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User:Brian Conner/Sandbox 1
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(Difference between revisions)
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== Disease == | == Disease == | ||
Deletions and mutations in the gene that encodes for elastin can result in supraventricular aortic stenosis, and autosomal dominant cutis laxa. Other disorders that are associated with defects in elastin are Marfan's Snydrome and emphysema, which is caused by an α<sub>1</sub>-antitrypsin deficiency. | Deletions and mutations in the gene that encodes for elastin can result in supraventricular aortic stenosis, and autosomal dominant cutis laxa. Other disorders that are associated with defects in elastin are Marfan's Snydrome and emphysema, which is caused by an α<sub>1</sub>-antitrypsin deficiency. | ||
| - | == Relevance == | ||
| - | == Structural highlights == | ||
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| - | This is a sample scene created with SAT to <scene name="/12/3456/Sample/1">color</scene> by Group, and another to make <scene name="/12/3456/Sample/2">a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes. | ||
</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
| - | <references/> | ||
Revision as of 20:13, 30 April 2014
Elastin
Elastin is a fibrous protein that can be found in human connective tissue and gives the tissue its elastic quality. This allows tissues that have been stretched to regain their original shape.
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