Zobrazeno 1 - 10
of 212
pro vyhledávání: '"Lysine transport"'
Autor:
Sana Latif, Young-Sook Kang
Publikováno v:
Biomolecules & Therapeutics
Amyotrophic lateral sclerosis (ALS) is a lethal neurological disorder characterized by the deterioration of motor neurons. The aim of this study was to investigate alteration of cationic amino acid transporter (CAT-1) activity in the transport of lys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6454cfaf64bf702a11db2554d033d78
https://doi.org/10.4062/biomolther.2021.037
https://doi.org/10.4062/biomolther.2021.037
Publikováno v:
Journal of Inherited Metabolic Disease. 43:952-959
Patients with lysine-related inborn errors of metabolism (pyridoxine-dependent epilepsy [PDE] and glutaric aciduria type 1 [GA1]), follow a lysine-restricted diet with arginine-fortified lysine-free amino acid formula and additional oral arginine sup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d911ea48e35b9e14f77ff3f9643b2a0c
https://doi.org/10.1002/jimd.12233
https://doi.org/10.1002/jimd.12233
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1995 Dec . 92(26), 12036-12040.
Externí odkaz:
https://www.jstor.org/stable/2369039
Autor:
Nicola Longo, Joy Lee, Nanda M. Verhoeven-Duif, Levinus A. Bok, Arushi Gahlot Saini, R. Lilje, Hanka Dekker, Erle Kristensen, Saikat Santra, Peter E. Clayton, Damayanti Rusli Sjarif, Flavia Balbo Piazzon, Clara D.M. van Karnebeek, Johan L.K. Van Hove, Frits A. Wijburg, Monica Boyer, Pasquale Striano, Barbara Plecko, Anibh M. Das, Emma Footitt, Daniela Buhas, Sylvia Stockler-Ipsiroglu, François Feillet, Hans Hartmann, Philippa B. Mills, Laura A. Tseng, François Boemer, Jose E. Abdenur, Athanasios Evangeliou, Curtis R. Coughlin, Catherine Ashmore, Sameer M. Zuberi, Phillip L. Pearl, Roelineke J. Lunsing, Sidney M. Gospe, Majdi Kara, Maria T. Papadopoulou
Publikováno v:
Journal of inherited metabolic disease, 44(1), 178-192. Springer Netherlands
Journal of Inherited Metabolic Disease, 44(1), 178-192. SPRINGER
Journal of Inherited Metabolic Disease, 44(1), 178-192. SPRINGER
Pyridoxine-dependent epilepsy (PDE-ALDH7A1) is an autosomal recessive condition due to a deficiency of alpha-aminoadipic semialdehyde dehydrogenase, which is a key enzyme in lysine oxidation. PDE-ALDH7A1 is a developmental and epileptic encephalopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd4287a08df287ea8d4a1d7feccc9924
http://hdl.handle.net/11567/1040301
http://hdl.handle.net/11567/1040301
Autor:
Joury van 't Klooster
During his promotion, Joury van ‘t Klooster studied the kinetics of lysine transport and the lateral organization of proteins and lipids in the plasma membrane of yeast.The plasma membrane of yeast is very robust. This is believed to be caused by t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1185e4999f3588d02063c78116bd5ba7
https://doi.org/10.33612/diss.119641587
https://doi.org/10.33612/diss.119641587
Autor:
Daniel J. Drucker, Mahroukh Rafii, Jasmine Bahrami, Jacqueline A. Koehler, Paul B. Pencharz, Bernardo Yusta, Dianne Matthews, Jennifer Lee
Publikováno v:
Molecular Metabolism, Vol 6, Iss 3, Pp 245-255 (2017)
Molecular Metabolism
Molecular Metabolism
Objective Glucagon-like peptide-2 (GLP-2) is co-secreted with GLP-1 from gut endocrine cells, and both peptides act as growth factors to expand the surface area of the mucosal epithelium. Notably, GLP-2 also enhances glucose and lipid transport in en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24982694b6fd9f9cc589ffd938323538
http://www.sciencedirect.com/science/article/pii/S221287781730011X
http://www.sciencedirect.com/science/article/pii/S221287781730011X
Autor:
Tiejun Li, Jie Yin, Liping Sun, Yulong Yin, Kai Wang, Hui Han, Fei Wu, Gang Liu, Xingguo Huang, Jie Zheng, Rejun Fang, Xin Wu, Wenkai Ren, Yurong Zhao, Yuying Li, Chunyong Li, Zhaojin Liu
Publikováno v:
Cellular Physiology and Biochemistry, Vol 44, Iss 5, Pp 1749-1761 (2017)
Background/Aims: Our previous reports suggested that dietary supplementation with lysine influenced intestinal absorption and metabolism of amino acids. In this study, we further investigated the effect of lysine restriction (30%) on feed intake and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b721c8bc9170f90f3fa558a674286b8e
https://doi.org/10.1159/000485782
https://doi.org/10.1159/000485782
Publikováno v:
Journal of Animal Science. 94:106-110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae1b509b7e84d40a1193588f65c5a136
https://doi.org/10.2527/jas.2015-0207
https://doi.org/10.2527/jas.2015-0207
Publikováno v:
Amino Acids. 48:2197-2204
L-homoarginine (hArg) is derived from enzymatic guanidination of lysine. It was demonstrated that hArg is a substrate for nitric oxide (NO) synthesis, blocks lysine transport and inhibits the uptake of arginine into synaptosomes and modulates GABA re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::445f71af42730c6404b9944b22a32470
https://doi.org/10.1007/s00726-016-2251-y
https://doi.org/10.1007/s00726-016-2251-y
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 16
International Journal of Molecular Sciences, Vol 21, Iss 5594, p 5594 (2020)
Volume 21
Issue 16
International Journal of Molecular Sciences, Vol 21, Iss 5594, p 5594 (2020)
Amino acids are known to play a key role in gene expression regulation. Amino acid signaling is mediated via two pathways: the mammalian target of rapamycin complex 1 (mTORC1) and the amino acid responsive (AAR) pathways. Cationic amino acid transpor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18094ae061e526a4e304c8a96d45007b
https://doi.org/10.3390/ijms21165594
https://doi.org/10.3390/ijms21165594