Riza K. Ozgul
Ankara, 06230, Turkey
Last Updated: 09/26/2026
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Found 16 publications
Genetic Variants in Early-Onset Inflammatory Bowel Disease: Monogenic Causes and Clinical Implications.
Journal: Children (Basel, Switzerland)
Published: March 14, 2025
Turning Trash Into Treasure: A Simple Protocol for Human Mesenchymal Stromal Cell Isolation From Used Bone Marrow Collection Kits.
Journal: Current protocols
Published: April 12, 2024
The bridge between cell survival and cell death: reactive oxygen species-mediated cellular stress.
Journal: EXCLI journal
Published: May 30, 2023
Immunodeficiency in a Child with Alström Syndrome.
Journal: Indian journal of pediatrics
Published: November 08, 2017
A New Chapter for Mesenchymal Stem Cells: Decellularized Extracellular Matrices.
Journal: Stem cell reviews and reports
Published: August 03, 2017
The genotypic and phenotypic spectrum of MTO1 deficiency.
Journal: Molecular genetics and metabolism
Published: July 28, 2017
A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation.
Journal: Clinical dysmorphology
Published: August 23, 2016
Allergy-specific Phenome-Wide Association Study for Immunogenes in Turkish Children.
Journal: Scientific reports
Published: May 20, 2016
Haplotype analysis of non-HLA immunogenetic loci in Turkish and worldwide populations.
Journal: Gene
Published: March 02, 2016
Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia.
Journal: Neurology. Genetics
Published: November 05, 2015
MCP1 2518 A/G polymorphism affects progression of childhood focal segmental glomerulosclerosis.
Journal: Renal failure
Published: September 04, 2015
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features.
Journal: Acta ophthalmologica
Published: January 08, 2014
Last Updated: 09/26/2026