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The Journal of Biological Chemistry|March 21, 2003
Mammalian fibroblasts lacking mitochondrial NAD+-dependent methylenetetrahydrofolate dehydrogenase-cyclohydrolase are glycine auxotrophsHarshila Patel, Erminia Di Pietro, Robert E MacKenzieGene Expression Patterns : GEP|March 8, 2005
Gene expression pattern of Claudin-1 during chick embryogenesisAnnie Simard, Erminia Di Pietro, Aimee K RyanBiochimica Et Biophysica Acta|September 3, 2004
The expression of mitochondrial methylenetetrahydrofolate dehydrogenase-cyclohydrolase supports a role in rapid cell growthErminia Di Pietro, Xiao-Ling Wang, Robert E MacKenzieArchives of Biochemistry and Biophysics|September 10, 2005
NAD- and NADP-dependent mitochondrially targeted methylenetetrahydrofolate dehydrogenase-cyclohydrolases can rescue mthfd2 null fibroblastsHarshila Patel, Erminia Di Pietro, Narciso Mejia, et al.American Journal of Medical Genetics. Part A|August 20, 2022
Expanding the genotypic and phenotypic landscapes of rhizomelic chondrodysplasia punctata type 3 (RCDP3) with two novel families, and a review of the literatureEzgi Gökpınar İli, Alper Gezdirici, Erminia Di Pietro, et al.Mechanisms of Development|February 28, 2006
Alterations in heart looping induced by overexpression of the tight junction protein Claudin-1 are dependent on its C-terminal cytoplasmic tailAnnie Simard, Erminia Di Pietro, Christopher R Young, et al.Journal of Lipid Research|March 9, 2025
Spatial characterization of RPE structure and lipids in the PEX1-p.Gly844Asp mouse model for Zellweger spectrum disorderSamy Omri, Catherine Argyriou, Rachel S Pryce, et al.Disease Models & Mechanisms|December 22, 2019
Oral administration of a synthetic vinyl-ether plasmalogen normalizes open field activity in a mouse model of rhizomelic chondrodysplasia punctataWedad Fallatah, Tara Smith, Wei Cui, et al.Biorxiv : the Preprint Server for Biology|May 25, 2026
Clinically relevant AAV8- PEX1 gene therapy preserves retinal integrity and function long-term in a murine model of Zellweger spectrum disorderSamy Omri, Erminia Di Pietro, Devin S McDougald, et al.Journal of Clinical Research in Pediatric Endocrinology|March 25, 2015
Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 GeneAbdullah Çim, Salih Coşkun, Orhan Görükmez, et al.Pageof 3