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Introduction | Niemann-Pick Disease
https://neimanpick.wordpress.com/2014/02/22/introduction
We will look at the research and biochemistry behind Niemann-Pick disease. February 22, 2014. Niemann-Pick disease is a lysosomal disease caused by genetic mutation. While there are different severities of the illness, the most severe lead to death during infancy. Those who exhibit the less severe form are able to live into their early teens or even adulthood. Niemann-Pick is caused by an enzyme functioning improperly, causing a buildup of sphingomyelin in the lysosomes of our cells. You are commenting u...
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References | Niemann-Pick Disease
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We will look at the research and biochemistry behind Niemann-Pick disease. Here is a list of commonly used references used throughout my research. As I utilize new sources, this page will be updated. Http:/ www.nnpdf.org/npdisease 01.html. Http:/ en.wikipedia.org/wiki/Niemann Pick disease. Http:/ themedicalbiochemistrypage.org/niemannpickdiseases.php. Http:/ www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0082879. Http:/ www.jbc.org/content/261/35/16769.full.pdf html. Enter your comment here.
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About | Niemann-Pick Disease
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We will look at the research and biochemistry behind Niemann-Pick disease. Throughout the next few months, we will attempt to understand what is behind Neimann-Pick disease. Not only will we look at the biochemistry of the genetic disorder, but also at the research and efforts put forth by the scientific community in order to better understand the illness. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public).
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Experimental Breakthrough – What causes NPC? | Niemann-Pick Disease
https://neimanpick.wordpress.com/2014/04/02/experimental-breakthrough-what-causes-npc
We will look at the research and biochemistry behind Niemann-Pick disease. Experimental Breakthrough – What causes NPC? April 2, 2014. Their results proved that NPC does, in fact, deal with a lack of esterification of cholesterol, leading to the accumulation that causes the symptoms. In addition, the characteristic of the accumulations (peri-nuclear) further suggests a lysosomal origin of the disease. The research done by these scientists led to a better understanding of the cause behind NPA and NPB....
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Biochemistry Behind NPC | Niemann-Pick Disease
https://neimanpick.wordpress.com/2014/03/18/biochemistry-behind-npc
We will look at the research and biochemistry behind Niemann-Pick disease. March 18, 2014. In a body with NPC, the cells filled with these important checks and balances have trouble regulating, as they are unable to respond to an accumulation of cholesterol. For example, the uptake of LDL continues far past the level of saturation of free cholesterol in a cell. This problem is now associated with the mutation I1061T along with an upregulated receptor gene (1.5 fold). Leave a Reply Cancel reply. Address n...
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April | 2014 | Niemann-Pick Disease
https://neimanpick.wordpress.com/2014/04
We will look at the research and biochemistry behind Niemann-Pick disease. April 14, 2014. Attempt to find a link between cognitive and coordination deficits and NPC. Experimental Breakthrough – What causes NPC? April 2, 2014. Their results proved that NPC does, in fact, deal with a lack of esterification of cholesterol, leading to the accumulation that causes the symptoms. In addition, the characteristic of the accumulations (peri-nuclear) further suggests a lysosomal origin of the disease. In a normal ...
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jacobmatano | Niemann-Pick Disease
https://neimanpick.wordpress.com/author/jacobmatano
We will look at the research and biochemistry behind Niemann-Pick disease. April 14, 2014. Attempt to find a link between cognitive and coordination deficits and NPC. Experimental Breakthrough – What causes NPC? April 2, 2014. Their results proved that NPC does, in fact, deal with a lack of esterification of cholesterol, leading to the accumulation that causes the symptoms. In addition, the characteristic of the accumulations (peri-nuclear) further suggests a lysosomal origin of the disease. In a normal ...