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pro vyhledávání: '"Kelsey A. Meacham"'
Autor:
Ugochukwu Kelvin Ihenacho, Kelsey A. Meacham, Megan Cleland Harwig, Michael E. Widlansky, R. Blake Hill
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Mitochondrial fission protein 1 (Fis1) was identified in yeast as being essential for mitochondrial division or fission and subsequently determined to mediate human mitochondrial and peroxisomal fission. Yet, its exact functions in humans, especially
Externí odkaz:
https://doaj.org/article/7f3518f105834c6e875afa31df4302b2
Autor:
Kelsey A. Meacham, John M. Egner, Megan C. Harwig, Maxx H. Tessmer, Elizabeth L. Noey, Ugochukwu K. Ihenacho, Francis C. Peterson, Michael E. Widlansky, Blake R. Hill
Publikováno v:
Biophysical Journal. 121:19a
Autor:
Mauricio Latorre, Martina Ralle, Eve M. Wiggins, Alejandro Maass, María Paz Cortés, Jason L. Burkhead, Kelsey A. Meacham
Publikováno v:
Metallomics. 10:1595-1606
Wilson disease (WD) is an autosomal recessive disorder caused by mutation in the ATP7B gene that affects copper transport in the body. ATP7B mutation damages copper transporter function, ultimately resulting in excessive copper accumulation and subse
Autor:
Kelsey A, Meacham, María Paz, Cortés, Eve M, Wiggins, Alejandro, Maass, Mauricio, Latorre, Martina, Ralle, Jason L, Burkhead
Publikováno v:
Metallomics : integrated biometal science. 10(11)
Wilson Disease (WD) is an autosomal recessive disorder caused by mutation in the ATP7B gene that affects copper transport in the body. ATP7B mutation damages copper transporter function, ultimately resulting in excessive copper accumulation and subse