Literatura académica sobre el tema "Inhibitor Activity"
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Artículos de revistas sobre el tema "Inhibitor Activity"
Sumanadasa, Subathdrage D. M., Christopher D. Goodman, Andrew J. Lucke, Tina Skinner-Adams, Ishani Sahama, Ashraful Haque, Tram Anh Do, Geoffrey I. McFadden, David P. Fairlie y Katherine T. Andrews. "Antimalarial Activity of the Anticancer Histone Deacetylase Inhibitor SB939". Antimicrobial Agents and Chemotherapy 56, n.º 7 (16 de abril de 2012): 3849–56. http://dx.doi.org/10.1128/aac.00030-12.
Texto completoBöhm, Martina, Manuela Krause, Charis Von Auer, Wolfgang Miesbach y Inge Scharrer. "The Frequency and the Significance of ADAMTS-13 Neutralising Inhibitors in 62 Patients with Non-Familial Thrombotic Thrombocytopenic Purpura." Blood 104, n.º 11 (16 de noviembre de 2004): 3945. http://dx.doi.org/10.1182/blood.v104.11.3945.3945.
Texto completoAghaali, Negar, Mohammad Ghadamyari, Vahid Hosseininaveh y Nasir Saberi Riseh. "PROTEASE INHIBITOR FROM THE CRUDE EXTRACT OF PLANT SEEDS AFFECTS THE DIGESTIVE PROTEASES IN HYPHANTRIA CUNEA (LEP.: ARCTIIDAE)". Journal of Plant Protection Research 53, n.º 4 (1 de octubre de 2013): 338–46. http://dx.doi.org/10.2478/jppr-2013-0051.
Texto completoJang, Seong, Bill Strickland, Lynda Finis, Jeffrey J. Koojiman, Janneke J. Melis, Guido J. Zaman y Jan V. Tornout. "Abstract 4014: Comparative biochemical kinase activity analysis identifies rivoceranib as the most selective VEGFR-2 inhibitor compared with other TKIs with known activity against VEGFR-2". Cancer Research 83, n.º 7_Supplement (4 de abril de 2023): 4014. http://dx.doi.org/10.1158/1538-7445.am2023-4014.
Texto completoLi, Qi, Hongyu Yang, Jun Mo, Yao Chen, Yue Wu, Chen Kang, Yuan Sun y Haopeng Sun. "Identification by shape-based virtual screening and evaluation of new tyrosinase inhibitors". PeerJ 6 (26 de enero de 2018): e4206. http://dx.doi.org/10.7717/peerj.4206.
Texto completoSato, Shun, Kana Yamamoto, Moeno Ito, Katsutoshi Nishino, Takanao Otsuka, Kazuhiro Irie y Masaya Nagao. "Enhancement of Inhibitory Activity by Combining Allosteric Inhibitors Putatively Binding to Different Allosteric Sites on Cathepsin K". Molecules 28, n.º 10 (19 de mayo de 2023): 4197. http://dx.doi.org/10.3390/molecules28104197.
Texto completoPintus, Francesca, Delia Spanò, Angela Corona y Rosaria Medda. "Antityrosinase activity ofEuphorbia characiasextracts". PeerJ 3 (13 de octubre de 2015): e1305. http://dx.doi.org/10.7717/peerj.1305.
Texto completoHs, Ranjini, Padmanabha Udupa Eg, Shobha U. Kamath, Manjunath Setty, Basavaraj Hadapad y Asha Kamath. "AN IN VITRO STUDY OF CINNAMOMUM ZEYLANICUM AS NATURAL INHIBITOR OF ANGIOTENSIN-CONVERTING ENZYME (ACE) ON SHEEP (OVIS ARIES) TISSUES". Asian Journal of Pharmaceutical and Clinical Research 9, n.º 5 (1 de septiembre de 2016): 249. http://dx.doi.org/10.22159/ajpcr.2016.v9i5.13424.
Texto completoCHEN, Ching-Jiunn, Hui-Sheng HUANG, Yu-Tsong LEE, Chia-Yi YANG y Wen-Chang CHANG. "Characterization and purification of a lipoxygenase inhibitor in human epidermoid carcinoma A431 cells". Biochemical Journal 327, n.º 1 (1 de octubre de 1997): 193–98. http://dx.doi.org/10.1042/bj3270193.
Texto completoMiao, Yuxi, Guanzhu Chen, Xinping Xi, Chengbang Ma, Lei Wang, James F. Burrows, Jinao Duan, Mei Zhou y Tianbao Chen. "Discovery and Rational Design of a Novel Bowman-Birk Related Protease Inhibitor". Biomolecules 9, n.º 7 (14 de julio de 2019): 280. http://dx.doi.org/10.3390/biom9070280.
Texto completoTesis sobre el tema "Inhibitor Activity"
Stott, Holly Rosannah. "MMP-12 activity during vascular remodelling". Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/23609.
Texto completoEckelman, Brendan P. "The regulation of caspase activity by the inhibitor of apoptosis proteins". Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC IP addresses, 2007. http://wwwlib.umi.com/cr/ucsd/fullcit?p3288846.
Texto completoTitle from first page of PDF file (viewed June 2, 2008). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 188-214).
Gora, Kasia G. (Kasia Gabriela). "SciP : a novel inhibitor of CtrA transcriptional activity in Caulobacter crescentus". Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/68426.
Texto completoCataloged from PDF version of thesis. "August 8, 2011."
Includes bibliographical references.
Cells must sense changes in their environment and respond appropriately in order to survive. A common survival strategy is for cells to translate an environmental signal into the activity of a transcription factor they effects a change in gene expression. In this way, cells can express a gene just-in-time for its biological function. In addition, cells can coordinate the activity of many transcription factors to construct genetic regulatory networks that integrate many inputs to control complex cellular behaviors. In this thesis, I use the model system Caulobacter crescentus to examine the regulation of CtrA, the essential transcription factor at the core of the Caulobacter cell cycle regulatory network. CtrA regulates the activity of approximately 100 cell cycle genes many of which are critical for cell cycle progression. CtrA activity is regulated at the level of abundance, post-transcriptional modification, and here I show that CtrA is also regulated by a novel protein-protein interaction. I identify SciP, a GI specific inhibitor of CtrA transcriptional activity and show that SciP forms a complex with CtrA at CtrA dependent promoters. The SciP/CtrA interaction likely prevents CtrA from recruiting RNA polymerase thereby blocking the activation of transcription. In addition, I show that SciP is restricted to G1 by regulated proteolysis. I identify the Lon as the SciP protease and show that Lon is required for SciP proteolysis in vivo and that E. coli Lon degrades SciP in vitro. Finally I engineer a stable allele of sciP and show SciP proteolysis is critical for proper cell cycle progression.
by Kasia G. Gora.
Ph.D.
Al-Yousuf, Karamallah. "Investigating the anti-melanoma activity of combinatorial paclitaxel and MEK inhibitor". Thesis, University of Dundee, 2018. https://discovery.dundee.ac.uk/en/studentTheses/1be821d2-2436-4c31-8485-e62b86d6d33b.
Texto completoSancho, Elena. "Conformation and activity of plasminogen activator inhibitor type 1 (PAI-1)". Thesis, University of Aberdeen, 1994. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU552562.
Texto completoGrundy, Martin. "Activity of the aurora kinase B inhibitor AZD1152 in acute myeloid leukaemia". Thesis, University of Nottingham, 2012. http://eprints.nottingham.ac.uk/12758/.
Texto completoSampathkumar, Yamuna. "Thermal processing effects on total phenolic content, antioxidant activity, trypsin inhibitor activity and in-vitro protein digestibility of lentils". Thesis, McGill University, 2012. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=107918.
Texto completoLe prétraitment thermique de lentilles avant de les moudre en farine peut faciliter son utilisation dans la préparation de produits à valeur ajoutée. Cette étude porte sur l'évaluation des effets des prétraitments thermiques par chauffage par torréfaction(CT), par chauffage par microondes (CM), ou par l'eau bouillante (EB), sur la teneur en composés phénoliques totaux (CPT), sur l'activité anti-oxydante totale (AAOT), sur les teneurs en inhibiteur de trypsine, et sur la digestibilité in-vitro des protéines (DIVP). Les essais ont été faits sur des farines obtenues à partir de lentilles rouges décortiquées et de lentilles vertes non decortiquées après l'application des prétraitment thermiques. Les deux varieties de lentilles ont été prétraitées selon des combinaisons déterminées de températures et de durées de traitment. Les teneurs en CPT et l'AAOT ont été évaluées par spectrophotométrie à 760 nm en utilisant la méthode de Folin-Ciocalteu et la méthode DPPH (1, 1- diphényl-2-picrylhydrazyle) de piégeage des radicaux libres. Les résultats ont démontré des différences significatives entre les deux types de lentilles étudiées. Le prétraitement CM (5 min) a conduit à une augumentation significative (P≤0.05) de la teneur en CPT dans les échantillons de farine de lentilles vertes [8.85 mg GAE/g de poids sec (ps) lorsque comparé aux échantillons de farine de lentilles vertes non-traitées [7.5 JEU mg/g ps]. Une tendance similaire a été observée auprés des farines de lentilles vertes torréfiées au four pendant 20 min. L'AAOT des farines de lentilles vertes non-traitées était d'environ 86% et elle était supérieure à celle obtenue à partir de lentilles rouges non-traitées. Les teneurs en CPT observées dans les échantillons traités soit par CT soit par CM étaient plus élevées que celles des échantillons non traitées et peuvent refléter des réductions en AAOT obetnues. Les teneurs en CPT et en AAOT des échantillons obtenues à la suite du prétraitment EB étainet nettement inférieures et peut être attributées à plusieurs facteurs dans la matrice. Bien que les lentilles soit riches en protéines, plusiers facteurs limitent leurs utilisation pour la consommation humaine. Ces principaux facteurs sont : la présence de composants antinutritionnels, le temps nécessaire à la préparation, les saveurs désagréables, et la digestibilité réduites des protéines. On peut réduire l'impacte des facteurs antinutritionnels comme les inhibiteurs de la trypsine par des traitements thermiques. Les résultats ont demontré que l'utilisation du pretraitment CM permettait de réduire significativement (P≤0.05) l'activité des inhibiteurs de trypsine lorsque comparés aux prétraitments CT et EB. Il a aussi été démontré que l'augmentation de la dureé des prétraitments thermiques par CT ou par EB permettait d'accroitre la DIVP. Dans tous les cas étudiés, l'application d'un prétraitment thermique sur les lentilles a permis d'améliorer la DIVP.Mots clés : Lentilles vertes, lentilles rouges, farines, traitements thermiques, composés phénoliques totaux (CPT), activité anti-oxydante totale (AAOT), digestibilité in-vitro des protéines (DIVP), équivalent en acide gallique, chauffage par torréfaction (CT), chauffage par microondes (CM), chauffage par trempage dans l'eau bouillante (EB).
Mendis, Mihiri Marini. "Variability in Arabinoxylan, Xylanase Activity and Xylanase Inhibitor Levels in Hard Spring Wheat". Thesis, North Dakota State University, 2012. https://hdl.handle.net/10365/26806.
Texto completoNational Science Foundation Grant (# HRD-0811239) to the NDSU Advance FORWARD program
North Dakota Wheat Commission
Zwahlen, Hugo. "Effects of low-dose "Factor VIII Inhibitor Bypassing Activity (FEIBA)" in resistant heamophilia /". [S.l : s.n.], 1986. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Texto completoRen, Zhongyuan. "Small molecules regulated bone resorption and enzyme activity in osseous cells". Thesis, Lyon 1, 2014. http://www.theses.fr/2014LYO10291/document.
Texto completoCathepsin K is among the most potent mammalian collagenase, capable of cleaving the triple helix in type-I collagen. We developed a series of azanitriles (CKI-8 and CKI-13) which are inhibitors of cathepsin K. CKI-8 (an isomer of CKI-13) and CKI-13 did not induce significant toxicity on osteoblasts Saos-2 and RAW 264.7 cells up to 1000 nM, while they were not toxic on mature osteoclasts up to 100 nM. Commercial E64 inhibitor was not toxic in primary osteoclast cells up to 1000 nM. CKI-8 did not affect alkaline phosphatase activity as well the mineralization induced by Saos-2 cells and by primary osteoblasts. CKI-13 decreased by 35% the mineralization induced by Saos-2 cells while it did not on mineralization induced by primary osteoblasts. Addition of CKI-13 decreased alkaline phosphatase activity by around 20% (Saos-2 cells) and 45% (primary osteoblasts). Bone resorption on bovine slices decreased significantly with 10 nM of CKI-13, with 100 nM of CKI-8 and commercial inhibitor E64. Our findings indicated that CKI-8 and CKI-13 inhibited bone resorption and affected the mobility of osteoclast. To monitor directly the PPi hydrolytic activity by alkaline phosphatase, we developed an infrared (IR) assay taking the advantage to use natural substrate under physiological pH in matrix vesicles and in living cells. PPi band located at 1107 cm-1 (∑= 2158 ± 211 M-1.cm-1) and Pi bands located at 1076 cm-1 (∑= 1346 ± 116 M-1.cm-1) and at 991 cm-1 (∑= 493 ± 49 M-1.cm-1) served to measure the substrate and the product concentrations
Libros sobre el tema "Inhibitor Activity"
Roué, Gael. Activity of the Novel BCR Kinase Inhibitor IQS019 in B-NHL. Saarbrücken: LAP LAMBERT Academic Publishing, 2017.
Buscar texto completoG, Cory Joseph y Cory Ann H, eds. Inhibitors of ribonucleoside diphosphate reductase activity. New York: Pergamon Press, 1989.
Buscar texto completoMerton, Sandler y Smith H. J. 1930-, eds. Design of enzyme inhibitors as drugs. Oxford: Oxford University Press, 1994.
Buscar texto completoMerton, Sandler y Smith H. J. 1930-, eds. Design of enzyme inhibitors as drugs. Oxford [England]: Oxford University Press, 1989.
Buscar texto completoGupta, Satya Prakash. Matrix metalloproteinase inhibitors: Specificity of binding and structure-activity relationships. Basel: Springer, 2012.
Buscar texto completo1935-, Tipper Donald J., ed. Antibiotic inhibitors of bacterial cell wall biosynthesis. Oxford [Oxfordshire]: Pergamon Press, 1987.
Buscar texto completoKiss, S. y M. Simihăian. Improving Efficiency of Urea Fertilizers by Inhibition of Soil Urease Activity. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-017-1843-1.
Texto completoAtwell, Mark M. Inhibition of secretary activity in cells isolated from the rat stomach. Birmingham: Aston University, Department of Pharmaceutical Sciences, 1990.
Buscar texto completoM, Simihǎian, ed. Improving efficiency of urea fertilizers by inhibition of soil urease activity. Dordrecht: Kluwer Academic Publishers, 2002.
Buscar texto completoJ, Cragoe Edward, Kleyman Thomas R y Simchowitz Louis, eds. Amiloride and its analogs: Unique cation transport inhibitors. New York, N.Y: VCH, 1992.
Buscar texto completoCapítulos de libros sobre el tema "Inhibitor Activity"
Kruithof, E. K. O. "Plasminogen activator inhibitor activity assay". En ECAT Assay Procedures A Manual of Laboratory Techniques, 147–50. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2992-3_18.
Texto completoTurecek, Peter y Hans Peter Schwarz. "Factor Eight Inhibitor Bypassing Activity". En Production of Plasma Proteins for Therapeutic Use, 49–63. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118356807.ch4.
Texto completoDarragh, A., M. Kenny, R. Lambe, T. Lenehan, I. Brick y C. Maulet. "Indalpine, A New Serotonin Uptake Inhibitor". En Biological Psychiatry, Higher Nervous Activity, 347–52. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-8329-1_50.
Texto completoKluft, C. y P. Meijer. "Plasmin inhibitor activity (previously α2-antiplasmin)". En Laboratory Techniques in Thrombosis - a Manual, 257–64. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4722-4_28.
Texto completoKaspari, Marion y Elke Bogner. "Antiviral Activity of Proteasome Inhibitors/Cytomegalovirus". En Viral Proteases and Antiviral Protease Inhibitor Therapy, 71–81. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2348-3_4.
Texto completoChelliah, Ramachandran, Eric Banan-MwineDaliri y Deog-Hwan Oh. "Screening of Actinobacteria for Enzyme Inhibitor Activity". En Methods in Actinobacteriology, 475–78. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1728-1_69.
Texto completoWalker, Mark C. y James K. Gierse. "In Vitro Assays for Cyclooxygenase Activity and Inhibitor Characterization". En Methods in Molecular Biology, 131–44. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-59745-364-6_11.
Texto completoMirsky, Arthur. "The Insulinase and Insulinase-Inhibitor Activity of the Liver". En Novartis Foundation Symposia, 263–77. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470718858.ch19.
Texto completoMaxwell, Robert A. y Helen L. White. "Tricyclic and Monoamine Oxidase Inhibitor Antidepressants: Structure-Activity Relationships". En Handbook of Psychopharmacology, 83–155. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-4045-4_3.
Texto completoLacroix-Desmazes, S., A. Moreau, M. P. Horn, M. D. Kazatchkine y S. V. Kaveri. "Factor VIII Inhibitor with Catalytic Activity towards Factor VIII". En Catalytic Antibodies, 102–14. Basel: KARGER, 2000. http://dx.doi.org/10.1159/000058800.
Texto completoActas de conferencias sobre el tema "Inhibitor Activity"
Liu, Keshun y Mike Woolman. "Developing an optimized method for measuring chymotrypsin inhibitor activity in protein products". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/yucc6741.
Texto completode Agostini, A., F. Barja, S. Carrel, P. C. Harpel y M. Schapira. "C1 -INHIBITOR: STRUCTURE-ACTIVITY RELATIONSHIPS". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642903.
Texto completoDonaldson, V. H. y M. D. B. H. Mitchell. "INTERACTIONS OF DYSFUNCTIONAL Cl-INHIBITORS FROM PATIENTS WITH TYPE II HEREDITARY ANGIONEUROTIC EDEMA (HANE) WITH ACTIVATED HAGEMAN FACTOR (FACTOR XIIa)." En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643302.
Texto completoBooth, N. A., A. Reith y B. Bennett. "A PLASMINOGEN ACTIVATOR INHIBITOR (PAI-2) CIRCULATES IN TWO HIGH MOLECULAR WEIGHT FORMS IN PREGNANCY". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644459.
Texto completoSaeki, T., K. HARADA, T. Youshimura, Y. Nakamura, T. Fujimori, K. E. Katayama, Y. Yamagish, I. Yamastu y I. Ikeda. "MODE OF ACTION OF A NOVEL ANTI-PLATELET AGENT (E-5510)". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643427.
Texto completoTans, G., T. Janssen-Claessen, J. Rosing y J. H. Griffin. "APPLICATION OF SPECIFIC SERINE PROTEASE INHIBITORS IN ASSAYS FOR ACTIVATED CONTACT FACTORS." En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643301.
Texto completoJansen, J. W. C. M. "EFFECTS OF INHIBITORS ON COLLAGEN INDUCED PLATELET AGGREGATION IN SIX DIFFERENT SPECIES." En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643445.
Texto completoAgarwal, Kailash C. "NEW INSIGHTS INTO THE ANTIPLATELET ACTIVITY OF FORSKOLIN: ROLE OF PLASMA ADENOSINE AND SPECIES DIFFERENCES". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643584.
Texto completoBeretz, A., F. Lanza, A. Stierlé y J.-P. Cazenave. "CYCLIC NUCLEOTIDE PHOSPHODIESTERASE INHIBITORS PREVENT AGGREGATION AND SECRETION OF HUMAN PLATELETS BY RAISING CYCLIC AMP AND REDUCING CYTOPLASMIC FREE CALCIUM MOBILIZATION". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643586.
Texto completoIwamoto, M., N. Sugiyama, T. Sasaki y Y. Abiko. "DOMAIN OF BINDING ACTIVITY WITH PLASMIN KRINGLE IN SYNTHESIZED C-TERMINAL PEPTIDES , OF α2-PLASMIN INHIBITOR". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644612.
Texto completoInformes sobre el tema "Inhibitor Activity"
Shea, Lonnie D. Identification of a PARP Inhibitor Sensitivity Signature in Breast Cancer Using a Novel Transcription Factor Activity Array. Fort Belvoir, VA: Defense Technical Information Center, marzo de 2012. http://dx.doi.org/10.21236/ada559941.
Texto completoOlszewski, Neil y David Weiss. Role of Serine/Threonine O-GlcNAc Modifications in Signaling Networks. United States Department of Agriculture, septiembre de 2010. http://dx.doi.org/10.32747/2010.7696544.bard.
Texto completoFarazi, Mena, Michael Houghton, Margaret Murray y Gary Williamson. Systematic review of the inhibitory effect of extracts from edible parts of nuts on α-glucosidase activity. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, agosto de 2022. http://dx.doi.org/10.37766/inplasy2022.8.0061.
Texto completoOri, Naomi y Mark Estelle. Specific mediators of auxin activity during tomato leaf and fruit development. United States Department of Agriculture, enero de 2012. http://dx.doi.org/10.32747/2012.7597921.bard.
Texto completoMoran, Nava, Richard Crain y Wolf-Dieter Reiter. Regulation by Light of Plant Potassium Uptake through K Channels: Biochemical, Physiological and Biophysical Study. United States Department of Agriculture, septiembre de 1995. http://dx.doi.org/10.32747/1995.7571356.bard.
Texto completoPrusky, Dov, Noel Keen y Rolf Christoffersen. Involvement of Epicatechin in the Regulation of Natural Resistance of Avocado Fruit against Postharvest Pathogens. United States Department of Agriculture, enero de 1997. http://dx.doi.org/10.32747/1997.7613028.bard.
Texto completoChamovitz, Daniel A. y Zhenbiao Yang. Chemical Genetics of the COP9 Signalosome: Identification of Novel Regulators of Plant Development. United States Department of Agriculture, enero de 2011. http://dx.doi.org/10.32747/2011.7699844.bard.
Texto completoGranot, David y Richard Amasino. Regulation of Senescence by Sugar Metabolism. United States Department of Agriculture, enero de 2003. http://dx.doi.org/10.32747/2003.7585189.bard.
Texto completoElroy-Stein, Orna y Dmitry Belostotsky. Mechanism of Internal Initiation of Translation in Plants. United States Department of Agriculture, diciembre de 2010. http://dx.doi.org/10.32747/2010.7696518.bard.
Texto completoGrafi, Gideon y Brian Larkins. Endoreduplication in Maize Endosperm: An Approach for Increasing Crop Productivity. United States Department of Agriculture, septiembre de 2000. http://dx.doi.org/10.32747/2000.7575285.bard.
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