Difference between revisions of "Team:New York City"

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{{New_York_City}}
 
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                                 <a class="dropdown-item" href="">Coming Soon</a>
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                                 <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/InterLab">InterLab</a>
 
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                                     Practices</a>
 
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                                <a class="dropdown-item" href="https://2018.igem.org/Team:New_York_City/Collaborations">Collaborations</a>
 
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                <h1 class="display-4">Testing the efficacy of mRNA displacement technique in huntingtin cell lines to
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            <h1 class="display-4">Testing the efficacy of mRNA displacement technique in huntingtin cell lines to
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                    treat Huntington's Disease</h1>
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                treat Huntington's Disease</h1>
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                    <h2 class="display-4">WHAT</h2>
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                    <p align="left" class="lead">Huntington's Disease (HD) is a genetic disorder that results in the
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                <h2 class="display-4">WHAT</h2>
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                        breakdown of nerve cells in the
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                <p align="left" class="lead">Huntington's Disease (HD) is a genetic disorder that results in the breakdown of nerve cells in the
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                        brain. Although the disease affects the whole brain, the basal ganglia, which plays a critical
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                    brain. Although the disease affects the whole brain, the basal ganglia, which plays a critical role in
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                        role in
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                    motor functions and behavior, is most severely affected. Thus, symptoms of HD include involuntary
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                        motor functions and behavior, is most severely affected. Thus, symptoms of HD include
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                    movements, personality changes, and cognitive problems. Over time, the effects of HD is extremely
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                        involuntary
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                    debilitating, eventually rendering a patient unable to speak, walk, or even reason.</p>
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                        movements, personality changes, and cognitive problems. Over time, the effects of HD is
+
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                        extremely
+
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                        debilitating, eventually rendering a patient unable to speak, walk, or even reason.</p>
+
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                </div>
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                <br>
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                <div class="container">
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                    <h2 class="display-4">WHY</h2>
+
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                    <p align="left" class="lead">HD is a result of a specific mutation in the huntingtin (HTT) gene,
+
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                        which results in a faulty production
+
−
                        of the HTT protein, mHTT. The mutation is a trinucleotide repeat of the codon CAG, where 40 or
+
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                        more will
+
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                        lead to the expression of HD.</p>
+
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            <br>
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                 <img src="https://static.igem.org/mediawiki/2018/d/d8/T--New_York_City--neuron.jpg" width=300>
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             <div class="container">
 +
                <h2 class="display-4">WHY</h2>
 +
                 <p align="left" class="lead">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>
 
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                    <h2 class="display-4">WHO</h2>
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             <img src="https://static.igem.org/mediawiki/2018/d/d8/T--New_York_City--neuron.jpg" width=300>
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                    <p align="left" class="lead">The most common form of HD is adult-onset, affecting people between
+
        </div>
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                        their 30s and 40s.
+
        <div class="col-sm-4">
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                        Many people form families and have children by the time they are diagnosed with HD, which
+
            <div class="container">
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                        automatically
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                <h2 class="display-4">WHO</h2>
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                        gives their children a 50% chance of inheriting the disease. HD affects about 1 in every 10,000
+
                <p align="left" class="lead">The most common form of HD is adult-onset, affecting people between their 30s and 40s.
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                        people worldwide.</p>
+
                    Many people form families and have children by the time they are diagnosed with HD, which automatically
−
                </div>
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                    gives their children a 50% chance of inheriting the disease. HD affects about 1 in every 10,000
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                <br>
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                    people worldwide.</p>
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                    <h2 class="display-4">HOW</h2>
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            <br>
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                    <p align="left" class="lead">Our goal is to develop a cure to Huntington's Disease by employing RNA
+
            <div class="container">
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                        strand displacement
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                <h2 class="display-4">HOW</h2>
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                        technology to target erroneous mRNA within the affected cells and replace it with the corrected
+
                <p align="left" class="lead">Our goal is to develop a cure to Huntington's Disease by employing RNA strand displacement
−
                        RNA
+
                    technology to target erroneous mRNA within the affected cells and replace it with the corrected RNA
−
                        strand for proper protein synthesis.
+
                    strand for proper protein synthesis.
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                    </p>
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        <video width="auto" height="300" controls>
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    <video height="320" width="auto" controls>
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            <source src="https://static.igem.org/mediawiki/2018/0/06/T--New_York_City--Video.mp4" type="video/mp4">
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        <source src="https://static.igem.org/mediawiki/2018/0/06/T--New_York_City--Video.mp4" type="video/mp4">
 
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            <a href="https://hdsa.org/"><img class="sponsor" src="https://static.igem.org/mediawiki/2018/a/a4/T--New_York_City--hdsa.png"/></a>
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            <a href="http://www.hdfoundation.org/"><img class="sponsor" src="https://static.igem.org/mediawiki/2018/8/86/T--New_York_City--hdf.png"/></a>
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            <a href="https://www.steptember.us/"><img class="sponsor" src="https://static.igem.org/mediawiki/2018/3/38/T--New_York_City--step.png"/></a>
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            <a href="https://hdsa.donordrive.com/index.cfm?fuseaction=donorDrive.participant&participantID=48528"><img class="sponsor" src="https://static.igem.org/mediawiki/2018/1/11/T--New_York_City--hope.png"/></a>
 
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Revision as of 03:21, 15 October 2018

Testing the efficacy of mRNA displacement technique in huntingtin cell lines to treat Huntington's Disease



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.