Relevant bibliographies by topics / Apg-1

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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 'Apg-1'

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

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Journal articles on the topic "Apg-1"

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Olszewski, Michael W., Samara J. Danan, and Thomas J. Boerth. "Effects of Enhanced APG Surfactant on Leaching and Wettability of Six Bark Substrates." HortTechnology 18, no. 2 (January 2008): 295–300. http://dx.doi.org/10.21273/horttech.18.2.295.

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Alkyl phenol ethoxylate (APE) surfactants are used in horticultural substrates but are considered nonbiodegradable, whereas others such as alkyl polyglucoside (APG) are derived from biodegradable sugar compounds. APE reduced total porosity (TP), container capacity (CC), and aeration porosity (AP) whereas APG with polyalkylene oxide block copolymer surfactant (APG/BLK) increased TP, CC, and AP for some substrates but other substrates remained unaffected by either surfactant. We determined substrate leaching fraction (LF) and wettability rating (WR) after drenches of 0.003 to 0.2 mL·L−1 APG/BLK for six bark substrates for three wetting cycles. After the third wetting cycle, five substrates had reduced LF and increased WR. Drenches of 0.2 mL·L−1 APE or APG/BLK for three wetting cycles indicated that APE was more efficacious than APG/BLK for reducing LF or increasing WR. APE was determined to be an effective surfactant for difficult-to-wet substrates, but drenching sometimes reduced TP. No reductions in TP were noted when using APG/BLK. Drenching rates of 0.003–0.2 mL·L−1 APG/BLK for three successive wetting cycles reduced LF and increased WR for most substrates, indicating potential usage for some horticultural applications.
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Vicens, Margarita, Amparo Caubet, and Virtudes Moreno. "Interaction of Pd(II) and Pt(II) Amino Acid Complexes With Dinucleotides." Metal-Based Drugs 4, no. 1 (January 1, 1997): 43–50. http://dx.doi.org/10.1155/mbd.1997.43.

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The interaction of the dinucleotides d(ApG) and d(ApA) with [Pd(aa)Cl2], where aa = L- or D-histidine or the methyl ester of L-histidine, and with [Pt(Met)Cl2], where Met = L-methionine was studied by H1 and C13 NMR and CD measurements. In the case of the L-histidine and L-histidineOMe, the reaction with d(ApG) appeared to give the bifunctional adducts Pd(L-Histidine)N1(1)N7(2) and Pd(L-HisOMe)N1(1)N7(2), but the behavior with D-histidine suggested the formation of the monofunctional adduct Pd(D-His)N7(2). The reaction of L-histidine with d(ApA) seemed to form the bimetallic adduct (L-His)PdN7(1)N7(2)Pd(L-His). The Pt(II)-L-methionine complex in both reactions with d(ApG) and d(ApA) seemed to yield mainly adducts Pt(L-Met)N7(1)N7(2) but the existence of adducts Pt(L-Met)N1(1)N7(2) cannot be ruled out.
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Modeß, Johannes M. "Apg 4,32–37 14.6.2020 1. Sonntag nach Trinitatis." Göttinger Predigtmeditationen 74, no. 3 (March 31, 2020): 332–36. http://dx.doi.org/10.13109/gpre.2019.74.3.332.

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Modeß, Johannes M. "Apg 4,32–37 14.6.2020 1. Sonntag nach Trinitatis." Pastoraltheologie 109, no. 5 (March 31, 2020): 332–36. http://dx.doi.org/10.13109/path.2020.109.5.332.

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Chen, Lihong, Chun Wang, Hengchuan Liu, Guanjian Liu, and Xingwu Ran. "Antibacterial Effect of Autologous Platelet-Rich Gel Derived from Subjects with Diabetic Dermal Ulcers In Vitro." Journal of Diabetes Research 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/269527.

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Background. Autologous platelet-rich gel (APG) is an effective method to improve ulcer healing. However, the mechanisms are not clear. This study aimed to investigate the antibacterial effect of APG in vitro.Methods. Platelet-rich plasma (PRP), platelet-poor plasma (PPP) and APG were prepared from whole blood of sixteen diabetic patients with dermal ulcers. Antibacterial effects againstStaphylococcus aureus,Escherichia coli, andPseudomonas aeruginosawere evaluated by bacteriostasis assay of APG, PRP, and APG-APO (APG combined with apocynin), with phosphate-buffered saline (PBS) and PPP as the control group.Results. (1) Compared to the PBS and PPP, the APG and APG-APO groups showed strong antibacterial activity againstStaphylococcus aureus. There was no significant difference(P>0.05)between APG and APG-APO. (2) Compared to PBS, APG, APG-APO, and PRP showed obvious antibacterial effects againstEscherichia coliandPseudomonas aeruginosa. No significant difference(P>0.05)was revealed among the three groups. Compared to the PPP group, they did not show antibacterial effect againstEscherichia coliandPseudomonas aeruginosa(P>0.05).Conclusions. APG has antibacterial effect againstStaphylococcus aureusmediated by platelet activation in the diabetic patients with dermal ulcer, and does not present obvious antibacterial effect againstEscherichia coliorPseudomonas aeruginosa. Combination of APG and antibiotics may have synergistic antibacterial effect.
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Plasger, Georg. "Apg 6, 1–7 17.8.2008 13. Sonntag nach Trinitatis." Göttinger Predigtmeditationen 62, no. 3 (April 2007): 364–69. http://dx.doi.org/10.13109/gpre.2007.62.3.364.

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Hadem, Eva. "Apg 3, 1-10 26.8.2012 12. Sonntag nach Trinitatis." Göttinger Predigtmeditationen 66, no. 3 (April 2011): 370–75. http://dx.doi.org/10.13109/gpre.2011.66.3.370.

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Gehring, Hans-Ulrich. "Apg 12, 1-11 23.9.2012 16. Sonntag nach Trinitatis." Göttinger Predigtmeditationen 66, no. 4 (July 2011): 406–12. http://dx.doi.org/10.13109/gpre.2011.66.4.406.

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Tsapara, Anna, Karl Matter, and Maria S. Balda. "The Heat-Shock Protein Apg-2 Binds to the Tight Junction Protein ZO-1 and Regulates Transcriptional Activity of ZONAB." Molecular Biology of the Cell 17, no. 3 (March 2006): 1322–30. http://dx.doi.org/10.1091/mbc.e05-06-0507.

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The tight junction adaptor protein ZO-1 regulates intracellular signaling and cell proliferation. Its Src homology 3 (SH3) domain is required for the regulation of proliferation and binds to the Y-box transcription factor ZO-1-associated nucleic acid binding protein (ZONAB). Binding of ZO-1 to ZONAB results in cytoplasmic sequestration and hence inhibition of ZONAB's transcriptional activity. Here, we identify a new binding partner of the SH3 domain that modulates ZO-1–ZONAB signaling. Expression screening of a cDNA library with a fusion protein containing the SH3 domain yielded a cDNA coding for Apg-2, a member of the heat-shock protein 110 (Hsp 110) subfamily of Hsp70 heat-shock proteins, which is overexpressed in carcinomas. Regulated depletion of Apg-2 in Madin-Darby canine kidney cells inhibits G1/S phase progression. Apg-2 coimmunoprecipitates with ZO-1 and partially localizes to intercellular junctions. Junctional recruitment and coimmunoprecipitation with ZO-1 are stimulated by heat shock. Apg-2 competes with ZONAB for binding to the SH3 domain in vitro and regulates ZONAB's transcriptional activity in reporter gene assays. Our data hence support a model in which Apg-2 regulates ZONAB function by competing for binding to the SH3 domain of ZO-1 and suggest that Apg-2 functions as a regulator of ZO-1–ZONAB signaling in epithelial cells in response to cellular stress.
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Bastian, Februadi, Ani Suryani, and Titi Candra Sunarti. "PENINGKATAN KECERAHAN PADA PROSES SINTESIS SURFAKTAN NONIONIK ALKIL POLIGLIKOSIDA (APG) BERBASIS TAPIOKA DAN DODEKANOL." Reaktor 14, no. 2 (August 8, 2012): 143. http://dx.doi.org/10.14710/reaktor.14.2.143-150.

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Alkylpolyglycosides (APG) is a nonionic surfactant that has been getting some green labels such asEcocert, EU Eco-flower and Green Seal as an environmentally friendly surfactant. Sugar is the mainraw material which is supplied the hydrophilic group, and fatty alcohol as hydrophobic group. Someundesirable compounds formed during the APG production and caused low quality. The aim of thisresearch to increase the quality and performance of APG, by controlling its process. Addition 0-10%of activated carbon and 0-0.3% of NaBH4 in APG pre-purification process; 2% (w/w) of H2O2, 35%and 500 ppm of MgO in the bleaching process were examined to process high quality and highperformance of APG. The best APG was obtained from purification step by addition 0% of activatedcarbon and 0.2% of NaBH4, with the characteristics of clarity of 59.02(%T); the ability to reducesurface and interfacial tensions at 1% concentration were 61.94% and 95.6% respectively; 81.71%of stability of emulsion, 62.5% of foam height and stable up to 315 minutes. Alkil Poliglikosida (APG) merupakan surfaktan nonionic yang telah mendapatkan beberapa greenlabel seperti Ecocert, EU Eco-flower Green Seal dan sebagainya sebagai surfaktan yang ramahlingkungan. Bahan dasar APG yaitu gula untuk membentuk gugus hidrofiliknya dan fatty alcoholuntuk membentuk gugus hidrofobiknya. Permasalahan dalam produksi APG adalah timbulnya warnagelap yang tidak dikehendaki yang menyebabkan penurunan mutu APG. Tujuan dari penelitian iniyaitu untuk meningkatkan mutu dan kinerja dari APG. Untuk meningkatkan kecerahan APG, makasebelum dilakukan proses destilasi dilakukan penambahan arang aktif 0-10% serta NaBH4 0-0,3%.Pada proses pemucatan ditambahkan 2% (b/b) H2O2 35% dan MgO 500 ppm. Hasil terbaik yaitupenambahan arang aktif 0% dan NaBH4 0,2% dengan karakteristik kecerahan 59,02(%T);kemampuan menurunkan tegangan permukaan dan antar muka pada konsentrasi 1% sebesar 61,94%dan 95,6%; kestabilan emulsi 81,71%, tinggi busa 62,5% dan umur busa 315 menit.
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Dissertations / Theses on the topic "Apg-1"

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Nonoguchi, Kosuke. "Cloning of human cDNAs for Apg-1 and Apg-2, menbers of the Hsp 110 family, and chromosomal assignment of their genes." Kyoto University, 2000. http://hdl.handle.net/2433/180836.

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Berglund, Carl Johan. "Det uppskjutna gränsöverskridandet : Apg 10:1–11:18, Luk 7:1–10 och frågan om narrativ enhet mellan Lukasevangeliet och Apostlagärningarna." Thesis, Uppsala universitet, Nya testamentets exegetik, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-288474.

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För att utvärdera H. J. Cadburys axiom att Luk och Apg utgör ett kontinuerligt verk i två delar, görs en översikt över frågorna om gemensamt författarskap, receptionshistoria, genre och narrativ enhet, samt en narrativ analys av Apg 10:1–11:18 och Luk 7:1–10 med syfte att bedöma om de två delberättelserna visar tecken på att tillhöra en samlad eller två skilda huvudberättelser. De två delberättelsernas narrativa värld och karaktärsgalleri är likartade, deras implice rade författares attityder och tendenser är desamma, och deras intriger passar väl in i en övergripande intrig, oavsett om Luk och Apg ses som en berättelse i två delar, eller som två berättelser med litterära relationer till varandra. Delberättelsernas radikalt olika narra tiva struktur, och att ingen i Apg 10:1–11:18 visar någon kunskap om att händelserna i Luk 7:1–10 ägt rum, talar för att de två delberättelserna tillhör två olika huvudberättelser.
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Carlbark, Linnea. "”Vad Gud har gjort rent skall inte du göra orent.” : Inkluderingen av hedningarna i den tidiga Jesusrörelsen En studie av Apg 10:1–48." Thesis, Uppsala universitet, Nya testamentets exegetik, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352363.

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Litterär och historisk studie av Apostlagärningarna 10:1-48 som försöker svara på frågeställningarna: Hur presenterar Apg 10:1–48 inkluderingen av hedningar i den tidiga judiska Jesusrörelsen? Vilka problem övervinns och vilka aktörer driver igenom förändringen? Uppstatsen studerar både perikopen i sitt historiska sammanhang och genom att studera narrativet. För att närma sig texten och se vilka bibliska motiv det finns för att möjliggöra den etiskt pluralistiska religion kristendomen är idag. Uppsatsen studerar litteratur historiska länkar, judiska renhetsföreskrifter, geografiska platser för perikopen, de olika karaktärerna och narrativets struktur.
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Stegh, Alexander H. "Effektormechanismen CD95-(APO-1-FAS)-vermittelter Apoptose." [S.l.] : [s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=961531592.

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Arias, Chávez Dennis, and Sevillano Luis Miguel Cangalaya. "Investigar y escribir con APA 7 [Capítulo 1]." Universidad Peruana de Ciencias Aplicadas (UPC), 2021. http://hdl.handle.net/10757/654533.

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El propósito de este libro es ayudar a los estudiantes, docentes y profesionales de las ciencias sociales y humanas a comunicar los resultados de investigación, ya sea en formato tesis o artículo científico. Para ello, el texto proporciona un conjunto de pautas formales para la organización, estructuración y redacción de estos dos géneros. Investigar y escribir con APA 7 toma como base los lineamientos establecidos en la séptima edición del Manual APA (2020) y desarrolla ejemplos reales y modélicos que ayudarán al lector a tener un mejor entendimiento de la forma de presentar estos textos. De esa manera, el libro es una herramienta que ayuda a dinamizar el proceso formativo de los estudiantes de pregrado y posgrado, mejorar los procesos de enseñanza y encaminar las actividades investigativas con miras a publicar los resultados.
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Rama, Nicolas. "La Nétrine-1, un facteur de guidage et de survie neuronale pendant le développement du système nerveux central." Thesis, Lyon 1, 2011. http://www.theses.fr/2011LYO10059/document.

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Le développement du système nerveux central fait intervenir de nombreux processus cellulaires comme la prolifération, la différenciation, l'apoptose, la migration neuronale et le guidage axonal. Ces processus sont finement régulés et aboutissent à la formation d'un système nerveux central fonctionnel. Au cours de cette thèse, je me suis principalement intéressé à une molécule chimiotropique, la Nétrine-1 et à ses récepteurs APP (Amyloïd-b Precursor Protein) et DCC (Deleted in Colorectal Cancer). La Nétrine-1 est impliquée à la fois dans le contrôle de la navigation neuronale (ie migration neuronale et guidage axonal) et dans celui de la survie neuronale. Un premier aspect de mon travail a consisté à étudier le rôle d'un nouveau récepteur à la Nétrine-1 : APP. Nous avons donc démontré que APP est un récepteur à la Nétrine-1 impliqué dans le guidage des axones commissuraux. En effet, APP collabore avec DCC afin de stimuler la croissance axonale en réponse à la Nétrine-1. Le second aspect de mon travail a été l'étude du rôle de la Nétrine-1 en tant que facteur de survie neuronale. En effet, son récepteur DCC appartient à la famille des récepteurs à dépendance. En absence de Nétrine-1, DCC ne reste pas inactif, mais déclenche une signalisation pro-apoptotique qui va éliminer la cellule. Nous avons démontré que pendant le développement du système nerveux, la Nétrine-1 inhibe cette signalisation et contrôle la survie des neurones commissuraux. Le contrôle de la signalisation pro-apoptotique de DCC par la Nétrine-1 pourrait ainsi réaliser un contrôle qualité des projections axonales et faciliter l'orientation du cône de croissance lors du guidage du cône de croissance
The development of the central nervous system requires several cellular processes such as proliferation, differentiation, apoptosis, neuronal migration and axon guidance. This whole process is finely regulated and leads to the formation of a functional central nervous system. During my thesis, I have mainly worked on a chemotropic molecule, Netrin-1 and its receptors APP (Amyloid-ß Precursor Protein) and DCC (Deleted in Colorectal Cancer). Netrin-1 is involved in both neuronal navigation (neuronal migration and axonal guidance) and neuronal survival. I have firstly investigated the role of a new Netrin-1 receptor, APP during axonal guidance. We have shown that APP is involved in the guidance of commissural axons. Indeed, APP collaborates with DCC in order to promote axonal outgrowth in response to Netrin-1. Thereafter, I have investigated the role of Netrin-1 as a neuronal survival factor. In fact, the Netrin-1 receptor DCC belongs to the dependence receptor family. In absence of Netrin-1, DCC does not remain inactive, since it triggers a pro-apoptotic signalling pathway. During the development of the central nervous system, we have shown that Netrin-1 blocks the pro-apoptotic signalling pathway and promotes neuronal survival. The Netrin-1 control of DCC pro-apoptotic signalling might carry out a “quality control” of the axonal projection or/and it could promote the steering of the growth cone during axonal guidance
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Jackson, David Brian. "Functional characterisation of Drosophila AP-1." Thesis, University of London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.407390.

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Mühlenbeck, Frank. "Aktivierung nicht-apoptotischer Signalwege durch TRAIL und anti-APO-1." [S.l.] : Universität Stuttgart , Fakultät Geo- und Biowissenschaften , Institut für Zellbiologie und Immunologie, 2000. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB8619084.

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Camus, Grégory. "Rôle du complexe AP1 dans la morphogenèse du VIH-1." Paris 7, 2008. http://www.theses.fr/2008PA077189.

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La formation de virions infectieux lors des étapes tardives de la réplication du VIH requiert trois composants structuraux du virus, (1) le précurseur Gag qui forme le corps des virions ; (2) la glycoprotéine d'enveloppe (Env) qui, incorporée dans les virions, leur confère leur infectiosité ; (3) les ARN génomiques viraux. Récemment, plusieurs liens ont été établis entre la biogenèse des rétrovirus et la voie endosomale : il a été montré que des interactions entre Gag et des facteurs cellulaires du transport vésiculaire étaient cruciales pour la production des virions. Durant ma thèse, nous avons rapporté une nouvelle interaction entre Gag du VIH-1, et le complexe d'adaptine AP1. Le domaine Matrice de Gag interagit directement avec la sous-unité mu d'AP1. De plus, l'absence d'AP1 réduit la libération de virions, alors qu'au contraire sa surexpression augmente la production virale. Enfin, nous avons montré qu'AP1 interagit avec Tsg101 : composant de la machinerie ESCRT indispensable au bourgeonnement du VIH. En conclusion, nos résultats suggèrent qu'AP1 est essentiel à la production virale du VIH-1. Au cours de ma thèse, je me suis également intéressé aux processus d'incorporation des glycoprotéines d'enveloppe virales. Nous avons, au laboratoire, montré que le cofacteur cellulaire TIP47 agit comme un connecteur entre Gag et Env du VIH-1 et est crucial pour l'incorporation d'Env dans les virions. Enfin, j'ai étudié les processus d'incorporation d'autres envefoppes virales. Nos résultats préliminaires suggèrent que l'incorporation des enveloppes de MLV et VSVg serait indépendante de TIP47 alors que celle du lentivirus VISmac nécessiterait la présence de ce cofacteur
Infectious virions morphogenesis during the late steps of HIV-1 replication cycle, requires three viral components: (1) Gag precursor, which forms the viral core; (2) the envelope glycoprotein (Env) which confers their infectivity to virions when incorporated ; (3) viral genomic RNA. Recently, several links have been made between retroviruses biogenesis and cellular proteins involved in the vesicular trafficking. During my PhD, we have found a new interaction between HIV-1 Gag and the adaptor complexe AP1. The matrix domain of Gag interacts directly with the mu subunit of AP1. Moreover, depletion of AP1 reduces virions production while overexpression increases it. Finally, we have shown that AP1 interacts with Tsg101, a component of the ESCRT machinery crucial to HIV-budding. In conclusion, our results suggest that AP1 is essential to HIV-1 virions production. I have also been interested in the incorporation process of the viral envelope glycoprotein. I have participated to a study, lead in the team, that shows that cellular factor TIP47 act as connector between HIV-1 Gag and Env proteins and is crucial for the incorporation of Env in virions. Finally, I have been interested in the incorporation process of other viral envelopes. Our first results indicate that incorporation of MLV Env ans VSVg would not be dependent on TIP47 while incorporation of SlVmac Env would require the presence of this cellular protein
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Gazon, Helène. "Étude de la régulation d’HBZ et son rôle sur la biogénèse des miARN chez les patients infectés par HTLV-1." Thesis, Antilles-Guyane, 2014. http://www.theses.fr/2014AGUY0806/document.

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HTLV-1, un rétrovirus endémique des Antilles-Guyane qui infecte plus de 10 millions de personnes dans le monde, est l’agent étiologique de l’ATL, une leucémie agressive des lymphocytes T CD4+ résistante aux traitements conventionnels actuels. Le rôle émergent des miARN dans la leucémogénèse et la résistance aux chimiothérapies a soulevé des interrogations quant à leurs rôles dans le développement de l’ATL. Les miARN sont de petits ARN non codant qui régulent l’expression génique. Récemment leur altération durant le cycle de vie du HTLV-1 a été mise en lumière. Une des caractéristiques de l’émergence de l’ATL est la perte d’expression des protéines virales codées par le promoteur en amont du génome proviral (LTR5’), à l’exception d’hbz dont l’expression est initiée dans le promoteur en aval du génome proviral (LTR3’). Dans une première étude, nous démontrons, dans un modèle mimant la cellule ATL, qu’HBZ module sa propre transcription à travers une boucle de rétrocontrôle qui implique une coopération avec le facteur de transcription de la famille AP-1 JunD. Nous montrons que l’expression d’HBZ induit des caractéristiques phénotypiques de fibroblastes transformés. Nous avons, ensuite, analysé l’effet d’HBZ sur les miARN dans les cellules ATL et montré qu’il induit une diminution des miARN cellulaires via l’inhibition d’un acteur clé de la maturation, Dicer. En accord avec notre première étude, nous montrons que l’induction d’HBZ dans les CD4+ de patients ATL corrèle avec une augmentation de la charge provirale (CPV) et donc l’évolution de l’ATL. Le traitement de ces cellules au VPA inhibe l’expression d’hbz, restaure celle de dicer et inverse la CPV et donc la prolifération des cellules malignes ex vivo
HTLV-1, a retrovirus endemic of Antilles-Guyana that infects more than 10 million people worldwide, is the etiological agent of ATL, an aggressive leukemia of CD4+ T lymphocytes resistant in currents treatments. The emerging role of miRNA in leukemogenesis and chemoresistance has risen questioning about their role in ATL development. MiRNAs are a class of non-coding RNAs that regulate gene expression. Involvement of their alteration in the HTLV-1 life cycle has recently come to light. One of the hallmarks of progression toward ATL is the emergence of LTR5’-deficient provirus and thereby eliminating the expression of all viral proteins on the sense strands in these cells, with the exception of the hbz gene regulated by an independent promoter in the 3’LTR. In a first study, using a provirus with the 5’LTR deleted, we found that HBZ modulates its own expression through a positive-feedback loop that involves cooperation with AP-1 transcription factor JunD. We also found that hbz-expressing fibroblasts displayed of a transformed phenotype. Then, we analyzed the effect of HBZ on miRNA expression in ATL patients and report that hbz reduce significantly expression of cellular miRNAs via inhibition of an enzyme essential for maturation, Dicer1. In agreement with our previous study, we show that hbz expression in ATL samples correlates with HTLV-1–provirus load (CPV) and consequently progression of the pathology. VPA treatment of these cells inhibits hbz expression, restores Dicer expression, and inverts the proviral charge thereby reducing cellular proliferation of malignant cells
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Books on the topic "Apg-1"

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Klein, Hans Hubert. Sie waren versammelt: Die Anfänge christlicher Versammlungen nach Apg 1-6. Münster: Aschendorff Verlag, 2015.

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Rettung für alle: Die Romreise des Paulus nach Apg 27, 1-28, 16. Berlin: Philo, 2003.

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1948-, Grilli Massimo, ed. Gottes Wort in menschlicher Sprache: Die Lektüre von Mt 18 und Apg 1-3 als Kommunikationsprozess. Stuttgart: Verlag Katholisches Bibelwerk, 2004.

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Gyurkovics, Tibor. Apa csak 1 van. Budapest: Móra, 1987.

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Kavvathas, Vasile s. 50 [syn] 1 grammata apo enan autocheira. Athe na: Ekd. "Gno se ", 1989.

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Dēmaras, K. Th. Symmikta 1: Apo tēn paideia stēn logotechnia. Athēna: Spoudastērio Neou Ellēnismou, 2000.

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Hartung, Paul J., Mark L. Savickas, and W. Bruce Walsh, eds. APA handbook of career intervention, Volume 1: Foundations. Washington: American Psychological Association, 2015. http://dx.doi.org/10.1037/14438-000.

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Anshel, Mark H., Trent A. Petrie, and Jesse A. Steinfeldt, eds. APA handbook of sport and exercise psychology, volume 1: Sport psychology (Vol. 1). Washington: American Psychological Association, 2019. http://dx.doi.org/10.1037/0000123-000.

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APL, Conference (1996 Lancaster England). Conference proceedings: APL 96, the Conference on APL, July 29-August 1, 1996, Lancaster, England. New York: Association for Computing Machinery, 1996.

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Sole trader and partnership accounts workbook (ap1): Accounts preparation 1. [Place of publication not identified]: Osborne Books Ltd, 2012.

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Book chapters on the topic "Apg-1"

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Angel, Peter, and Jochen Hess. "AP-1." In Encyclopedia of Cancer, 222–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_341.

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Böning, Dieter, Michael I. Lindinger, Damian M. Bailey, Istvan Berczi, Kameljit Kalsi, José González-Alonso, David J. Dyck, et al. "AP-1." In Encyclopedia of Exercise Medicine in Health and Disease, 88. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_2107.

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Angel, Peter, and Jochen Hess. "AP-1." In Encyclopedia of Cancer, 1–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27841-9_341-2.

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Angel, Peter, and Jochen Hess. "AP-1." In Encyclopedia of Cancer, 306–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-46875-3_341.

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Chauveau, M. "Accuracy of Venous Compliance Measurements with Air Plethysmography (APG)." In Phlebology ’95, 292–94. London: Springer London, 1995. http://dx.doi.org/10.1007/978-1-4471-3095-6_134.

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Freeman, Adam. "Creating an Angular App, Part 1." In Essential TypeScript, 419–42. Berkeley, CA: Apress, 2019. http://dx.doi.org/10.1007/978-1-4842-4979-6_17.

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Freeman, Adam. "Creating a Vue.js App, Part 1." In Essential TypeScript, 501–25. Berkeley, CA: Apress, 2019. http://dx.doi.org/10.1007/978-1-4842-4979-6_21.

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Freeman, Adam. "Creating a Vue.js App, Part 1." In Essential TypeScript 4, 515–39. Berkeley, CA: Apress, 2021. http://dx.doi.org/10.1007/978-1-4842-7011-0_21.

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Freeman, Adam. "Creating an Angular App, Part 1." In Essential TypeScript 4, 435–55. Berkeley, CA: Apress, 2021. http://dx.doi.org/10.1007/978-1-4842-7011-0_17.

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Riesen, Kaspar. "Klassen des Java API Verwenden (Teil 1)." In Java in 14 Wochen, 53–74. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-30313-6_3.

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Conference papers on the topic "Apg-1"

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Chen, Jianyong, Chengzhe Wu, Lingling Jiao, Leilei Zhao, Yunlong Zhou, Dongbo Li, Guozhi Tang, et al. "Abstract 73: Development of APG-3526 as a novel and highly efficacious MCL-1 inhibitor." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-73.

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Rachman, A., D. U. C. Rahayu, A. P. Gustianthy, and Y. K. Krisnandi. "Optimization of butanolysis reaction: Synthesis of alkyl polyglycoside (APG) from 1-butanol and glucose for enhanced oil recovery (EOR) application." In PROCEEDINGS OF THE 5TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0008004.

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Nicoson, Rodney, and Julian Knudsen. "Design and Analysis of the Waukesha APG1000 Engine." In ASME 2006 Internal Combustion Engine Division Fall Technical Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/icef2006-1517.

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Waukesha Engine, in cooperation with the Department of Energy, has designed a new high efficiency natural gas engine designed specifically for the power generation market. The APG1000 (Advance Power Generation) engine is capable of achieving 1 MW output at 42% thermal efficiency and less than 1 g/bhp-hr Nox. A design method using modern tools such as 3-D modeling, rapid prototyping and computer simulation have, in a large part, contributed to the success of this engine. This paper discusses the methodology and tools used in the design of the APG engine.
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Zing, Carlos, and Shadi Mahjoob. "Numerical Analysis of Thermal Transport in Nano Fluidic Porous Filled Heat Exchangers for Electronics Cooling." In ASME 2017 Heat Transfer Summer Conference. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/ht2017-4966.

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The exponential growth in electronic power has brought amazing technology but with it also comes a burden in high heat production that threatens the safety of the product since electronics’ failure rate increases by its operating temperature. As such, cooling techniques have a key role to keep the temperature of electronics devices, such as processors, memory and graphics chips, below a maximum operating temperature. In this work, a porous filled heat exchanger has been numerically modeled to investigate the cooling effectiveness and temperature distribution on the base of the heat exchanger subjected to high heat flux leaving these devices. The effects of different nanofluid coolants (0.75% double walled carbon nanotube in water (DWCNT), 1% alumina in water, and 1% diamond in 20:80 ethylene glycol/water), porous materials (copper and annealed pyrolytic graphite (APG)), and porosity values are investigated. The coolant enters from an inlet channel normal to the base, moves through the porous field, and then leaves the heat exchanger through two opposite exit channels parallel to the base. The study is performed for two and three dimensional geometries in which two different designs are studied for 3D cases. One of the designs has a rectangular cross sectional inlet channel (along transverse direction) and the other design has square one. The results indicate that utilizing APG porous matrix, for all studied coolants of pure water and water based nano fluidics, improves substantially the cooling of the base of the heat exchanger in 2D and 3D with rectangular inlet. The results also show that utilizing carbon nanofluids (DWCNT) as coolant for high porosity structures, in both copper and APG porous matrices, improves cooling efficiency and temperature uniformity over the base, for all 2D and 3D cases. The effect of inlet channel geometry, square and rectangular, is also investigated for either similar velocity or similar mass flow rate at the inlet channel entrances.
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Fang, Douglas D., Qiuqiong Tang, Yanhui Kong, Qixin Wang, Jiaxing Gu, Xu Fang, Peng Zou, et al. "Abstract 3192: Activation of p53 in the tumor microenvironment by MDM2 inhibitor APG-115 synergizes with PD-1 blockade independently of p53 status of tumor cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-3192.

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Fang, Douglas D., Qiuqiong Tang, Yanhui Kong, Qixin Wang, Jiaxing Gu, Xu Fang, Peng Zou, et al. "Abstract 3192: Activation of p53 in the tumor microenvironment by MDM2 inhibitor APG-115 synergizes with PD-1 blockade independently of p53 status of tumor cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-3192.

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Reinbold, Ed, and Daniel Mather. "Development of the Waukesha 16V150 LTD Advanced Power Generation Engine." In ASME 2006 Internal Combustion Engine Division Fall Technical Conference. ASMEDC, 2006. http://dx.doi.org/10.1115/icef2006-1510.

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Waukesha Engine has developed an advanced power generation engine using technologies that were developed as part of the Department of Energy-Advanced Reciprocating Engine Systems (ARES) program. The engine uses lean-burn technologies for high efficiency, and low NOx emissions. The technical goals for the ARES program were 50% Brake Thermal Efficiency (BTE) and 0.075 g/kW-hr NOx emissions (with aftertreatment). The goals for the Waukesha Engine Phase 1 Advanced Power Generation (APG) engine are 42% Brake Thermal Efficiency (BTE) and 0.75 g/kW-hr (1.0 g/Bhp-hr) NOx emissions, capable of 0.075 g/kW-hr (0.1 g/Bhp-hr) with aftertreatment. The barriers and technical paths applied to achieve this performance are discussed in this paper.
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Fang, Douglas D., Hengrui Zhu, Qiuqiong Tang, Qixin Wang, Na Li, Xu Fang, Ping Min, Guangfeng Wang, Dajun Yang, and Yifan Zhai. "Abstract 1096: FMS-like tyrosine kinase 3 (FLT3) inhibition by olverembatinib (HQP1351) downregulates MCL-1 and synergizes with BCL-2 inhibitor APG-2575 in preclinical models of FLT3-mutant acute myeloid leukemia (AML)." In Proceedings: AACR Annual Meeting 2021; April 10-15, 2021 and May 17-21, 2021; Philadelphia, PA. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1538-7445.am2021-1096.

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Frey, Joe, and Peter Carter. "API 579-1 / ASME FFS-1 Power Industry Examples." In ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-26070.

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The use of the fitness-for-service (FFS) standard API 579-1/ASME FFS-1 is increasing in the power industry. A fitness-for-service evaluation in a power plant can be performed to determine whether a unit can run safely until the next planned outage. This evaluation can save a significant amount of money. Examples of the effective application of API 579-1/ASME FFS-1 in the power industry are provided in this paper.
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Osage, David A., and Jeremy L. Janelle. "API 579-1/ASME FFS-1 2007: A Joint API/ASME Fitness-for-Service Standard for Pressurized Equipment." In ASME 2008 Pressure Vessels and Piping Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/pvp2008-61796.

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The first edition of API 579 Recommended Practice for Fitness-For-Service was published in 2000. Work on the second edition of API 579 was initiated the same year with many planned technical improvements. In addition to technical improvements, API and ASME agreed to form a joint committee to produce a joint API/ASME FFS Standard that can be used for pressure-containing equipment. This new standard designated as API 579-1/ASME FFS-1 2007 Fitness-For-Service is based on the first edition of API 579, incorporates all planned technical enhancements originally slated for the second edition, and also includes modifications to address the special needs of other industries such as the fossil electric power industry, and the pulp and paper industry. Insights into the driving force to create API 579 and an overview of the technical enhancements that will be incorporated into API 579-1/ASME FFS-1 are presented in this paper. The use of the API 579-1/ASME FFS-1 fitness-for-service assessment procedure models to establish a probability of failure for use with the API Risk Based Inspection Planning Technology is also provided.
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Reports on the topic "Apg-1"

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Fenner, Richard B. APS Science 2018 Vol. 1. Office of Scientific and Technical Information (OSTI), December 2018. http://dx.doi.org/10.2172/1490823.

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Fenner, Richard B. APS Science 2019 Volume 1. Office of Scientific and Technical Information (OSTI), January 2019. http://dx.doi.org/10.2172/1598338.

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Fenner, Richard. APS Science 2020 Volume 1. Office of Scientific and Technical Information (OSTI), January 2021. http://dx.doi.org/10.2172/1817911.

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Hahn, U., D. Shu, and T. M. Kuzay. APS beamline standard components handbook, Version 1. 3. Office of Scientific and Technical Information (OSTI), February 1993. http://dx.doi.org/10.2172/6712866.

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Benaroya, R., and B. Roop. APS storage ring vacuum chamber: Section 1, Evaluation. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/93503.

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Hahn, U., D. Shu, and T. M. Kuzay. APS beamline standard components handbook, Version 1.3. Revision 1. Office of Scientific and Technical Information (OSTI), February 1993. http://dx.doi.org/10.2172/10136996.

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Shadday, M. A. APT Blanket Thermal Analyses of Top Horizontal Row 1 Modules. Office of Scientific and Technical Information (OSTI), September 1999. http://dx.doi.org/10.2172/12338.

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Reynolds, R., and R. Hink. APT cooling water supply make-up trade study. Revision 1. Office of Scientific and Technical Information (OSTI), August 1996. http://dx.doi.org/10.2172/289378.

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Nian, H. L. T., T. M. Kuzay, and I. C. A. Sheng. Thermo-mechanical optimization of photon shutter 1 for APS front ends. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/87839.

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Morgan, James, and /Fermilab. Proposed Magnet Alignment Changes for AP-1. Office of Scientific and Technical Information (OSTI), February 2001. http://dx.doi.org/10.2172/984582.

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