PXE, a Mysterious Inborn Error Clarified-Reference-Cited by-同舟云学术

PXE, a Mysterious Inborn Error Clarified

Published:2019-02 Issue:2 Volume:44 Page:125-140
ISSN:0968-0004
Container-title:Trends in Biochemical Sciences
language:en
Short-container-title:Trends in Biochemical Sciences

Author:

Borst Piet,Váradi András,van de Wetering Koen

Funder

National Institutes of Health/National Institute of Arthritis and Musculoskeletal and Skin Diseases

Hungarian Academy of Sciences

Publisher

Elsevier BV

Subject

Molecular Biology,Biochemistry

Reference92 articles.

1. An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancy;Le Boulanger;Am. J. Med. Genet.,2009

2. Insights into pathomechanisms and treatment development in heritable ectopic mineralization disorders: summary of the PXE International Biennial Research Symposium 2016;Uitto;J. Invest. Dermatol.,2017

3. Etidronate for prevention of ectopic mineralization in patients with pseudoxanthoma elasticum;Kranenburg;J. Am. Coll. Cardiol.,2018

4. Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum;Le Saux;Nat. Genet.,2000

5. Mutations in ABCC6 cause pseudoxanthoma elasticum;Bergen;Nat. Genet.,2000

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2. The 2023 PXE Calcification Meeting in Budapest: A Focus on Clinical Trials for this Disease;Journal of Investigative Dermatology;2024-08

3. Plasma lipids in Pseudoxanthoma Elasticum (PXE) patients: A comparative study with population-based reference values and Non-PXE controls;Atherosclerosis Plus;2024-03

4. A new perspective on intervertebral disc calcification—from bench to bedside;Bone Research;2024-01-22

5. A Regulator Role for the ATP-Binding Cassette Subfamily C Member 6 Transporter in HepG2 Cells: Effect on the Dynamics of Cell–Cell and Cell–Matrix Interactions;International Journal of Molecular Sciences;2023-11-16