Publications

2021

  • Kural-Mangıt E, Dinçer PR. Physical evidence on desmin–lamin B interaction. Cytoskeleton. 2021; 78:14–17, doi: https://doi.org/10.1002/cm.21651)
  • Kayman-Kurekci G., Kural Mangit E., Koyunlar C., Unsal S., Saglam B., Ergin B., Gizer M., Düz N., Korkusuz P., Talim B., Purali N., Hughes S.M., Dincer P. Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux. 17 October 2020, bioRxiv, doi: https://doi.org/10.1101/2020.10.16.342485.

2018

  • Balci-Hayta B., Talim B, Dincer P. LARGE expression in different types of muscular dystrophies other than dystroglycanopathies. BMC Neurology 2018, 18:207.

2017

  • Cali-Daylan AE, Dincer P. Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1, a novel muscular dystrophy gene. Neuromuscul Disord. 2017 Mar;27(3):269-277. doi: 10.1016/j.nmd.2016.10.011.

2016

  • Yaylacioglu Tuncay F, Kayman Kurekci G, Guntekin Ergun S, Pasaoglu OT, Akata RF, Dincer PR. 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.

2015

  • Hayta B, Erdem Ozdamar S, Dincer P.  Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line. Turkish Journal of Biochemistry 2015, 40 (1): 31-36.

2014

  • 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. Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies. Neuromuscul Disord. 2014, 24: 624-33.

2013

  • Cetin N, Balci-Hayta B, Gundesli H, Korkusuz P, Purali N, Talim B, Tan E, Selcen D, Erdem-Ozdamar S, Dincer P. A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies. J Med Genet. 2013 Jul; 50(7): 437-43.
  • Balcı-Hayta B, Talim B, Dinçer P, Topaloğlu H. Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy. Neuromuscul Disord. 2013 Jan; 23(1):15-8.

2011

  • Hara Y, Balcı-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 MBA, Accardi A, Talim B, Muntoni F, Topaloğlu H, Dinçer P, Campbell KP. A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy. N Engl J Med. 2011 Mar 10; 364 (10):939-46.
  • Balcı-Hayta B, Erdem-Özdamar S, Dinçer P. Overexpression of Amyloid beta precursor protein enhances expression and secretion of ST6GalI in C2C12 myogenic cell line. Cell Biol Int. 2011 Jan; 35 (1): 9-13.
  • Akyüz MD, Balcı-Hayta B, Dinçer PR. An efficient method for stable transfection of mouse myogenic C2C12 cell line using nonviral transfection approach. Turk J Med Sci. 2011; 41 (5): 821-825.

2010

  • Gündeşli H, Talim B, Korkusuz P, Balci-Hayta B, Çirak S, Akarsu NA, Topaloğlu H, Dinçer P. Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal recessive limb-girdle muscular dystrophy. Am. J. Hum. Genet. 2010. Dec 10; 87 (6):834-41.

2009

  • Oflazer PS, Gundesli H, Zorludemir S, Sabuncu T, Dinçer P. Eosinophilic myositis in calpainopathy: could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease? Neuromuscul Disord. 2009 Apr;19(4):261-3. Epub 2009 Mar 13.
  • Balcı B, Dinçer P. Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrix. Biotechnol J. 2009 Apr 9.
  • Balci B, Morris-Rosendahl DJ, Celebi A, Talim B, Topaloglu H, Dincer P. Prenatal diagnosis of muscle-eye-brain disease. Prenat Diagn. 2007 Jan; 27(1):51-54.

2006

  • Balcı B, Talim B, Haliloğlu G, Aurino S, Akçören Z, Leturcq F, Kale G, Nigro V, Kaplan JC, Richard I, Topaloğlu H, Dinçer P. Calpain-3 Mutations in Turkey: 10 years experience. Eur J Pediatr. 2006 May; 165(5): 293-298.

2005

  • Balcı B, Özbaş Gerçeker F, Aksoy S, Sennaroğlu G, Kalay E, Sennaroğlu L, Dinçer P. Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (Connexin 26) gene responsible for autosomal recessive nonsyndromic hearing loss in families from the Eastern Black Sea Region in Turkey. Turkish Journal of Pediatrics, 47:213-221, 2005.
  • Balcı B, Uyanik G, Dinçer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloglu H.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. Neuromuscular Disorders.2005 Apr; 15(4):271-5.

2004

  • Balcı B, Wilichowski E, Haliloglu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloglu H, Bonnemann C, Dinçer P. Beta-sarcoglycan gene mutations in Turkey. Acta Myol. 2004 Dec; 23(3):154-8.

2003

  • Dinçer P, Balcı B, Yuva Y, Talim B, Brockington B, Dinçel D, Torelli S, Brown S, Akçören Z, Haliloğlu G, Özbaş Gerçeker F, Çetin Atalay R, Yakıcıer C, Longman C, Muntoni F, Topaloğlu H. A novel form of recessive limb-girdle muscular dystrophy with mental retardation and abnormal expression of α-dystroglycan. Neuromuscul Disord 2003; 13(10): 771-778.

2000

  • Dinçer P, Bonnemann CG, Erdir Aker O, Akcoren Z, Nigro V, Kunkel LM,Topaloglu H.A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F. Neuromuscular Disorders. 2000 Jun;10(4-5):247-50.
  • Dinçer P, Akcoren Z, Demir E, Richard I, Sancak O, Kale G, Ozme S, Karaduman A, Tan E, Urtizberea JA, Beckmann JS, Topaloglu H.A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. Journal Medical Genetics. 2000 May;37(5):361-7.

1998

  • Dinçer P, Topaloğlu H, Ayter Ş.DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis. Turkish Journal of Pediatrics. 1998 40: 347-356.
  • Dinçer P, Piccolo F, Leturcq F, Kaplan JC, Pierre MJ, Topaloğlu H.Prenatal diagnosis of limb-girdle muscular dystrophy type 2C. Prenatal Diagnosis. 1998 18: 1300-1303.

1997

  • Topaloğlu H, Dinçer P, Richard I, Akçören Z, Alehan D, Özme Ş, Çağlar M, Karaduman A, Urtizberea JA, Beckmann JS. Calpain-3 deficiency causes a mild muscular dystrophy in childhood. Neuropediatrics. 1997 28: 1-5.

1996

  • Dinçer P, Topaloglu H, Ayter S, Ozguc M, Tasdemir HA, Renda Y. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. Brain Dev. 1996 Mar-Apr;18(2):91-4.

1995

  • Topaloglu H, Tan E, Dinçer P, Erdem S, Akcoren Z. Good clinical observation is essential before molecular studies.Lancet. 1995 Dec 2;346(8988):1490.

1993

  • Topaloglu H, Dinçer P, Gogus S, Ayter S, Topcu M. An unusual case of Duchenne muscular dystrophy. Brain Dev. 1993 Jul-Aug;15(4):313-5.