These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. 7-Dehydrocholesterol-derived oxysterols and retinal degeneration in a rat model of Smith-Lemli-Opitz syndrome. Xu L; Sheflin LG; Porter NA; Fliesler SJ Biochim Biophys Acta; 2012 Jun; 1821(6):877-83. PubMed ID: 22425966 [TBL] [Abstract][Full Text] [Related]
5. Novel oxysterols observed in tissues and fluids of AY9944-treated rats: a model for Smith-Lemli-Opitz syndrome. Xu L; Liu W; Sheflin LG; Fliesler SJ; Porter NA J Lipid Res; 2011 Oct; 52(10):1810-20. PubMed ID: 21817059 [TBL] [Abstract][Full Text] [Related]
6. Assays of plasma dehydrocholesteryl esters and oxysterols from Smith-Lemli-Opitz syndrome patients. Liu W; Xu L; Lamberson CR; Merkens LS; Steiner RD; Elias ER; Haas D; Porter NA J Lipid Res; 2013 Jan; 54(1):244-53. PubMed ID: 23072947 [TBL] [Abstract][Full Text] [Related]
7. Lipid biomarkers of oxidative stress in a genetic mouse model of Smith-Lemli-Opitz syndrome. Korade Z; Xu L; Mirnics K; Porter NA J Inherit Metab Dis; 2013 Jan; 36(1):113-22. PubMed ID: 22718275 [TBL] [Abstract][Full Text] [Related]
9. Probes for protein adduction in cholesterol biosynthesis disorders: Alkynyl lanosterol as a viable sterol precursor. Tallman KA; Kim HH; Korade Z; Genaro-Mattos TC; Wages PA; Liu W; Porter NA Redox Biol; 2017 Aug; 12():182-190. PubMed ID: 28258022 [TBL] [Abstract][Full Text] [Related]
10. Sterols and oxysterols in plasma from Smith-Lemli-Opitz syndrome patients. Griffiths WJ; Abdel-Khalik J; Crick PJ; Ogundare M; Shackleton CH; Tuschl K; Kwok MK; Bigger BW; Morris AA; Honda A; Xu L; Porter NA; Björkhem I; Clayton PT; Wang Y J Steroid Biochem Mol Biol; 2017 May; 169():77-87. PubMed ID: 26976653 [TBL] [Abstract][Full Text] [Related]
11. 7-Dehydrocholesterol-derived oxysterols cause neurogenic defects in Smith-Lemli-Opitz syndrome. Tomita H; Hines KM; Herron JM; Li A; Baggett DW; Xu L Elife; 2022 Sep; 11():. PubMed ID: 36111785 [TBL] [Abstract][Full Text] [Related]
12. DHCEO accumulation is a critical mediator of pathophysiology in a Smith-Lemli-Opitz syndrome model. Xu L; Mirnics K; Bowman AB; Liu W; Da J; Porter NA; Korade Z Neurobiol Dis; 2012 Mar; 45(3):923-9. PubMed ID: 22182693 [TBL] [Abstract][Full Text] [Related]
13. Biochemical and Clinical Effects of Vitamin E Supplementation in Hungarian Smith-Lemli-Opitz Syndrome Patients. Koczok K; Horváth L; Korade Z; Mezei ZA; Szabó GP; Porter NA; Kovács E; Mirnics K; Balogh I Biomolecules; 2021 Aug; 11(8):. PubMed ID: 34439893 [TBL] [Abstract][Full Text] [Related]
14. 7-Dehydrocholesterol metabolites produced by sterol 27-hydroxylase (CYP27A1) modulate liver X receptor activity. Endo-Umeda K; Yasuda K; Sugita K; Honda A; Ohta M; Ishikawa M; Hashimoto Y; Sakaki T; Makishima M J Steroid Biochem Mol Biol; 2014 Mar; 140():7-16. PubMed ID: 24269243 [TBL] [Abstract][Full Text] [Related]
15. Cholesterol deficiency in a mouse model of Smith-Lemli-Opitz syndrome reveals increased mast cell responsiveness. Kovarova M; Wassif CA; Odom S; Liao K; Porter FD; Rivera J J Exp Med; 2006 May; 203(5):1161-71. PubMed ID: 16618793 [TBL] [Abstract][Full Text] [Related]
16. The Effect of Small Molecules on Sterol Homeostasis: Measuring 7-Dehydrocholesterol in Dhcr7-Deficient Neuro2a Cells and Human Fibroblasts. Korade Z; Kim HY; Tallman KA; Liu W; Koczok K; Balogh I; Xu L; Mirnics K; Porter NA J Med Chem; 2016 Feb; 59(3):1102-15. PubMed ID: 26789657 [TBL] [Abstract][Full Text] [Related]
17. Cholesterol biosynthesis from birth to adulthood in a mouse model for 7-dehydrosterol reductase deficiency (Smith-Lemli-Opitz syndrome). Marcos J; Shackleton CH; Buddhikot MM; Porter FD; Watson GL Steroids; 2007 Oct; 72(11-12):802-8. PubMed ID: 17714750 [TBL] [Abstract][Full Text] [Related]
18. Oxysterols from free radical chain oxidation of 7-dehydrocholesterol: product and mechanistic studies. Xu L; Korade Z; Porter NA J Am Chem Soc; 2010 Feb; 132(7):2222-32. PubMed ID: 20121089 [TBL] [Abstract][Full Text] [Related]
19. Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome. Wassif CA; Maslen C; Kachilele-Linjewile S; Lin D; Linck LM; Connor WE; Steiner RD; Porter FD Am J Hum Genet; 1998 Jul; 63(1):55-62. PubMed ID: 9634533 [TBL] [Abstract][Full Text] [Related]
20. Oxidative stress, serotonergic changes and decreased ultrasonic vocalizations in a mouse model of Smith-Lemli-Opitz syndrome. Sharif NF; Korade Z; Porter NA; Harrison FE Genes Brain Behav; 2017 Jul; 16(6):619-626. PubMed ID: 28220990 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]