標(biāo)題: Titlebook: Microfluidic and Compartmentalized Platforms for Neurobiological Research; Emilia Biffi Book 2015 Springer Science+Business Media New York [打印本頁(yè)] 作者: Jejunum 時(shí)間: 2025-3-21 18:52
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research影響因子(影響力)
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research影響因子(影響力)學(xué)科排名
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書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research被引頻次
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research被引頻次學(xué)科排名
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research年度引用
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書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research讀者反饋
書(shū)目名稱Microfluidic and Compartmentalized Platforms for Neurobiological Research讀者反饋學(xué)科排名
作者: HOWL 時(shí)間: 2025-3-21 20:20 作者: 貧困 時(shí)間: 2025-3-22 00:34
Microfluidic and Compartmentalized Platforms for Neurobiological Research978-1-4939-2510-0Series ISSN 0893-2336 Series E-ISSN 1940-6045 作者: 單獨(dú) 時(shí)間: 2025-3-22 07:18 作者: OUTRE 時(shí)間: 2025-3-22 11:48
https://doi.org/10.1007/978-1-4939-2510-0arraying neurons; cell populations; drug discovery; electrophysiology recordings; hydraulically controll作者: 陳列 時(shí)間: 2025-3-22 14:41
The Fabrication of Microfluidic Platforms with Pneumatically/Hydraulically Controlled PDMS Valves anusly to transfect neurons with different fluorescent presynaptic and postsynaptic markers and then observe in real-time the subsequent process of synapse formation. Additionally, the platform has been an effective tool for investigating the role of glia–neuron communication on synaptic formation and作者: Entirety 時(shí)間: 2025-3-22 18:33 作者: Malleable 時(shí)間: 2025-3-23 01:13 作者: engrave 時(shí)間: 2025-3-23 02:33 作者: CLASP 時(shí)間: 2025-3-23 07:59
Development of Microfluidic Devices for the Manipulation of Neuronal Synapsesng neurons in highly controlled environments wherein different regions of a network, or even a cell, are cultured in fluidically isolated compartments. Enhanced strategies such as highly regulated manipulations of fluid flow and physical guidance cues when combined with this compartmentalization pro作者: 外來(lái) 時(shí)間: 2025-3-23 10:19 作者: glucagon 時(shí)間: 2025-3-23 15:50 作者: 襲擊 時(shí)間: 2025-3-23 20:46
0893-2336 dics and compartmentalized platforms with neuronal cell cultures as well as the strengths of these exciting devices and their precious contribution in the field of Neuroscience..978-1-4939-5561-9978-1-4939-2510-0Series ISSN 0893-2336 Series E-ISSN 1940-6045 作者: 袋鼠 時(shí)間: 2025-3-23 23:35
Bryson M. Brewer,Donna J. Webb,Deyu Li. Measurements are made at specified locations and depths on each part. NSRS data from the hole drilling and slotting measurements were comparable; NSRS data from X-ray diffraction differed and was less repeatable. NSRS data for different milling parameters shows that the depth of NSRS increases wit作者: 試驗(yàn) 時(shí)間: 2025-3-24 05:01 作者: 預(yù)示 時(shí)間: 2025-3-24 09:46
Jonathan West,Ngoc-Duy Dinh,Heike Hardelauf,Ya-Yu Chiang,Tracey A. Newman,Mariana Vargas-Caballero,AVD, and then directly identify modal parameters, i.e., omitting the additional process of constructing the generalized Hankel matrix, which provides a more efficient method of identification of modal parameter. Also, in this paper, the SVD algorithm is introduced to the identification process of Ibr作者: 百科全書(shū) 時(shí)間: 2025-3-24 12:18
Prasanna Sakha,Cecilia Brunello,Joonas Heikkinen,Ville Jokinen,Henri J. Huttunen作者: extract 時(shí)間: 2025-3-24 15:16
Ting Huang,Russell K. Pirlo,Wan Qin,Yongliang Lin,Lina Wei,Lucas Schmidt,Nick Erdman,Tingfei Xi,Maur作者: giggle 時(shí)間: 2025-3-24 19:18
Sara J. Fenstermacher,Maria F. Pazyra-Murphy,Rosalind A. Segal作者: BYRE 時(shí)間: 2025-3-25 02:54 作者: 難解 時(shí)間: 2025-3-25 05:17
Katherine A. Southam,Anna E. King,Catherine A. Blizzard,Graeme H. McCormack,Tracey C. Dickson作者: Myocyte 時(shí)間: 2025-3-25 08:11 作者: CYN 時(shí)間: 2025-3-25 15:22 作者: BROW 時(shí)間: 2025-3-25 17:12 作者: hauteur 時(shí)間: 2025-3-25 22:57
Book 2015nd Compartmentalized Platforms for Neurobiological Research.?provides practical skills needed to fabricate, use microfluidics and compartmentalized platforms with neuronal cell cultures as well as the strengths of these exciting devices and their precious contribution in the field of Neuroscience..作者: 放大 時(shí)間: 2025-3-26 03:19
Asymmetric Genetic Manipulation and Patch Clamp Recording of Neurons in a Microfluidic Chipdies that require specific expression of for example optogenetic tools in presynaptic neurons or for studying the entry of pathogenic particles, such as viruses or oligomers of misfolded proteins, into presynaptic structures.作者: Mendicant 時(shí)間: 2025-3-26 07:46
Development of a Compartmentalized Biochip for Axonal Isolation and Neuronal-Circuit Formation at thtudy glia–neuron interaction at the single-cell level is necessary. In this chapter we describe a biochip-microfabrication technique and a unique laser cell-micropatterning system for creation of a compartmentalized, axon-isolating, polarized neuron-growth platform at the single-cell level.作者: HEDGE 時(shí)間: 2025-3-26 11:02 作者: 特別容易碎 時(shí)間: 2025-3-26 12:55
Compartmentalized Microfluidic Platforms as Tool of Choice to Study the Interaction Between Neurons tandardize the major proceedings to ensure the success of the coculture model for neurons and osteoblasts and further recommend the qualitative and quantitative analysis for two- or three-dimensional cocultures.作者: 項(xiàng)目 時(shí)間: 2025-3-26 20:31
Selective Biochemical Manipulation of Twin Neuronal Networks on Microelectrode Arraysally independent but fluidically connected neuronal networks can be grown. This platform improves biological comparability between cultures and allows to perform selective and temporally controlled stimulations to neurons, running parallel pharmacological tests on the same device.作者: occult 時(shí)間: 2025-3-27 00:30 作者: 認(rèn)識(shí) 時(shí)間: 2025-3-27 03:16
A Novel In Vitro Primary Culture Model of the Lower Motor Neuron–Neuromuscular Junction Circuittomical and cellular interactions of this circuit in compartmented microfluidic devices, such that the glial cells are located with motor neuron cell bodies in the cell body chamber and motor neuron axons extend to a distal chamber containing skeletal muscle cells whilst simultaneously allowing targeted intervention.作者: dominant 時(shí)間: 2025-3-27 05:30 作者: 貧窮地活 時(shí)間: 2025-3-27 12:10
The Fabrication of Microfluidic Platforms with Pneumatically/Hydraulically Controlled PDMS Valves aners to investigate neurobiological phenomena in ways previously unachievable using traditional cell biology techniques. Here we detail the fabrication of a microfluidic cell coculture platform that uses pneumatically or hydraulically controlled valves to reversibly separate cell populations. Using t作者: Additive 時(shí)間: 2025-3-27 15:12
A Reliable Reversible Bonding Method for Perfused Microfluidic Devicessurface properties of the material itself. Bulk properties include optical transparency, gas permeability, and ease of fabrication, to name a few. On the other hand, silanol groups (SiOH) present on the surface can be easily activated through air/oxygen plasma treatments, and used to permanently bon作者: 飛鏢 時(shí)間: 2025-3-27 20:24 作者: fluoroscopy 時(shí)間: 2025-3-27 23:02
Asymmetric Genetic Manipulation and Patch Clamp Recording of Neurons in a Microfluidic Chippartmentalized cell culture systems offer a simple yet powerful solution for isolation of axons from dendrites and cell somas. This chapter describes how to manufacture and use a microfluidic chip with a modular design for highly defined isolation of axons, asymmetric genetic manipulation, and whole作者: Generator 時(shí)間: 2025-3-28 05:08
Development of a Compartmentalized Biochip for Axonal Isolation and Neuronal-Circuit Formation at thy with the development of microelectrode arrays. Most current techniques used to form a defined neuronal network are based on microcontact-printing, but the intercellular connections in the patterned low-density network are formed randomly, systematic study of a specific network is not possible. For作者: NAV 時(shí)間: 2025-3-28 08:38
Campenot Cultures and Microfluidics Provide Complementary Platforms for Spatial Study of Dorsal Root These pseudo-unipolar neurons extend a single axon that bifurcates to innervate the periphery and spinal cord, allowing sensory information from the environment to be transferred rapidly to the central nervous system. During development, these DRG neurons rely on peripheral target-derived neurotrop作者: Rheumatologist 時(shí)間: 2025-3-28 13:15
Development of Microfluidic Devices for the Manipulation of Neuronal Synapsesamong these extracellular factors is the presence and influence of neighboring cells. It is crucial, therefore, in studying development to be able to replicate in vitro these network-like conditions. This is especially true of neuroscience, tissue engineering, and clinical biology, where network for作者: nuclear-tests 時(shí)間: 2025-3-28 17:54 作者: ARCHE 時(shí)間: 2025-3-28 19:00
Multi-compartment Neuron–Glia Coculture Microsystem cells that allow detailed investigation into axon–glia interactions and spatial regulation of functions. Here, we describe a multi-compartment neuron–glia coculture microsystem platform where axons can be fluidically and physically isolated from neuronal somata and dendrites so that interactions be作者: 蛙鳴聲 時(shí)間: 2025-3-28 23:41
Compartmentalized Microfluidic Platforms as Tool of Choice to Study the Interaction Between Neurons research. Compartmentalized microfluidic devices, initially applied in the neuroscience field for the simplest biochemical tests, is presently used at the most complex assays such as cocultures for developmental and regeneration studies. Excitingly, these devices have emerged as a potential tool to 作者: 木訥 時(shí)間: 2025-3-29 03:49 作者: 刀鋒 時(shí)間: 2025-3-29 08:26
Compartmentalized Microfluidics for In Vitro Alzheimer’s Disease Studies chambers can be expanded to induce co-pathological cell cultures, where one cell population expresses a specific disease state, while being in direct-cell or metabolic contact to a second or third unaffected cell population. A typical example for co-pathological cell states in the brain is the well作者: DAMP 時(shí)間: 2025-3-29 12:38
Selective Biochemical Manipulation of Twin Neuronal Networks on Microelectrode Arraysharmacological assays. Here, we describe the fabrication and the use of a device for long-term growth of twin neuronal networks and for their controlled biochemical stimulation. The device is formed by a PDMS microfluidic chamber coupled to a flat Microelectrode Array (MEA), which provides the elect作者: VOK 時(shí)間: 2025-3-29 17:41 作者: fatty-streak 時(shí)間: 2025-3-29 22:56
Bryson M. Brewer,Donna J. Webb,Deyu Liex geometries with tight tolerance requirements where large distortion is undesirable. The understanding and characterization of NSRS in milled aluminum parts is important and should be included in the design and manufacturing process. There exists a variety of experimental tests for characterizing 作者: 樸素 時(shí)間: 2025-3-30 03:08 作者: 小爭(zhēng)吵 時(shí)間: 2025-3-30 06:26
Jonathan West,Ngoc-Duy Dinh,Heike Hardelauf,Ya-Yu Chiang,Tracey A. Newman,Mariana Vargas-Caballero,Ato effectively identify the modal parameters. In this study, the MIMO concept is extended to the time domain for system identification of systems with modal interference. When performing a modal analysis of a structural system with close modes or high damping, the results of identification may be po作者: 策略 時(shí)間: 2025-3-30 08:57
Book 2023s geographically constrained Earth systems.? It contributes to the ongoing discussion of human transformation of the world, and the current debate about the designation of a new geological epoch, the Anthropocene.? It concludes by supporting the proposition that the Anthropocene is best understood a作者: 演講 時(shí)間: 2025-3-30 15:45
