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Burcu Balci

Showing results (1-10 of 27) with videos related to

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Biotechnology Journal|April 11, 2009
Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrixBurcu Balci, Pervin Dinçer
Cell Biology International|August 28, 2010
Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell lineBurcu Balci-Hayta, Sevim Erdem-Özdamar, Pervin Dinçer
Neuromuscular Disorders : NMD|September 19, 2012
Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular DystrophyBurcu Balci-Hayta, Beril Talim, Pervin Dinçer, et al.
BMC Neurology|December 17, 2018
LARGE expression in different types of muscular dystrophies other than dystroglycanopathyBurcu Balci-Hayta, Beril Talim, Gulsev Kale, et al.
Stem Cell Reviews and Reports|July 29, 2010
Reprogramming of human umbilical cord stromal mesenchymal stem cells for myogenic differentiation and muscle repairCetin Kocaefe, Deniz Balci, Burcu Balci Hayta, et al.
Journal of Fluorescence|February 11, 2023
Synthesis and Characterization of a Luminol Based Chemiluminescent Trimeric SystemBusra Kesimal, Burcu Balci, Deniz Cakal, et al.
Journal of Cellular and Molecular Medicine|January 20, 2025
Hypotonic Swelling Method for the Isolation of Pure Mitochondria From Primary Human Skeletal Myoblasts for Proteomic StudiesEvrim Aksu-Menges, Eray Taha Kumtepe, Gurler Akpinar, et al.
Biologia Futura|September 23, 2021
Biologia Futura: the importance of 3D organoids-a new approach for research on neurological and rare diseasesTayfun Hilmi Akbaba, Can Ebru Bekircan-Kurt, Banu Balci-Peynircioglu, et al.
Prenatal Diagnosis|December 13, 2006
Prenatal diagnosis of muscle-eye-brain diseaseBurcu Balci, Deborah J Morris-Rosendahl, Asli Celebi, et al.
The Turkish Journal of Pediatrics|October 28, 2005
Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in TurkeyBurcu Balci, Filiz Ozbaş Gerçeker, Songül Aksoy, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Biotechnology Journal|April 11, 2009
Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrixBurcu Balci, Pervin Dinçer
Cell Biology International|August 28, 2010
Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell lineBurcu Balci-Hayta, Sevim Erdem-Özdamar, Pervin Dinçer
Neuromuscular Disorders : NMD|September 19, 2012
Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular DystrophyBurcu Balci-Hayta, Beril Talim, Pervin Dinçer, et al.
BMC Neurology|December 17, 2018
LARGE expression in different types of muscular dystrophies other than dystroglycanopathyBurcu Balci-Hayta, Beril Talim, Gulsev Kale, et al.
Stem Cell Reviews and Reports|July 29, 2010
Reprogramming of human umbilical cord stromal mesenchymal stem cells for myogenic differentiation and muscle repairCetin Kocaefe, Deniz Balci, Burcu Balci Hayta, et al.
Journal of Fluorescence|February 11, 2023
Synthesis and Characterization of a Luminol Based Chemiluminescent Trimeric SystemBusra Kesimal, Burcu Balci, Deniz Cakal, et al.
Journal of Cellular and Molecular Medicine|January 20, 2025
Hypotonic Swelling Method for the Isolation of Pure Mitochondria From Primary Human Skeletal Myoblasts for Proteomic StudiesEvrim Aksu-Menges, Eray Taha Kumtepe, Gurler Akpinar, et al.
Biologia Futura|September 23, 2021
Biologia Futura: the importance of 3D organoids-a new approach for research on neurological and rare diseasesTayfun Hilmi Akbaba, Can Ebru Bekircan-Kurt, Banu Balci-Peynircioglu, et al.
Prenatal Diagnosis|December 13, 2006
Prenatal diagnosis of muscle-eye-brain diseaseBurcu Balci, Deborah J Morris-Rosendahl, Asli Celebi, et al.
The Turkish Journal of Pediatrics|October 28, 2005
Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in TurkeyBurcu Balci, Filiz Ozbaş Gerçeker, Songül Aksoy, et al.
Pageof 3