Relevant bibliographies by topics / Modified fragment of neuropeptide Y

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Modified fragment of neuropeptide Y'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Modified fragment of neuropeptide Y"

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Ihnat, Havrylov, and Shtrygol’ Sergіy. "Investigation of the effect of a modified fragment of neuropeptide Y on memory phases and extrapolation escape of animals." Česká a slovenská farmacie 70, no. 3 (2021): 91–99. http://dx.doi.org/10.5817/csf2021-3-91.

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The article presents a study of the effect of a modified fragment of neuropeptide Y (H-L-Ile-L-Asn-L-Leu-L-Nle-L-SerL-Arg-L-Asn-L-Arg-L-Tyr-NH2 ) named nonapeptide NP9 on the memory phases and extrapolation escape of animals. The study was performed in th
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Ihnat, Havrylov, Shtrygol' Sergey, and Kavraiskyi Dmytryi. "The effect of a modified fragment of neuropeptide Y on spatial memory and learning in the Morris water maze." ScienceRise: Pharmaceutical Science, no. 1(35) (February 28, 2022): 22–27. https://doi.org/10.15587/2519-4852.2022.253372.

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Neuropeptide Y (NPY) is a biologically active neuropeptide that is responsible for a large list of physiological processes. We propose a short modified fragment of NPY that should at least partially have a spectrum of biological activity of the original peptide. The compound was named nonapeptide NP9. <strong>The aim of our study</strong>&nbsp;was to investigate the ability of the modified fragment of NPY to influence spatial memory and learning. <strong>Materials and methods:</strong>&nbsp;the study was performed on 24 one-year-old random-bred female rats weight 220&ndash;250 g. The animals w
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Havrylov, Ihnat, Sergey Shtrygol’, and Dmytryi Kavraiskyi. "The effect of a modified fragment of neuropeptide y on spatial memory and learning in the Morris water maze." ScienceRise: Pharmaceutical Science, no. 1(35) (February 28, 2022): 22–27. http://dx.doi.org/10.15587/2519-4852.2022.253372.

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Neuropeptide Y (NPY) is a biologically active neuropeptide that is responsible for a large list of physiological processes. We propose a short modified fragment of NPY that should at least partially have a spectrum of biological activity of the original peptide. The compound was named nonapeptide NP9.&#x0D; The aim of our study was to investigate the ability of the modified fragment of NPY to influence spatial memory and learning.&#x0D; Materials and methods: the study was performed on 24 one-year-old random-bred female rats weight 220–250 g. The animals were divided into 3 groups of 8 rats ea
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Caddy, Judy, Ulrich Hoffmanns, and Nils Metzler-Nolte. "Introduction of Phosphine-Gold(I) Precursors into a Cys-modified Enkephalin Neuropeptide as Part of Solid Phase Peptide Synthesis." Zeitschrift für Naturforschung B 62, no. 3 (2007): 460–66. http://dx.doi.org/10.1515/znb-2007-0321.

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The synthesis and full characterization of a series of (triphenylphosphine)gold complexes with thiol-containing amino acids and peptides is reported. Boc-Cys-Au(PPh3) was prepared in solution by reaction of Boc-Cys-OH with (Ph3P)AuCl. The related Ac-Cys-Au(PPh3) and an Au derivative of the cysteine-modified neuropeptide enkephalin (Enk), [Cys]5-Au(PPh3)-Enk, were prepared on the resin, using the orthogonal trityl-protecting group on Cys. For comparison, the metal-free [Cys]5-Enk and an S-tert-butyl-protected [Cys]5-Enk were also prepared. Most noteworthy, gold complexation works best when carr
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Havrylov, I. O., and S. Yu Shtrygol’. "The study of the antidepressant and actoprotective activity of a synthetic analog of the terminal region of neuropeptide Y." Ukrainian biopharmaceutical journal, no. 1(66) (April 12, 2021): 28–35. http://dx.doi.org/10.24959/ubphj.21.301.

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Topicality. Neuropeptide Y (NPY), which is significantly widespread in the human body, is responsible for various physiological processes, in particular it is involved in the regulation of the emotional behavior, memory and metabolism. The modified short fragment of NPY proposed – NP9 nonapeptide for intranasal administration – shows certain biological properties of the native peptide, in particular the anxiolytic and antiamnesic action. The effect of NP9 on affective disorders of depressive nature and physical endurance remains unknown. Aim. To study the antidepressant and actoprotective acti
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Boublik, J. H., N. A. Scott, M. R. Brown, and J. E. Rivier. "Synthesis and hypertensive activity of neuropeptide Y fragments and analogs with modified N- or C-termini or D-substitutions." Journal of Medicinal Chemistry 32, no. 3 (1989): 597–601. http://dx.doi.org/10.1021/jm00123a014.

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Numao, T., and D. K. Agrawal. "Neuropeptides modulate human eosinophil chemotaxis." Journal of Immunology 149, no. 10 (1992): 3309–15. http://dx.doi.org/10.4049/jimmunol.149.10.3309.

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Abstract To investigate the role of neuropeptides in allergic inflammation, we examined the effect of peptides on eosinophil chemotaxis. Eosinophils were purified from the blood of allergic and normal subjects using a discontinuous Percoll density gradients. Chemotaxis was induced by platelet-activating factor (PAF) and leukotriene B4, and was assayed by a modified Boyden's chamber technique. Four neuropeptides were examined in this study: substance P (SP), neurokinin A, calcitonin gene-related peptide (CGRP), and cholecystokinin octapeptide. Peptides alone (10 nM to 10 microM) were not chemot
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Leban, Johann J., Dennis Heyer, Antonio Landavazo, Jessica Matthews, Ann Aulabaugh, and Alejandro J. Daniels. "Novel Modified Carboxy Terminal Fragments of Neuropeptide Y with High Affinity for Y2-Type Receptors and Potent Functional Antagonism at the Y1-Type Receptor." Journal of Medicinal Chemistry 38, no. 7 (1995): 1150–57. http://dx.doi.org/10.1021/jm00007a012.

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Orosz, F., K. Liliom, N. A. Barkhudaryan, L. Horváth, and J. Ovádi. "Effects of calmodulin antagonists on antibody binding to calmodulin. Distinct conformers of calmodulin induced by the binding of drugs." Biochemical Journal 284, no. 3 (1992): 803–8. http://dx.doi.org/10.1042/bj2840803.

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An indirect enzyme-linked immunosorbent assay has been used to study the interactions between calmodulin and two calmodulin antagonists, trifluoperazine and a neuropeptide isolated from the hypothalamus. The binding of a monospecific anti-calmodulin antibody, raised in rabbit against dinitrophenylated calmodulin, to calmodulin was tested at various concentrations of these drugs under equilibrium conditions. Trifluoperazine at low concentrations stimulated, but at relatively high concentrations inhibited, immunocomplex formation. The neuropeptide displaced the antibody from calmodulin at nanomo
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Hiltz, Melanie E., та James M. Lipton. "Antiinflammatory activity of a COOH‐terminal fragment of the neuropeptide α‐MSH". FASEB Journal 3, № 11 (1989): 2282–84. http://dx.doi.org/10.1096/fasebj.3.11.2550304.

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Dissertations / Theses on the topic "Modified fragment of neuropeptide Y"

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Jonsson, Anna. "The Impact of the Neuropeptide Substance P (SP) Fragment SP1-7 on Chronic Neuropathic Pain." Doctoral thesis, Uppsala universitet, Institutionen för farmaceutisk biovetenskap, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-241637.

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There is an unmet medical need for the efficient treatment of neuropathic pain, a condition that affects approximately 10% of the population worldwide. Current therapies need to be improved due to the associated side effects and lack of response in many patients. Moreover, neuropathic pain causes great suffering to patients and puts an economical burden on society. The work presented in this thesis addresses SP1-7, (Arg-Pro-Lys-Pro-Gln-Gln-Phe-OH), a major metabolite of the pronociceptive neuropeptide Substance P (SP). SP is released in the spinal cord following a noxious stimulus and binds to
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Toney, Karen 1967. "Characterization of post-translationally modified forms of the joining peptide fragment of pro-opiomelanocortin." Thesis, McGill University, 1994. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=28934.

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The aim of these studies was the identification and characterization of the micro-heterogeneity present within the joining peptide fragment of POMC. The joining peptide (JP) from various animal species was resolved into major and minor components by RP-HPLC and characterized in terms of amino acid composition. Amino acid analyses revealed that no apparent sequence variations occur in any of the JP forms, indicating that post-translational modifications were responsible for the heterogeneity. Using a combination of biochemical and analytical techniques, including RP-HPLC, mass spectrometry, Edm
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González-Alemán, Roy. "Computational fragment-based design of chemically modified oligonucleotides for selective protein inhibition : BACE1 as a case study." Electronic Thesis or Diss., université Paris-Saclay, 2023. http://www.theses.fr/2023UPASL149.

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La conception de médicaments à base de fragments (FBDD) est devenue une approche de plus en plus populaire dans la conception de ligand, avec de nombreuses réussites dans le processus de découverte de médicaments. Malgré certains défis liés à l'accessibilité synthétique et aux stratégies de conception de ligand, le FBDD reste une méthode prometteuse pour aborder l'espace chimique, la complexité moléculaire, la probabilité de liaison et l'efficacité des ligands. Les thérapies à ARN se développent rapidement, subissant une résurgence en raison des nombreux avantages de ces molécules par rapport
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Doyon, Christian. "Corticotropin-releasing factor (CRF) and neuropeptide Y (NPY) mRNA levels are modified by stress and glucocorticoids in rainbow trout (Oncorhynchus mykiss)." Thesis, University of Ottawa (Canada), 2003. http://hdl.handle.net/10393/29014.

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The studies described in this thesis were designed to address the hypothesis that stress and glucocorticoids modify the levels of corticotropin-releasing factor (CRF) and neuropeptide Y (NPY) mRNA in the rainbow trout ( Oncorhynchus mykiss) brain. Standard cloning techniques provided the full-length cDNA sequences coding for trout NPY and two CRF paralogues. Using a ribonuclease protection assay (RPA), a tissue distribution demonstrated that both CRF paralogues are primarily abundant in the preoptic area of the trout brain, whereas NPY mRNA is more abundant in the telencephalon. The effects of
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rob, abdur. "Protein-Nucleic Acid Interactions in Nuclease and Polymerases." Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/54.

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DNA polymerase binds to the double stranded DNA and extends the primer strand by adding deoxyribonucletide to the 3’-end. Several reactions in the polymerase active site have been reported by Kornberg in addition to the polymerization. We observed DNA polymerase I can act as a pyrophosphatase and hydrolyze deoxyribonucletide. In performing the pyrophosphatase activity, DNA polymerase I requires to interact with RNA. RNA in general, was found to activate the DNA polymerase I as pyrophosphatase. This hydrolysis causes depletion of dNTP and inhibits DNA polymeration synthesis in vitro. In this RN
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Tarli, Lorenzo. "Tumour targeting and therapy experiments using a chemically-modified human antibody fragment directed against the ED-B domain of fibronectin, a marker of angiogenesis /." [S.l.] : [s.n.], 2000. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=13680.

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Wu, Ming-Ju, and 吳明儒. "Conformational studies of synthesized neuropeptide fragment hPP【17-24】by CD and NMR." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/96jee5.

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碩士<br>淡江大學<br>化學學系碩士班<br>96<br>The human pancreatic polypeptide(hPP), a 36-residue, polypeptide hormone is a member of the neuropeptide Y(NPY)family. In the central nervous system PP promotes food intake and gastric emptying by activation of the Y4 and probably Y5 receptors. The C-terminal is a well-defined α-helical region and the N terminus is an extended polyproline helix which bent back onto the the C-terminalα-helix. The structural motif of pp has been named as the PP-fold. hPP in solution exists as a dimer and when bound to micelle, it exists as a monomer. Therefore, to elucidate the mon
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Lin, Chia-Hao, and 林嘉豪. "Conformational studies of synthesized neuropeptide fragment hNPY[21-31] by CD and NMR." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/50985876967206541276.

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碩士<br>淡江大學<br>化學學系碩士班<br>96<br>Human Neuropeptide Y(hNPY) has a well-defined α-helical structure in solution, and is monomer at low concentration, dimer at high concentration. It has specific binding mechanism: First, the monomer structure binds with membrane micelle, and further interacts with G protein-coulpled receptors(GPCRs). We synthesize neuropeptide fragment hNPY[21-31] by solid phase peptide synthesis, purified by RP-HPLC and made sure the molecular weight by Mass. The conformation and dynamics of hNPY[21-31] in difference solvent condition is studied by CD and 2D NMR experiment. 2D N
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Books on the topic "Modified fragment of neuropeptide Y"

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Tarli, Lorenzo. Tumour targeting and therapy experiments using a chemically-modified human antibody fragment directed against the ED-B domain of fibronectin, a marker of angiogenesis. 2000.

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Book chapters on the topic "Modified fragment of neuropeptide Y"

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Murase, S., N. Yumoto, H. Yamamoto, Y. Tatsu, T. Taguchi, and S. Yoshikawa. "Disulfide-bond contribution to secondary structure formation of the C-terminal fragment of neuropeptide Y." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_251.

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Yumoto, N., S. Murase, M. G. Petukhov, et al. "Effect of the N-terminal modification on the stability of α-helix in the C-terminal fragment of neuropeptide Y." In Peptides 1994. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-1468-4_252.

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Battachariyya, Sanchari, Ruslana Tytarenko, Christoph Heuck, John Greally, and Amit Verma. "Genome Wide Mapping of Methylated and Hydroxyl-Methylated Cytosines Using a Modified HpaII Tiny Fragment Enrichment by Ligation Mediated PCR Tagged Sequencing Protocol." In Methods in Molecular Biology. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7865-6_12.

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Bouyer, Patricia, B. Srivathsan, and Vaishnavi Vishwanath. "Model-Checking Real-Time Systems: Revisiting the Alternating Automaton Route." In Lecture Notes in Computer Science. Springer Nature Switzerland, 2025. https://doi.org/10.1007/978-3-031-90897-2_19.

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Abstract Alternating timed automata (ATA) are an extension of timed automata, that are closed under complementation and hence amenable to logic-to-automata translations. Several timed logics, including Metric Temporal Logic (MTL), can be converted to equivalent 1-clock ATAs (1-ATAs). Satisfiability of an MTL formula reduces to checking emptiness of a 1-ATA. Furthermore, algorithms for 1-ATA emptiness can be adapted for model-checking timed automata models against 1-ATA specifications. However, existing emptiness algorithms for 1-ATA proceed by an extended region construction, and are not suita
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Erster, Oran, and Moti Liscovitch. "A Modified Inverse PCR Procedure for Insertion, Deletion, or Replacement of a DNA Fragment in a Target Sequence and Its Application in the Ligand Interaction Scan Method for Generation of Ligand-Regulated Proteins." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-652-8_12.

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Kalinichenko, Elena. "Modified (2′,5′)Oligonucleotides: The Influence of Structural and Steriochemical Factors on Biological and Immunotropic Activity." In Oligonucleotides - Overview and Applications [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108630.

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The synthesis of a large number of analogs of natural 2-5A and the results of studies to clarify the relationship between the structure and spatial organization (stereochemistry) and the biological properties of analogs 2-5A have convincingly demonstrated that by changing the structure and/or stereochemistry of molecules, it is possible to achieve either strengthening of known properties or giving new ones. The replacement of the adenosine fragment with 1-deazaadenosine (c1A) or 3-deazaadenosine (c3A) at various positions of the 2-5A chain demonstrated the role of each of the nitrogen atoms of
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Harris, Eva. "Rapid Cloning of PCR Products." In A Low-Cost Approach To PCR. Oxford University PressNew York, NY, 1998. http://dx.doi.org/10.1093/oso/9780195119268.003.0006.

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Abstract PCR products can be visualized directly or cloned by ligating the amplified product into the vector of choice. Cloning of PCR products is useful for many purposes; for instance, the cloned fragment can then be sequenced, modified, expressed, labeled, or used as a DNA probe. While PCR methods have been described to perform many of these functions without cloning, it is often useful to have a cloned stock of PCR product (modified or unmodified) as a permanent source of the material. PCR products can be notoriously difficult to clone, and numerous PCR cloning strategies have been develop
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Pudo, Dorota. "Le Maroc francophone en classe du FLE en Pologne : état des lieux et proposition didactique." In Pensées orientale et occidentale: influences et complémentarité II. Ksiegarnia Akademicka Publishing, 2021. http://dx.doi.org/10.12797/9788381383950.10.

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The article contains an idea for a lesson of French as a foreign language and focuses on the reading of a fragment from the Moroccan writer Tahar Ben Jelloun’s novel Enfant de sable. In the theoretical part, the author of the text analyses modern conceptions of interculturality in a language class as well as the place of literature in teaching foreign languages. The author also analyses the presence of Moroccan culture in French classes in Poland and the reasons why this presence seems so scarce. The objectives of the proposed lesson target communication skills (reading comprehension, oral int
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Oy-Marra, Elisabeth. "Conceptualising Schools of Art: Giovanni Battista Agucchi’s (1570–1632) Theory and Its Afterlife." In Art and Its Geographies. Amsterdam University Press, 2024. http://dx.doi.org/10.5117/9789463728140_ch04.

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This essay features a close reading of Giovanni Battista Agucchi’s concept of artistic schools, which he develops in his uncomplete treatise, published 1646 by Giovanni Antonio Massani. From this fragment, it can be shown that an artistic geography, which had been formulated to a large extent by Giorgio Vasari and which is seen here from a different perspective, has been modified and developed further. In particular, I focus on the goals Agucchi pursued in his conception of artistic schools. While he regarded these schools as a historical development, he seeks to praise the Carracci for their
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Inouye, Sumiko, and Masayori Inouye. "Site-directed mutagenesis using gapped-heteroduplex plasmid DNA." In Directed Mutagenesis. Oxford University PressOxford, 1991. http://dx.doi.org/10.1093/oso/9780199631414.003.0004.

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Abstract Oligonucleotide-directed site-specific mutagenesis is the most effective and powerful method to create desired mutations at a specific site in a gene. The method involves the use of a short, synthetic oligonucleotide carrying the appropriate mutation, which acts as a primer of in vitro DNA synthesis on a complementary single-stranded circular DNA template. There are two basic methods to create a complementary single-stranded circular DNA template; one utilizes double-stranded plasmid (the plasmid method) and the other utilizes single-stranded M13 or phagemid vectors (the M13 method).
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Conference papers on the topic "Modified fragment of neuropeptide Y"

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Okamoto, Shogo, Yusuhide Ohno, Kenzo Maehashi, Koichi Inoue, and Kazuhiko Matsumoto. "6.1.3 Fragment-Modified Graphene FET for Highly Sensitive Detection of Antigen-Antibody Reaction." In 14th International Meeting on Chemical Sensors - IMCS 2012. AMA Service GmbH, Von-Münchhausen-Str. 49, 31515 Wunstorf, Germany, 2012. http://dx.doi.org/10.5162/imcs2012/6.1.3.

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Soria, J., C. Soria, Me Mirshahi, et al. "DDE COMPLEX DETERMINATION AS A SPECIFIC MARKER FOR FIBRINOLYSIS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643653.

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Monoclonal antibodies (McAb) reacting with fibrin degradation products (FbDP), but not with fibrinogen have been produced in order to determine specifically FbDP directly in plasma. Most of the McAb available however do also react with fragment D. Our anti D neo McAb reacts about 10 times less with fragment D than with FbDP but does not react with fibrinogen, fragment X or Y.In clinical investigation, even in pathological conditions in which there is a great release of tissue-type plasminogen activator (tpA), we have shown that fragment D is not generated in patients plasma. Therefore, the rea
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LEUS, VITALY, ROY CEDER, VALENTIN OGNEV, and MEIR MAYSELESS. "THE ROLE OF TANGENTIAL VELOCITY IN EXPLOSIVE INITIATION BY FRAGMENT IMPACT." In 32ND INTERNATIONAL SYMPOSIUM ON BALLISTICS. Destech Publications, Inc., 2022. http://dx.doi.org/10.12783/ballistics22/36170.

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An initiation study is presented in which we examine the effect of the normal and the tangential velocity components of a fragment that impacts a covered and a bare Comp-B explosive. The study is based on calibrated numerical Lagrangian simulations using the LS-Dyna hydrocode. The influence of the fragment strength and the steel cover thickness on the detonation threshold were also examined, for different impact angles. The velocity threshold results are presented and compared to a modified Jacobs-Roslund initiation model, obtained by substituting the orientation angle by the impact angle. Up
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Dubrovskaya, E. V., D. I. Ivkina, and A. R. Imatdinov. "RECOMBINANT INFLUENZA A VIRUS REASSORTANT VACCINE STRAIN EXPRESSING MODIFIED RBD FRAGMENT OF SARS-COV-2 CORONAVIRUS SPIKE GLYCOPROTEIN." In OpenBio-2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-244.

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Influenza A virus and SARS-CoV-2 virus have a high pandemic potential. Vaccination is an effective method of prevention, but existing vaccines cannot be quickly updated to match circulating virus variants. This paper describes a recombinant reassortant strain of influenza A virus expressing SARS-CoV-2 trimerized RBD, which can be used as a component of candidate multivalent vaccines.
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Arikawa, Keisuke. "Kinematic Modeling and Inverse Kinematics of Serial 6R Fragment of Molecule." In ASME 2021 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/detc2021-70853.

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Abstract Depending on their mobilities around bond axes, molecules (e.g., proteins, DNA, and RNA) can be modeled as robotic manipulators. We focus on the serial 6R fragments, or the fragments containing six revolute joints connected in series, extracted from these molecules. We solved the inverse kinematics problems of the fragments. We obtained multiple conformations that maintained the relative position and orientation between both ends. Raghavan and Roth’s solution effectively conveys all real solutions. However, the solution is not directly applicable when some link lengths are zeros. To c
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Zhang, Ya, Xiaobin Li, and Siyu Li. "Research on the Velocity Attenuation Characteristics of the Fragments During High-Speed Water Entry." In ASME 2018 37th International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/omae2018-78665.

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When fragments entering water at high speed, velocity attenuation coefficients of the fragments calculated by different scholars were quite different. Through theoretical analysis and numerical simulation, the velocity attenuation characteristics of the fragments with different head shapes, water entry angles and aspect ratios are studied in this paper. Numerical results show that for the fragments with different head shapes, the main factors affecting the velocity attenuation of the fragments are different. In particular, the influences of the pier’s rough effect on the velocity attenuation o
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Price, David W., Benjamin L. Adams, Alexander Harding, Callan Corbett, and Steven Calverley. "COPPER LuREx: COMPARISON OF THE FRAGMENTATION OF COPPER- AND STEEL-CASED EXPLOSIVE DEVICES." In 34th International Symposium on Ballistics. Destech Publications, Inc., 2025. https://doi.org/10.12783/ballistics25/37089.

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Data from safety justification trials (SJTs) and calculations are used to predict the threats to the facility infrastructure from explosively-driven experiments. We aim to remove the requirement for future costly SJTs and rely solely on simulation, which necessitates validation and verification of our modelling methodology. To improve our fragment formation modelling and to test mitigation schemes, a range of simple steel-cased explosive devices have been designed and fielded in experiments. The devices were designed using leadingedge modelling techniques and gave us information regarding frag
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Hartley, Adam, Michelle Greene, Mikhail Caga-Anan, et al. "BS15 In vivo whole-body fluorescence molecular imaging of experimental atherosclerosis using anti-malondialdehyde-modified low-density lipoprotein humanised antibody fragment targeted nanoparticles." In British Cardiovascular Society Annual Conference, ‘100 years of Cardiology’, 6–8 June 2022. BMJ Publishing Group Ltd and British Cardiovascular Society, 2022. http://dx.doi.org/10.1136/heartjnl-2022-bcs.195.

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Hartley, Adam, Michelle Greene, Mikhail Caga-Anan, et al. "BS15 In vivo whole-body fluorescence molecular imaging of experimental atherosclerosis using anti-malondialdehyde-modified low-density lipoprotein humanised antibody fragment targeted nanoparticles." In British Cardiovascular Society Annual Conference, ‘100 years of Cardiology’, 6–8 June 2022. BMJ Publishing Group Ltd and British Cardiovascular Society, 2022. http://dx.doi.org/10.1136/heartjnl-2022-bcs.195.

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Kirby, Edward P., Mary Ann Mascelli, Carol Silverman, and Daniel W. Karl. "LOCALIZATION OF THE PLATELET-BINDING AND HEPARIN-BINDING DOMAINS OF BOVINE VON WILLEBRAND FACTOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644097.

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Bovine von Willebrand Factor (vWF) binds directly to human platelets and also to heparin-agarose. Cleavage of vWF with Protease I, a metalloenzyme isolated from the venom of the western diamondback rattlesnake, produces two major fragments with apparent Mr of 250 kD and 200 kD. The 200 kD fragment competes with native vWF for binding to the GPIb-associated vWF receptor on formalin-fixed human platelets and has weak platelet-agglutinating activity. It is composed of three polypeptide chains of apparent Mr of 97 kD, 61 kD, and 35 kD. Monoclonal antibodies #2 and H-9, which inhibit binding of vWF
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Reports on the topic "Modified fragment of neuropeptide Y"

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Ohad, Itzhak, and Himadri Pakrasi. Role of Cytochrome B559 in Photoinhibition. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7613031.bard.

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The aim of this research project was to obtain information on the role of the cytochrome b559 in the function of Photosystem-II (PSII) with special emphasis on the light induced photo inactivation of PSII and turnover of the photochemical reaction center II protein subunit RCII-D1. The major goals of this project were: 1) Isolation and sequencing of the Chlamydomonas chloroplast psbE and psbF genes encoding the cytochrome b559 a and b subunits respectively; 2) Generation of site directed mutants and testing the effect of such mutation on the function of PSII under various light conditions; 3)
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