Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Christopher M. Mulligan"'
Autor:
Stephanie R. Wesolowski, Christopher M. Mulligan, Rachel C. Janssen, Peter R. Baker, II, Bryan C. Bergman, Angelo D'Alessandro, Travis Nemkov, Kenneth N. Maclean, Hua Jiang, Tyler A. Dean, Diana L. Takahashi, Paul Kievit, Carrie E. McCurdy, Kjersti M. Aagaard, Jacob E. Friedman
Publikováno v:
Molecular Metabolism, Vol 18, Iss , Pp 25-41 (2018)
Objective: Non-alcoholic fatty liver disease (NAFLD) risk begins in utero in offspring of obese mothers. A critical unmet need in this field is to understand the pathways and biomarkers underlying fetal hepatic lipotoxicity and whether maternal dieta
Externí odkaz:
https://doaj.org/article/a28561519af14a2b8a154ec639481f85
Autor:
Carrie E. McCurdy, Kenneth N. Maclean, Paul Kievit, Bryan C. Bergman, Rachel C. Janssen, Peter R. Baker, Christopher M. Mulligan, Tyler Dean, Diana L. Takahashi, Travis Nemkov, Kjersti Aagaard, Hua Jiang, Stephanie R. Wesolowski, Angelo D'Alessandro, Jacob E. Friedman
Publikováno v:
Molecular Metabolism, Vol 18, Iss, Pp 25-41 (2018)
Molecular Metabolism
Molecular Metabolism
Objective Non-alcoholic fatty liver disease (NAFLD) risk begins in utero in offspring of obese mothers. A critical unmet need in this field is to understand the pathways and biomarkers underlying fetal hepatic lipotoxicity and whether maternal dietar
Autor:
Lance C. Li Puma, Adam J. Chicco, Jessica E. Prenni, Christopher M. Mulligan, Adam L. Heuberger, Kathryn C. Chatfield, Genevieve C. Sparagna, Catherine H. Le, Lindsay G. Benage, Steven M. Claypool, Kalyn S. Specht
Publikováno v:
J Biol Chem
Barth syndrome is a mitochondrial myopathy resulting from mutations in the tafazzin (TAZ) gene encoding a phospholipid transacylase required for cardiolipin remodeling. Cardiolipin is a phospholipid of the inner mitochondrial membrane essential for t
Autor:
Adam J Chicco, Christopher M Mulligan, Catherine H Le, Melissa A Routh, Dina Nemr, Lance C Li Puma, Peter E Linde, Gerrit J Bouma, Daniel P Regan, Manabu T Nakamura, Karen S Moulton
Publikováno v:
Circulation Research. 121
Single nucleotide polymorphisms of the FADS2 gene associate with cardiometabolic risk in humans. Additionally, serum fatty acid profiles reflecting hepatic hyperactivity of the FADS2 gene product, delta-6 desaturase (D6D), correspond to cardiometabol
Publikováno v:
The Journal of endocrinology. 235(1)
Transmission of metabolic diseases from mother to child is multifactorial and includes genetic, epigenetic and environmental influences. Evidence in rodents, humans and non-human primates support the scientific premise that exposure to maternal obesi
Autor:
Catherine H. Le, Robert C. Murphy, Christopher M. Mulligan, Gerrit J. Bouma, Melissa A. Routh, Michael R. Bristow, Russell L. Moore, Genevieve C. Sparagna, Kimberly M. Jeckel, Sylvia A. McCune, Simona Zarini, Adam J. Chicco, Melinda A. Frye, Joshua M. Lynch
Publikováno v:
Circulation: Heart Failure. 7:172-183
Background— Remodeling of myocardial phospholipids has been reported in various forms of heart failure for decades, but the mechanism and pathophysiological relevance of this phenomenon have remained unclear. We examined the hypothesis that δ-6 de
Autor:
Amanda J. Evans, Connor M. Whitaker, Lance C. Li Puma, Christopher M. Mulligan, Adam J. Chicco
Publikováno v:
The FASEB Journal. 30
Autor:
Jessica E. Prenni, Adam J. Chicco, Christopher M. Mulligan, Adam L. Heuberger, Lindsay G. Benage, Catherine H. Le
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857:e75
Autor:
Kimberly M. Jeckel, Phillip J Chapman, Christopher M. Mulligan, Jennifer R. Hegarty, D.N.R. Veeramachaneni, Melinda A. Frye, Michael J. Pagliassotti, Adam J. Chicco
Publikováno v:
The FASEB Journal. 26
Publikováno v:
The FASEB Journal. 26