Oral and Poster Presentations (2016-2021)

 

National

  1. Yaylacıoğlu Tuncay, F., Kural Mangıt, E., Kayman Kürekçi, G., Güntekin Ergün, S., & Dinçer, P. R. , (2021).Creating Rare Disease Specific CRISPR-Cas9 Platforms in Zebrafish and Ensuring Their Sustainability in Hacettepe University Zebrafish Research Laboratory: Challenges in mimicking missense variants. 2nd Zebrafish Workshop, Turkey, Sözlü sunum
  2. Kayman Kürekçi, G., Kural Mangıt, E., Sağlam, B., Ergin, B., Uyanık, İ., Korkusuz, P.,Talim, B. Dinçer, P.R., (2021). Characterization of zebrafish desmin orthologs and incomplete penetrance in CRISPR/Cas9-generated stable knockouts . The 2nd Zebrafish Workshop in Turkey, Sözlü sunum
  3. Güntekin Ergün, S., Ünsal, Ş., Dinçer, P.R.(2021). Effect of MST1 kinase inhibitor in hepatocellular cancer. Ankara Hematology and Oncology Days. Ankara, Oral presentation.
  4. Yaylacıoğlu Tuncay, F., Talim, B.,& Dinçer, P. R. , (2020). Investigation of the phenotypic effects of the variations generated by genome editing technique in the TGFBI gene in the zebrafish cornea . 14th National Congress of Medical Genetics. Ankara, Turkey, Oral presentation
  5. Kural Mangıt, E., Ünver, N.,& Dinçer, P. R. , (2020). Desmin and Lamin B: Proteomic analysis of binding partners of two differently positioned proteins. 3. Ulusal Proteomik Kongresi. İstanbul, Turkey, Sözlü sunum
  6. Güntekin Ergün, S.,& Dinçer, P. R. , (2020). Effect of MST1/2 kinase inhibitor on LGMD2R phenotype. 14th National Congress of Medical Genetics. Ankara, Turkey, Oral presentation
  7. Kayman Kürekçi, G., Acar, A. C. ,& Dinçer, P. R. , (2019). 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 (pp.5). Muğla, Turkey, Sözlü sunum
  8. Güntekin Ergün, S., Akay Güven, G., Ergün, A., S, Perçin F., Dinçer, P.R. (2019). Osteoporosis pseudoglioma syndrome related to LRP5 gene mutation. 2nd Symposium on Current Treatments in Genetics, Konya, Oral presentation
  9. Kural-Mangıt E, Kayman-Kürekçi G, Koyunlar C, Yaylacıoğlu-Tuncay F, Ünsal Ş, Dinçer P (2017). Modeling of rare diseases in zebrafish using genome editing tools. 15th National Congress of Medical Biology and Genetics, Fethiye, Turkey, Oral presentation
  10. Kural Mangıt, E., Kayman Kürekçi, G., Koyunlar, C., Yayıcıoğlu Tuncay, F., Ünsal, Ş.,& Dinçer, P. R. , (2017). Modeling LGMD2R in zebrafish using genome editing tool. 15. National Congress of Medical Biology and Genetics, Muğla, Turkey, Oral presentation

International

  1. Kural Mangıt E., Dinçer P.R. 06-11 July 2019. No compartment for proteins: an approach for isolating differentially located intermediate filaments. 44th FEBS Congress, Krakow, Poland.
  2. Ünsal Ş., Dinçer P.R., 06-11 July 2019. Loss of mechanosensitivity causes skeletal muscle degeneration in LGMD2R. 44th FEBS Congress, Krakow, Poland
  3. Çinar, Z., & Dinçer, P. R. , (2019). Intramuscular drug application in zebrafish. Türkiye Moleküler Biyoloji Derneği 7.Uluslararası Kongresi, İstanbul, Turkey
  4. Kural-Mangıt Ecem, Dinçer P. 5-8 September 2018. Tale of two proteins: interaction between desmin and lamin B. 6th International Congress of the Molecular Biology Association of Turkey, Sözlü sunum
  5. Ergin, B., Saglam B., Unsal,Ş., Purali,N., Dincer P.R., 7-11 July 2018. A novel method for monitoring Ca2+ transients in zebrafish muscle fibers. 11th FENS Forum of Neuroscience, Berlin, Germany.
  6. Ünsal Ş., Kayman-Kürekçi G., Kural-Mangıt E., Talim B., Yersal N., Ergin B., Düz N., Çinar Z., Korkusuz P., Puralı N., Dinçer P. 5-8 September 2018. Disease modeling in zebrafish: Limb-Girdle Muscular Dystrophy 2R. 6th International Congress of the Molecular Biology Association of Turkey, İzmir, Turkey.
  7. Kayman-Kurekci, G, Kural-Mangıt, E, Unsal, Ş, Yersal, N, Ergin, B, Sağlam, B, Duz,N, Cınar, Z, Talim, B,  Korkusuz, P, Purali, N, DincerP,  11-14 November 2018. Limb-Girdle muscular dystrophy 2R modelling in zebrafish to determine a novel mechanism related to desmin-lamin B interaction. Keystone Symposia meeting on From Rare to Care: Discovery, Modeling and Translation of Rare Diseases, Vienna, Austria.
  8. Kayman Kürekçi G., Dinçer P. R.09.2018. Myogenic differentiation and fusion defects in myoblasts lacking LAP1B, 6th International Congress of the Molecular Biology Association of Turkey, Türkiye
  9. Kayman-Kürekçi G, Kural-Mangıt E, Koyunlar C, Ünsal Ş, Dinçer P. R. (24-27 October 2017). LGMD2R disease modeling in zebrafish by genome editing tools. Mammalian Genetics and Genomics: From Molecular Mechanisms toTranslational Applications, Heidelberg, Germany
  10. Kayman-Kürekçi G, Ünsal Ş, Dinçer P (2017). In vivo targeted mutagenesis via CRISPR/Cas9 and TALEN in zebrafish enables rapid screening of candidate rare diseases genes. 42nd FEBS congress, Jerusalem, Israel.
  11. Daylan, A., & Dinçer, P. R. , (2017). 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
  12. Ünsal Ş, Kural-Mangıt E, Koyunlar C, Kayman-Kürekçi G, Ergin B, Sağlam B, Puralı N, Dinçer P (2017). Defining the role of mechanotransduction in limb-girdle muscular dystrophy type 2R. Mechanical Forces in Biology,EMBO-EMBL Symposia, Almanya.
  13. Yaylacıoğlu Tuncay, F., Kayman Kürekçi, G., Güntekin Ergün, S., Paşaoğlu, Ö. T. , Akata, R. F. , & Dinçer, P. R. , (2017). Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6 . ESHG Conference, Vienna, Austria
  14. Kural-Mangıt E, Kayman-Kürekçi G, Koyunlar C, Yaylacıoğlu-Tuncay F, Ünsal Ş, Dinçer P (2017). Zebrafish disease modeling of rare disorders by genome editing tools in Turkey. 10th European Zebrafish Meeting.
  15. Koyunlar C, Kayman-Kürekçi G, Kural-Mangıt E, Talim B, Puralı N, Dinçer P (2017). Analysing the expression profiles of human DES orthologous desma and desmb by using knockout zebrafish models. ESHG Conference.
  16. Kayman-Kürekçi G, Koyunlar C, Kural-Mangıt E, Talim B, Ergin B, Ünsal Ş, Puralı N, Korkusuz P, Erdem-Özdamar S, Dinçer Pervin (27-30 May 2017). Modeling of a unique desmin mutation in zebrafish by using genome editing brings new insights into desmin function. European Human Genetics Conference, Copenhagen, Denmark
  17. Kural-Mangıt E, Koyunlar C, Kayman-Kürekçi G, Ünsal Ş, Dinçer Pervin (27-30 May 2017). Hacettepe University Zebrafish Research Laboratory: Rare diseases modeling in zebrafish by using genome editing tools. ESHG Conference, Copenhagen, Denmark
  18. Kayman-Kürekçi G, Koyunlar C, Kural-Mangıt E, Talim B, Korkusuz P, ErdemÖzdamar S, Puralı N, Dinçer P (3-5 August 2017). Desmin mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model. Rare and Undiagnosed Diseases: Discovery and Models of Precision Therapy, Boston, USA
  19. Kural-Mangıt E, Kayman-Kürekçi G, Koyunlar C, Tuncay Yaylacıoğlu F, Ünsal Ş, Dinçer P (3-7 Temmuz 2017). Zebrafish disease modeling by genome editing tools. 10th European Zebra Fish Meeting, Macaristan, The 41st FEBS Congress, Turkey.
  20. Hayta, B., Puralı, N., Tan, M. E. , Erdem Özdamar, S., Talim, B., Korkusuz, P., Dinçer, P. R. (2016). A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology. ESHG. Barcelona, Spain
  21. Aksu E, Talim B, Dinçer PR, Hayta B (2016) Activation of the mitochondrial unfolded protein responce pathway in C2C12 myoblast cell line. ESHG Barseleno, Spain.