Relevant bibliographies by topics / Vamps

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  2. Dissertations / Theses
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Academic literature on the topic 'Vamps'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Vamps"

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Rose, Adam J., Jacob Jeppesen, Bente Kiens, and Erik A. Richter. "Effects of contraction on localization of GLUT4 and v-SNARE isoforms in rat skeletal muscle." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 297, no. 5 (November 2009): R1228—R1237. http://dx.doi.org/10.1152/ajpregu.00258.2009.

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In skeletal muscle, contractions increase glucose uptake due to a translocation of GLUT4 glucose transporters from intracellular storage sites to the surface membrane. Vesicle-associated membrane proteins (VAMPs) are believed to play an important role in docking and fusion of the GLUT4 transporters at the surface membrane. However, knowledge about which VAMP isoforms colocalize with GLUT4 vesicles in mature skeletal muscle and whether they translocate during muscle contractions is incomplete. The aim of the present study was to further identify VAMP isoforms, which are associated with GLUT4 vesicles and examine which VAMP isoforms translocate to surface membranes in skeletal muscles undergoing contractions. VAMP2, VAMP3, VAMP5, and VAMP7 were enriched in immunoprecipitated GLUT4 vesicles. In response to 20 min of in situ contractions, there was a redistribution of GLUT4 (+64 ± 13%), transferrin receptor (TfR; +75 ± 22%), and insulin-regulated aminopeptidase (IRAP; +70 ± 13%) to fractions enriched in heavy membranes away from low-density membranes (−32 ± 7%; −18 ± 12%; −33 ± 9%; respectively), when compared with the resting contralateral muscle. Similarly, there was a redistribution of VAMP2 (+240 ± 40%), VAMP5 (+79 ± 9%), and VAMP7 (+79 ± 29%), but not VAMP3, to fractions enriched in heavy membranes away from low-density membranes (−49 ± 10%, −54 ± 9%, −14 ± 11%, respectively) in contracted vs. resting muscle. In summary, VAMP2, VAMP3, VAMP5, and VAMP7 coimmunoprecipitate with intracellular GLUT4 vesicles in muscle, and VAMP2, VAMP5, VAMP7, but not VAMP3, translocate to the cell surface membranes similar to GLUT4, TfR, and IRAP in response to muscle contractions. These findings suggest that VAMP2, VAMP5, and VAMP7 may be involved in translocation of GLUT4 during muscle contractions.
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Sadler, Jessica B. A., Nia J. Bryant, and Gwyn W. Gould. "Characterization of VAMP isoforms in 3T3-L1 adipocytes: implications for GLUT4 trafficking." Molecular Biology of the Cell 26, no. 3 (February 2015): 530–36. http://dx.doi.org/10.1091/mbc.e14-09-1368.

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The fusion of GLUT4-containing vesicles with the plasma membrane of adipocytes is a key facet of insulin action. This process is mediated by the formation of functional soluble N-ethylmaleimide–sensitive factor attachment protein receptor (SNARE) complexes between the plasma membrane t-SNARE complex and the vesicle v-SNARE or VAMP. The t-SNARE complex consists of Syntaxin4 and SNAP23, and whereas many studies identify VAMP2 as the v-SNARE, others suggest that either VAMP3 or VAMP8 may also fulfil this role. Here we characterized the levels of expression, distribution, and association of all the VAMPs expressed in 3T3-L1 adipocytes to provide the first systematic analysis of all members of this protein family for any cell type. Despite our finding that all VAMP isoforms form SDS-resistant SNARE complexes with Syntaxin4/SNAP23 in vitro, a combination of levels of expression (which vary by >30-fold), subcellular distribution, and coimmunoprecipitation analyses lead us to propose that VAMP2 is the major v-SNARE involved in GLUT4 trafficking to the surface of 3T3-L1 adipocytes.
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Jeff Bursey. "Estonian Vamps." American Book Review 31, no. 2 (2010): 15. http://dx.doi.org/10.1353/abr.0.0026.

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TIMMERS, Kim I., Avril E. CLARK, Mariko OMATSU-KANBE, Sidney W. WHITEHEART, Mark K. BENNETT, Geoffrey D. HOLMAN, and Samuel W. CUSHMAN. "Identification of SNAP receptors in rat adipose cell membrane fractions and in SNARE complexes co-immunoprecipitated with epitope-tagged N-ethylmaleimide-sensitive fusion protein." Biochemical Journal 320, no. 2 (December 1, 1996): 429–36. http://dx.doi.org/10.1042/bj3200429.

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The vesicle-associated membrane proteins [VAMPs; vesicle SNAP receptors (v-SNAREs)] present on GLUT4-enriched vesicles prepared from rat adipose cells [Cain, Trimble and Lienhard (1992) J. Biol. Chem. 267, 11681–11684] have been identified as synaptobrevin 2 (VAMP 2) and cellubrevin (VAMP 3) by using isoform-specific antisera. Additional antisera identify syntaxins 2 and 4 as the predominant target membrane SNAP receptors (t-SNAREs) in the plasma membranes (PM), with syntaxin 3 at one-twentieth the level. Syntaxins 2 and 4 are enriched 5–10-fold in PM compared with low-density microsomes (LDM). Insulin treatment results in an 11-fold increase in immunodetectable GLUT4 in PM and smaller (approx. 2-fold) increases in VAMP 2 and VAMP 3, whereas the subcellular distributions of the syntaxins are not altered by insulin treatment. To determine which of the SNAP receptors (SNAREs) in PM might participate in SNARE complexes with proteins from GLUT4 vesicles, complexes were immunoprecipitated with anti-myc antibody from solubilized membranes after the addition of myc-epitope-tagged N-ethylmaleimide-sensitive fusion protein (NSF) and recombinant α-soluble NSF attachment protein (α-SNAP). These complexes contain VAMPs 2 and 3 and syntaxin 4, but not syntaxins 2 or 3. Complex formation requires ATP and is disrupted by ATP hydrolysis. When all membrane fractions are prepared from basal cells, few or no VAMPs and no syntaxin 4 are immunoprecipitated in SNARE complexes obtained from LDM alone (or from immunoisolated GLUT4 vesicles). The content of syntaxin 4 depends on the presence of PM, and participation of VAMPs 2 and 3 is enhanced 4–6-fold by the addition of solubilized GLUT4 vesicles to PM. The latter increase is greater than can be explained by the 2-fold higher levels of VAMPs added to the reaction mixture. When all membrane fractions are prepared from insulin-stimulated cells, SNARE complexes formed from PM alone contain similar levels of syntaxin 4 but 5–6-fold higher levels of VAMPs 2 and 3 compared with PM alone from basal cells. Addition of GLUT4 vesicle proteins to PM from insulin-treated cells results in a further 2-fold increase in VAMP 2 recovered in SNARE complexes. Therefore the VAMPs in PM of insulin-treated but not basal cells, and in GLUT4-vesicles from cells in either condition, are in a form that readily forms a SNARE complex with PM t-SNAREs and NSF. Insulin seems to activate PM and/or GLUT4 vesicles so as to increase the efficiency of SNARE complex formation.
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Zeng, Qi, V. Nathan Subramaniam, Siew Heng Wong, Bor Luen Tang, Robert G. Parton, Shane Rea, David E. James, and Wanjin Hong. "A Novel Synaptobrevin/VAMP Homologous Protein (VAMP5) Is Increased during In Vitro Myogenesis and Present in the Plasma Membrane." Molecular Biology of the Cell 9, no. 9 (September 1998): 2423–37. http://dx.doi.org/10.1091/mbc.9.9.2423.

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cDNA clones encoding a novel protein (VAMP5) homologous to synaptobrevins/VAMPs are detected during database searches. The predicted 102–amino acid VAMP5 harbors a 23-residue hydrophobic region near the carboxyl terminus and exhibits an overall amino acid identity of 33% with synaptobrevin/VAMP1 and 2 and cellubrevin. Northern blot analysis reveals that the mRNA for VAMP5 is preferentially expressed in the skeletal muscle and heart, whereas significantly lower levels are detected in several other tissues but not in the brain. During in vitro differentiation (myogenesis) of C2C12 myoblasts into myotubes, the mRNA level for VAMP5 is increased ∼8- to 10-fold. Immunoblot analysis using antibodies specific for VAMP5 shows that the protein levels are also elevated ∼6-fold during in vitro myogenesis of C2C12 cells. Indirect immunofluorescence microscopy and immunoelectron microscopy reveal that VAMP5 is associated with the plasma membrane as well as intracellular perinuclear and peripheral vesicular structures of myotubes. Epitope-tagged versions of VAMP5 are similarly targeted to the plasma membrane.
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Garcia, Edwin A., Giampaolo Trivellin, Elena D. Aflorei, Michael Powell, Joana Grieve, Ghassan Alusi, Luis Pobereskin, et al. "Characterization of SNARE Proteins in Human Pituitary Adenomas: Targeted Secretion Inhibitors as a New Strategy for the Treatment of Acromegaly?" Journal of Clinical Endocrinology & Metabolism 98, no. 12 (December 1, 2013): E1918—E1926. http://dx.doi.org/10.1210/jc.2013-2602.

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Context: Targeted secretion inhibitors (TSIs), a new class of recombinant biotherapeutic proteins engineered from botulinum toxin, represent a novel approach for treating diseases with excess secretion. They inhibit hormone secretion from targeted cell types through cleavage of SNARE (soluble N-ethylmaleimide-sensitive factor-activating protein receptor) proteins. qGHRH-LHN/D is a TSI targeting pituitary somatotroph through binding to the GHRH-receptor and cleavage of the vesicle-associated membrane protein (VAMP) family of SNARE proteins. Objective: Our objective was to study SNARE protein expression in pituitary adenomas and to inhibit GH secretion from somatotropinomas using qGHRH-LHN/D. Design: We analyzed human pituitary adenoma analysis for SNARE expression and response to qGHRH-LHN/D treatment. Setting: The study was conducted in University Hospitals. Patients: We used pituitary adenoma samples from 25 acromegaly and 47 nonfunctioning pituitary adenoma patients. Outcome: Vesicle-SNARE (VAMP1–3), target-SNARE (syntaxin1, SNAP-23, and SNAP-25), and GHRH-receptor detection with RT-qPCR, immunocytochemistry, and immunoblotting. Assessment of TSI catalytic activity on VAMPs and release of GH from adenoma cells. Results: SNARE proteins were variably expressed in pituitary samples. In vitro evidence using recombinant GFP-VAMP2&3 or pituitary adenoma lysates suggested sufficient catalytic activity of qGHRH-LHN/D to degrade VAMPs, but was unable to inhibit GH secretion in somatotropinoma cell cultures. Conclusions: SNARE proteins are present in human pituitary somatotroph adenomas that can be targeted by TSIs to inhibit GH secretion. qGHRH-LHN/D was unable to inhibit GH secretion from human somatotroph adenoma cells. Further studies are required to understand how the SNARE proteins drive GH secretion in human somatotrophs to allow the development of novel TSIs with a potential therapeutic benefit.
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d'Hugues, Philippe. "Le temps des vamps." Commentaire Numéro 84, no. 4 (October 1, 1998): 1167–68. http://dx.doi.org/10.3917/comm.084.1167.

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Williams, Dumaine, and Jeffrey E. Pessin. "Mapping of R-SNARE function at distinct intracellular GLUT4 trafficking steps in adipocytes." Journal of Cell Biology 180, no. 2 (January 28, 2008): 375–87. http://dx.doi.org/10.1083/jcb.200709108.

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The functional trafficking steps used by soluble NSF attachment protein receptor (SNARE) proteins have been difficult to establish because of substantial overlap in subcellular localization and because in vitro SNARE-dependent binding and fusion reactions can be promiscuous. Therefore, to functionally identify the site of action of the vesicle-associated membrane protein (VAMP) family of R-SNAREs, we have taken advantage of the temporal requirements of adipocyte biosynthetic sorting of a dual-tagged GLUT4 reporter (myc-GLUT4-GFP) coupled with small interfering RNA gene silencing. Using this approach, we confirm the requirement of VAMP2 and VAMP7 for insulin and osmotic shock trafficking from the vesicle storage sites, respectively, and fusion with the plasma membrane. Moreover, we identify a requirement for VAMP4 for the initial biosynthetic entry of GLUT4 from the Golgi apparatus into the insulin-responsive vesicle compartment, VAMP8, for plasma membrane endocytosis and VAMP2 for sorting to the specialized insulin-responsive compartment after plasma membrane endocytosis.
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Peters, Christian G., and Robert Flaumenhaft. "Localization of VAMP Isoforms In Platelets Reveals Separate Granule Populations with Distinct Functions." Blood 116, no. 21 (November 19, 2010): 2015. http://dx.doi.org/10.1182/blood.v116.21.2015.2015.

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Abstract Abstract 2015 Secretion of granules from platelets is essential for normal platelet activity in hemostasis and thrombosis. Platelet granules have different morphologies and different granule subpopulations contain distinct cargos. Platelet granules not only participate in the release of granule contents, but also appear to function to increase plasma membrane surface area during platelet spreading, morphogenesis, tether formation, and membrane repair. Whether different granule subpopulations mediate these distinct functions of the granule is currently not known. To judge whether specific subpopulations of granules are involved in different granule functions, we evaluated the subcellular localization of vesicle-associated membrane proteins (VAMPs) in resting and spread platelets using immunofluorescence confocal microscopy. Imaging showed that VAMP 3- and VAMP 8-containing granules segregate from one another into distinct granule populations (Pearson (R) correlation values (R = 0.143 ± .039, n=25). Fibrinogen and von Willebrand factor (vWF) also segregated from one another (R= 0.099 ± .027, n=15), but associated with granules containing either VAMP 3 or 8 (R = 0.447 ± 0.065 and R = 0.5485 ± 0.62, n=20, respectively). To visualize the granule contribution to membrane remodeling during spreading, granule membranes were selectively labeled using the membrane dye FM 1–43 followed by washout of external dye. Following platelet spreading, FM 1–43-labeled granules coalesced at the ends of pseudopodia and appeared as punctate areas of FM-1-43 staining on the plasma membrane. Quantitation of staining within spread platelets demonstrated that 92% of granules expressing VAMP 8 translocated with their associated cargo (vWF or fibrinogen) to the central granulomere. VAMP 3 also translocated with vWF and fibrinogen to the granulomere in spread platelets. In contrast, only 31% of granules expressing VAMP 5 localized to the granulomere of spread platelets, while 69% of VAMP 5 staining localized to pseudopodia and lamellipodia at the platelet periphery. Granules expressing VAMP 5 demonstrated little colocalization with vWF and fibrinogen in spread platelets. Similarly, VAMP 7 translocated to pseudopodia and lamellipodia during spreading, displaying punctuate staining at the leading edge of plasma membrane. Studies evaluating the expression of VAMP isoforms in nonpermeabilized platelets demonstrated that a portion of VAMP 5, but not VAMPs 3, 7, or 8, resides on the extracellular face of the plasma membrane. Flow cytometry confirmed the presence of VAMP 5 on the extracellular surface of platelets. These data demonstrate that different VAMP isoforms segregate to distinct platelet granule subpopulations and subcellular locals. The colocalization of VAMPs 3 and 8 with vWF and fibrinogen is consistent with previous data demonstrating a role for these VAMP isoforms in cargo release. In contrast, granules expressing VAMP 5 or VAMP 7, which contains an actin-binding login domain, translocate to areas of cytoskeletal remodeling and may contribute membrane to growing cytoskeletal structures as the platelet spreads. These studies indicate that separate granule populations defined by expression of distinct VAMP isoforms perform different functions in platelets. Disclosures: No relevant conflicts of interest to declare.
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Schemenauer, Ellie. "Victims and Vamps, Madonnas and Whores." International Feminist Journal of Politics 14, no. 1 (March 2012): 83–102. http://dx.doi.org/10.1080/14616742.2011.631277.

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Dissertations / Theses on the topic "Vamps"

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Petrescu, Mihaela. "Vamps, Eintaenzer, and desperate housewives social dance in Weimar literature and film /." [Bloomington, Ind.] : Indiana University, 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3297124.

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Thesis (Ph.D.)--Indiana University, Dept. of Germanic Studies, 2007.
Title from dissertation home page (viewed Sept. 25, 2008). Source: Dissertation Abstracts International, Volume: 69-02, Section: A, page: 0622. Adviser: William Rasch.
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Wang, Guan. "Roles of substrate rigidity and composition in membrane trafficking." Thesis, Sorbonne Paris Cité, 2016. http://www.theses.fr/2016USPCC195.

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Du cerveau à l’os, la rigidité et la composition de la matrice extracellulaire varient énormément et jouent un rôle dans les réponses cellulaires. La rigidité influe également sur la tension de la membrane plasmique, elle-même régulée par le trafic membranaire. Comment la rigidité et la composition du substrat peuvent réguler l'exocytose, qui à son tour régule la tension de la membrane, reste largement inconnu. Ici, j'ai utilisé l’imagerie pHluorin d’évènements uniques d’exocytose de cellules cultivées sur des substrats de rigidité et de composition contrôlée pour explorer la régulation de VAMP2 et VAMP7. J'ai développé un logiciel informatique pour identifier automatiquement les évènements de fusion, permettant une analyse rapide de données. J'ai contribué à l'étude montrant que l’exocytose VAMP7 est régulée par la kinase src, qui phosphoryle VAMP7 dans son domaine Longin (LD) (Burgo et al. JBC 2013). De plus, j’ai trouvé que la rigidité du substrat stimule l’exocytose, en présence de la laminine, de VAMP7, mais pas VAMP7 sans LD ni VAMP2. VAMP7 et VAMP7 sans LD sont par ailleurs également sensibles aux variations de la tension membranaire induites par chocs osmotiques. Enfin, j'ai identifié que LRRK1 est un partenaire du LD, et contrôle le transport rétrograde de VAMP7.Ces approches m’ont permis de révéler un nouveau mécanisme par lequel la rigidité, agissant sur la signalisation des intégrines, contrôle le transport de VAMP7 via LRRK1 et Rab21 (Wang et al. soumis). Ce mécanisme pourrait avoir un large intérêt potentiel pour comprendre la dynamique de la membrane dans des conditions normales et pathologiques, en particulier le cancer
From brain to bones, stiffness and composition of the extracellular matrix vary greatly and play a role in cell responses. Substrate rigidity also impacts plasma membrane tension, which has a close relationship with membrane trafficking. How substrate rigidity and chemistry sensing may regulate exocytosis, which in turn regulates membrane tension, is still largely unknown. Here, I used pHluorin imaging of single vesicle exocytosis in cells cultured on substrates of controlled rigidity and composition to explore the regulation of VAMP2 and VAMP7-mediated exocytosis. I developed a computer software to automatically identify fusion events thus allowing quick analysis of batch data. I contributed to the study showing that VAMP7 exocytosis is regulated by src kinase which phosphorylates VAMP7 in its Longin domain (LD) (Burgo et al. JBC 2013). I further found that VAMP7 but not VAMP7 lacking LD- or VAMP2-mediated secretion was stimulated by substrate stiffness on laminin. VAMP7 and VAMP7 lacking LD were similarly sensitive to osmotic chock-induced membrane tension changes. Finally, i showed that LRRK1, a regulator of egf receptor transport, is a partner of the LD, and controls the retrograde transport of VAMP7. These approaches allowed me to reveal a new mechanism whereby substrate rigidity, by acting on integrin signalling, enhances VAMP7 exocytosis via LRRK1- and Rab21-dependent regulation of its peripheral readily-releasable pool (Wang et al. submitted). This mechanism may have broad potential relevance for plasma membrane dynamics in normal conditions and diseases, particularly cancer
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Krapivkina, Julia. "Identification de protéines SNARE de l'exocytose des endosomes de recyclage dans les dendrites neuronales." Thesis, Bordeaux, 2016. http://www.theses.fr/2016BORD0343/document.

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Le trafic membranaire est un processus universel qui est essentiel pour la fonction neuronale dans un large spectre de fonctions. De la croissance neuronale et le développement morphologique à la libération des neurotransmetteurs et la plasticité synaptique, il prend en charge l'activité neuronale et donne d'innombrables questions qui animent la recherche sur la neurobiologie d'aujourd'hui. Notamment, l’exocytose des endosomes de recyclage (ER) dans les compartiments somatodendritiques participe à la transmission synaptique et à la potentialisation synaptique à long terme (PLT). Cependant la machine moléculaire sous-tendant l’exocytose des ER reste encore méconnue. Afin d’identifier les protéines SNAREs vésiculaires (v-SNARE) impliquées dans les différentes formes d’exocytose des ER postsynaptiques, nous avons d'abord imagé les protéines VAMP neuronales fusionnées avec la pHluorine, une GFP mutée sensible au pH dans les neurones de l’hippocampe en culture. Nous avons constaté que seulement VAMP2 et VAMP4, mais pas VAMP7, rapportaient des événements d’exocytose somatodendritique dans les neurones matures. Après avoir identifié ces deux protéines candidates, nous avons utilisé la combinaison de différentes techniques de régulation négative chronique ou aiguë pour désactiver leur fonction et observer les conséquences sur l’exocytose des ER, la transmission synaptique basale ou la PLT. Nos résultats suggèrent que VAMP2 est impliqué dans une forme d’exocytose régulée importante pour la PLT, mais pas l’exocytose constitutive des récepteurs AMPA, qui stabilise la transmission basale. VAMP4 est nécessaire pour l'exocytose constitutive d'une grande partie des endosomes, mais l'implication fonctionnelle de ces endosomes doit encore être explorée, car la régulation négative de VAMP4 ne modifie pas la transmission basale
Membrane trafficking is a universal process that is essential for neuronal function in a wide spectrum of applications. From neuronal growth and morphological development to neurotransmitter release and synaptic plasticity, it supports neuronal activity and gives countless questions that drive today’s neurobiology research. Notably, the trafficking of recycling endosomes (REs) in somatodendritic compartments participates in synaptic transmission and plasticity, such as long-term synaptic potentiation (LTP). However, the fusion machinery mediating RE exocytosis is still unclear. To identify the vesicular SNAREs (v-SNAREs) involved in different forms of postsynaptic RE exocytosis, we first imaged neuronal VAMP proteins fused with pH-sensitive pHluorin in cultured hippocampal neurons, and found that only VAMP2 and VAMP4, but not VAMP7, underwent somatodendritic exocytosis in mature neurons. After identifying these two candidate proteins, we used a combination of different downregulation techniques to chronically or acutely deactivate their function and observe consequences on REs exocytosis, basal synaptic transmission and LTP. Our results suggest that VAMP2 is involved in activity-regulated exocytosis important for LTP, but not constitutive postsynaptic AMPARs exocytosis, supporting basal transmission. VAMP4 is required for constitutive exocytosis of at least a large proportion of REs, but the functional implication of these endosomes still need to be explored, as VAMP4 downregulation did not alter basal synaptic transmission
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Lynch, Jordan. "Where Have I Known This Before? An Exploration of Harmony and Voice Leading in the Compositions of Chick Corea." Bowling Green State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1333991067.

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Jullié, Damien. "Les endosomes de recyclage fusionnent transitoirement avec la membrane plasmique des dendrites neuronales." Thesis, Bordeaux 2, 2012. http://www.theses.fr/2012BOR21942/document.

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Le trafic membranaire est essentiel dans les neurones pour la morphogénèse, le recyclage des vésicules synaptiques et des récepteurs. L’exocytose des récepteurs AMPA contenus dans les endosomes de recyclage (ER) est nécessaire pour l’expression de la plasticité synaptique à long terme (PLT). Pour étudier ce mécanisme, nous avons visualisé l’exocytose par microscopie de fluorescence sur des neurones en culture transfectés avec le récepteur de la transferrine (TfR), un marqueur des ER, fusionné à la phluorine. Un examen systématique des événements d'exocytose a révélé des différences de comportement. Dans la plupart des cas, les récepteurs diffusent rapidement dans la membrane plasmique après exocytose (discharge), mais dans environ 25% des cas, les récepteurs restent concentrés (display). L’utilisation de changements rapides de pH extracellulaire autour de la cellule montre que l’exocytose est transitoire : après quelques secondes (médiane 2.6s) les récepteurs sont réinternalisés. Ce mécanisme a pu être étendu aux récepteurs AMPA et β2-adrenergique, pour lesquels l’exocytose de type display avait déjà été décrite. L’imagerie deux couleurs montre que Rab11, un marqueur des ER, est enrichie au site d’exocytose. L’expression d’un dominant négatif de Rab11 connu pour inhiber la PLT provoque une diminution spécifique de la fréquence des évènements discharge. Dans nos recherches sur le mécanisme de l’exocytose, nous avons testé l’implication des protéines SNARE dans la fusion membranaire. Ainsi VAMP4 est enrichie avec le TfR dans les ER qui sont exocytés à une fréquence équivalente. De plus, elle est requise pour le recyclage du TfR
Membrane trafficking is essential for neuronal function: from growth of neurons and synapse formation to recycling of synaptic vesicles and receptors, questions concerning exocytosis and endocytosis are stimulating neurobiology research. In particular, trafficking of glutamate receptors present in recycling endosomes (REs) is necessary for the expression of long term potentiation (LTP). To investigate the mechanism of exocytosis in dendrites, we have imaged cultured rat hippocampal neurons transfected with transferrin receptor, a classical marker of REs, tagged with phluorin. As for AMPA receptors or β2-adrenegric receptors, single exocytic events has revealed two main behaviors: in most cases, receptors diffuse quickly in the plasma membrane after exocytosis (discharge events), but receptors can also remain clustered (display events). Using fast extracellular pH changes around the recorded cell, we show that for display events exocytosis is transient: after a few seconds (median 2.6 s) receptors are internalized. Moreover, using two color imaging of single exocytosis events with markers of neuronal compartments, we found that Rab11 is enriched at the exocytosis site, confirming the endosomal origin of the vesicles. Overexpression of a dominant negative form of Rab11 known to impair LTP decreases selectively the frequency of discharge events. As SNARE proteins are involved in virtually all membrane fusion processes, we investigated the role of Vamp proteins in somatodendritic exocytosis events. We found that Vamp4, unlike Vamp2 or Vamp7, is enriched in TfR containing compartments and can undergo exocytosis at high frequency and is required for TfR exocytosis
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Chaineau, Mathilde. "Régulation du trafic vésiculaire : rôle de la protéine Hrb dans l'endocytose de la SNARE vésiculaire TI-VAMP/VAMP7." Paris 6, 2009. http://www.theses.fr/2009PA066022.

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Le trafic membranaire assure la communication entre les différents compartiments intracellulaires ainsi qu’entre les cellules et leur environnement via l’exocytose et l’endocytose. Les protéines SNARE vésiculaires (v-SNARE) et leurs partenaires à la membrane cible (t-SNARE) sont responsables de la fusion membranaire. Des travaux antérieurs ont montré le rôle de la v-SNARE TI-VAMP dans une voie d’exocytose impliquée dans la croissance neuritique et le remodelage de la membrane plasmique. Le domaine amino-terminal Longin de TI-VAMP régule l'activité fusogénique de la protéine et son ciblage. J'ai montré que ce domaine interagit avec la protéine Hrb, un nouveau partenaire de TI-VAMP. Hrb est localisée dans des structures membranaires recouvertes de clathrine et régule l’internalisation de TI-VAMP. Le domaine Longin interagit également avec certains lipides, indiquant que ces derniers pourraient réguler le ciblage ou l'activité de TI-VAMP. Ces nouvelles données moléculaires et cellulaires établissent des liens moléculaires inédits entre une protéine responsable de la fusion membranaire, une protéine régulatrice de l'endocytose et les lipides.
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Gonzalez, i. Llinares Bernat. "Presynaptic mechanisms of short-term plasticity at hippocampal mossy fibersynapses." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0424/document.

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Les synapses fibres moussues de l‘hippocampe entre le gyrus denté et les cellulespyramidales de CA3 sont caractérisées par leur morphologie particulière, et par leurspropriétés distinctives de transmission synaptique et de plasticité présynaptique. Cessynapses sont parfois appelées «détonatrices» pour leur rôle fonctionnel dansl‘encodage de la mémoire épisodique. Cependant, les mécanismes moléculaires à labase des propriétés spécifiques de ces synapses restent peu connus. Ce travail estcomposé de deux parties principales:1) Phénotypage des synapses fibres moussues de l'hippocampe chez les sourisVAMP7 KOVAMP7 est une protéine SNARE vésiculaire de la famille des longins, qui joue unrôle dans la croissance des neurites durant le développement. Dans le cerveauadulte, VAMP7 est enrichi dans un sous-ensemble de terminaisons nerveuses, enparticulier dans les fibres moussues de l‗hippocampe. Nous avons analysé lafonction de VAMP7 dans la libération de neurotransmetteurs par une caractérisationextensive de la transmission synaptique et des mécanismes de plasticité de cettesynapse. L'absence de VAMP7 ne cause pas de graves déficits développementauxou neuronaux (Sato et al., 2011; Danglot et al., 2012). Les mécanismesprésynaptiques de la plasticité à court terme de la fibre moussue de l‘hippocampesemblent également normaux, pour des raisons éventuelles qui seront discutées.2) Circuits du CA3 examinés par traçage viral et enregistrements de pairesNous avons développé une technique pour établir des enregistrements en pairesentre cellules en grain du gyrus denté connectées et cellules pyramidales CA3 (GCCA3),sur des cultures organotypiques de tranches d'hippocampe de souris. Pouridentifier les partenaires présynaptiques directs à une cellule pyramidale CA3 ciblée,nous avons combiné l‘électroporation cellulaire unitaire et le traçage mono-transsynaptiquebasé sur un virus de la rage recombinant et pseudotypé. Nous avonstransfecté une cellule pyramidale CA3 unique par tranche avec les plasmides codantla glycoprotéine d‘enveloppe du virus de la rage (RG), un rapporteur fluorescent, etla protéine TVA (récepteur de surface apparenté au EnvA, qui n'a pas d‘homologuechez les cellules de mammifères). Les tranches ont ensuite été infectées avec levirus de la rage recombinant et pseudotypé. Après 3-4 jours, le traçage mono-transsynaptiquerévèle les entrées présynaptiques de ce neurone unique. Ensuite, nousavons pu établir des enregistrements de paires entre les cellules en grain-CA3connectés, ainsi que de quantifier les partenaires présynaptiques de la cellulepyramidale CA3 de départ
The hippocampal mossy fiber is characterized by its particular morphology, distinctsynaptic transmission and presynaptic plasticity. Moreover, this synapse has beencalled ―teacher‖ or ―detonator‖ for its proposed functional role in episodic memoryencoding. Nevertheless, the molecular mechanisms underlying its specific functionalproperties remain elusive. This work is composed of two main parts:1) Phenotyping Hippocampal Mossy Fiber Synapses in VAMP7 KO MiceVAMP7 is a vesicle SNARE of the longin family important in neurite growth duringdevelopment. In the adult brain, VAMP7 is enriched in a subset of nerve terminals,particularly at the hippocampal mossy fiber. We analyzed VAMP7 function inneurotransmitter release by characterizing basal and evoked transmission at thissynapse in KO mice and fully tested hypotheses relevant to short-term plasticity.Loss of VAMP7 has been previously reported not to cause major developmental orneurological deficits (Sato et al., 2011; Danglot et al., 2012). Presynapticmechanisms of short-term plasticity at the hippocampal mossy fiber also seemunaffected for potential reasons that will be discussed.2) CA3 Circuits Probed with RABV-Tracing and Paired RecordingsWe developed a technique to establish paired recordings between connected dentategyrus granule cells and CA3 pyramidal cells (GC-CA3) in mouse hippocampalorganotypic slice cultures. To identify direct presynaptic partners to a defined targetCA3 pyramidal cell, we combined single-cell electroporation (SCE) and mono-transsynaptictracing based on a pseudotyped, recombinant rabies virus (EnvApseudotyped RABV ΔG). Using SCE we transfected a single CA3 pyramidal cell perslice with the plasmids encoding: the RABV envelope glycoprotein (RG), afluorescent reporter, and TVA (the EnvA cognate surface receptor, which has nohomologue in mammalian cells). The slices were subsequently infected with EnvApseudotyped RABV ΔG. After 3-4 days, the RABV mono-trans-synaptic tracingrevealed the presynaptic inputs of that single neuron. Then, we were able toestablish paired recordings between connected GC-CA3 cells, as well as to quantifythe presynaptic partners of the starter CA3 pyramidal cell
De mosvezel van de hippocampus kenmerkt zich door een bijzondere morfologie,uitzonderlijke synaptische transmissie en presynaptische plasticiteit. De synapswordt ook wel "leraar" of "detonator" genoemd vanwege zijn waarschijnlijke rol in decodering van het episodisch geheugen. Toch blijven de specifieke moleculairemechanismen van dit synaps onbekend. Dit werk bestaat uit twee delen:1) Fenotypering van mosvezel synapsen van de hippocampus in VAMP7 KO muizenVAMP7 is een vesicle-SNARE van de longin familie van belang bij de groei vanneurieten tijdens de ontwikkeling. In de volwassen hersenen, wordt VAMP7 verrijkt ineen subset van zenuwuiteinden, vooral in de mosvezel van de hippocampus. Weanalyseerden VAMP7 functie in neurotransmitter afgifte door het karakteriseren vanbasale en opgeroepen transmissie bij deze synaps in KO muizen. Eerder is algesteld dat gebrek aan VAMP7 niet leidt tot grote ontwikkelings- of neurologischeafwijkingen (Sato et al., 2011; Danglot et al., 2012). Presynaptische mechanismenvan korte termijn plasticiteit in de mosvezel van de hippocampus lijken ookonaangetast te zijn, de mogelijke redenen hiervoor zullen worden besproken.2) CA3 circuits onderzocht met behulp van RABV-tracing en gekoppelde opnamesWe ontwikkelden een techniek om gekoppelde opnames tussen korelcellen van degyrus dentatus en aangesloten CA3 piramidale cellen (KC-CA3) op zogenaamde‗mouse hippocampal organotypic slice cultures‘ te meten. Om rechtstreeksepresynaptische partners te identificeren van een specifieke CA3 piramidale cel,combineerden we single-cell electroporation (SCE) en mono-trans-synaptic tracingop basis van een pseudo-typed, recombinant rabiësvirus (EnvA pseudogetypedRABV ΔG). Met behulp van SCE transfecteerde we één CA3 piramidale cel per slicemet plasmiden die coderen voor: het RABV glycoproteïne-envelop (RG), eenfluorescerende reporter, en TVA (de aan EnvA verwante oppervlakte receptor diegeen homoloog in zoogdiercellen heeft). De slices werden vervolgens geïnfecteerdmet ENVA pseudogetyped RABV ΔG. Na 3-4 dagen bracht de RABV mono-transsynaptischetracing de presynaptische ingangen van die ene neuron aan het licht.Hierna konden we gekoppelde opnames doen tussen verbonden KC-CA3 cellen.Daarnaast konden we de presynaptische partners van de starter CA3 pyramidale celkwantificeren
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Añaños, Gamarra Eduardo Martín, Burgos Piero Chichizola, Loro Abel Israel Colmenares, Rivera Gianella Chávez, and Guillén Ernesto Alonso Sosa. "¡Vamos app!" Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2021. http://hdl.handle.net/10757/656837.

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En esta investigación se analiza el desarrollo de la aplicación llamada “Vamos App”, que permite medir el aforo de los locales en tiempo real. La idea surge dada la coyuntura en la que se encuentra el país, donde estamos en un proceso constante de adaptación a las necesidades actuales, con aforos reducidos y distanciamiento social obligatorio. Además, el estilo de vida en general es cada vez más dinámico y la gente tiene menos tiempo para esperar. Por ello, esta aplicación permitirá a los usuarios conocer el aforo de los locales y conocer cuáles son los que tienen espacio disponible según la ubicación de la persona. Además, en nuestra versión “Premium” se podrá acceder a otros beneficios como descuentos, la posibilidad de hacer reservas, entre otros. La investigación nos ha permitido confirmar la viabilidad del proyecto, incursionando nuestra aplicación en el mercado peruano. Para ello, hemos utilizado las redes sociales como nuestro canal de ventas principal, lo que nos permitió obtener resultados satisfactorios expresados en las ventas realizadas. Posteriormente, se realizó el proceso de validación de problema y de la idea de negocio, para luego realizar los planes a futuro, con lo que se obtuvo el plan financiero. Los resultados de nuestra investigación se pueden resumir en que nuestro VAN es de 53,933.27, con retorno en el año 2 y nuestro TIR es de 57.70%, lo que demuestra la viabilidad del proyecto.
This research analyzes the development of the application called "Vamos App", which allows measuring the capacity of the premises in real time. The idea arises given the current situation in the country, where we are in a constant process of adaptation to current needs, with reduced capacity and mandatory social distancing. In addition, the lifestyle in general is increasingly dynamic and people have less time to wait. Therefore, this application will allow users to know the capacity of the premises and to know which ones have available space according to the location of the person. In addition, in our "Premium" version you can access other benefits such as discounts, the possibility of making reservations, among others. The research has allowed us to confirm the viability of the project, entering our application in the Peruvian market. For this, we have used social networks as our main sales channel, which allowed us to obtain satisfactory results expressed in the sales made. Subsequently, the process of validation of the problem and the business idea was carried out, to then carry out the future plans, with which the financial plan was obtained. The results of our research can be summarized in that our NPV is 53,933.27, with a return in year 2 and our IRR is 57.70%, which shows the viability of the project.
Trabajo de investigación
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Ortiz, Encalada Rafael. "¿Hacia dónde vamos?" IUS ET VERITAS, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/122522.

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Olmedo, Juan Pablo. "Probono : ¿Hacia dónde vamos?" IUS ET VERITAS, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/123142.

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Books on the topic "Vamps"

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Collins, Nancy A. Vamps. New York: HarperTeen, 2008.

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Collins, Nancy A. Vamps. New York: HarperCollins, 2009.

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Vamps. New York, NY: DC Comics, 1994.

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Hinson, Lorna. Vamps. Round Rock, TX: Torquere Press, 2009.

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Sklavounakos, Stathēs. Vamps. Athēna: Hermēs, 2001.

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Paglia, Camille. Vamps & tramps. Madrid: Valdemar, 2001.

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Ostinato vamps: Poems. Pittsburgh, Pa: University of Pittsburgh Press, 2003.

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Sparks, Kerrelyn. Vamps and the city. New York: Avon Books, 2006.

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Sparks, Kerrelyn. Vamps and the city. New York: Avon Books, 2006.

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Vamps & tramps: New essays. New York: Vintage Books, 1994.

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Book chapters on the topic "Vamps"

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Wagner, Kristen Anderson. "Pie Queens and Virtuous Vamps." In A Companion to Film Comedy, 39–60. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781118327821.ch2.

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Clarke, Liz. "Vamps and Virgins: The Women of 1920s Hollywood War Romances." In New Perspectives on the War Film, 39–57. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-23096-8_3.

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George, Susan A. "Saturday Matinee Cautionary Tales: Science Fiction Vamps and Promethean Scientists." In Gendering Science Fiction Films, 47–84. New York: Palgrave Macmillan US, 2013. http://dx.doi.org/10.1057/9781137321589_3.

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Tracy, Robert. "Loving You All Ways: Vamps, Vampires, Necrophiles and Necrofilles in Nineteenth-Century Fiction." In Sex and Death in Victorian Literature, 32–59. London: Palgrave Macmillan UK, 1990. http://dx.doi.org/10.1007/978-1-349-10280-8_3.

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Clarke, Robert. "¿Adónde vamos?" In Mastering Spanish, 111–24. London: Macmillan Education UK, 1995. http://dx.doi.org/10.1007/978-1-349-13467-0_9.

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Carreres, Ángeles, María Noriega-Sánchez, and Carme Calduch. "Vamos a traducir." In Mundos en palabras, 23–54. New York : Routledge, 2017.: Routledge, 2018. http://dx.doi.org/10.4324/9781315162379-3.

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Gontijo, Viviane. "Vamos às compras!" In Colloquial Portuguese of Brazil, 211–28. Third Edition / Viviane Gontijo. | Milton Park, Abingdon, Oxon; New York, NY: Routledge, [2016] | Series: The Colloquial Series | English and Portuguese. | Second edition was written by: Esmenia Simäoes Osborne, Joäao Sampaio and Barbara McIntyre, 2003.: Routledge, 2016. http://dx.doi.org/10.4324/9781315813301-12.

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Gontijo, Viviane. "Vamos nos divertir!" In Colloquial Portuguese of Brazil, 43–64. Third Edition / Viviane Gontijo. | Milton Park, Abingdon, Oxon; New York, NY: Routledge, [2016] | Series: The Colloquial Series | English and Portuguese. | Second edition was written by: Esmenia Simäoes Osborne, Joäao Sampaio and Barbara McIntyre, 2003.: Routledge, 2016. http://dx.doi.org/10.4324/9781315813301-3.

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Nielsen, Aldon Lynn. "Vamp Till Ready." In The Inside Songs of Amiri Baraka, 1–19. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-75758-8_1.

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Vázquez-Cedeira, Marta, Diana M. Monsalve, Marta Sanz-García, Pedro A. Lazo, Thierry Galli, Véronique Proux-Gillardeaux, Xosé R. Bustelo, et al. "VAMP1/2/3/7." In Encyclopedia of Signaling Molecules, 1957–63. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_627.

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Conference papers on the topic "Vamps"

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Leshchyshyn Mykolaivna, Maryna, Svitlana Stepanivna Garkavenko, and Antonina Ivanivna Babich. "Studying the similarities of deformation properties of leather materials in the process of creating a model of shoes." In The 8th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2020. http://dx.doi.org/10.24264/icams-2020.i.10.

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Determination of values and dependencies of deformation and physical and mechanical properties of materials of shoe models and finished products. According to the results of theoretical, analytical and marketing research, a number of experimental tests of materials have been carried out to prove the practical significance of the work, namely tests for: deformation of the vamp part of the product, uniaxial and biaxial stretching, bending, dry and wet friction, adhesion, elongation and tearing. There has been established the nature of the distribution of the total elongations of the samples of the vamps cut from different areas of the leather, as well as the ability of the leather material to be formed when improving the shape of the product or changing the shape of the shoetree. The processes of deformation of the vamp part of shoe blanks, physical and mechanical properties of different groups of modern materials and values analysis of similarity of their deformation properties have been studied. There has been created a working model-transformer for carrying out preliminary measurement of clients’ feet at the individual order. The expediency of these works has been proved experimentally. A working version of a model-transformer for foot measurements has been made and as a result of the works approbation, a sample of shoes has been made. The ergonomic properties of the manufactured footwear have been improved due to the use of materials with enhanced physical and mechanical properties. The article investigates the deformation of the most vulnerable vamp part of the men's model of a typical model, as well as the physical and mechanical characteristics of leather materials for manufacturing models and shoes of this type. Providing high quality and comfort of footwear, accuracy of parameters selection of foot measurement, zones of beams and achievement of form stability of footwear with a top from genuine leathers has been predicted.
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Hoang, O., Z. Azzegagh, C. Garcia, J. R. Flores Gonzalez, A. M. Jaramillo, M. J. Tuvim, and B. F. Dickey. "VAMP3 and VAMP8 in Airway Mucin Secretion." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a7467.

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Iriarte, A., L. A. Martínez, and R. Alfaro. "VAMOS." In SPIE Astronomical Telescopes + Instrumentation, edited by Tadayuki Takahashi, Stephen S. Murray, and Jan-Willem A. den Herder. SPIE, 2012. http://dx.doi.org/10.1117/12.925757.

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Currano, Rebecca, So Yeon Park, Lawrence Domingo, Jesus Garcia-Mancilla, Pedro C. Santana-Mancilla, Victor M. Gonzalez, and Wendy Ju. "¡Vamos!" In AutomotiveUI '18: 10th International Conference on Automotive User Interfaces and Interactive Vehicular Applications. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3239060.3241680.

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Wunder, Bernhard, Gunther Lehmann, and Klaus D. Müller-Glaser. "VAMP." In the 33rd annual conference. New York, New York, USA: ACM Press, 1996. http://dx.doi.org/10.1145/240518.240541.

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Burke, Robin, Gediminas Adomavicius, Ido Guy, Jan Krasnodebski, Luiz Pizzato, Yi Zhang, and Himan Abdollahpouri. "VAMS 2017." In RecSys '17: Eleventh ACM Conference on Recommender Systems. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3109859.3109957.

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Thimmaraju, Kashyap, Bhargava Shastry, Tobias Fiebig, Felicitas Hetzelt, Jean-Pierre Seifert, Anja Feldmann, and Stefan Schmid. "The vAMP Attack." In CCS '17: 2017 ACM SIGSAC Conference on Computer and Communications Security. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3140649.3140651.

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Schmitt, C. "VAMOS: HOT NEWS AND PERSPECTIVES." In Proceedings of the French–Japanese Symposium. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814417952_0049.

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Budura, Georgeta, and Cornel Balint. "Pairing strategy for VAMOS downlink transmission." In 2014 11th International Symposium on Electronics and Telecommunications (ISETC). IEEE, 2014. http://dx.doi.org/10.1109/isetc.2014.7010768.

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Ferrel, P. J., and R. F. Meyer. "Vamp: the Aldus application framework." In Conference proceedings. New York, New York, USA: ACM Press, 1989. http://dx.doi.org/10.1145/74877.74897.

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Reports on the topic "Vamps"

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Author, Not Given. VAMAS Nb{sub 3}Sn test conductor. Office of Scientific and Technical Information (OSTI), January 1994. http://dx.doi.org/10.2172/426088.

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Creuziger, Adam, and Mark Vaudin. Report on VAMAS round robin of ISO 13067 :. Gaithersburg, MD: National Institute of Standards and Technology, 2011. http://dx.doi.org/10.6028/nist.ir.7814.

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Roach, C. A., and J. R. Cantrell. Vamp{trademark} coverage area for personnel protection. Office of Scientific and Technical Information (OSTI), January 1995. http://dx.doi.org/10.2172/102492.

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Gnanapragasam, E. K., and C. Yu. Application of the RESRAD computer code to VAMP scenario S. Office of Scientific and Technical Information (OSTI), March 1997. http://dx.doi.org/10.2172/469181.

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Dubivsky, Paul M., and Richard W. Bukowski. False alarm study of smoke detectors in Department of Veterans Affairs Medical Centers (VAMCS). Gaithersburg, MD: National Institute of Standards and Technology, 1989. http://dx.doi.org/10.6028/nist.ir.89-4077.

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González-Mahecha, Esperanza, Livia Minoja, Lucas Rosse Caldas, and Clémentine Tribouillard. Vamos construir verde?: Guia prático para edificações, espaços públicos e canteiros sustentáveis no Brasil. Inter-American Development Bank, June 2020. http://dx.doi.org/10.18235/0002417.

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Tribouillard, Clémentine, Esperanza González-Mahecha, Lucas Rosse Caldas, and Livia Minoja. Vamos construir verde?: Guia prático para edificaçoes, espaços públicos e canteiros sustentáveis no Brasil (Resumo executivo). Banco interamericano de Desarrollo, November 2020. http://dx.doi.org/10.18235/0002847.

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Cosmelli, Liz, and Raissa Ferreira, eds. MAPI Monitors – Os desafios sociais, ambientais e econômicos na pandemia: onde estamos e para onde vamos? E-papers Servicos Editoriais Ltda, December 2020. http://dx.doi.org/10.48207/23181818/bm0906.

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Betsill, J. D., and R. D. Gruebel. VAMOS: The verification and monitoring options study: Current research options for in-situ monitoring and verification of contaminant remediation and containment within the vadose zone. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/120929.

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Kleinman, LI, SR Springston, PH Daum, Y.-N. Lee, AJ Sedlacek, G. Senum, and J. Wang. Pre-Cloud Aerosol, Cloud Droplet Concentration, and Cloud Condensation Nuclei from the VAMOS Ocean-Cloud-Atmosphere Land Study (VOCALS) Field Campaign First Quarter 2010 ASR Program Metric Report. Office of Scientific and Technical Information (OSTI), August 2011. http://dx.doi.org/10.2172/1023451.

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