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Burcu Balci

Showing results (11-20 of 27) with videos related to

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Turkish Journal of Medical Sciences|January 9, 2026
Diagnostic yield of clinical exome sequencing in patients with suspected hereditary neuropathyCan Ebru Bekircan-Kurt, Doruk Arslan, Naz Güleray, et al.
Journal of the Neurological Sciences|August 29, 2018
Establishment of primary myoblast cell cultures from cryopreserved skeletal muscle biopsies to serve as a tool in related research & development studiesBurcu Balci-Hayta, Can Ebru Bekircan-Kurt, Evrim Aksu, et al.
American Journal of Human Genetics|November 27, 2010
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophyHulya Gundesli, Beril Talim, Petek Korkusuz, et al.
Acta Neurologica Belgica|July 9, 2021
Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALSEvrim Aksu-Menges, Burcu Balci-Hayta, Can Ebru Bekircan-Kurt, et al.
Journal of Pregnancy|August 29, 2018
Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular DystrophyMehmet Sinan Beksac, Atakan Tanacan, Duygu Aydin Hakli, et al.
Scientific Reports|September 14, 2021
Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular DystrophyEvrim Aksu-Menges, Cemil Can Eylem, Emirhan Nemutlu, et al.
Pediatric Cardiology|May 10, 2022
Mitochondrial Dysfunction in Cyanotic Congenital Heart Disease: A Promising Therapeutic Approach for the FutureZeynep Ucar, Tayfun Hilmi Akbaba, Ayse Tulay Aydinoglu, et al.
The American Journal of Pathology|July 11, 2020
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular DystrophiesEvrim Aksu-Menges, Yeliz Z Akkaya-Ulum, Didem Dayangac-Erden, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Journal of Medical Genetics|May 21, 2013
A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathiesNilgun Cetin, Burcu Balci-Hayta, Hulya Gundesli, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Turkish Journal of Medical Sciences|January 9, 2026
Diagnostic yield of clinical exome sequencing in patients with suspected hereditary neuropathyCan Ebru Bekircan-Kurt, Doruk Arslan, Naz Güleray, et al.
Journal of the Neurological Sciences|August 29, 2018
Establishment of primary myoblast cell cultures from cryopreserved skeletal muscle biopsies to serve as a tool in related research & development studiesBurcu Balci-Hayta, Can Ebru Bekircan-Kurt, Evrim Aksu, et al.
American Journal of Human Genetics|November 27, 2010
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophyHulya Gundesli, Beril Talim, Petek Korkusuz, et al.
Acta Neurologica Belgica|July 9, 2021
Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALSEvrim Aksu-Menges, Burcu Balci-Hayta, Can Ebru Bekircan-Kurt, et al.
Journal of Pregnancy|August 29, 2018
Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular DystrophyMehmet Sinan Beksac, Atakan Tanacan, Duygu Aydin Hakli, et al.
Scientific Reports|September 14, 2021
Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular DystrophyEvrim Aksu-Menges, Cemil Can Eylem, Emirhan Nemutlu, et al.
Pediatric Cardiology|May 10, 2022
Mitochondrial Dysfunction in Cyanotic Congenital Heart Disease: A Promising Therapeutic Approach for the FutureZeynep Ucar, Tayfun Hilmi Akbaba, Ayse Tulay Aydinoglu, et al.
The American Journal of Pathology|July 11, 2020
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular DystrophiesEvrim Aksu-Menges, Yeliz Z Akkaya-Ulum, Didem Dayangac-Erden, et al.
Neuromuscular Disorders : NMD|March 29, 2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 geneBurcu Balci, Gökhan Uyanik, Pervin Dincer, et al.
Journal of Medical Genetics|May 21, 2013
A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathiesNilgun Cetin, Burcu Balci-Hayta, Hulya Gundesli, et al.
Pageof 3