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This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison.

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This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison.
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1 gene
2 gene homology
3 gene phylogeny
4 gene ontology
5 protein
6 protein homology
7 protein phylogeny
8 domains
9 interaction network
10 protein modifications
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This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison.

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Protein

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Conclusions and Future Directions. CHARGE Syndrome and the CHD7 Protein. Chromodomain Helicase DNA Binding Protein 7 (CHD7. Chromodomain helicase DNA binding protein 7 (. Figure 1: Schematic of the domains present in CHD7 (Modified from SMART). Figure 2: CHD7 Crystallized Structure of CHD7. Observe the similarity between. The human CHD7 protein and that possessed by other organisms. Learn more about the evolutionary history and relatedness of different organisms' CHD7 proteins. Create a free website.

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Gene

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Conclusions and Future Directions. CHARGE Syndrome and the. This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. Figure 1: the cytogenetic location of CHD7. Observe the similarity between. Gene and that present in other organisms. Learn more about the evolutionary history and relatedness of different organisms'. Genetics Home reference: CHD7." 10 Feb. 2015 Web. February 10, 2016. Http:/ ghr.nlm.nih.gov/gene/CHD7. Create a free website.

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Microarrays

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Conclusions and Future Directions. The differences in the transcriptome of individuals with CHARGE Syndrome are still poorly characterized. Transcriptomics, and microarrays specifically, can be used to compare the RNA profile between diseased and normal tissue to provide information about the genes that should, but are not, being expressed [. CHARGE Syndrome Transcriptome Profile. Http:/ homes.cs.washington.edu/ dcjones/talks/cse427-rna-seq-quantification/#/1. Am J Hum Genet. Create a free website.

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Domains

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Conclusions and Future Directions. Domains confer important structural functions when the. Protein conforms into its three-dimensional shape. This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. A few examples of domain function include: DNA binding, protein-protein interactions, ATP synthesis, amino acid breakdown, etc. Proteins may have one or many domains that work together or independently [ 2. These domains are responsible for binding to chroma...

5

Model Organisms

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Conclusions and Future Directions. For Studying CHARGE Syndrome and the. There are many merits to using a mouse model. Mice are a mammalian system that is highly applicable to human disease pathology. Mice also have large litter sizes, and transgenic mouse varieties can be made to conduct large scale, highly controlled experiments with many genetically identical animals [ 2. CHD7 Mutant Mouse Models for studying CHARGE Syndrome. CHD7 Mutant Zebrafish Models for studying CHARGE Syndrome. This zebrafish st...

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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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Conclusions and Future Directions. CHARGE Syndrome and the. Despite these seemingly insurmountable obstacles, children with CHARGE syndrome. Often far surpass their medical, physical, educational, and social expectations.". A word from the CHARGE Syndrome Foundation. This webpage was produced as an assignment for Genetics 564, an undergraduate capstone course at UW-Madison. A brief discussion of CHARGE Syndrome. Oloboma in the eye; H. Eart Defects; A. Tresia of the Choanae; R. Enital Abnormalities; E.

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