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Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B51 and ERAP1

Nature genetics, 2013-02, Vol.45 (2), p.202-207

2013

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Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

Proceedings of the National Academy of Sciences - PNAS, 2013-05, Vol.110 (20), p.8134-8139

2013

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Water as Source of Francisella tularensis Infection in Humans, Turkey

Emerging infectious diseases, 2015-12, Vol.21 (12), p.2213-2216

2015

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The Immunostimulatory Effect of Lactic Acid Bacteria in a Rat Model

Iranian journal of immunology, 2016-09, Vol.13 (3), p.220-228

2016

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Microfluidics and nanoparticles based amperometric biosensor for the detection of cyanobacteria (Planktothrix agardhii NIVA-CYA 116) DNA

Biosensors & bioelectronics, 2015-08, Vol.70, p.426-432

2015

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MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever

Turkish journal of medical sciences, 2021-08, Vol.51 (4), p.1702-1705

2021

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Recombinant plasmid-based quantitative Real-Time PCR analysis of Salmonella enterica serotypes and its application to milk samples

Journal of microbiological methods, 2016-03, Vol.122, p.50-58

2016

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Determination of a New Mutation in MT-ND1 Gene of a Patient With Dextrocardia, Ventriculoarterial Discordance, and Tricuspid Atresia

Artificial organs, 2015-01, Vol.39 (1), p.83-84

2015

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Association of Enteric Protist Blastocystis spp. and Gut Microbiota with Hepatic Encephalopathy

Journal of gastrointestinal and liver diseases : JGLD, 2016-12, Vol.25 (4), p.489-497

2016

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Characterization of H3K9me3- and H4K20me3-associated circulating nucleosomal DNA by high-throughput sequencing in colorectal cancer

Tumor biology, 2013-02, Vol.34 (1), p.329-336

2013

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Draft Genome Sequence of Halomonas smyrnensis AAD6T

Journal of Bacteriology, 2012-10, Vol.194 (20), p.5690-5691

2012

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Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis

Balkan medical journal, 2019-01, Vol.36 (1), p.23-31

2019

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Alix Protein Is Substrate of Ozz-E3 Ligase and Modulates Actin Remodeling in Skeletal Muscle

The Journal of biological chemistry, 2012-04, Vol.287 (15), p.12159-12171

2012

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The association between P selectin glycoprotein ligand 1 gene variable number of tandem repeats polymorphism and risk of thrombosis in Behçet's disease

International journal of rheumatic diseases, 2018-12, Vol.21 (12), p.2175-2179

2018

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BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy

Molecular syndromology, 2022-02, Vol.13 (1), p.12-22

2022

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Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next‑generation sequencing technology and matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry

Molecular medicine reports, 2019-05, Vol.19 (5), p.3912-3922

2019

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Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993T>C mutation in the MT-ATP6 gene

Molecular genetics and metabolism, 2012-11, Vol.107 (3), p.389-393

2012

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Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from turkey with McArdle disease

Neuromuscular disorders : NMD, 2017-11, Vol.27 (11), p.997-1008

2017

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Spleen Tyrosine Kinase Inhibitor TAK-659 Prevents Splenomegaly and Tumor Development in a Murine Model of Epstein-Barr Virus-Associated Lymphoma

mSphere, 2018-08, Vol.3 (4)

2018

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Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology

Cardiology in the young, 2015-04, Vol.25 (4), p.705-711

2015

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A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

Journal of clinical research in pediatric endocrinology, 2015-12, Vol.7 (4), p.323-328

2015

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MEFV gene variations in patients with systemic lupus erythematosus

Modern rheumatology, 2014-01, Vol.24 (1), p.93-96

2014

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Investigation of ErbB and Insulin Signaling Pathways in the Pathogenesis of Multiple Myeloma

Haseki tıp bülteni, 2018-06, Vol.56 (2), p.109-113

2018

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A Novel Partial Sequence Alignment Tool for Finding Large Deletions

TheScientificWorld, 2012-01, Vol.2012, p.694813-6

2012

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Real-Time Polymerase Chain Reaction Versus Conventional PCR: A Comparison between two Methods for the Detection of Fusobacterium Nucleatum in Saliva, Nasopharyngeal Secretion and Middle Ear Effusion Samples

Biotechnology, biotechnological equipment, 2013, Vol.27 (3), p.3825-3828

2013

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Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B51 and ERAP1

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

Water as Source of Francisella tularensis Infection in Humans, Turkey

The Immunostimulatory Effect of Lactic Acid Bacteria in a Rat Model

Microfluidics and nanoparticles based amperometric biosensor for the detection of cyanobacteria (Planktothrix agardhii NIVA-CYA 116) DNA

MEFV mutation frequencies in a Turkish cohort with low prevalence of familial Mediterranean fever

Recombinant plasmid-based quantitative Real-Time PCR analysis of Salmonella enterica serotypes and its application to milk samples

Determination of a New Mutation in MT-ND1 Gene of a Patient With Dextrocardia, Ventriculoarterial Discordance, and Tricuspid Atresia

Association of Enteric Protist Blastocystis spp. and Gut Microbiota with Hepatic Encephalopathy

Characterization of H3K9me3- and H4K20me3-associated circulating nucleosomal DNA by high-throughput sequencing in colorectal cancer

Draft Genome Sequence of Halomonas smyrnensis AAD6T

Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis

Alix Protein Is Substrate of Ozz-E3 Ligase and Modulates Actin Remodeling in Skeletal Muscle

The association between P selectin glycoprotein ligand 1 gene variable number of tandem repeats polymorphism and risk of thrombosis in Behçet's disease

BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy

Identification of red blood cell membrane defects in a patient with hereditary spherocytosis using next‑generation sequencing technology and matrix‑assisted laser desorption/ionization time‑of‑flight mass spectrometry

Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993T>C mutation in the MT-ATP6 gene

Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from turkey with McArdle disease

Spleen Tyrosine Kinase Inhibitor TAK-659 Prevents Splenomegaly and Tumor Development in a Murine Model of Epstein-Barr Virus-Associated Lymphoma

Mitochondrial mutations in patients with congenital heart defects by next generation sequencing technology

A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

MEFV gene variations in patients with systemic lupus erythematosus

Investigation of ErbB and Insulin Signaling Pathways in the Pathogenesis of Multiple Myeloma

A Novel Partial Sequence Alignment Tool for Finding Large Deletions

Real-Time Polymerase Chain Reaction Versus Conventional PCR: A Comparison between two Methods for the Detection of Fusobacterium Nucleatum in Saliva, Nasopharyngeal Secretion and Middle Ear Effusion Samples

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