Gülsüm Kayman Kürekçi. 2021. Investigation of the role of LAP1B in Transcriptional Regulation in Muscle Cells. Ph.D. Thesis.

Zeynep Çınar. 2021. Therapeutic XMU-MP-1 Application in Desma Mutant Zebrafish Model. Master Thesis.

Seyda Unsal. 2019. Defining the Role of Mechanotransduction in Limb-Girdle Muscular Dystrophy 2R (LGMD2R). Master Thesis.

Ecem Kural. 2017. Investigation of desmin and lamin b interaction using zebrafish. Master Thesis.

Cansu Koyunlar. 2017. Examination of desmin expression on desma and desmb knockout zebrafish models. Master Thesis.

Ayşe Ece Çalı Daylan. 2015. Investigation of muscular dystrophies with allelic heterogeneity using bioinformatics tools. PhD Thesis.

Gülsüm Kayman Kürekçi. 2014. Genetic study of families diagnosed with autosomal recessive limb-girdle muscular dystrophy. Master Thesis.

Nilgün Çetin. 2012. Investigation of the effects of c.1289-2A>G desmin mutation at the protein level. PhD Thesis.

Hülya Gündeşli. 2011. Identification of a locus responsible for limb-girdle muscular dystrophy phenotype. PhD Thesis.

Mehmet Deniz Akyüz. 2009. Establishment of stable transfection in C2C12 mouse myoblast cell line. Master Thesis.

Burcu Balcı. 2008. Identification of the role of beta galactoside alpha-2,6-sialyltransferase (ST6Gal1) in the pathogenesis of Sporadic Inclusion Body Myositis (s-IBM) by the use of an in-vitro culture model. PhD Thesis.

Hülya Gündeşli. 2006. Searching of 2p25 cytoband for candidate genes in the nonsyndromic hearing loss. Master Thesis.

Burcu Balcı. 2002. Identification of the ancestral haplotype of 35delG mutation in the connexin 26 (Cx26/GJB2) gene responsible for hearing loss in Turkish population. Master Thesis.