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Niemann-Pick Disease | We will look at the research and biochemistry behind Niemann-Pick disease.

We will look at the research and biochemistry behind Niemann-Pick disease.

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Niemann-Pick Disease | We will look at the research and biochemistry behind Niemann-Pick disease. | neimanpick.wordpress.com Reviews

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We will look at the research and biochemistry behind Niemann-Pick disease.

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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 ...

2

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...

3

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....

4

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 ...

5

About | Niemann-Pick Disease

https://neimanpick.wordpress.com/about

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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About | Albinism

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This is an example of a page. Unlike posts, which are displayed on your blog’s front page in the order they’re published, pages are better suited for more timeless content that you want to be easily accessible, like your About or Contact information. Click the Edit link to make changes to this page or add another page. 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). Notify me of new comments via email.

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March | 2014 | Albinism

https://hannahmasengale.wordpress.com/2014/03

Monthly Archives: March 2014. March 19, 2014. Image taken from: Carden, Susan M., Raymond E. Boissy, Pamela J. Schoettker, and William V. Good. “Albinism: Modern Molecular Diagnosis.” British Journal of Ophthalmology. Np, nd. Web. 18 Mar. 2014. Carden, Susan M., Raymond E. Boissy, Pamela J. Schoettker, and William V. Good. “Albinism: Modern Molecular Diagnosis.” British Journal of Ophthalmology. Np, nd. Web. 18 Mar. 2014. Create a free website or blog at WordPress.com.

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February | 2014 | Albinism

https://hannahmasengale.wordpress.com/2014/02

Monthly Archives: February 2014. February 28, 2014. Albinism is an autosomal recessive genetic disorder that causes people to have little or no pigment in their eyes, skin, or hair. In the United States 1 out of 17,000 people has some form of albinism. There are four forms of Oculocutaneous albinisms (OCA) and one other form called ocular albinism (OA). OA is caused by a defect of the GPR143 gene that plays a signaling role that is important to pigmentation of the eye. This is also the only sex-linke...

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hannahmasengale | Albinism

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April 15, 2014. Current research over Oculocutaneous albinism (OCA) involves understanding the wide variety of mutations to tyrosinase, how those play a role in OCA1A and OCA1B forms of albinism, how these mutations have such dramatic effects, and why some are temperature-sensitive. April 3, 2014. 8220;The technique consisted of immersing frozen sections of skin into a dilute solution of dopa buffered at physiological pH and noting the melanin deposition which occurred after. At this time, not much was k...

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Biochemistry | Albinism

https://hannahmasengale.wordpress.com/2014/03/19/biochemistry

Experimental Breakthrough →. March 19, 2014. Image taken from: Carden, Susan M., Raymond E. Boissy, Pamela J. Schoettker, and William V. Good. “Albinism: Modern Molecular Diagnosis.” British Journal of Ophthalmology. Np, nd. Web. 18 Mar. 2014. Carden, Susan M., Raymond E. Boissy, Pamela J. Schoettker, and William V. Good. “Albinism: Modern Molecular Diagnosis.” British Journal of Ophthalmology. Np, nd. Web. 18 Mar. 2014. 2 thoughts on “ Biochemistry. March 29, 2014 at 6:45 pm. April 15, 2014 at 2:10 am.

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About | Albinism

https://hannahmasengale.wordpress.com/2014/02/28/about

February 28, 2014. Albinism is an autosomal recessive genetic disorder that causes people to have little or no pigment in their eyes, skin, or hair. In the United States 1 out of 17,000 people has some form of albinism. There are four forms of Oculocutaneous albinisms (OCA) and one other form called ocular albinism (OA). OCA3 is rarely described and results from a defect in TYRP1, a protein related to tyrosinase. Individuals with this can still have substantial amounts of pigment produced. OA is caused b...

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February | 2014 | Scurvy

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Discovery of the Cause of Scurvy. On Introduction to Scurvy. On Introduction to Scurvy. Monthly Archives: February 2014. February 23, 2014. Al-Dabagh, A., Milliron, B., Strowd, L., and Feldman, S.R. (2013). A disease of the present: Scurvy in well-nourished patients. Journal of the American Academy of Dermatology. 5), 246-247. http:/ dx.doi.org/10.1016/j.jaad.2013.04.051. Crosta, P. (2013, January 23). What Is Scurvy? Retrieved from http:/ www.medicalnewstoday.com/articles/155758.php.

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An Experimental Breakthrough: The Cause of Pellagra | Pellagra

https://pellagradisease.wordpress.com/2014/04/02/an-experimental-breakthrough-the-cause-of-pellagra

A nutritional deficiency disorder. Biochemical Consequences of Pellagra. Current Research: Pellagra in Unexpected Places ». An Experimental Breakthrough: The Cause of Pellagra. April 2, 2014. During the Southern United States pellagra epidemic in the early 20. Lanska, Douglas J. The Discovery of Niacin, Biotin, and Pantothenic Acid. Annals of Nutrition and Metabolism. 61 (2012): 246-253. Web. 31 March 2014. DOI: 10.1159/000343115. 2 thoughts on “ An Experimental Breakthrough: The Cause of Pellagra.

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Experimental Breakthrough | Albinism

https://hannahmasengale.wordpress.com/2014/04/03/experimental-breakthrough/comment-page-1

Current Research →. April 3, 2014. 8220;The technique consisted of immersing frozen sections of skin into a dilute solution of dopa buffered at physiological pH and noting the melanin deposition which occurred after. 24 hours at room temperature. The deposition of melanin was the most intense in the. He concluded that this dopa reaction was a reliable indicator of the active capacity of. Cells to form pigment.”. 103 (1958): 250-67. Print. One thought on “ Experimental Breakthrough. Enter your comment here.

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Niemann-Pick Disease | We will look at the research and biochemistry behind Niemann-Pick disease.

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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