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Journal of Inherited Metabolic Disease
|
December 11, 2025
Lipid Metabolism Alterations in Hereditary Inorganic Pyrophosphate Deficiency Syndromes: A Narrative Review of Insights and Controversies
Robbe Derudder, Olivier M Vanakker
Biomolecules
|
November 25, 2023
Significance of Premature Vertebral Mineralization in Zebrafish Models in Mechanistic and Pharmaceutical Research on Hereditary Multisystem Diseases
Judith Van Wynsberghe, Olivier M Vanakker
International Journal of Molecular Sciences
|
December 11, 2022
Mitochondrial Dysfunction and Oxidative Stress in Hereditary Ectopic Calcification Diseases
Lukas L Nollet, Olivier M Vanakker
World Journal of Clinical Cases
|
August 6, 2015
From variome to phenome: Pathogenesis, diagnosis and management of ectopic mineralization disorders
Eva Yg De Vilder, Olivier M Vanakker
Stroke Research and Treatment
|
February 19, 2011
Hereditary connective tissue diseases in young adult stroke: a comprehensive synthesis
Olivier M Vanakker, Dimitri Hemelsoet, Anne De Paepe
International Journal of Molecular Sciences
|
February 15, 2022
Minocycline Counteracts Ectopic Calcification in a Murine Model of Pseudoxanthoma Elasticum: A Proof-of-Concept Study
Elise Bouderlique, Lukas Nollet, Emmanuel Letavernier, et al.
Frontiers in Genetics
|
October 19, 2013
The ABCC6 transporter: what lessons can be learnt from other ATP-binding cassette transporters?
Olivier M Vanakker, Mohammad J Hosen, Anne De Paepe
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 29, 2021
Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a model
Wouter Steyaert, Shana Verschuere, Paul J Coucke, et al.
FEBS Letters
|
November 1, 2020
From membrane to mineralization: the curious case of the ABCC6 transporter
Shana Verschuere, Matthias Van Gils, Lukas Nollet, et al.
International Journal of Molecular Sciences
|
January 27, 2017
GGCX-Associated Phenotypes: An Overview in Search of Genotype-Phenotype Correlations
Eva Y G De Vilder, Jens Debacker, Olivier M Vanakker
Page
of 6
Search research articles
Search
Showing results (1-10 of 54) with videos related to
Sort By:
Page
of 6
Journal of Inherited Metabolic Disease
|
December 11, 2025
Lipid Metabolism Alterations in Hereditary Inorganic Pyrophosphate Deficiency Syndromes: A Narrative Review of Insights and Controversies
Robbe Derudder, Olivier M Vanakker
Biomolecules
|
November 25, 2023
Significance of Premature Vertebral Mineralization in Zebrafish Models in Mechanistic and Pharmaceutical Research on Hereditary Multisystem Diseases
Judith Van Wynsberghe, Olivier M Vanakker
International Journal of Molecular Sciences
|
December 11, 2022
Mitochondrial Dysfunction and Oxidative Stress in Hereditary Ectopic Calcification Diseases
Lukas L Nollet, Olivier M Vanakker
World Journal of Clinical Cases
|
August 6, 2015
From variome to phenome: Pathogenesis, diagnosis and management of ectopic mineralization disorders
Eva Yg De Vilder, Olivier M Vanakker
Stroke Research and Treatment
|
February 19, 2011
Hereditary connective tissue diseases in young adult stroke: a comprehensive synthesis
Olivier M Vanakker, Dimitri Hemelsoet, Anne De Paepe
International Journal of Molecular Sciences
|
February 15, 2022
Minocycline Counteracts Ectopic Calcification in a Murine Model of Pseudoxanthoma Elasticum: A Proof-of-Concept Study
Elise Bouderlique, Lukas Nollet, Emmanuel Letavernier, et al.
Frontiers in Genetics
|
October 19, 2013
The ABCC6 transporter: what lessons can be learnt from other ATP-binding cassette transporters?
Olivier M Vanakker, Mohammad J Hosen, Anne De Paepe
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 29, 2021
Comprehensive validation of a diagnostic strategy for sequencing genes with one or multiple pseudogenes using pseudoxanthoma elasticum as a model
Wouter Steyaert, Shana Verschuere, Paul J Coucke, et al.
FEBS Letters
|
November 1, 2020
From membrane to mineralization: the curious case of the ABCC6 transporter
Shana Verschuere, Matthias Van Gils, Lukas Nollet, et al.
International Journal of Molecular Sciences
|
January 27, 2017
GGCX-Associated Phenotypes: An Overview in Search of Genotype-Phenotype Correlations
Eva Y G De Vilder, Jens Debacker, Olivier M Vanakker
Page
of 6