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ETS1 mediates MEK1/2-dependent overexpression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancer cells

PloS one, 2011-03, Vol.6 (3), p.e17979

2011

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Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis

Cogent medicine, 2019-01, Vol.6 (1), p.1582400

2019

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The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

BMB Reports, 2010, 43(8), , pp.530-534

2010

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Why Crossmatch Tests are Very Important and What Do They Tell Us?

Turkish journal of nephrology, 2020-01, Vol.29 (1), p.77-81

2020

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Comparison of Cytotoxic Flow Cytometric Cross Match With Complement Dependent Lymphocytotoxicity and Flow Cytometric Cross Match in Renal Transplant Patients

Transplantation proceedings, 2019-05, Vol.51 (4), p.1021-1023

2019

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Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism

The journal of obstetrics and gynaecology research, 2008-02, Vol.34 (1), p.73-77

2008

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Myxoma Virus Combination Therapy Enhances Lenalidomide and Bortezomib Treatments for Multiple Myeloma

Pathogens (Basel), 2024-01, Vol.13 (1), p.72

2024

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Protective effects of Acetobacter ghanensis against gliadin toxicity in intestinal epithelial cells with immunoregulatory and gluten-digestive properties

European journal of nutrition, 2023-03, Vol.62 (2), p.605-614

2023

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The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

BMB reports, 2010-08, Vol.43 (8), p.530-534

2010

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Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study

Medicine (Baltimore), 2022-08, Vol.101 (32), p.e29881-e29881

2022

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First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population

Turkish journal of haematology, 2015-12, Vol.32 (4), p.374-375

2015

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FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center

Gazi tıp dergisi, 2022-10, Vol.33 (4)

2022

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First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population

Turkish journal of haematology, 2016-03, Vol.33 (1), p.71-72

2016

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Prevalence and significance of the MEFV gene mutations in childhood Henoch–Schönlein purpura without FMF symptoms

Rheumatology international, 2013-02, Vol.33 (2), p.377-380

2013

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Chk1 Targeting Reactivates PP2A Tumor Suppressor Activity in Cancer Cells

Cancer research (Chicago, Ill.), 2013-11, Vol.73 (22), p.6757-6769

2013

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A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C

Hemoglobin, 2016-07, Vol.40 (4), p.280-282

2016

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hMLH1 Gene is not Methylated in Osteosarcoma

Laboratory medicine, 2011-05, Vol.42 (5), p.280-282

2011

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Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya

Turkish journal of haematology, 2016-06, Vol.33 (2), p.107-111

2016

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788: The association between inherited thrombophilias and pregnancy-related hypertension recurrence

American journal of obstetrics and gynecology, 2009-12, Vol.201 (6), p.S283-S283

2009

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The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population

Blood cells, molecules, & diseases, 2011-03, Vol.46 (3), p.226-229

2011

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ETS1 Mediates MEK1/2-Dependent Overexpression of Cancerous Inhibitor of Protein Phosphatase 2A

PloS one, 2011-03, Vol.6 (3), p.e17979

2011

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Investigation of the Effects of Piperlongumine and Doxorubicin Combined Treatment on Cell Death via PTEN in HeLa Cells

Yüzüncü Yıl Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2024-04, Vol.29 (1), p.1-11

2024

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The association between inherited thrombophilias and pregnancy-related hypertension recurrence

Archives of gynecology and obstetrics, 2011-10, Vol.284 (4), p.837-841

2011

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Alloreactive memory B cell detection by flow cytometric cross match using polyclonally activated memory B cell culture supernatants

Transplant immunology, 2022-08, Vol.73, p.101642-101642, Article 101642

2022

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Complement Factor H Y403H Polymorphism in the Turkish Population

Balkan journal of medical genetics, 2010-01, Vol.13 (2), p.41-45

2010

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ETS1 mediates MEK1/2-dependent overexpression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancer cells

Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

Why Crossmatch Tests are Very Important and What Do They Tell Us?

Comparison of Cytotoxic Flow Cytometric Cross Match With Complement Dependent Lymphocytotoxicity and Flow Cytometric Cross Match in Renal Transplant Patients

Effects of hormone replacement therapy on bone mineral density in Turkish patients with or without COL1A1 Sp1 binding site polymorphism

Myxoma Virus Combination Therapy Enhances Lenalidomide and Bortezomib Treatments for Multiple Myeloma

Protective effects of Acetobacter ghanensis against gliadin toxicity in intestinal epithelial cells with immunoregulatory and gluten-digestive properties

The effect of CYP1A2 gene polymorphisms on Theophylline metabolism and chronic obstructive pulmonary disease in Turkish patients

Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study

First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population

FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center

First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population

Prevalence and significance of the MEFV gene mutations in childhood Henoch–Schönlein purpura without FMF symptoms

Chk1 Targeting Reactivates PP2A Tumor Suppressor Activity in Cancer Cells

A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C

hMLH1 Gene is not Methylated in Osteosarcoma

Gap-PCR Screening for Common Large Deletional Mutations of β-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (δβ)0 Mutation in Antalya

788: The association between inherited thrombophilias and pregnancy-related hypertension recurrence

The association between intragenic SNP haplotypes and mutations of the beta globin gene in a Turkish population

ETS1 Mediates MEK1/2-Dependent Overexpression of Cancerous Inhibitor of Protein Phosphatase 2A

Investigation of the Effects of Piperlongumine and Doxorubicin Combined Treatment on Cell Death via PTEN in HeLa Cells

The association between inherited thrombophilias and pregnancy-related hypertension recurrence

Alloreactive memory B cell detection by flow cytometric cross match using polyclonally activated memory B cell culture supernatants

Complement Factor H Y403H Polymorphism in the Turkish Population

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