Temporal changes in the brain lipidome during neurodevelopment of Smith–Lemli–Opitz syndrome mice
Author:
Affiliation:
1. Department of Medicinal Chemistry, University of Washington, Seattle, WA, USA
2. Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA, USA
Abstract
Funder
National Institute of Environmental Health Sciences
National Institute of General Medical Sciences
National Institute of Child Health and Human Development
National Center for Advancing Translational Sciences
Publisher
Royal Society of Chemistry (RSC)
Subject
Electrochemistry,Spectroscopy,Environmental Chemistry,Biochemistry,Analytical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/AN/D2AN00137C
Reference64 articles.
1. Carrier Frequency of the Common Mutation IVS8-1G>C in DHCR7 and Estimate of the Expected Incidence of Smith–Lemli–Opitz Syndrome
2. Frequency and ethnic distribution of the commonDHCR7 mutation in Smith-Lemli-Opitz syndrome
3. SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutations
4. Malformation syndromes caused by disorders of cholesterol synthesis
5. Defective Cholesterol Biosynthesis Associated with the Smith-Lemli-Opitz Syndrome
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. MALDI-IM-MS Imaging of Brain Sterols and Lipids in a Mouse Model of Smith-Lemli-Opitz Syndrome;2023-10-02
2. Smith-Lemli-Opitz syndrome: A pathophysiological manifestation of the Bloch hypothesis;Frontiers in Molecular Biosciences;2023-01-12
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