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Calvin News

Finding answers and building network for rare disease community

Wed, Jun 13, 2018
Connor Bechler

How can mutations in one supposedly single-function protein result in four unique diseases with symptoms ranging from strangely textured hair to early death?

That鈥檚 the question that biochemistry professor聽Rachael Baker and biology professor聽Amy Wilstermann are seeking to answer through three linked research projects this summer. Working with three student researchers to conduct experiments on the mitochondria of yeast and zebrafish, the professors are examining the effects of mutations in the protein鈥檚 gene to determine its other roles within the cell.

By discovering how each mutation results in each disease, Baker says they hope to more fully understand the mitochondrial system, leading to both 鈥渂etter treatments for people affected by rare diseases and a better understanding about health and wellness in general that could lead to treatments for things like cancer and other disorders.鈥

Beyond the lab

Baker and Wilstermann, however, view these direct applications as only one step in the larger process of improving the lives of those with rare diseases.

鈥淭here鈥檚 just a lot of uncertainty [around rare disease]; even when you get a diagnosis, you might not know what the prognosis is,鈥 said Wilstermann. She and Baker aim to help remedy this through two key routes: improving the readability of scholarly work on rare disease and providing a website to collect information for patients and their families.

During the summer, Wilstermann says, the students will work toward both goals by reviewing the literature around a specific rare disease and writing a condensed summary for the website, giving them practice in 鈥渢aking really complicated ideas and mak[ing] them accessible but still completely accurate.鈥 Wilstermann says that the students will most likely start by covering the diseases which were represented at the聽rare disease symposium (in March 2018) and are present in the local community.

The website is broadly intended to function as a network for members of the rare disease community, including patients, families, clinicians, and researchers. 鈥淲e want it to be a place where we can connect people with resources; we want it to be a place where people can connect with one another,鈥 Wilstermann said. 鈥淭here鈥檚 opportunity to bring people together and help build a supportive community around common experiences, and the common experience of being rare.鈥

A faith-driven approach

鈥淭his project, for me, encapsulates why I came to be a professor at Calvin college,鈥 said Baker. 鈥淭he way we do science looks different here,鈥 she added. 鈥淲e eat together each week, we value each other, and we [work] in a body of Christ model where different people have different strengths and interests [which we] bring together to be a functioning whole. We鈥檝e employed various practices that are really rooted in Christian principles, and we鈥檝e used those to shape how we run our research team.

鈥淭o me," Baker said, "it鈥檚 really exciting that I get to do that and think about it explicitly."