Literatura académica sobre el tema "Molecular Modifications"
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Artículos de revistas sobre el tema "Molecular Modifications"
Rehpenn, Andreas, Alexandra Walter y Golo Storch. "Molecular Editing of Flavins for Catalysis". Synthesis 53, n.º 15 (22 de marzo de 2021): 2583–93. http://dx.doi.org/10.1055/a-1458-2419.
Texto completoLi, Yinglu, Zhiming Li y Wei-Guo Zhu. "Molecular Mechanisms of Epigenetic Regulators as Activatable Targets in Cancer Theranostics". Current Medicinal Chemistry 26, n.º 8 (16 de mayo de 2019): 1328–50. http://dx.doi.org/10.2174/0929867324666170921101947.
Texto completoEichler, Jerry y Michael W. W. Adams. "Posttranslational Protein Modification in Archaea". Microbiology and Molecular Biology Reviews 69, n.º 3 (septiembre de 2005): 393–425. http://dx.doi.org/10.1128/mmbr.69.3.393-425.2005.
Texto completoWinter, Stefan y Wolfgang Fischle. "Epigenetic markers and their cross-talk". Essays in Biochemistry 48 (20 de septiembre de 2010): 45–61. http://dx.doi.org/10.1042/bse0480045.
Texto completoChukwuma Sr, Chrysanthus. "Characterization of the Clinical and Molecular Perspectives of Epigenetics". Archives of Clinical Investigation 1, n.º 1 (17 de octubre de 2022): 01–07. http://dx.doi.org/10.31579/2834-8087/003.
Texto completoMiki, Keishu, Takeshi Watanabe y Shinji Koh. "Electrochemical Characterization of CVD-Grown Graphene for Designing Electrode/Biomolecule Interfaces". Crystals 10, n.º 4 (26 de marzo de 2020): 241. http://dx.doi.org/10.3390/cryst10040241.
Texto completoWang, Ya-Nan, Chen-Yang Yu y Hong-Zhong Jin. "RNA N6-Methyladenosine Modifications and the Immune Response". Journal of Immunology Research 2020 (21 de enero de 2020): 1–6. http://dx.doi.org/10.1155/2020/6327614.
Texto completoHan, Dali y Meng Michelle Xu. "RNA Modification in the Immune System". Annual Review of Immunology 41, n.º 1 (26 de abril de 2023): 73–98. http://dx.doi.org/10.1146/annurev-immunol-101921-045401.
Texto completoWölk, Michele, Theres Schröter, Ralf Hoffmann y Sanja Milkovska-Stamenova. "Profiling of Low-Molecular-Weight Carbonyls and Protein Modifications in Flavored Milk". Antioxidants 9, n.º 11 (23 de noviembre de 2020): 1169. http://dx.doi.org/10.3390/antiox9111169.
Texto completoOgihara, Takuo, Kenta Mizoi y Akiko Ishii-Watabe. "Pharmacokinetics of Biopharmaceuticals: Their Critical Role in Molecular Design". Biomedicines 11, n.º 5 (16 de mayo de 2023): 1456. http://dx.doi.org/10.3390/biomedicines11051456.
Texto completoTesis sobre el tema "Molecular Modifications"
Pattarini, Lucia. "Post-translational modifications and molecular interactions regulating VEGFR2 activity". Doctoral thesis, Scuola Normale Superiore, 2009. http://hdl.handle.net/11384/85997.
Texto completoMotleleng, Liabo Lilian. "Histone modifications and the Arabidopsis thaliana circadian clock". Master's thesis, University of Cape Town, 2010. http://hdl.handle.net/11427/14719.
Texto completoThe circadian system has a regulatory role in almost all aspects of a plant's life. In Arabidopsis thaliana, almost 36% of the genome has been shown to be circadianly regulated and many genes that are circadianly regulated have been shown to be light responsive or involved in light responses. Rhythmic histone acetylation has been demonstrated in the promoter of TIMING OF CAB EXPRESSION1 (TOC1). Here, I used semi-quantitative Reverse Transcriptase Polymerase Chain Reaction (semi-quantitative RT -PCR) to investigate which enzymes are involved in the rhythmic expression of TOC1. I also determined whether loss-of-function histone acetylation and methylation mutants could affect the overall functioning of the circadian oscillator by measuring their circadian leaf movement and delayed fluorescence (DF) rhythms. GCN5/ HAG1 mutant plants (gcn5) exhibited erratic TOC1 expression in both constant dark (DD) and constant light (LL) conditions. Although TOC1 expression appeared to be rhythmic in both DD and LL conditions, the waveform of the rhythm was altered in TATA-binding protein associated factor 1 (taf1) mutants. This suggested that TAF1 and GCN5 might play different roles in the rhythmic histone acetylation affecting TOC1 expression. DF data and leaf movement data indicated that both TAF1 and GCN5 might play a role in the overall functioning of the A. thaliana circadian clock. Arrhythmic TOC1 expression and DF was observed in histone deacetylase 1 (hd1) mutants, suggesting that HD1 is not only involved in the rhythmic histone deacetylation affecting TOC1 expression but in the overall functioning of the circadian clock. Semi-quantitative RTPCR, DF and leaf movement studies demonstrated that CURLY LEAF (CLF), a histone methylase is involved in both the histone methylation affecting TOC1 expression and in the overall functioning of the A. thaliana circadian clock.
Zheng, Gang Gang Zheng. "A molecular 'switchboard' - lysine modifications and their impact on transcription". Connect to text online, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1131636831.
Texto completoZheng, Gang. "A MOLECULAR ‘SWITCHBOARD’-LYSINE MODIFICATIONS AND THEIR IMPACT ON TRANSCRIPTION". Case Western Reserve University School of Graduate Studies / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=case1131636831.
Texto completoBaker, Daniel Lindley. "Relaxation dynamics in molecular glass-formers with systematic structure modifications". Thesis, University of Leeds, 2014. http://etheses.whiterose.ac.uk/8734/.
Texto completoChen, Peng. "Function of wobble nucleoside modifications in tRNAs of Salmonella enterica Serovar Typhimurium". Doctoral thesis, Umeå universitet, Molekylärbiologi (Teknat- och Medfak), 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-328.
Texto completoColl, San Martín Laia. "Genetic disruption of transfer RNA modifications in human cancer". Doctoral thesis, Universitat de Barcelona, 2021. http://hdl.handle.net/10803/672905.
Texto completoLas modificaciones del ARN son claves en multitud de procesos celulares que al verse alteradas pueden participar en el proceso de tumorogénesis. En la presente tesis se aborda el efecto de estas alteraciones implicadas en la transformación celular en a las moléculas de los ARN de transferencia (ARNt). Se identificó la amplificación génica de TRIT1 exclusivamente en líneas celulares de cáncer de pulmón microcítico (SCLC). La amplificación de TRIT1 también fue detectada en pacientes de SCLC. La enzima TRIT1 que se encarga de introducir la modificación i6A la posición A37 de ciertos ARNt. La amplificación de TRIT1 lleva a un aumento de su expresión a nivel transcripcional y traduccional. Se generó un modelo celular de pérdida de expresión empleando una línea celular de SCLC con amplificación de TRIT1, y se realizaron ensayos in vitro. También se evaluaron las consecuencias funcionales in vivo mediante la inyección de las células en ratón, se observó una reducción del crecimiento tumoral en los tumores derivados de las células con pérdida de expresión de TRIT1. El análisis transcriptómico del modelo celular, mediante secuenciación masiva de ARN (RNA-seq), mostro una desregulación de procesos biológicos relacionados con la diferenciación celular debido a la amplificación de TRIT1. Este hallazgo condujo a la identificación del trióxido de arsénico como un posible candidato como tratamiento para SCLC por su acción en la diferenciación celular. Ensayos in vitro e in vivo indican que la amplificación de TRIT1 confiere sensibilidad al trióxido de arsénico, proponiendo un nuevo candidato terapéutico para el tratamiento de una enfermedad con tan pocas opciones terapéuticas como es SCLC.
Hartsough, Edward J. "Molecular regulation of VEGFR-2 function and expression through post-translational modifications". Thesis, Boston University, 2012. https://hdl.handle.net/2144/12417.
Texto completoVascular endothelial growth factor receptor-2 (VEGFR-2) is an endothelial cell receptor tyrosine kinase (RTK) whose activity is an obligate requirement for both normal development and pathological angiogenesis. A critical post-translational modification (PTM) of RTKs such as VEGFR-2 is tyrosine phosphorylation, which regulates these proteins at multiple levels including, tyrosine kinase activation, signaling, trafficking, and degradation. Similarly, growing evidence now suggests that protein methylation is another important type of PTM that plays a role in protein-protein interaction and signal transduction. In an effort to explore the possibility that methylation plays a role in regulation of VEGFR-2 function, we have employed mass spectrometry analysis coupled with pharmacological inhibitors of the methylation pathway. Our analysis revealed the presence of five methylated residues, three lysine and two arginine. Particularly, methylation of lysine 1041 (K1041), which is proximal to the conserved activation loop of the kinase domain, significantly contributed to VEGFR-2 kinase activation. Mutation of K1041 to multiple different amino acids rendered VEGFR-2 inactive and inhibited the activation of key downstream signaling proteins. Moreover, these mutations reduced VEGFR-2 mediated cell proliferation and capillary tube formation. Single mutations of R817, K856, K861 and R1115 yielded no apparent effect on tyrosine phosphorylation of VEGFR-2, however compounding the methyl deficiencies with triple and quadruple mutations markedly weakened tyrosine phosphorylation and the ligand-mediated downregulation of VEGFR-2. Furthermore, treatment of endothelial cells with global methylation inhibitors including adenosine dialdehyde (AdOx) and 3-deazaneplanocin A (DZNep) decreased ligand mediated tyrosine phosphorylation of VEGFR-2. The study presented here provides evidence that arginine and lysine methylation of VEGFR-2 through both combinatorial and non-combinatorial mechanisms regulate VEGFR-2 phosphorylation and function. This study also demonstrates that RNF121, an endoplasmic reticulum (ER) resident ubiquitin E3 ligase, binds to nascent VEGFR-2 protein and controls the abundance of cell surface VEGFR-2. Taken together, our data describes a novel role for arginine and lysine methylation in the regulation of VEGFR-2 functions and identifies a link between RNF121 ubiquitin E3 ligase and cell surface expression of VEGFR-2.
Di, Antonio Marco. "New Molecular Devices for Selective Structural Modifications of G-Quadruplex Folded Oligonucleotides". Doctoral thesis, Università degli studi di Padova, 2011. http://hdl.handle.net/11577/3427493.
Texto completoNell’ultimo decennio un sempre più crescente interesse è stato rivolto nei confronti del riconoscimento selettivo dei quartetti di guanina (G-quadruplex), strutture supramolecolari in grado di auto-assemblarsi in condizioni fisiologiche da oligonucleotidi ricchi di residui guaninici. La ragione di ciò risiede nel fatto che tali strutture sembrano agire come regolatori di processi a livello cellulare. Infatti, esistono svariati esempi in cui, soprattutto in vitro, molecole o anticorpi in grado di riconoscere e stabilizzare quartetti di guanina influenzino drasticamente il processo biologico in cui l’oligonucleotide stesso è implicato. L’inibizione indiretta della telomerasi e gli studi dell’effetto sulla trascrizione di oncogeni ne rappresentano le applicazioni più importati, assieme ai più recenti effetti sulla traduzione di RNA. Ciò rende G-quadruplex un vero e proprio target terapeutico per lo sviluppo di nuove terapie antitumorali. Questo lavoro nasce con lo scopo di creare una nuova generazione di leganti di G-4 che manifestino proprietà alchilanti attivabili mediante protocolli biocompatibili. Proprietà alchilanti non intrinseche, ma attivabili attraverso modifiche chimiche e fisiche, permetterebbero un controllo temporale del processo di alchilazione. Tali molecole agirebbero pertanto da veri e propri dispositivi molecolari preconcentrandosi sul target e stabilizzando il complesso attraverso interazioni non covalenti per poi, mediante attivazione, generare la specie alchilante così da ancorare fortemente la molecola all’oligonucleotide. Queste caratteristiche renderebbero il danno indotto irreversibile o non riparabile dai comuni processi cellulari, aumentando notevolmente l’efficacia di azione in termini di effetti farmaco-biologici. L’idea pertanto è quella di sfruttare le proprietà di riconoscimento di alcuni tra i leganti noti in letteratura equipaggiandoli, però, con una specie alchilante silente, il cui rilascio può essere controllato temporalmente mediante azione fisica o chimica. Questo nuovo tipo di molecole rappresenterebbe pertanto una classe di leganti irreversibili di G-4, mai progettata in precedenza. Per far ciò la molecola da sintetizzare deve possedere: 1) una superficie aromatica estesa ed elettron-povera che conferisca le proprietà di riconoscimento molecolare attraverso interazioni di π stacking con il target biologico. 2) un precursore di una specie alchilante che presenti una scarsa o assente reattività intrinseca modulabile mediante attivazione, possibilmente compatibile con condizioni fisiologiche. 3) una porzione molecolare facilmente modificabile per interazioni con il substrato o per attivazione chimica, che funga da “grilletto” della reattività del precursore alchilante. Nella fattispecie ci siamo concentrati sulla derivatizzazione di strutture, che dalla letteratura risultano dei buoni leganti di G-4, come Naftalendiimidi (NDI) o Naftalimmidi (NI), variamente sostituite con dei precursori di alchilanti tipo chinone metide (QM). Questi ultimi risultano particolarmente adatti a questo scopo in quanto posso essere generati da precursori molto stabili, attraverso dei protocolli di attivazione biocompatibili. Soprattutto risultano elettrofili la cui reattività è modulabile variando la natura elettronica del precursore stesso. In questo lavoro di tesi descriviamo la sintesi, la reattività e gli studi di interazione con oligonucleotidi ripegabili a strutture tipo G-4, delle molecole progettate e preparate nel corso del dottorato di ricerca. Particolare enfasi verrà posta sull’effetto indotto dal danno da alchilazione osservato e sulle potenziali applicazioni sia terapeutiche che diagnostiche. Inoltre descriveremo brevemente un progetto parallelo svolto durante il periodo trascorso all’Università di Cambridge, presso il gruppo di ricerca del Prof. Balasubramanian.
Ali, Ibraheem Irfan. "Role of Post-translational Protein Modifications in Regulating HIV-1 and Mammalian Transcription". Thesis, University of California, San Francisco, 2019. http://pqdtopen.proquest.com/#viewpdf?dispub=13423596.
Texto completoThe molecular gatekeepers of nearly all gene expression in living cells are the proteins that function in the process of transcription. Transcription occurs when a cell must respond to a signal. These signals can be in the form of metabolic responses, signals for growth or differentiation, signals to defend against stress or pathogenic invasion, to name a few. The fundamentals of transcription have been extensively studied in bacterial systems and model organisms, but technical limitations have hindered their studies in mammalian and human systems. Recent developments in mass spectrometric methodologies, next-generation sequencing and techniques to study difficult-to-detect post-translational protein modifications are extensively reviewed here to highlight an important regulatory network through which gene expression is regulated. In addition, I present two vignettes: the first, a study of the regulatory mechanisms of monomethylation of the HIV-1 Tat protein in regulating HIV-1 gene expression and latency; the second, a study investigating the role of acetylation in regulating RNA Polymerase II protein modifications and gene expression in mammalian systems. Together, these studies combine new mass spectrometric techniques, modification-specific antibodies, protein purification methods, and next generation sequencing to better understand the role of these modifications in regulating the transcriptional response in mammalian systems. These findings can be applied to better understand mechanisms that regulate HIV-1 viral latency, along with fundamentally shifting the field of mammalian transcription by pinpointing unique modes of regulation only found in higher eukaryotes relevant to HIV-1 infection and cancer.
Libros sobre el tema "Molecular Modifications"
Geological Survey (U.S.), ed. Modifications of two palynological processing techniques: Ultrasonic processing and early-stage sieving. [Reston, VA]: Dept. of the Interior, U.S. Geological Survey, 1992.
Buscar texto completoOverweg, Arian. The preparation, modification and characterization of some molecular sieve materials. Eindhoven: Eindhoven University, 1998.
Buscar texto completoHenri, Grosjean, ed. DNA and RNA modification enzymes: Structure, mechanism, function, and evolution. Austin, Tex: Landes Bioscience, 2009.
Buscar texto completoBlair, Mary Elizabeth. Habitat modification and gene flow in Saimiri oerstedii: Landscape genetics, intraspecific molecular systematics, and conservation. [New York, N.Y.?]: [publisher not identified], 2011.
Buscar texto completoSusanne, Brakmann y Johnsson Kai, eds. Directed molecular evolution of proteins: Or how to improve enzymes for biocatalysis. Weinheim: Wiley-VCH, 2002.
Buscar texto completoThor, G. Bioprocesses of biopharmaceuticals: The obligatory role of post translational modifications to create functional bioactive molecules. Westborough, MA: D&MD Publications, 2005.
Buscar texto completoZhou, Xiufen. Molecular genetic analysis of an unusual DNA modification and a phage defence system of streptomyces lividans 66. Norwich: University of East Anglia, 1993.
Buscar texto completoA 'Toolkit' of Small Molecules for Polymer Assembly and Post-Synthetic Modification Using 'Click' and Photoactive Chemistries. [New York, N.Y.?]: [publisher not identified], 2011.
Buscar texto completo1952-, Zouali Moncef, ed. The epigenetics of autoimmune diseases. Chichester: Wiley-Blackwell, 2009.
Buscar texto completoLamond, Angus I. Pre-mRNA processing. New York: Springer-Verlag, 1995.
Buscar texto completoCapítulos de libros sobre el tema "Molecular Modifications"
Carlberg, Carsten, Eunike Velleuer y Ferdinand Molnár. "Histone Modifications". En Molecular Medicine, 101–15. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-27133-5_7.
Texto completoBross, Peter. "Posttranslational Modifications". En SpringerBriefs in Molecular Science, 53. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-26088-4_11.
Texto completoGait, Michael J. y Sudhir Agrawal. "Introduction and History of the Chemistry of Nucleic Acids Therapeutics". En Methods in Molecular Biology, 3–31. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_1.
Texto completoCullen, Bryan R. y Kevin Tsai. "Mapping RNA Modifications Using Photo-Crosslinking-Assisted Modification Sequencing". En Methods in Molecular Biology, 123–34. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1374-0_8.
Texto completoYu, Bin y Xuemei Chen. "Analysis of miRNA Modifications". En Methods in Molecular Biology, 137–48. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-005-2_10.
Texto completoLavitrano, Marialuisa, Laura Farina, Maria Grazia Cerrito y Roberto Giovannoni. "Sperm-Mediated Genetic Modifications". En Methods in Molecular Biology, 125–32. New York, NY: Springer US, 2019. http://dx.doi.org/10.1007/978-1-4939-9837-1_11.
Texto completoTreffon, Patrick, Michael Liebthal, Wilena Telman y Karl-Josef Dietz. "Probing Posttranslational Redox Modifications". En Methods in Molecular Biology, 195–219. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7136-7_12.
Texto completoWidłak, Wiesława. "Synthesis and Posttranslational Modifications of Proteins". En Molecular Biology, 93–107. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-45361-8_6.
Texto completoRoy, Bijoyita. "Effects of mRNA Modifications on Translation: An Overview". En Methods in Molecular Biology, 327–56. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1374-0_20.
Texto completoKarijolich, John, Athena Kantartzis y Yi-Tao Yu. "Quantitative Analysis of RNA Modifications". En Methods in Molecular Biology, 21–32. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-657-3_2.
Texto completoActas de conferencias sobre el tema "Molecular Modifications"
Chao, Chih-Ming y Kerwin Wang. "Surface modifications for iron oxide nanoparticle assembly". En 2011 IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS). IEEE, 2011. http://dx.doi.org/10.1109/nems.2011.6017460.
Texto completoHamlow, Lucas, J. Oomens, Giel Berden, M. Rodgers, Bo Yang, Ranran Wu, Lin Fan y Chenchen He. "STRUCTUAL EFFECTS OF CYTIDINE 2′ RIBOSE MODIFICATIONS AS DETERMINED BY IRMPD ACTION SPECTROSCOPY". En 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.mi13.
Texto completoShao, Hao-Chiang. "UNVEILING VESTIGES OF MAN-MADE MODIFICATIONS ON MOLECULAR-BIOLOGICAL EXPERIMENT IMAGES". En 2018 IEEE Global Conference on Signal and Information Processing (GlobalSIP). IEEE, 2018. http://dx.doi.org/10.1109/globalsip.2018.8646594.
Texto completoRothman, Laurence S. "The HITRAN Molecular Database: Enhancements for Remote Sensing". En Optical Remote Sensing of the Atmosphere. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/orsa.1993.thc.1.
Texto completoArčon, D., R. Blinc, P. Cevc, A. Omerzu y D. Mihailovič. "Comparative study of ferromagnetic and non-ferromagnetic modifications of TDAE-". En ELECTRONIC PROPERTIES OF NOVEL MATERIALS--SCIENCE AND TECHNOLOGY OF MOLECULAR NANOSTRUCTURES. ASCE, 1999. http://dx.doi.org/10.1063/1.59814.
Texto completoVernier, P. T. "Molecular modeling of membrane modifications after exposure to nanosecond, pulsed electric fields". En SPIE BiOS, editado por Gerald J. Wilmink y Bennett L. Ibey. SPIE, 2013. http://dx.doi.org/10.1117/12.2005996.
Texto completoAngioni, MM, A. Denotti, S. Pinna, C. Sanna, A. Floris, M. Piga, A. Loi y A. Cauli. "SAT0528 Molecular modifications induced by mud-bath therapy in patients with osteoarthritis". En 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.6874.
Texto completoAdamek, Maksimiljan. "Molecular Grammar of RNA-binding Protein Interactions in Formation and Function of Ribonucleoprotein Complexes". En Socratic Lectures 8. University of Lubljana Press, 2023. http://dx.doi.org/10.55295/psl.2023.ii15.
Texto completoRodgers, M., Jos Oomens, Giel Berden, Chase Leslie, Erik Soley, Harrison Roy, Zachary Devereaux et al. "INFLUENCE OF NATURALLY-OCCURRING AND SYNTHETIC MODIFICATIONS ON THE STRUCTURES AND GLYCOSIDIC BOND STABILITIES OF DNA AND RNA NUCLEOSIDES". En 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.ma02.
Texto completoRodgers, M., Jos Oomens, Giel Berden, Chase Leslie, Erik Soley, Harrison Roy, Zachary Devereaux et al. "INFLUENCE OF NATURALLY-OCCURRING AND SYNTHETIC MODIFICATIONS ON THE STRUCTURES AND GLYCOSIDIC BOND STABILITIES OF DNA AND RNA NUCLEOSIDES". En 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.rg02.
Texto completoInformes sobre el tema "Molecular Modifications"
Library, Spring. Where Does Current Quorum Sensing Research Stand. Spring Library, diciembre de 2020. http://dx.doi.org/10.47496/sl.blog.16.
Texto completoClough, S. B., S. Kumar, X. F. Sun, S. Tripathy y H. Matsuda. Molecular and Crystal Engineering of Polydiacetylenes: Modification of Optical Properties. Fort Belvoir, VA: Defense Technical Information Center, octubre de 1988. http://dx.doi.org/10.21236/ada200808.
Texto completoLópez-Valverde, Nansi, Javier Aragoneses, Antonio López-Valverde, Cinthia Rodríguez y Juan Manuel Aragoneses. Role in the osseointegration of titanium dental implants, of bioactive surfaces based on biomolecules: A systematic review and meta-analysis of in vivo studies. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, junio de 2022. http://dx.doi.org/10.37766/inplasy2022.6.0076.
Texto completoSchaffer, Arthur, Jack Preiss, Marina Petreikov y Ilan Levin. Increasing Starch Accumulation via Genetic Modification of the ADP-glucose Pyrophosphorylase. United States Department of Agriculture, octubre de 2009. http://dx.doi.org/10.32747/2009.7591740.bard.
Texto completoPorat, Ron, Gregory T. McCollum, Amnon Lers y Charles L. Guy. Identification and characterization of genes involved in the acquisition of chilling tolerance in citrus fruit. United States Department of Agriculture, diciembre de 2007. http://dx.doi.org/10.32747/2007.7587727.bard.
Texto completoAnderson, Olin, Gad Galili y Ann Blechl. Heterologous Expression of Wheat High Molecular Weight Glutenin Subunit Genes: Analysis and Modification of Protein Sequences Affecting Dough Quality. United States Department of Agriculture, enero de 1993. http://dx.doi.org/10.32747/1993.7603826.bard.
Texto completoBrown Horowitz, Sigal, Eric L. Davis y Axel Elling. Dissecting interactions between root-knot nematode effectors and lipid signaling involved in plant defense. United States Department of Agriculture, enero de 2014. http://dx.doi.org/10.32747/2014.7598167.bard.
Texto completoWeiss, David y Neil Olszewski. Manipulation of GA Levels and GA Signal Transduction in Anthers to Generate Male Sterility. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7580678.bard.
Texto completoTzfira, Tzvi, Michael Elbaum y Sharon Wolf. DNA transfer by Agrobacterium: a cooperative interaction of ssDNA, virulence proteins, and plant host factors. United States Department of Agriculture, diciembre de 2005. http://dx.doi.org/10.32747/2005.7695881.bard.
Texto completoCohen, Jerry D. y Ephraim Epstein. Metabolism of Auxins during Fruit Development and Ripening. United States Department of Agriculture, agosto de 1995. http://dx.doi.org/10.32747/1995.7573064.bard.
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