Academic literature on the topic 'Ser/Thr protein kinases'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Ser/Thr protein kinases.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Ser/Thr protein kinases"
PHALIP, Vincent, Jian-Hong LI, and Cheng-Cai ZHANG. "HstK, a cyanobacterial protein with both a serine/threonine kinase domain and a histidine kinase domain: implication for the mechanism of signal transduction." Biochemical Journal 360, no. 3 (December 10, 2001): 639–44. http://dx.doi.org/10.1042/bj3600639.
Full textMizunuma, Masataka, Atsushi Kaneko, Shunta Imai, Kazuhiro Furukawa, and Yoshiro Chuman. "Methods for Identification of Substrates/Inhibitors of FCP/SCP Type Protein Ser/Thr Phosphatases." Processes 8, no. 12 (December 4, 2020): 1598. http://dx.doi.org/10.3390/pr8121598.
Full textSongyang, Z., K. P. Lu, Y. T. Kwon, L. H. Tsai, O. Filhol, C. Cochet, D. A. Brickey, et al. "A structural basis for substrate specificities of protein Ser/Thr kinases: primary sequence preference of casein kinases I and II, NIMA, phosphorylase kinase, calmodulin-dependent kinase II, CDK5, and Erk1." Molecular and Cellular Biology 16, no. 11 (November 1996): 6486–93. http://dx.doi.org/10.1128/mcb.16.11.6486.
Full textSeok, Seung-Hyeon. "Structural Insights into Protein Regulation by Phosphorylation and Substrate Recognition of Protein Kinases/Phosphatases." Life 11, no. 9 (September 13, 2021): 957. http://dx.doi.org/10.3390/life11090957.
Full textBlume, Constanze, Peter M. Benz, Ulrich Walter, Joohun Ha, Bruce E. Kemp, and Thomas Renné. "AMP-activated Protein Kinase Impairs Endothelial Actin Cytoskeleton Assembly by Phosphorylating Vasodilator-stimulated Phosphoprotein." Journal of Biological Chemistry 282, no. 7 (November 2, 2006): 4601–12. http://dx.doi.org/10.1074/jbc.m608866200.
Full textPrasad, Jayendra, and James L. Manley. "Regulation and Substrate Specificity of the SR Protein Kinase Clk/Sty." Molecular and Cellular Biology 23, no. 12 (June 15, 2003): 4139–49. http://dx.doi.org/10.1128/mcb.23.12.4139-4149.2003.
Full textTHELEN, Jay J., Jan A. MIERNYK, and Douglas D. RANDALL. "Pyruvate dehydrogenase kinase from Arabidopsis thaliana: a protein histidine kinase that phosphorylates serine residues." Biochemical Journal 349, no. 1 (June 26, 2000): 195–201. http://dx.doi.org/10.1042/bj3490195.
Full textGangwal, Aakriti, Nitika Sangwan, Neha Dhasmana, Nishant Kumar, Chetkar Chandra Keshavam, Lalit K. Singh, Ankur Bothra, et al. "Role of serine/threonine protein phosphatase PrpN in the life cycle of Bacillus anthracis." PLOS Pathogens 18, no. 8 (August 1, 2022): e1010729. http://dx.doi.org/10.1371/journal.ppat.1010729.
Full textByrne, Dominic P., Safal Shrestha, Martin Galler, Min Cao, Leonard A. Daly, Amy E. Campbell, Claire E. Eyers, Elizabeth A. Veal, Natarajan Kannan, and Patrick A. Eyers. "Aurora A regulation by reversible cysteine oxidation reveals evolutionarily conserved redox control of Ser/Thr protein kinase activity." Science Signaling 13, no. 639 (July 7, 2020): eaax2713. http://dx.doi.org/10.1126/scisignal.aax2713.
Full textLutterbach, B., and S. R. Hann. "Hierarchical phosphorylation at N-terminal transformation-sensitive sites in c-Myc protein is regulated by mitogens and in mitosis." Molecular and Cellular Biology 14, no. 8 (August 1994): 5510–22. http://dx.doi.org/10.1128/mcb.14.8.5510-5522.1994.
Full textDissertations / Theses on the topic "Ser/Thr protein kinases"
Lee, Guinevere Kwun Wing Queenie. "Serine/threonine phosphorylation in mycobacterium tuberculosis : identification of protein kinase B (PknB) substrates." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/693.
Full textHaj, Slimane Ammar Zeineb. "Dynamique Spatiotemporelle de la protéine kinase AMPc dépendante dans les myocytes cardiaques." Phd thesis, Université Paris Sud - Paris XI, 2012. http://tel.archives-ouvertes.fr/tel-00954406.
Full textGONZALEZ, MAYA LETICIA. "Etude de la transduction du signal impliquant la phospho-proteine pii et des ser/thr-kinases chez les cyanobacteries." Université Louis Pasteur (Strasbourg) (1971-2008), 2000. http://www.theses.fr/2000STR13092.
Full textKobir, Ahasanul. "Physiological roles of Eukaryotic Hanks type Ser/Thr kinase in transition to stationary phase in Bacillus subtilis." Phd thesis, Université Paris Sud - Paris XI, 2012. http://tel.archives-ouvertes.fr/tel-00911812.
Full textWehenkel, Annemarie. "Etude structurale et fonctionnelle de Ser/Thr kinases et phosphates mycobactériennes." Paris 6, 2007. http://www.theses.fr/2007PA066177.
Full textMacaccaro, Paolo. "Immunophenotypic characterization of B-lymphopoiesis in KO mice for oncogenic Ser / Thr kinases by multiparameter flow cytometry." Doctoral thesis, Università degli studi di Padova, 2017. http://hdl.handle.net/11577/3422901.
Full textProtein kinase CK2 and CK1 are a pleiotropic and evolutionary conserved serin-threonin kinase that is involved in several cellular processes. A number of studies revealed many mechanisms through which this kinase regulates cell cycle, apoptosis, cell survival and tumorigenesis. CK2 participates in many developmental pathways, of which particularly relevant for hemo-lymphopoiesis are those dependent on Hedgehog, NF-κB and STAT3, which regulate cell differentiation, proliferation, self-renewal as well as lineage choice commitment.. CK1 regulates also molecular pathways which are important for multiple myeloma plasma cells survival, like WNT/β-catenin pathway and PI3K/AKT pathway. However, despite all this data, little is known about the role of CK2 and CK1 in B-lymphopoiesis and lymphomagenesis. To elucidate the physiological and pathogenetic role of CK2 and CK1 in B-lymphocytes, we generated B cell specific conditional KO mice, were we studied the effects of deletion during normal B cell development with multiparameter flow cytometry analysis. In the bone marrow (BM), CK2β KO mice displayed a reduction of B cells, especially of the recirculating population of transitional and follicular (FO) B-cells. In peripheral blood and spleen the number of B-cells was markedly reduced. In the spleen of CK2β KO we observed an imbalance between the amount of FO and marginal zone (MZ) B-cells was found with an absolute reduction of FO B cells by approximately 2-folds and an increase of MZ B-cells and MZB cell precursors by up to three folds.. In vitro class-switch recombination assays demonstrated impairment in IgG1 and IgG3 class-switch and a marked reduction of the generation of antibody-producing cells. In CK1 KO mice we observed the totally absence of mature B cells and the presence of early precursors B cells. CK1 HET mice showed a reduction of B cells in bone marrow and an light imbalance of FO B cells an MZB cells in spleen. In vitro class-switch recombination assays doesn’t showed significant difference between HET and CTRL mice in IgG1 and IgG3 class-switch. Here, we found that the β subunit of protein kinase CK2 is a novel regulator of peripheral B cell differentiation. CK2β has a role in regulation of the GC reaction and in homeostasis of FOB and MZB cells. Furthermore we found that CK1 has a pivotal role in early B cells development. On one side our data enrich the knowledge on the mechanisms regulating B-cell development, on the other side they inform about the potential mechanisms altered by CK2 and CK1 during B-cell tumorigenesis.
石崎, 敏理. "The small GTP-binding protein Rho binds to and activates a 160kDa Ser/Thr protein kinase homologous to myotonic dystrophy kinaseに関する研究(myotonic dystrophy kinaseに相同性を有し,低分子量GTP結合蛋白質Rhoに結合,活性化される160kDaセリン/スレオニンキナーゼ)." Kyoto University, 1997. http://hdl.handle.net/2433/202205.
Full text0048
新制・課程博士
博士(医学)
甲第6788号
医博第1888号
新制||医||664(附属図書館)
15860
UT51-97-H172
京都大学大学院医学研究科分子医学系専攻
(主査)教授 月田 承一郎, 教授 永田 和宏, 教授 中西 重忠, 教授 成宮 周
学位規則第4条第1項該当
Deupí, i. Corral Xavier. "Influence of Ser and Thr residues in the geometry of transmembrane helices: implications on the structure and function of G protein-coupled receptors." Doctoral thesis, Universitat Autònoma de Barcelona, 2003. http://hdl.handle.net/10803/4426.
Full textSe sap que determinats residus, com prolina, serina o treonina, provoquen distorsions locals en l'estructura de les hèlices a. L'anàlisi de bases de dades de seqüències de segments transmembrana mostra com certes combinacions d'aquests residus són més comunes que d'altres, i que algunes d'elles estan sobre-representades de manera significativa, mentre que d'altres estan clarament sots-representades. La restricció d'aquesta anàlisi de seqüències a la regió transmembrana dels GPCRs de la Classe A mostra com aquestes combinacions es troben en posicions específiques i, a més, es troben conservades en certes subfamílies de receptors.
L'estructura i la dinàmica de les hèlices transmembrana que contenen aquestes combinacions de prolina i serina o treonina s'han estudiat mitjançant simulacions de dinàmica molecular en un entorn hidrofòbic explícit. Els resultats mostren com algunes d'aquestes combinacions indueixen distorsions importants en l'estructura de l'hèlix a, degut al seu efecte desestabilitzador de la xarxa de ponts d'hidrogen que dóna estabilitat a l'hèlix.
Aquests resultats s'han aplicat a la construcció d'un model tridimensional del receptor de quimiocines CCR5 , utilitzant tècniques de modelització molecular per homologia. En aquest model es proposa que les hèlices transmembrana (TMH) 2 i 3 del receptor CCR5 són estructuralment diferents del patró de rodopsina. TMH2 està més doblegada degut a la presència d'un motiu Thr-X-Pro, que, a més, fa que aquesta hèlix es doblegui cap a TMH3. Així doncs, es proposa que, en aquest receptor, aquestes dues hèlices interaccionen. Aquesta interacció estaria mediada per la presència de residus hidrofòbics conservats i específics en les dues hèlices. Aquestes hipòtesis han estat posades a prova mitjançant experiments de mutagènesi dirigida, gràcies a la col·laboració amb l'Institut de Recherche Interdisciplinaire en Biologie Humaine et Nucléaire (IRIBHN), Université Libre de Bruxelles. Els resultats experimentals permeten establir la hipòtesi que la interfície TMH2-TMH3 participa en l'activació induïda per quimiocines del receptor CCR5.
Com a conclusió, aquesta tesi pretén mostrar com, mitjançant la utilització d'eines bioinformàtiques, és possible traduir les seqüències primàries de proteïnes i les interaccions a nivell atòmic en estructures tridimensionals de proteïnes. A més, aquesta tesi mostra que, encara que l'estructura tridimensional de la rodopsina bovina és un patró útil per la modelització per homologia de GPCRs, s'han de tenir en compte de manera explícita les especificitats de seqüència de cada receptor per tal de construir models de receptors particulars. Aquestes especificitats de seqüència consisteixen en patrons de seqüència conservats en determinades famílies, que es tradueixen en divergències estructurals. Entre aquests patrons de seqüència, es proposa que els residus de serina i treonina, sols o combinats amb residus de prolina propers, poden modular la geometria de les TMHs, degut a la seva capacitat d'interferir amb la xarxa de ponts d'hidrogen que dóna estabilitat a les hèlices a.
Finalment, es proposa que la influència dels motius de serina, treonina i prolina en l'estructura de les TMHs pot estar relacionada amb els processos d'activació dels GPCRs de la Classe A i, possiblement, d'altres proteïnes de membrana. En els GPCRs, aquests motius poden haver evolucionat per tal d'adaptar uns mecanismes d'activació conservats als lligands característics de cada família de receptors.
This thesis is framed in the study of particular biological systems through the use of bioinformatics. In particular, the theoretical study of the influence of certain amino acids on the structure and dynamics of the secondary structure elements of proteins has been applied to homology modelling of G protein-coupled receptors (GPCRs) and to the study of their mechanisms of activation.
Certain residues, as proline, serine or threonine, are known to induce local distortions in the a-helical structure. Analysis of sequence databases of transmembrane segments evidence that certain combinations of these residues are more common than others, and that some of them are significantly over-represented, while others are clearly under-represented. The focusing this sequence analysis on the transmembrane region of Class A GPCRs illustrates that these combinations are located in some specific locations and conserved within certain subfamilies of receptors.
The structure and dynamics of transmembrane a-helices containing these combinations of proline and serine or threonine have been studied using molecular dynamics simulations in an explicit hydrophobic environment. The results show how some of these combinations induce significant distortions in the a-helical structure, due to their effect on the hydrogen bond network that stabilizes the helix.
These results have been applied to the building of a three-dimensional model of the chemokine CCR5 receptor, using homology modelling techniques. In this model, transmembrane helices (TMH) 2 and 3 of CCR5 are proposed to be different from the bovine rhodopsin template. TMH2 is more bent due to the presence of a Thr-X-Pro motif, which, in turn, induces this helix to lean towards TMH3. As a consequence, an interaction between these two helices is proposed for this particular receptor. This interaction would be mediated through the presence of specific and conserved hydrophobic and aromatic residues in both helices. These hypothesis have been tested through site-directed mutagenesis experiments, thanks to a collaboration with the Institut de Recherche Interdisciplinaire en Biologie Humaine et Nucléaire (IRIBHN), Université Libre de Bruxelles. The experimental results let us to hypothesize that the TMH2-TMH3 interface is involved in the chemokine-induced activation of the CCR5 receptor.
As a conclusion, this thesis aims to show how through the use of bioinformatics tools, primary sequences of proteins and interactions at an atomic level can be translated to three-dimensional protein structures. In addition, this thesis illustrates that, even though the three-dimensional structure of bovine rhodopsin is a very useful template for homology modelling of GPCRs, the sequence specificities of each receptor have to be explicitly taken into account in order to build models. These sequence specificities consist in sequence patterns conserved within certain families, which are translated into structural divergences. Among these sequence patterns, we hypothesize that serine and threonine, alone or combined with nearby proline residues, can modulate the geometry of TMHs, due to its capability to interfere with the hydrogen bond network that stabilize a-helices.
Finally, we propose that the influence of serine, threonine and proline motifs in the structure of TMHs may be related to processes of activation in the Class A of GPCRs, and, possibly, other membrane proteins as well. In GPCRs, these motifs may have evolved in order to adapt a conserved mechanism of activation of the G protein to the cognate ligands of each receptor family.
Shor, Audrey Cathryn. "Src kinase inhibitors for the treatment of sarcomas : cellular and molecular mechanisms of action." [Tampa, Fla] : University of South Florida, 2007. http://purl.fcla.edu/usf/dc/et/SFE0001906.
Full textUnsworth, Amanda J. "The role of protein kinase C in platelet activation." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:114582b8-185a-41f5-958c-77038fb185df.
Full textBooks on the topic "Ser/Thr protein kinases"
Takao, Kumazawa, Kruger Lawrence, and Mizumura Kazue, eds. The polymodal receptor: A gateway to pathological pain. Amsterdam: Elsevier, 1996.
Find full textKung, Hsien-Jien. Protein Kinases (Journal of Biomedical Science Ser. 2). S Karger Pub, 1998.
Find full textJournal of Molecular Microbiology and Biotechnology: Ser/Thr/tyr Protein Phosphorylation in Bacteria (Journal of Molecular Microbiology and Biotechnology). Not Avail, 2006.
Find full textJohnston, Michael V. Coffin-Lowry Syndrome. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0057.
Full text(Editor), T. Kumazawa, L. Kruger (Editor), and K. Mizumura (Editor), eds. The Polymodal Receptor - A Gateway to Pathological Pain (Progress in Brain Research). Elsevier Science, 1996.
Find full textBook chapters on the topic "Ser/Thr protein kinases"
Inouye, Sumiko, Hirofumi Nariya, and José Muñoz-Dorado. "Protein Ser/Thr Kinases and Phosphatases in Myxococcus xanthus." In Myxobacteria, 191–210. Washington, DC, USA: ASM Press, 2014. http://dx.doi.org/10.1128/9781555815677.ch11.
Full textZorina, Anna A., Galina V. Novikova, and Dmitry A. Los. "Participation of Ser-Thr Protein Kinases in Regulation of Heat Stress Responses inSynechocystis." In Stress and Environmental Regulation of Gene Expression and Adaptation in Bacteria, 766–80. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119004813.ch74.
Full textAriño, Joaquin, Francesc Posas, and Josep Clotet. "The Search for the Biological Function of Novel Yeast Ser/Thr Phosphatases." In Protein Phosphatase Protocols, 305–13. Totowa, NJ: Humana Press, 1998. http://dx.doi.org/10.1385/0-89603-468-2:305.
Full textShen, Sheldon S. "Protein Kinase C and Regulation of the Na+−H+ Antiporter Activity During Fertilization of the Sea Urchin Egg." In Mechanisms of Egg Activation, 173–99. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0881-3_9.
Full text"Ser/Thr-Specific Protein Kinases and Protein Phosphatases." In Biochemistry of Signal Transduction and Regulation, 269–309. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2004. http://dx.doi.org/10.1002/3527601864.ch7.
Full text"Ser/Thr-Specific Protein Kinases and Protein Phosphatases." In Biochemistry of Signal Transduction and Regulation, 417–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667475.ch09.
Full text"Ser-Thr Protein Kinase PK428." In Encyclopedia of Signaling Molecules, 4913. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_103474.
Full text"Ser-Thr Protein Kinase Related to the Myotonic Dystrophy Protein Kinase." In Encyclopedia of Signaling Molecules, 4913. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_103475.
Full textHuff, Janice, and Thomas Parsons. "Sea." In The Protein Kinase FactsBook, 221–22. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012324719-3/50200-4.
Full textGeoghegan, Kieran F., and Mary E. Kelly. "Selective Sequencing of Peptides with N-Terminal Ser or Thr in Mixtures." In Techniques in Protein Chemistry, 151–58. Elsevier, 1994. http://dx.doi.org/10.1016/b978-0-12-194710-1.50022-9.
Full textConference papers on the topic "Ser/Thr protein kinases"
Liang, Chengwei, and Xiaowen Zhang. "Evidence for Positive Selection in Ser/Thr Protein Kinases (STKs) Genes of Trichodesmium erythraeum." In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5162808.
Full textVasilevich, Natalya, Elena Aksenova, Denis Kazyulkin, and Ilya Afanasyev. "Search For Potent And Selective Aurora A Inhibitors Based On General Ser/Thr Kinases Pharmacophore Model." In 1st International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a036.
Full textGear, LR A., D. Freas, and J. D. Carty. "EARLY (< 5 SEC) PHOSPHORYLATIONS OF PLATELET PROTEINS FOLLOWING ACTIVATION BY ADP AND ADRENALIN, SEPARATELY AND IN COMBINATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643640.
Full textSuzuki, Koji, Yoshihiro Deyashiki, Junji Nishioka, Kazunori Toma, and Shuji Yamamoto. "THE INHIBITOR OF ACTIVATED PROTEIN C: STRUCTURE AND FUNCTION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642963.
Full textWilliams, Christopher Charles, Michelyn C. Patton, and Melody M. Campbell. "Abstract B67: Phenotype-specific role for protein kinase CK2 in luminal and basal-like breast cancer cells." In Abstracts: AACR International Conference on the Science of Cancer Health Disparities‐‐ Sep 18-Sep 21, 2011; Washington, DC. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1055-9965.disp-11-b67.
Full textDemolle, D., E. J. Cragoe, and J. M. Boeynaems. "MECHANISMS INVOLVED IN 5-HT STIMULATION OF PROSTACYCLIN PRODUCTION BY BOVINE AORTIC SMOOTH MUSCLE CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642841.
Full textWallace, Robert W., E. Ann Tallant, and Lynn M. Brumley. "POSSIBLE ROLE FOR THE CA2+-DEPENDENT PROTEASE (CALPAIN I) AS AN IRREVERSIBLE ACTIVATOR OF CA2+/CALMODULIN-MEDIATED REACTIONS IN THE HUMAN PLATELET." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644528.
Full textPiliouras, Teresa, Kun Zack Liu, Yiwei Jia, Pui Lam Raymond Yu, Qian Zeng, Jeanne Lauer, Maigh Attre, and Julie Ortiz. "“Others may see someone eating a cookie — I see the start of a protein kinase cascade reaction”." In 2014 IEEE Integrated STEM Education Conference (ISEC). IEEE, 2014. http://dx.doi.org/10.1109/isecon.2014.6891042.
Full textHolderness, Nina, Howard Donninger, Michael J. Birrer, and Virna Leaner. "The role of p21-activated kinase 3 (PAK3) in activating protein 1 (AP-1) induced oncogenesis." In AACR International Conference: Molecular Diagnostics in Cancer Therapeutic Development– Sep 27-30, 2010; Denver, CO. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/diag-10-a36.
Full textBaker, J. B., M. P. McGrogan, C. Simonsen, R. L. Gronke, and B. W. Festoff. "STRUCTURE AND PROPERTIES OF PROTEASE NEXIN I." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644765.
Full textReports on the topic "Ser/Thr protein kinases"
Dickman, Martin B., and Oded Yarden. Regulation of Early Events in Hyphal Elongation, Branching and Differentiation of Filamentous Fungi. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7580674.bard.
Full textDickman, Martin B., and Oded Yarden. Role of Phosphorylation in Fungal Spore Germination. United States Department of Agriculture, August 1993. http://dx.doi.org/10.32747/1993.7568761.bard.
Full textEpel, Bernard L., Roger N. Beachy, A. Katz, G. Kotlinzky, M. Erlanger, A. Yahalom, M. Erlanger, and J. Szecsi. Isolation and Characterization of Plasmodesmata Components by Association with Tobacco Mosaic Virus Movement Proteins Fused with the Green Fluorescent Protein from Aequorea victoria. United States Department of Agriculture, September 1999. http://dx.doi.org/10.32747/1999.7573996.bard.
Full textSessa, Guido, and Gregory Martin. A functional genomics approach to dissect resistance of tomato to bacterial spot disease. United States Department of Agriculture, January 2004. http://dx.doi.org/10.32747/2004.7695876.bard.
Full text