A. Z3280894 You need to add pictures to your page. Also I suggest reordering your page so that it flows better, like making function below structure. Great job on referencing, you seemed to have done a lot of research. Maybe it would improve your page if you made the cited text link down to the references.
B. z3217578: An image on your page linking to one or more sections would be helpful for the reader, as well as make your page look nicer. Otherwise, the information is presented well, and clearly explained.
C. z3189925: Well written. Would have added some images to the page to better understand the topic and of course add some colour. First impressions are important. As to referencing, although it is not major issue, I would have used the wiki reference list style. This would help readers focus on the content rather than skim past references.
D. hey, u got content but a bit not helpful to have no pictures to understand what you're trying to say.
E. Quite informative - images would definitely help though! If you can't find any, maybe draw your own? Especially under the heading "TNF-α Receptors & Signaling". It's good that you linked to a video though. A glossary would also be helpful if people without cell-bio background were to read it...
F. Probably, the best written project I have reviewed so far. It provides quite a good overview of Tumor Necrosis Factor Alpha and the progression of the scientific knowledge of it. The page may benefit from some pictures, to demonstrate a function of TNF alpha as a multifunctional ligand (draw an example maybe?). Aside from that it was well formatted.
G. Appropriate information was given about this particular protein. I have a question: known to be one of the most significant members of its class. --> do you mean out of all TNF family? What does it mean by significant? It will be better if you can put pictures on page so that the reader will have some visual information about this protein. Nonetheless, it a well structured page from well background research. (3222840)
H. You have all the important information here, maybe just a bit more on the current research. It would also be good to have images of the protein and diagrams to help with the understanding. (3221652)
LECTURE 4: Outline something new that you learnt from this lecture.
I learnt about Nuclear Bodies (Cajal and PML) that, to my recollection, I hadn't heard of previously. I also learnt some things about chromosomes that were fairly new. Also, I liked the picture of Nuclear Pores. I had heard about them for a good while but could never really visualise what they might look like - kinda cool.
LECTURE 5: What did you find difficult to understand?
Everything was pretty understandable because you have a nice voice that's very easy to listen to; like the voices on TV. Perhaps when we study the Cytoskeleton and ECM later on I can build on my knowledge of the structural role of intermediate filaments.
LECTURE 7: What are the main energy processes in the cell?
Mitochondria is an organelle in cells. The main function of mitochondria is to produce energy (ATP) for the cell using raw materials such as oxygen and fatty acids. In plant cells chloroplasts are highly involved in energy production.
LECTURE 8: There are different types of Cell Adhesion Molecules present within the Nervous System that each serve a different role
N-CAMs are Neuronal Cell Adhesion Molecules.
Ng-CAMs are Neuron-glia Cell Adhesion Molecules involved in promoting the regeneration of a nerve subsequent to damage. In addition to this Ng-CAMs are associated with adhesion across the axon.
L-CAMs are Liver Cell Adhesion Molecules that are involved in maintaining the architectural integrity of the liver with cell-cell adhesion.
I-CAMs are Intercellular Adhesion Molecules that are closely associated with the inflammatory response. They often mediate adhesive interactions important for antigen-specific immune responses and are are involved in WBC recirculation when they act to block cell ahesion.
LECTURE 10: What is the layer of the skin that contains a high concentration of intermediate filaments that form desmosomes?
(Hint: between the Statum Granulosum and Stratum Basale layer of the skin). This layer is the Stratum Spinosum.
LAB 6: If you've seen differences in the distribution of phenotypes in Tm4 over-expressing B35 cells versus control B35 cells, describe these differences. Formulate a hypothesis with regards to what changes on the molecular level may have occurred due to the over-expression of Tm4 that lead to morphological changes that you have observed
LECTURE 14: What are the 2 main forms of generating confocal microscopy?
1 - Laser scanning
2 - Spinning Disc
LECTURE 11:What does "S" stand for in the S phase?