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UBE3A -Angelman Syndrome - Introduction | mokgen677s12.weebly.com Reviews
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Literature Review - UBE3A -Angelman Syndrome
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Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. The Angelman Syndrome Protein Ube3A Regulates Synapse Development by Ubiquitinating Arc. Cell, Volume 140, Issue 5, 704-716, 2010. By Greer, P.L.,. 101016/j.cell.2010.01.026. Angelman Syndrome (AS) is a neurodevelopmental disorder. Although the. In this experiment, the researchers sought to seek how disruption in. Create your...
Subcellular Localization - UBE3A -Angelman Syndrome
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Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. Dindot et al. found that the. In the neuronal cell population, the E6-AP protein was found to localize mainly to the nucleus, and also in the cytoplasm of the cell body as well as in dendrites. 1] Dindot, S. V., Antalffy, B. A., Bhattacharjee. M B, Beaudet. 17(1): 111-118. doi:10.1093/hmg/ddm288. Created by Jonathan Mok.
Protein Interactions - UBE3A -Angelman Syndrome
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Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. Here, we used 2 protein interactions databases, STRING 9.0. To generate the UBE3A protein interaction network. Figure 1: Protein Interaction Networks generated by STRING 9.0. Found 10 proteins that the UBE3A protein interacts with:. Figure 2: The 28 proteins identified by MINT. Identified 28 proteins that interact with UBE3A.
UBE3A -Angelman Syndrome - Introduction
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Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. What is Angelman syndrome? It is a neurodevelopmental disorder,where patients usually show signs of intellectual and development delay, difficulties in balance and movement, epilepsy, sleep disturbance, frequent laughter, and a small head size (microcephaly) [1,6]. How common is Angelman syndrome? About 70-75% of this syndrom...
DNA Motifs - UBE3A -Angelman Syndrome
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Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. DNA has short, recurring sequences, known as DNA motifs [4]. In general, they are presumed to have a biological function, such as binding sites for nucleases and transcription factors [4]. By looking at the sequence motifs, we could deduce the function of the gene or how the gene interacts with other genes. Motif Name: EGF 1.
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UBE3A -Angelman Syndrome - Introduction
Conclusion and Future Directions. The picture in the header was taken from here. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. What is Angelman syndrome? It is a neurodevelopmental disorder,where patients usually show signs of intellectual and development delay, difficulties in balance and movement, epilepsy, sleep disturbance, frequent laughter, and a small head size (microcephaly) [1,6]. How common is Angelman syndrome? About 70-75% of this syndrom...
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