Yayınlar & Eserler

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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) Creative Commons License identifier identifier identifier

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) identifier identifier identifier

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) identifier

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) identifier

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) identifier identifier identifier

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 identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

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 , 2024 (Hakemli Dergi)

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) identifier

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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 identifier

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 identifier

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 identifier

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 identifier

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 Creative Commons License identifier

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 identifier

Metrikler

Yayın

16

Atıf (WoS)

23

H-İndeks (WoS)

1

Atıf (Scopus)

9

H-İndeks (Scopus)

2

Açık Erişim

2
BM Sürdürülebilir Kalkınma Amaçları