Burcu Hayta-Balcı
Ankara, 06100, Turkey
Last Updated: 09/26/2026
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Found 20 publications
Exploratory proteomic analysis of Megaconial congenital muscular dystrophy skeletal myoblasts suggests cytoskeletal and contractile alterations.
Journal: BMC neurology
Published: March 23, 2026
Diagnostic yield of clinical exome sequencing in patients with suspected hereditary neuropathy.
Journal: Turkish journal of medical sciences
Published: August 06, 2025
Hypotonic Swelling Method for the Isolation of Pure Mitochondria From Primary Human Skeletal Myoblasts for Proteomic Studies.
Journal: Journal of cellular and molecular medicine
Published: May 20, 2024
Mitochondrial Dysfunction in Cyanotic Congenital Heart Disease: A Promising Therapeutic Approach for the Future.
Journal: Pediatric cardiology
Published: February 15, 2022
Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALS.
Journal: Acta neurologica Belgica
Published: May 05, 2021
Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular Dystrophy.
Journal: Scientific reports
Published: March 06, 2021
Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature.
Journal: The journal of allergy and clinical immunology. In practice
Published: January 03, 2021
Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy.
Journal: Human molecular genetics
Published: July 27, 2020
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular Dystrophies.
Journal: The American journal of pathology
Published: March 06, 2020
Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect.
Journal: Molecular immunology
Published: December 15, 2019
Last Updated: 09/26/2026