Prof. Dr. Kıvanç ÇEFLE

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Curcumin suppresses cell viability in breast cancer cell line by affecting the expression of miR-15a-5p

Suer İ., Abuaisha A., Kaya M., Abanoz F., Çefle K., Palanduz Ş., et al.

TURKISH JOURNAL OF BIOCHEMISTRY , cilt.1, sa.1, ss.1-10, 2024 (SCI-Expanded)

Long-term efficacy of canakinumab in hyperimmunoglobulin D syndrome

Ozdemir Isik O., Karadag D. T., Tekeoglu S., YAZICI A., Cefle K., ÇEFLE A.

International Journal of Rheumatic Diseases , cilt.27, sa.1, 2024 (SCI-Expanded)

CDR1as/miR-7-5p/IGF1R axis contributes to the suppression of cell viability in prostate cancer

Kaya M., Suer I., Aytatli A., Karatas O. F., Palanduz S., Cefle K., et al.

Turkish Journal of Biochemistry , 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

miR-145-5p suppresses cell proliferation by targeting <i>IGF1R </i>and <i>NRAS </i>genes in multiple myeloma cells

Kaya M., Suer İ., Ozgur E., Capik O., Karatas O. F., Ozturk Ş., et al.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , cilt.48, sa.5, ss.563-569, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.

Dirim A. B., Kalayci T., Safak S., Garayeva N., Gultekin B., Hurdogan O., et al.

Clinical rheumatology , cilt.42, sa.2, ss.597-606, 2023 (SCI-Expanded)

The effect of Anzer honey on X-ray induced genotoxicity in human lymphocytes: An in vitro study

Bagatir G., Kaya M., Suer İ., Çefle K., Palanduz A., Palanduz Ş., et al.

MICROSCOPY RESEARCH AND TECHNIQUE , cilt.85, sa.6, ss.2241-2250, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

OCT-1 Expression in Patients with Chronic Myeloid Leukemia: A Comparative Analysis with Respect to Response to Imatinib Treatment

Bozkurt Bulakçı B., Aday A., Gürtekin B., Yavuz A. S., Öztürk Ş., Çefle K., et al.

INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION , cilt.1, sa.1, ss.1-7, 2022 (SCI-Expanded)

Clinical Characteristics and Mutation Spectrum of Neurofibromatosis Type 1 in 27 Turkish Families

Sharifi S., Kalayci T., Palanduz S., Ozturk S., Cefle K.

BALKAN MEDICAL JOURNAL , cilt.38, sa.6, ss.365-373, 2021 (SCI-Expanded)

Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey

Berkay E. G., Elkanova L., Kalayci T., ULUDAĞ ALKAYA D., Altunoglu U., Cefle K., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.185, sa.8, ss.2488-2495, 2021 (SCI-Expanded)

Dysregulation of MS4A3 and PRDX5 Gene Expression in Multiple Myeloma Patients

Suer İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., Ekmekci S. S., et al.

UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , cilt.31, sa.4, ss.205-213, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

RELATIONSHIP BETWEEN CHROMOSOMAL ABERRATIONS AND GENE EXPRESSIONS IN THE p53 PATHWAY IN CHRONIC LYMPHOCYTIC LEUKEMIA

ÖZTAN G., Aktan M., Palanduz Ş., İŞSEVER H., ÖZTÜRK Ş., Nikerel E., et al.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.23, sa.1, ss.15-23, 2020 (SCI-Expanded)

DNA damage effects of inhalation anesthetics in human bronchoalveolar cells

ÇUKUROVA Z., Cetingok H., Ozturk S., Gedikbasi A., HERGÜNSEL O., Ozturk D., et al.

MEDICINE , cilt.98, sa.32, 2019 (SCI-Expanded)

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

Sariman M., Abaci N., Ekmekci S., Cakiris A., Pacal F., Ustek D., et al.

Balkan medical journal , cilt.36, sa.1, ss.23-31, 2019 (SCI-Expanded)

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

Kurklu E., Ozturk S., Cassidy A. J., Ak G., Koray M., Cefle K., et al.

MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL , sa.2, 2018 (SCI-Expanded)

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

BAYRAM Y., WHITE J. J., Elcioglu N., CHO M. T., ZADEH N., Gedikbasi A., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , cilt.101, sa.1, ss.149-156, 2017 (SCI-Expanded)

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

Yokote K., Chanprasert S., Lee L., EIRICH K., Takemoto M., Watanabe A., et al.

HUMAN MUTATION , cilt.38, sa.1, ss.7-15, 2017 (SCI-Expanded)

The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.

Bagatır G., Sırma S. Ö., Palanduz S., Ozturk Ş., Cefle K., Ozbek U., et al.

Cellular and molecular biology (Noisy-le-Grand, France) , cilt.62, sa.7, ss.61-5, 2016 (SCI-Expanded)

Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

BONORA E., BIANCO F., Cordeddu L., Bamshad M., Francescatto L., Dowless D., et al.

GASTROENTEROLOGY , cilt.148, sa.4, ss.771-793, 2015 (SCI-Expanded)

Evaluation of micronuclear frequencies in both circulating lymphocytes and buccal epithelial cells of patients with oral lichen planus and oral lichenoid contact reactions

Saruhanoglu A., Ergun S., Kaya M. O., Warnakulasuriya S., Erbagci M., Öztürk S., et al.

ORAL DISEASES , cilt.20, sa.5, ss.521-527, 2014 (SCI-Expanded)

Genotoxicity of fixation devices analyzed by the frequencies of sister chromatid exchange

Aydil B. A., Kocak Berberoglu H., Ozturk S., Cefle K., Palanduz S., Erkal H.

ULUSAL TRAVMA VE ACIL CERRAHI DERGISI-TURKISH JOURNAL OF TRAUMA & EMERGENCY SURGERY , cilt.19, sa.4, ss.299-304, 2013 (SCI-Expanded)

A Turkish trichothiodystrophy patient with homozygous XPD mutation and genotype-phenotype relationship

Pehlivan D., Cefle K., Raams A., Ozturk Ş., Baykal C., Kleijer W. J., et al.

JOURNAL OF DERMATOLOGY , cilt.39, sa.12, ss.1016-1021, 2012 (SCI-Expanded)

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Diggle C. P., Parry D. A., Logan C. V., Laissue P., Rivera C., Martin Restrepo C., et al.

HUMAN MUTATION , cilt.33, sa.8, ss.1175-1181, 2012 (SCI-Expanded)

A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man.

CARIDI G., DAGNINO M., Di D., AKYÜZ F., BOZTAS G., BESISIK F., et al.

Clinica chimica acta; international journal of clinical chemistry , cilt.413, sa.9-10, ss.950-1, 2012 (SCI-Expanded)

A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man.

ÇEFLE K.

CLINICA CHIMICA ACTA , cilt.413, ss.950-1, 2012 (SCI-Expanded)

Investigation of Arg399Gln and Arg194Trp Polymorphisms of the XRCC1 (X-Ray Cross-Complementing Group 1) Gene and Its Correlation to Sister Chromatid Exchange Frequency in Patients with Chronic Lymphocytic Leukemia

Duman N., Aktan M., Ozturk S., Palanduz S., Cakiris A., Ustek D., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.16, sa.4, ss.287-291, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

A novel frameshift deletion in the albumin gene causes analbuminemia in a young Turkish woman

Dagnino M., Caridi G., Aydin Z., Ozturk S., Karaali Z., Kazancioglu R., et al.

Clinica Chimica Acta , cilt.411, ss.1711-1715, 2010 (SCI-Expanded)

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Friedrich K., Lee L., Leistritz D. F., Nuernberg G., Saha B., Hisama F. M., et al.

HUMAN GENETICS , cilt.128, sa.1, ss.103-111, 2010 (SCI-Expanded)

A POSSIBLE DELETERIOUS EFFECT OF INCREASED SERUM COPPER ON MYOCARDIAL FUNCTION IN PATIENTS WITH DILATED CARDIOMYOPATHY AWAITING TRANSPLANTATION

Cefle K., Ercag E., Gezertas S., Uzer A., Oeztuerk Ş., Cefle A., et al.

NOBEL MEDICUS , cilt.6, sa.2, ss.32-36, 2010 (SCI-Expanded)

NILOTINIB EFFICACY IN 21 IMATINIB-RESISTANT OR-INTOLERANT T (9;22) POSITIVE CHRONIC MYELOID LEUKEMIA PATIENTS WITH AND WITHOUT ADDITIONAL CHROMOSOMAL CHANGES

Yavuz A. S., Elcioglu O. C., Akpinar T. S., Cosan F., Ucur A., Bayrak A., et al.

NOBEL MEDICUS , cilt.6, sa.2, ss.57-62, 2010 (SCI-Expanded)

TRANSPLANTASYON BEKLEYEN DİLATE KARDİYOMİYOPATİLİ HASTALARDA YÜKSEK SERUM BAKIR DÜZEYİNİN MİYOKARD İŞLEVİ ÜZERİNDEKİ MUHTEMEL KÖTÜ ETKİSİ

PALANDUZ Ş., ÇEFLE K.

NOBEL MEDICUS , sa.6, ss.32-36, 2010 (SCI-Expanded)

İMATİNİBE DİRENÇLİ VEYA ENTOLERANS GÖSTEREN, KROMOZOMAL DEĞİŞİKLİKLERİ OLAN VE OLMAYAN T(9;22) POZİTİF KRONİK MYELOİD LÖSEMİLİ 21 HASTADA NİLOTİNİB’İN ETKİNLİĞİ

PALANDUZ Ş., ÇEFLE K.

NOBEL MEDICUS , sa.6, ss.57-62, 2010 (SCI-Expanded)

Cytogenetic Analysis and Examination of SOS1 Gene Mutation in a Turkish Family with Hereditary Gingival Fibromatosis

Pehlivan D., Abe S., Ozturk S., Kayhan K., Gunduz E., Cefle K., et al.

JOURNAL OF HARD TISSUE BIOLOGY , cilt.18, sa.3, ss.131-134, 2009 (SCI-Expanded)

Micronuclear and sister chromatid exchange analyses in peripheral lymphocytes of patients with oral lichen planus - a pilot study

Ergun S., Warnakulasuriya S., Duman N., Saruhanoglu A., Sevinc B., Öztürk S., et al.

ORAL DISEASES , cilt.15, sa.7, ss.499-504, 2009 (SCI-Expanded)

Comparison of the Cytogenetic and Molecular Analyses in the Assessment of Imatinib Response in Chronic Myelocytic Leukemia

Palanduz S., Bayrak A., Sirma S., Vural B., Cefle K., Ucur A., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.13, sa.5, ss.599-602, 2009 (SCI-Expanded)

Left Ventricular Thickness Is Increased in Nonhypertensive Turner's Syndrome

Sozen A. B., Cefle K., Kudat H., Ozturk Ş., Oflaz H., Akkaya V., et al.

ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES , cilt.26, sa.8, ss.943-949, 2009 (SCI-Expanded)

ALTERATIONS IN LYMPHOCYTE MEMBRANE PROTEIN CONTENT AND INCREASED LYMPHOCYTE RIGIDITY IN CATS WITH DIABETES MELLITUS

ÇEFLE K.

JOURNAL OF PHYSIOLOGICAL SCIENCES , sa.59, ss.505, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

The effect of parental consanguinity on the clinical and laboratory findings of rheumatoid arthritis

Cefle K., ÇEFLE A., YAZICI A., SELEK A.

INTERNATIONAL JOURNAL OF CLINICAL PRACTICE , cilt.63, sa.7, ss.1056-1060, 2009 (SCI-Expanded)

ALTERATIONS IN LYMPHOCYTE MEMBRANE PROTEIN CONTENT AND INCREASED LYMPHOCYTE RIGIDITY IN CATS WITH DIABETES MELLITUS

Tamer S. A., Cefle K., Kaymaz A. A., Albeniz I.

JOURNAL OF PHYSIOLOGICAL SCIENCES , cilt.59, ss.505, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

The effects of etodolac, nimesulid and naproxen sodium on the frequency of sister chromatid exchange after enclused third molars surgery.

Koeseoglu B., Oeztuerk Ş., Kocak H., Palanduz S., Cefle K.

Yonsei medical journal , cilt.49, sa.5, ss.742-7, 2008 (SCI-Expanded)

Effect of Cyclosporin A and Tacrolimus on sister chromatid exchange frequency in renal transplant patients

Ozturk Ş., Ayna T. K., Cefle K., Palanduz S., Ciftci H., Kaya Ş., et al.

GENETIC TESTING , cilt.12, sa.3, ss.427-430, 2008 (SCI-Expanded)

Atrial and ventricular arryhthmogenic potential in Turner syndrome

Sozen A. B., Cefle K., Kudat H., Ozturk Ş., Oflaz H., Pamukcu B., et al.

PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY , cilt.31, sa.9, ss.1140-1145, 2008 (SCI-Expanded)

A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24

Deglincerti A., De Giorgio R., Cefle K., Devoto M., Pippucci T., Castegnaro G., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , cilt.15, sa.8, ss.889-897, 2007 (SCI-Expanded)

The genotoxic effects in lymphocyte cultures of children treated with radiosynovectomy by using yttrium-90 citrate colloid

Turkmen C., Ozturk Ş., Unal S. N., Zulrikar B., Taser O., Sanfi Y., et al.

CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS , cilt.22, sa.3, ss.393-399, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey

Yoenal O., Hatirnaz O., Akyuez F., KOROGLU G., Ozbeik U., Cefle K., et al.

TURKISH JOURNAL OF GASTROENTEROLOGY , cilt.18, sa.1, ss.53-57, 2007 (SCI-Expanded)

Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male

Baumer A., Basaran S., Taralczak M., Cefle K., Ozturk S., Palanduz S., et al.

CYTOGENETIC AND GENOME RESEARCH , cilt.118, sa.1, ss.38-41, 2007 (SCI-Expanded)

Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis

Turkmen C., Ozturk Ş., Unal N., Zulfikar B., Taser O., Sanli Y., et al.

HAEMOPHILIA , cilt.13, sa.1, ss.57-64, 2007 (SCI-Expanded)

Lens opacities in Bloom syndrome: Case report and review of the literature

Cefle K., Ozturk Ş., Gozum N., Duman N., Mantar F., Guler K., et al.

OPHTHALMIC GENETICS , cilt.28, sa.3, ss.175-178, 2007 (SCI-Expanded)

Comparison of rheological parameters in patients with post hepatitic and alcoholic cirrhosis

Tamer S., Cefle K., Gokkusu C., Ademoglu E., Ozturk Ş., Vatansever S., et al.

CLINICAL HEMORHEOLOGY AND MICROCIRCULATION , cilt.36, sa.3, ss.247-252, 2007 (SCI-Expanded)

Increased sister chromatid exchange frequency in young women with breast cancer and in their first-degree relatives.

Cefle K., Ucur A., Guney N., Ozturk S., Palanduz S., Tas F., et al.

Cancer genetics and cytogenetics , cilt.171, ss.65-7, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade

Cefle A., Cefle K., Tunaci M., Ozturk S., Palanduz S.

INTERNATIONAL JOURNAL OF CLINICAL PRACTICE , cilt.60, sa.10, ss.1306-1309, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

The genotoxic effects in lymphocyte cultures of infants treated with radiosynovectomy by using Yittrium-90 citrate colloid.

ÇEFLE K.

EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING , sa.33, 2006 (SCI-Expanded)

A different approach to telomere analysis with ddPRINS in chronic lymphocytic leukemia

Palanduz S., Serakinci N., Cefle K., Aktan M., Tutkan G., Ozturk S., et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.49, sa.1, ss.63-69, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

Two siblings with distal pachydermodactyly

Saka B., Mezdegi A., Ozturk A., Erten N., Cefle K., Palanduz S.

CLINICAL AND EXPERIMENTAL DERMATOLOGY , cilt.30, sa.6, ss.707-709, 2005 (SCI-Expanded)

A solitary calvarial lytic lesion with typical histopathological findings of juvenile hyaline fibromatosis.

BAS N., GÜZEY F., EMEL E., CEFLE K., TURGUT H. Z., ALATAS I., et al.

Journal of neurosurgery , cilt.103, ss.285-8, 2005 (SCI-Expanded)

Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome

Tufan F., Cefle K., Turkmen S., Turkmen A., Zorba U., Dursun M., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , sa.2, ss.185-189, 2005 (SCI-Expanded)

Genotoxicity and sister chromatid exchange in patients with myelodysplastic disorders.

Oztürk S., PALANDUZ S., CEFLE K., TUTKAN G., UCUR A., DINCOL G., et al.

Cancer genetics and cytogenetics , cilt.159, ss.148-50, 2005 (SCI-Expanded)

Alterations in rheological properties and erythrocyte membrane proteins in cats with diabetes mellitus.

KAYMAZ A., TAMER S., ALBENIZ I., CEFLE K., PALANDUZ S., Ozturk S., et al.

Clinical hemorheology and microcirculation , cilt.33, ss.81-8, 2005 (SCI-Expanded) Sürdürülebilir Kalkınma

In vitro effects of selective and non-selective nonsteroidal anti-inflammatory drugs on the frequency of sister chromatid exchanges.

PALANDUZ Ş., ÇEFLE K.

Drugs R D , sa.5, ss.327-30, 2004 (SCI-Expanded)

Peutz-Jeghers syndrome: report of 6 cases in a family and management of polyps with intraoperative endoscopy.

ÇEFLE K.

TURKISH JOURNAL OF GASTROENTEROLOGY , sa.15, ss.164-8, 2004 (SCI-Expanded)

A case of mandibuloacral dysplasia presenting with features of scleroderma

Cefle A., Cefle K.

INTERNATIONAL JOURNAL OF CLINICAL PRACTICE , cilt.58, sa.6, ss.635-638, 2004 (SCI-Expanded)

In vitro effects of selective and non-selective nonsteroidal anti-inflammatory drugs on the frequency of sister chromatid exchanges.

Oztürk S., Köseoglu B., Koçak H., Palanduz S., Cefle K., Erkal H.

Drugs in R&D , cilt.5, ss.327-30, 2004 (SCI-Expanded)

Sister chromatid exchange and mitotic index in patients with cirrhosis related to hepatitis B and C viruses and in chronic carriers

Ucur A., Palanduz S., Cefle K., Ozturk Ş., Tutkan G., Vatansever S., et al.

HEPATO-GASTROENTEROLOGY , cilt.50, sa.54, ss.2137-2140, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

Acute wood or coal exposure with carbon monoxide intoxication induces sister chromatid exchange

ÇEFLE K.

JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY , sa.40, ss.115-120, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

Relationship between insulin-like growth factor-I and bone mineral density in men aged over 65 years

ÇEFLE K.

OSTEOPOROSIS INTERNATIONAL , sa.13, 2002 (SCI-Expanded)

Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families.

GALLIANO M., CAMPAGNOLI M., ROSSI A., Wirsing v., LYON A., CEFLE K., et al.

Clinical chemistry , cilt.48, ss.844-9, 2002 (SCI-Expanded)

The effect of atorvastatin on hemorheological parameters in rabbits fed on a normal diet

Cefle K., Tamer S., Kaymaz A., Balci M., Ahmetov S., Palanduz S., et al.

CLINICAL HEMORHEOLOGY AND MICROCIRCULATION , cilt.26, sa.4, ss.265-271, 2002 (SCI-Expanded)

Rheological properties of blood in patients with chronic liver disease

Tamer S., Cefle K., Palanduz S., Vatansever S.

CLINICAL HEMORHEOLOGY AND MICROCIRCULATION , cilt.26, sa.1, ss.9-14, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

Acute wood or coal exposure with carbon monoxide intoxication induces sister chromatid exchange.

Oztürk S., VATANSEVER S., CEFLE K., PALANDUZ S., GÜLER K., ERTEN N., et al.

Journal of toxicology. Clinical toxicology , cilt.40, ss.115-20, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

Sister chromatid exchange frequency in B-cells stimulated by TPA in chronic lymphocytic leukemia

Ozturk S., Palanduz S., Aktan M., Cefle K., Serakinci N., Perkcelen Y.

CANCER GENETICS AND CYTOGENETICS , cilt.123, sa.1, ss.49-51, 2000 (SCI-Expanded) Sürdürülebilir Kalkınma

A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia

Ozturk Ş., Cefle K., Palanduz S., Erten N., Karan M., Tascioglu C., et al.

INTERNATIONAL JOURNAL OF CLINICAL PRACTICE , cilt.54, sa.4, ss.274-276, 2000 (SCI-Expanded)

A case of turner syndrome with a rare reciprocal translocation between an autosome and the X chromosome

PALANDUZ Ş., ÖZTÜRK Ş., ÇEFLE K., KARAMAN B., ÜSTEK D., BAŞARAN S.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.3, ss.45-48, 2000 (AHCI)

A case of chronic lymphocytic leukemia with a constitutional pericentric inversion of chromosome 1

Palanduz S., Cefle K., Aktan M., Tutkan G., Ozturk S., Pekcelen Y.

CANCER GENETICS AND CYTOGENETICS , cilt.118, sa.1, ss.62-64, 2000 (SCI-Expanded)

A case of mental retardation associated with a partial tetrasomy of chromosome 15

PALANDUZ Ş., ÇEFLE K.

CYTOGENETICS AND CELL GENETICS , sa.85, 1999 (SCI-Expanded)

A case of Turner syndrome with a rare reciprocal translocation between an autosome and the X chromosome

ÇEFLE K.

CYTOGENETICS AND CELL GENETICS , sa.85, 1999 (SCI-Expanded)

Rheological properties of blood in patients with ischaemic heart disease

Palanduz S., Tamer S., Vatansever S., Karan M., Cefle K., Ozturk Ş., et al.

MEDICAL SCIENCE RESEARCH , cilt.27, sa.5, ss.327-329, 1999 (SCI-Expanded)

A case of McCune-Albright syndrome mimicking Paget's disease of bone

Palanduz S., Cefle K., Ozturk S., Tanakol R., Tascioglu C., Koldas T., et al.

BONE , cilt.24, sa.2, ss.157-158, 1999 (SCI-Expanded)

47,XYY karyotype in acute myeloid leukemia

Palanduz S., Aktan M., Ozturk S., Tutkan G., Cefle K., Pekcelen Y.

CANCER GENETICS AND CYTOGENETICS , cilt.106, sa.1, ss.76-77, 1998 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Akut Miyeloid Lösemi’li Olgularda inv(3)/t(3;3) ile 7.Kromozomun Anomalilerinin Prognoza Etkisi

Bayrak Tokaç A. G., Bağatır G., Erdem S., Çefle K., Öztürk Ş., Yenerel M. N., et al.

Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi , cilt.11, sa.3, ss.334-339, 2024 (Hakemli Dergi)

EFFECT of CURCUMIN on BREAST CANCER CELLS THROUGH miR-145-5p AND ITS TARGET GENES

Abuaisha A., Kaya M., Suer İ., Emiroğlu S., Abanoz F., Palanduz Ş., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , sa.3, ss.235-245, 2024 (ESCI) Sürdürülebilir Kalkınma

Expression patterns of eighteen genes involved in crucial cellular processes in the TP53 pathway in Multiple Myeloma

Öztan G., Suer İ., Aday A., Ayer M., Öztürk Ş., Çefle K., et al.

GAZI UNIVERSITY JOURNAL OF SCIENCE , cilt.37, sa.3, ss.1066-1082, 2024 (ESCI) Sürdürülebilir Kalkınma

ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

İstanbul Kanuni Sultan Süleyman Tıp Dergisi , cilt.14, sa.2, ss.120-124, 2022 (Hakemli Dergi) Sürdürülebilir Kalkınma

A Rare Variant Translocation (t(5922)(q13q34q11.2)) In A Case With Chronic Myeloid Leukemia

ERKAL H., ÖZTÜRK Ş., YÜCEL S., ÇEFLE K., BAGATIR G., BAYRAK A., et al.

Tıp Fakültesi Klinikleri Dergisi , 2019 (Hakemli Dergi)

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

Ozturk D., Coskunpinar E. M., Osmanbasoglu E., ÇETİN G., Yenerel M. N., Ayer M., et al.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.56, sa.2, ss.109-113, 2018 (ESCI)

THE PROGNOSTIC EFFECT OF GENES IN THE P53 PATHWAY IN CHRONIC LYMPHOCYTIC LEUKEMIA

Oztan G., Palanduz S., Cefle K.

NOBEL MEDICUS , cilt.14, sa.2, ss.5-16, 2018 (ESCI)

Could the ENPP1 p.D85H Mutation be Associated with Hypophosphatemic Rickets?

Coskunpinar E., Tekin S., Palanduz S., Avci H., Cefle K., Tiryakioglu N. O., et al.

BEZMIALEM SCIENCE , cilt.6, sa.2, ss.126-129, 2018 (ESCI)

Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene

Coskunpinar E., Ozvarnali A., Cefle K., Palanduz A., Gül A., Ozturk D., et al.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , cilt.56, sa.1, ss.42-49, 2018 (ESCI)

Diabetes Mellituslu Kedilerde Lenfosit Membran Protein İçeriğinde Değişiklikler ve Artmış Lenfosit Rijiditesi

ÇEFLE K.

Turkiye Klinikleri J Med Sci , sa.31, ss.816-822, 2011 (Hakemli Dergi) Sürdürülebilir Kalkınma

Investigation of Genomic Instability in Patients with Sjögren’s Syndrome by Using Sister Chromatid Exchange Analysis

ERGÜN S., TANYERİ H., ÖZTÜRK Ş., Duman N., KAMALI S., GÜL A., et al.

ACTA STOMATOLOGICA CROATICA , cilt.42, sa.4, ss.318-325, 2008 (ESCI)

ARTERIAL OBSTRUCTION IN A KLINEFELTER SYNDROME PATIENT WITH RARE KARYOTYPE (48, XXYY)

Pehlivan D., Cefle K., Ozturk S., Akbulut M. F., Palazduz S.

TURKISH JOURNAL OF UROLOGY , cilt.34, sa.4, ss.491-494, 2008 (ESCI)

MULTİPL EKZOSTOZ SENDROMLU İKİ KARDEŞ

ÇEFLE K.

İSTANBUL TIP FAKÜLTESİ DERGİSİ , sa.71, ss.14-18, 2008 (Hakemli Dergi)

Two sisters with hereditary multiple exositosis

Palanduz Ş., Öztürk Ş., Palanduz A., Çefle K., Erden S., Odabaş A. R., et al.

Medical Bulletin of Istanbul Medical Faculty , cilt.32, sa.2, ss.196-199, 1999 (Hakemli Dergi)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Optical Genome Mapping in Newly Diagnosed Chronic Lymphocytic Leukemia

ERDEM S., BAYRAK TOKAÇ A. G., ADAY A., KARACA D., ÖZTÜRK Ş., ÇEFLE K., et al.

66th ASH Annual Meeting and Exposition, San Diego, CA, Amerika Birleşik Devletleri, 7 - 10 Aralık 2024, ss.6758

DE NOVO 46,XX,t(5;7)(p15.2;q11.2) VE 46,XX,t(1;9)(q23;q21) DENGELİ RESIPROKAL TRANSLOKASYONLARI VE HABITUEL ABORTUS İLİŞKİSİ

Alptekin M. S., Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.

17th International Medical and Health Sciences Research Congress, 19 - 20 Ekim 2024

inv(5)(q15q33) in both parents associated with recurrent pregnancy loss

Kuntsal E., SUER İ., Kaya M., KALAYCI T., ÖZTÜRK Ş., ÇEFLE K.

10th South East European Congress of Perinatal Medicine (SEESPM), İstanbul, Türkiye, 25 Ekim 2024

De Novo 46,XX,t(5;7)(p15.2;q11.2) ve 46,XX,t(1;9)(q23;q21) Dengeli Resiprokal Translokasyonları ve Habituel Abortus İlişkisi

Alptekin M. S., Kaya M., Suer İ., Çefle K., Öztürk Ş.

17. Uluslararası Tıp ve Sağlık Bilimleri Araştırmaları Kongresi, Ankara, Türkiye, 19 - 20 Ekim 2024, ss.172-176

Akut miyeloid lösemi hücrelerinde EIF4E, PIM1 ve IGF1R ekspresyonunun miRNA aracılı baskılanması

Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.

26. Ulusal İç Hastalıkları Kongresi, Kıbrıs (Kktc), 2 - 06 Ekim 2024

A Novel FBN1 Variant in A Large Marfan Family with High Penetrance of Aortic Features

ERBİLGİN Y., ÇEFLE K., ÖZTÜRK Ş., EKIJI L., KADIOĞLU P., Kocaağa S., et al.

Avrupa İnsan Genetiği Kongresi 2024, Berlin, Almanya, 01 Haziran 2024

Curcumin inhibits breast cancer cell proliferation by regulating ciRS-7/miR-7-5p/CKS2 axis

Abuaisha A., Kaya M., Suer İ., Emiroğlu S., Abanoz F., Tükenmez M., et al.

2023 San Antonio Breast Cancer Symposium, San-Antonio, Kuzey Mariana Adaları, 5 - 09 Aralık 2023, ss.101-102

Şiddetli Oligospermi ve Tekrarlayan Gebelik Kaybıyla İlişkili Perisentrik Inv(1)(p34.1q25)

Kuntsal E., Suer İ., Kaya M., Bayrak Tokaç A. G., Palanduz Ş., Öztürk Ş., et al.

14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Türkiye, 23 - 24 Aralık 2023, cilt.1, ss.586-591

Şiddetli Oligospermi ve Tekrarlayan Gebelik Kaybıyla İlişkili Perisentrik Inv(1)(p34.1q25)

Kuntsal E., SUER İ., Kaya M., Bayrak A. G., PALANDUZ Ş., ÖZTÜRK Ş., et al.

14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Türkiye, 23 - 24 Aralık 2023, cilt.1, ss.586-591

Curcumin inhibits breast cancer cell proliferation by regulating ciRS-7/miR-7-5p/CKS2 axis

Abuaisha A., Kaya M., SUER İ., EMİROĞLU S., Abanoz F., TÜKENMEZ M., et al.

2023 San Antonio Breast Cancer Symposium, San-Antonio, Kuzey Mariana Adaları, 5 - 09 Aralık 2023

Wilson Hastalığında Aile İçi Genetik Taramanın Kliniğe Önemli Katkıları

Şahin A., ÇİFCİBAŞI ÖRMECİ A., SUER İ., DEMİR K., KALAYCI T., ÇEFLE K., et al.

40. Ulusal Gastroenteroloji Haftası ve 11. Gastroenteroloji Cerrahisi Kongresi, Antalya, Türkiye, 21 - 26 Kasım 2023

The Phenotypic Effect of X;Autosome Balanced Chromosomal Translocations: A Case with Premature Ovarian Failure and Familial t(X;9)(q22;q34)

Abuaisha A., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, İstanbul, Türkiye, 26 - 28 Mayıs 2022, cilt.1, ss.42-43

miR-16-5p/CCNE1 Relation in AML Cells

Teomete Ş., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.

VIII. INSAC International Congress on Health Sciences (ICHES-2022), Konya, Türkiye, 18 - 20 Mart 2022, cilt.1, ss.116-122 Sürdürülebilir Kalkınma

Miyeloid maligniteli hastalarda TET2 gen varyasyonları

Aday A., Sırma Ekmekci S., Bayrak A. G., Çefle K., Öztürk Ş., Nalçacı M., et al.

XVII. Tıbbi Biyoloji ve Genetik Kongresi, 28 - 31 Ekim 2021, cilt.52, ss.242-243

Investigation Of Some Candidate Genes Determined From Multiple Myeloma Whole Genome Transcriptome Data

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

EACR 2021 Virtual Congress-Innovative Cancer Science: Better Outcomes through Research, 9 - 12 Haziran 2021, ss.1

CEBPA c.584_589dup p.His195Pro196dup variant in myeloid malignancies

SUER İ., SIRMA EKMEKCİ S., Aday A., Bayrak A. G., ÇEFLE K., ÖZTÜRK Ş., et al.

The Virtual Conference on Current Challenges in Hematology (C-HEM2021), İstanbul, Türkiye, 18 - 19 Mart 2021

Investigation Of Possibly Related Genes Determined From Bioinformatic Analysis Of Multiple Myeloma Whole Genome Transcriptome Data

Sariman M., KARAÇAM B., AYER M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

8th Multidisciplinary Cancer Research Congress, İstanbul, Türkiye, 16 - 17 Ocak 2021, ss.123

Overexpression of FUS and PRDX5 Genes In Multiple Myeloma Patients

SUER İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., SIRMA EKMEKCİ S., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Türkiye, 20 - 23 Kasım 2020, ss.23 Sürdürülebilir Kalkınma

Steroide duyarlı kronik anemisi ve osteosklerozu olan erişkin olguda moleküler tanının klinik izleme etkisi

Sharifi S., Kalaycı T., Kaya M., SUER İ., ÖZTÜRK Ş., ÇEFLE K., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Türkiye, 20 - 23 Kasım 2020, ss.37

46,XX,t(8;9)(q12;q12) translokasyon taşıyıcısı tekrarlayan gebelik kayıp öykülü olgu sunumu

SUER İ., Kaya M., Sharifi S., Kalaycı T., ÖZTÜRK Ş., ÇEFLE K., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Türkiye, 20 - 22 Kasım 2020, ss.89

Investigation of miR-145 target genes in multiple myeloma cell lines

Kaya M., SUER İ., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.

V. International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Türkiye, 20 - 22 Şubat 2020, cilt.2584, ss.37 Sürdürülebilir Kalkınma

Evaluation of Spermatogenesis Process in Cases with Azospermic and Oligospermic Normal Karyotype and Azospermic Klinefelter Syndrome

ÖZTAN G., PALANDUZ Ş., ÇEFLE K., ÖZTÜRK Ş.

Cell Death Symposium, Türkiye, 3 - 04 Ekim 2019

Investigation of TMD-ERAP1 Candidate Gene Expressions Obtained from Multiple Myeloma Transcriptome Data by RT-PCR

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Türkiye, 18 - 22 Eylül 2019, cilt.1, ss.96

Investigation of miR-34a target genes in multiple myeloma cell lines

SUER İ., Kaya M., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.

VII. International Congress of Molecular Medicine, İstanbul, Türkiye, 5 - 07 Eylül 2019, cilt.1, ss.141

A Case of a Variant Philadelphia Translocation Involving Chromosomes (7;9;22)(q22;q34;q11) in Chronic Myeloid Leukemia

BAYRAK A. G., ADAY A., UÇUR A., ÖZBALAK M. M., NALÇACI M., ÇEFLE K., et al.

13th Balkan Congress of Human Genetics, Edirne, Türkiye, 17 - 20 Nisan 2019, cilt.BJMG, sa.39, ss.76

KML Hastalarında Moleküler Monitorizasyon-Klinik Seyir İlişkisinin ve SLC22A1 MRNA Ekspresyonunun Araştırılması

Bulakçı B., Dağlar Aday A., YAVUZ A. S., Gürtekin B., ÇEFLE K., ÖZTÜRK Ş., et al.

44. Ulusal Hematoloji Kongresi, Türkiye, 21 Ekim - 03 Kasım 2018

Akut Myeloid Lösemi ve 3q Kromozomal Yeniden Düzenlenmeleri

Bagatir G., Kaya M., Dön B., SUER İ., NALÇACI M., YENEREL M. N., et al.

3. Ulusal Uygulamalı Biyolojik Bilimler Kongresi (UBBK), Eskişehir, Türkiye, 3 - 05 Mayıs 2018, cilt.1, ss.35

idic(Y)(q11.2) ABNORMALITY IN CASES WITH MIXT GONADAL DYSGENESIS AND INFERTILITY

Kaya M., SUER İ., KALAYCI T., KARAMAN B., Dön B., Bagatir G., et al.

Erciyes Medical Genetics Days, Kayseri, Türkiye, 7 - 10 Mart 2018, cilt.1, ss.16

A Novel Insertional Translocation in a Patient with Infertility and Undiagnosed Mild Intellectual Disability

SUER İ., Kaya M., Bagatir G., KARAMAN B., ÇEFLE K., ÖZTÜRK Ş., et al.

Erciyes Medical Genetics Days, Kayseri, Türkiye, 7 - 10 Mart 2018, ss.32

Multiple Myeloma hastalarının Myeloma hücrelerinde RNA dizileme ve insilico analizler.

Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Paçal F., Üstek D., et al.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi , Muğla, Türkiye, 26 - 29 Ekim 2017, ss.108-109

Investigation of gene expression of myeloma cells in bone marrow of multiple myeloma patients by transcriptome analysis

Sarıman M., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., PAÇAL F., ÜSTEK D., et al.

ESHG 2016, Barcelona, İspanya, 21 - 24 Mayıs 2016, ss.153

Habituel Abortus Nedeniyle Başvuran 46,XX,inv(12)(p11.2q14) Karyotip Özelliği Saptanan Olgu

Kaya M., Dön B., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.102

46,XY,t(11;22)(q23;q11) Dengeli Translokasyonunu Taşıyan İnfertil Bir Olgu

Kaya M., Bağatır G., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.100-101

İnhalasyon Anestezisi ile Oluşan Genotoksik Etkilerin Bronkoalveoler Lavaj Sıvısında "Tek Hücre Jel Elektroforezi, Komet" Yöntemi il İncelenmesi

Çukurova Z., Gedikbaşı A., Öztürk Ş., Çetingök H., Öztürk D., Eren G., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.107-108

Kleidokranial Displazi: Olgu Sunumu

Gedikbaşı A., Çefle K., Kaya M., Öztürk Ş., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.67-68

47,XXY,inv(12)(q15q24) Karyotip Özelliği Gösteren Klinefelter Sendromlu Bir Olgu

Kaya M., Gedikbaşı A., Bağatır G., Öztürk Ş., Çefle K., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.101

46,XY,t(4;6)(p15.3;q23) Kriptik Dengeli Resiprokal Translokasyonunu Taşıyan İnfertil Olgu

Kaya M., Bağatır G., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.100

Büyük Yq Delesyonlu [46,X,del(Yq)] İnfertil Olguda Sadece AZFc Delesyonu

Kaya M., Öztan G., Gedikbaşı A., Bağatır G., Coşkunpınar E., Öztürk Ş., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.108

mos 46,XX/47,XXX/48,XXXX Karyotipli Cinsel Kimlik Bozukluğu Tanılı Olgu

Kaya M., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.100

Habituel Abortus Nedeniyle Başvuran ve 46,XX,t(1;6)(p35;p21) Dengeli Resiprokal Translokasyonu Saptanan Olgu

Kaya M., Bağatır G., Gedikbaşı A., Dön B., Öztürk Ş., Çefle K., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.101

Sistemik Lupus Eritematozus ve Romatoid Artritin Eşlik Ettiği Klinefelter Sendromu Olgusu

Gedikbaşı A., ÇEFLE K., Bayrak A., Tutkan G., Uçur A., Kamalı S., et al.

10. Ulusal Tıbbi Genetik Kongresi, Bursa, Türkiye, 19 - 23 Aralık 2012, ss.314

‘‘Micronucleus and Sister Chromatid Exchange Analyses in Peripheral Lymphocytes of Patients with Oral Leukoplakia – A Pilot Study’’

SARUHANOĞLU A., Tanyeri H., ERGUN S., ÇEFLE K., ÖZTÜRK Ş., PALANDUZ Ş.

10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, Birleşik Krallık, 23 - 25 Eylül 2010, ss.518-519

‘‘No Difference in Micronuclear Scores in both Circulating Lymphocytes and Buccal Epithelial Cells between Patients with Oral Lichen Planus and Oral Lichenoid Stomatitis’

ERGUN S., SARUHANOĞLU A., ÇEFLE K., Warnakulasuriya S., ÖZTÜRK Ş., PALANDUZ Ş.

10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, Birleşik Krallık, 23 - 25 Eylül 2010, ss.524-525

Variant philadelphia translocations in patients with chronic myeloid leukemia

Satkın B. N., PALANDUZ Ş., KARAMAN B., ÖZTÜRK Ş., ÇEFLE K., Bagatır G., et al.

European Cytogenetic Conference (7th), Stockholm, İsveç, 4 - 07 Temmuz 2009, ss.161-162

Determination of genomic instability of patients with oral lichen planus’’

ERGUN S., SARUHANOĞLU A., TANYERİ H., ÇEFLE K., DUMAN N., ÖZEL YILDIZ S., et al.

9th Biennal Congress European Association of Oral Medicine (EAOM),, Salzburg, Avusturya, 18 - 20 Eylül 2008, ss.35

‘‘Ligneous Periodontitis with Conjunctival Involvement: A Case Report’’

kürklü e., ERGUN S., TANYERİ H., ÇEFLE K., Mete Ö., ÖZTÜRK Ş., et al.

1st International Congress of Oral and Maxillofacial Surgery Society, Antalya, Türkiye, 16 - 20 Mayıs 2007, ss.42

. Is there any relation between the NQO1 C609T polymorphism and cytogenetics abnormalities in MDS?

Bağatır G., Sırma Ekmekci S., Palandüz Ş., Özbek U., Nalçacı M., Öztürk Ş., et al.

7th Balkan Meeting on Human Genetics konferansı, Skopje, Makedonya, 20 Eylül 2008, cilt.9, sa.3, ss.75

‘Investigation of Genomic Instability of Patients with Sjögren’s Syndrome by Using Sister Chromatide Exchange Analysis’

ERGUN S., TANYERİ H., ÇEFLE K., DUMAN N., PALANDUZ S., Özel S., et al.

8th Biennal Congress European Association of Oral Medicine (EAOM, Zagreb, Hırvatistan, 31 Ağustos - 02 Eylül 2006, ss.24

Primer Hiperparatroidizm ile İlgili Poliostotik Fibröz Displazi: Olgu Sunumu

Kocaelli H., Emes Y., Günhan Ö., Bilgiç M. B., Çefle K., Yalçın S.

Türk Oral ve Maksillofasiyal Cerrahi Derneği 12. Uluslararası Bilimsel Kongresi, İstanbul, Türkiye, 10 - 13 Ekim 2004, ss.135

A Novel Mutation in Keratin 13 Gene in a Turkish Family with White Sponge Nevus

KÜRKLÜ E., CASSIDY A., ÖZTÜRK Ş., KORAY M., AK G., ÇEFLE K., et al.

7th Biennial Congress of the European Association of Oral Medicine & 26th Annual Scientific Meeting of the Academy of Oral Pathology and Oral Medicine (AKOPOM), Almanya, ss.29

Çiftçi HŞ. Diler AS. Öztürk Ş. Önal EA. Kaya S. Ayna T. Cefle K. Karahan G. Palandüz Ş. Gürtekin M. Çarin M. Effects of cyclosporin A and tacrolimus on sister chromatid exchange frequency in renal transplant patients. 18. European Immunogenetics and Histocompatibility Conference 08-11 May 2004, Sofia; Bulgaria NPG Volume 5. suplement 1. May 2004.

Şentürk Çiftçi H., Diler A. S., Öztürk Ş., Önal A. E., Kaya S., Kılıçaslan Ayna T., et al.

18. European Immunogenetics and Histocompatibility Conference, Sofija, Bulgaristan, 8 - 11 Mayıs 2004

GÖMÜK 20 YAŞ AMELİYATLARINDAN SONRA KULLANILAN ETODOLAC(ETOL), NİMESULİD (MESULİD), NAPROKSEN SODYUM (APRANAX)'IN KARDEŞ KROMATİD DEĞİŞİKLİK(KKD) SIKLIĞI ÜZERİNE ETKİSİ

AYDİL B. A., KOÇAK BERBEROĞLU H., GÜRKAN KÖSEOĞLU B., KOÇAK BERBEROĞLU H., ÇEFLE K., ÖZTÜRK Ş., et al.

7. ANKEM KLİNİKLER VE TIP BİLİMLERİ KONGRESİ, Antalya, Türkiye, 26 - 30 Mayıs 2002, ss.76

THE IN VITRO EFFECTS OF SELECTIVE AND NON-SELECTIVE NON-STEROIDAL ANTI-INFLAMMATORY DRUGS ON THE FREQUENCY OF SISTER CHROMATID EXCHANGES

AYDİL B. A., KOÇAK BERBEROĞLU H., PALANDUZ Ş., ÇEFLE K.

10TH INTERNATIONAL CONGRESS OF HUMAN GENETICS, Viyana, Avusturya, 15 - 19 Mayıs 2001, ss.161

Hallerman-Streff sendromlu bir olgu

PALANDUZ Ş., ÖZTÜRK Ş., ÇEFLE K., KATİPOĞLU A. B., KIR MERCÜL N., AKKAYA V. A.

3.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Muğla, Türkiye, 26 - 30 Nisan 1998, ss.97

The effect of propafenone on signal averaged electrocardiogram

ÇEFLE K., Koylan N., ADALET K.

36th Annual World Congress, New York, Amerika Birleşik Devletleri, 2 - 09 Temmuz 1994, ss.76-77

Kitap & Kitap Bölümleri

Diğer Yayınlar

Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability

Kaya M., Suer İ., Öztürk Ş., Çefle K., Karaman B., Palanduz Ş.

Diğer, ss.1-12, 2019

AML’ DE APAF-1 PROMOTÖR METİLASYONU, KARDEŞ KROMATİD DEĞİŞİMİ, K ROMOZOMAL ANOMALİLER İLE KLİNİK VE LABORATUVAR PARAMETRELERİ ARASINDAKİ İLİŞKİ

Özgen Ö., Bağatır G., Bayrak A., Uçur A., Öztürk Ş., Palanduz Ş., et al.

Diğer, ss.1-93, 2012

Metrikler

Yayın

152

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710

H-İndeks (WoS)

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841

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H-İndeks (Scholar)

Atıf (TrDizin)

H-İndeks (TrDizin)

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BM Sürdürülebilir Kalkınma Amaçları

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