Lect. PhD EYLÜL AKBAL

Publication Network

Articles 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 , vol.11, pp.11-18, 2025 (TRDizin)

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 , vol.241, no.3, pp.765-775, 2022 (SCI-Expanded, Scopus)

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 , vol.47, no.7, pp.5377-5383, 2020 (SCI-Expanded, Scopus)

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 , vol.91, pp.185, 2019 (SCI-Expanded, Scopus)

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 , vol.32, 2017 (SCI-Expanded, Scopus)

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 , vol.25, no.2, pp.176-186, 2015 (SCI-Expanded, Scopus)

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 , vol.36, no.2, pp.178-182, 2015 (SCI-Expanded, Scopus) Sustainable Development

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 , vol.18, no.1, pp.85-92, 2015 (SCI-Expanded, Scopus)

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 , vol.38, no.1, pp.15-21, 2013 (TRDizin)

Papers Presented at Peer-Reviewed Scientific Conferences 21

1. Hepatoselüler Karsinom Manyetik Rezonans Görüntülerinde Renk Uzaylarının Attention Tabanlı Segmentasyon Performansına Etkisi

AKBAL E.

26. ULUSAL VE 9. ULUSLARARASI BİYOİSTATİSTİK KONGRESİ, 5 - 08 November 2025, pp.151-152, (Summary Text)

2. 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, Turkey, 20 - 22 June 2024, (Summary Text)

3. 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 March 2024, (Summary Text)

4. 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), Turkey, 27 - 30 October 2019, (Summary Text)

5. 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, Hungary, 13 - 16 June 2019, vol.34, pp.199-201, (Summary Text)

6. 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, United Kingdom, 24 - 27 May 2018, vol.33, pp.168-169, (Summary Text)

7. 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, Turkey, 3 - 05 May 2018, pp.96, (Summary Text)

8. 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, Denmark, 24 - 27 May 2018, vol.33, (Summary Text)

9. 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 October 2016, (Full Text)

10. 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, Turkey, 26 - 28 October 2016, (Summary Text)

11. 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 May 2016

12. 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, Austria, 21 - 24 May 2016, vol.31, pp.1468, (Summary Text)

13. 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 October 2015, (Full Text)

14. 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 May 2015

15. 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, Canada, 28 - 31 May 2015, (Full Text)

16. 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 May 2015

17. 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, Canada, 28 - 31 May 2015, vol.30, (Summary Text)

18. 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, Canada, 28 - 31 May 2015, vol.30, (Summary Text)

19. 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 March 2015, (Full Text)

20. 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 May - 03 June 2014

21. 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, Netherlands, 31 May - 03 June 2014, vol.29, pp.381, (Summary Text)

Books 1

1. FERROPTOZ, PİROPTOZ VE YENİ HÜCRESEL ÖLÜM YOLLARININ KANSER TEDAVİSİNDEKİ ROLÜ

AKBAL E.

in: KANSERİN MOLEKÜLER TEMELLERİ, KANLI AYLİN, İSKENDER İZGİ BANU, Editor, EFE AKADEMİK YAYINCILIK, pp.68-79, 2025

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