Zobrazeno 1 - 10
of 362
pro vyhledávání: '"Carnitine transport"'
Autor:
Robert Olek
Publikováno v:
Kosmos. 69:777-784
Utrwalona od kilku lat opinia, że suplementacja karnityną nie zmienia metabolizmu, szczególnie metabolizmu wysiłkowego, opiera się głównie na protokołach suplementacji krótkoterminowej. Ostatnie badania sugerują, że kluczowymi czynnikami m
Autor:
Janet Haasjes, Frédéric M. Vaz, Sacha Ferdinandusse, Merel S. Ebberink, Ronald J.A. Wanders, Jos P.N. Ruiter, W. Oostheim, Henk van Lenthe, Hans R. Waterham, Heleen te Brinke, Lodewijk IJlst
Publikováno v:
Human Mutation
Human Mutation, 40(10), 1899-1904. Wiley-Liss Inc.
Human mutation, 40(10), 1899-1904. Wiley-Liss Inc.
Human Mutation, 40(10), 1899-1904. Wiley-Liss Inc.
Human mutation, 40(10), 1899-1904. Wiley-Liss Inc.
Primary carnitine deficiency is caused by a defect in the active cellular uptake of carnitine by Na+‐dependent organic cation transporter novel 2 (OCTN2). Genetic diagnostic yield for this metabolic disorder has been relatively low, suggesting that
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Han-Wook Yoo
Publikováno v:
Journal of Lipid and Atherosclerosis
Mitochondrial fatty acid β-oxidation (mFAO), which is the major pathway for the degradation of fatty acids and is critical for maintaining energy homeostasis in the human body, consists of carnitine transport, the carnitine shuttle, and fatty acid
Autor:
Robert S. Jones, Melanie A. Felmlee, Marilyn E. Morris, Kristin E. Follman, Vivian Rodriguez-Cruz
Publikováno v:
Pharmacol Rev
The solute carrier family 16 (SLC16) is comprised of 14 members of the monocarboxylate transporter (MCT) family that play an essential role in the transport of important cell nutrients and for cellular metabolism and pH regulation. MCTs 1–4 have be
Autor:
Kate Lichkus, Michel Tchan, Beena Devanapalli, Troy Dalkeith, Susan Thompson, Kaustuv Bhattacharya, Walid Matar, Adviye Ayper Tolun
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Ketone bodies form a vital energy source for end organs in a variety of physiological circumstances. At different times, the heart, brain and skeletal muscle in particular can use ketones as a primary substrate. Failure to generate ketones
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 2, Pp 58-62 (2012)
Carnitine (β-hydroxy-γ-trimethylaminobutyric acid) is involved in the transport of long-chain fatty acids into the mitochondrial matrix and the removal of potentially toxic acylcarnitine esters. Transient carnitine transport defect is a rare condit
Externí odkaz:
https://doaj.org/article/256e30770d204581876e4912b27752e8
Publikováno v:
Toxicology and Applied Pharmacology. 368:18-25
In spite of remarkable reduction in the number of children born with HIV due to antiretroviral therapy, concerns remain on the short- and long-term effects of antiretroviral drugs at the feto-placental unit. Cardio- and skeletal myopathies have been
Autor:
Si Chen, Jin Lin, Xiaojian Zhou, Shangqin Chen, Yan Nan, Zhenlang Lin, Yumei Huang, Yingying Hu
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-7 (2019)
BMC Pediatrics
BMC Pediatrics
Background Maternofetal carnitine transport through the placenta is the main route of fetal carnitine uptake. Decreased free carnitine levels discovered by newborn screening has identified many asymptomatic adult women with systemic primary carnitine
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.