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The evaluation of possible role of endocrine disruptors in central and peripheral precocious puberty

Toxicology Mechanisms and Methods · Eylül 2016

Özet
Exposure to environmental chemicals can affect genetic and epigenetic molecular pathways and may cause altered growth and development. Among those exposures, endocrine-disrupting chemicals (EDCs) are of particular concern as humans are abundantly exposed to these chemicals by various means in every period of life. Several well-known environmental chemicals, including phthalates and bisphenol A (BPA), are classified as EDCs. These EDCs are suggested to play roles in early onset of puberty in girls. The aim of this study is to determine plasma phthalate (di(2-ethylhexyl)phthalate [DEHP] and its main metabolite mono(2-ethylhexyl)phthalate [MEHP]) and urinary BPA levels in girls with idiopathic central precocious puberty (CPP) and peripheral precocious puberty (PPP). This study was performed on newly diagnosed idiopathic central precocious puberty (CPP) patients (n = 42) and peripheral precocious puberty (PPP) (n = 42) patients, who were admitted to Keçiören Training and Research Hospital, Clinic of Pediatric Endocrinology between August 2012 and –July 2013. Nonobese healthy girls (n = 50) were used as the control group. Urinary BPA levels were not statistically different in control, PPP and CPP groups (medians 10.91, 10.63 and 10.15 μg/g creatinine, respectively; p > 0.05). Plasma DEHP levels were significantly higher in PPP group when compared to control. Plasma MEHP levels were not significantly different in control and PPP groups (p > 0.05). However, in CPP group, both plasma DEHP and MEHP levels were significantly higher than control and PPP groups. This study showed that phthalates might play a role in the occurence of CPP in girls.
62 atıf Eylül 2016 DOI
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The evaluation of possible role of endocrine disruptors in central and peripheral precocious puberty
Toxicology Mechanisms and Methods · 2016 SCI-Expanded
Dr. Öğr. Üyesi ALİ AŞCI →
YÖKSİS Kayıtları — ISSN Eşleşmesi
Bu dergide (ISSN eşleşmesi) kurumun 7 kaydı bulundu.
The evaluation of possible role of endocrine disruptors in central and peripheral precocious puberty
2016 ISSN: 1537-6516 SCI-Expanded
Dr. Öğr. Üyesi ALİ AŞCI →
Eucalyptol regulates Nrf2 and NF-kB signaling and alleviates gentamicin-induced kidney injury in rats by downregulating oxidative stress, oxidative DNA damage, inflammation, and apoptosis
2024 ISSN: 1537-6516 SCI-Expanded Q2
Arş. Gör. ZEYNEP ÇELİK KENAR →
Investigation of the effects of Theranekron and Sorafenib treatments on carcinogenesis, apoptosis and biochemical profile in hepatocellular carcinoma in rats
2024 ISSN: 1537-6516 SCI Q2
Prof. Dr. FİRUZE KURTOĞLU →
Eucalyptol regulates Nrf2 and NF-kB signaling and alleviates gentamicin-induced kidney injury in rats by downregulating oxidative stress, oxidative DNA damage, inflammation, and apoptosis
2024 ISSN: 1537-6516 SCI-Expanded Q2
Prof. Dr. MEHMET TUZCU →
Investigation of the effects of Theranekron and Sorafenib treatments on carcinogenesis, apoptosis and biochemical profile in hepatocellular carcinoma in rats.
2024 ISSN: 1537-6516 SCI-Expanded Q2
Dr. Öğr. Üyesi BEYZA SUVARIKLI ALAN →
Eucalyptol regulates Nrf2 and NF-kB signaling and alleviates gentamicin-induced kidney injury in rats by downregulating oxidative stress, oxidative DNA damage, inflammation, and apoptosis
2024 ISSN: 1537-6516 SCI-Expanded Q2
Prof. Dr. ÖZGÜR ÖZDEMİR →
Investigation of the effects of Theranekron and Sorafenib treatments on carcinogenesis, apoptosis and biochemical profile in hepatocellular carcinoma in rats
2024 ISSN: 1537-6516 SCI-Expanded Q2
Prof. Dr. ÖZGÜR ÖZDEMİR →

Makale Bilgileri

Toplam Atıf 62 atıf · Scopus
ISSN15376516
Yayın TarihiEylül 2016
Cilt / Sayfa26 · 493-500

Kurumlar

Ankara Yildirim Beyazit University
Ankara Turkey
Hacettepe Üniversitesi
Ankara Turkey
T.C. Sağlık Bakanlığı,
Ankara Turkey

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Scimago Dergi (ISSN Eşleşmesi)
Toxicology Mechanisms and Methods
Q3
SJR Skoru0,636
H-Index62
YayıncıTaylor and Francis Ltd.
ÜlkeUnited Kingdom
Health, Toxicology and Mutagenesis (Q3)
Toxicology (Q3)
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62
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