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Ligia Mateiu

Showing results (11-20 of 34) with videos related to

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Pediatric Neurology|August 30, 2024
The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric StudyLiene Thys, Diane Beysen, Berten Ceulemans, et al.
Mitochondrion|September 13, 2011
Nuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studiesAmanda Ramos, Elena Barbena, Ligia Mateiu, et al.
Calcified Tissue International|December 5, 2023
An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone RemodelingGretl Hendrickx, Eveline Boudin, Ligia Mateiu, et al.
Nucleic Acids Research|January 9, 2013
Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domainsNiels Van der Aa, Jiqiu Cheng, Ligia Mateiu, et al.
Acta Neuropathologica Communications|January 13, 2017
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative diseaseThomas Geuens, Vicky De Winter, Nicholas Rajan, et al.
European Journal of Human Genetics : EJHG|January 25, 2024
Identification of a DLG3 stop mutation in the MRX20 familyJolien Huyghebaert, Ligia Mateiu, Ellen Elinck, et al.
Brain : a Journal of Neurology|June 15, 2021
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunctionJonas Van Lent, Peter Verstraelen, Bob Asselbergh, et al.
International Journal of Molecular Sciences|November 25, 2023
Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and CholestophagyClaudia Theys, Joe Ibrahim, Ligia Mateiu, et al.
Frontiers in Molecular Medicine|August 1, 2024
Loss of PPARα function promotes epigenetic dysregulation of lipid homeostasis driving ferroptosis and pyroptosis lipotoxicity in metabolic dysfunction associated Steatotic liver disease (MASLD)Claudia Theys, Tineke Vanderhaeghen, Evelien Van Dijck, et al.
European Journal of Human Genetics : EJHG|October 21, 2025
A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndromeClaudio Peter D'Incal, Bram Dierickx, Claudia Vingerhoets, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Pediatric Neurology|August 30, 2024
The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric StudyLiene Thys, Diane Beysen, Berten Ceulemans, et al.
Mitochondrion|September 13, 2011
Nuclear insertions of mitochondrial origin: Database updating and usefulness in cancer studiesAmanda Ramos, Elena Barbena, Ligia Mateiu, et al.
Calcified Tissue International|December 5, 2023
An Additional Lrp4 High Bone Mass Mutation Mitigates the Sost-Knockout Phenotype in Mice by Increasing Bone RemodelingGretl Hendrickx, Eveline Boudin, Ligia Mateiu, et al.
Nucleic Acids Research|January 9, 2013
Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domainsNiels Van der Aa, Jiqiu Cheng, Ligia Mateiu, et al.
Acta Neuropathologica Communications|January 13, 2017
Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative diseaseThomas Geuens, Vicky De Winter, Nicholas Rajan, et al.
European Journal of Human Genetics : EJHG|January 25, 2024
Identification of a DLG3 stop mutation in the MRX20 familyJolien Huyghebaert, Ligia Mateiu, Ellen Elinck, et al.
Brain : a Journal of Neurology|June 15, 2021
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunctionJonas Van Lent, Peter Verstraelen, Bob Asselbergh, et al.
International Journal of Molecular Sciences|November 25, 2023
Mitochondrial GpC and CpG DNA Hypermethylation Cause Metabolic Stress-Induced Mitophagy and CholestophagyClaudia Theys, Joe Ibrahim, Ligia Mateiu, et al.
Frontiers in Molecular Medicine|August 1, 2024
Loss of PPARα function promotes epigenetic dysregulation of lipid homeostasis driving ferroptosis and pyroptosis lipotoxicity in metabolic dysfunction associated Steatotic liver disease (MASLD)Claudia Theys, Tineke Vanderhaeghen, Evelien Van Dijck, et al.
European Journal of Human Genetics : EJHG|October 21, 2025
A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndromeClaudio Peter D'Incal, Bram Dierickx, Claudia Vingerhoets, et al.
Pageof 4