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Write a 2000-3000 word paper OR record a 10-15 minute presentation. The presentation must be recorded so that we can see your face and verify that you completed the assignment. In your paper or presentation, you must reference at least two ideas from each of the following six topic areas: 1.Consciousness (lecture on 2/19) https://mediasite.csom.umn.edu/Mediasite/Play/621c821150dd4999878f9ab6fa07e30b1d This is the lecture link for consciousness 2.Memory (textbook Ch7 and lectures on 2/21 & 2/24) 3.Cognition (textbook Ch8 and lectures on 2/26 & 2/28) 4.Intelligence/Individual Differences (textbook Ch9, lectures on 3/2, 3/4 and 3/6) 5.Behavioral Psychology (textbook Ch6 and lecture from 3/16) 6.Industrial/Organizational Psychology (lecture from 3/18) https://mediasite.csom.umn.edu/Mediasite/Play/dc4fc47594be44a0a894acdcc5cd2dfa1d? catalog=3502a188ee14476ca9532380105a0e6921 This is the ling for industrial/organizational psychology
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1. Presentation Liver disappointment is a significant clinical test since itand is one of the main sources of death in the around the world. As of now, entire organ liver transplantation is the main healing treatment. Benefactor lack and conceivable resistant dismissal limit the proficiency of transplantation and accordingly increment the quantity of individuals living with end phase of liver ailment [1]. As an option in contrast to liver transplantation, tissue designing has concentrated on creating cell-based treatments to beat the shortage of liver benefactors, so that hepatocytes produced by separation of undeveloped immature microorganisms (ESCs) or prompted pluripotent foundational microorganisms (iPSCs) in culture can give a boundless stockpile of such cells for transplantation [2]. iPSCs, which have been produced by Yamanaka and associates, are fundamentally the same as ESCs in morphology, separation potential, telomerase action, surface markers and quality articulation profiles [3]. These cells are pluripotent and have separation potential into three germ layers genealogies, including endodermal hepatocyte-like cells [4], [5]. Significantly, a few examinations have indicated that the hepatocyte-like cells produced from iPSCs express numerous interpretation elements and markers of hepatocytes [6],[7],[8]. Thusly, with because of their one of a kind properties, iPSCs have been proposed as an entirely significant and boundless transplantable wellspring of hepatic cells hotspot for patients with end-organize liver ailments [9]. While Since the hepatocytes separated from understanding explicit iPSCs are hereditarily indistinguishable cells, resistant dismissal just as moral issues related with human ES cells would be forestalled and an in vitro model for liver illness would be given [10]. Tissue building has been utilized to create perfect frameworks that possesseswith comparable structure and properties to coordinate with local extracellular grid (ECM), which includes a mind boggling system of nanoscale strands shaping profoundly organized neighborhood microenvironments [11]. Electrospinning is an important and promptly controllable technique for arrangement of these frameworks, which has been generally read for creation of nanofibers with a high surface territory and porosity [12]. Nanofibers improve the supplement move just as trade of oxygen and different metabolites. A few nanofibrous frameworks, for example, collagen covered poly(L-lactic corrosive) and PCL/collagen/polyethersulfone (PES) composite have been accounted for as appropriate substrates for hepatocytes [13-15]. As a biocompatible and non-biodegradable polymer, PES had has been basically utilized in layer materials with applications, for example, filtration and hemodialysis [16>
1. Presentation Liver disappointment is a significant clinical test since itand is one of the main sources of death in the around the world. As of now, entire organ liver transplantation is the main healing treatment. Benefactor lack and conceivable resistant dismissal limit the proficiency of transplantation and accordingly increment the quantity of individuals living with end phase of liver ailment [1]. As an option in contrast to liver transplantation, tissue designing has concentrated on creating cell-based treatments to beat the shortage of liver benefactors, so that hepatocytes produced by separation of undeveloped immature microorganisms (ESCs) or prompted pluripotent foundational microorganisms (iPSCs) in culture can give a boundless stockpile of such cells for transplantation [2]. iPSCs, which have been produced by Yamanaka and associates, are fundamentally the same as ESCs in morphology, separation potential, telomerase action, surface markers and quality articulation profiles [3]. These cells are pluripotent and have separation potential into three germ layers genealogies, including endodermal hepatocyte-like cells [4], [5]. Significantly, a few examinations have indicated that the hepatocyte-like cells produced from iPSCs express numerous interpretation elements and markers of hepatocytes [6],[7],[8]. Thusly, with because of their one of a kind properties, iPSCs have been proposed as an entirely significant and boundless transplantable wellspring of hepatic cells hotspot for patients with end-organize liver ailments [9]. While Since the hepatocytes separated from understanding explicit iPSCs are hereditarily indistinguishable cells, resistant dismissal just as moral issues related with human ES cells would be forestalled and an in vitro model for liver illness would be given [10]. Tissue building has been utilized to create perfect frameworks that possesseswith comparable structure and properties to coordinate with local extracellular grid (ECM), which includes a mind boggling system of nanoscale strands shaping profoundly organized neighborhood microenvironments [11]. Electrospinning is an important and promptly controllable technique for arrangement of these frameworks, which has been generally read for creation of nanofibers with a high surface territory and porosity [12]. Nanofibers improve the supplement move just as trade of oxygen and different metabolites. A few nanofibrous frameworks, for example, collagen covered poly(L-lactic corrosive) and PCL/collagen/polyethersulfone (PES) composite have been accounted for as appropriate substrates for hepatocytes [13-15]. As a biocompatible and non-biodegradable polymer, PES had has been basically utilized in layer materials with applications, for example, filtration and hemodialysis [16>
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