Autumn Brown - Profile and Journalist Details

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Total articles 7

• A community-science approach identifies genetic variants associated with three color morphs in ball pythons (Python regius)

  By Autumn Brown, Eastern Michigan, Kaylee Comai, Dominic Mannino| PLOS@ The Ultramel color morph is associated with a missense variant and a putative deletion in TYRP1The Ultramel color morph is characterized by skin patches that are tan or light brown, rather than dark brown or black. This phenotype suggests a mild loss of melanin. We hypothesized that this phenotype was caused by loss of function of one of five genes: TYRP1, TYRP2, SLC7A11, SLC24A5, and SLC45A2 (Table 1). TYRP1 and TYRP2 encode enzymes involved in synthesizing melanin [87].

  By Autumn Brown, Eastern Michigan, Kaylee Comai, Dominic Mannino · PLOS

  Oct. 19, 2022

• Remote data-collection during COVID 19: Thing of the past or the way of the future?

  By Sharon G. Wolf, Elisabetta Aurino, Autumn Brown, Edward Tsinigo| World Bank Blogs@ The COVID-19 pandemic pushed the process of collecting learning data from in-person to remote in just a few weeks, mobilizing researchers and practitioners alike to learn new systems, adapt instruments, and engage in a great deal of trial and error. Today, nearly two years after the first shutdowns, the education sector is cautiously moving back to in-person activities with new expertise and new questions, including: “What will we continue to do remotely? What can’t we do remotely?

  By Sharon G. Wolf, Elisabetta Aurino, Autumn Brown, Edward Tsinigo · World Bank Blogs

  Apr. 13, 2022

• A community-science approach identifies genetic variants associated with three color morphs in ball pythons (Python regius)

  By Autumn Brown, Eastern Michigan, Kaylee Comai, Dominic Mannino| PLOS@ The Ultramel color morph is associated with a missense variant and a putative deletion in TYRP1The Ultramel color morph is characterized by skin patches that are tan or light brown, rather than dark brown or black. This phenotype suggests a mild loss of melanin. We hypothesized that this phenotype was caused by loss of function of one of five genes: TYRP1, TYRP2, SLC7A11, SLC24A5, and SLC45A2 (Table 1). TYRP1 and TYRP2 encode enzymes involved in synthesizing melanin [87].

  By Autumn Brown, Eastern Michigan, Kaylee Comai, Dominic Mannino · PLOS

  Oct. 19, 2022

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