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of 3
pro vyhledávání: '"Ann E. Frazier"'
Autor:
Ann E. Frazier, David A. Stroud, Nicholas A. Jamnick, David R. Thorburn, Adrienne Laskowski, Melinda T. Coughlan, Javier Botella, Nikeisha J. Caruana, Boris Reljic, Kevin Huynh, Tegan Stait, David Bishop, H. Janssen, Cesare Granata, Natalie A. Mellett, Peter J. Meikle, Jujiao Kuang
SUMMARYMitochondrial defects are implicated in multiple diseases and aging. Exercise training is an accessible and inexpensive therapeutic intervention improving mitochondrial bioenergetics and quality of life. By combining a multi-omics approach wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a43cd52864b89b8d72d6b2fa6680950
https://doi.org/10.1101/2021.02.19.431993
https://doi.org/10.1101/2021.02.19.431993
Rothmund-Thomson Syndrome (RTS) is an autosomal recessive disorder characterized by poikiloderma, sparse or absent hair, and defects in the skeletal system such as bone hypoplasia, short stature, low bone mass, and an increased incidence of osteosarc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9dcfab24a0fd1a0d325910115205ec2
https://doi.org/10.1101/2020.11.11.379214
https://doi.org/10.1101/2020.11.11.379214
Autor:
Diana Stojanovski, Alexander J Anderson, David A. Stroud, Dedreia Tull, Malcolm J. McConville, Ann E. Frazier, Michael T. Ryan, Yilin Kang, Nicholas J. Clemons, Catherine S Palmer, Kenji M Fujihara, Tegan Stait, David P De Souza, David R. Thorburn
Human Tim8a is a member of an intermembrane space chaperone network, known as the small TIM family, which transport hydrophobic membrane proteins through this compartment. Mutations in TIMM8A cause a neurodegenerative disease, Mohr-Tranebjærg syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ee7d049f5e69a1cb2a946a3bb22baeb