Association of Endothelin-1 rs5370 G>T gene polymorphism with the risk of nephrotic syndrome in children

Mohammad Hashemi ^1,2, Simin Sadeghi-Bojd ^3,4 * , Soheib Aryanezhad ⁴, Maryam Rezaei ²

Cited by CrossRef: 6

1- Zhang R, Yang H, Zhu B, Yuan T, Peng Q, Lv J, Qiu S, Zhou S, Li Y, Zhong Z. Endothelin‐1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome. Clinical Laboratory Analysis. 2020;34(4) [Crossref]

2- Sadeghi-Bojd S, Teimouri A, Zarifi E. Platelet Indices in Children with Nephrotic Syndrome. Nephro-Urol Mon. 2024;16(2) [Crossref]

3- Rizk H, Hammad A, El-Said A, Wahba Y. Polimorfismo rs5370 del gen de la endotelina-1 en el síndrome nefrótico primario: estudio de casos y controles. Anales de Pediatría. 2021;95(6):406 [Crossref]

4- Tantawy A, Tadros M, Adly A, Ismail E, Ibrahim F, Salah Eldin N, Hussein M, Alfeky M, Ibrahim S, Hashem M, Ebeid F. Endothelin-1 gene polymorphism (G8002A) and endothelial monocyte-activating polypeptide II: Role in vascular dysfunction in pediatric patients with β-thalassemia major. Cytokine. 2023;161:156048 [Crossref]

5- Rizk H, Hammad A, El-Said A, Wahba Y. Endothelin-1 RS5370 gene polymorphism in primary nephrotic syndrome: A case-control study. Anales de Pediatría (English Edition). 2021;95(6):406 [Crossref]