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Methylation of SOCS3 in myeloproliferative neoplasms and secondary erythrocytosis/thrombocythemia / Miyeloproliferatif Neoplazmlar ve Sekonder Eritrositoz/Trombositemide SOCS3 Metilasyonu

Turkish journal of haematology, 2013-03, Vol.30 (1), p.13

2013

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New approaches in studying biological mechanisms in psychiatric diseases

Gülhane tıp dergisi, 2021-03, Vol.63 (1), p.1-7

Guran, Sefik

2021

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Uptake of high-dose folic acid decreases cell viability and proliferation via JAK/STAT pathway in human prostate cancer cells

Gülhane tıp dergisi, 2023-03, Vol.65 (1), p.1-6

2023

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Specific Polymorphisms of IL-1β Genes (-511, +3953) and Their Probable Effects on IL-1β Production in Idiopatic Hypogonadotropic Hypogonadism

Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi, 2010-12, Vol.30 (6), p.1814-1819

2010

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Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

American journal of medical genetics. Part A, 2013-07, Vol.161A (7), p.1737-1742

2013

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Imatinib mesylate therapy may cause additional chromosomal instability by a feedback mechanism in chronic myeloid leukemia treatment

Bioscience hypotheses, 2009-01, Vol.2 (6), p.396-398

Guran, Sefik

2009

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In vitro effects of zinc and folic acid on the expressions of Neurogenin 3, Kruppel-like factor 4, c-Myc, Nanog, Nestin and POU class 5 homeobox 1 genes

Journal of experimental and integrative medicine, 2015, Vol.5 (2), p.75

2015

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Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts

Prenatal diagnosis, 2009-05, Vol.29 (5), p.536-537

2009

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The progeny of homozygous identical reciprocal translocation carrier mother

American journal of medical genetics. Part A, 2010-11, Vol.152A (11), p.2886-2887

2010

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Importance of Myc-related microRNAs in induced pluripotency

Cell biology international, 2015-09, Vol.39 (9), p.987-994

2015

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Chitin increases the angiogenesis in chorioallantoic membrane model in the presence of testosterone and progesterone.(ORIGINAL ARTICLE)

Gülhane tıp dergisi, 2019-03, Vol.61 (1), p.20

2019

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Cell viability in SH-SY5Y neuroblastoma cells in folic acid application by using JACK-STAT pathway

Gülhane tıp dergisi, 2019-12, Vol.61 (4), p.157

2019

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Melatonin hormone stimulates human clock genes on neuroblastoma cell line

Gülhane tıp dergisi, 2019-12, Vol.61 (4), p.172

2019

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Hyperhomocysteinemia and homozygous MTHFR 677C>T mutation finding in an Alzheimer's disease case with metabolic syndrome diagnosis

Folia neuropathologica, 2010, Vol.48 (1), p.64

2010

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Rare chromosomal complement of trisomy 21 in a boy conceived only by IVF

Reproductive biomedicine online, 2010-11, Vol.21 (5), p.721-722

2010

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BDNF and Gad^sub 65^ Responses of Primary Auditory Cortex and Inferior Colliculus to Noise Exposure and Cochlear Ablation

The journal of international advanced otology, 2012-05, Vol.8 (2), p.187

2012

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Periodontal Status in Two Siblings With Severe Congenital Neutropenia: Diagnosis and Mutational Analysis of the Cases

Journal of periodontology (1970), 2005-05, Vol.76 (5), p.837-844

2005

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Identification of polymorphisms on the MDR1 gene among Turkish population and their effects on multidrug resistance in acute leukemia patients

American journal of hematology, 2005-09, Vol.80 (1), p.26-34

2005

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Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia

Turkish journal of haematology, 2013-03, Vol.30 (1), p.13-18

2013

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Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation-Dependent Probe Amplification Assay

Cancer investigation, 2011-01, Vol.29 (1), p.73-77

2011

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Donor cell leukemia in a patient developing 11 months after an allogeneic bone marrow transplantation for chronic myeloid leukemia

American journal of hematology, 2006-05, Vol.81 (5), p.370-373

2006

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A papillary thyroid carcinoma case associated with hereditary colon carcinoma due to familial adenomatous polyposis with no hereditary mutation finding

International journal of colorectal disease, 2007-06, Vol.22 (6), p.725-726

2007

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New phenotype with generalized platyspondyly, large mandible, hypoplastic teeth, strabismus, hyperopia and low cholesterol levels

Genetic counseling, 2011-01, Vol.22 (2), p.129

2011

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Gene correction applications in cell replacement therapy and use in neurodegenerative diseases

Gülhane Tip Dergisi, 2018, Vol.60 (2), p.60

Güran, Şefik

2018

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A New Syndrome Associated with Absence of Lower Lid Lacrimal Punctum, Ptosis, Elevation Deficiency of Both Eyes and Mild Facial Dysmorphism

Ophthalmic genetics, 2009, Vol.30 (3), p.146-151

2009

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Methylation of SOCS3 in myeloproliferative neoplasms and secondary erythrocytosis/thrombocythemia / Miyeloproliferatif Neoplazmlar ve Sekonder Eritrositoz/Trombositemide SOCS3 Metilasyonu

New approaches in studying biological mechanisms in psychiatric diseases

Uptake of high-dose folic acid decreases cell viability and proliferation via JAK/STAT pathway in human prostate cancer cells

Specific Polymorphisms of IL-1β Genes (-511, +3953) and Their Probable Effects on IL-1β Production in Idiopatic Hypogonadotropic Hypogonadism

Gorlin-chaudhry-moss syndrome revisited: Expanding the phenotype

Imatinib mesylate therapy may cause additional chromosomal instability by a feedback mechanism in chronic myeloid leukemia treatment

In vitro effects of zinc and folic acid on the expressions of Neurogenin 3, Kruppel-like factor 4, c-Myc, Nanog, Nestin and POU class 5 homeobox 1 genes

Prenatal diagnosis of Cri-du chat syndrome following high maternal serum human chorionic gonodotrophin and choroid plexus cysts

The progeny of homozygous identical reciprocal translocation carrier mother

Importance of Myc-related microRNAs in induced pluripotency

Chitin increases the angiogenesis in chorioallantoic membrane model in the presence of testosterone and progesterone.(ORIGINAL ARTICLE)

Cell viability in SH-SY5Y neuroblastoma cells in folic acid application by using JACK-STAT pathway

Melatonin hormone stimulates human clock genes on neuroblastoma cell line

Hyperhomocysteinemia and homozygous MTHFR 677C>T mutation finding in an Alzheimer's disease case with metabolic syndrome diagnosis

Rare chromosomal complement of trisomy 21 in a boy conceived only by IVF

BDNF and Gad^sub 65^ Responses of Primary Auditory Cortex and Inferior Colliculus to Noise Exposure and Cochlear Ablation

Periodontal Status in Two Siblings With Severe Congenital Neutropenia: Diagnosis and Mutational Analysis of the Cases

Identification of polymorphisms on the MDR1 gene among Turkish population and their effects on multidrug resistance in acute leukemia patients

Methylation of SOCS3 in Myeloproliferative Neoplasms and Secondary Erythrocytosis/Thrombocythemia

Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation-Dependent Probe Amplification Assay

Donor cell leukemia in a patient developing 11 months after an allogeneic bone marrow transplantation for chronic myeloid leukemia

A papillary thyroid carcinoma case associated with hereditary colon carcinoma due to familial adenomatous polyposis with no hereditary mutation finding

New phenotype with generalized platyspondyly, large mandible, hypoplastic teeth, strabismus, hyperopia and low cholesterol levels

Gene correction applications in cell replacement therapy and use in neurodegenerative diseases

A New Syndrome Associated with Absence of Lower Lid Lacrimal Punctum, Ptosis, Elevation Deficiency of Both Eyes and Mild Facial Dysmorphism

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