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disorder of lysine and hydroxylysine metabolism相关文献:
Neutrophil Adhesion and the Release of the Free Amino Acid Hydroxylysine.
Galkina SI, Fedorova NV, Ksenofontov AL, Serebryakova MV, Golenkina EA, Stadnichuk VI, Baratova LA, Sud'ina GF.
Cells. 2021 Mar 5;10(3):563. doi: 10.3390/cells10030563.
PMID:33807594
Glutaric acidemia type 1.
Hedlund GL, Longo N, Pasquali M.
Am J Med Genet C Semin Med Genet. 2006 May 15;142C(2):86-94. doi: 10.1002/ajmg.c.30088.
PMID:16602100
Collagen IV biosynthesis: Intracellular choreography of post-translational modifications.
Ishikawa Y, Lennon R, Forneris F, Myllyharju J, Salo AM.
Matrix Biol. 2025 Sep;140:59-77. doi: 10.1016/j.matbio.2025.07.002. Epub 2025 Jul 4.
PMID:40618934
Molecular identification of hydroxylysine kinase and of ammoniophospholyases acting on 5-phosphohydroxy-L-lysine and phosphoethanolamine.
Veiga-da-Cunha M, Hadi F, Balligand T, Stroobant V, Van Schaftingen E.
J Biol Chem. 2012 Mar 2;287(10):7246-55. doi: 10.1074/jbc.M111.323485. Epub 2012 Jan 12.
PMID:22241472
Estimation of hydroxylysine in urine and serum of patients with chronic uremia.
Dubovsky J, Geary WT Jr, Chilcutt DA.
Clin Chim Acta. 1977 Apr 1;76(1):41-53. doi: 10.1016/0009-8981(77)90117-6.
PMID:856503
Prediction and analysis of protein hydroxyproline and hydroxylysine.
Hu LL, Niu S, Huang T, Wang K, Shi XH, Cai YD.
PLoS One. 2010 Dec 31;5(12):e15917. doi: 10.1371/journal.pone.0015917.
PMID:21209839
Urinary excretion of hydroxylysine and its glycosides as an index of collagen degradation.
Krane SM, Kantrowitz FG, Byrne M, Pinnell SR, Singer FR.
J Clin Invest. 1977 May;59(5):819-27. doi: 10.1172/JCI108704.
PMID:404321
Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism.
Zhang X, Nemeria NS, Leandro J, Houten S, Lazarus M, Gerfen G, Ozohanics O, Ambrus A, Nagy B, Brukh R, Jordan F.
J Biol Chem. 2020 Jun 5;295(23):8078-8095. doi: 10.1074/jbc.RA120.012761. Epub 2020 Apr 17.
PMID:32303640
Reducible crosslinks in hydroxylysine-deficient collagens of a heritable disorder of connective tissue.
Eyre DR, Glimcher MJ.
Proc Natl Acad Sci U S A. 1972 Sep;69(9):2594-8. doi: 10.1073/pnas.69.9.2594.
PMID:4506780
New mechanistic insights to PLOD1-mediated human vascular disease.
Koenig SN, Cavus O, Williams J, Bernier M, Tonniges J, Sucharski H, Dew T, Akel M, Baker P, Madiai F, De Giorgi F, Scietti L, Faravelli S, Forneris F, Mohler PJ, Bradley EA.
Transl Res. 2022 Jan;239:1-17. doi: 10.1016/j.trsl.2021.08.002. Epub 2021 Aug 13.
PMID:34400365
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