Ichthyosis in Sjögren–Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Ichthyosis in Sjögren–Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion

Published:2010-01-05 Issue:6 Volume:302 Page:443-451
ISSN:0340-3696
Container-title:Archives of Dermatological Research
language:en
Short-container-title:Arch Dermatol Res

Author:

Rizzo William B.,S’Aulis Dana,Jennings M. Anitia,Crumrine Debra A.,Williams Mary L.,Elias Peter M.

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,General Medicine

Link

http://www.springerlink.com/index/pdf/10.1007/s00403-009-1022-y

Reference40 articles.

1. Brash AR, Yu Z, Boeglin WE, Schneider C (2007) The hepoxilin connection in the epidermis. FEBS J 274:3494–3502

2. De Laurenzi V, Rogers GR, Hamrock DJ, Marekov LN, Steinert PM, Compton JG, Markova N, Rizzo WB (1996) Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene. Nat Genet 12:52–57

3. Demerjian M, Crumrine DA, Milstone LM, Williams ML, Elias PM (2006) Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis (Chanarin–Dorfman syndrome). J Invest Dermatol 126:2032–2038

4. Elias PM (1983) Epidermal lipids, barrier function, and desquamation. J Invest Dermatol 80(Suppl):44s–49s

5. Elias PM, Cullander C, Maura T, Rassner U, Kömüves L, Brown BE, Menon GK (1998) The secretory granular cell: the outermost granular cell as a specialized secretory cell. J Invest Dermatol Symp Proc 3:87–100

Cited by 37 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. Sjögren Larsson syndrome: A case study with unique mutation;Brain Disorders;2024-03

2. Untargeted Metabolomic Analysis of Sjögren–Larsson Syndrome Reveals a Distinctive Pattern of Multiple Disrupted Biochemical Pathways;Metabolites;2023-05-23

3. Sjögren-Larsson Syndrome: A Rare Presentation With Developmental Delay;Cureus;2023-02-18

4. Novel ALDH3A2 mutations in structural and functional domains of FALDH causing diverse clinical phenotypes in Sjögren–Larsson syndrome patients;Human Mutation;2021-06-15

5. Sjögren‐Larsson syndrome: Anesthetic considerations and practical recommendations;Pediatric Anesthesia;2020-10-26

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3