Relevant bibliographies by topics / Transition G1

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
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Academic literature on the topic 'Transition G1'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Transition G1"

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Chen, Zihao, and Chunhe Li. "Quantifying the Landscape and Transition Paths for Proliferation–Quiescence Fate Decisions." Journal of Clinical Medicine 9, no. 8 (2020): 2582. http://dx.doi.org/10.3390/jcm9082582.

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The cell cycle, essential for biological functions, experiences delicate spatiotemporal regulation. The transition between G1 and S phase, which is called the proliferation–quiescence decision, is critical to the cell cycle. However, the stability and underlying stochastic dynamical mechanisms of the proliferation–quiescence decision have not been fully understood. To quantify the process of the proliferation–quiescence decision, we constructed its underlying landscape based on the relevant gene regulatory network. We identified three attractors on the landscape corresponding to the G0, G1, an
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Zwijsen, R. M., R. Klompmaker, E. B. Wientjens, P. M. Kristel, B. van der Burg, and R. J. Michalides. "Cyclin D1 triggers autonomous growth of breast cancer cells by governing cell cycle exit." Molecular and Cellular Biology 16, no. 6 (1996): 2554–60. http://dx.doi.org/10.1128/mcb.16.6.2554.

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Cyclin D1 controls G1-associated processes, including G0-to-G1 and G1-to-S transitions. This study demonstrates a novel aspect of cyclin D1 as a regulator of the transition between G1 and G0. Overexpression of cyclin D1 in MCF7 breast tumor cells resulted in a continued proliferation under low-serum conditions, whereas nonoverexpressing cells ceased to grow. This difference in growth was due to a reduced exit from G1 to G0 in cyclin D1-overexpressing cells. Our data therefore suggest a model in which cyclin D1 overexpression in tumor cells is responsible for hyperproliferation under growth fac
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Mattaloni, Stella M., Anabela C. Ferretti, Facundo M. Tonucci, Cristián Favre, James R. Goldenring, and M. Cecilia Larocca. "Centrosomal AKAP350 modulates the G1/S transition." Cellular Logistics 3, no. 4 (2013): e26331. http://dx.doi.org/10.4161/cl.26331.

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Bekkal-Brikci, Fadia, Giovanna Chiorino, and Khalid Boushaba. "G1/S transition and cell population dynamics." Networks & Heterogeneous Media 4, no. 1 (2009): 67–90. http://dx.doi.org/10.3934/nhm.2009.4.67.

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Dittmer, D., and E. S. Mocarski. "Human cytomegalovirus infection inhibits G1/S transition." Journal of virology 71, no. 2 (1997): 1629–34. http://dx.doi.org/10.1128/jvi.71.2.1629-1634.1997.

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Prathapam, T., S. Tegen, T. Oskarsson, A. Trumpp, and G. S. Martin. "Activated Src abrogates the Myc requirement for the G0/G1 transition but not for the G1/S transition." Proceedings of the National Academy of Sciences 103, no. 8 (2006): 2695–700. http://dx.doi.org/10.1073/pnas.0511186103.

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Ortega, S., M. Malumbres, and M. Barbacid. "Cell Cycle and Cancer: The G1 Restriction Point and the G1 / S Transition." Current Genomics 3, no. 4 (2002): 245–63. http://dx.doi.org/10.2174/1389202023350444.

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Ohtsubo, M., A. M. Theodoras, J. Schumacher, J. M. Roberts, and M. Pagano. "Human cyclin E, a nuclear protein essential for the G1-to-S phase transition." Molecular and Cellular Biology 15, no. 5 (1995): 2612–24. http://dx.doi.org/10.1128/mcb.15.5.2612.

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Cyclin E was first identified by screening human cDNA libraries for genes that would complement G1 cyclin mutations in Saccharomyces cerevisiae and has subsequently been found to have specific biochemical and physiological properties that are consistent with it performing a G1 function in mammalian cells. Most significantly, the cyclin E-Cdk2 complex is maximally active at the G1/S transition, and overexpression of cyclin E decreases the time it takes the cell to complete G1 and enter S phase. We have now found that mammalian cells express two forms of cyclin E protein which differ from each o
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Orr, Stephen J., Rong Wang, Nicholas C. Lea, et al. "Systems Biology Analysis of Human Primary T Cells Identifies SAP145 as Rate Limiting for the G1→S Phase Transition." Blood 110, no. 11 (2007): 3350. http://dx.doi.org/10.1182/blood.v110.11.3350.3350.

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Abstract We identified a G0→G1 commitment point in primary human T cells that controls entry into the cell cycle from quiescence. We demonstrated proof of principle that cellular pathways regulating cell cycle progression and effector functions that normally coincide during CD3/CD28 stimulation can be uncoupled experimentally. We have now used systems biology approaches to identify nuclear protein networks in primary human T cells that are regulated during the transition from quiescence into the cell cycle (G0→G1→S-phase). First we sequenced proteins that became bound to chromatin & nuclea
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Chiorino, G., and M. Lupi. "Variability in the timing of G1/S transition." Mathematical Biosciences 177-178 (May 2002): 85–101. http://dx.doi.org/10.1016/s0025-5564(02)00085-8.

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Dissertations / Theses on the topic "Transition G1"

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Cariou, Sandrine. "Mecanismes controlant la progression en g1 et la transition g1/s du cycle cellulaire des hepatocytes normaux et transformes." Paris 5, 1996. http://www.theses.fr/1996PA05S010.

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La progression des cellules de mammiferes dans le cycle cellulaire est soumise a differents points de controle ou points de restriction qui pour certains d'entre eux definissent des regulations specifiques de la proliferation en fonction des types cellulaires. Au niveau des points de restriction, les parametres nutritionnels, la presence des facteurs de croissance, l'integrite du genome et sa replication, la segregation correcte des composants nucleaires et cytoplasmiques sont controles. Par ailleurs, au cours des dernieres annees, la comprehension des mecanismes moleculaires qui gouvernent la
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Ramsey, Matthew Robert Sharpless Norman E. "Regulation of the G1-S transition by cyclin-dependent kinase inhibitors." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1001.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.<br>Title from electronic title page (viewed Dec. 18, 2007). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Curriculum of Genetics and Molecular Biology." Discipline: Genetics and Molecular Biology; Department/School: Medicine.
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Kersey, Paul Julian. "Control of gene expression during the G1-S transition in Schizosaccharomyces pombe." Thesis, University of Edinburgh, 1994. http://hdl.handle.net/1842/15156.

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Control over the mitotic cell division cycle of the fission yeast <I>Schizosaccharomyces pombe</I> is exerted at two main points, mitotic entry and an earlier point, situated prior to DNA replication, known as Start. At Start, cells become committed to one of a number of developmental pathways. The genes <I>cdc2</I><SUP>+</SUP> and <I>cdc10</I><SUP>+</SUP> are both required for commitment to the mitotic pathway. The <I>cdc22</I><SUP>+</SUP> gene encodes an enzyme which functions in S phase, and is periodically expressed at the G1/S boundary. Cdc10 binds elements in the <I>cdc22</I><SUP>+</SUP>
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Jensen, Bryan. "Regulation of the G1 to S-phase transition in S. cerevisiae by CDC4 /." Thesis, Connect to this title online; UW restricted, 1997. http://hdl.handle.net/1773/10257.

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Le, Frère-Belda Marie-Aude. "Les inhibiteurs de la transition G1-Sp14arf, p15 et p16 dans le cancer de vessie." Paris 11, 2002. http://www.theses.fr/2002PA11T063.

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Drougat, Ludivine. "Etude de la dynamique de O-GlcNAcylation et identification de protéines différentiellement O-GlcNAcylées au cours de la transition G1/S du cycle cellulaire de cellules épithéliales humaines." Thesis, Lille 1, 2012. http://www.theses.fr/2012LIL10086/document.

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La O-GlcNAcylation est une glycosylation dynamique et réversible sous le contrôle de la O-GlcNAc Transférase (OGT) qui transfère un résidu de GlcNAc sur les Ser/Thr de protéines intracellulaires, et de la O-GlcNAcase (OGA). Plusieurs travaux dont ceux de notre équipe ont montré l'importance de la dynamique de O-GlcNAcylation pour la progression normale du cycle cellulaire, et plus particulièrement de la mitose. L’objectif de mes travaux de thèse était de comprendre comment la balance O-GlcNAc participe au contrôle des étapes précoces du cycle cellulaire. J’ai d’abord montré dans différentes li
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Thacker, Urvi. "Analysis of cyclin-CDK mediated regulation of the G1/S transition in post quiescent murine fibroblasts." Thesis, Lancaster University, 2017. http://eprints.lancs.ac.uk/88802/.

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Eukaryotic cells have evolved a complex set of regulatory proteins to maintain genome stability by regulating DNA replication once and once per cell cycle. Despite intensive investigation, a precise understanding of the proteins that are phosphorylated during the initiation phase of DNA replication remains to be identified. Here we investigate the roles of cyclin E and cyclin A in the G1 to S-phase transition and reconstitute initiation of DNA replication in cyclin depleted nuclei using an in vitro DNA replication system. Using a murine 3T3 fibroblast model, chemical and genetic inhibition of
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Havens, Courtney Guiheen. "Regulation of late G1/S phase transition and the anaphase promoting complex-Cdh1 by reactive oxygen species /." Diss., Connect to a 24 p. preview or request complete full text in PDF formate. Access restricted to UC campuses, 2006. http://wwwlib.umi.com/cr/ucsd/fullcit?p3236627.

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Conradie, Riaan. "A comparative analysis of the G1/S transition control in kinetic models of the eukaryotic cell cycle." Thesis, Stellenbosch : University of Stellenbosch, 2009. http://hdl.handle.net/10019.1/1236.

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Thesis (PhD (Biochemistry))--University of Stellenbosch, 2009.<br>ENGLISH ABSTRACT: The multiplication of cells proceeds through consecutive phases of growth and division (G1, S, G2 and M phases), in a process known as the cell cycle. The transition between these phases is regulated by so-called checkpoints, which are important to ensure proper functioning of the cell cycle. For instance, mutations leading to faulty regulation of the G1/S transition point are seen as one of the main causes of cancer. Traditionally, models for biological systems that show rich dynamic behavior, such as
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Pontier, Garance. "Caractérisation fonctionnelle de TCTP et CSN4 dans la régulation de la progression du cycle cellulaire et de la croissance mitotique chez Arabidopsis thaliana." Thesis, Lyon, 2020. http://www.theses.fr/2020LYSEN065.

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Chez les plantes comme chez les animaux, la taille des organes est une caractéristique cruciale dépendant de différents processus que sont la prolifération, la croissance, la différentiation et la mort cellulaires. Ces processus sont très précisément contrôlés et beaucoup de leurs régulateurs clefs sont fortement conservés chez les eucaryotes. Parmi eux, TRANSLATIONNALLY CONTROLLED TUMOR PROTEIN (TCTP), une protéine régulée lors de sa traduction, est connue pour jouer un rôle essentiel dans le développement des organes. Ma thèse vise à préciser la voie d'action de TCTP sur la progression du cy
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Books on the topic "Transition G1"

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Costanzo, Michael Anthony. Transcriptional regulation at the G1/S transition in Saccharomyces cerevisiae. 2003.

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Book chapters on the topic "Transition G1"

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Shen, Wen-Hui. "G1/S Transition and the Rb-E2F Pathway." In Plant Cell Monographs. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/7089_2007_122.

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Thwaites, Michael J., Matthew J. Cecchini, and Frederick A. Dick. "Analyzing RB and E2F During the G1–S Transition." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0888-2_24.

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Knudsen, Karen, Anne F. Fribourg, Christin Petre, and Yelena Wetherill. "Androgen Mediated Regulation of the G1-S Transition in Prostate Cancer." In Steroid Hormones and Cell Cycle Regulation. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0965-3_6.

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Sekine, Masami, and Atsuhiko Shinmyo. "Control of the G1/S Phase Transition in Tobacco BY-2 Cells." In Tobacco BY-2 Cells. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-10572-6_4.

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Ferrari, S., and G. Thomas. "The Mitogen/Oncogene-Activated p70s6k: Its Role in the G0/G1 Transition." In DNA Replication and the Cell Cycle. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77040-1_13.

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Welsh, Catherine F. "Regulation of G1 to S Phase Transition by Adhesion and Growth Factor Signaling." In Steroid Hormones and Cell Cycle Regulation. Springer US, 2002. http://dx.doi.org/10.1007/978-1-4615-0965-3_2.

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Zilhão, João. "Szeletian, Not Aurignacian: A Review of the Chronology and Cultural Associations of the Vindija G1 Neandertals." In Sourcebook of Paleolithic Transitions. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-76487-0_27.

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McClymont, Juliet, and Robin H. Crompton. "Repetition Without Repetition: A Comparison of the Laetoli G1, Ileret, Namibian Holocene and Modern Human Footprints Using Pedobarographic Statistical Parametric Mapping." In Reading Prehistoric Human Tracks. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-60406-6_3.

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AbstractIt is traditionally held that early hominins of the genusAustralopithecushad a foot transitional in function between that of the other great apes and our own but that the appearance of genusHomowas marked by evolution of an essentially biomechanically modern foot, as well as modern body proportions. Here, we report the application of whole foot, pixel-wise topological statistical analysis, to compare four populations of footprints from across evolutionary time:Australopithecusat Laetoli (3.66 Ma, Tanzania), early AfricanHomofrom Ileret (1.5 Ma, Kenya) and recent modern (presumptively habitually barefoot) pastoralistHomo sapiensfrom Namibia (Holocene), with footprints from modern Western humans. Contrary to some previous analyses, we find that only limited areas of the footprints show any statistically significant difference in footprint depth (used here as an analogy for plantar pressure). A need for this comparison was highlighted by recent studies using the same statistical approach, to examine variability in the distribution of foot pressure in modern Western humans. This study revealed very high intra-variability (mean square error) step-to-step in over 500 steps. This result exemplifies the fundamental movement characteristic of dynamic biological systems, whereby regardless of the repetition in motor patterns for stepping, and even when constrained by experimental conditions, each step is unique or non-repetitive; hence, repetition without repetition. Thus, the small sample sizes predominant in the fossil and ichnofossil record do not reveal the fundamental neurobiological driver of locomotion (variability), essentially limiting our ability to make reliable interpretations which might be extrapolated to interpret hominin foot function at a population level. However, our need for conservatism in our conclusions does not equate with a conclusion that there has been functional stasis in the evolution of the hominin foot.
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"G1/S Transition." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_2291.

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"SECTION G – SOME METALS IN BIOLOGY G1 The early transition metals." In BIOS Instant Notes in Chemistry for Biologists. Taylor & Francis, 2020. http://dx.doi.org/10.1201/9780203079522-20.

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Conference papers on the topic "Transition G1"

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BARBERIS, MATTEO, and EDDA KLIPP. "INSIGHTS INTO THE NETWORK CONTROLLING THE G1/S TRANSITION IN BUDDING YEAST." In Proceedings of the 7th Annual International Workshop on Bioinformatics and Systems Biology (IBSB 2007). IMPERIAL COLLEGE PRESS, 2007. http://dx.doi.org/10.1142/9781860949920_0009.

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Schmidt, Keon R., Yingjia Ni, and Siyuan Zhang. "Abstract LB-321: Cytoplasmic DEDD promotes G1- to S-phase cell cycle transition." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-lb-321.

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Zhang, Bingyuan, Tianqiang Song, Pingzhou Yang, et al. "Abstract 4607: G1/S transition-related gene mutations associated with survival of hepatocellular carcinoma patients." In 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.am2018-4607.

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Taira, Naoe, Rei Mimoto, Yoshio Miki, and Kiyotsugu Yoshida. "Abstract 3060: DYRK2-mediated phosphorylation of c-Jun and c-Myc is requisite for proper control of the G1/S transition." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3060.

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Kusuma, Mayang Fati, and Fajar Adi-Kusumo. "A mathematical modelling for estradiol influence on DNA damage response and G1/S transition phase regulations in early stage of breast cancer." In PROCEEDINGS OF THE 8TH SEAMS-UGM INTERNATIONAL CONFERENCE ON MATHEMATICS AND ITS APPLICATIONS 2019: Deepening Mathematical Concepts for Wider Application through Multidisciplinary Research and Industries Collaborations. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5139158.

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Verduci, Ivan, Valentina Carlini, Federica M. Raciti, et al. "Abstract 304: CLIC1 membrane insertion is a pivotal regulator of glioblastoma stem cell G1-S transition by promoting an increase of chloride permeability." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-304.

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Tajima, Shingo, and Burak Sencer. "Smooth Cornering Strategy for High Speed CNC Machine Tools With Confined Contour Error." In ASME 2016 11th International Manufacturing Science and Engineering Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/msec2016-8529.

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Conventional tool-paths for CNC (computer numerical controlled) machine tools or NC positioning systems are mainly composed of linear motion segments, or so called the G1 commands. Interpolating along linear tool-paths exhibits serious limitations in terms of achieving the desired part geometry and productivity in high-speed machining. Velocity and acceleration discontinuities occur at the junction points of consecutive segments. In order to generate smooth and continuous feed motion, a kinematic corner smoothing algorithm is proposed in this paper, which plans smooth acceleration and jerk pro
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Zhou, P., W. Sun, and Z.-M. Shao. "Abstract P4-04-16: Long non-coding RNA DSCAM-AS1 regulates G1/S cell cycle transition and is an independent poor prognosis factor in luminal breast cancer with endocrine therapy." In Abstracts: 2017 San Antonio Breast Cancer Symposium; December 5-9, 2017; San Antonio, Texas. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.sabcs17-p4-04-16.

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Mohamed, Islam, Ahmed Moahmed, Mennatallah Abdelkader, Alaaeldin Saleh, and Ala-Eddin Al-Moustafa. "Elaeagnus Angustifolia: a Promising Medicinal Plant for Cancer Theraby." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0124.

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Introduction: Elaeagnus angustifolia (EA) is a medicinal plant that has been used for centuries in treating many human diseases, in the Middle East, including fever, amoebic dysentery, gastrointestinal problems. However, the effect of EA plant extract on human cancer progression especially oral malignancy has not been investigated yet. Thus, first we examined the effect of EA flower extract on angiogenesis in ovo, and on selected parameters in human oral cancer cells. Materials and methods: Chorioallantoic membranes (CAMs) of chicken embryos at 3-7 days of incubation were used to assess the ef
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Reports on the topic "Transition G1"

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Evans, Julie, Kendra Sikes, and Jamie Ratchford. Vegetation classification at Lake Mead National Recreation Area, Mojave National Preserve, Castle Mountains National Monument, and Death Valley National Park: Final report (Revised with Cost Estimate). National Park Service, 2020. http://dx.doi.org/10.36967/nrr-2279201.

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Vegetation inventory and mapping is a process to document the composition, distribution and abundance of vegetation types across the landscape. The National Park Service’s (NPS) Inventory and Monitoring (I&amp;M) program has determined vegetation inventory and mapping to be an important resource for parks; it is one of 12 baseline inventories of natural resources to be completed for all 270 national parks within the NPS I&amp;M program. The Mojave Desert Network Inventory &amp; Monitoring (MOJN I&amp;M) began its process of vegetation inventory in 2009 for four park units as follows: Lake Mead
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