Previously classified as the congenital variant of Rett Syndrome, FOXG1 syndrome is a rare genetic nuerodevelopmental disorder characterized by severe mental retardation, limited cognitive function,...
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FOXG1 Syndrome - Home | ramirezgen564s16.weebly.com Reviews
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Previously classified as the congenital variant of Rett Syndrome, FOXG1 syndrome is a rare genetic nuerodevelopmental disorder characterized by severe mental retardation, limited cognitive function,...
ramirezgen564s16.weebly.com
Gene - FOXG1 Syndrome
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This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. 8203;The FOXG1 gene is crucial for normal development and plays a major role in FOXG1 syndrome. For more information on this gene and its respective protein, start by learning about its gene ontology and continue by exploring other pages of this website. Figure 1: Types of mutations that give rise to FOXG1 syndrome. 1] http:/ geneontology.org. Create a free website.
Interactions - FOXG1 Syndrome
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This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. What are protein interactions? 8203;FOXG1 interacts primarily with the proteins depicted in color. Majority of these other proteins are either other proteins in the forkhead family or protein kinases which are involved with phosphorylation. These interactions intrigued me because it suggests that the protein must be phosphorylated to function properly. Phosphorylation of FOXG1 can be ...The prote...
Conclusions - FOXG1 Syndrome
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This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. Conclusions and Future Direction. Figure 1: FOXG1 homologs. Figure 2: Protein interaction networks in the human and the zebrafish with similar proteins circled in the same colors. Figure 3: Example of tandem mass spectrometry results. I would expect interactions of FOXG1p to be over expressed in the mutant zebrafish. Figure 4: Example of the yeast 2 hybrid model with FOXG1p as the bait. 2] Manuel...
Specific Aims - FOXG1 Syndrome
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This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. 8203; Elucidating FOXG1 protein interactors for future drug development to treat infantile spasms. However the exact effects of over-expressed FOXG1 on the proteome have not been explored. Of this study is to understand the role that FOXG1 plays in the pathway that gives rise to infantile spasms. The. This study will test the central hypothesis. Quantitate the results by measuring the relative ab...
Chemical Genetics - FOXG1 Syndrome
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This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. There are databases such as PubChem. That store all of the information known about small molecules that have been screened. This site was used to see if any small molecules had been shown to produced the normal phenotype in mutants but no results were obtained. Figure 1: A visual of a typical chemical genetic screen. 8203; [1]PubChem: http:/ pubchem.ncbi.nlm.nih.gov/search/. Create a free website.
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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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FOXG1 Syndrome - Home
This web page was produced as an assignment for Genetics 564. An undergraduate capstone course at UW-Madison. Previously classified as the congenital variant of Rett Syndrome, FOXG1 syndrome is a rare genetic nuerodevelopmental disorder characterized by severe mental retardation, limited cognitive function, postnatal microcephaly, and seizures [ 1. These symptoms arise from a dysfuntional FOXG1 gene and can range from mild to severe[ 2. Figure 1: The telencephalon in an embryo and an adult brain. Arm of ...
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