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+ | <div class="container"> | ||
+ | <nav class="navbar navbar-expand-lg navbar-light mr-auto"> | ||
+ | <a class="navbar-brand" href="index.html">HD Resolution</a> | ||
+ | <div class="collapse navbar-collapse" id="navbarSupportedContent"> | ||
+ | <ul class="navbar-nav mr-auto"> | ||
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+ | <a class="nav-link dropdown-toggle" href="#" id="navbarPR" role="button" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false"> | ||
+ | Project | ||
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+ | <div class="dropdown-menu" aria-labelledby="navbarPR"> | ||
+ | <a class="dropdown-item" href="HD.html">What is HD?</a> | ||
+ | <a class="dropdown-item" href="#">Coming Soon</a> | ||
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+ | Notebook | ||
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+ | <div class="dropdown-menu" aria-labelledby="navbarNB"> | ||
+ | <a class="dropdown-item" href="#">Coming Soon</a> | ||
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+ | <a class="nav-link dropdown-toggle" href="#" id="navbarHP" role="button" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false"> | ||
+ | Human Practices | ||
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+ | <div class="dropdown-menu" aria-labelledby="navbarHP"> | ||
+ | <a class="dropdown-item" href="#">Coming Soon</a> | ||
+ | </div> | ||
+ | </li> | ||
+ | <li class="nav-item"> | ||
+ | <a class="nav-link" href="#">Team (Coming Soon)</a> | ||
+ | </li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </nav> | ||
+ | </div> | ||
− | <div class=" | + | <div class="container" align="center" width=50%> |
− | < | + | <div class="row"> |
− | < | + | <div class="col-sm-4 vcl"> |
− | < | + | <h1 >Using genomics<br> to search for a <span class="shiny">Resolution</span> to Huntington's Disease (<span class="shiny">HD</span>)</h1> |
− | + | </div> | |
− | </div> | + | <div class="col-sm-4"> |
− | + | <img src="brain.gif" width=200% style="border-radius: 15px"> | |
− | <div class=" | + | </div> |
− | + | </div> | |
− | < | + | </div> |
− | < | + | |
+ | <div class="container" align="center"> | ||
+ | <div class="row"> | ||
+ | <div class="col-sm-4"> | ||
+ | <div class="container bg-light"> | ||
+ | <h2>WHAT</h2> | ||
+ | <p align="left">Huntington's Disease (HD) is a genetic disorder that results in the breakdown of nerve cells in the | ||
+ | brain. Although the disease affects the whole brain, the basal ganglia, which plays a critical role in | ||
+ | motor functions and behavior, is most severely affected. Thus, symptoms of HD include involuntary | ||
+ | movements, personality changes, and cognitive problems. Over time, the effects of HD is extremely | ||
+ | debilitating, eventually rendering a patient unable to speak, walk, or even reason.</p> | ||
+ | </div> | ||
+ | <br> | ||
+ | <div class="container bg-light"> | ||
+ | <h2>WHY</h2> | ||
+ | <p align="left">HD is a result of a specific mutation in the huntingtin (HTT) gene, which results in a faulty production | ||
+ | of the HTT protein, mHTT. The mutation is a trinucleotide repeat of the codon CAG, where 40 or more will | ||
+ | lead to the expression of HD.</p> | ||
+ | </div> | ||
+ | </div> | ||
+ | <div class="col-sm-4" align="center"> | ||
+ | <img src="img/neuron.jpg" width=300> | ||
+ | </div> | ||
+ | <div class="col-sm-4"> | ||
+ | <div class="container bg-light"> | ||
+ | <h2>WHO</h2> | ||
+ | <p align="left">The most common form of HD is adult-onset, affecting people between their 30s and 40s. | ||
+ | Many people form families and have children by the time they are diagnosed with HD, which automatically | ||
+ | gives their children a 50% chance of inheriting the disease. HD affects about 1 in every 10,000 | ||
+ | people worldwide.</p> | ||
+ | </div> | ||
+ | <br> | ||
+ | <div class="container bg-light"> | ||
+ | <h2>HOW</h2> | ||
+ | <p align="left">Our goal is to develop a cure to Huntington's Disease by employing RNA strand displacement | ||
+ | technology to target erroneous mRNA within the affected cells and replace it with the corrected RNA | ||
+ | strand for proper protein synthesis. | ||
+ | </p> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
</div> | </div> | ||
</body> | </body> | ||
</html> | </html> |
Revision as of 19:29, 23 August 2018
Using genomics
to search for a Resolution to Huntington's Disease (HD)
WHAT
Huntington's Disease (HD) is a genetic disorder that results in the breakdown of nerve cells in the brain. Although the disease affects the whole brain, the basal ganglia, which plays a critical role in motor functions and behavior, is most severely affected. Thus, symptoms of HD include involuntary movements, personality changes, and cognitive problems. Over time, the effects of HD is extremely debilitating, eventually rendering a patient unable to speak, walk, or even reason.
WHY
HD is a result of a specific mutation in the huntingtin (HTT) gene, which results in a faulty production of the HTT protein, mHTT. The mutation is a trinucleotide repeat of the codon CAG, where 40 or more will lead to the expression of HD.
WHO
The most common form of HD is adult-onset, affecting people between their 30s and 40s. Many people form families and have children by the time they are diagnosed with HD, which automatically gives their children a 50% chance of inheriting the disease. HD affects about 1 in every 10,000 people worldwide.
HOW
Our goal is to develop a cure to Huntington's Disease by employing RNA strand displacement technology to target erroneous mRNA within the affected cells and replace it with the corrected RNA strand for proper protein synthesis.