We are proudly a Ukrainian website. Our country was attacked by Russian Armed Forces on Feb. 24, 2022.
You can support the Ukrainian Army by following the link: https://u24.gov.ua/.
Even the smallest donation is hugely appreciated!
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Striated".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Antony Gormley's Another Place and Olafur Eliasson's Your watercolour machine exemplify passages and combinations of smooth and striated space as beings of sensation on planes of technical and aesthetic composition. They are frames which striate the smoothness of light, water, molten iron, etc., using scientific planes of reference. Smooth and striated mix as boundaries between visitors’ bodies and installation become permeable. Optic becomes tactile, becomes haptic, generative engagement. Both artists experiment with the interface between striated and smooth to encourage visitors to experiment and experience sensation. The installations are liquid spaces; forms of perpetual non-permanence which affect and react with others’ behaviours in processes of co-emergence.
2
Huang, Haibo, Jinpeng Liu, Binbin Fan, Xing Chen, Aibing Yu, and Xuedao Shu. "Wear resistance behavior of striated tool for cross wedge rolling." Industrial Lubrication and Tribology 70, no. 6 (August 13, 2018): 942–52. http://dx.doi.org/10.1108/ilt-09-2016-0204.
Purpose The purpose of this paper is to investigate the wear resistance behavior of the striated tool for cross wedge rolling (CWR). Design/methodology/approach A mechanical-thermal coupled, temperature-dependent FE wear model was developed to explore the wear behaviors for striated CWR tools. To verify the proposed FE model, a newly developed measuring device was also developed to measure wear on the tool ridge. To find the impact order of the parameters of striate unit, orthogonal experiment was carried out. Findings The experimental and numerical results both indicate that the wear resistance of striated tool is better than that of smooth tool. Minimum tool ridge wear can be achieved by choosing proper tool contact temperature with striated units on crossed ridge. The order of the striation geometrical factors’ impact on ridge wear is striation width > striation interval > striation length. Research limitations/implications Because of the specified tool, the research results may lack generalizability. Therefore, researchers are encouraged to test the proposed propositions further. Originality/value It is shown that the wear resistance of striated CWR tool is better than that of smooth tool. The information may help CWR manufactures to design and produce tools with less wear.
3
Hering, Jens. "Melanistic Striated Heron Butorides striata in Djibouti." Bulletin of the African Bird Club 21, no. 2 (2014): 234–38. http://dx.doi.org/10.5962/p.310060.
Piechowiak, H., F. Goebel, U. Hirche, and R. Tyrell. "Cranial Sclerosis with Striated Bone Disease (Osteopathia Striata)." Klinische Pädiatrie 198, no. 05 (September 1986): 418–24. http://dx.doi.org/10.1055/s-2008-1033900.
Morris, Tessa Altair, Sarah Eldeen, Richard Duc Hien Tran, and Anna Grosberg. "A comprehensive review of computational and image analysis techniques for quantitative evaluation of striated muscle tissue architecture." Biophysics Reviews 3, no. 4 (December 2022): 041302. http://dx.doi.org/10.1063/5.0057434.
Unbiased evaluation of morphology is crucial to understanding development, mechanics, and pathology of striated muscle tissues. Indeed, the ability of striated muscles to contract and the strength of their contraction is dependent on their tissue-, cellular-, and cytoskeletal-level organization. Accordingly, the study of striated muscles often requires imaging and assessing aspects of their architecture at multiple different spatial scales. While an expert may be able to qualitatively appraise tissues, it is imperative to have robust, repeatable tools to quantify striated myocyte morphology and behavior that can be used to compare across different labs and experiments. There has been a recent effort to define the criteria used by experts to evaluate striated myocyte architecture. In this review, we will describe metrics that have been developed to summarize distinct aspects of striated muscle architecture in multiple different tissues, imaged with various modalities. Additionally, we will provide an overview of metrics and image processing software that needs to be developed. Importantly to any lab working on striated muscle platforms, characterization of striated myocyte morphology using the image processing pipelines discussed in this review can be used to quantitatively evaluate striated muscle tissues and contribute to a robust understanding of the development and mechanics of striated muscles.
Silva, Marcio André, Hilda Fátima Jesus Pena, Herbert Sousa Soares, Juliana Aizawa, Solange Oliveira, Bruna Farias Alves, Dênisson Silva Souza, et al. "Isolation and genetic characterization of Toxoplasma gondii from free-ranging and captive birds and mammals in Pernambuco state, Brazil." Revista Brasileira de Parasitologia Veterinária 27, no. 4 (August 30, 2018): 481–87. http://dx.doi.org/10.1590/s1984-296120180059.
Abstract Recent genetic population studies on Toxoplasma gondii in Brazil have shown large genetic variability. The objective of the present study was to isolate and genotypically characterize T. gondii from free-ranging and captive wild mammals and birds in Pernambuco state, Brazil. Fragments of heart, brain, skeletal muscle and diaphragm tissue from 71 birds and 34 mammals, which were either free-ranging or captive, were collected. Samples from 32 of these animals were subjected to bioassays in mice. Samples from the remaining 73 animals underwent biomolecular diagnosis, using PCR technique, targeting a repetitive DNA fragment of 529 bp in T. gondii. A non-virulent isolate (TgButstBrPE1) was obtained from a free-ranging striated heron (Butorides striata) and, based on primary samples, seven animals were found to be positive. The primary samples and the isolate obtained were subjected to PCR-RFLP using the markers SAG1, 5’3’SAG2, alt.SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1, Apico and CS3. ToxoDB-RFLP genotype #13 from the striated heron isolate and Type BrIII genotype from a captive otter ( Lontra longicaudis) (PS-TgLonloBrPE1) were obtained. The present study describes the first isolation and genotypic characterization of T. gondii in free-ranging striated heron, and the first genotypic characterization of T. gondii in a captive otter.
9
Swynghedauw, B., K. Schwartz, B. Lauer, A. M. Lompre, J. J. Mercadier, J. L. Samuel, and L. Rappaport. "Striated muscle overload." European Heart Journal 9, suppl E (April 2, 1988): 1–6. http://dx.doi.org/10.1093/eurheartj/9.suppl_e.1.
Azibani, Feriel, Antoine Muchir, Nicolas Vignier, Gisèle Bonne, and Anne T. Bertrand. "Striated muscle laminopathies." Seminars in Cell & Developmental Biology 29 (May 2014): 107–15. http://dx.doi.org/10.1016/j.semcdb.2014.01.001.
North, Alison Jane. "Spectrin localisation in mammalian striated muscle." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276872.
Palmer, Roy Emmet. "Striated muscle relaxation : a caged compound study." Thesis, University of Oxford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315026.
Hallett, Peter C. "Scanning force microscopy of striated muscle proteins." Thesis, University of Bristol, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296600.
Caruel, Matthieu. "Mechanics of Fast Force Recovery in striated muscles." Phd thesis, Ecole Polytechnique X, 2011. http://pastel.archives-ouvertes.fr/pastel-00668301.
Cette thèse est consacrée à la modélisation de la réponse transitoire d'une fibre musculaire squelettique soumise à des sollicitations mécaniques rapides. A l'échelle du nanomètre, la fibre musculaire contient des filaments d'actine et de myosine regroupés en unités contractiles appelées "sarcomères". Le filament de myosine est un assemblage de moteurs mol ́eculaires qui, en présence d'ATP, s'attachent et se d ́etachent p ́eriodiquement au filament d'actine. Au cours de ce processus d'attachement-détachement, la myosine génère une force lors d'un changement de conformation appelé "power-stroke". Ses caractéristiques peuvent être étudiées lors de la réponse transitoire de la fibre soumise à des sollicitations mécaniques rapides. Nous proposons un modèle mécanique innovant du demi-sarcomere permettant de relier les caractéristiques de la myosine à la réponse de la fibre complète. A la différence des modèles existants, privilégiant une approche discrète, ce modèle s'appuie sur la définition d'un potentiel d'énergie continu qui prend en compte une interaction de champ moyen entre les moteurs moléculaires. Ce système présente des réponses radicallement différentes à longueur imposée et à force imposée. Nous proposons en particulier une explication à la différence de cinétique observée expérimentalement. Nous montrons également que le demi-sarcomere est m ́ecaniquement instable ce qui explique les inhomogénéités de longueurs observées dans une myofibrille.
5
Ankrett, Richard Joseph. "Conformers of myosin from scallop striated adductor muscle." Thesis, University of Leicester, 1992. http://hdl.handle.net/2381/35712.
Myosin from the striated adductor muscle of scallop (Pecten maximus) folds into a compact 10S conformer, as has been characterized for smooth muscle and non-muscle myosins. The 10S conformer of scallop myosin is favoured at physiological ionic strengths in the absence of Ca2+ and in the presence of nucleotide triphoshate. The folded transition is accompanied by the trapping of the nucleotide at the active site to give a species with a half-time of about an hour at 20C. Ca2+ binding to the specific, regulatory sites on a myosin head promotes unfolding to the extended 6S conformer and activates product release by around 60-fold. The unfolding transition, however, remains much slower than the contraction-relaxation cycle of scallop striated muscle and could not play a role in the regulation of these events. The turnover of nucleotide by the 10S conformer is an order of magnitude slower than the turnover by native scallop filaments. The latter have very similar kinetic properties to that of scallop heavy meromyosin suggesting that the myosin-linked regulatory system requires only the head and neck domain to function properly. Thus there is no evidence, from nucleotide turnover measurements, for an intermolecular interaction occurring between the neck and tail regions of neighbouring myosin in the filament equivalent to that observed as an intramolecular interaction in the 10S conformer. The role of the 10S conformer in striated muscle may therefore be associated with events which occur on a slower time-scale than the contraction-relaxation cycle, such as transport of myosin molecules from their site of synthesis to the myofibril during growth and development of the muscle. Removal of either one or both of the regulatory light chains from scallop myosin prevents, or at least disfavours, formation of the folded 10S conformer. Readdition of the native regulatory light chains, or those from other other molluscan species, restores to the myosin its ability to fold. Labelling the reactive heavy chain thiol of myosin also disfavours formation of the 10S conformer and allows separation of the modified protein from the native molecules.
6
Ochmann, Constanze. "Investigating the role of Klhl31 in striated muscle." Thesis, University of East Anglia, 2013. https://ueaeprints.uea.ac.uk/45561/.
Members of the Kelch-like family display various functions at the cellular level, such as being involved in signalling pathways, as mediators of cytoskeletal changes and most prominently by targeting specific substrates for proteasomal degradation. Previous studies suggested a role for Kelch-like 31 (Klhl31) during myogenesis, as its expression is dependent on signals responsible for the induction of myogenesis in the somites and is slightly delayed compared to the expression of early myogenic regulatory factors. With this study we wanted to analyse the function of Klhl31 during myogenesis in more detail. Using C2C12 mouse myotubes as our model cell line to study myogenic differentiation and myofibrillogenesis, we found that Klhl31 is closely associated with Actin fibres in differentiated, multi-nucleated myotubes and that observed co-localisation can be linked to C2C12 differentiation. Furthermore, we used a Yeast-2-Hybrid screen approach and GST-pull downs to find interaction partners for Klhl31. Putative interacting proteins for Klhl31 were analysed and found to be structural components of the sarcomere with many of them also being involved in myofibrillogenesis, such as Nebulin, Actin, CapZ and tropomyosin. We also analysed a possible role of Klhl31 in proteasomal degradation, as Klhl31 was shown to negatively regulate canonical Wnt-signalling. We gathered evidence that Klhl31 might interact with components of E3-Ubiquitin ligase complexes and might target specific substrates including itself for degradation by the 26S proteasome. Furthermore, we analysed the expression of Klhl31 during heart development in chick embryos, where it was restricted to the myocardium. We concluded that Klhl31 might be important during myofibrillogenesis in striated muscles. A role for Klhl31 in mature muscle might involve providing structural stabilisation in sarcomeres and during muscle contraction.
7
Schuster, Joseph M. "The contribution of titin to striated muscle shortening." Diss., Columbia, Mo. : University of Missouri-Columbia, 2008. http://hdl.handle.net/10355/5758.
Thesis (M.S.)--University of Missouri-Columbia, 2008. The entire dissertation/thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file (which also appears in the research.pdf); a non-technical general description, or public abstract, appears in the public.pdf file. "December 2008" Includes bibliographical references.
8
Briggs, Dustin L. "NATURALLY STRIATED MUSCLE: EXAMINING THE IDEOGRAPHIC CRYSTALLIZATION OF." OpenSIUC, 2016. https://opensiuc.lib.siu.edu/dissertations/1161.
In U.S. America and much of the Western world, natural is a venerated symbolic placeholder for any number of assumed virtues and ideals. Present conflicts have brought forward questions about what natural (which I argue functions as an ideograph) should mean in contexts that seem to call for a formal, enforceable definition. In this study, I use the vocabulary of Deleuze and Guattari (1987) and the context of bodybuilding to work towards a theory of how ambiguous ideographs become "striated" or “crystallized.” Within this discussion I present instances where natural has been employed as a vehicle to cause harm, and I offer an advisement to rhetorical scholars on how we might approach striated ideographs in the future.
9
Essackjee, Hafejee Cassim. "The influence of contraction, pH and enzyme inhibition on the release of adenosine from rat gracilis muscle." Thesis, Hong Kong : University of Hong Kong, 1998. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20565914.
Rogers, Brendan James. "Arrangement and structure of α-actinins in striated muscle". Thesis, University of Leeds, 2018. http://etheses.whiterose.ac.uk/22905/.
The smallest contractile unit within striated muscle cells are called sarcomeres. The boundary regions between sarcomeres are called Z-discs, which contain over 30 different proteins, organised within a narrow ~100 nm wide structure. Standard fluorescence microscopy approaches do not reveal the arrangement of Z-disc proteins, as the width of the Z-disc is below the resolution limit (~250 nm). The arrangement of the actin filaments and the cross-linking proteins α-actinin in the Z-discs are well characterised by electron microscopy (EM) studies, however other Z-disc proteins are not. With the development of super-resolution fluorescence microscopy techniques, it is now possible to obtain Z-disc protein localisation information. Here, dSTORM (direct Stochastic Optical Reconstruction Microscopy) was used, to investigate the arrangement of α-actinins in Z-discs of cardiomyocytes, and then the arrangement of the N-terminal ends of the giant protein titin in the Z-discs. Affimers were generated to bind α-actinin 2 and the N-terminal titin domains (Z1/Z2), to use as binders in dSTORM. Affimers are small (~12 kDa) non-antibody binding proteins, about 1/10th the size of antibodies, that can be selected to bind to a specific protein. The localisation data of dSTORM using the Affimer binders showed the same regular arrangement of α-actinins observed in EM studies. The use of dSTORM with Affimers also suggests the titin Z1/Z2 domains do not only localise at the edges of the Z-discs but arranged throughout the Z-disc with regular spacing (~25 nm) in the transverse plane of the Z-discs. Also, three mutations located in the actin binding domain of α-actinin 2 associated to hypertrophic cardiomyocytes (G111V, A119T and M228T) were characterised by in vitro co-sedimentation assays with actin. The mutants G111V and A119T did not show a significant difference in binding affinity to actin compared to the wild-type. The co-sedimentation assays did however suggest the mutation M228T significantly increases the binding affinity of α-actinin 2.
John, Solaro R., and Moss, Richard L. Ph.D., eds. Molecular control mechanisms in striated muscle contraction. Dordrecht: Kluwer Academic Publishers, 2002.
Solaro, R. John, and Richard L. Moss, eds. Molecular Control Mechanisms in Striated Muscle Contraction. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-015-9926-9.
Lieber, Richard L. Skeletal muscle structure, function, and plasticity: The physiological basis of rehabilitation. 3rd ed. Baltimore: Lippincott Williams & Wilkins, 2010.
Lynch, Gordon S., David G. Harrison, Hanjoong Jo, Charles Searles, Philippe Connes, Christopher E. Kline, C. Castagna, et al. "Striated Muscle Tissue." In Encyclopedia of Exercise Medicine in Health and Disease, 824. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_3085.
Hargitai, Henrik. "Radially Striated Ejecta (Mars)." In Encyclopedia of Planetary Landforms, 1–2. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9213-9_641-1.
Picci, Piero, and Angelo Paolo Dei Tos. "Smooth and Striated Muscle." In Diagnosis of Musculoskeletal Tumors and Tumor-like Conditions, 277–84. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-29676-6_44.
Hargitai, Henrik. "Radially Striated Ejecta (Mars)." In Encyclopedia of Planetary Landforms, 1703–4. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4614-3134-3_641.
Wetzel, Petra, and Gerolf Gros. "Carbonic anhydrases in striated muscle." In The Carbonic Anhydrases, 375–99. Basel: Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8446-4_18.
Edman, K. A. P. "Contractile Performance of Striated Muscle." In Advances in Experimental Medicine and Biology, 7–40. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-6366-6_2.
Kam, Peter, Ian Power, Michael J. Cousins, and Philip J. Siddal. "Striated MusclesSkeletal and Cardiac Muscles." In Principles of Physiology for the Anaesthetist, 73–80. Fourth edition. | Boca Raton : CRC Press, Taylor & Francis Group, 2020.: CRC Press, 2020. http://dx.doi.org/10.1201/9780429288210-12.
Gomes, Aldrin V., Keita Harada, and James D. Potter. "Cation Signaling in Striated Muscle Contraction." In Molecular Control Mechanisms in Striated Muscle Contraction, 163–97. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-015-9926-9_5.
Kinosita, Kazuhiko, Katsuyuki Shiroguchi, M. Yusuf Ali, Kengo Adachi, and Hiroyasu Itoh. "On the Walking Mechanism of Linear Molecular Motors." In Regulatory Mechanisms of Striated Muscle Contraction, 369–84. Tokyo: Springer Japan, 2007. http://dx.doi.org/10.1007/978-4-431-38453-3_31.
F., Fan S., Yun W. B., Rosser R. J., Kirz J., Sayre D., Dewey M. M., and Colflesh D. "Soft X-Ray Diffraction Of Striated Muscle." In Soft X-Rays Optics and Technology, edited by E. Koch and Guenther A. Schmahl. SPIE, 1986. http://dx.doi.org/10.1117/12.964943.
Kozlov, Alexei A., James B. Oliver, John Spaulding, Christopher Smith, Sara MacNally, David Coates, Kyle R. P. Kafka, Amy L. Rigatti, and Stavros G. Demos. "Striated composite layers for high-fluence applications." In Laser-Induced Damage in Optical Materials 2022, edited by Christopher W. Carr, Detlev Ristau, and Carmen S. Menoni. SPIE, 2022. http://dx.doi.org/10.1117/12.2642334.
Wood, J. E. "On statistical-mechanical models for the molecular dynamics of striated muscle." In Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 1988. http://dx.doi.org/10.1109/iembs.1988.94680.
Keglevic, M., and R. Sablatnig. "Learning a Similarity Measure for Striated Toolmarks using Convolutional Neural Networks." In 7th International Conference on Imaging for Crime Detection and Prevention (ICDP 2016). Institution of Engineering and Technology, 2016. http://dx.doi.org/10.1049/ic.2016.0069.
Liu, Xiaoli, Sean Hall, Su Wol Chung, Annarosa Leri, Jan Kajstura, Piero Anversa, and Mark A. Perrella. "Striated Preferentially Expressed Gene Is Transcriptionally Regulated By Differentiation Of Cardiomyocytes." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a4958.
Dobson, John. "Theory of Cohesive Forces in Layered and Striated Nanostructures: Some Surprises." In 2006 International Conference on Nanoscience and Nanotechnology. IEEE, 2006. http://dx.doi.org/10.1109/iconn.2006.340706.
Chen, Jian-Zhang. "Thermally Actuated Droplet Motion on Chemically Homogeneous, Striated, and Defected Surfaces." In 2008 Second International Conference on Integration and Commercialization of Micro and Nanosystems. ASMEDC, 2008. http://dx.doi.org/10.1115/micronano2008-70096.
Experiments have demonstrated thermocapillary actuation on uniformly grafted partial-wettable surfaces. Droplet mobilization only occurs above a threshold thermal gradient or threshold droplet radius [1]. We characterized the motion instead in terms of a threshold depinning force, which successfully describes all the liquids tested. Above the depinning transition, the droplet speed, which is controlled by thermocapillary, capillary and viscous forces, increases monotonically with this reduced force parameterization. These results agree well to numerical predictions of a generalized Ford and Nadim model by using two fitting parameters, the slip coefficient and the magnitude of contact angle hysteresis [2–3]. In this follow-up study, we developed a doubly grafted surface, on which alkyltrichlorosilane coated stripes are surrounded by a more hydrophobic coating, perfluoroctyl-trichlorosilane. The quality of alkyltrichlorosilane coated stripes was still good for the thermocapillary droplet actuation, in which droplets were driven on the alkyltrichlorosilane surface and confined by the perfluoroctyl-trichlorosilane. The experimental results are also well described by a derived approximate three-dimensional model equation, which resembles the parameterization. The droplets are driven by thermocapillary force and retarded by contact angle hysteretic force, represented as contact angle hysteresis. This contact angle hysteresis is caused by chemical heterogeneity, surface roughness etc [4]. In the last part of this presentation, we will also present the thermocapillary droplet motion on a designed defected surface, which shows a tiny defect can severely hinge the droplet.
8
Baltoiu, Andra, Alexandru Nistorescu, Pierre de Hillerin, Mirel Vasiliu, Vlad Valeanu, Tudor Ion, and Calin Marin. "Preliminary qualitative analysis of mechanical impulse propagation dynamics in human striated muscle." In 2015 E-Health and Bioengineering Conference (EHB). IEEE, 2015. http://dx.doi.org/10.1109/ehb.2015.7391413.
BRAUNER, C., G. NAMAH, P. FIFE, C. SCHMIDT-LAINE, B. GOSSANT, and G. UHRIG. "Solid propellant combustion in striated media with application to the hump effect." In 28th Joint Propulsion Conference and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1992. http://dx.doi.org/10.2514/6.1992-3508.
Zhao, Heng, Chao Cai, Xiang He, Ping Ma, and Jinyong Huang. "Generating mechanism and eliminating method of striated haze in advanced mitigation process." In Advanced Optical Manufacturing Technologies, edited by William T. Plummer, Bin Fan, Xiong Li, Xiangang Luo, Mingbo Pu, and Yongjian Wan. SPIE, 2019. http://dx.doi.org/10.1117/12.2504849.
Sun, Lushan, and Jean Parsons. Striated. Ames: Iowa State University, Digital Repository, 2014. http://dx.doi.org/10.31274/itaa_proceedings-180814-1001.
Spotts, Ryan E. Objective forensic analysis of striated, quasi-striated and impressed toolmarks. Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1227283.
Amemiya, Naoyuki. AC Loss Characterization of Striated Multifilamentary YBCO Coated Conductors. Fort Belvoir, VA: Defense Technical Information Center, June 2005. http://dx.doi.org/10.21236/ada451863.
Veillette, J. J., and M. Roy. The spectacular cross-striated outcrops of James Bay, Quebec. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/202923.
Hoeksema, Amy Beth. Statistical methods for the forensic analysis of striated tool marks. Office of Scientific and Technical Information (OSTI), January 2013. http://dx.doi.org/10.2172/1226173.
Heller, Alfred, Martin Gross, and Lisa Won. Characterization of a Dopaminergic Stimulatory Factor Derived From Monoclonal Cell Lines of Striated Origin. Fort Belvoir, VA: Defense Technical Information Center, December 2004. http://dx.doi.org/10.21236/ada430419.
Neve, Rachael L., and Mark F. Bear. Visual Experience Regulates Gene Expression in the Developing Striate Cortex. Fort Belvoir, VA: Defense Technical Information Center, December 1989. http://dx.doi.org/10.21236/ada216149.
Wereszczak, Andrew A., Alicia T. Mayville, S. Toller, Mattison K. Ferber, and Benjamin L. Hackett. Glass Striae and Laser Shock Damage. Office of Scientific and Technical Information (OSTI), December 2018. http://dx.doi.org/10.2172/1484998.
Smith, Yoland. Kainate Receptors in the Striatum: Implications for Excitotoxicity in Huntington's Disease. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada426787.
Smith, Yoland. Kainate Receptors in the Striatum: Implications for Excitoxicity in Huntington's Disease. Fort Belvoir, VA: Defense Technical Information Center, August 2002. http://dx.doi.org/10.21236/ada415869.
