Publications by authors named "Munis Dundar"

77Publications

Natural compounds as inhibitors of SARS-CoV-2 endocytosis: A promising approach against COVID-19.

Acta Biomed 2020 11 9;91(13-S):e2020008. Epub 2020 Nov 9.

MAGI EUREGIO, Bolzano, Italy; EBTNA-LAB, Rovereto (TN), Italy; MAGI'S LAB, Rovereto (TN), Italy.

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http://dx.doi.org/10.23750/abm.v91i13-S.10520DOI Listing
November 2020

Genetic testing for autonomic dysfunction or dysautonomias.

Acta Biomed 2020 Nov 9;91(13-S):e2020002. Epub 2020 Nov 9.

MAGI'S LAB, Rovereto (TN), Italy; MAGI EUREGIO, Bolzano, Italy; EBTNA-LAB, Rovereto (TN), Italy.

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http://dx.doi.org/10.23750/abm.v91i13-S.10518DOI Listing
November 2020

Bacteriophages in food supplements obtained from natural sources.

Acta Biomed 2020 Nov 9;91(13-S):e2020025. Epub 2020 Nov 9.

MAGI EUREGIO, Bolzano, Italy; EBTNA-LAB, Rovereto (TN), Italy; MAGI'S LAB, Rovereto (TN), Italy.

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http://dx.doi.org/10.23750/abm.v91i13-S.10834DOI Listing
November 2020

Bacteriophages presence in nature and their role in the natural selection of bacterial populations.

Acta Biomed 2020 Nov 9;91(13-S):e2020024. Epub 2020 Nov 9.

EBTNA-LAB, Rovereto (TN), Italy; MAGI EUREGIO, Bolzano, Italy; MAGI'S LAB, Rovereto (TN), Italy.

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http://dx.doi.org/10.23750/abm.v91i13-S.10819DOI Listing
November 2020

Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift.

Sleep Med 2020 09 5;73:101-105. Epub 2020 Jun 5.

Department of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.sleep.2020.04.027DOI Listing
September 2020

Diagnostic and therapeutic implements based on advanced Biotechnology should be available in low-income countries.

Acta Biomed 2019 09 30;90(10-S):5-6. Epub 2019 Sep 30.

EBTNA-LAB, Rovereto (TN), Italy; MAGI EUREGIO, Bolzano, Italy; Alliance for Health Promotion - in Official Relations with the World Health Organization (WHO), Geneva, Switzerland.

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http://dx.doi.org/10.23750/abm.v90i10-S.8771DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233641PMC
September 2019

Current state and prospects of biotechnology in Central and Eastern European countries. Part I: Visegrad countries (CZ, H, PL, SK).

Crit Rev Biotechnol 2019 Feb 29;39(1):114-136. Epub 2018 Oct 29.

Faculty of Natural Sciences, Department of Biotechnology, University of SS. Cyril and Methodius in Trnava, Trnava, Slovakia.

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https://www.tandfonline.com/doi/full/10.1080/07388551.2018.1
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http://dx.doi.org/10.1080/07388551.2018.1523131DOI Listing
February 2019

The association of endothelin-1 levels with renal survival in polycystic kidney disease patients.

J Nephrol 2019 Feb 18;32(1):83-91. Epub 2018 Jul 18.

Department of Nephrology, Erciyes University Medical Faculty, 38039, Kayseri, Turkey.

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http://dx.doi.org/10.1007/s40620-018-0514-2DOI Listing
February 2019

The frequencies of Y chromosome microdeletions in infertile males.

Turk J Urol 2018 Sep 4;44(5):389-392. Epub 2018 Jan 4.

Department of Urology, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.5152/tud.2018.73669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134974PMC
September 2018

Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder.

Mol Biol Rep 2018 Aug 18;45(4):541-546. Epub 2018 May 18.

Department of Medical Genetics, Erciyes University School of Medicine, Kayseri, Turkey.

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http://dx.doi.org/10.1007/s11033-018-4191-yDOI Listing
August 2018

Evaluation of aortic intima-media thickness in newborns with Down syndrome.

Adv Clin Exp Med 2017 Nov;26(8):1253-1256

Department of Biochemistry, Faculty of Medicine, Acıbadem University, Istanbul, Turkey.

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http://www.advances.umed.wroc.pl/en/article/2017/26/8/1253/
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http://dx.doi.org/10.17219/acem/68677DOI Listing
November 2017

Research of genetic bases of hereditary non-syndromic hearing loss.

Turk Pediatri Ars 2017 Sep 1;52(3):122-132. Epub 2017 Sep 1.

Department of Medical Genetics, Erciyes University Faculty of Medicine, Kayseri, Turkey.

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http://dx.doi.org/10.5152/TurkPediatriArs.2017.4254DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644578PMC
September 2017

Prenatal diagnosis of upper extremity malformations with ultrasonography: Diagnostic features and perinatal outcome.

J Clin Ultrasound 2017 Jun 22;45(5):267-276. Epub 2016 Nov 22.

Department of Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.1002/jcu.22429DOI Listing
June 2017

Genetic expressions of thrombophilic factors in patients with Sheehan's syndrome.

Gynecol Endocrinol 2016 Nov 16;32(11):908-911. Epub 2016 Jul 16.

a Department of Endocrinology.

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http://dx.doi.org/10.1080/09513590.2016.1198763DOI Listing
November 2016

The effect of parental 5,10-methylenetetrahydrofolate reductase 677C/T and 1298A/C gene polymorphisms on response to single-dose methotrexate in tubal ectopic pregnancy.

J Matern Fetal Neonatal Med 2017 May 2;30(10):1232-1237. Epub 2016 Aug 2.

b Department of Medical Genetics , Faculty of Medicine, Erciyes University , Kayseri , Turkey.

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http://dx.doi.org/10.1080/14767058.2016.1209652DOI Listing
May 2017

Ameliorative effects of pentoxifylline on NOS induced by diabetes in rat kidney.

Ren Fail 2016 24;38(4):605-13. Epub 2016 Feb 24.

b Department of Medical Genetics, Faculty of Medicine , Erciyes University , Kayseri , Turkey.

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http://dx.doi.org/10.3109/0886022X.2016.1149688DOI Listing
January 2017

Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndrome.

Ann Saudi Med 2015 Nov-Dec;35(6):462-7

Dr. Seda Orenay-Boyacioglu, Department of Medical Genetics,, Celal Bayar University Faculty of Medicine,, Celal Bayar University,, Manisa 45010, Turkey,

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http://dx.doi.org/10.5144/0256-4947.2015.462DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074473PMC
September 2016

Nitric oxide synthase in diabetic rat testicular tissue and the effects of pentoxifylline therapy.

Syst Biol Reprod Med 2016 13;62(1):22-30. Epub 2015 Nov 13.

d Erciyes University , Faculty of Medicine, Department of Medical Genetics , Kayseri , Turkey.

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http://dx.doi.org/10.3109/19396368.2015.1085605DOI Listing
October 2016

The Effects of Long-Term Diabetes on Ghrelin Expression in Rat Stomachs.

Adv Clin Exp Med 2015 May-Jun;24(3):401-7

Department of Medical Genetics, Faculty of Medicine, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.17219/acem/43723DOI Listing
November 2015

Is idiopathic hirsutism (IH) really idiopathic? mRNA expressions of skin steroidogenic enzymes in women with IH.

Eur J Endocrinol 2015 Oct 20;173(4):447-54. Epub 2015 Jul 20.

Departments of Medical BiologyStatisticsEndocrinologyDermatologyObstetrics and GynecologyGeneticsErciyes University Medical School, Kayseri 38039, TurkeyBetul-Ziya Eren Genome and Stem Cell CenterErciyes University, Kayseri, Turkey

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http://dx.doi.org/10.1530/EJE-15-0460DOI Listing
October 2015

A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia.

Mol Syndromol 2015 Feb 29;6(1):50-3. Epub 2015 Jan 29.

Department of Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

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http://dx.doi.org/10.1159/000370337DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369121PMC
February 2015

Progress in biotechnology: EuroBiotech 2014.

J Biotechnol 2015 May 14;202:1-2. Epub 2015 Mar 14.

Life Sciences, Glasgow Caledonian University, Glasgow G4 0BA, Scotland, United Kingdom. Electronic address:

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http://dx.doi.org/10.1016/j.jbiotec.2015.03.003DOI Listing
May 2015

The effects of streptozotocin-induced diabetes on ghrelin expression in rat testis: biochemical and immunohistochemical study.

Folia Histochem Cytobiol 2015 13;53(1):26-34. Epub 2015 Mar 13.

Erciyes University, Faculty of Medicine, Department of Histology and Embryology, Kayseri, Turkey.

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http://dx.doi.org/10.5603/FHC.a2015.0006DOI Listing
January 2016

Genetic background of supernumerary teeth.

Eur J Dent 2015 Jan-Mar;9(1):153-158

Department of Medical Genetics, Medical Faculty, Erciyes University, Kayseri, Turkiye.

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http://dx.doi.org/10.4103/1305-7456.149670DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319293PMC
February 2015

Circulating microRNAs in patients with non-alcoholic fatty liver disease.

World J Hepatol 2014 Aug;6(8):613-20

Mehmet Celikbilek, Mevlut Baskol, Serkan Dogan, Sebnem Gursoy, Kadri Guven, Omer Ozbakır, Mehmet Yucesoy, Department of Gastroenterology, Erciyes University, Medical School, 38039 Kayseri, Turkey.

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http://dx.doi.org/10.4254/wjh.v6.i8.613DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163744PMC
August 2014

Etiopathogenesis of Sheehan's Syndrome: Roles of Coagulation Factors and TNF-Alpha.

Int J Endocrinol 2014 10;2014:514891. Epub 2014 Apr 10.

Department of Medical Genetics, Erciyes University Medical School, 38039 Kayseri, Turkey.

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http://dx.doi.org/10.1155/2014/514891DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003783PMC
June 2014

A c.1244G>A (p.Arg415Gln) mutation in SH3BP2 gene causes cherubism in a Turkish family: report of a family with review of the literature.

Med Oral Patol Oral Cir Bucal 2014 Jul 1;19(4):e340-4. Epub 2014 Jul 1.

Erciyes University, Faculty of Dentistry, Department of Oral and Maxillofacial Radiology, Kayseri-Turkey,

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4119308PMC
http://dx.doi.org/10.4317/medoral.19496DOI Listing
July 2014

Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage?

Childs Nerv Syst 2014 Mar 7;30(3):419-24. Epub 2013 Dec 7.

Department of Obstetrics and Gynecology, Erciyes University, Faculty of Medicine, Gevher Nesibe Hospital, 38039, Kayseri, Turkey,

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http://dx.doi.org/10.1007/s00381-013-2338-7DOI Listing
March 2014

Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome.

Hum Mol Genet 2013 Sep 23;22(18):3761-72. Epub 2013 May 23.

Department of Pediatrics I, Division of Human Genetics, Innsbruck Medical University, Anichstrasse 35, Innsbruck, Austria.

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http://dx.doi.org/10.1093/hmg/ddt227DOI Listing
September 2013

A novel COL4A3 mutation causes autosomal-recessive Alport syndrome in a large Turkish family.

Genet Test Mol Biomarkers 2013 Mar 8;17(3):260-4. Epub 2013 Jan 8.

Department of Medical Genetics, Erciyes University School of Medicine, Kayseri, Turkey.

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http://dx.doi.org/10.1089/gtmb.2012.0340DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582275PMC
March 2013

The role of TNF-α and PAI-1 gene polymorphisms in familial Mediterranean fever.

Mod Rheumatol 2013 Jan 27;23(1):140-5. Epub 2012 Jun 27.

Medical Faculty, Department of Medical Genetics, Erciyes University, Melikgazi, Kayseri, 38039, Kayseri, Turkey.

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http://dx.doi.org/10.1007/s10165-012-0687-9DOI Listing
January 2013

A new syndrome of microtia with unilateral renal agenesis and short stature.

Am J Med Genet A 2012 Aug 18;158A(8):1837-40. Epub 2012 Jun 18.

Department of Medical Genetics, Kayseri Education and Research Hospital, Kayseri, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.33653DOI Listing
August 2012

Current state of biotechnology in Turkey.

Curr Opin Biotechnol 2011 Sep 15;22 Suppl 1:S3-6. Epub 2011 Jun 15.

Department of Medical Genetics, Faculty of Medicine, Erciyes University, 38039, Kayseri, Turkey.

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http://dx.doi.org/10.1016/j.copbio.2011.05.509DOI Listing
September 2011

Idiopathic hirsutism: local and peripheral expression of aromatase (CYP19A) and 5α-reductase genes (SRD5A1 and SRD5A2).

Fertil Steril 2011 Aug 15;96(2):479-82. Epub 2011 Jun 15.

Department of Medical Genetics, School of Medicine, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.1016/j.fertnstert.2011.05.040DOI Listing
August 2011

Common Familial Mediterranean Fever gene mutations in a Turkish cohort.

Mol Biol Rep 2011 Nov 14;38(8):5065-9. Epub 2010 Dec 14.

Department of Medical Genetics, Erciyes University Medicine Faculty Kayseri, 38039 Kayseri, Turkey.

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http://dx.doi.org/10.1007/s11033-010-0652-7DOI Listing
November 2011

Healthcare in overview of Turkey.

EPMA J 2010 Dec 8;1(4):587-94. Epub 2010 Oct 8.

Medical Faculty, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.1007/s13167-010-0049-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405350PMC
December 2010

Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome.

Am J Med Genet A 2010 Nov;152A(11):2791-5

Department of Medical Genetics, Erciyes University Medical Faculty, Kayseri, Turkey.

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http://dx.doi.org/10.1002/ajmg.a.33249DOI Listing
November 2010

Cytogenetic results of patients with infertility in middle anatolia, Turkey: do heterochromatin polymorphisms affect fertility?

J Reprod Infertil 2010 Oct;11(3):179-81

Department of Medical Genetics, Kayseri Education and Research Hospital, Kayseri, Turkey.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719298PMC
October 2010

Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency.

Dev Med Child Neurol 2010 Sep 22;52(9):868-72. Epub 2010 Jun 22.

Department of Pediatric Neurology, Erciyes University Medical Faculty, Kayseri, Turkey.

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http://doi.wiley.com/10.1111/j.1469-8749.2010.03724.x
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http://dx.doi.org/10.1111/j.1469-8749.2010.03724.xDOI Listing
September 2010

Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users.

Cancer Epidemiol 2009 Jul 27;33(1):47-50. Epub 2009 May 27.

Erciyes University, Medical Faculty, Department of Medical Genetics, Kayseri, Turkey.

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http://dx.doi.org/10.1016/j.canep.2009.04.018DOI Listing
July 2009

Frank-ter Haar syndrome with unusual clinical features.

Eur J Med Genet 2009 Jul-Aug;52(4):247-9. Epub 2009 Mar 19.

Erciyes University, Medical Faculty, Department of Medical Genetics, Talas Cad., 38039 Kayseri, Turkey.

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http://linkinghub.elsevier.com/retrieve/pii/S176972120900024
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http://dx.doi.org/10.1016/j.ejmg.2009.03.005DOI Listing
November 2009

Inherited diseases and syndromes leading to aortic aneurysms and dissections.

Eur J Cardiothorac Surg 2009 Jun 23;35(6):931-40. Epub 2009 Feb 23.

Kayseri Education and Research Hospital, Department of Medical Genetics, Kayseri 38010, Turkey.

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http://dx.doi.org/10.1016/j.ejcts.2009.01.006DOI Listing
June 2009

Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2).

Ann Saudi Med 2008 May-Jun;28(3):209-12

Departmentsof Medical Genetics, Erciyes University, School of Medicine, Kayseri, Turkey.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074418PMC
http://dx.doi.org/10.5144/0256-4947.2008.209DOI Listing
October 2008

ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features.

J Pediatr Endocrinol Metab 2008 Jan;21(1):59-62

Institute of Human Genetics, RWTH Aachen, Germany.

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http://dx.doi.org/10.1515/jpem.2008.21.1.59DOI Listing
January 2008

Genotype-phenotype correlation in children with familial Mediterranean fever in a Turkish population.

Pediatr Int 2008 Apr;50(2):208-12

Department of Pediatric Nephrology and Rheumatology, Erciyes University Faculty of Medicine, Kayseri, Turkey.

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http://dx.doi.org/10.1111/j.1442-200X.2008.02554.xDOI Listing
April 2008

The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue.

J Toxicol Environ Health A 2008 ;71(6):396-404

Department of Medical Genetics, Erciyes University Medical Faculty, Kayseri, Turkey.

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http://www.tandfonline.com/doi/abs/10.1080/15287390701801661
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http://dx.doi.org/10.1080/15287390701801661DOI Listing
February 2008

Megarbane syndrome.

Indian J Hum Genet 2008 Jan;14(1):27-9

Erciyes University Medical Faculty Department of Medical Genetics, Kayseri, Turkey.

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http://dx.doi.org/10.4103/0971-6866.42325DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2840786PMC
January 2008

How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population.

Cancer Genet Cytogenet 2007 Sep;177(2):95-7

Department of Medical Genetics, Medical Faculty, Erciyes University, Talas Caddesi, 38039, Kayseri, Turkey.

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http://dx.doi.org/10.1016/j.cancergencyto.2007.05.015DOI Listing
September 2007

Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter).

Prenat Diagn 2007 Apr;27(4):365-8

Department of Obstetrics and Gynecology, Erciyes University, Faculty of Medicine, Kayseri, Turkey.

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http://dx.doi.org/10.1002/pd.1653DOI Listing
April 2007

Prenatal diagnosis of a fetus with partial trisomy 7p.

Fetal Diagn Ther 2007 17;22(3):229-32. Epub 2007 Jan 17.

Department of Obstetrics and Gynecology, Erciyes University, Kayseri, Turkey.

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http://dx.doi.org/10.1159/000098724DOI Listing
May 2007

Hereditary isolated ankyloblepharon filiforme adnatum.

Plast Reconstr Surg 2005 Jan;115(1):363-4

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January 2005

Isolated congenital anonychia cases with coincident chromosomal fragility.

Ann Genet 2004 Oct-Dec;47(4):381-6

Department of Plastic and Reconstructive Surgery, Faculty of Medicine, Erciyes University, Melikgazi, Kayseri 38039, Turkey.

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http://dx.doi.org/10.1016/j.anngen.2004.03.004DOI Listing
May 2005

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype.

Ann Genet 2002 Oct-Dec;45(4):181-3

Department of Genetics, School of Medicine, Erciyes University, 38039, Kayseri, Turkey

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http://dx.doi.org/10.1016/s0003-3995(02)01139-5DOI Listing
November 2003