Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Anna A. Dickson"'
Autor:
Anna S. Dickson, Tekle Pauzaite, Esther Arnaiz, Brian M. Ortmann, James A. West, Norbert Volkmar, Anthony W. Martinelli, Zhaoqi Li, Niek Wit, Dennis Vitkup, Arthur Kaser, Paul J. Lehner, James A. Nathan
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Cholesterol biosynthesis is a highly regulated, oxygen-dependent pathway, vital for cell membrane integrity and growth. In fungi, the dependency on oxygen for sterol production has resulted in a shared transcriptional response, resembling pr
Externí odkaz:
https://doaj.org/article/c87d491caba847fcaeae18fb670de9f1
Autor:
Anna S. Dickson, Tekle Pauzaite, Esther Arnaiz, Brian M. Ortmann, James A. West, Norbert Volkmar, Anthony W. Martinelli, Zhaoqi Li, Niek Wit, Dennis Vitkup, Arthur Kaser, Paul J. Lehner, James A. Nathan
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/1e8df5e5952f458ba4cea0c1b5668fea
Autor:
Anna S. Dickson, Tekle Pauzaite, Esther Arnaiz, Brian M. Ortmann, James A. West, Norbert Volkmar, Anthony W. Martinelli, Zhaoqi Li, Niek Wit, Dennis Vitkup, Arthur Kaser, Paul J. Lehner, James A. Nathan
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/2599fb5071604775b7eff4fa0c444bd5
Autor:
Alba Signes, Raffaele Cerutti, Anna S Dickson, Cristiane Benincá, Elizabeth C Hinchy, Daniele Ghezzi, Rosalba Carrozzo, Enrico Bertini, Michael P Murphy, James A Nathan, Carlo Viscomi, Erika Fernandez‐Vizarra, Massimo Zeviani
Publikováno v:
EMBO Molecular Medicine, Vol 11, Iss 1, Pp 1-21 (2018)
Abstract Loss‐of‐function mutations in APOPT1, a gene exclusively found in higher eukaryotes, cause a characteristic type of cavitating leukoencephalopathy associated with mitochondrial cytochrome c oxidase (COX) deficiency. Although the genetic
Externí odkaz:
https://doaj.org/article/215a8a7301c4477ba2ac4a4276753ce7
Autor:
Sam A Menzies, Norbert Volkmar, Dick JH van den Boomen, Richard T Timms, Anna S Dickson, James A Nathan, Paul J Lehner
Publikováno v:
eLife, Vol 7 (2018)
Mammalian HMG-CoA reductase (HMGCR), the rate-limiting enzyme of the cholesterol biosynthetic pathway and the therapeutic target of statins, is post-transcriptionally regulated by sterol-accelerated degradation. Under cholesterol-replete conditions,
Externí odkaz:
https://doaj.org/article/f84da21acd8c46149f6d640a9199b032
Autor:
Rafael Musayev, Lamia Hauter, Ashif I. Bhuiyan, Asha R. Santha, Anna A. Dickson, Alan J. Finkelstein, Tanaji T. Talele, Sanjai K. Pathak
Publikováno v:
The FASEB Journal. 36
Autor:
Faiza Rafi, Karl R. Fath, Anna A. Dickson, Tuhin Das, Guoshen Li, Gopal Subramaniam, Sarbani Ghoshal, Sanjai K. Pathak, Pratikkumar Rathod, Dibyendu Dana, Suneeta Paroly, Ashif I. Bhuiyan, Emmanuel J. Chang
Publikováno v:
Bioorganic Chemistry. 117:105463
Human cathepsin B is a cysteine-dependent protease whose roles in both normal and diseased cellular states remain yet to be fully delineated. This is primarily due to overlapping substrate specificities and lack of unambiguously annotated physiologic
Autor:
Elizabeth C. Hinchy, Raffaele Cerutti, Rosalba Carrozzo, James A. Nathan, Erika Fernandez-Vizarra, Michael P. Murphy, Carlo Viscomi, Alba Signes, Daniele Ghezzi, Cristiane Benincá, Massimo Zeviani, Anna S Dickson, Enrico Bertini
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
EMBO Molecular Medicine, Vol 11, Iss 1, Pp n/a-n/a (2019)
Loss‐of‐function mutations in APOPT1, a gene exclusively found in higher eukaryotes, cause a characteristic type of cavitating leukoencephalopathy associated with mitochondrial cytochrome c oxidase (COX) deficiency. Although the genetic associati
Autor:
Dick J. H. van den Boomen, James A. Nathan, Anna S Dickson, Richard T. Timms, Paul J. Lehner, Norbert Volkmar, Sam A. Menzies
Publikováno v:
eLife, Vol 7 (2018)
eLife
eLife
Mammalian HMG-CoA reductase (HMGCR), the rate-limiting enzyme of the cholesterol biosynthetic pathway and the therapeutic target of statins, is post-transcriptionally regulated by sterol-accelerated degradation. Under cholesterol-replete conditions,