Littérature scientifique sur le sujet « Lhc protein »
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Articles de revues sur le sujet "Lhc protein"
Darr, S. C., S. C. Somerville et C. J. Arntzen. « Monoclonal antibodies to the light-harvesting chlorophyll a/b protein complex of photosystem II. » Journal of Cell Biology 103, no 3 (1 septembre 1986) : 733–40. http://dx.doi.org/10.1083/jcb.103.3.733.
Texte intégralRochaix, Jean-David, et Roberto Bassi. « LHC-like proteins involved in stress responses and biogenesis/repair of the photosynthetic apparatus ». Biochemical Journal 476, no 3 (14 février 2019) : 581–93. http://dx.doi.org/10.1042/bcj20180718.
Texte intégralJackowski, Grzegorz, et Ewa Kluck. « The Oligomeric Arrangement of the Light-Harvesting Chlorophyll a/6-Protein Complex of Photosystem II ». Zeitschrift für Naturforschung C 49, no 5-6 (1 juin 1994) : 337–42. http://dx.doi.org/10.1515/znc-1994-5-610.
Texte intégralNield, Jon, Christiane Funk et James Barber. « Supermolecular structure of photosystem II and location of the PsbS protein ». Philosophical Transactions of the Royal Society of London. Series B : Biological Sciences 355, no 1402 (29 octobre 2000) : 1337–44. http://dx.doi.org/10.1098/rstb.2000.0695.
Texte intégralSprague, S. G., E. L. Camm, B. R. Green et L. A. Staehelin. « Reconstitution of light-harvesting complexes and photosystem II cores into galactolipid and phospholipid liposomes. » Journal of Cell Biology 100, no 2 (1 février 1985) : 552–57. http://dx.doi.org/10.1083/jcb.100.2.552.
Texte intégralTakeuchi, TS, et JP Thornber. « Heat-Induced Alterations in Thylakoid Membrane Protein Composition in Barley ». Functional Plant Biology 21, no 6 (1994) : 759. http://dx.doi.org/10.1071/pp9940759.
Texte intégralSchuster, G., M. Dewit, L. A. Staehelin et I. Ohad. « Transient inactivation of the thylakoid photosystem II light-harvesting protein kinase system and concomitant changes in intramembrane particle size during photoinhibition of Chlamydomonas reinhardtii. » Journal of Cell Biology 103, no 1 (1 juillet 1986) : 71–80. http://dx.doi.org/10.1083/jcb.103.1.71.
Texte intégralEvans, JR. « Acclimation by the Thylakoid Membranes to Growth Irradiance and the Partitioning of Nitrogen Between Soluble and Thylakoid Proteins ». Functional Plant Biology 15, no 2 (1988) : 93. http://dx.doi.org/10.1071/pp9880093.
Texte intégralGaneteg, Ulrika, Frank Klimmek et Stefan Jansson. « Lhca5 – an LHC-Type Protein Associated with Photosystem I ». Plant Molecular Biology 54, no 5 (mars 2004) : 641–51. http://dx.doi.org/10.1023/b:plan.0000040813.05224.94.
Texte intégralLyon, M. K., et K. R. Miller. « Crystallization of the light-harvesting chlorophyll a/b complex within thylakoid membranes. » Journal of Cell Biology 100, no 4 (1 avril 1985) : 1139–47. http://dx.doi.org/10.1083/jcb.100.4.1139.
Texte intégralThèses sur le sujet "Lhc protein"
Engelken, Johannes [Verfasser]. « Evolution of the extended LHC protein superfamily in photosynthesis / Johannes Engelken ». Konstanz : Bibliothek der Universität Konstanz, 2010. http://d-nb.info/1023210401/34.
Texte intégralBradburne, James Andrew. « Gibberellic acid and reflected light mediated changes in the content of light - harvesting chlorophyll protein (LHC - II) ». Thesis, Georgia Institute of Technology, 1989. http://hdl.handle.net/1853/25394.
Texte intégralHey, Daniel. « Die Funktion LHC-ähnlicher Proteine in der Assemblierung der Photosysteme und der Regulation der Chlorophyllbiosynthese ». Doctoral thesis, Humboldt-Universität zu Berlin, 2019. http://dx.doi.org/10.18452/19963.
Texte intégralThe plant light-harvesting complex protein family comprises different members with a variety of functions. However, the function of the light-harvesting-like 3 proteins (LIL3) as well as the one-helix proteins (OHPs) is largely unknown. In this thesis, an interaction of LIL3 not only with geranylgeranyl-reductase (CHLP), but also with protochlorophyllide-oxidoreductase (POR) could be established. LIL3 tethers CHLP and POR to the thylakoid membrane, thereby conferring stability to both enzymes. Both CHLP and POR are synthesizing the direct chlorophyll precursors which are combined to chlorophyll by the subsequent chlorophyll synthase (CHLG). In addition to the chlorophyll binding ability of LIL3 reported earlier, an affinity of LIL3 towards the chlorophyll biosynthesis intermediates Proto IX, MgP, MgPMME, and Pchlide could be shown. Interestingly, the highest affinity of LIL3 was exerted towards Pchlide which is the substrate of POR. Therefore, LIL3 is postulated to shuffle the intermediates between enzymes and brings CHLP and POR in close proximity, which may help to supply CHLG with its substrates. Regarding the function of the OHPs an exclusive heterodimer formation of both the OHP1 and OHP2 variants could be shown. The OHP1-OHP2-heterodimer is able to bind chlorophyll and carotenoids in an approximate 3:1 ratio and pigment binding depends on dimer formation as well as the presence of the conserved amino acids in the chlorophyll binding motif. The PSII-assembly factor HCF244 is anchored to the thylakoid membrane by binding to both OHPs, thereby stabilizing the OHP-heterodimer. The heterotrimeric OHP1-OHP2-HCF244-complex is essential for D1 biosynthesis, although the exact molecular function of HCF244 is still unknown. It is suggested that the OHP-dimer is responsible for co-translational loading of (p)D1 with pigments as well as photoprotection of early PSII assembly intermediates.
Molson, James. « Proton scattering and collimation for the LHC and LHC luminosity upgrade ». Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/proton-scattering-and-collimation-for-the-lhc-and-lhc-luminosity-upgrade(3c4fab61-2d9d-4575-8874-15d91c95523f).html.
Texte intégralWorthen, Denise Lynne. « Lactose binding to the E. coli symport protein Lac permease ». Diss., Pasadena, Calif. : California Institute of Technology, 1989. http://resolver.caltech.edu/CaltechTHESIS:11242009-093118312.
Texte intégralDE, BIANCHI Silvia. « The function of monomeric Lhcb proteins ofPhotosystem II analyzed by reverse genetic ». Doctoral thesis, Università degli Studi di Verona, 2010. http://hdl.handle.net/11562/341729.
Texte intégralIn eukaryotes the photosynthetic antenna system is composed by subunits encoded by the light harvesting complex (Lhc) multigene family. These proteins play a key role in photosynthesis and are involved in both light harvesting and photoprotection. In particular, antenna protein of PSII, the Lhcb subunits, have been proposed to be involved in the mechanism of thermal dissipation of excitation energy in excess (NPQ, non-photochemical quenching). Elucidating the molecular details of NPQ induction in higher plants has proven to be a major challenge. In my phD work, I decided to investigate the role of Lhcbs in energy quenching by using a reverse genetic approach: I knocked out each subunit in order to understand their involvement in the mechanism. Here below the major results obtained are summarized. Section A. Mutants of monomeric Lhc and photoprotection: insights on the role of minor subunits in thermal energy dissipation. In this section I investigate the function of chlorophyll a/b binding antenna proteins, CP26, CP24 and CP29 in light harvesting and regulation of photosynthesis by isolating Arabidopsis thaliana knockout (ko) lines that completely lacked one or two of these proteins. In particular in Section A.1 I focused on single mutant koCP24, koCP26 and double mutant koCP24/26. All these three mutant lines have a decreased efficiency of energy transfer from trimeric light-harvesting complex II (LHCII) to the reaction center of photosystem II (PSII) due to the physical disconnection of LHCII from PSII. We observed that photosynthetic electron transport is affected in koCP24 plants but not in plants lacking CP26: the former mutant has decreased electron transport rates, a lower pH gradient across the grana membranes, a reduced capacity for non-photochemical quenching, and a limited growth. Furthermore, the PSII particles of these plants are organized in unusual two-dimensional arrays in the grana membranes. Surprisingly, the double mutant koCP24/26, lacking both CP24 and CP26 subunits, restores overall electron transport, non-photochemical quenching, and growth rate to wild type levels. We further analysed the koCP24 phenotype to understand the reasons for the photosynthetic defection. Fluorescence induction kinetics and electron transport measurements at selected steps of the photosynthetic chain suggested that koCP24 limitation in electron transport was due to restricted electron transport between QA and QB, which retards plastoquinone diffusion. We conclude that CP24 absence alters PSII organization and consequently limits plastoquinone diffusion. The limitation in plastoquinone diffusion is restore in koCP24/26. In Section A.2 I characterized the function of CP29 subunits, extending the analyses to the different CP29 isoforms. To this aim, I have constructed knock-out mutants lacking one or more Lhcb4 isoforms and analyzed their performance in photosynthesis and photoprotection. We found that lacks of CP29 did not result in any significant alteration in linear/cyclic electron transport rate and maximal extent of state transition, while PSII quantum efficiency and capacity for NPQ were affected. Photoprotection efficiency was lower in koCP29 plants with respect to either WT or mutants retaining a single Lhcb4 isoform. Interestingly, while deletion of either isoforms Lhcb4.1 or Lhcb4.2 get into a compensatory accumulation of the remaining subunit, photoprotection capacity in the double mutant Lhcb4.1/4.2 was not restored by Lhcb4.3 accumulation. Section B. Membrane dynamics and re-organization for the quenching events: B4 dissociation and identification of two distinct quenching sites. Antenna subunits are hypothesized to be the site of energy quenching, while the trigger of the mechanism is mediated by PsbS, a PSII subunit that is involved in detection of luminal acidification. In this section we investigate the molecular mechanism by which PsbS regulates light harvesting efficiency by studying Arabidopsis mutants specifically devoid of individual monomeric Lhcbs. In Section B.1 we showed that PsbS controls the association/dissociation of a five-subunit membrane complex, composed of two monomeric Lhcb proteins, CP29 and CP24 and the trimeric LHCII-M (namely Band 4 Complex - B4C). We demonstrated that the dissociation of this supercomplex is indispensable for the onset of non-photochemical fluorescence quenching in high light. Consistently, we found that knock-out mutants lacking the two subunits participating to the B4C, namely CP24 and CP29, are strongly affected in heat dissipation. Direct observation by electron microscopy showed that B4C dissociation leads to the redistribution of PSII within grana membranes. We interpret these results proposing that the dissociation of B4C makes quenching sites, possibly CP29 and CP24, available for the switch to an energy-quenching conformation. These changes are reversible and do not require protein synthesis/degradation, thus allowing for changes in PSII antenna size and adaptation to rapidly changing environmental conditions. In Section B.2 we studied this quenching mechanism by ultra-fast Chl fluorescence analysis. Recent results based on fluorescence lifetime analysis in vivo proposed that two independent quenching sites are activated during NPQ: Q1 is located in the major LHCII complexes, which are functionally detached from the PSII/RC (reaction centre) supercomplex with a mechanism that strictly requires PsbS but not Zea; Q2 is located in and connected to the PSII complex and is dependent on the Zea formation. These two quenching events could well originate in each of the two physical domains of grana revealed by electron microscopy analysis previously reported. We thus proceeded to investigate the modulation of energy quenching in knock out mutants by comparing the fluorescence lifetimes under quenched and unquenched conditions in intact leaves: we obtained results that are consistent with the model of two quenching sites located, respectively, in the C2S2 domain and in the LHCII-enriched domain. Data reported suggest that Q1 site is released in the koCP24 mutant while Q2 is attenuated in the koCP29 mutant. On the bases of the results of this section, we conclude that during the establishment of NPQ in vivo the PSII supercomplex dissociates into two moieties, which segregates into distinct domain of the grana membrane and are each protected from over-excitation by the activity of quenching sites probably located in CP24 and CP29. Section C. Excitation energy transfer and membrane organization: role of PSII antenna subunits. In this section we investigated the role of individual photosynthetic antenna complexes of PSII both in membrane organization and excitation energy transfer, by using the knock out mutants previously isolated. Thylakoid membranes from wild-type and three mutants lacking light harvesting complexes CP24, CP26 or CP29 respectively, were studied by ps-fluorescence spectroscopy on thylakoids, using different combination of excitation and detection wavelengths in order to separate PSI and PSII kinetics. Spectroscopic measurements revealed that absence of CP26 did not alter PSII organization. In contrast, the absence of CP29 and especially CP24 lead to substantial changes in the PSII organization as evidenced by a significant increase of the apparent migration time, demonstrating a bad connection between a significant part of the peripheral antenna and the RCs. Section D.
Lee, Sarah Angeline. « Curcumin Protects against Renal Ischemia by Activating the Unfolded Protein Response and Inducing HSP70 ». Yale University, 2009. http://ymtdl.med.yale.edu/theses/available/etd-04062009-215154/.
Texte intégralLaos, Roberto. « Protein directed evolution ». Revista de Química, 2012. http://repositorio.pucp.edu.pe/index/handle/123456789/99875.
Texte intégralDirected evolution allows us to explore protein functionalities not required in the natural environment. It mimics natural genetic processes and selective pressures. This approach is used when the molecular basis is not completely understood and rational design is a difficult task. This approach consists of serial cycles of consecutive diversification and selection which eventually lead to the accumulation of beneficial mutations. Here are presented two cases where directed evolution is used to modify two different proteins: Taq polymerase, enzyme used for DNA extension in PCR, and the LacI repressor protein which regulates gene expression on E.coli.
Taddei, Lucilla. « The role of the LHCX light-harvesting complex protein family in diatom photoprotection ». Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066219/document.
Texte intégralDiatoms dominate phytoplanktonic communities in contemporary oceans, contributing to 20% of global primary productivity. In their extremely variable environment, diatoms are especially efficient in adjusting their photosynthetic activity by dissipating as heat the light energy absorbed in excess, through a process called “Non-Photochemical Quenching of chlorophyll fluorescence”, (NPQ). In the model diatom Phaeodactylum tricornutum, it has been shown that LHCX1, a photosynthetic antenna-related gene, is involved in the NPQ process. Through integrated approaches of genetics, molecular biology, biochemistry, study of the kinetics of chlorophyll fluorescence yields and ultrafast spectroscopy, I studied the role of the LHCX family in the photoprotection activity of P. tricornutum. I first correlated a differential regulation of the 4 P. tricornutum LHCX genes with different dynamics of NPQ and photosynthetic activity, in different light and nutrient conditions. By localizing the LHCXs in fractioned photosynthetic complexes and the different sites of energy dissipation, I was able to propose a model of dynamic regulation of NPQ capacity involving mainly the LHCX1 in the reaction centers, during short-term high light responses. During prolonged high light stress, the quenching occurs mainly in the antennas, potentially mediated by the LHCX3 isoform. Finally, using photosynthetic parameters, I screened a series of transgenic lines putatively deregulated in their LHCX amount, and I identified lines with altered NPQ, which could represent novel investigation tools. Altogether, this work highlighted the functional diversification and the importance of the LHCX protein family in the fine-tuning of light harvesting and photoprotection capacity, possibly contributing to explain diatoms success in their highly fluctuating environment
Benson, Samuel Lee. « Light harvesting and state transitions in Arabidopsis thaliana deficient in Lhca proteins ». Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289600.
Texte intégralLivres sur le sujet "Lhc protein"
Brüning, O. LHC design report. Sous la direction de European Organization for Nuclear Research. Geneva : European Organization for Nuclear Research, 2004.
Trouver le texte intégralAlejandro, Ayala, et Universidad Nacional Autónoma de México. Instituto de Ciencias Nucleares, dir. 5th International Workshop on High-pT Physics at LHC : Instituto de Ciencias Nucleares, UNAM, Mexico, 27 September - 1 October 2010. Melville, N.Y : American Institute of Physics, 2011.
Trouver le texte intégralAlvarez-Gaumé, Luis. From the PS to the LHC - 50 Years of Nobel Memories in High-Energy Physics. Berlin, Heidelberg : Springer Berlin Heidelberg, 2012.
Trouver le texte intégralLee, See-Lai. Studies on regulation of expression of the verotoxin operon and of the 39K replication protein of plasmid pFA3 using gene and operon fusions to lac Z. Ottawa : National Library of Canada, 1990.
Trouver le texte intégralStep-By-Step Guide to Starting a Limited Liability Company (LLC) and Protect Your LLC. Independently Published, 2021.
Trouver le texte intégralDow, Bonnie J. Magazines and the Marketing of the Movement. University of Illinois Press, 2017. http://dx.doi.org/10.5406/illinois/9780252038563.003.0004.
Texte intégralAlvarez-Gaumé, Luis, Michelangelo Mangano et Emmanuel Tsesmelis. From the PS to the LHC - 50 Years of Nobel Memories in High-Energy Physics. Springer, 2015.
Trouver le texte intégralAlvarez-Gaumé, Luis, Michelangelo Mangano et Emmanuel Tsesmelis. From the PS to the LHC - 50 Years of Nobel Memories in High-Energy Physics. Springer, 2013.
Trouver le texte intégralBogue, Ronald. Deleuze and Roxy : The Time of the Intolerable and Godard’s Adieu au langage. Edinburgh University Press, 2018. http://dx.doi.org/10.3366/edinburgh/9781474422734.003.0015.
Texte intégralChapitres de livres sur le sujet "Lhc protein"
Hind, Geoffrey, et Sean Coughlan. « Reconstitution of LHC Phosphorylation by a Protein Kinase Isolated from Spinach Thylakoids ». Dans Progress in Photosynthesis Research, 801–4. Dordrecht : Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3535-8_189.
Texte intégralEngelken, Johannes, Christiane Funk et Iwona Adamska. « The Extended Light-Harvesting Complex (LHC) Protein Superfamily : Classification and Evolutionary Dynamics ». Dans Functional Genomics and Evolution of Photosynthetic Systems, 265–84. Dordrecht : Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1533-2_11.
Texte intégralKuang, T. Y., J. G. Yuan, C. Q. Tang, Q. D. Zhang et S. Q. Lin. « Reversal Movement of Sub-Population of Light Harvesting Chlorophyll Protein Complexes LHC-II and LHC-I between Grana and Stroma Lamellae under Different Conditions ». Dans Progress in Photosynthesis Research, 729–32. Dordrecht : Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3535-8_171.
Texte intégralPeter, Gary F., et J. Philip Thornber. « The Antenna Components Of Photosystem ii With Emphasis On The Major Pigment-Protein, Lhc IIb ». Dans Photosynthetic Light-Harvesting Systems. Organization and Function, sous la direction de Hugo Scheer et Siegfried Schneider, 175–86. Berlin, Boston : De Gruyter, 1988. http://dx.doi.org/10.1515/9783110861914-019.
Texte intégralTsuchiya, Tohru, Tatsuya Tomo, Seiji Akimoto, Akio Murakami et Mamoru Mimuro. « Unique Optical Properties of LHC II Isolated from Codium fragile – Its Correlation to Protein Environment ». Dans Photosynthesis. Energy from the Sun, 343–46. Dordrecht : Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6709-9_78.
Texte intégralForti, Giorgio, Cesare Resta et Alessandra Sangalli. « On the Phosphorylation and Dephosphorylation of LHC-II and of the Protein Kinase of Spinach Thylakoids ». Dans Current Research in Photosynthesis, 1735–38. Dordrecht : Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_396.
Texte intégralMorishige, Daryl T., et J. Philip Thornber. « The Major Light-Harvesting Chlorophyll a/b Protein (LHC IIb) : The Smallest Subunit is a Novel Cab Gene Product ». Dans Current Research in Photosynthesis, 1221–24. Dordrecht : Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_282.
Texte intégralSiefermann-Harms, D., et A. Angerhofer. « An O2 -Barrier in the Light-Harvesting Chl-a/b-Protein Complex LHC II Protects Chlorophylls and Carotenoids from Photooxidation ». Dans Photosynthesis : from Light to Biosphere, 3035–38. Dordrecht : Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_711.
Texte intégralDavies, Paul N., Jens Forsberg et John F. Allen. « Localisation of a Thylakoid Protein Kinase and its Relation to the 64 kDa LHC-II Kinase and Reverse Redox Titrator ». Dans Photosynthesis : from Light to Biosphere, 4213–16. Dordrecht : Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_992.
Texte intégralPflitsch, Svenja Karen. « The LHC and the CMS Experiment ». Dans Associated Production of W + Charm in 13 TeV Proton-Proton Collisions Measured with CMS and Determination of the Strange Quark Content of the Proton, 47–56. Cham : Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-52762-4_3.
Texte intégralActes de conférences sur le sujet "Lhc protein"
Ide, J. P., D. R. Klug, W. Kuhlbrandt et G. Porter. « Detergent effects upon the picosecond dynamics of higher plant light harvesting chlorophyll complex (LHC). » Dans International Conference on Ultrafast Phenomena. Washington, D.C. : Optica Publishing Group, 1986. http://dx.doi.org/10.1364/up.1986.mf1.
Texte intégralde Vries, C. J. M., N. K. Veerman et H. Pannekoek. « ARTIFICIAL EXON SHUFFLING : CONSTRUCTION OF HYBRID cDNAS CONTAINING DOMAINS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR (T-PA) AND UROKINASE (u-PA) ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643940.
Texte intégralJakobs, K. « The physics prospects of the ATLAS experiment at LHC ». Dans The 10th topical workshop on proton−antiproton collider physics. AIP, 1996. http://dx.doi.org/10.1063/1.49652.
Texte intégralChachisvilis, M., T. Pullerits, M. R. Jones, C. N. Hunter et V. Sundstrom. « Coherent Nuclear Motions and Exciton State Dynamics in Photosynthetic Light-Harvesting Pigments. » Dans International Conference on Ultrafast Phenomena. Washington, D.C. : Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.tub.6.
Texte intégralPannekok, H., A. J. Van Zonneveid, C. J. M. de vries, M. E. MacDonald, H. Veerman et F. Blasi. « FUNCTIONAL PROPERTIES OF DELETION-MUTANTS OF TISSUE-TYPE PLASMINOGEN ACTIVATOR ». Dans XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643724.
Texte intégralLillian, Todd D. « An Elastic Rod Representation for the LacI-DNA Loop Complex ». Dans ASME 2011 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/detc2011-47407.
Texte intégralMallakin, Ali, Kazushi Inoue et Martin Guthold. « In-Situ Quantitative Analysis of Tumor Suppressor Protein (hDMP1) Using a Nanomechanical Cantilever Beam ». Dans ASME 2005 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2005. http://dx.doi.org/10.1115/detc2005-84503.
Texte intégralIslam, Nazmul, Davood Askari et Tarek Trad. « Biocompatible Nanocomposite for Lab-on-a-Chip Application ». Dans ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-64119.
Texte intégralZambalde, Erika Pereira, Ana Carolina Rodrigues, Rubens Silveira Lima, Enilze Maria Souza Fonseca Ribeiro et Jaqueline Carvalho Oliveira. « TLNC-UC.147, A NOVEL LONG RNA (lncRNA) FROM AN ULTRACONSERVED REGION AS POTENTIAL BIOMARKER IN LUMINAL A BREAST CANCER ». Dans Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1052.
Texte intégralLegchenko, E., B. Liu, J. West, P. Vangheluwe, P. Upton et N. Morrell. « Protein truncating mutations in ATP13A3 promote pulmonary arterial hypertension in mice ». Dans ERS Lung Science Conference 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/23120541.lsc-2020.83.
Texte intégralRapports d'organisations sur le sujet "Lhc protein"
Nechushtai, Rachel, et Parag Chitnis. Role of the HSP70 Homologue from Chloroplasts in the Assembly of the Photosynthetic Apparatus. United States Department of Agriculture, juillet 1993. http://dx.doi.org/10.32747/1993.7568743.bard.
Texte intégralLi, Wei. Exploring novel QCD matter in proton-proton and proton-nucleus collisions at the LHC. Office of Scientific and Technical Information (OSTI), juillet 2019. http://dx.doi.org/10.2172/1577131.
Texte intégralWittich, Peter. Searches for Physics Beyond the Standard Model and Triggering on Proton-Proton Collisions at 14 TEV LHC. Office of Scientific and Technical Information (OSTI), octobre 2011. http://dx.doi.org/10.2172/1045792.
Texte intégralFitterer, Miriam, Giulio Stancari et Alexander Valishev. Effect of pulsed hollow electron-lens operation on the proton beam core in LHC. Office of Scientific and Technical Information (OSTI), novembre 2016. http://dx.doi.org/10.2172/1408326.
Texte intégralDucimetiere, L., U. Jansson, G. H. Schroeder, E. B. Vossenberg, M. J. Barnes et G. D. Wait. Design of the injection kicker magnet system for CERN`s 14 TeV proton collider LHC. Office of Scientific and Technical Information (OSTI), août 1995. http://dx.doi.org/10.2172/132743.
Texte intégralVitev, Ivan Mateev. Future physics opportunities for high-density QCD at the LHC with heavy-ion and proton beams. Office of Scientific and Technical Information (OSTI), mars 2019. http://dx.doi.org/10.2172/1501772.
Texte intégralFluhr, Robert, et Maor Bar-Peled. Novel Lectin Controls Wound-responses in Arabidopsis. United States Department of Agriculture, janvier 2012. http://dx.doi.org/10.32747/2012.7697123.bard.
Texte intégralChen, Yi. Extraction of CP Properties of the H(125) Boson Discovered in Proton-Proton Collisions at√s = 7 and 8 TeV with the CMS Detector at the LHC. Office of Scientific and Technical Information (OSTI), janvier 2015. http://dx.doi.org/10.2172/1249491.
Texte intégralTucker, Mark L., Shimon Meir, Amnon Lers, Sonia Philosoph-Hadas et Cai-Zhong Jiang. Elucidation of signaling pathways that regulate ethylene-induced leaf and flower abscission of agriculturally important plants. United States Department of Agriculture, janvier 2012. http://dx.doi.org/10.32747/2012.7597929.bard.
Texte intégralMeidan, Rina, et Robert Milvae. Regulation of Bovine Corpus Luteum Function. United States Department of Agriculture, mars 1995. http://dx.doi.org/10.32747/1995.7604935.bard.
Texte intégral