Fragile X Syndrome, a lack of FMR1 protein. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. Introduction to Fragile X Syndrome. According to The Fragile X Association of Australia. Until the discovery of the .

This web page was produced as an assignment for Genetics 677, an undergraduate course at UW-Madison. SMN1 - Survival Motor Neuron 1, telomeric. Type I Acute - 6 months after birth. Type II Intermediate - age 6 - 18 months. Type III Mild - 18 months - early adulthood. Type IV Adult Onset - adulthood.

This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. For more information about the HLA-DQA1 gene click here. Or see the gene tab in the main menu.

This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. Many famous people have been diagnosed, or thought to have battled with the disease, including Robert Downey Jr. , Britney Spears, Ben Stiller, Mozart, Beethoven, Vincent Van Gogh, Winston Churchill, Abraham Lincoln, Edgar Allen Poe, and possibly Charles Darwin. Twin studies have been limite.

Summary of popular press article. This web page was produced as an assignment for Gen677 at UW-Madison Spring 2010. Please click on images themselves for a larger view. CFH and Age-Related Macular Degeneration.

Popular Press vs Scientific Review. This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. Image is courtesy of healthscape. The following video shows animations for describing the symptoms, causes, and hope for those living with PD. 1 How do I prevent myself from getting PD? There is currently no known way to prevent getting PD. 2 Who is more at risk from getting PD? .

Homology, Phylogeny and Alignments. This web page was produced as an assignment for. Gene on the X chromosome. The type of SCID caused by mutations to the. Gene is autosomal recessive and is the second most common T B SCID. Located on the short arm of chromosome 19 at band 13. 1, as seen in Figure 2,. Gene codes for the JAK3 protein, .

This web page was produced as an assignment for Genetics 677. An undergraduate course at UW-Madison. The goal of this project is to perform an in depth analysis of the MeCP2 gene and its impact on Rett Syndrome using genomic and bioinformatics tools. Seizures and mental retardation are also common features.

This page was produced as an assignment for Genetics 677. 5 Mb on human chromosome 7q11. 23, as depicted in figure 1.

Protein motifs, homology, phylogeny. This web page was produced as an assignment for Gen677. SIRT6 and its link to aging. From Mostoslavsky et al Genomic instability and agind like phenotype in the absence of mammalian SIRT6 cell paper.