Publications by authors named "Pervin Dincer"

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Precision rewriting of muscle genetics: therapeutic horizons of base and prime editing in skeletal muscle disorders.
Selin Saydam, Pervin Dinçer

Gene Ther· December 2025

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Tissue-Selective Effects of PLEC Isoform Deficiency: Insights From A Muscle Only Phenotype.
Hulya Gundesli, Haluk Topaloglu, Pervin Dincer

Muscle Nerve· December 2025

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Unveiling the strain uniformity challenge: design and evaluation of a PDMS membrane for precise mechanobiology studies.
Nilüfer Düz, Yasin Gülsüm, Waleed Odeibat, Ismail Uyanık, Samet Akar

Comput Methods Biomech Biomed Engin· April 2025

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Mimicking TGFBI Hot-Spot Mutation Did Not Result in Any Deposit Formation in the Zebrafish Cornea.
Fulya Yaylacıoğlu Tuncay, Beril Talim, Pervin Rukiye Dinçer

Curr Eye Res· May 2024

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Applications of CRISPR Epigenome Editors in Tumor Immunology and Autoimmunity.
Berkay Yahsi, Fahreddin Palaz, Pervin Dincer

ACS Synth Biol· February 2024

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RSPO4 is a potential risk gene of stages III-IV, grade C periodontitis through effects on innate immune response and oral barrier integrity.
Avneesh Chopra, Jiahui Song, January Weiner, Huseyin G Keceli, Pervin R Dincer

J Clin Periodontol· April 2023

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Angiotensin receptor blocker use is associated with upregulation of the memory-protective angiotensin type 4 receptor (ATR) in the postmortem brains of individuals without cognitive impairment.
Caglar Cosarderelioglu, Lolita S Nidadavolu, Claudene J George, Ruth Marx-Rattner, Laura Powell, Pervin Dincer

Geroscience· February 2023

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Clinical trials and promising preclinical applications of CRISPR/Cas gene editing.
Barış Çerçi, Ihsan Alp Uzay, Mustafa Kemal Kara, Pervin Dinçer

Life Sci· January 2023

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Loss of the Nuclear Envelope Protein LAP1B Disrupts the Myogenic Differentiation of Patient-Derived Fibroblasts.
Gülsüm Kayman Kürekçi, Aybar C Acar, Pervin R Dinçer

Int J Mol Sci· November 2022

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Higher Angiotensin II Type 1 Receptor Levels and Activity in the Postmortem Brains of Older Persons with Alzheimer's Dementia.
Caglar Cosarderelioglu, Lolita S Nidadavolu, Claudene J George, Ruth Marx-Rattner, Laura Powell, Pervin Dincer

J Gerontol A Biol Sci Med Sci· April 2022

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A cytoplasmic escapee: desmin is going nuclear.
Ecem Kural Mangit, Niloufar Boustanabadimaralan Düz, Pervin Dinçer

Turk J Biol· December 2021

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Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux.
Gülsüm Kayman Kürekçi, Ecem Kural Mangit, Cansu Koyunlar, Seyda Unsal, Berk Saglam, Pervin R Dincer

Sci Rep· April 2021

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Physical evidence on desmin-lamin B interaction.
Ecem Kural-Mangıt, Pervin Rukiye Dinçer

Cytoskeleton (Hoboken)· January 2021

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Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular Dystrophy.
Mehmet Sinan Beksac, Atakan Tanacan, Duygu Aydin Hakli, Gokcen Orgul, Burcu Soyak, Pervin Dincer

J Pregnancy· January 2019

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LARGE expression in different types of muscular dystrophies other than dystroglycanopathy.
Burcu Balci-Hayta, Beril Talim, Gulsev Kale, Pervin Dincer

BMC Neurol· December 2018

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Genetic analysis of and in Turkish patients with corneal dystrophies: Five novel variations in .
Fulya Yaylacioglu Tuncay, Gülsüm Kayman Kurekci, Sezen Guntekin Ergun, Ozge Tugce Pasaoglu, Rustu Fikret Akata, Pervin Rukiye Dincer

Mol Vis· January 2018

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Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1, a novel muscular dystrophy gene.
Ayse Ece Cali-Daylan, Pervin Dincer

Neuromuscul Disord· March 2017

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Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies.
Gulsum Kayman-Kurekci, Beril Talim, Petek Korkusuz, Nilufer Sayar, Turkan Sarioglu, Pervin Dincer

Neuromuscul Disord· July 2014

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A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.
Nilgun Cetin, Burcu Balci-Hayta, Hulya Gundesli, Petek Korkusuz, Nuhan Purali, Pervin Dincer

J Med Genet· July 2013

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Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy.
Burcu Balci-Hayta, Beril Talim, Pervin Dinçer, Haluk Topaloğlu

Neuromuscul Disord· January 2013

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Pitfall of identifying a disease locus by using low-resolution SNP arrays.
Hulya Gundesli, Sebahattin Cirak, Pervin Dincer

J Mol Genet Med· October 2012

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A dystroglycan mutation associated with limb-girdle muscular dystrophy.
Yuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, Motoi Kanagawa, Daniel Beltrán-Valero de Bernabé

N Engl J Med· March 2011

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Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line.
Burcu Balci-Hayta, Sevim Erdem-Özdamar, Pervin Dinçer

Cell Biol Int· January 2011

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Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy.
Hulya Gundesli, Beril Talim, Petek Korkusuz, Burcu Balci-Hayta, Sebahattin Cirak, Pervin Dincer

Am J Hum Genet· December 2010

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Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrix.
Burcu Balci, Pervin Dinçer

Biotechnol J· July 2009

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