Beren Karaosmanoglu
Ankara, Turkey
Last Updated: 09/26/2026
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Found 37 publications
Transcriptome analysis of unmedicated heterozygous familial Mediterranean fever patients reveals a type I interferon signature driving increasing Pyrin expression.
Journal: Annals of the rheumatic diseases
Published: May 08, 2025
Hierarchical TiO2 nanotube arrays enhance mesenchymal stem cell adhesion and regenerative potential through surface nanotopography.
Journal: Journal of the Royal Society, Interface
Published: February 25, 2025
ERF-Related Craniosynostosis in a Patient With Hypochondroplasia: A Case Report.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: February 19, 2025
Unraveling the Role of RSPRY1 in TGF-β Pathway Dysregulation: Insights into the Pathogenesis of Spondyloepimetaphyseal Dysplasia.
Journal: International journal of molecular sciences
Published: December 19, 2024
Ex vivo disease modelling of Rett syndrome: the transcriptomic and metabolomic implications of direct neuronal conversion.
Journal: Molecular biology reports
Published: July 09, 2024
A Novel Pathogenic TSPEAR Variant in a Family with Clinical Variability: Definition of Dental Anomalies and Review of the Literature.
Journal: Molecular syndromology
Published: July 03, 2024
The effect of LARP7 on gene expression during osteogenesis.
Journal: Molecular biology reports
Published: June 26, 2024
Microfluidic Fabrication of Gelatin-Nano Hydroxyapatite Scaffolds for Enhanced Control of Pore Size Distribution and Osteogenic Differentiation of Dental Pulp Stem Cells.
Journal: Macromolecular bioscience
Published: June 13, 2024
Two cases with undefined childhood interstitial lung disease: Can it be related to telomere variants?
Journal: Journal of paediatrics and child health
Published: May 20, 2024
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia.
Journal: American journal of medical genetics. Part A
Published: February 04, 2024
AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis.
Journal: Pathology, research and practice
Published: January 04, 2024
A Novel ZBTB20 Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive Features.
Journal: Molecular syndromology
Published: December 18, 2023
Last Updated: 09/26/2026