Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

Effect of MST1/2 kinase inhibitor on LGMD2R phenotype

14. Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.56

Cells lacking LAP1B are defective in withdrawal from the cell cycle during myogenic differentiation.

XVI. Congress of the Medical Biology and Genetics Society of Turkey, Muğla, Turkey, 27 October 2019, pp.5

Intramuscular drug application in zebrafish

Moleküler Biyoloji Derneği 7.Uluslararası Kongresi, İstanbul, Turkey, 27 September 2019

Modeling of a unique desmin mutation in zebrafish by using genome editing brings new insights into desmin function

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.427 identifier

Myogenic Differentiation and Fusion Defects in Myoblasts Lacking LAP1B

6th International Congress of the Molecular Biology Association of Turkey, İzmir, Turkey, 05 September 2018, vol.1, pp.162

Disease Modeling in Zebrafish: Limb-Girdle MuscularDystrophy 2R

6th International Congress of the Molecular Biology Association of Turkey, Turkey, 5 - 08 September 2018, pp.5-6

LGMD2R disease modeling in zebrafish by genome editing tools

Mammalian Genetics and Genomics: From Molecular Mechanisms to Translational Applications, Heidelberg, Germany, 24 - 27 October 2017

In vivo targeted mutagenesis via CRISPR/Cas9 and TALEN in zebrafish enables rapid screening of candidate rare diseases genes

42nd Congress of the Federation-of-European-Biochemical-Societies (FEBS) on From Molecules to Cells and Back, Jerusalem, Israel, 10 - 14 September 2017, vol.284, pp.171 identifier

Co-expression Network of a Rare Disease: Significant Genes in Dysferlinopathy and Functional Prediction of TOR1AIP1

Rare and Undiagnosed Diseases: Discovery and Models of Precision Therapy (Keystone Symposia), Massachusetts, United States Of America, 3 - 08 May 2017

Hacettepe University Zebrafish Research Laboratory: zebrafish disease modeling by genome editing tools

41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Turkey, 3 - 08 September 2016, vol.283, pp.116 identifier

Çekirdek zarfı hastalıkları ile ilişkili yeni bir gen: TOR1AIP1 ve kas distrofisi

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 October 2015, pp.23

Histopathological characteristics of muscular dystrophy caused by mutation in the nuclear envelope protein LAP1B

7th UK Conference on the Nuclear Envelope in Disease and Chromatin Organization, Sheffield, United Kingdom, 22 June 2015

A Novel Nuclear Envelopathy-Related Gene: Mutation İn Tor1aip1 Encoding Lap1b Causes Muscular Dystrophy

Türkiye Moleküler Biyoloji Derneği 3. Uluslararasi Kongresi, İzmir, Turkey, 11 September 2014, pp.15

Reduction of LARGE expression in different types of muscular dystrophies other than dystroglycanopathy

18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.780 identifier

A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy

18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.851-852 identifier

Inflammatory effect of AbetaPP induced ST6Gal1 secretion from myogenic cell line

16th International Congress of the World-Muscle-Society, Algarve, Portugal, 18 - 22 October 2011, vol.21, pp.746 identifier

Mutation screening of CAPN3 gene in 13 Turkish LGMD2A patients

12th International Congress of the World-Muscle-Society, Giardini Naxos, Italy, 17 - 20 October 2007, vol.17, pp.791 identifier

Limb-girdle muscular dystrophy and mental retardation (LGMD2M) has a heterogeneous background

11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.679-680 identifier

The first successful prenatal diagnosis in two different forms of muscular dystrophies: MEB and LGMD2M

11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.678-679 identifier

Autosomal recessive limb-girdle muscular dystrophies (LGMD2s) in Turkey

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

Consanguinity and neuromuscular disorders in Turkey

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

The first prenatal diagnosis in Muscle-Eye-Brain Disease

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

Muscle pathology in childhood cases of calpainopathy

9th International Congress of the World-Muscle-Society, Goteborg, Sweden, 1 - 04 September 2004, vol.14, pp.605 identifier

Books & Book Chapters