Öğr. Gör. Dr. EYLÜL AKBAL

Yayın Ağı

Makaleler 9

1. Investigation of the relationship between prolactin and infertility by expression levels of kisspeptin (KISS1), KISS1 receptor, neurokinin (NK), NK receptor genes

AKBAL E., YILMAZ M. B.

THE EUROPEAN RESEARCH JOURNAL , cilt.11, ss.11-18, 2025 (Hakemli Dergi)

2. Modifications of the locomotor system in habitually quadrupedal humans

Tardieu C., Demirhan O., Akbal E., Ozgozen L., Biçer Ö. S., Delapre A., et al.

JOURNAL OF ANATOMY , cilt.241, sa.3, ss.765-775, 2022 (SCI-Expanded)

3. Calcium hypochlorite on mouse embryonic fibroblast cells (NIH3T3) in vitro cytotoxicity and genotoxicity: MTT and comet assay.

Yilmaz Ş., Yoldas O., Dumani A., Guler G., Ilgaz S., Akbal E., et al.

Molecular biology reports , cilt.47, sa.7, ss.5377-5383, 2020 (SCI-Expanded)

4. The Role of Rat Hypothalamus Kisspeptin, Neurokinin and their respective Receptors in the Prolactin-Infertility Interaction

Isik E., USLU İ. N., AY G., Cetinel N., CÖMERTPAY G., Oksuz H., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.185, 2019 (SCI-Expanded)

5. MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME

SAGLIKER Y., DEMİRHAN O., Arslan A., SAGLIKER H. S., AKBAL E., Ergun S., et al.

NEPHROLOGY DIALYSIS TRANSPLANTATION , cilt.32, 2017 (SCI-Expanded)

6. Gene Mutations in Chronic Kidney Disease Patients With Secondary Hyperparathyroidism and Sagliker Syndrome

DEMİRHAN O., Arslan A., Sagliker Y., Akbal E., Ergun S., Bayraktar R., et al.

JOURNAL OF RENAL NUTRITION , cilt.25, sa.2, ss.176-186, 2015 (SCI-Expanded)

7. Estrogen receptor alpha (Esr1) regulates aromatase (Cyp19a1) expression in the mouse brain

Yilmaz M. B., Zhao H., Brooks D. C., Fenkci I. V., Imir-Yenicesu G., Attar E., et al.

NEUROENDOCRINOLOGY LETTERS , cilt.36, sa.2, ss.178-182, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

8. REPORT OF A NEW CASE WITH PENTASOMY X AND NOVEL CLINICAL FINDINGS

DEMİRHAN O., TANRIVERDİ N., YILMAZ M., Kocaturk-Sel S., INANDIKLIOGLU N., Luleyap U., et al.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.18, sa.1, ss.85-92, 2015 (SCI-Expanded)

9. Differential Regulation of Diabetes-Induced Rat Aorta ATP-Sensitive Potassium Channels, Kir 6.1 And Kir 6.2, by Pulsed Magnetic Field Therapy

Yilmaz M., Öcal I., Akbal E., Mert T., Tufan T., Cömertpay G., et al.

CUKUROVA MEDICAL JOURNAL , cilt.38, sa.1, ss.15-21, 2013 (Hakemli Dergi)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 20

1. EVALUATION OF THE RELATIONSHIP BETWEEN ANGIOPOIETIN-2 LEVELS AND SURVIVAL IN HEPATOCELLULAR CARCINOMA PATIENTS

AKBAL E., BALLI H. T.

7TH INTERNATIONAL ACHARAKA CONGRESS ON MEDICINE, NURSING, MIDWIFERY, AND HEALTH SCIENCES, Türkiye, 20 - 22 Haziran 2024, (Özet Bildiri)

2. 736 Molecular classification and clinical significance in recurrent endometrial adenocarcinomas

KÜÇÜKGÖZ GÜLEÇ Ü., PAYDAŞ S., KILIÇ BAĞIR E., AKBAL E., KÜÇÜKBİNGÖZ E., KHATİB G., et al.

İnternational Journal of Gynecologic Cancer, 10 Mart 2024, (Özet Bildiri)

3. Result of karyotype analysis of 8475 pregnancies in prenataly identified cases with amniosentesis from south of Turkey.

PAZARBAŞI A., ALPTEKİN D., ILGAZ N. S., USLU İ. N., CÖMERTPAY G., AY G., et al.

16. Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Türkiye, 27 - 30 Ekim 2019, (Özet Bildiri)

4. STRIKING NOVEL MULTI- MISMUTATIONS ON GNAS1, FGF23 AND FGFR3 GENES IN CKD WITH SECONDARY HYPERPARATHYROIDISM(SH) . SAGLIKER SYNDROME(SS) . SS IS A COMBINATION -COMPULSION OF BONE DISPLASIAS-HEREDITARY OSTEODYSTROPHIES AND SH AND CKD

SAGLIKER Y., DEMİRHAN O., Arslan A., AKBAL E., Ergun S., Bayraktar R., et al.

56th Congress of the European-Renal-Association (ERA)-European-Dialysis-and-Transplant-Association (EDTA) - Burden, Access and Disparities in Kidney Disease, Budapest, Macaristan, 13 - 16 Haziran 2019, cilt.34, ss.199-201, (Özet Bildiri)

5. MULTIPLE GNAS1, FGF23, FGFR3 GENES’xx STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS)

SAĞLIKER Y., DEMİRHAN O., ARSLAN A., SAĞLIKER H. S., BAYRAKTAR R., DOĞAN E., et al.

55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA, Birleşik Krallık, 24 - 27 Mayıs 2018, cilt.33, ss.168-169, (Özet Bildiri)

6. Determining The Mediators of GnRH Release Upon Prolactin Induction in GT1-7 Cells

KOCATÜRK SEL S., PAZARBAŞI A., Öksüz H., Öztecik E., EVRAN M., Akbal E., et al.

4th INTERNATIONAL CONGRESS ON APPLIED BIOLOGICAL SCIENCES, Eskişehir, Türkiye, 3 - 05 Mayıs 2018, ss.96, (Özet Bildiri)

7. MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS)

SAGLIKER Y., DEMİRHAN O., Arslan A., SAGLIKER H. S., Bayraktar R., Dogan E., et al.

55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA), Copenhagen, Danimarka, 24 - 27 Mayıs 2018, cilt.33, (Özet Bildiri)

8. Leptinin pubertal KİSS1 KİSS1R TAC2 ve TACR3 genlerinin ekspresyonlarına etkisinin gt 1 7hipotalamik hücre hattında değerlendirilmesi

ILGAZ N. S., cömertpay g., ÖZPAK L., akbal E., öksüz h., yılmaz m., et al.

1. Uluslararası Akdeniz Bilim ve Mühendislik Kongresi, 26 - 28 Ekim 2016, (Tam Metin Bildiri)

9. Leptinin pubertal Kiss1 Kiss1R TacR ve TacR3 genlerinin ekspresyonlarına etkisinin GT 1 7 hipotalamik hücre hattında değerlendirilmesi

ILGAZ N. S., Cömertpay G., AKBAL E., ÖKSÜZ H., ÖZPAK L., TOPALOĞLU A. K., et al.

1st International Mediterranean Science and Engineering Congress. October 26-28, 2016. Adana, Turkey, Adana, Türkiye, 26 - 28 Ekim 2016, (Özet Bildiri)

10. KALSİYUM HİPOKLORİTİN İN VİTRO BİYOLOJİK ÖZELLİKLERİ

YILMAZ A. Ş., DUMANİ A., YOLDAŞ H. O., Akbal E., Öksüz H., Güler G., et al.

Türk Endodonti Derneği 13. Uluslararası Kongresi, 26 - 29 Mayıs 2016

11. MULTIPLE GENE MUTATIONS IN GNAS1, FGF23 AND FGFR3 GENES IN CKD PATIENTS WITH SH SAGLIKER SYNDROME

DEMİRHAN O., Arslan A., SAGLIKER Y., AKBAL E., Ergun S., Bayraktar R., et al.

53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.1468, (Özet Bildiri)

12. Quadrupedal subjects in a family Adana Turkey comparision between two adult brothers skeletons one bipedal one quadrupedal Are they similar or different

Tardieu C., Bonneau N., akbal E., Özgüven L., biçer Ö. S., DEMİRHAN O., et al.

5th Annual Meeting of the European Society for the study of human evolution, 10 - 12 Ekim 2015, (Tam Metin Bildiri)

13. Whole 13 exons of gnas1 gene in Sagliker syndrome ss Combınatıon compulsion of bone dysplasıas hereditary osteodistrophies bd chronic kidney diseases ckd and secondary hyperparathyroidism sh

DEMİRHAN O., Sağlıker Y., Akbal E., Paylar N., Sağlıker H. S., Sağlıker Özkaynak P., et al.

52nd Congress of the European-Renal-Association-European-Dialysis-andTransplant-Assocation, 28 - 31 Mayıs 2015

14. Novel striking mismutations on GNAS1 FGF23 and FGF3 genes in CKD with secondary hyperparathroidism and Sağlıker syndrome is a combination compulsion of bone displasias hereditary osteodystrophies and CKD

DEMİRHAN O., Sağlıker Y., Akbal E., Ergun S., BAYRAKTAR R., Sağlıker H. S., et al.

52nd European Renal Association- European Dialysis and Transplant Association (ERA-EDTA) Congress, London, Kanada, 28 - 31 Mayıs 2015, (Tam Metin Bildiri)

15. Whole 13 exons of GNAS1 gene in saglıker syndrome ss combınatıon compulsıon of bone dysplasıas heredıtary osteodıstrophıes bd chronıc kıdney dıseases ckd and secondary hyperparathyroıdısm

DEMİRHAN O., SAĞLIKER Y., AKBAL E., ERGÜN S., BAYRAKTAR R., SAĞLIKER H. S., et al.

52nd European Renal Association - European Dialysis and Transplant Association (ERA-EDTA) Congress, 28 - 31 Mayıs 2015

16. NOVEL STRIKING MISMUTATIONS ON GNAS1, FGF23 AND FGFR3 GENES IN CKD WITH SECONDARY HYPERPARATHYROIDISM (SH) AND SAGLIKER SYNDROME (SS). SS IS ACOMBINATION-COMPULSION OF BONE DISPLASIAS-HEREDITARY OSTEODYSTROPHIES AND CKD

DEMİRHAN O., Arslan A., SAGLIKER Y., AKBAL E., Ergun S., Bayraktar R., et al.

52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri)

17. WHOLE 13 EXONS OF GNAS1 GENE IN SAGLIKER SYNDROME(SS). COMBINATION-COMPULSION OF BONE DYSPLASIAS-HEREDITARY OSTEODISTROPHIES(BD), CHRONIC KIDNEY DISEASES (CKD) AND SECONDARY HYPERPARATHYROIDISM(SH)

DEMİRHAN O., SAGLIKER Y., AKBAL E., PAYLAR N., Sagliker H. S., Ozkaynak P. S., et al.

52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri)

18. Saglıker Syndrome Strıkıng Mutatıons on GNAS1 FGF23 FGFR3 Genes A Unıque Combınatıon Compulsıon of Bone Dısplasıas Osteodıstrophıes and Secondary Hyperparathyroıdısm in Ckd

DEMİRHAN O., Sağlıker Y., Akbal E., Ergun S., BAYRAKTAR R., Sağlıker H. S., et al.

ISN World Congress Of Nephrology, 13 - 17 Mart 2015, (Tam Metin Bildiri)

19. The whole 13 exons of gnas1 gene and the genes for hereditary osteodıstrophıas ho in Saglıker syndrome ss Combinatıon compulsion of hereditary osteodistrophias and chronıc kidney diseases ckd

Sağlıker Y., DEMİRHAN O., Yıldız İ., Paylar N., İNANDIKLIOĞLU BAŞGÜL N., Akbal E., et al.

51st Congress of the European-Renal-Association(ERA)/European-Dialysis-and-Transplant-Association (EDTA), 31 Mayıs - 03 Haziran 2014

20. THE WHOLE 13 EXONS OF GNAS1 GENE AND THE GENES FOR HEREDITARY OSTEODISTROPHIAS(HO) IN SAGLIKER SYNDROME(SS). COMBINATION-COMPULSION OF HEREDITARY OSTEODISTROPHIAS AND CHRONIC KIDNEY DISEASES (CKD) ?

SAGLIKER Y., DEMİRHAN O., YILDIZ İ., PAYLAR N., INANDIKLIOGLU N., AKBAL E., et al.

51st Congress of the European-Renal-Association(ERA)/European-Dialysis-and-Transplant-Association (EDTA), Amsterdam, Hollanda, 31 Mayıs - 03 Haziran 2014, cilt.29, ss.381, (Özet Bildiri)

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