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Academic literature on the topic 'ASTN1'

Author: Grafiati

Published: 6 September 2023

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Journal articles on the topic "ASTN1"

Horn, Zachi, Hourinaz Behesti, and Mary E. Hatten. "N-cadherin provides a cis and trans ligand for astrotactin that functions in glial-guided neuronal migration." Proceedings of the National Academy of Sciences 115, no. 42 (September 27, 2018): 10556–63. http://dx.doi.org/10.1073/pnas.1811100115.

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Prior studies demonstrate that astrotactin (ASTN1) provides a neuronal receptor for glial-guided CNS migration. Here we report that ASTN1 binds N-cadherin (CDH2) and that the ASTN1:CDH2 interaction supports cell–cell adhesion. To test the function of ASTN1:CDH2 binding in glial-guided neuronal migration, we generated a conditional loss of Cdh2 in cerebellar granule cells and in glia. Granule cell migration was slowed in cerebellar slice cultures after a conditional loss of neuronal Cdh2, and more severe migration defects occurred after a conditional loss of glial Cdh2. Expression in granule cells of a mutant form of ASTN1 that does not bind CDH2 also slowed migration. Moreover, in vitro chimeras of granule cells and glia showed impaired neuron–glia attachment in the absence of glial, but not neuronal, Cdh2. Thus, cis and trans bindings of ASTN1 to neuronal and glial CDH2 form an asymmetric neuron–glial bridge complex that promotes glial-guided neuronal migration.

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Behesti, Hourinaz, Taylor R. Fore, Peter Wu, Zachi Horn, Mary Leppert, Court Hull, and Mary E. Hatten. "ASTN2 modulates synaptic strength by trafficking and degradation of surface proteins." Proceedings of the National Academy of Sciences 115, no. 41 (September 21, 2018): E9717—E9726. http://dx.doi.org/10.1073/pnas.1809382115.

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Surface protein dynamics dictate synaptic connectivity and function in neuronal circuits. ASTN2, a gene disrupted by copy number variations (CNVs) in neurodevelopmental disorders, including autism spectrum, was previously shown to regulate the surface expression of ASTN1 in glial-guided neuronal migration. Here, we demonstrate that ASTN2 binds to and regulates the surface expression of multiple synaptic proteins in postmigratory neurons by endocytosis, resulting in modulation of synaptic activity. In cerebellar Purkinje cells (PCs), by immunogold electron microscopy, ASTN2 localizes primarily to endocytic and autophagocytic vesicles in the cell soma and in subsets of dendritic spines. Overexpression of ASTN2 in PCs, but not of ASTN2 lacking the FNIII domain, recurrently disrupted by CNVs in patients, including in a family presented here, increases inhibitory and excitatory postsynaptic activity and reduces levels of ASTN2 binding partners. Our data suggest a fundamental role for ASTN2 in dynamic regulation of surface proteins by endocytic trafficking and protein degradation.

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Chang, Hao, Philip M. Smallwood, John Williams, and Jeremy Nathans. "Intramembrane Proteolysis of Astrotactins." Journal of Biological Chemistry 292, no. 8 (January 18, 2017): 3506–16. http://dx.doi.org/10.1074/jbc.m116.768077.

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Astrotactins are vertebrate-specific membrane proteins implicated in neuron-glia interactions during central nervous system development and in hair follicle polarity during skin development. By studying epitope-tagged derivatives of mouse astrotactin-2 (Astn2) produced in transfected cells, we determined that the amino and carboxyl termini reside in the extracellular space and are initially linked by two transmembrane segments and a single cytoplasmic domain. We further show that Astn2 undergoes proteolytic cleavage in the second transmembrane domain (TM2) and that a disulfide bond holds the resulting two fragments together. Recombinant Astn1 also undergoes TM2 cleavage, as does Astn2 isolated from mouse cerebellum. Astn2 intramembrane proteolysis is insensitive to replacement of TM2 by the transmembrane domain of CD74 or by 21 alanines. However, replacement of TM2 by the transmembrane domain of CD4, the asialoglycoprotein receptor, or the transferrin receptor eliminates intramembrane proteolysis, as does leucine substitution of residues that overlap or are immediately upstream of the cleavage site. Replacement of the transmembrane domain of CD74 or the asialoglycoprotein receptor with Astn2 TM2 leads to the appearance of a carboxyl-terminal fragment consistent with intramembrane proteolysis. These experiments define a highly unusual transmembrane topology for the astrotactins, reveal intramembrane proteolysis as a feature of astrotactin maturation, and constrain the substrate sequences that are permissive for cleavage of one type 2 transmembrane segment.

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Wilson, P. M., R. H. Fryer, Y. Fang, and M. E. Hatten. "Astn2, A Novel Member of the Astrotactin Gene Family, Regulates the Trafficking of ASTN1 during Glial-Guided Neuronal Migration." Journal of Neuroscience 30, no. 25 (June 23, 2010): 8529–40. http://dx.doi.org/10.1523/jneurosci.0032-10.2010.

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McDougall, Annie R. A., Vanny Wiradjaja, Aminath Azhan, Anqi Li, Nadia Hale, Mary E. Wlodek, Stuart B. Hooper, Megan J. Wallace, and Mary Tolcos. "Intrauterine Growth Restriction Alters the Postnatal Development of the Rat Cerebellum." Developmental Neuroscience 39, no. 1-4 (2017): 215–27. http://dx.doi.org/10.1159/000470902.

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Intrauterine growth restriction (IUGR) is a major cause of antenatal brain injury. We aimed to characterize cerebellar deficits following IUGR and to investigate the potential underlying cellular and molecular mechanisms. At embryonic day 18, pregnant rats underwent either sham surgery (controls; n = 23) or bilateral uterine vessel ligation to restrict blood flow to fetuses (IUGR; n = 20). Offspring were collected at postnatal day 2 (P2), P7, and P35. Body weights were reduced at P2, P7, and P35 in IUGR offspring (p < 0.05) compared with controls. At P7, the width of the external granule layer (EGL) was 30% greater in IUGR than control rats (p < 0.05); there was no difference in the width of the proliferative zone or in the density of Ki67-positive cells in the EGL. Bergmann glia were disorganized at P7 and P35 in IUGR pups, and by P35, there was a 10% decrease in Bergmann glial fiber density (p < 0.05) compared with controls. At P7, trophoblast antigen-2 (Trop2) mRNA and protein levels in the cerebellum were decreased by 88 and 40%, respectively, and astrotactin 1 mRNA levels were increased by 20% in the IUGR rats (p < 0.05) compared with controls; there was no difference in ASTN1 protein. The expressions of other factors known to regulate cerebellar development (astrotactin 2, brain-derived neurotrophic factor, erb-b2 receptor tyrosine kinase 4, neuregulin 1, sonic hedgehog and somatostatin) were not different between IUGR and control rats at P7 or P35. These data suggest that damage to the migratory scaffold (Bergmann glial fibers) and alterations in the genes that influence migration (Trop2 and Astn1) may underlie the deficits in postnatal cerebellar development following IUGR.

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Hill, Shirley Y., Daniel E. Weeks, Bobby L. Jones, Nicholas Zezza, and Scott Stiffler. "ASTN1 and alcohol dependence: Family-based association analysis in multiplex alcohol dependence families." American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B, no. 4 (April 9, 2012): 445–55. http://dx.doi.org/10.1002/ajmg.b.32048.

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Yi, Sheng, Shanshan Wang, Qing Zhao, Chun Yao, Yun Gu, Jie Liu, Xiaosong Gu, and Shiying Li. "miR-sc3, a Novel MicroRNA, Promotes Schwann Cell Proliferation and Migration by Targeting Astn1." Cell Transplantation 25, no. 5 (May 2016): 973–82. http://dx.doi.org/10.3727/096368916x690520.

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Fan, Chunli, Quanfu Ma, Xufeng Wu, Xuan Dai, Qiuzi Peng, and Hongning Cai. "Detection of DNA Methylation in Gene Loci ASTN1, DLX1, ITGA4, RXFP3, SOX17, and ZNF671 for Diagnosis of Cervical Cancer." Cancer Management and Research Volume 15 (July 2023): 635–44. http://dx.doi.org/10.2147/cmar.s417877.

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Amaya-Ramirez, Diego, Laura Camila Martinez-Enriquez, and Carlos Parra-López. "Usefulness of Docking and Molecular Dynamics in Selecting Tumor Neoantigens to Design Personalized Cancer Vaccines: A Proof of Concept." Vaccines 11, no. 7 (June 29, 2023): 1174. http://dx.doi.org/10.3390/vaccines11071174.

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Personalized cancer vaccines based on neoantigens are a new and promising treatment for cancer; however, there are still multiple unresolved challenges to using this type of immunotherapy. Among these, the effective identification of immunogenic neoantigens stands out, since the in silico tools used generate a significant portion of false positives. Inclusion of molecular simulation techniques can refine the results these tools produce. In this work, we explored docking and molecular dynamics to study the association between the stability of peptide–HLA complexes and their immunogenicity, using as a proof of concept two HLA-A2-restricted neoantigens that were already evaluated in vitro. The results obtained were in accordance with the in vitro immunogenicity, since the immunogenic neoantigen ASTN1 remained bound at both ends to the HLA-A2 molecule. Additionally, molecular dynamic simulation suggests that position 1 of the peptide has a more relevant role in stabilizing the N-terminus than previously proposed. Likewise, the mutations may have a “delocalized” effect on the peptide–HLA interaction, which means that the mutated amino acid influences the intensity of the interactions of distant amino acids of the peptide with the HLA. These findings allow us to propose the inclusion of molecular simulation techniques to improve the identification of neoantigens for cancer vaccines.

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Wang, Zhi, Cheng Feng, Hao Liu, Tian Meng, Wei-Qing Huang, Ke-Xin Song, and You-Bin Wang. "Exosomes from circ-Astn1-modified adipose-derived mesenchymal stem cells enhance wound healing through miR-138-5p/SIRT1/FOXO1 axis regulation." World Journal of Stem Cells 14, no. 10 (October 26, 2022): 777–90. http://dx.doi.org/10.4252/wjsc.v14.i10.777.

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Dissertations / Theses on the topic "ASTN1"

Bohman, Adam. "Webbaserat gränssnitt till en ASN1 Common-Decoder." Thesis, Luleå tekniska universitet, Institutionen för system- och rymdteknik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-61461.

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When you, as a company, works alongside other companies such as Telia, where information about calls, text messages and internetsurf are saved as files and gets encrypted according to security policies, it’s important that you have a good and trustworthy software that can decode these files. Transforming(decoding) them back to their original state, so that bills etc. can be properly produced. This project has used a decoder that does exactly that as a starting point, and a web-based graphical interface(GUI) has been created with the decoder as a base. This GUI can deocde these particual files and it also allows the user to search for specific information in those files after they have been decoded. It’s a very simple and user friendly construction that will simplify future processes. Instead of using a command-line(CMD), there is now a GUI where you can do exactly what you can in CMD, only simpler and faster.

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Junkunlo, Kingkamon. "Regulation of hematopoiesis in the freshwater crayfish, Pacifastacus leniusculus : role of transglutaminase." Doctoral thesis, Uppsala universitet, Jämförande fysiologi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-327921.

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The freshwater crayfish, Pacifastacus leniusculus, has been used as a model for studying hematopoiesis or blood cell production or hematopoiesis and immunity. The work of this thesis aims to investigate the impact of factors such as ROS signaling, Ast1, and the PVF/PVR signaling pathway in controlling stem cell behavior during hematopoiesis and specifically the role of the crosslinking enzyme transglutaminase (TGase) in regulation of hematopoiesis. The role of ROS in crayfish hematopoiesis was characterized by using the antioxidant named NAC to inhibit ROS production. Low ROS level resulted in a prolonged decrease in hemocyte numbers and a combined injection of LPS and NAC caused a slower rate of new hemocyte production. A low ROS level in cell cultures supplemented with crude Ast1 was found to inhibit cell spreading and a high extracellular TGase activity was detected on the surfaces of APC and HPT cells. We suggest that ROS serves as a prime signal to control proliferation and differentiation of progenitor cells by affecting extracellular TGase activity. We reported an inhibitory effect of Ast1 on TGase enzyme activity and on its crosslinking activity and consequently Ast1 affects the clot formation and thus coagulation by inhibiting the crosslinking activity of the TGase enzyme. Secretion of the clot protein (CP) and the production of CP filament network between spreading cells were observed in HPT cell cultures in vitro. In the presence of CP together with Ast1 in 3D-collagen-I cultures, HPT cells were found to be more elongated and they formed chains of cells throughout the surrounding matrix. In the HPT tissue, CP was located around the HPT cells or around the lobules of HPT, and thus, CP was demonstrated to be a part of ECM and to possibly function together with collagen in generating a suitable environment for HPT progenitor cells. The inhibition of PVF/PVR downstream signaling pathway by Sunitinib malate resulted in a dramatic change of cell morphology and induction of an increase cell surface area during cell culture. The addition of crude Ast1 into the cell cultures in vitro enhanced this effect. Consequently, cell migration was stimulated and a high extracellular TGase activity on HPT cell surface was found after this inhibition. In conclusion, the work in this thesis provides new insight in understanding the role of the extracellular matrix (ECM) and extracellular TGase activity in controlling stem cell activity.

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Jilläng, Emil. "Making ASN.1 (Abstract Syntax Notation One) human-readable : Investigative and practical study to generalize decoding and manual validation of ASN.1 from the cellular network during run time." Thesis, Luleå tekniska universitet, Institutionen för system- och rymdteknik, 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-67595.

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ASN.1 is a powerful formal notation divided into two parts, a specification of the data and the data itself in binary form. Creating decoders for these files can often be tedious. The purpose of this degree work is to extend current tools at Arctic Group to make an application that decodes a range of different ASN.1 specifications and data. This should be done during runtime, without needing to rebuild the application for each specification, while generating human-readable data and abstracting unwanted information. Two ways to create ASN.1 decoders were identified, and the application was designed taking heavy inspiration from a solution that stores intermediate data in a list. By not including encoding as a feature of the application a few shortcuts could be made, and the desired result could be achieved during runtime. The application was designed to include three parts. The first part was an ASN.1 parser using the Java-based tool ANTLR4. The second part matched the binary data to the information in the specification. The final part was an output formatter that abstracts and prettifies the output data to text files. The result was an application that parses at least three of the most commonly used specifications of the employer and does only have to be rebuilt when a new data type is present in the specifications. Problems arose when matching the data to the ASN.1 specifications, thus the matching and output formatting was only partially implemented. The application was evaluated by testing many different ASN.1 specifications, making sure everything was generated correctly during runtime and extending the parser to support more syntax as it was introduced in new specifications. Although the application did not support any arbitrary ASN.1 specification, it could serve as a foundation for further development to make the application truly generalized.
ASN.1 är en kraftfull formell notation uppdelad i två delar. En specifikation av data och medföljande data i binär form. Att skapa avkodare till dessa filer kan ofta vara tidskrävande. Syftet med det här examensarbetet är att vidareutveckla nuvarande verktyg på Arctic Group till en applikation som avkodar ett flertal olika ASN.1-specifikationer och data. Detta skall göras under körning och skall inte kräva att applikationen byggs om för varje specifikation. Applikationen skall även generera mänskligt läsbar utdata och abstrahera bort oönskad information. Två sätt att bygga en ASN.1-avkodare hittades under förstudien och applikationen designades med inspiration av en lösning som sparar data i en mellanliggande lista. Genom att inte inkludera kodning av data i applikationen kunde genvägar tas och det önskade resultatet kunde uppnås under körning. Applikationen designades med tre delar. Den första delen var en ASN.1-läsare som använde verktyget ANTLR4 byggt i Java, den andra en del som matchade informationen från specifikationen till den binära datan. Den sista delen var en formaterare för utdata som även abstraherade bort oönskad information. Resultatet blev en applikation som korrekt läser av minst tre av de mest använda ASN.1-specifikationerna hos uppdragsgivaren och som bara behöver byggas om då en ny datatyp introduceras i specifikationerna. Problem uppstod vid matching av data till specifikationen vilket ledde till att matchningen och formateringen blev bara delvis implementerat. Applikationen utvärderades genom att testa många olika ASN.1 specifikationer, kontrollera att allt genererades korrekt under körning och att utöka läsaren efterhand för att kunna hantera mer syntax då den introducerades i de nya specifikationerna. Även om applikationen inte än stödjer godtycklig ASN.1-specifikation kan den verka som en bas för vidareutveckling mot en mer komplett generaliserad lösning.

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"Overexpression of the ASN1 gene enhances nitrogen status in arabidopsis thaliana." 2000. http://library.cuhk.edu.hk/record=b5890346.

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Chan Hiu-ki.
Thesis (M.Phil.)--Chinese University of Hong Kong, 2000.
Includes bibliographical references (leaves 97-112).
Abstracts in English and Chinese.
Thesis Committee --- p.i
摘要 --- p.ii
Abstract --- p.iii
Acknowledgements --- p.v
Abbreviations --- p.vi
Table of Contents --- p.vii
List of figures --- p.xi
List of tables --- p.xiii
Chapter Chapter 1 --- Literature Review --- p.1
Chapter 1.1 --- Nitrogen assimilation in plants --- p.1
Chapter 1.2 --- Importance of asparagine in plants --- p.5
Chapter 1.3 --- Enzymatic reaction of asparagine synthetase (AS) --- p.8
Chapter 1.4 --- Asparagine synthetase of non-plant organisms --- p.10
Chapter 1.5 --- Biochemistry background of plant asparagine synthetases --- p.12
Chapter 1.6 --- Molecular studies of asparagine synthetase genes in plants --- p.15
Chapter 1.7 --- Arabidopsis thaliana as a model plant --- p.24
Chapter 1.8 --- ASN studies in Arabidopsis thaliana --- p.24
Chapter 1.9 --- Hypothesis --- p.27
Chapter Chapter 2 --- Materials and Methods --- p.29
Chapter 2.1 --- Chemicals --- p.29
Chapter 2.2 --- Plant materials and growth conditions --- p.29
Chapter 2.2.1 --- Surface sterilization of Arabidopsis seeds --- p.29
Chapter 2.2.2 --- "Growth conditions of Arabidopsis seeds for total RNA extraction, enzyme assay, chlorophyll content measurement and dry weight measurement" --- p.30
Chapter 2.3 --- Agrobacterium mediated transformation via vacuum infiltration method --- p.30
Chapter 2.3.1 --- Principles --- p.30
Chapter 2.3.2 --- Plant materials and bacterial strains of Agrobacterium mediated transformation --- p.31
Chapter 2.3.2.1 --- Plant materials --- p.31
Chapter 2.3.2.2 --- Gene constructs --- p.31
Chapter 2.3.2.2 --- Bacterial strains --- p.32
Chapter 2.3.3 --- Agrobacterium mediated transformation via vacuum infilitration --- p.32
Chapter 2.4 --- Screening of transformants --- p.33
Chapter 2.5 --- DNA and RNA manipulation --- p.34
Chapter 2.5.1 --- DNA extraction and quantitation --- p.34
Chapter 2.5.2 --- PCR amplification and detection of transgenes --- p.36
Chapter 2.5.2.1 --- PCR amplification and detection of transgenes --- p.36
Chapter 2.5.2.2 --- Primer sequence --- p.37
Chapter 2.6 --- RNA analysis of transormants --- p.38
Chapter 2.6.1 --- General introduction --- p.38
Chapter 2.6.2 --- RNA extraction --- p.39
Chapter 2.6.3 --- Making single-strand DIG PCR probes --- p.40
Chapter 2.6.4 --- Quantitation of single-strand DIG-labeled probes --- p.42
Chapter 2.7 --- Northern blot analysis --- p.42
Chapter 2.7.1 --- Detection --- p.43
Chapter 2.7.2 --- Film development --- p.43
Chapter 2.8 --- "Amino acid, protein, dry weight and total nitrogen analysis" --- p.43
Chapter 2.8.1 --- Extraction of free amino acids --- p.43
Chapter 2.8.2 --- Protein assay --- p.44
Chapter 2.8.3 --- Determination of nitrogen and carbon content in seeds --- p.45
Chapter 2.8.4 --- Dry weight measurement --- p.45
Chapter 2.8.5 --- Seed storage protein analyses --- p.45
Chapter 2.8.6 --- Detection of chlorophyll content --- p.46
Chapter 2.9 --- Asparagine synthetase activity analysis --- p.46
Chapter 2.9.1 --- Crude extracts preparation --- p.46
Chapter 2.9.2 --- AS enzyme assay --- p.47
Chapter 2.9.3 --- Asparagine content measurement --- p.47
Chapter 2.10 --- In situ hybridization --- p.48
Chapter 2.10.1 --- Making cRNA probe --- p.48
Chapter 2.10.2 --- In situ hybridization --- p.48
Chapter Chapter 3 --- Results --- p.50
Chapter 3.1 --- Construction of ASN1 overexpressing lines --- p.50
Chapter 3.2 --- Changes in nitrogen status during vegetative growth of ASN1 overexpressing lines --- p.53
Chapter 3.3 --- Changes in nitrogen status during seed development of ASN1 overexpressing lines --- p.55
Chapter Chapter 4 --- Discussion --- p.76
Chapter Chapter 5 --- Conclusion --- p.85
Chapter Chapter 6 --- Perspective --- p.86
Appendix --- p.87
References --- p.97

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Books on the topic "ASTN1"

Semonin, Holleran Reneé, and Air & Surface Transport Nurses Association (U.S.), eds. ASTNA patient transport: Principles and practice. 4th ed. St. Louis, Mo: Mosby, 2010.

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Semonin, Holleran Reneé, and Air & Surface Transport Nurses Association (U.S.), eds. ASTNA patient transport: Principles and practice. 4th ed. St. Louis, Mo: Mosby, 2010.

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ba, Mirko Fry. Ume ni z i t s t astne: Buddhova Abhidhamma v praxi meditace a zvla da ni z ivota. Praha: Argo, 2003.

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Ljubková, Marie. Št´astná generace. Režiséři z alterny. Praha, Pražská scéna, 2014, 2013.

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Conference papers on the topic "ASTN1"

Zhou, Michael M. "Planning algorithms of ASTN architectures." In Asia-Pacific Optical and Wireless Communications, edited by S. J. Ben Yoo, Kwok-wai Cheung, Yun-Chur Chung, and Guangcheng Li. SPIE, 2004. http://dx.doi.org/10.1117/12.520636.

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Aquilina, Michael, Peter Dower, Peter Farrell, and Kerry Hinton. "Taking the physical layer seriously in ASTNs." In 2006 Australian Conference on Optical Fibre Technology (ACOFT). IEEE, 2006. http://dx.doi.org/10.1109/acoft.2006.4519233.

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Zhang, Mengjiao, Huimin Zhu, Xin Chang, Zijian Wang, and Honglin Wang. "ASTNN-Based System for Auditing PHP Code." In 2023 IEEE 3rd International Conference on Electronic Communications, Internet of Things and Big Data (ICEIB). IEEE, 2023. http://dx.doi.org/10.1109/iceib57887.2023.10170290.

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Chahine, R., A. Kirstadter, A. Iselt, and S. Pasqualini. "Operational cost reduction using ASON/ASTN." In 2005 Optical Fiber Communications Conference Technical Digest. IEEE, 2005. http://dx.doi.org/10.1109/ofc.2005.192573.

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Wellbrock, Glenn, Marc Barry, Stefan Bodamer, Jan Spath, and Christoph Glingener. "IP over OTH/ASTN: from concepts to real deployments." In Optics East, edited by Benjamin B. Dingel, Werner Weiershausen, Achyut K. Dutta, and Ken-Ichi Sato. SPIE, 2004. http://dx.doi.org/10.1117/12.572393.

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Zhang, Hui, Yuanyuan Ma, Dongfeng Mao, Jie Zhang, and Wanyi Gu. "Comparative study of signaling and routing schemes in ASTN." In Asia-Pacific Optical Communications, edited by Cedric F. Lam, Wanyi Gu, Norbert Hanik, and Kimio Oguchi. SPIE, 2005. http://dx.doi.org/10.1117/12.575083.

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Li, Jingcong, Feng Gao, Jinhua Gao, and Sheping Shi. "Analysis of bandwidth requirements for ASON/ASTN signaling networks." In Asia-Pacific Optical Communications, edited by S. J. Ben Yoo, Gee-Kung Chang, Guangcheng Li, and Kwok-wai Cheung. SPIE, 2005. http://dx.doi.org/10.1117/12.576046.

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Grandy, Holger, Robert Bertossi, Kurt Stenzel, and Wolfgang Reif. "ASN1-light: A Verified Message Encoding for Security Protocols." In Fifth IEEE International Conference on Software Engineering and Formal Methods (SEFM 2007). IEEE, 2007. http://dx.doi.org/10.1109/sefm.2007.8.

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Ni, Haobin, Antoine Delignat-Lavaud, Cédric Fournet, Tahina Ramananandro, and Nikhil Swamy. "ASN1*: Provably Correct, Non-malleable Parsing for ASN.1 DER." In CPP '23: 12th ACM SIGPLAN International Conference on Certified Programs and Proofs. New York, NY, USA: ACM, 2023. http://dx.doi.org/10.1145/3573105.3575684.

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Laborczi, P., and T. Cinkler. "Efficient algorithms for physically-disjoint routing in survivable GMPLS/ASTN networks." In 11th International Telecommunications Network Strategy and Planning Symposium. IEEE, 2004. http://dx.doi.org/10.1109/netwks.2004.240884.

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