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BRD2 & Juvenile Myoclonic Epilepsy - Home

What is juvenile myoclonic epilepsy? Epilepsy is the fourth most common neurological disorder and is otherwise known as a seizure disorder [ 2 ]. The severity and type of seizures vary among those...

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BRD2 & Juvenile Myoclonic Epilepsy - Home | praskagen564s16.weebly.com Reviews
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What is juvenile myoclonic epilepsy? Epilepsy is the fourth most common neurological disorder and is otherwise known as a seizure disorder [ 2 ]. The severity and type of seizures vary among those...
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3 phylogeny
4 domains
5 interactions
6 model organisms
7 sequence consensus
8 specific aims
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BRD2 & Juvenile Myoclonic Epilepsy - Home | praskagen564s16.weebly.com Reviews

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What is juvenile myoclonic epilepsy? Epilepsy is the fourth most common neurological disorder and is otherwise known as a seizure disorder [ 2 ]. The severity and type of seizures vary among those...

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Domains - BRD2 & Juvenile Myoclonic Epilepsy

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BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. Protein domains are distinct units in a protein that have a particular function and/or structure [ 1. An understanding of protein domains can provide insight into the function of the protein. Domains can also be examined for evolutionary conservation among species. Generally speaking, BRD2 is well-conserved between different species. Create a free website.

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Sequence Consensus - BRD2 & Juvenile Myoclonic Epilepsy

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BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. To understand sequence conservation at particular regions in the genome, online databases can be used to visualize this. Using the UCSC Genome Browser. The SNPs in the BRD2 promoter can be visualized and compared among species. The above figure shows the. Create a free website.

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Model Organisms - BRD2 & Juvenile Myoclonic Epilepsy

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BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. Model Organisms for BRD2. Model organisms can be used to study diseases or alterations. They provide insight into mechanisms of disease, genotype/phenotype effects, and much more information. Due to high sequence conservation, mice provide a good model organism for studying. 8203; A knockout model has been made. Create a free website.

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Specific Aims - BRD2 & Juvenile Myoclonic Epilepsy

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BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. Two single nucleotide polymorphisms (SNPs) in the promoter region of. Are of particular interest [2]. Is a gene involved in transcriptional regulation and is thought to play a role in neural development. However, the actual functional relevance of the SNPs in the. Promoter region is unknown. Interestingly, knocking out the. Is that the SNPs found in. Promoter...

5

Protein - BRD2 & Juvenile Myoclonic Epilepsy

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BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. This protein is a nuclear transcriptional regulator belonging to the BET (bromine and extra terminal domain) family of proteins. BRD2 localizes to the nucleus and associates with acetylated chromatin and transcription complexes, particularly those involved in neuronal development [. Image: http:/ www.proteinatlas.org/ENSG00000204256-BRD2/tissue.

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Projects - Genetics 564

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Spring 2016 Student Projects. Matthew Busalacchi: Familial Melanoma and Pigmentation (MC1R). Salvador Carranza: Cystinosis (CTNS). Mikayla Gallenberger: Acute Lymphoblastic Leukemia (PAX5). Sara Grange: Synesthesia (KIAA0319). Aidan Holmes: Wilson Disease (ATP7B). Bailey Marquardt: Developmental Dyslexia (ROBO1). Troy Meikle: Autoimmune lymphoproliferative syndrome (FAS). Mary Mohr: Cardiovascular Disease in Women (BCAR1/p130CAS). Kathryn Ness: CHARGE Syndrome (CHD7). Tia Ramirez: FOXG1 Syndrome (FOXG1).

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BRD2 & Juvenile Myoclonic Epilepsy - Home

BRD2 and Juvenile Myoclonic Epilepsy. This web page was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. Site is under construction. What is juvenile myoclonic epilepsy? Epilepsy is the fourth most common neurological disorder and is otherwise known as a seizure disorder [ 2. Juvenile myoclonic epilepsy (JME) is the most common form of idiopathic generalized epilepsy, and it presents in mid-to-late childhood between the ages of 12 and 18. Absence seizures (forme...

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