Publications & Works

Publication Network
Published journal articles indexed by SCI, SSCI, and AHCI

Desmin's conformational modulation by hydrophobicity

KURAL MANGIT E., CEVHEROĞLU O., Dincer P.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.49, no.2, pp.236-243, 2024 (SCI-Expanded) Creative Commons License Sustainable Development identifier identifier identifier

Assessment of myogenic potency in patient-derived fibroblasts with c.1289-2A>G Desmin mutation

Duz N., Unsal S., Eerdem-Ozdamar S., Dincer P.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.49, no.2, pp.244-251, 2024 (SCI-Expanded) Creative Commons License Sustainable Development identifier identifier identifier

Applications of CRISPR Epigenome Editors in Tumor Immunology and Autoimmunity

Yahsi B., Palaz F., DİNÇER P. R.
ACS Synthetic Biology , vol.13, no.2, pp.413-427, 2024 (SCI-Expanded) identifier identifier

Mimicking TGFBI Hot-Spot Mutation Did Not Result in Any Deposit Formation in the Zebrafish Cornea

Yaylacıoğlu Tuncay F., TALİM B., DİNÇER P. R.
Current Eye Research , vol.49, no.5, pp.458-466, 2024 (SCI-Expanded) identifier identifier

Angiotensin receptor blocker use is associated with upregulation of the memory-protective angiotensin type 4 receptor (AT(4)R) in the postmortem brains of individuals without cognitive impairment

Cosarderelioglu C., Nidadavolu L. S., George C. J., Marx-Rattner R., Powell L., Xue Q., et al.
GEROSCIENCE , vol.45, no.1, pp.371-384, 2023 (SCI-Expanded) identifier identifier identifier

Clinical trials and promising preclinical applications of CRISPR/Cas gene editing

Çerçi B., Uzay I. A., KARA M., DİNÇER P. R.
Life Sciences , vol.312, 2023 (SCI-Expanded) identifier identifier identifier

Higher Angiotensin II Type 1 Receptor Levels and Activity in the Postmortem Brains of Older Persons with Alzheimer's Dementia

Cosarderelioglu C., Nidadavolu L. S., George C. J., Marx-Rattner R., Powell L., Xue Q., et al.
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES , vol.77, no.4, pp.664-672, 2022 (SCI-Expanded) identifier identifier identifier

Could TGFBI-related corneal dystrophies be mimicked in zebrafish via CRISPR/Cas9-mediated hot spot arginine variations?

Tuncay F. Y., TALİM B., DİNÇER P. R.
EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.140, 2022 (SCI-Expanded) identifier

Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux.

Kayman Kürekçi G., Kural Mangit E., Koyunlar C., Unsal S., Saglam B., Ergin B., et al.
Scientific reports , vol.11, no.1, pp.7505, 2021 (SCI-Expanded) Creative Commons License identifier identifier identifier

Physical evidence on desmin-lamin B interaction

Kural Mangıt E., Dinçer P. R.
CYTOSKELETON , vol.78, no.1, pp.14-17, 2021 (SCI-Expanded) identifier identifier identifier

No compartment for proteins - an approach for isolating differentially located intermediate filaments

Mangit E. K., Dincer P. R.
FEBS OPEN BIO , vol.9, pp.424, 2019 (SCI-Expanded) identifier

Loss of mechanosensitivity causes skeletal muscle degeneration in LGMD2R

Unsal S., Dincer P. R.
FEBS OPEN BIO , vol.9, pp.199-200, 2019 (SCI-Expanded) identifier

LARGE expression in different types of muscular dystrophies other than dystroglycanopathy

Balci-Hayta B., TALİM B., KALE G., Dincer P.
BMC NEUROLOGY , vol.18, 2018 (SCI-Expanded) identifier identifier identifier

Gene co-expression network analysis of dysferlinopathy: Altered cellular processes and functional prediction of TOR1AIP1 a novel muscular dystrophy gene

Cali-Daylan A. E., Dincer P.
NEUROMUSCULAR DISORDERS , vol.27, no.3, pp.269-277, 2017 (SCI-Expanded) identifier identifier identifier

Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6

TUNCAY F. Y., KUREKCI G. K., Ergun S. G., Pasaoglu O. T., Akata R. F., DİNÇER P. R.
MOLECULAR VISION , vol.22, pp.1267-1279, 2016 (SCI-Expanded) identifier identifier identifier

Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line

HAYTA B., ERDEM ÖZDAMAR S., Dincer P.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.40, no.1, pp.31-36, 2015 (SCI-Expanded) identifier identifier

Response (to Sewry and Goebel).

Kayman-Kurekci G., Korkusuz P., Dincer P. R.
Neuromuscular disorders : NMD , vol.24, pp.1122, 2014 (SCI-Expanded) identifier identifier

Mutation in <i>TOR1AIP1</i> encoding LAP1B in a form of muscular dystrophy: A novel gene related to nuclear envelopathies

Kayman-Kurekci G., TALİM B., KORKUSUZ P., Sayar N., Sarioglu T., Oncel İ. H., et al.
NEUROMUSCULAR DISORDERS , no.7, pp.624-633, 2014 (SCI-Expanded) Creative Commons License Sustainable Development identifier identifier identifier

A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.

Cetin N., Balci-Hayta B., Gundesli H., KORKUSUZ P., PURALI N., TALİM B., et al.
Journal of medical genetics , vol.50, no.7, pp.437-43, 2013 (SCI-Expanded) identifier identifier identifier

Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy

Balci-Hayta B., TALİM B., Dincer P., Topaloglu H.
NEUROMUSCULAR DISORDERS , vol.23, no.1, pp.15-18, 2013 (SCI-Expanded) identifier identifier identifier

An efficient method for stable transfection of mouse myogenic C2C12 cell line using a nonviral transfection approach

Akyuz M. D., Hayta B., Dincer P. R.
TURKISH JOURNAL OF MEDICAL SCIENCES , vol.41, no.5, pp.821-825, 2011 (SCI-Expanded) Creative Commons License identifier identifier

BRIEF REPORT A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy

Hara Y., Balci-Hayta B., Yoshida-Moriguchi T., Kanagawa M., de Bernabe D. B., Gundesli H., et al.
NEW ENGLAND JOURNAL OF MEDICINE , vol.364, no.10, pp.939-946, 2011 (SCI-Expanded) Creative Commons License identifier identifier

Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line.

BALCI-HAYTA B., Erdem-Ozdamar S., DINCER P. R.
Cell biology international , vol.35, no.1, pp.9-13, 2011 (SCI-Expanded) identifier identifier identifier

Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy.

Gundesli H., TALİM B., KORKUSUZ P., Balci-Hayta B., Cirak S., Akarsu N. A., et al.
American journal of human genetics , vol.87, no.6, pp.834-41, 2010 (SCI-Expanded) Creative Commons License identifier identifier identifier

Efficient transfection of mouse-derived C2C12 myoblasts using a matrigel basement membrane matrix.

Balci B., Dinçer P. R.
Biotechnology journal , vol.4, pp.1042-5, 2009 (SCI-Expanded) identifier identifier

Eosinophilic myositis in calpainopathy: Could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?

Oflazer P. S., Gundesli H., ZORLUDEMİR S., Sabuncu T., Dincer P.
NEUROMUSCULAR DISORDERS , vol.19, no.4, pp.261-263, 2009 (SCI-Expanded) identifier identifier identifier

Linkage Analysis in a Large Primary Osteoporosis Family

Balci B., Yildiz B. O., Ofir R., Dincer P., BAYRAKTAR M.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.33, no.4, pp.215-222, 2008 (SCI-Expanded) identifier

Prenatal diagnosis of muscle-eye-brain disease

Balci B., Morris-Rosendahl D. J., Celebi A., Talim B., Topaloglu H., Dincer P. R.
PRENATAL DIAGNOSIS , vol.27, no.1, pp.51-54, 2007 (SCI-Expanded) identifier identifier identifier

Calpain-3 mutations in Turkey

Balci B., Aurino S., Haliloglu G., Talim B., Erdem S., Akcoren Z., et al.
EUROPEAN JOURNAL OF PEDIATRICS , vol.165, no.5, pp.293-298, 2006 (SCI-Expanded) identifier identifier identifier

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

Balci B., Gerceker F., Aksoy S., Sennaroglu G., Kalay E., Sennaroglu L., et al.
TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3, pp.213-221, 2005 (SCI-Expanded) identifier identifier

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

Balci B., Uyanik G., Dincer P. R., Gross C., Willer T., Talim B., et al.
NEUROMUSCULAR DISORDERS , vol.15, no.4, pp.271-275, 2005 (SCI-Expanded) identifier identifier identifier

A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan

Dincer P. R., Balci B., Yuva Y., Talim B., Brockington M., Dincel D., et al.
NEUROMUSCULAR DISORDERS , vol.13, no.10, pp.771-778, 2003 (SCI-Expanded) Creative Commons License identifier identifier identifier

A large consanguineous osteoporosis family with 20 affected individuals

Dincer P. R., YILDIZ O. B., Balci B., Bayraktar M.
BONE , vol.28, no.5, 2001 (SCI-Expanded) identifier

A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F

Dincer P. R., Bonnemann C., Aker O., Akcoren Z., Nigro V., Kunkel L., et al.
NEUROMUSCULAR DISORDERS , vol.10, pp.247-250, 2000 (SCI-Expanded) identifier

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families

Dincer P. R., Akcoren Z., Demir E., Richard I., Sancak O., Kale G., et al.
JOURNAL OF MEDICAL GENETICS , vol.37, no.5, pp.361-367, 2000 (SCI-Expanded) Creative Commons License identifier

Heterogeneity within subgroups of the autosomal recessive limb girdle muscular dystrophy in Turkey.

Dincer P. R., Akcoren Z., Demir E., Richard I., Sancak O., Kale G., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , vol.65, no.4, 1999 (SCI-Expanded) identifier

Prenatal diagnosis of limb-girdle muscular dystrophy type 2C.

Dinçer P. R., Piccolo F., Leturcq F., Kaplan J. C., Jeanpierre M., Topaloğlu H.
Prenatal diagnosis , vol.18, pp.1300-3, 1998 (SCI-Expanded) identifier identifier identifier

DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.

Dinçer P. R., Topaloğlu H., Ayter S.
The Turkish journal of pediatrics , vol.40, pp.347-55, 1998 (SCI-Expanded) identifier identifier identifier

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Dincer P. R., Leturcq F., Richard I., Piccolo F., Yalnizoglu D., deToma C., et al.
ANNALS OF NEUROLOGY , vol.42, no.2, pp.222-229, 1997 (SCI-Expanded) identifier identifier identifier

Calpain-3 deficiency causes a mild muscular dystrophy in childhood

Topaloglu H., Dincer P. R., Richard I., Akcoren Z., Alehan D., Ozme S., et al.
NEUROPEDIATRICS , vol.28, no.4, pp.212-216, 1997 (SCI-Expanded) identifier identifier identifier

Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy.

Taşdemir H. A., Topaloğlu H., Dinçer P. R., Göğüş S., Kotiloğlu E., Ozdirim E., et al.
The Turkish journal of pediatrics , vol.39, pp.317-24, 1997 (SCI-Expanded) identifier identifier identifier

Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins

Richard I., Brenguier L., Dincer P., Roudaut C., Bady B., Burgunder J., et al.
AMERICAN JOURNAL OF HUMAN GENETICS , vol.60, no.5, pp.1128-1138, 1997 (SCI-Expanded) identifier identifier identifier

Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

Beckmann J., Richard I., Broux O., Fougerousse F., Allamand V., Chiannilkulchai N., et al.
NEUROMUSCULAR DISORDERS , vol.6, no.6, pp.455-462, 1996 (SCI-Expanded) identifier identifier identifier

Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients

Dincer P. R., Topaloglu H., Ayter S., Ozguc M., Tasdemir H., Renda Y.
BRAIN & DEVELOPMENT , vol.18, no.2, pp.91-94, 1996 (SCI-Expanded) identifier identifier identifier

GOOD CLINICAL OBSERVATION IS ESSENTIAL BEFORE MOLECULAR STUDIES

TOPALOGLU H., TAN E., DINCER P. R., ERDEM S., AKCOREN Z.
LANCET , vol.346, no.8988, pp.1490, 1995 (SCI-Expanded) identifier identifier identifier

An unusual case of Duchenne muscular dystrophy.

Topaloğlu H., Dinçer P. R., Göğüş S., Ayter S., Topçu M.
Brain & development , vol.15, pp.313-5, 1993 (SCI-Expanded) identifier identifier identifier
Articles Published in Other Journals

Could autosomal dominant TGFBI-related corneal dystrophies be modelled in zebrafish by using CRISPR/Cas9: Challenges and Possibilities

Yaylacıoğlu Tuncay F., Dinçer P. R.
World Journal of Ophthalmology and Vision Research , vol.1, no.3, pp.1-13, 2019 (Peer-Reviewed Journal) Creative Commons License

Genome Editing Technologies: From Bench Side to Bedside

Yaylacıoğlu Tuncay F., Dinçer P. R.
Acta Medica , vol.49, no.3, pp.30-40, 2018 (Peer-Reviewed Journal) Sustainable Development

Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular Dystrophy

BEKSAÇ M. S., TANAÇAN A., AYDIN HAKLI D., ÖRGÜL G., SOYAK B., HAYTA B., et al.
JOURNAL OF PREGNANCY , vol.2018, 2018 (ESCI) Creative Commons License Sustainable Development identifier identifier identifier

INHERITANCE OF ACQUIRED EPIGENETIC MODIFICATIONS AND ITS ROLE IN DISEASE SUSCEPTIBILITY

Kayman Kürekçi G., Dinçer P. R.
İstanbul Tıp Fakültesi Dergisi , vol.80, no.1, pp.45-53, 2017 (Peer-Reviewed Journal)

INHERITANCE OF ACQUIRED EPIGENETIC MODIFICATIONS AND ITS ROLE IN DISEASE SUSCEPTIBILITY

KUREKCI G. K., BUNSUZ M., Onal G., DINCER P. R.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.80, no.1, pp.45-53, 2017 (ESCI) Sustainable Development identifier

Exome Sequencing for The Identification of Mendelian Disease Genes

KAYMAN KÜREKÇİ G., Dincer P.
ERCIYES MEDICAL JOURNAL , vol.36, no.4, pp.139-143, 2014 (ESCI) Creative Commons License identifier identifier

Next-Generation DNA Sequencing Technologies

KAYMAN KÜREKÇİ G., Dincer P.
ERCIYES MEDICAL JOURNAL , vol.36, no.3, pp.99-103, 2014 (ESCI) Creative Commons License identifier identifier

The new era in therapeutic approaches: Non-coding RNAs and diseases

AKKAYA ULUM Z. Y., Dincer P.
MARMARA MEDICAL JOURNAL , vol.26, no.1, pp.5-10, 2013 (ESCI) Sustainable Development identifier identifier

Pitfall of identifying a disease locus by using low-resolution SNP arrays.

Gundesli H., Cirak S., Dincer P. R.
Journal of molecular and genetic medicine : an international journal of biomedical research , vol.5, pp.264-5, 2010 (Peer-Reviewed Journal) identifier

Beta-sarcoglycan gene mutations in Turkey.

Balci B., Wilichowski E., Haliloğlu G., Talim B., Aurino S., Kremer E., et al.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology , vol.23, pp.154-8, 2004 (Scopus) identifier identifier
Refereed Congress / Symposium Publications in Proceedings

Mechanical strain stimulates the cytonuclear shuttling of the desmin intermediate protein in skeletal muscle cells

Duz N., Driessen R., Bouten C., DİNÇER P. R.
56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, England, 10 - 13 June 2023, pp.397-398 identifier

A Novel Membrane with Soft Sensors to Directly Measure Mechanical Strain

Kumbay Yildiz Ş., Düz N., Aydın E. Y., Akar S., Artuner H., Dinçer P. R., et al.
Neuroscience 2023 - Society for Neuroscience, Washington, Kiribati, 11 November 2023

Desmin in the nucleus of the skeletal muscle

KURAL MANGIT E., DİNÇER P. R.
14th International Congress of Human Genetics (ICHG2023), 22 February 2023

Hepatosellüler kanserde YAP proteini hedefli yeni bileşiklerin belirlenmesi

GÜNTEKİN ERGÜN S., SARI S., AVCI A., DİNÇER P. R.
17. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, 28 - 31 October 2021

TGFBI geninde genom düzenleme tekniği ile oluşturulan varyasyonların zebra balığı korneasındaki fenotipik etkilerinin incelenmesi

Yaylacıoğlu Tuncay F., Dinçer P. R.
53. Türk Oftalmoloji Derneği Ulusal Kongresi, Antalya, Turkey, 06 November 2019

Defining the role of mechanotransduction in limb-girdle muscular dystrophy type 2R

Ünsal Ş., Kural Mangıt E., Koyunlar C., Kayman Kürekçi G., Ergin B., Sağlam B., et al.
Mechanical Forces in Biology (EMBO-EMBL Symposia), Heidelberg, Germany, 12 - 15 July 2017

Hepatosellüler kanserde MST1/2 kinaz inhibitörünün etkisi

GÜNTEKİN ERGÜN S., DİNÇER P. R.
Ankara Hematoloji ve Onkoloji Günleri, Ankara, Turkey, 2 - 04 April 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

Yaylacıoğlu Tuncay F., Kural Mangıt E., Kayman Kürekçi G., Güntekin Ergün S., Dinçer P. R.
2nd Zebrafish Workshop, Turkey, Ankara, Turkey, 18 March 2021, pp.7

Characterization of zebrafish desmin orthologs and incomplete penetrance in CRISPR/Cas9-generated stable knockouts

Kayman Kürekçi G., Kural Mangıt E., Sağlam B., Ergin B., Uyanık İ., Korkusuz P., et al.
The 2nd Zebrafish Workshop in Turkey, İzmir, Turkey, 18 March 2021

Effect of MST1/2 kinase inhibitor on LGMD2R phenotype

Güntekin Ergün S., Dinçer P. R.
14. Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.56

TGFBI geninde Genom Düzenleme Tekniği ile Oluşturulan Varyasyonların Zebra Balığı Korneasındaki Fenotipik Etkilerinin İncelenmesi

Yaylacıoğlu Tuncay F., Talim B., Dinçer P. R.
14. Ulusal Tıbbi Genetik Kongresi, Ankara, Turkey, 20 - 22 November 2020, pp.57-58

OSTEOPOROSIS PSEUDOGLIOMA SYNDROME DUE TO LRP5 GENE MUTATION

Güntekin Ergün S., Gümüş-Akay G., Ergün M. A., Perçin F. E., Dinçer P. R.
2. Genetikte Güncel Tedaviler, Konya, Turkey, 5 - 06 October 2019, pp.3

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

Kayman Kürekçi G., Acar A. C., Dinçer P. R.
XVI. Congress of the Medical Biology and Genetics Society of Turkey, Muğla, Turkey, 27 October 2019, pp.5

Intramuscular drug application in zebrafish

Çinar Z., Dinçer P. R.
Moleküler Biyoloji Derneği 7.Uluslararası Kongresi, İstanbul, Turkey, 27 September 2019

Loss of mechanosensitivity causes skeletal muscle degeneration in LGMD2R

Ünsal Ş., Dinçer P. R.
44th FEBS Congress, Krakow, Poland, 6 - 11 July 2019

Limb-Girdle Muscular Dystrophy 2R modelling in zebrafishto determine a novel mechanism related to desmin-lamin B interaction

KAYMAN KÜREKÇİ G., KURAL MANGIT E., ÜNSAL Ş., YERSAL N., ERGİN B., SAĞLAM B., et al.
Keystone Symposia, 11 - 15 November 2018

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

Kurekci G. K., Koyunlar C., Kural E., Talim B., Ergin B., Unsal S., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.427 identifier

Analysing the expression profiles of human DES orthologous desma and desmb by using knockout zebrafish models

Koyunlar C., Kayman-Kurekci G., Kural E., Talim B., Purali N., Dincer P. R.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.618 identifier

Hacettepe University Zebrafish Research Laboratory: Rare diseases modeling in zebrafish by using genome editing tools

Kural E., Kurekci G. K., Koyunlar C., Tuncay F. Y., Unsal S., Dincer P. R.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.987 identifier

Myogenic Differentiation and Fusion Defects in Myoblasts Lacking LAP1B

Kayman Kürekçi G., Dinçer P. R.
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

ÜNSAL Ş., KAYMAN KÜREKÇİ G., KURAL MANGIT E., TALİM B., YERSAL N., ERGİN B., et al.
6th International Congress of the Molecular Biology Association of Turkey, Turkey, 5 - 08 September 2018, pp.5-6

A novel method for monitoring Ca2+ transients in zebrafish muscle fibers

Ergin B., Sağlam B., Ünsal Ş., Puralı N., Dinçer P. R.
11th FENS Forum of Neuroscience, Berlin, Germany, 7 - 11 July 2018

Rare disease modeling by genome editing tools in zebrafish

Kural Mangıt E., Kayman Kürekçi G., Koyunlar C., Yaylacıoğlu Tuncay F., Önal G., Ünsal Ş., et al.
15. Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 October 2017, pp.149

Modeling LGMD2R in Zebrafish Using Genome Editing Tools

Kural Mangıt E., Kayman Kürekçi G., Koyunlar C., Yayıcıoğlu Tuncay F., Ünsal Ş., Dinçer P. R.
Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017

LGMD2R disease modeling in zebrafish by genome editing tools

Kayman Kürekçi G., Kural Mangıt E., Koyunlar C., Ünsal Ş., Dinçer P. R.
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

Kurekci G. K., Unsal S., Dincer P. R.
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

Desmin Mutation with an ultra rare and unique phenotype: Genome editing for a patient specific zebrafish model

Kayman Kürekçi G., Koyunlar C., Kural Mangıt E., Talim B., Korkusuz P., Erdem Özdamar S., et al.
keystone symposia Rare and Undiagnosed Diseases, Massachusetts, United States Of America, 3 - 05 August 2017

Defining the role of mechanotransduction in limb-girdle muscular dystrophy 2R

ÜNSAL Ş., KURAL MANGIT E., Koyunlar C., KAYMAN KÜREKÇİ G., ERGİN B., SAĞLAM B., et al.
Mechanical Forces in Biology (EMBO-EMBL Symposium), 12 - 15 July 2017

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

KAYMAN KÜREKÇİ G., Koyunlar C., KURAL MANGIT E., TALİM B., ERGİN B., ÜNSAL İ., et al.
European Human Genetics Conference, 27 - 30 May 2017

Hacettepe University Zebrafish Research Laboratory: Rare Disease Modeling in Zebrafish by Using Genome Editing Tools

KURAL E., KAYMAN KÜREKÇİ G., KOYUNLAR C., ÜNSAL Ş., DİNÇER P. R.
ESHG Conference, 27 - 30 May 2017

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

Daylan A., Dinçer P. R.
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

KURAL E., KAYMAN-KUREKCI G., KOYUNLAR C., DİNÇER P. R.
41st FEBS Congress on Molecular and Systems Biology for a Better Life, Kusadasi, Turkey, 3 - 08 September 2016, vol.283, pp.116 identifier

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.

Hayta B., Puralı N., Tan M. E., Erdem Özdamar S., Talim B., Korkusuz P., et al.
ESHG, Barcelona, Spain, 21 May 2016, pp.45

Activation of the mitochondrial unfolded protein responce pathway in C2C12 myoblast cell lin

Aksu Mengeş E., Talim B., Dinçer P. R., Hayta B.
ESHG, Barcelona, Spain, 21 May 2016, pp.15

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

Dinçer P. R.
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

Kayman Kürekçi G., Talim B., Korkusuz P., Hayta B., Puralı N., Dinçer P. R.
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

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

Torsin A-interacting protein 1/Lamina-associated polypeptide 1B in a form of limb-girdle muscular dystrophy: a novel gene related to nuclear envelopathies

Kayman Kürekçi G., Hayta B., Talim B., Puralı N., Dinçer P. R.
18. International Meeting of the World Muscle Society, California, United States Of America, 05 October 2013, pp.64

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

Cetin N., Balci-Hayta B., Gundesli H., KORKUSUZ P., PURALI N., TALİM B., et al.
18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.851-852 identifier

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

Balci-Hayta B., Talim B., Topaloglu H., Kale G., Dincer P. R.
18th International Congress of the World-Muscle-Society (WMS), California, United States Of America, 1 - 05 October 2013, vol.23, pp.780 identifier

Inflammatory effect of AbetaPP induced ST6Gal1 secretion from myogenic cell line

Balci-Hayta B., Erdem-Ozdamar S., Dincer P. R.
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

Guendesli H., Balci B., Talim B., Topaloglu H., Dincer P. R.
12th International Congress of the World-Muscle-Society, Giardini Naxos, Italy, 17 - 20 October 2007, vol.17, pp.791 identifier

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

Balci B., Topaloglu H., Dincer P. R.
11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.678-679 identifier

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

Haliloglu G., Balci B., Talim B., Dincer P. R., Topaloglu H.
11th International Congress of the World-Muscle-Society, Bruges, Belgium, 4 - 07 October 2006, vol.16, pp.679-680 identifier

The first prenatal diagnosis in Muscle-Eye-Brain Disease

Balci B., Celebi A., Talim B., Dincer P., Topaloglu H.
11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

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

Balci B., Talim B., Akcoeren Z., Caglar M., Kale G., Topaloglu H., et al.
11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

Consanguinity and neuromuscular disorders in Turkey

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

Muscle pathology in childhood cases of calpainopathy

Talim B., Dincer P. R., Richard I., Aurino S., Akcoren Z., Haliloglu G., et al.
9th International Congress of the World-Muscle-Society, Goteborg, Sweden, 1 - 04 September 2004, vol.14, pp.605 identifier

Autosomal recessive limb-girdle muscular dystrophy with severe mental retardation: a new phenotype with glycosylation defects of alpha-dystroglycan

Dincer P. R., Balci B., Yuva Y., Talim B., Brockington M., Dincel D., et al.
7th International Congress of the World-Muscle-Society, Rotterdam, Netherlands, 2 - 05 October 2002, vol.12, pp.721 identifier
Books

Human Molecular Genetics

Dinçer P. R. (Editor)
CRC, Ghent, Belgium , Ankara, 2020 Creative Commons License

Molecular biology of the cell

Dinçer P. R., Altungöz O., Akçalı K. C., Çırakoğlu A., Engin E., Erdal Ş. E., et al.
Tuba Kitabevi, Ankara, 2008

THOMPSON & THOMPSON TIBBİ GENETİK

Dinçer P. R., Alikaşifoğlu M. (Editor)
Güneş Kitabevi, Ankara, 2005

Obstetrik Maternal-Fetal Tıp & Perinatoloji

Dinçer P. R., Beksaç M. S. (Editor), Demir N. (Editor), Koç A. (Editor), Yüksel A. (Editor)
NOBEL, Ankara, 2001

Kas Distrofilerinin Moleküler Patolojisindeki Son Gelişmeler

Dinçer P. R.
in: Obstetrik Maternal-Fetal Tıp & Perinatoloji, MEHMET SİNAN BEKSAÇ, Editor, Nobel Yayın Dağıtım, Ankara, pp.188-210, 2001

Fetal Tıp: Prenatal Tanı

Dinçer P. R., Alikaşifoğlu M., Alpay M., Altay Ç., Ataç F. B., Aytepe N., et al.
Medical Networt & Nobel, Ankara, 1996
Metrics

Publication

123

Citation (WoS)

798

H-Index (WoS)

12

Citation (Scopus)

934

H-Index (Scopus)

12

Citation (Scholar)

387

H-Index (Scholar)

5

Project

48

Thesis Advisory

16

Open Access

13
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