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Статті в журналах з теми "Γ-peptides"
Bracci, Laura, David F. Stroncek, Stefanie Slezak, Giulio C. Spagnoli, and Maurizio Provenzano. "Comprehensive Analysis of CD8 T Cell Immune Response Specific for Two Novel HLA-A*0201 Restriced CMV pp65 Peptides." Blood 106, no. 11 (November 16, 2005): 3928. http://dx.doi.org/10.1182/blood.v106.11.3928.3928.
Повний текст джерелаMöller, Carolina, та Frank Marí. "A vasopressin/oxytocin-related conopeptide with γ-carboxyglutamate at position 8". Biochemical Journal 404, № 3 (29 травня 2007): 413–19. http://dx.doi.org/10.1042/bj20061480.
Повний текст джерелаMujtaba, Mustafa. "Antiviral inducing properties of staphylococcal enterotoxin mimetic peptides (VAC9P.1065)." Journal of Immunology 194, no. 1_Supplement (May 1, 2015): 145.5. http://dx.doi.org/10.4049/jimmunol.194.supp.145.5.
Повний текст джерелаSaini, Chaman, H. K. Prasad, Rajni Rani, A. Murtaza, Namita Misra, N. P. Shanker Narayan, and Indira Nath. "Lsr2 of Mycobacterium leprae and Its Synthetic Peptides Elicit Restitution of T Cell Responses in Erythema Nodosum Leprosum and Reversal Reactions in Patients with Lepromatous Leprosy." Clinical and Vaccine Immunology 20, no. 5 (February 27, 2013): 673–82. http://dx.doi.org/10.1128/cvi.00762-12.
Повний текст джерелаPassero, Christopher J., Marcelo D. Carattino, Ossama B. Kashlan, Mike M. Myerburg, Rebecca P. Hughey, and Thomas R. Kleyman. "Defining an inhibitory domain in the gamma subunit of the epithelial sodium channel." American Journal of Physiology-Renal Physiology 299, no. 4 (October 2010): F854—F861. http://dx.doi.org/10.1152/ajprenal.00316.2010.
Повний текст джерелаHuang, Xiao-Li, Zheng Fan, LuAnn Borowski, and Charles R. Rinaldo. "Multiple T-Cell Responses to Human Immunodeficiency Virus Type 1 Are Enhanced by Dendritic Cells." Clinical and Vaccine Immunology 16, no. 10 (August 19, 2009): 1504–16. http://dx.doi.org/10.1128/cvi.00104-09.
Повний текст джерелаHirano, Naoto, Marcus O. Butler, Zhinan Xia, Seiji Kojima та Lee M. Nadler. "γ-Globin, a Tumor-Associated Antigen for Juvenile Myelomonocytic Leukemia (JMML): A Cell-Based Approach To Identify Tumor Antigenic Epitopes That Are Naturally Processed and Presented." Blood 104, № 11 (16 листопада 2004): 3418. http://dx.doi.org/10.1182/blood.v104.11.3418.3418.
Повний текст джерелаBECERRIL, Baltazar, Miguel CORONA, Fredy I. V. CORONAS, Fernando ZAMUDIO, Emma S. CALDERONARANDA, Paul L. FLETCHER, Brian M. MARTIN та Lourival D. POSSANI. "Toxic peptides and genes encoding toxin γ of the Brazilian scorpions Tityus bahiensis and Tityus stigmurus". Biochemical Journal 313, № 3 (1 лютого 1996): 753–60. http://dx.doi.org/10.1042/bj3130753.
Повний текст джерелаZeng, Yi, Michael W. Graner, Sylvia Thompson, Marilyn Marron, and Emmanuel Katsanis. "Induction of BCR-ABL–specific immunity following vaccination with chaperone-rich cell lysates derived from BCR-ABL+ tumor cells." Blood 105, no. 5 (March 1, 2005): 2016–22. http://dx.doi.org/10.1182/blood-2004-05-1915.
Повний текст джерелаStaska, Lauren M., Christopher J. Davies, Wendy C. Brown, Travis C. McGuire, Carlos E. Suarez, Joo Youn Park, Bruce A. Mathison, Jeffrey R. Abbott, and Timothy V. Baszler. "Identification of Vaccine Candidate Peptides in the NcSRS2 Surface Protein of Neospora caninum by Using CD4+ Cytotoxic T Lymphocytes and Gamma Interferon-Secreting T Lymphocytes of Infected Holstein Cattle." Infection and Immunity 73, no. 3 (March 2005): 1321–29. http://dx.doi.org/10.1128/iai.73.3.1321-1329.2005.
Повний текст джерелаДисертації з теми "Γ-peptides"
Qureshi, Muhammad Khurram Naseem. "Foldamers based on γ-peptides". Thesis, University of Cambridge, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.611289.
Повний текст джерелаStanovych, Andrii. "Synthèse et études structurales de γ-peptides synthétisés à partir d’acides β,γ-diaminés". Thesis, Paris 11, 2014. http://www.theses.fr/2014PA112310/document.
Повний текст джерелаThe design of a new oligopeptides, capable to mimic the properties of natural proteins, is an important field not only for structural studies but also in the developpement of new efficient drugs. The peptides featuring β-amino acids have been extensively explored, whereas the research in γ-peptides is more recent. The studies of γ-peptides show their ability to adopt stable secondary structures and also to have a promising biological activity. Our laboratory is interested in the synthesis of new β,γ-diaminoacids.The aim of this work is a developpement of new synthetic route starting from different natural α -amino acids and to use obtained β,γ-diaminoacids to access novel unnatural peptides having specific conformational properties.The synthetic strategy, developed and optimized in our laboratory during this work, gives access to diastereomers cis and trans from L-leucine, L- and D-phenylalanine which were used in the synthesis of a new hybrid α/γ-peptides. The structural studies were performed on two series of hybrid α/γ-peptides consisting of β,γ-aminoacid from L-leucine and L- or D-α-amino acids. In the first case, the peptides are able to adopt stable secondary structures stabilized by intramolecular hydrogen bonds involving the nitrogen on the β-position. In addition, we present the synthesis of an analogue of gramicidine S, a naturally occuring antibiotic cyclic peptide. The dipeptide pattern D-Phe-L-Pro has been replaced with the β,γ-diaminoacid synthesized from D-phenylalanine
Bouillère, Francelin. "Synthèse stéréosélective d'acides β,γ-diaminés : applications à l'étude structurale de nouveaux peptides". Paris 11, 2010. http://www.theses.fr/2010PA112359.
Повний текст джерелаInterest in unnatural oligomers with strong conformational propensities (« foldamers ») akin to those of proteins has led to numerous recent explorations in this field. These oligomers are interesting targets as they can be valuable for specific applications such as protein-protein interactions or antibodies activity. The aim of this work is both to allow the development of a new synthetic route to enantiopure β,γ-diaminoacids and to use them to access to novel peptides having specific conformational properties
Migliore, Mattia. "Recherche par modélisaion moléculaire de signatures RMN et DC caractéristiques pour les coudes β et y dans les peptides bioactifs. Characterization of β-turns by electronic circular dichroism spectroscopy : a coupled molecular dynamics and time-dependent density functional theory computational study". Thesis, Normandie, 2020. http://www.theses.fr/2020NORMR001.
Повний текст джерелаThe aim of this work is to identify NMR and CD characteristic patterns for β- and γ-turns in bioactive peptides by molecular modelling. With helices, β- and γ-turns constitute favoured recognition motifs in bioactive peptides by their targets. Even though several classes of turns with different geometries exist in polypeptide structures (2 γ-turn types and 12 β-turn types), few experimental tools are available for their characterization. Thus, only 4 types of β-turns (I, I’, II et II’) have been, at present, described by NMR and there are no reliable reference CD spectra for turns. In order to extend the NMR data for all β- and γ-turn types, we analyzed NMR structural parameters (inter-hydrogen distances and ᶾJʜɴ-ʜꭤ coupling constants) in a representative peptide model dataset extracted from the PDB. The inter-hydrogen distance analysis allowed to identify specific NMR patterns for the two γ-turn types and for four β-turn types (IV₁, IV₂,, VIb and VIII). ᶾJʜɴ-ʜꭤ coupling constant may be used to confirm the identification and to remove ambiguities. Then, we simulated the reference CD spectra of model peptides adopting type I, I’, II and II’ β-turn conformations by combining molecular dynamic simulations and TDDFT computations. These computations allowed to determine two families of specific CD spectra : types I/II’, on one side and types I’/II, on the other. All these results indicate that the turns do not present the same patterns in both techniques. The combination of NMR and CD could therefore allow a better identification of the nature and the different types of turns
Itkin, Anna. "Multidisniplinary study of Alzheimer's disease-related peptides : from amyloid precursor protein (APP) to amyloid β-oligomers and γ-secretase modulators". Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAF051/document.
Повний текст джерелаA histopathological characteristic of Alzheimer’s disease (AD) is the presence of amyloid plaques formed by amyloid β(A) peptides of 40 and 42 residues-long, which are the cleavage products of APP by proteases. To understand the role of structural changes in the TM domain of APP, APP_TM4K peptides were studied in the lipid bilayer using ATR-FTIR and ssNMR. While the overall secondary structure of the APP_TM4K peptide is helical, conformational and orientational heterogeneity was observed for the y- and for the -cleavage sites, which may have implications for the cleavage mechanism and therefore the production of Aβ. Starting from its monomeric form, Aβ peptides aggregate into fibrils and / or oligomers, the latter being the most neurotoxic. We found that in the presence of Ca2 +, Aβ (1-40) preferably forms oligomers, whereas in the absence of a2 + Aβ (1-40) aggregates into fibrils. In samples without Ca2 +, ATR-FTIR shows conversion from antiparallel β sheet conformation of oligomers into parallel β sheets, characteristic of fibrils. These results led us to conclude that Ca2 +stimulates the formation of oligomers of Aβ (1-40), that have been implicated in the pathogenesis of AD. Position and precise orientation of two new drugs powerful modulators of γ-secretase benzyl-carprofen and carprofen sulfonyl in the lipid bilayer were obtained from neutron scattering and ssNMR experiments. These results indicate that carprofen-derivatives can directly interact with APP. Such interaction would interfere with proper APP-dimer formation, which is necessary for the sequential cleavage by β -secretase, diminishing or greatly reducing Aβ42 production
Rosés, Subirós Cristina. "Solid-phase synthesis of cell-penetrating γ-peptide/antimicrobial peptide conjugates and of cyclic lipodepsipeptides derived from fengycins". Doctoral thesis, Universitat de Girona, 2016. http://hdl.handle.net/10803/393895.
Повний текст джерелаAquesta tesi doctoral s’ha centrat en el desenvolupament d’estratègies sintètiques útils per a l’obtenció de nous pèptids bioactius. Primerament, s’han dissenyat nous pèptids conjugats antitumorals a través de la unió d’un pèptid antimicrobià i un cell-pentrating peptide. Aquesta conjugació augmenta l’activitat antitumoral del pèptid mantenint la toxicitat baixa. Aquests conjugats són interessants pel desenvolupament de nous agents antitumorals. A continuació, s’ha desenvolupat una metodologia per a la preparació de pèptids cíclics derivats de les fengicines. Aquesta metodologia representa la primera estratègia sintètica descrita per a l’obtenció en fase sòlida d’aquesta família de ciclolipodepsipèptids i pot ser fàcilment adaptada per a l’obtenció d’una àmplia varietat d’anàlegs.
Claudel, Stéphanie. "Les peptides Vinylogues : des nouveaux outils pour la préparation d'analogues contraints de la substance P, de γ-aminoacides α, β-hydroxylés et de dihydroxylactames". Nancy 1, 2004. http://www.theses.fr/2004NAN10039.
Повний текст джерелаThis work concerns conception and synthesis of modified peptides and is divided in two parts. Firstly, it's the insertion of vinylogous amino acids with cis and trans conformation in neuropeptide of eleven amino acids which is substance P in order to understand its interaction with NK-1 receptor. A second study has been oriented on the preparation of g-amino peptides by hydrogenation of previous vinylogous amino acids. This structural modification has given a new SP's analog which has been tested. The second part is the methodology of synthesis using vinylogous peptides and is divided in three chapters. First one presents dihydroxylation's results of these residues with an asymmetric induction using chiral catalyst to obtain dihydroxylated g-amino acids. Second one is an application of these studies with a total synthesis of natural product extracted from nyctinastic plant. And the last one deals with preparation of dihydroxylated lactams leading to the synthesis of new azasugars
Mazzier, Daniela. "Functionalized short peptides and polypeptides: from organic reactions, through secondary structure control, to supramolecular applications." Doctoral thesis, Università degli studi di Padova, 2016. http://hdl.handle.net/11577/3424844.
Повний текст джерелаPeptidi elicoidali corti In questo lavoro di tesi sono stati studiati diversi peptidi caratterizzati da una ben definita conformazione elicoidale con lo scopo di stabilizzarne la struttura secondaria oppure di sfruttare la loro conformazione rigida come mezzo per controllare l’induzione asimmetrica su lunghe distanze. Il primo esempio, un sistema oligopeptidico biciclico doppiamente stabilizzato, è stato ottenuto tramite due reazioni di macrociclizzazione che hanno coinvolto le catene laterali dei residui in posizione i e i+4 di un peptide lineare. Un’indagine conformazionale dettagliata, condotta utilizzando le spettroscopie CD ed NMR, ha rivelato che la conformazione mista 310/α-elica, osservata per il peptide lineare, risulta completamente convertita in una struttura ad elevato contributo α-elicoidale nel peptide biciclico. In parallelo, sia il contenuto totale di elica sia la stabilità risultano significativamente aumentati. Nel secondo caso, un foldamero achirale elicoidale a base di Aib è stato opportunamente funzionalizzato con il gruppo fotoisomerizzabile fumarammide/maleammide contenente un residuo chirale. In questo modo è stato ottenuto un sistema in cui è stato possibile influenzare il senso di spiralizzazione dell’elica grazie all’uso di luce ultravioletta. La configurazione trans nella fumarammide, infatti mantiene il residuo chirale lontano dal segmento achirale dell’oligomero, rendendo impossibile l’induzione di una conformazione preferenziale. Tuttavia dopo l’isomerizzazione, la configurazione cis della maleammide consente alla parte chirale e a quella achirale di essere spazialmente vicine, con conseguente induzione di chiralità e adozione di un senso preferenziale di spiralizzazione. Sfruttando questo principio è stato quindi possibile utilizzare la luce per accendere o spegnere la capacità del sistema di reagire stereoselettivamente, oppure di modulare la comunicazione di chiralità tra due segmenti elicoidali. Polipeptidi elicoidali funzionalizzati Con lo scopo di ottenere tramite self-assembly microstrutture con differenti caratteristiche, forme e funzioni sono stati sintetizzati diversi sistemi coniugati a base di poli(γ-benzil-L-glutammato) (PBLG). Sistemi polipeptidici contenenti una o due unità di fullerene sono stati ottenuti tramite reazione tiol-ene one-pot. Questi due polimeri hanno mostrato una diversa propensione ad auto-assemblarsi in ambiente acquoso, formando microstrutture di forma toroidale oppure di tipo vescicolare. Come ulteriore esempio è stata riportata la sintesi di sistemi coniugati a base di PBLG e carbon quantum dots. I CQDs, preparati per trattamento in microonde a partire da una soluzione acquosa di arginina e 1,2-etilendiammina, sono stati usati come iniziatore, ottenendo una struttura polimerica a forma di stella, oppure come agente cappante, portando alla formazione di microstrutture più complesse. I sistemi ottenuti sono in grado di autoassemblarsi formando aggregati supramolecolari di forma sferica che mantengono le caratteristiche proprietà di emissione dei dots originali. Infine, microstrutture “smart” con comportamento fotoresponsivo sono state ottenute inserendo amminoacidi a base di azobenzene all’interno del sistema polipeptidico. Sono state quindi sintetizzate due strutture polipeptidiche con simmetria C2 e C3 che hanno evidenziato la formazione di strutture sferiche tramite self-assembly. Il cambiamento della loro struttura tridimensionale in seguito ad irraggiamento è accompagnato da una variazione nella morfologia degli aggregati. Peptidi corti auto-assemblanti In questo ultimo capitolo sono discusse la sintesi e le peculiari proprietà di self-assembly mostrate da due diversi sistemi peptidici. La prima serie di composti contiene l’amminoacido fotoisomerizzabile bis[p-(fenilazo)benzil]glicina, che è in grado di isomerizzare reversibilmente tra le due forme cis/trans in seguito ad irraggiamento con luce di adeguata lunghezza d’onda. Derivati e peptidi corti contenenti questo amminoacido sono in grado di promuovere la formazione di strutture supramolecolari ordinate. Inoltre, grazie alla presenza delle due unità di azobenzene sulle catene lineari, la transizione morfologica osservata in seguito ad irraggiamento si è dimostrata essere reversibile. Nella seconda parte di questo studio è stato esaminato il comportamento del dipeptide idrofobico protetto Boc-L-Cys(Me)-L-Leu-OMe. La formazione di nano-, micro- e macro- architetture complesse, tra cui bacchette caratterizzate da una cavità interna, è stata osservata in diverse condizioni sperimentali. I risultati ottenuti suggeriscono che le proprietà di self-assembly sono correlate all’organizzazione delle molecole nel cristallo singolo in cui è stata osservata la presenza di una particolare struttura supramolecolare elicoidale formata da sei molecole. Successivamente è stato deciso di modificare il dipeptide in modo da ottenere un derivato diacetilenico. Questo derivato è in grado di formare un organogel o delle strutture sferiche che possono subire polimerizzazione topochimica per irraggiamento UV.
Romero, Eugénie. "Synthèse et étude conformationnelle d’α-hydrazinopeptides linéaires et cycliques". Thesis, Université de Lorraine, 2015. http://www.theses.fr/2015LORR0232/document.
Повний текст джерелаThe formation of nanostructures with well-defined organic brick self-assembly has received much attention due to their potential applications in chemistry and biology. Among all these organic elements, peptides and pseudopeptides are among the most promising because of their similarity to proteins. We can enumerate many peptides self-assembly, such as nanotubes, nonafibres, vesicles, nanospheres etc … In this context, we are interested by the synthesis and overall structural study of hydrazinopeptides. Thanks to the additional nitrogen, these bis-nitrogen pseudopeptides are able to self-assemble into new structuring. The 1:1[α/α-Nα-Bn-hydrazino] linear peptides showed coalesce into hydrazinoturn and γ-turn in solution. We have highlighted the ability of analogues of 1:1[ß/α-Nα-Bn-hydrazino] linear peptides to be structured in hydrazinoturn only, in solution. Similarly, we have demonstrated the ability of pure α-Nα-Bn-hydrazino pseudopeptides to be structured in a very solid solution structure formed of hydrazinoturn observable also in crystal state. Secondly, and as part of the development of nanotube structures, we have studied a serie of 1:1[α/α-Nα-hydrazino] cyclic peptides, and especially cyclotetrameres. In this context, we have sought to highlight the various parameters that may affect the organization in nanotubes, in order to develop the best strategy to achieve this potential application in nanostructuring views. The various parameters studied are: the synthetic strategy, the chirality, the orientation of side chains, and finally the ability to form gels
Wan, Yang. "Synthesis of β,γ-diamino acids and their use to design new analogues of the antimicrobial peptide Gramicidin Septide antimicrobien, la Gramicidine S". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS407/document.
Повний текст джерелаIn our group, we are interested in developing peptides containing β,γ-diamino acids . Along with many other peptides containing unnatural amino acids, they have shown the ability to possess stable conformations and/or interesting biological activities. Moreover, those peptides are usually more resistant to proteolysis. In order to synthesize stereopure γ-amino acids, we have developed a synthetic route using Blaise reaction and subsequent diastereoselective reduction as key reactions. Through applying this method, we have synthesized β,γ-diamino acids derived from D-phenylalanine and L-glutamic acid. The former β,γ-diamino acid was used for designing antimicrobial peptide gramicidin S analogues. Compared with mother molecule, the analogues exerted much less host cell cytotoxicity while remaining interesting antibacterial activity. Meanwhile, it gave us more knowledge for further developing analogues of gramicidin S as well as other antimicrobial peptides. We also paid lots of effort to efficiently synthesize cyclic β,γ-diamino acids starting from L-glutamic acid. Interestingly, when oligomers incorporating this β,γ-diamino acids and α-amino acids, they have shown the potential to adopt stable conformations. The following studies will be continuously investigated
Частини книг з теми "Γ-peptides"
Pavone, V., A. Lombardi, G. D’Auria, M. Saviano, B. Blasio, L. Paolillo, and C. Pedone. "Molecular tools for the design of γ-turn in peptides." In Peptides, 366–67. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_135.
Повний текст джерелаZerkout, S., M. P. Golinelli, V. Grand, J. Vidal, A. Collet, A. Aubry, and M. Marraud. "Hydrazino peptide mimics of the γ- and β-turns." In Peptides 1994, 690–91. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_317.
Повний текст джерелаColpitts, T., and F. J. Castellino. "Ca2+ Binding properties of synthetic γ-carboxyglutamic acid containing peptides homologous to protein C." In Peptides, 932–33. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_312.
Повний текст джерелаBernatowicz, Michael S., Catherine E. Costello, and Gary R. Matsueda. "Synthesis of an є-(γ-Glu) Lys cross-linked peptide in human fibrin." In Peptides, 187–88. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9595-2_53.
Повний текст джерелаBlumenstein, Michael, and Gary R. Matsueda. "Correlation of conformation with antibody affinity for fibrinogen γ-chain carboxyl terminal peptide segment." In Peptides, 237–38. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_82.
Повний текст джерелаGuichard, Gilles. "β-Peptides, γ-Peptides and Isosteric Backbones: New Scaffolds with Controlled Shapes for Mimicking Protein Secondary Structure Elements." In Pseudo-Peptides in Drug Development, 33–120. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527601902.ch2.
Повний текст джерелаSeebach, Dieter. "Homologs of Amino Acids and Explorations into the Worlds of β- and γ-Peptides." In Peptides: The Wave of the Future, 569–71. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_264.
Повний текст джерелаRueping, Magnus, Bernhard Jaun, and Dieter Seebach. "Folding of β- and γ-Peptides — the Influence of Substitution Patterns on the Formation of Secondary Structures." In Peptides: The Wave of the Future, 383–84. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_177.
Повний текст джерелаv.d. Muelbe, Florian, Thomas Mothes, Holm Uhlig, A. A. Osman, Toni Weinschenk, Dietmar G. Schmid, Günther Jung, and Burkhard Fleckenstein. "Deamidation within a γ-Gliadin-Derived Peptide Enhances Its Recognition by Serum Antibodies of CD Patients." In Peptides: The Wave of the Future, 1037–38. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_485.
Повний текст джерелаNishiuchi, Yuji, Masayuki Nakao, Makoto Nakata, and Shumpei Sakakibara. "Synthesis of γ-carboxyglutamic acid-containing peptides by Boc strategy using HF for final deprotection." In Peptide Chemistry 1992, 61–64. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1474-5_18.
Повний текст джерелаТези доповідей конференцій з теми "Γ-peptides"
Fresslnaud, E., J. E. Sadler, J. P. Girma, H. R. Baumgartner, and D. Meyer. "SYNTHETIC RGD-CONTAINING PEPTIDES OF VON WILLEBRAND FACTOR INHIBIT PLATELET ADHESION TO COLLAGEN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643591.
Повний текст джерелаLam, S., E. F. Plow, A. L. Frelinger III, M. A. Smith, J. C. Loftus, and M. H. Ginsberg. "ARG-GLY-ASP (RGD) PEPTIDES INCREASE THE EXPOSURE OF THE CARBOXYL TERMINAL REGION OF THE HEAVY CHAIN OF GPIIB ON THE PLATELET SURFACE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643698.
Повний текст джерелаD’Souza, S. E., M. H. Ginaberg, S. Lam, and E. A. Plow. "ACTIVATION DEPENDENT ALTERATIONS IN THE CHEMICAL CROSSLINKING OF ARGINYL-GLYCYL-ASPARTIC ACID (RGD) PEPTIDES WITH PLATELET GLYCOPROTEIN (GP) GPIIb-IIIa." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643699.
Повний текст джерелаYoshida, N., S. Terukina, M. Matsuda, M. Moroi, M. Okuma та N. Aoki. "FIBRINOGENS KYOTO AND TOCHIGI, EACH WITH AN APPARENT ABNORMAL MOL. WT. γ CHAIN, ARE CHARACTERIZED BY REPLACEMENT OF γ ASN-308 BY LYS AND γ ARG-275 BY CYS, RESPECTIVELY". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644702.
Повний текст джерелаCharon, M. H., L. Tranqui, A. Andrieux, G. Hudry-Clergeon, and G. Marguerie. "FIBRINOGEN BINDING TO ENDOTHELIAL CELLS AND INTERFERING PEPTIDES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644735.
Повний текст джерелаGuha, Snigdha. "Efficacy of Great Northern Beans-derived γ-glutamyl Peptides in Reducing Vascular Inflammation". У 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/pykq1684.
Повний текст джерелаAndrieux, A., M. H. Charon, G. Hudry-Clergeon, and G. Marguerie. "FIBRINOGEN SEQUENCES INTERACTING WITH PLATELET GPIIbIIIa." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643519.
Повний текст джерелаTerukina, S., M. Matsuda, N. Yoshida, K. Yamazumi, Y. Takeda та T. Takano. "TWO ABNORMAL FIBRINOGENS DESIGNATED AS OSAKA II AND MORIOKA WITH A HITHERTO UNIDENTIFIED AMINO ACID SUBSTITUTION; γARG-275 BY CYS". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644701.
Повний текст джерелаCierniewski, C. S., та A. Z. Budzynski. "CONFORMATIONAL EQUILIBRIA IN THE γ CHAIN COOH-TERMINUS OF HUMAN FIBRINOGEN". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642935.
Повний текст джерелаGuha, Snigdha, та Kaustav Majumder. "Efficacy of Great Northern Beans-derived γ-glutamyl Peptides in Reducing Vascular Inflammation". У Virtual 2021 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2021. http://dx.doi.org/10.21748/am21.308.
Повний текст джерелаЗвіти організацій з теми "Γ-peptides"
Baszler, Timothy, Igor Savitsky, Christopher Davies, Lauren Staska, and Varda Shkap. Identification of bovine Neospora caninum cytotoxic T-lymphocyte epitopes for development of peptide-based vaccine. United States Department of Agriculture, March 2006. http://dx.doi.org/10.32747/2006.7695592.bard.
Повний текст джерела