Heritable Ectopic Mineralization Disorders: The Paradigm of Pseudoxanthoma Elasticum
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference46 articles.
1. MOAT-E (ARA) is a full-length MRP/cMOAT subfamily transporter expressed in kidney and liver;Belinsky;Br J Cancer,1999
2. Mutations in ABCC6 cause pseudoxanthoma elasticum;Bergen;Nat Genet,2000
3. Does the absence of ABCC6 (multidrug resistance protein 6) in patients with Pseudoxanthoma elasticum prevent the liver from providing sufficient vitamin K to the periphery?;Borst;Cell Cycle,2008
4. Vitamin K does not prevent soft tissue mineralization in a mouse model of pseudoxanthoma elasticum;Brampton;Cell Cycle,2011
5. A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structure;Cai;J Mol Med,2000
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1. Clinical and subclinical findings in heterozygous ABCC6 carriers: results from a Belgian cohort and clinical practice guidelines;Journal of Medical Genetics;2021-04-05
2. From membrane to mineralization: the curious case of the ABCC6 transporter;FEBS Letters;2020-11-21
3. Étude du fond d’œil en fonction de l’âge dans le pseudoxanthome élastique chez 158 patients;Journal Français d'Ophtalmologie;2018-09
4. Subretinal fibrosis is associated with fundus pulverulentus in pseudoxanthoma elasticum;Graefe's Archive for Clinical and Experimental Ophthalmology;2018-02-26
5. Pathology of the Elastic Matrix;Elastic Fiber Matrices;2016-05-19
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