Publications

  1. Uzay İA, Dinçer PR (2021) CRISPR-based approaches for the point-of-care diagnosis of COVID19, Acta Medica (in press)
  2. Kayman Kürekçi G, Kural Mangit E, Koyunlar C, Unsal S, Saglam B, Ergin B, Gizer M, Uyanik I, Boustanabadimaralan Düz N, Korkusuz P, Talim B, Purali N, Hughes SM, Dincer PR. (2021) Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux. Sci Rep, Apr 5;11(1):7505. doi: 10.1038/s41598-021-86974-w.PMID: 33820917, Supported by TÜBİTAK 214S174 (Q1).
  3. Kural-Mangıt E, Dinçer PR (2021) Physical evidence on desmin-lamin B interaction. Cytoskeleton (Hoboken), Jan;78(1):14-17. doi: 10.1002/cm.21651. Epub 2021 Jan 28.PMID: 33475247, Supported by TÜBİTAK 214S174 (Q3).
  4. Yaylacıoğlu Tuncay F, Dinçer PR. (2019) Could autosomal dominant TGFBI related corneal dystrophies be modelled in zebrafish by using CRISPR/Cas9: Challenges and Possibilities. World Journal of Opthalmology Vision Research, 1 (3), 1-13, Supported by HÜ-BAP-TAY-2017-12735 .
  5. Yaylacıoğlu Tuncay F, Dincer PR (2018) Genome Editing Technologies:From Bench Side to Bedside. Acta Medica, 49(3): 30 – 40.
  6. Balci-Hayta B, Talim B, Kale G, Dincer PR (2018) LARGE expression in different types of muscular dystrophies other than dystroglycanopathy. BMC Neurol., Dec 15;18(1):207. doi: 10.1186/s12883-018-1207-0.PMID: 30553274, Supported by HÜ-BAP- 011 D01 101 003 (Q2).
  7. Beksac MS, Tanacan A, Aydin Hakli D, Orgul G, Soyak B, Balci Hayta B, Dincer PR, Topaloğlu H (2018) Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular Dystrophy. J Pregnancy, Jul 30;2018:9718316. doi: 10.1155/2018/9718316. eCollection 2018.PMID: 30151283 (Q2).
  8. Cali-Daylan AE, Dincer PR (2017) Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1, a novel muscular dystrophy gene. Neuromuscul Disord., Mar;27(3):269-277. doi: 10.1016/j.nmd.2016.10.011. Epub 2016 Nov 3.PMID: 28110863, Supported by TÜBİTAK 112S271 (Q1).
  9. Kayman Kürekçi G, Bunsuz M, Önal G, Dinçer PR (2017) Kazanılmıs Epigenetik Degisikliklerin Kalıtımı ve Hastalıklara Yatkınlıktaki Rolü. İstanbul Tıp Fakültesi Dergisi, 80(1), 45-53.
  10. Yaylacioglu Tuncay F, Kayman Kurekci G, Guntekin Ergun S, Pasaoglu OT, Akata RF, Dincer PR (2016) Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6. Mol Vis., 2016 Oct 26;22:1267-1279. eCollection 2016.PMID: 27829782, Supported by TÜBİTAK 114S126 (Q2).
  11. Hayta B, Erdem Özdamar S, Dinçer PR (2015) Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line. Turk J Biochem., 2015, 40(1), 31-36., Doi: 10.5505/tjb.2015.46547, Supported by TÜBİTAK 111S320 (Q4).
  12. Kayman-Kurekci G, Talim B, Korkusuz P, Sayar N, Sarioglu T, Oncel I, Sharafi P, Gundesli H, Balci-Hayta B, Purali N, Serdaroglu-Oflazer P, Topaloglu H, Dincer P (2014) Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies. Neuromuscul Disord., Jul;24(7):624-33. doi: 10.1016/j.nmd.2014.04.007. Epub 2014 May 2.PMID: 24856141, Supported by TÜBİTAK 112S271 (Q1).
  13. Kayman-Kurekci G, Korkusuz P, Dincer P (2014) Response (to Sewry and Goebel).Neuromuscul Disord., Dec;24(12):1122. doi: 10.1016/j.nmd.2014.08.001. Epub 2014 Aug 4.PMID: 2519333, Supported by TÜBİTAK 112S271 (Q1).
  14. Kayman Kürekçi G, Dinçer PR (2014) Next Generation DNA SequencingTechnologies. Erciyes Medical Journal, 36(3), 99-103., Doi:10.5152/etd.2014.7803
  15. Akkaya ZY,  Dinçer P (2013) Tedavi yaklaşımlarında yeni bir dönem: Kodlamayan RNA’lar ve hastalıklar, Marmara Tıp Dergisi, 26:5-DOI:10.5472/MMJ.2012.02596 (Q4).
  16. Cetin N, Balci-Hayta B, Gundesli H, Korkusuz P, Purali N, Talim B, Tan E, Selcen D, Erdem-Ozdamar S, Dincer P (2013) A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies. J Med Genet., Jul;50(7):437-43. doi: 10.1136/jmedgenet-2012-101487. Epub 2013 May 18.PMID: 23687351, Supported by TÜBİTAK 108S124 (Q1).
  17. Balci-Hayta B, Talim B, Dinçer P, Topaloğlu H (2013) Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy. Neuromuscul Disord., Jan;23(1):15-8. doi: 10.1016/j.nmd.2012.07.001. Epub 2012 Sep 15.PMID: 22985905 (Q1).
  18. Hara Y, Balci-Hayta B, Yoshida-Moriguchi T, Kanagawa M, Beltrán-Valero de Bernabé D, Gündeşli H, Willer T, Satz JS, Crawford RW, Burden SJ, Kunz S, Oldstone MB, Accardi A, Talim B, Muntoni F, Topaloğlu H, Dincer P, Campbell KP (2011) A dystroglycan mutation associated with limb-girdle muscular dystrophy. N Engl J Med., Mar 10;364(10):939-46. doi: 10.1056/NEJMoa1006939.PMID: 21388311, Supported by TÜBİTAK 197S055 (Q1).
  19. Balci-Hayta B, Erdem-Özdamar S, Dinçer P (2011) Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line. Cell Biol Int., Jan;35(1):9-13. doi: 10.1042/CBI20100159.PMID: 20795944, Supported by TÜBİTAK 107S228 (Q2).
  20. Akyüz MD, Hayta Balcı B, Dinçer PR (2011) An efficient method for stable transfection of mouse myogenic C2C12 cell line using a nonviral transfection approach, Turk J Med Sci; 41 (5): 821-825, Supported by HÜ-BAP 03.02.101.009 (Q3).
  21. Gundesli H, Talim B, Korkusuz P, Balci-Hayta B, Cirak S, Akarsu NA, Topaloglu H, Dincer P (2010) Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy.Am J Hum Genet., Dec 10;87(6):834-41. doi: 10.1016/j.ajhg.2010.10.017. Epub 2010 Nov 25.PMID: 21109228, Supported by TÜBİTAK 108S124 (Q1).
  22. Gundesli H, Cirak S, Dincer P (2010) Pitfall of identifying a disease locus by using low-resolution SNP arrays. J Mol Genet Med., 5:264-5. Epub 2011 Nov 22.PMID: 22190979,  Supported by TÜBİTAK 108S124.
  23. Balcı-Hayta B, Gündeşli H, Dinçer P. (2010) D/BMD, LGMD2 ve distroglikanopatilerde moleküler genetic çalışmalar. Turkiye Klinikleri J Neurol-Special Topics, 3(2):22-27.
  24. Balci B, Dinçer P (2009) Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrix. Biotechnol J., Jul;4(7):1042-5. doi: 10.1002/biot.200800269.PMID: 19360711 (Q1).
  25. Oflazer PS, Gundesli H, Zorludemir S, Sabuncu T, Dincer P (2009) Eosinophilic myositis in calpainopathy: could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease? Neuromuscul Disord., Apr;19(4):261-3. doi: 10.1016/j.nmd.2009.01.010. Epub 2009 Mar 13.PMID: 19285864 (Q1).
  26. Balcı B, Yıldız B, Ofir R, Dincer P, Bayraktar M (2009) Linkage analysis in a large primary osteoporosis family J. Biochem., 33, 4, 215-222, WOS:000264746100014, ISSN; 0250-4685, Supported by TÜBİTAK 100S024 (Q4).
  27. Gündeşli H, Dinçer PR (2008) Endoplazmik retikulum stresinin molekuler mekanizması ve kas patolojisi arasındaki ilişki, Hacettepe Tıp Dergisi 39:109-11.
  28. Balci B, Morris-Rosendahl DJ, Celebi A, Talim B, Topaloglu H, Dinçer P (2007)Prenatal diagnosis of muscle-eye-brain disease. Prenat Diagn., Jan;27(1):51-4. doi: 10.1002/pd.1622.PMID: 17154333 (Q2).
  29. Balcı B, Gündeşli H, Dinçer P (2006) Popülasyonumuzdaki nonsendromik işitme kayıplarında 35delG mutasyonunun önemi. Hacettepe Tıp Dergisi, 37(2).
  30. Balci B, Aurino S, Haliloglu G, Talim B, Erdem S, Akcören Z, Tan E, Caglar M, Richard I, Nigro V, Topaloglu H, Dincer P (2006) Calpain-3 mutations in Turkey.Eur J Pediatr., May;165(5):293-8. doi: 10.1007/s00431-005-0046-3. Epub 2006 Jan 13.PMID: 16411092 (Q1).
  31. Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H (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 gene. Neuromuscul Disord., Apr;15(4):271-5. doi: 10.1016/j.nmd.2005.01.013.PMID: 15792865 (Q1).
  32. Balci B, Gerçeker FO, Aksoy S, Sennaroğlu G, Kalay E, Sennaroğlu L, Dinçer P (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 Turkey. Turk J Pediatr., Jul-Sep;47(3):213-21.PMID: 16250304, Supported by HÜBAB- 99.01.101.014 (Q3).
  33. Balci B, Wilichowski E, Haliloğlu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloğlu H, Bonnemann C, Dinçer P (2004) Beta-sarcoglycan gene mutations in Turkey. Acta Myol., Dec;23(3):154-8.PMID: 15938573 (Q2).
  34. Dinçer P, Balci B, Yuva Y, Talim B, Brockington M, Dinçel D, Torelli S, Brown S, Kale G, Haliloglu G, Gerçeker FO, Atalay RC, Yakicier C, Longman C, Muntoni F, Topaloglu H (2003) A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan. Neuromuscul Disord., Dec;13(10):771-8. doi: 10.1016/s0960-8966(03)00161-5.PMID: 14678799 (Q1).
  35. Balcı B, Sennaroğlu L, Dinçer P (2003) Connexin 26 ve nonsendromik işitme kayıpları.Hacettepe Tıp Dergisi, 34(1):25-29.
  36. Dinçer P, Bönnemann CG, Erdir Aker O, Akçoren Z, Nigro V, Kunkel LM, Topaloglu H (2000) A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F. Neuromuscul Disord., Jun;10(4-5):247-50. doi: 10.1016/s0960-8966(00)00100-0.PMID: 10838250, Supported by TÜBİTAK 197S055 (Q1).
  37. Dinçer P, Akçören Z, Demir E, Richard I, Sancak O, Kale G, Ozme S, Karaduman A, Tan E, Urtizberea JA, Beckmann JS, Topaloğlu H (2000) A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. J Med Genet., May;37(5):361-7. doi: 10.1136/jmg.37.5.361.PMID: 10807695, Supported by TÜBİTAK 197S055 (Q1).
  38. Dinçer P (1999) The recent advances in muscular dystrophies. Balkan Journal of Medical Genetics, Vol2, 1, 15;1-5 (Q4).
  39. Dinçer P, Piccolo F, Leturcq F, Kaplan JC, Jeanpierre M, Topaloğlu H (1998) Prenatal diagnosis of limb-girdle muscular dystrophy type 2C. Prenat Diagn., Dec;18(12):1300-3. doi: 10.1002/(sici)1097-0223(199812)18:12<1300::aid-pd436>3.0.co;2-h.PMID: 9885023 (Q2).
  40. Dinçer P, Topaloğlu H, Ayter S (1998) DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis..Turk J Pediatr., Jul-Sep;40(3):347-55.PMID: 9763898, Supported by TÜBİTAK 195S317 (Q3).
  41. Dinçer P, Topaloğlu H, Ayter Ş (1997) Kas distrofilerinin moleküler tanısı. Hacettepe Tıp Dergisi, 28(4);71-6.
  42. Dinçer P (1997) X’e bağlı ve otozomal resesif kalıtım gösteren kas distrofilerinin moleküler tekniklerle analizi. KATKI Pediatri Dergisi, 18(4);476-86.
  43. Taşdemir HA, Topaloğlu H, Dinçer P, Göğüş S, Kotiloğlu E, Ozdirim E, Yalaz K (1997) Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy. Turk J Pediatr., Jul-Sep;39(3):317-24.PMID: 9339110 (Q3).
  44. Topaloğlu H, Dinçer P, Richard I, Akçören Z, Alehan D, Ozme S, Cağlar M, Karaduman A, Urtizberea JA, Beckmann JS (1997) Calpain-3 deficiency causes a mild muscular dystrophy in childhood.Neuropediatrics., Aug;28(4):212-6. doi: 10.1055/s-2007-973702.PMID: 930971 (Q2).
  45. Richard I, Brenguier L, Dinçer P, Roudaut C, Bady B, Burgunder JM, Chemaly R, Garcia CA, Halaby G, Jackson CE, Kurnit DM, Lefranc G, Legum C, Loiselet J, Merlini L, Nivelon-Chevallier A, Ollagnon-Roman E, Restagno G, Topaloglu H, Beckmann JS (1997) Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. Am J Hum Genet., May;60(5):1128-38.PMID: 9150160 (Q1).
  46. Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H (1997) A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Ann Neurol., Aug;42(2):222-9. doi: 10.1002/ana.410420214.PMID: 9266733 (Q1).
  47. Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, Dinçer P, Lefranc G, Merlini L, Topaloglu H, Tomé FM, Cohen D, Jackson CE, Campbell KP, Fardeau M (1996) Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.Neuromuscul Disord., Dec;6(6):455-62. doi: 10.1016/s0960-8966(96)00386-0.PMID: 9027855 (Q1).
  48. Dinçer P (1996) Genetik Varyantlar (Gen Mutasyonları ve DNA Polimorfizmleri). Medikal Biyoteknoloji ve Moleküler Tıp Dergisi, 89-95.
  49. Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients (1996) Brain. Dev.,Mar-Apr;18(2):91-4.doi:10.1016/0387-7604(95)00128-x.PMID: 8733896 (Q1).
  50. Topaloglu H, Tan E, Dinçer P, Erdem S, Akçören Z (1995) Good clinical observation is essential before molecular studies. Lancet, 1995 Dec 2;346(8988):1490. doi: 10.1016/s0140-6736(95)92507-4.PMID: 7491011 (Q1).
  51. Topaloğlu H, Dinçer P, Göğüş S, Ayter S, Topçu M (1993) An unusual case of Duchenne muscular dystrophy. Brain Dev., Jul-Aug;15(4):313-5. doi: 10.1016/0387-7604(93)90032-.PMID: 825015 (Q2).