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Статті в журналах з теми "Array segment"
Commins, Deirdre, Sanjeev Gupta, and Joseph Cartwright. "Deformed streams reveal growth and linkage of a normal fault array in the Canyonlands graben, Utah." Geology 33, no. 8 (August 1, 2005): 645–48. http://dx.doi.org/10.1130/g21433ar.1.
Повний текст джерелаМистонов, А. А., И. С. Дубицкий, А. Х. А. Елмекави, Е. Г. Яшина, С. В. Сотничук, K. С. Напольский та Д. Менцель. "Изменение направления оси легкого намагничивания массивов сегментированных нанонитей Ni/Cu с увеличением длины сегмента Ni". Физика твердого тела 63, № 7 (2021): 881. http://dx.doi.org/10.21883/ftt.2021.07.51037.237.
Повний текст джерелаZheng, Fuzhong, Shaochun Huang, Yuan Zhai, Yi Xiang, and Ying Wu. "LED Device Based on Single-Walled Carbon Nanotube Arrays." Journal of Nanoelectronics and Optoelectronics 16, no. 3 (March 1, 2021): 368–73. http://dx.doi.org/10.1166/jno.2021.2963.
Повний текст джерелаGarcía Fernández, Javier, Víctor Vega Martínez, Andy Thomas, Víctor de la Prida Pidal, and Kornelius Nielsch. "Two-Step Magnetization Reversal FORC Fingerprint of Coupled Bi-Segmented Ni/Co Magnetic Nanowire Arrays." Nanomaterials 8, no. 7 (July 19, 2018): 548. http://dx.doi.org/10.3390/nano8070548.
Повний текст джерелаZheng, M., Z. Z. Wu, and Z. Q. Zhu. "Partitioned stator flux reversal machines having Halbach array PMs." COMPEL: The International Journal for Computation and Mathematics in Electrical and Electronic Engineering 35, no. 2 (March 7, 2016): 396–406. http://dx.doi.org/10.1108/compel-12-2015-0442.
Повний текст джерелаTomčík, Peter, and Dušan Bustin. "Interdigitated Array Diffusion Layer Titration of Dithiocarbamates with Electrogenerated Hypobromite." Collection of Czechoslovak Chemical Communications 65, no. 6 (2000): 1029–34. http://dx.doi.org/10.1135/cccc20001029.
Повний текст джерелаTimofeev, Evgeniy Alexandrovich. "On a Segment Partition for Entropy Estimation." Modeling and Analysis of Information Systems 27, no. 1 (March 23, 2020): 40–47. http://dx.doi.org/10.18255/1818-1015-2020-1-40-47.
Повний текст джерелаLandschulz, WH, PF Johnson, and SL McKnight. "The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins." Science 240, no. 4860 (June 24, 1988): 1759–64. http://dx.doi.org/10.1126/science.3289117.
Повний текст джерелаIriarte, Juan Carlos, IÑigo Ederra, RamÓn Gonzalo, Yan Brand, Aurelien Fourmault, Yves Demers, Luca Salgetti-Drioli, and Peter de Maagt. "EBG Superstrate Array Configuration for the WAAS Space Segment." IEEE Transactions on Antennas and Propagation 57, no. 1 (January 2009): 81–93. http://dx.doi.org/10.1109/tap.2008.2009732.
Повний текст джерелаBernards, A., J. M. Kooter, and P. Borst. "Structure and transcription of a telomeric surface antigen gene of Trypanosoma brucei." Molecular and Cellular Biology 5, no. 3 (March 1985): 545–53. http://dx.doi.org/10.1128/mcb.5.3.545.
Повний текст джерелаДисертації з теми "Array segment"
Eclache-Saudreau, Virginie. "Analyse des altérations structurales du génome dans la Leucémie Lymphoïde Chronique : apport de l’hybridation génomique comparative sur puces à ADN (CGH –array)." Paris 13, 2011. http://www.theses.fr/2011PA132047.
Повний текст джерелаB-cell chronic lymphocytic leukemia (CLL) is the most frequent leukemia in western countries. Genomic abnormalities detected by Fluorescence in situ hybridization (FISH) are emerging prognostic indicators important in CLL. These ones are observed in about 80% of CLL patients and have been associated to defined subgroups with different clinical outcomes. In this project, different techniques have been performed aiming at the identification of new genetic abnormalities in CLL. FISH was the most sensitive one, identifying deletion del13q14 in 54% of 314 patients with a restriction to the D13S319 marker. We showed that the del13q deletion was heterogeneous and the clonality of the deletion was highly variable, ranging from 7 to 90 %, monoallelic in most cases but biallelic in 9. 5% and concomitantly mono and bi-allelic in 15% of the cases. We also used Comparative Genomic Hybridization performed on DNA array (CGH-a) that measured differences in DNA copy number between patients and reference genomes. We observed variable sizes of deletion ranging from a Minimal deleted region (BCMS) including microRNAs 15 /16 to a very large region of 60 Mb, including RB1 or protocadherin in the opposite sides. CGH-array allowed to detect a deletion del14q in 3 cases, with a fusion between Immunoglobulin gene and a new partner that we identified as ZFP36L1 a member of the tris tetrapolin family of proteins involved in mRNA decay. The functional role of this new fusion gene in leukemogenesis is currently under study
Shen, Yang. "Novel permanent magnet brushless machines having segmented Halbach array." Thesis, University of Sheffield, 2013. http://etheses.whiterose.ac.uk/3376/.
Повний текст джерелаCatelani, Ana Lúcia Pereira Monteiro. "Variação no número de cópias de segmentos de DNA (CNV) em pacientes com surdez sindrômica." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-28062010-123759/.
Повний текст джерелаHearing loss is the most common congenital deficiency and about 70 million people worldwide present some degree of hearing impairment. In addition to its high incidence, hearing loss impacts language, cognition and social and emotional development. However, in a large proportion of patients, the cause of the hearing deficiency cannot be elucidated. We screened copy number changes by 1 Mb-array Comparative Genomic Hybridization (aCGH) in 31 individuals with syndromic hearing impairment whose clinical features were untypical for known disorders. The choice of evaluating syndromic rather than non-syndromic individuals was based on the assumption that they are more likely to carry larger genomic alterations which could be more easily detected by the comparatively low resolution 1 Mb aCCG, which was the available platform when this project started. Copy number changes (CNV) not documented in the database of normal individuals were detected in eight patients, four de novo imbalances and four inherited from a normal parent. The de novo alterations define candidate chromosome segments likely to harbor dosage sensitive genes related to hearing impairment, namely 1q23.3-q25.2, 2q22q23, 6p25.3 and 11q13.2- q13.4. The rare imbalances also present in normal parents might be casually associated with hearing impairment, but also have a possible role as a predisposition factor. When only the de novo CNVs were considered causative for the disease phenotypes, our study revealed relevant copy number changes in 4 patients (13%). If we also count the rare CNVs that had been inherited as possibly causative, the frequency of chromosome imbalances associated with syndromic deafness in our sample becomes 26%. These figures are probably underestimates and will probably become larger when high resolution oligoarray platforms are applied. These results indicate that aCGH is an efficient tool for defining the etiology of syndromic deafness and its use in routine diagnosis of hearing impairment and for genetic counseling is highly recommended.
Locke, Devin Paul. "SEGMENTAL DUPLICATIONS PROMOTE GENOMIC INSTABILITY IN HUMAN CHROMOSOME 15q11-q13." Case Western Reserve University School of Graduate Studies / OhioLINK, 2004. http://rave.ohiolink.edu/etdc/view?acc_num=case1088114861.
Повний текст джерелаGinsz, Michaël. "Characterization of high-purity, multi-segmented germanium detectors." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAE047/document.
Повний текст джерелаRecent developments of electrical segmentation of HPGe detectors, coupled with digital electronics have led to promising applications such as γ-ray tracking, γ-ray imaging or low-background measurements which will benefit from a fine knowledge of the detector response. The IPHC has developed a new scanning table which uses a collimated γ-ray beam to investigate the detector response as a function of the location of the γ-ray interaction. It is designed to use the Pulse Shape Comparison Scan technique, which has been simulated in order to prove its efficiency. An AGATA detector has been thoroughly scanned. 2D classical scans brought out, for example, local charge collection modification effects such as charge sharing, due to the segmentation. For the first time, a 3D, complete pulse-shape database has been established. It will especially allow to improve the overall AGATA array performances
Kohl, Ilana. "Pesquisa de genes e/ou segmentos cromossômicos em pacientes com obesidade, e/ou hiperfagia, atraso do desenvolvimento neuropsicomotor e/ou dificuldades de aprendizado e distúrbios de comportamento." Universidade de São Paulo, 2010. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-07102010-134828/.
Повний текст джерелаSyndromic obesity is defined as obesity occurring in association with several distinct clinical features and mental retardation (MR). Prader-Willi syndrome (PWS) is the most frequent syndromic form of obesity and is characterized by hypotonia, poor sucking in the neonatal period, developmental delay, hyperphagia, obesity, short stature in adolescence, small hands and feet, hypogonadism, learning disabilities and behavior disturbances. Herein, we studied 141 patients with obesity and/or hyperphagia, psychomotor developmental delay and/or learning disabilities and behavior disturbances with the technique of MLPA (multiplex ligation-dependent probe amplification), and 19 patients by SNP-array technique (\"The GeneChip 174; Mapping 100K Set, Affymetrix) to identify copy number variations. By using both techniques we detected deletions or duplications of the genome in ten patients: two deletions at 1p36, two deletions at 12q15q21.1 (twins), a deletion of chromosomes 2p25.3, 6q16.1-q21, and Xp22.13p22.12, a duplication of chromosomes 14q11.2 and Xq26.3, and an unbalanced translocation between chromosomes 3p26.3 and 11q22.3. Monosomy 1p36 and monosomy 6q16 are well-known syndromes and had already been related with obesity. Both syndromes are considered as differential diagnosis of PWS. Several genes related to obesity are mapped in the altered chromosome segments: DRD2, MCHR2, PLCH2, PRKCZ, RAB21, RAB2B, RAB39, TPO and SIM1. Eleven parents were studied by MLPA, SNP array, and / or karyotype analyses, and chromosomal rearrangements were not identified. Therefore, we consider these rearrangements to be causative of the patients´ phenotype. The diagnosis of patients with syndromic obesity is a challenge due to the overlapping of the phenotypes, except for Prader-Willi syndrome that is a clinically recognizable syndrome, mainly in its second phase. The use of techniques that detect copy number variations of the human genome will increase the recognition of new syndromes and also the description of the spectrum of phenotypic variability of known syndromes. These syndromes are a potential source for the understanding of the etiology of the common forms of obesity.
Villela, Darine Christina Maia. "Alterações genômicas e epigenômicas nas manifestações anatomopatológicas e cognitivas da doença de Alzheimer." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-16012015-143817/.
Повний текст джерелаAlzheimer\'s disease (AD) is the most common form of dementia in the population, corresponding to 50-60% of all cases. Although clinical diagnosis seems to be accurate, the definitive diagnosis of the disease can only be made by a post mortem neuropathological exam that certifies the presence of the two hallmarks of AD: the accumulation of extracellular senile plaques containing β-amyloid (Aβ) and the intracellular neurofibrillary tangles containing hyperphosphorylated tau protein. Four genes are known to be involved in the etiology of AD, three of them (APP, PSEN1 and PSEN2) are associated to the familial form of the disease, which show autosomal dominant inheritance and correspond to the more severe and rare type of AD. Despite many genome wide association studies (GWAS), APOE still remains the only unequivocal genetic risk factor associated to the multifactorial form of AD. The discoveries from GWAS using SNPs collectively explain only a small percentage of heritable variation that may contribute in AD risk. Currently, new approaches have been used to investigate the genetic basis of the phenotypical variability inheritance that can influence the susceptibility of complex diseases. The important role of DNA copy number variation (CNV) has been demonstrated by several studies over the last years and shows that genomic imbalances may also significantly contribute to resistance or susceptibility to various complex diseases. Additionally, there is now increasing interest in exploring how epigenetic modifications, in particular DNA methylation, could influence complex diseases etiology. Thus, the major aim of this work were to investigate two aspects related to the multifactorial form of AD: (1) identification of rare CNVs, using array-CGH, that could contribute to the development of the disease, and (2) analysis of the DNA methylation pattern in frontal cortex of individuals with AD. In our study, we identified 6 rare CNVs with relevant gene content to the investigated phenotype. Two distinct subjects with AD from our casuistic presented microduplications in genes that encode different subunits of the same type of Ca2+ voltage channel, the L-type. Furthermore, among the other selected genes, four are involved in different inflammatory process and one encodes the nicotinamide phosphoribosyltransferase enzyme, important mediator of nicotinamide adenine dinucleotide (NAD) biosynthesis. The implication of a possible involvement of Ca2+ intracellular signaling mediators and NAD biosynthesis pathway in the etiology of AD was also reinforced by our analysis of DNA methylation pattern. Interestingly, two important genes, one to intracellular Ca2+ homeostasis and the other to NAD biosynthesis pathway presented CpGs sites differently methylated in the AD subjects
De, Canditiis Bartolomeo. "3D characterization of multi-segmented HPGe detectors : simulation and validation of the PSCS technique and its application for different energies with a 152 Eu source." Thesis, Strasbourg, 2020. http://www.theses.fr/2020STRAE008.
Повний текст джерелаNew generation gamma-ray detectors arrays, such as AGATA, employ multi-segmented high purity germanium detectors in experiments of nuclear physics that require high resolution and efficiency which are obtained thanks to the application of pulse-shape analysis and gamma-ray tracking. These techniques require full volume characterization of the position sensitive detectors. The IPHC developed a scanning table that uses the Pulse Shape Comparison Scan (PSCS) technique to perform this task. Simulations are performed to quantify the accuracy of the PSCS and to validate it.They are applied on a pixelated 3x3 planar detector and a symmetrical S-type AGATA detector. The method is tested with different gamma-ray energies and input statistics. Several real scans are performed as well on both detectors, which are fully characterized. In particular a scan with agamma-ray source of 152Eu, the first ever done, prove some assumptions on which the tracking technique is based
Tsai-MeiHu and 胡采梅. "Contactless Power Array Track with Segment-excited Overlapping-circle Inductive Coupled Structure." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/g36nu8.
Повний текст джерела國立成功大學
電機工程學系
104
This thesis is aimed to utilize the technology of contactless power transmission and implement contactless power array track with segment -excited overlapping-circle inductive coupled structure for power supply of public transportation. First, to improve the stability of power transmission for moving EVs, overlapping-circle inductive coupled structure array is used to provide a uniform distribution of magnetic field. Second, to raise efficiency of overall system, we designed that segment-excited array track controlled by MCU. After that, the transmitting ability is improved by analyzing resonant circuit. Moreover, overlapping-circle inductive coupled structure array is proposed to provide a smooth magnetic field. Proper parameters of coils and lapping way are decided based on magnetic simulation results, so as to increase tolerance of vertical and horizontal offset for EVs on the power track. Based on the experimental results with 15-cm distance, the maximum efficiency comes up to 89.9% with 360-W output power, and the maximum output power of overall system is 759 W with efficiency of 82.95%.
Chang, Ruey-Shyan, and 張瑞賢. "Characteristics Study of Multi-Segment RF-excited CO2 Slab Waveguide and its Array Lasers." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/99590407958505736142.
Повний текст джерела國立清華大學
電機工程學系
89
Abstract Electrical discharge is a common method for the excitation of a gas laser. The RF excitation especially has outstanding performance for uniform discharge. The discharge tube has the characteristic of capacitive loading due to the property of the ion sheath. Without the existence of the ballast resistor, the discharge can still be maintained stably and efficiently. The RF excitation accommodates more input power level than the DC discharge. The operating pressure of the gas can be raised and the laser power will be increased accordingly. With the superior performance mentioned above, the RF excitation still has many advantages such as the lower firing voltage, the electrodeless operation to avoid the sputtering pollution and so on. The standing wave effect in the RF excitation causes the voltage to distribute nonuniformly along the longitudinal electrodes. Segmented excitation can improve the uniformity of the discharge and enhance the laser efficiency. The segmented discharge used in our experiments has the advantages such as uniform discharge, easy power transform to the load, less ohm loss in matching circuit. Reliable components and compact elements make the entire setup more efficient and lower coat. The large area discharge (area-scaling) and the arrayed structure (volume-scaling) have been developed to increase the laser power per unit length. The characteristics of multi-segment RF-excited CO2 slab waveguide and its array lasers with effects of additional xenon gas have been investigated in this thesis. The laser efficiency of 20.5% with 10% xenon is obtained in multi-segmented slab waveguide laser. And in the segmented coupled slab waveguide array, the efficiency is 19.5% with 10% xenon. The efficiency of our segmented structures is superior to the others. The segmented laser structure has shown to be suitable for the RF excitation of CO2 and other gas lasers.
Книги з теми "Array segment"
Fallah, Bahram. Time-driven routing and segment length assignment in field-programmable gate arrays. 1992, 1992.
Знайти повний текст джерелаEasterbrooks, Susan R., and Hannah M. Dostal, eds. The Oxford Handbook of Deaf Studies in Literacy. Oxford University Press, 2020. http://dx.doi.org/10.1093/oxfordhb/9780197508268.001.0001.
Повний текст джерелаMetcalf, Michael, John Reid, and Malcolm Cohen. Coarrays. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198811893.003.0017.
Повний текст джерелаLi, Jing, and Xiao-Ying Huang. Nanostructured crystals: An unprecedented class of hybrid semiconductors exhibiting structure-induced quantum confinement effect and systematically tunable properties. Edited by A. V. Narlikar and Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.16.
Повний текст джерелаЧастини книг з теми "Array segment"
Mehta, Ajay Kumar. "Dynamic Segment Array and Search." In Algorithms for Intelligent Systems, 489–98. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5077-5_44.
Повний текст джерелаBojesen, Jesper, and Jyrki Katajainen. "Interchanging Tw Segments of an Array in a Hierarchical Memory System." In Algorithm Engineering, 159–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/3-540-44691-5_14.
Повний текст джерелаLiu, Zhen, Tim Foresman, John van Genderen, and Lizhe Wang. "Understanding Digital Earth." In Manual of Digital Earth, 1–21. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-32-9915-3_1.
Повний текст джерелаKorstanje, Maximiliano Emanuel. "The Lost Paradise." In Global Perspectives on Religious Tourism and Pilgrimage, 129–41. IGI Global, 2018. http://dx.doi.org/10.4018/978-1-5225-2796-1.ch008.
Повний текст джерелаMatilda S. "Big Data in Social Media Environment." In Social Media Listening and Monitoring for Business Applications, 70–93. IGI Global, 2017. http://dx.doi.org/10.4018/978-1-5225-0846-5.ch004.
Повний текст джерелаSchram, Frederick R., and Stefan Koenemann. "Anostraca." In Evolution and Phylogeny of Pancrustacea, 627–44. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780195365764.003.0042.
Повний текст джерелаL. Yurchenko, Alexander, and Maria O. Zamulina. "Basic Tools and Techniques for Assessing Strength and General Endurance." In Contemporary Advances in Sports Science. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96993.
Повний текст джерелаGardner, Caleb, Reginald A. Watson, Anes Dwi Jayanti, Suadi, Mohsen AlHusaini, and Gordon H. Kruse. "Crustaceans as Fisheries Resources: General Overview." In Fisheries and Aquaculture, 2–20. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780190865627.003.0001.
Повний текст джерелаAjmal Khan, M., and Yasuaki Ishikawa. "Indium (In)-Catalyzed Silicon Nanowires (Si NWs) Grown by the Vapor–Liquid–Solid (VLS) Mode for Nanoscale Device Applications." In Nanowires - Recent Progress. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.97723.
Повний текст джерелаТези доповідей конференцій з теми "Array segment"
Hough, Jessandra, Ryan S. McGinnis, and N. C. Perkins. "Benchmarking the Accuracy of Inertial Measurement Units for Estimating Kinetic Energy." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-63303.
Повний текст джерелаBusuioc, D., M. Shahabadi, A. Borji, and S. Safavi-Naeini. "G/T of multi-segment active arrays - dependence on array configuration." In IEEE Antennas and Propagation Society Symposium, 2004. IEEE, 2004. http://dx.doi.org/10.1109/aps.2004.1329571.
Повний текст джерелаChengcheng Li and Hong Wu. "Study of segment dictionary based on two-dimensional array." In Multimedia Technology (IC-BNMT 2010). IEEE, 2010. http://dx.doi.org/10.1109/icbnmt.2010.5705175.
Повний текст джерелаSumali, Hartono, and Harley Cudney. "Segmented Two-Dimensional Modal-Filtering Sensors." In ASME 1993 Design Technical Conferences. American Society of Mechanical Engineers, 1993. http://dx.doi.org/10.1115/detc1993-0221.
Повний текст джерелаAin, Mohd Fadzil Bin, Ubaid Ullah, Seyi Stephen Olokede, and ZainalArifin Ahmad. "Dual-segment corporate feed four elements array antenna for broadband application." In 2012 IEEE Asia-Pacific Conference on Antennas and Propagation (APCAP). IEEE, 2012. http://dx.doi.org/10.1109/apcap.2012.6333231.
Повний текст джерелаGuo, Jianqiang, Lin Chen, Yu Zhang, Kai Yang, Jinlong Li, and Xiaorong Gao. "Method of ultrasonic phased array imaging based on segment amplitude apodization." In 2013 Far East Forum on Nondestructive Evaluation/Testing: New Technology & Application (FENDT). IEEE, 2013. http://dx.doi.org/10.1109/fendt.2013.6635552.
Повний текст джерелаMerčep, Elena, Neal C. Burton, Xosé Luís Deán-Ben, and Daniel Razansky. "Multi-segment detector array for hybrid reflection-mode ultrasound and optoacoustic tomography (Conference Presentation)." In Multimodal Biomedical Imaging XII, edited by Fred S. Azar and Xavier Intes. SPIE, 2017. http://dx.doi.org/10.1117/12.2251170.
Повний текст джерелаLee, Jia-You, Chih-Yi Liao, and Ming-Han Tsai. "Design and Implementation of Contactless Power Array Track with Segment-excited Inductively Coupled Structure." In 2018 IEEE International Power Electronics and Application Conference and Exposition (PEAC). IEEE, 2018. http://dx.doi.org/10.1109/peac.2018.8590297.
Повний текст джерелаDas, Gourab, Anand Sharma, and Ravi Kumar Gangwar. "Two elements dual segment cylindrical dielectric resonator antenna array with annular shaped microstrip feed." In 2016 Twenty Second National Conference on Communication (NCC). IEEE, 2016. http://dx.doi.org/10.1109/ncc.2016.7561168.
Повний текст джерелаPalunas, Povilas, James R. Fowler, John A. Booth, George Damm, and Greg H. Ames. "Control of the Hobby-Eberly Telescope primary mirror array with the segment alignment maintenance system." In SPIE Astronomical Telescopes + Instrumentation. SPIE, 2004. http://dx.doi.org/10.1117/12.552410.
Повний текст джерелаЗвіти організацій з теми "Array segment"
Dr. Ethan L. Hull. Segmented Monolithic Germanium Detector Arrays for X-ray Absorption Spectroscopy. Office of Scientific and Technical Information (OSTI), March 2011. http://dx.doi.org/10.2172/937096.
Повний текст джерелаErlandson, A., H. Powell, and R. McCracken. Measurements of the radiant efficiency of the flashlamp arrays used in the multi-segment amplifier (MSA). Office of Scientific and Technical Information (OSTI), May 1990. http://dx.doi.org/10.2172/7051214.
Повний текст джерелаJoel, Daniel M., Steven J. Knapp, and Yaakov Tadmor. Genomic Approaches for Understanding Virulence and Resistance in the Sunflower-Orobanche Host-Parasite Interaction. United States Department of Agriculture, August 2011. http://dx.doi.org/10.32747/2011.7592655.bard.
Повний текст джерелаFuruta, Naoki, K. R. Brushwyler, and Gary M. Hieftje. Flow-Injection Analysis Utilizing a Spectrally Segmented Photodiode- Array Inductively Coupled Plasma Emission Spectrometer 1. Microcolumn Preconcentration for the Determination of Molybdenum. Fort Belvoir, VA: Defense Technical Information Center, February 1989. http://dx.doi.org/10.21236/ada205687.
Повний текст джерелаTobias, Benjamin John. A parameterized ray-tracing model for evaluation of hemispherical lensing of a uniform, telecentric object aperture -- performance improvement estimates for segmented scintillators with miniature lens arrays. Office of Scientific and Technical Information (OSTI), April 2018. http://dx.doi.org/10.2172/1431105.
Повний текст джерела