Relevant bibliographies by topics / Stem growth

Academic literature on the topic 'Stem growth'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 January 2023

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Journal articles on the topic "Stem growth"

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Keller, Jonathan R., Sten E. W. Jacobsen, Claire M. Dubois, Kjetil Hestdal, and Francis W. Ruscetti. "Transforming growth factor-β: A bidirectional regulator of hematopoietic cell growth." International Journal of Cell Cloning 10, no. 1 (1992): 2–11. http://dx.doi.org/10.1002/stem.5530100103.

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Quesenberry, Peter J. "Synergistic hematopoietic growth factors." International Journal of Cell Cloning 4, no. 1 (1986): 3–15. http://dx.doi.org/10.1002/stem.5530040102.

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Brizzi, Maria F., G. Carlo Avanzi, and Luigi Pegoraro. "Hematopoietic growth factor receptors." International Journal of Cell Cloning 9, no. 4 (1991): 274–300. http://dx.doi.org/10.1002/stem.5530090404.

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Whipker, Brian E., and P. Allen Hammer. "Growth and Yield Characteristics of Field-grown Limonium sinuatum (L.)." HortScience 29, no. 6 (June 1994): 638–40. http://dx.doi.org/10.21273/hortsci.29.6.638.

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Field studies were conducted on the potential of annual statice as an outdoor cut-flower crop for the Midwestern United States. Data was collected on seven cultivars in 1989 and 42 in 1990. In 1989, total fresh stem weight, stem count, and average stem weight differed significantly among cultivars. Yellow cultivars had more stems harvested than the rose, apricot, and blue cultivars, but stems of the yellow cultivars weighed less. The number of stems harvested over time tended to be concentrated in the first 8 weeks after flowering begins. In 1990, the average stem fresh weight was significantly different among the apricot, blue, and rose cultivars, but the number of stems harvested was significantly different only between the blue and rose cultivars.
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Parks, Brian M., Kevin M. Folta, and Edgar P. Spalding. "Photocontrol of stem growth." Current Opinion in Plant Biology 4, no. 5 (October 2001): 436–40. http://dx.doi.org/10.1016/s1369-5266(00)00197-7.

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Sikström, U., Hans-Örjan Nohrstedt, Folke Pettersson, and Staffan Jacobson. "Stem-growth response of." Trees 12, no. 4 (1998): 208. http://dx.doi.org/10.1007/s004680050142.

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Golde, David W. "Hematopoietic growth factors-An overview." International Journal of Cell Cloning 8, S1 (1990): 4–10. http://dx.doi.org/10.1002/stem.5530080702.

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Eva Singletary, S., Didier Frappaz, Susan L. Tucker, Lillie Larry, William A. Brock, and Gary Spitzer. "Epidermal growth factor effect on serum-free growth of primary and metastatic human tumors." International Journal of Cell Cloning 7, no. 1 (1989): 59–66. http://dx.doi.org/10.1002/stem.5530070108.

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Deuel, Thomas F. "Growth factors, wound healing, and neoplasia platelet-derived growth factor as a model cytokine." International Journal of Cell Cloning 9, S1 (May 1991): 60–71. http://dx.doi.org/10.1002/stem.5530090709.

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Konôpka, B., and J. Pajtík. "Foliage and fine roots in terms of growth efficiency – a comparison between European beech and Norway spruce at early growth stages." Journal of Forest Science 59, No. 11 (November 29, 2013): 436–46. http://dx.doi.org/10.17221/56/2013-jfs.

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The quantification of stems (under- and overbark), foliage and fine roots in 14-year-old stands of European beech and Norway spruce grown on the same site were evaluated. Therefore, 60 trees of each species were sampled, dry masses of stems and foliage were established and expressed by allometric equations with stem diameter as an independent variable. The spruce allocated a much larger portion of biomass into the foliage than beech. The equations on a tree level were constructed also for specific leaf area and one-sided projected leaf area. Moreover, the quantity and morphological characteristics of fine roots in both stands were surveyed through soil coring. While standing stocks of fine roots were similar in the stands of both tree species, significant interspecies differences occurred in morphological properties of roots. Growth efficiency, expressing annual stem production on a variety of foliage and fine root parameters was calculated. The largest differences, specifically fivefold in favour of spruce, were found in growth efficiency based on a number of root tips.
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Dissertations / Theses on the topic "Stem growth"

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Amarachintha, Surya P. "Optimal Growth Conditions for Tracheal Epithelial Stem Cells." Bowling Green State University / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1187395530.

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Ringstedt, Thomas. "Neurotrophins during development : overexpression in neural stem cells /." Stockholm, 1998. http://diss.kib.ki.se/search/diss.se.cfm?19980605ring.

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Culme-Seymour, E. J. "Engineering the growth substrate for embryonic stem cell processing." Thesis, University College London (University of London), 2010. http://discovery.ucl.ac.uk/20449/.

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Embryonic stem cells (ESCs) are pluripotent cells that represent a potentially unlimited supply of specialised cells for drug testing and cell therapy. However, a more robust, reproducible and efficient process is required for successful expansion and differentiation of these cells. One variable that exhibits a large effect on ESC culture is the growth substrate. Modifications to the currently accepted standard culture system have been made and a novel feeder layer system for human (h) ESC maintenance has been created in the research presented here. Standard hESC culture involves maintenance on supportive feeder layers of mitotically inactivated mouse embryonic fibroblasts (mEFs). The presence of these cocultured cells in pluripotent hESC cultures and during differentiation does pose technical challenges to large-scale production, thus there is a need for biphasic scalable coculture systems. Here, alginate modified with the RGD peptide sequence (commonly utilised for stimulated cell adhesion onto synthetic surfaces) has been used to immobilise mEFs into a biphasic culture system as a possible replacement to the traditional feeder layer. Analysis of proliferation, viability and ECM production of mEFs within alginate is described in this project, as well as results from both short- and long-term maintenance of hESCs on the modified layer. Apart from the choice of substrate, there are other variables within the culture system that affect ESC growth and lineage specification. Upon characterisation of the Young’s modulus (E) of an elastically tuneable glutaraldehyde cross-linked gelatin culture system, mouse (m) ESCs have been cultured on surfaces exhibiting varying degrees of stiffness. Investigations into the effect of E on the expression of pluripotency markers, regulation of spontaneous differentiation and efficiency of directed neuronal differentiation have been carried out. The results strongly suggest that adequate control of E may be critical in order to increase the yield of stem cell bioprocesses.
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Anilkumar, Thapasimuthu Vijayamma. "The pathobiology of hepatic stem cells (oval cells)." Thesis, Imperial College London, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244072.

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Yeoh, Joyce Siew Gaik. "Regulatory role of fibroblast growth factors on hematopoietic stem cells." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2007. http://irs.ub.rug.nl/ppn/299000842.

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Houlihan, Diarmaid Dominic. "Growth factors direct mesenchymal stem cell fate and therapeutic potential." Thesis, University of Birmingham, 2015. http://etheses.bham.ac.uk//id/eprint/5551/.

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Murine mesenchymal stem cells (MSCs) isolated by plastic adherence contain contaminating cells and have poor growth and differentiation. I report a detailed protocol outlining the steps to prospectively isolate a pure and potent MSC population from murine bone marrow based on their expression of stem cell antigen-1 (Sca-1) and platelet derived growth factor- alpha (PDGFRα) (PαS cells) using flow cytometry. PαS MSCs have augmented growth potential and robust tri-lineage differentiation compared to plastic adherent cells. They exert potent immunosuppressive effects on proliferating naive CD4+ T cells, which is mediated via the production of nitric oxide (NO). Nevertheless, prolonged culture results in cellular senescence, loss of adipogenic differentiation and reduced immunosuppressive properties. Addition of growth factors to standard media (SM) produced significant genotypic and phenotypic changes. Cells cultured in SM supplemented with basic fibroblast growth factor (bFGF) and platelet derived growth factor-BB (PDGF-BB) were primed towards fat and cartilage, but had reduced immunosuppressive potential. In contrast, cells cultured with transforming growth factor-beta (TGF-β) had reduced tri-lineage potential but potent immunosuppressive properties that endured despite long term culture. I demonstrate using novel tissue engineering techniques that bFGF PαS MSCs generate substantial 3-D cartilage pellets. These data have implications for MSC therapy in humans.
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Jennings, Adam Edward. "Control of growth and differentiation of human liver stem cells." Thesis, University of Birmingham, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.403607.

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Ham, Trevor Richard. "Covalent Growth Factor Tethering to Guide Neural Stem Cell Behavior." University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1555347467862553.

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Benjamin, Corey Antonio. "Growth Factors and Chondrogenic Differentiation of Adipose-Derived Stem Cells." Thesis, The University of Arizona, 2015. http://hdl.handle.net/10150/578983.

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Osteoarthritis is the result of the breakdown of articular cartilage, which often begins with a traumatic injury to the joint. The loss of cartilage leads to joint pain, stiffness, and reduced physical mobility and activity. Although joint replacement with artificial joints is currently the standard of care for osteoarthritis, there are drawbacks that limit the types of activity the patient can be involved in after surgery and other side effects that can lead to failure of the artificial joint. Infection following surgery, loss of proprioception (the ability to know where the joint is in space), and the possibility of a failure of parts of the synthetic joint that requires additional surgeries are all risks that this treatment presents.One possible alternative to total joint replacement is tissue engineering that can be used to regenerate the damaged joint. Stem cells that are differentiated into cartilage cells and reintroduced into the area or areas with cartilage defects will form cartilage tissue. The conversion of stem cells into cartilage cells (chondrocytes) can be induced through the use of growth factors, including TGF-β3, TGF-β1, BMP-2, and BMP-6. [4, 10] The differentiation of stem cells into chondrocytes will be examined with each growth factor separately as well as in combination. Safranin-O staining results will be compared to determine which growth factor or combination of growth factors most effectively converts stem cells into chondrocytes.
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Neumann, John A. P. "Variability in the relationship between leaf area and selected stem measures in Douglas fir." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/28819.

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Variability in the relationship between tree leaf area (TLA) and selected stem measurements was examined in three Douglas-fir stands (Pseudotsuga menziesii (Mirb.) Franco, var. menziesii) that were less than 50 years-old, spaced to approximately 550 to 650 stems/ha, and differed in soil moisture and nutrients. Attention was given to the effect of mean annual ring width (MARW), cross-sectional area of the live bark (ALB - a surrogate measure of relative nutrient storage in the stem), and cross-sectional area of the most recent annual rings equal in number to the number of whorls in the live crown (ALC), on variability in the relationship between TLA and cross-sectional area of sapwood (ASW). At breast height, basal area, ASW, and cross-sectional area of sapwood plus live bark (ASWLB) were not linearly related to TLA, and linear regression equations using log transformed variables varied significantly between sites. Nonlinear regression equation for ASW at breast height was: TLA = 0.064ASẆ¹•³³ (I² = 0.856). Including D (the distance between breast height and the center of the live crown) in the nonlinear equation, did not significantly improve the regression. Tree leaf area prediction models using stem measures from the base of live crown (blc) had higher adjusted R² values than models using stem measures from breast height. At the blc, basal area, ASW, and ASWLB were linearly related to TLA (adjusted R² = 0.926, 0.908, and 0.934, respectively). Multiplying ASW by MARW did not improve the fit of the regression models. Multiplying ASW by ALB improved the linearity of the relationship of ASW at breast height to TLA. The best fitting TLA model overall used the product of ASW at blc and ALB at blc as the independent variable (adjusted R² = 0.967). The results indicate that research into the allometric relationship of TLA to stem measures should give consideration to more than hydraulic measures and include measures of bark function. At breast height and the blc, the independent variable ALC was linearly related to tree leaf area and had higher adjusted R² values than did ASW. In most trees the ALC stem measure was found to include a portion of heartwood area. The strong relationship between TLA and ALC suggests that a given transpiring leaf mass or area is related to a proportional amount of conducting stemwood and physical support stemwood. A quick alternative approach for estimating individual tree leaf area using photographs taken at fixed distance and angle from the target tree did not result in a reliable tree leaf area prediction technique. The difficulty of obtaining views of the tree crown which were not obstructed by adjacent tree crowns was the major obstacle. Using a fixed distance and camera angle was a problem because of variable tree heights. However, altering these fixed positions introduced additional variation into the tree leaf area estimation. Mean specific leaf area (SLA) varied significantly by site, needle age class, and crown position. Mean SLA per needle age class per branch can be predicted with 95% confidence and a 10% allowable error using six 10-needle samples.
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Books on the topic "Stem growth"

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Stem cell biology in health and disease. Dordrecht: Springer, 2009.

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Sell, Stewart. Liver stem cells. Austin: Landes Bioscience, 1997.

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Bormann, Bernard T. Early wide spacing in red alder (Alnus rubra Bong.): Effects on stem form and stem growth. [Portland, Or.?]: U.S. Dept. of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station, 1985.

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Bormann, Bernard T. Early wide spacing in red alder (Alnus rubra Bong.): Effects on stem form and stem growth. Portland, Or.?]: U.S. Dept. of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station, 1985.

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Regenerative medicine: Stem cells and the liver. Boca Raton, FL: CRC Press/Taylor & Francis Group, 2012.

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Taupin, Philippe. Adult neurogenesis and neural stem cells in mammals. New York: Nova Science Publishers, 2006.

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1950-, Gage F., ed. Stem cells in the nervous system: Functional and clinical implications. New York: Springer, 2004.

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Magin, Angela Susanne. Humane Primärzellen als Feederzellen für die Kokultur mit hämatopoetischen Stammzellen aus Nabelschnurblut. Jülich: Forschungszentrum Jülich, Zentralbibliothek, 2006.

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J, Barrett A., and Gordon-Smith E. C, eds. Bone marrow disorders: The biological basis of clinical problems. Oxford: Blackwell Scientific Publications, 1985.

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Kempermann, Gerd. Adult neurogenesis: Stem cells and neuronal development in the adult brain. New York, NY: Oxford University Press, 2006.

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Book chapters on the topic "Stem growth"

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Niles, Walter D., Dustin R. Wakeman, and Evan Y. Snyder. "Growth Dynamics of Fetal Human Neural Stem Cells." In Stem Cells Handbook, 75–89. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7696-2_5.

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Stocum, David L. "Urodele Limb Regeneration: Mechanisms of Blastema Formation and Growth." In Stem Cells Handbook, 107–17. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-7696-2_7.

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Macken, Catherine A., and Alan S. Perelson. "Characterization of Colony Growth with Time." In Stem Cell Proliferation and Differentiation, 27–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-93396-7_3.

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Ghensi, Paolo. "Dental Stem Cells and Growth Factors." In Dental Stem Cells: Regenerative Potential, 85–103. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33299-4_5.

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Semeano, Ana Teresa, Talita Glaser, Henning Ulrich, and Denise Freitas Siqueira Petri. "Scaffolds for Embryonic Stem Cell Growth and Differentiation." In Working with Stem Cells, 347–65. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30582-0_20.

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Hussain, Anwar, Husna, Ihsan Ullah, and Muhammad Naseem. "Plant-Associated Microbes Alter Root Growth by Modulating Root Apical Meristem." In Plant Stem Cells, 49–58. New York, NY: Springer US, 2019. http://dx.doi.org/10.1007/978-1-0716-0183-9_6.

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Coleman, William B., and Joe W. Grisham. "Epithelial stem-like cells of the rodent liver." In Liver Growth and Repair, 50–99. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4932-7_3.

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Oh, Steve. "Human Embryonic Stem Cells in Serum-Free Media: Growth and Metabolism." In Stem Cells and Cancer Stem Cells,Volume 3, 103–12. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-2415-0_10.

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Gimble, Jeffrey M., Bruce A. Bunnell, Farshid Guilak, Steven R. Smith, and Adam J. Katz. "Isolation and Growth of Stem Cells." In Tissue Engineering, 93–111. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02824-3_6.

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Sellheyer, Klaus. "5. Stem cells and growth factors." In Cosmetic Medicine and Surgery, 29–42. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315382364-6.

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Conference papers on the topic "Stem growth"

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Neacsu, Ioan, and Nicoleta Samarescu. "STEM Strategies for Economic Growth." In New Trends in Sustainable Business and Consumption. Editura ASE, 2022. http://dx.doi.org/10.24818/basiq/2022/08/108.

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McDougall, Bailey A. "How Climate Change Affects Coral Growth." In 2019 IEEE Integrated STEM Education Conference (ISEC). IEEE, 2019. http://dx.doi.org/10.1109/isecon.2019.8882076.

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Natarajan, Roshan S. "What Effects Do Ultra Violet Rays Have on Yeast Colony Growth." In 2020 IEEE Integrated STEM Education Conference (ISEC). IEEE, 2020. http://dx.doi.org/10.1109/isec49744.2020.9397813.

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Reid, Kenneth J., and Daniel M. Ferguson. "Do design experiences in engineering build a “growth mindset” in students?" In 2014 IEEE Integrated STEM Education Conference (ISEC). IEEE, 2014. http://dx.doi.org/10.1109/isecon.2014.6891046.

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BARRIO, R. A., S. OROZCO-FUENTES, and R. ROMERO-ARIAS. "MODELLING THE EARLY GROWTH OF STEM CELL TISSUES." In 15th International Symposium on Mathematical and Computational Biology. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789813141919_0009.

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Cadle, Chuck. "Exponential STEM Growth is Leaving Our Future Workforce Unprepared." In AIAA SPACE 2015 Conference and Exposition. Reston, Virginia: American Institute of Aeronautics and Astronautics, 2015. http://dx.doi.org/10.2514/6.2015-4433.

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Kahlen, Katrin, Jana Zinkernagel, and Hartmut Stutzel. "Modeling temperature-modulated stem growth of cucumber plants (Cucumis sativus L.)." In 2012 IEEE 4th International Symposium on Plant Growth Modeling, Simulation, Visualization and Applications (PMA). IEEE, 2012. http://dx.doi.org/10.1109/pma.2012.6524832.

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LI, Meizhang. "Abstract 5337: Laminin alpha 2 enables glioblastoma stem cell growth." 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.am2012-5337.

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Maynard, Jacqueline A., Ahmad S. Arabiyat, Anna Elefante, Lucas Shearer, Eoin King, and Andrea Kwaczala. "Using Acoustic Waves to Modulate Stem Cell Growth and Differentiation." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-71341.

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During spaceflight, the loss of mechanical loads due to microgravity leads to rapid bone loss, where bone deteriorates at a rate of 1–2% per month, where some astronauts can lose as much as 20% of their skeletal mass in a single expedition [NASA, 2001]. In order to prevent muscle and bone loss, long-term space flight exercise regimes are strictly implemented [Shackleford, 2004]. Current research has demonstrated that mechanical vibrations can help to maintain or improve bone mass [Chan, 2013] and reduce adiposity [Chen, 2015, Sen, 2011] when signals are applied at the appropriate frequency and amplitude. We have developed an acoustic sound chamber that can apply sound waves to stem cells grown in vitro. Characterization of the culture conditions inside the vibration chamber showed considerable variance across the culture plates where an applied acceleration of 0.6g varied at different spots in a 12-well tissue culture plate from as low as 0.47g to 0.78g. We believe the variance is caused by differences in the rigidity of the culture plates that makes the waves transmit inconsistently through the plastic. We hypothesized acoustic waves would induce osteogenic differentiation when applied to stem cells. We utilized pre-osteoblastic stem cells (MC3T3-E1-Subclone 4) to observe the effects of acoustic waves when applied at 0.3g and 0.6g, compared to non-vibrated controls. Cells were vibrated for 30 minutes a day for either 6 days (n = 24/group) or 12 days (n = 12/group). Cellular changes were characterized by assessing well-by-well cell number by a manual cell count and mineral content by Alizarin Red S staining. Differences between groups were determined using One-Way ANOVA with a post hoc test: Student’s t-test. To assess the effects of the variance across the culture plates, correlative analysis was conducted for well-by-well variation using Regression Analysis. Acoustically vibrated wells had 10x more cells after 6 days and showed more mineralization than non-vibrated wells at both 6 and 12 days. Acoustic waves have the ability to increase cell proliferation and can drive stem cell differentiation towards an osteoblastic lineage, this could lead to therapies that prevent bone loss during spaceflight.
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Jin, Xiuhong, Thierry Fourcaud, Baoguo Li, and Yan Guo. "Towards Modeling and Analyzing Stem Lodging for Two Contrasting Rice Cultivars." In 2009 Third International Symposium on Plant Growth Modeling, Simulation, Visualization and Applications (PMA). IEEE, 2009. http://dx.doi.org/10.1109/pma.2009.16.

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Reports on the topic "Stem growth"

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Zwetsloot, Remco, Jack Corrigan, Emily Weinstein, Dahlia Peterson, Diana Gehlhaus, and Ryan Fedasiuk. China is Fast Outpacing U.S. STEM PhD Growth. Center for Security and Emerging Technology, August 2021. http://dx.doi.org/10.51593/20210018.

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Since the mid-2000s, China has consistently graduated more STEM PhDs than the United States, a key indicator of a country’s future competitiveness in STEM fields. This paper explores the data on STEM PhD graduation rates and projects their growth over the next five years, during which the gap between China and the United States is expected to increase significantly.
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Alexander, Caroline M. Implications of Stem Cell Growth Regulation for Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2007. http://dx.doi.org/10.21236/ada474690.

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Bormann, Bernard T. Early wide spacing in red alder (Alnus rubra Bong.): effects on stem form and stem growth. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Forest and Range Experiment Station, 1985. http://dx.doi.org/10.2737/pnw-rb-423.

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Kloepper, Joseph W., and Ilan Chet. Endophytic Bacteria of Cotton and Sweet Corn for Providing Growth Promotion and Biological Disease Control. United States Department of Agriculture, January 1996. http://dx.doi.org/10.32747/1996.7613039.bard.

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Endophytes were isolated from 16.7% of surface-disinfested seeds and 100% of stems and roots of field-growth plants. Strains from Israel with broad-spectrum in vitro antibiosis were mainly Bacillus spp., and some were chitinolytic. Following dipping of cut cotton roots into suspensions of these strains, endophytes were detected up to 72 days later by isolation and by autoradiograms of 14C-labelled bacteria. Selected endophytes exhibited biological control potential based on significant reductions in disease severity on cotton inoculated with Rhizoctonia solani or Fusarium oxysporum f. sp. vasinfectum as well as control of Sclerotium rolfsii on bean. Neither salicylic acid nor chitinase levels increased in plants as a result of endophytic colonization, suggesting that the observed biocontrol was not accounted for by PR protein production. Some biocontrol endophytes secreted chitinolytic enzymes. Model endophytic strains inoculated into cotton stems via stem injection showed only limited movement within the stem. When introduced into stems at low concentrations, endophytes increased in population density at the injection site. After examining several experimental and semi-practical inoculation systems, seed treatment was selected as an efficient way to reintroduce most endophytes into plants.
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Watabe, Kounosuke. The Role of Tumor Associated Macrophage in Recurrent Growth of Tumor Stem Cell. Fort Belvoir, VA: Defense Technical Information Center, September 2012. http://dx.doi.org/10.21236/ada569375.

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Betancourt, Aline M. The Role of Mesenchymal Stem Cells in Promoting Ovarian Cancer Growth and Spread. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada590590.

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Silcox, J., and E. J. Kirkland. Uhv-stem studies on nucleation and growth of thin metal silicide films on silicon. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/6207328.

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8

Griend, Donald Vander. Isolation and Growth of Prostate Stem Cells and Establishing Cancer Cell Lines from Human Prostate Tumors. Fort Belvoir, VA: Defense Technical Information Center, May 2009. http://dx.doi.org/10.21236/ada511041.

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9

Thiede, M. E. Effects of an acute dose of gamma radiation exposure on stem diameter growth, carbon gain, and biomass partitioning in Helianthus annuus. Office of Scientific and Technical Information (OSTI), May 1988. http://dx.doi.org/10.2172/6316100.

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Silcox, J., and E. J. Kirkland. Uhv-stem studies on nucleation and growth of thin metal silicide films on silicon. Progress report, June 12, 1990--December 31, 1992. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10166349.

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