc167 cells caused a reduction in the level of Lozenge protein and a concomitant decrease in Lozenge transactivation activity, which were very similar to those caused by MLF knock-down. Similarly, over-expression of two DnaJ-1 mutants that are unable to stimulate the chaperone activity of Hsc70-4 also decreased Lozenge level and impaired its capacity to activate transcription. These results suggest that MLF could act within a chaperone complex composed of DnaJ-1 and Hsc70-4 to control Lozenge stability and activity. Along that line, we showed by co-immunoprecipitation that Lozenge interacts with MLF, DnaJ-1 and Hsc70-4, respectively. Using various truncated mutants of MLF or DnaJ-1, we showed that MLF and DnaJ-1 interact and together with Lozenge through their conserved MLF homology domain (MHD) and C-terminal region, respectively. Furthermore, in vitro GST pull-down assays suggested that the interactions between MLF, DnaJ-1 and Lozenge are direct. Thus, we propose that MLF and DnaJ-1 control Lozenge protein level by interacting with it and by promoting its folding and/or solubility via the Hsc70 chaperone machinery. In parallel, we assessed DnaJ-1 function in Drosophila blood cells in vivo using a null allele of dnaj-1 generated by CRISPR/Cas9 technique. We found that, like mlf, dnaj-1 mutation leads to an increase in the number and size of LZ+ blood cells, as well as to an over-activation of the Notch signaling pathway in these cells. Moreover, our data suggested that high levels of active Lozenge are required to control the number and size of LZ+ blood cells, and to down-regulate Notch expression. We propose that the MLF/DnaJ-1 complex controls LZ+ blood cell development in vivo by regulating Lozenge protein level/activity and thereby Notch pathway activation. In sum, our results establish a functional link between MLF, the Hsp40 co-chaperone DnaJ-1 and the RUNX transcription factor Lozenge, which could be conserved in other species
Antony-Debré, Iléana. "Fpd/aml : diagnostic et modélisation d'anomalies de Runx 1". Paris 7, 2013. http://www.theses.fr/2013PA077049.
Pełny tekst źródłaFPD/AML (familial platelet disorder with predisposition to acute myeloid leukemia) results from constitutive alterations of RUNX1, a hematopoietic transcription factor essential to definitive hematopoiesis. In the first part of our work, we proposed a new diagnostic test to detect RUNX1 alterations. We showed that MYH10, which is regulated negatively by RUNX1 during megakaryopoiesis, persisted in platelets from FPD/AML patients. MYHIO persistence was not detected in platelets from patients with other constitutional thrombocytopenia, except from patients with Paris-Trousseau syndrome. This new test could be used also to detect RUNX1 alterations in acquired haematological disorders like chronic myelomonocytic leukemia. In a second work, we generated induced pluripotent stem cells (iPSC) from fibroblasts of FPD/AML patients with different RUNX1 alterations, in order to model the pathology. We reproduced the phenotype already described in patients with defect in megakaryocytic lineage whatever RUNX1 alterations and increase in granulo-monocytic compartment only with the mutation which predisposes to leukemia. We highlighted for the first time that RUNX1 is necessary also for erythroid lineage. We confirmed these results after RUNX1 knock down in an embryonic stem cell line. In conclusion we validated our model and now we can use it to study the mechanisms leading to dysmegakaryopoiesis and predisposition to leukemia in FPD/AML patients
Pande, Sandhya. "Regulation of Runx Proteins in Human Cancers: A Dissertation". eScholarship@UMMS, 2011. https://escholarship.umassmed.edu/gsbs_diss/559.
Pełny tekst źródłaStephens, Alexandre, i N/A. "Genetic and Functional Characterization of RUNX2". Griffith University. School of Medical Science, 2007. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20070823.100953.
Pełny tekst źródłaStephens, Alexandre. "Genetic and Functional Characterization of RUNX2". Thesis, Griffith University, 2007. http://hdl.handle.net/10072/365677.
Pełny tekst źródłaThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
School of Medical Science
Faculty of Health
Full Text
Ferguson, Alison Mary. "The Role of RUNX Transcription Factors in Prostate Development and Tumorigenesis". Thesis, The University of Sydney, 2016. http://hdl.handle.net/2123/16898.
Pełny tekst źródłaFerrari, Nicola. "Investigating RUNX transcription factors in mammary gland development and breast cancer". Thesis, University of Glasgow, 2013. http://theses.gla.ac.uk/4790/.
Pełny tekst źródłaKsiążki na temat "RUNX"
Groner, Yoram, Yoshiaki Ito, Paul Liu, James C. Neil, Nancy A. Speck i Andre van Wijnen, red. RUNX Proteins in Development and Cancer. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2.
Pełny tekst źródłaSammy Sosa: Home-run hitter = bateador de home runs. New York: Rosen Pub. Group's PowerKids Press & Buenas Letras, 2001.
Znajdź pełny tekst źródłaClub, Colorado Mountain, red. Run the Rockies: Classic trail runs in Colorado's Front Range. Golden, Colo: Colorado Mountain Club Press, 2004.
Znajdź pełny tekst źródłaWhen the rivers run dry: What happens when our water runs out? London: Eden Project, 2007.
Znajdź pełny tekst źródłaHow to run: [from fun runs to marathons and everything in between. London: Simon & Schuster Illustrated, 2011.
Znajdź pełny tekst źródłaPearce, Fred. When the rivers run dry: What happens when our water runs out? London: Eden Project, 2006.
Znajdź pełny tekst źródłaRun, run, run away. Oregon?]: [publisher not identified], 2015.
Znajdź pełny tekst źródłaChukhov, Petŭr. Runi. [Bulgaria?]: Ab Izdatelsko Atelie, 1998.
Znajdź pełny tekst źródłaGriffiths, Niall. Runt. London: Jonathan Cape, 2007.
Znajdź pełny tekst źródłaRuna. New York, N.Y: Atheneum, 1993.
Znajdź pełny tekst źródłaCzęści książek na temat "RUNX"
Ito, Yoshiaki. "RUNX". W Encyclopedia of Signaling Molecules, 4773–81. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101825.
Pełny tekst źródłaIto, Yoshiaki. "RUNX". W Encyclopedia of Signaling Molecules, 1–9. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4614-6438-9_101825-1.
Pełny tekst źródłaHughes, S., i A. Woollard. "RUNX in Invertebrates". W Advances in Experimental Medicine and Biology, 3–18. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_1.
Pełny tekst źródłaChuang, Linda Shyue Huey, Kosei Ito i Yoshiaki Ito. "Roles of RUNX in Solid Tumors". W Advances in Experimental Medicine and Biology, 299–320. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_19.
Pełny tekst źródłaWest, Michelle J., i Paul J. Farrell. "Roles of RUNX in B Cell Immortalisation". W Advances in Experimental Medicine and Biology, 283–98. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_18.
Pełny tekst źródłaPassaniti, Antonino, Jessica L. Brusgard, Yiting Qiao, Marius Sudol i Megan Finch-Edmondson. "Roles of RUNX in Hippo Pathway Signaling". W Advances in Experimental Medicine and Biology, 435–48. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_26.
Pełny tekst źródłaEbihara, Takashi, Wooseok Seo i Ichiro Taniuchi. "Roles of RUNX Complexes in Immune Cell Development". W Advances in Experimental Medicine and Biology, 395–413. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_24.
Pełny tekst źródłaBlumenthal, Ezra, Sarah Greenblatt, Guang Huang, Koji Ando, Ye Xu i Stephen D. Nimer. "Covalent Modifications of RUNX Proteins: Structure Affects Function". W Advances in Experimental Medicine and Biology, 33–44. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_3.
Pełny tekst źródłaWang, Jae Woong, i Stefano Stifani. "Roles of Runx Genes in Nervous System Development". W Advances in Experimental Medicine and Biology, 103–16. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_8.
Pełny tekst źródłaWang, Chelsia Qiuxia, Michelle Meng Huang Mok, Tomomasa Yokomizo, Vinay Tergaonkar i Motomi Osato. "Runx Family Genes in Tissue Stem Cell Dynamics". W Advances in Experimental Medicine and Biology, 117–38. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3233-2_9.
Pełny tekst źródłaStreszczenia konferencji na temat "RUNX"
Chu, Jinn P., i C. H. Lin. "High Performance Cu Containing Ru or RuNx for Barrierless Metallization". W 2008 International Interconnect Technology Conference - IITC. IEEE, 2008. http://dx.doi.org/10.1109/iitc.2008.4546914.
Pełny tekst źródłaYong, T., S. Meyers, N. Davis i A. Sun. "Involvement of notch and RUNX pathways in human breast cancer." W CTRC-AACR San Antonio Breast Cancer Symposium: 2008 Abstracts. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-6021.
Pełny tekst źródłaFelcher, Carla M., Johanna M. Tocci, Martin E. Garcia Sola, John H. Bushweller, Lucio H. Castilla i Edith C. Kordon. "Abstract 5041: Inhibition of RUNX-CBFβ binding reduces RSPO3 expression and EMT features in breast cancer cells". W Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-5041.
Pełny tekst źródłaMatsuo, Junichi, Naing Naing Mon, Akihiro Yamamura, Dede L. Heng, Linda SH Chuang, Motomi Osato i Yoshiaki Ito. "Abstract 5110: Runx knockout in breast luminal stem/progenitor cells induced precancerous lesion via robust expression of ERα". W Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-5110.
Pełny tekst źródłaSasaski, Asami, Youhei Yanagida, Hiroshi Sugiyama, Souichi Adachhi i Yasuhiko Kamikubo. "Abstract 2937: The regulation of FGFR signaling by RTK adaptor protein down-regulation through CROX (cluster regulation of RUNX) theory in DNPC". W Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-2937.
Pełny tekst źródłaBattula, Venkata Lokesh, Phuong M. Le, Jeff Sun, Christopher B. Benton, Teresa Mc.Queen, Elizabeth J. Shpall, Carlos E. Bueso-Ramos, Marina Konopleva i Michael Andreeff. "Abstract 5085: Acute myeloid leukemia cells induce osteogenic differentiation in mesenchymal stem cells through bone morphogenetic protein- and RUNX-2- mediated signaling". W Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-5085.
Pełny tekst źródłaPérez-García, S., I. Gutiérrez-Cañas, R. Villanueva-Romero, J. Leceta, J. Fernández, I. González-Άlvaro, Y. Juarranz i RP Gomariz. "FRI0016 Involvement of runx-2 and β-catenin signaling in the production of adamts-7 and adamts-12 in osteoarthritic synovial fibroblasts". W Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.5808.
Pełny tekst źródłaCobb, Michael G., Dana M. Austin, Dapeng Xu i Antonio T. Baines. "Abstract B56: The role of Pim kinases and RUNX transcription factors as potential molecular targets of K-Ras signaling in pancreatic cancer cells." W Abstracts: AACR Special Conference on Pancreatic Cancer: Progress and Challenges; June 18-21, 2012; Lake Tahoe, NV. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.panca2012-b56.
Pełny tekst źródłaOkoli, Uzoamaka A. "Abstract PO-150: Comparison of RUNX1, RUNX2, RUNX3 and CBFβ gene expression in breast tumors Indicate ethnic differences and similarities by receptor status". W Abstracts: AACR Virtual Conference: 14th AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; October 6-8, 2021. American Association for Cancer Research, 2022. http://dx.doi.org/10.1158/1538-7755.disp21-po-150.
Pełny tekst źródłaLa Rosa, Alessandro. "ATLAS Pixel Detector: Operational Experience and Run1$\rightarrow$Run2 Transition". W The 23rd International Workshop on Vertex Detectors. Trieste, Italy: Sissa Medialab, 2015. http://dx.doi.org/10.22323/1.227.0001.
Pełny tekst źródłaRaporty organizacyjne na temat "RUNX"
Zhang S. Y. i V. Ptitsyn. Proton Beam Emittance Growth in Run5 and Run6. Office of Scientific and Technical Information (OSTI), listopad 2006. http://dx.doi.org/10.2172/1061848.
Pełny tekst źródłaZhang S. Y. i D. Trbojevic. Observation of Experimental Background in Proton Run5 and Run6. Office of Scientific and Technical Information (OSTI), listopad 2006. http://dx.doi.org/10.2172/1061849.
Pełny tekst źródłaDonaldson, Jason, i Giorgia Piacentino. Money Runs. Cambridge, MA: National Bureau of Economic Research, wrzesień 2019. http://dx.doi.org/10.3386/w26298.
Pełny tekst źródłaAndolfatto, David, Ed Nosal i Bruno Sultanum. Preventing Bank Runs. Federal Reserve Bank of St. Louis, 2014. http://dx.doi.org/10.20955/wp.2014.021.
Pełny tekst źródłaAndolfatto, David, i Ed Nosal. Shadow Bank Runs. Federal Reserve Bank of St. Louis, 2020. http://dx.doi.org/10.20955/wp.2020.012.
Pełny tekst źródłaBernardo, Antonio, i Ivo Welch. Financial Market Runs. Cambridge, MA: National Bureau of Economic Research, październik 2002. http://dx.doi.org/10.3386/w9251.
Pełny tekst źródłaHe, Zhiguo, i Wei Xiong. Dynamic Debt Runs. Cambridge, MA: National Bureau of Economic Research, listopad 2009. http://dx.doi.org/10.3386/w15482.
Pełny tekst źródłaGutiérrez, José E., i Luis Fernández Lafuerza. Credit line runs and bank risk management: evidence from the disclosure of stress test results. Madrid: Banco de España, grudzień 2022. http://dx.doi.org/10.53479/25006.
Pełny tekst źródłaGutiérrez, José E., i Luis Fernández Lafuerza. Credit line runs and bank risk management: evidence from the disclosure of stress test results. Madrid: Banco de España, styczeń 2023. http://dx.doi.org/10.53479/24998.
Pełny tekst źródłaRode, C. A1 cryogenic magnet runs. Office of Scientific and Technical Information (OSTI), lipiec 1994. http://dx.doi.org/10.2172/1155894.
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