Molecular characterization of two patients with severe LCAT deficiency-Reference-Cited by-同舟云学术

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Molecular characterization of two patients with severe LCAT deficiency

Published:2007-03-29 Issue:8 Volume:22 Page:2379-2382
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Charlton-Menys V.,Pisciotta L.,Durrington P. N.,Neary R.,Short C. D.,Calabresi L.,Calandra S.,Bertolini S.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/22/8/2379/5194520/gfm311.pdf

Cited by 13 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. Targeting host-specific metabolic pathways—opportunities and challenges for anti-infective therapy;Frontiers in Molecular Biosciences;2024-02-22

2. Familial LCAT Deficiency and Low HDL-C Levels: In silico Characterization of Two Rare LCAT Missense Mutations;The Application of Clinical Genetics;2024-02

3. A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency;Journal of Lipid Research;2022-03

4. LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred;Lipids in Health and Disease;2021-07-13

5. Molecular basis for activation of lecithin:cholesterol acyltransferase by a compound that increases HDL cholesterol;eLife;2018-11-27

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