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Endocrinology|November 24, 2019
Extra-Large Gα Protein (XLαs) Deficiency Causes Severe Adenine-Induced Renal Injury with Massive FGF23 ElevationJulia Matthias, Qiuxia Cui, Lauren T Shumate, et al.
Neuropharmacology|December 27, 2005
D2 dopamine receptor-induced sensitization of adenylyl cyclase type 1 is G alpha(s) independentTimothy A Vortherms, Chau H Nguyen, Murat Bastepe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2005
Effect of zinc supplementation on growth hormone secretion, IGF-I, IGFBP-3, somatomedin generation, alkaline phosphatase, osteocalcin and growth in prepubertal children with idiopathic short statureSebahat Imamoğlu, Abdullah Bereket, Serap Turan, et al.
Pediatrics|June 15, 2011
Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend?Zeynep Atay, Serap Turan, Tulay Guran, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 23, 2011
The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girlsZeynep Atay, Serap Turan, Tulay Guran, et al.
Hormone Research in Paediatrics|August 28, 2019
Restoration of Height after 11 Years of Letrozole Treatment in 11β-Hydroxylase DeficiencyZeynep Atay, Serap Turan, Onur Buğdaycı, et al.
Hormone Research in Paediatrics|March 19, 2020
Fibroblast Growth Factor-23 and Matrix Extracellular Phosphoglycoprotein Levels in Healthy Children and, Pregnant and Puerperal WomenAhu Ozsen, Andrzej Furman, Tulay Guran, et al.
Bone|October 23, 2010
Paternal uniparental isodisomy of the entire chromosome 20 as a molecular cause of pseudohypoparathyroidism type Ib (PHP-Ib)Murat Bastepe, Ozge Altug-Teber, Chhavi Agarwal, et al.
Molecular Endocrinology (Baltimore, Md.)|July 30, 2002
Receptor-mediated adenylyl cyclase activation through XLalpha(s), the extra-large variant of the stimulatory G protein alpha-subunitMurat Bastepe, Yasemin Gunes, Beatriz Perez-Villamil, et al.
The American Journal of the Medical Sciences|July 16, 2008
Molecular diagnosis and clinical characterization of pseudohypoparathyroidism type-Ib in a patient with mild Albright's hereditary osteodystrophy-like features, epileptic seizures, and defective renal handling of uric acidUgur Unluturk, Ayla Harmanci, Melih Babaoglu, et al.
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