Ugur Akpulat
Kastamonu, 37150, Turkey
Last Updated: 09/26/2026
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Found 10 publications
Postmortem Temporal Changes in Liver and Spleen Stiffness: Evaluation with Shear Wave Elastography in a Rat Model.
Journal: Diagnostics (Basel, Switzerland)
Published: March 03, 2025
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
Journal: American journal of human genetics
Published: December 03, 2021
LC-MS/HRMS Analysis, Anti-Cancer, Anti-Enzymatic and Anti-Oxidant Effects of Boerhavia diffusa Extracts: A Potential Raw Material for Functional Applications.
Journal: Antioxidants (Basel, Switzerland)
Published: November 14, 2021
Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey.
Journal: American journal of medical genetics. Part A
Published: November 02, 2020
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
Journal: American journal of human genetics
Published: November 03, 2018
Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMD.
Journal: Molecular therapy. Nucleic acids
Published: April 20, 2018
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome.
Journal: American journal of human genetics
Published: April 16, 2018
Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization.
Journal: Brain : a journal of neurology
Published: April 21, 2017
Tenotomy immobilization as a model to investigate skeletal muscle fibrosis (with emphasis on Secreted frizzled-related protein 2).
Journal: Physiological genomics
Published: February 01, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026