Association of endothelin-1 gene polymorphisms with the clinical phenotype in primary nephrotic syndrome of children-Reference-Cited by-同舟云学术

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Association of endothelin-1 gene polymorphisms with the clinical phenotype in primary nephrotic syndrome of children

Published:2014-11 Issue:2 Volume:118 Page:446-450
ISSN:0024-3205
Container-title:Life Sciences
language:en
Short-container-title:Life Sciences

Author:

Yang Fang,Lai Xinlong,Deng Li,Liu Xiaoxiao,Li Jian,Zeng Shuixiu,Zhang Cheng,Hocher Carl-Friedrich,Hocher Berthold

Funder

Guangdong Medical Science and Technology Foundation

Ministry of Education of China

Publisher

Elsevier BV

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference31 articles.

1. Endothelin-1 gene variant associates with blood pressure in obese Japanese subjects: the Ohasama Study;Asai;Hypertension,2001

2. Structural organization and chromosomal assignment of the gene encoding endothelin;Bloch;J Biol Chem,1989

3. Endothelin-1 and F2-isoprostane relate to and predict renal dysfunction in hypertensive patients;Cottone;Nephrol Dial Transplant,2009

4. Urinary endothelin-1 in chronic kidney disease and as a marker of disease activity in lupus nephritis;Dhaun;Am J Physiol Renal Physiol,2009

5. Assessment of urinary endothelin-1 and nitric oxide concentrationss and their relationship with clinical and pathologic types in primary glomerulonephritis;Duan;Yonsei Med J,1999

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1. Epigenetic Alteration of Smooth Muscle Cells Regulates Endothelin-Dependent Blood Pressure and Hypertensive Arterial Remodeling;2024-07-10

2. Uteroglobin gene polymorphism (G38A) as a potential risk factor for nephrotic syndrome in Egyptian children;Egyptian Journal of Basic and Applied Sciences;2024-06-08

3. Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children;Molecular Biology Reports;2023-04-04

4. An Overview of Gene Variants of Endothelin-1: A Critical Regulator of Endothelial Dysfunction;Endothelial Dysfunction - A Novel Paradigm;2023-03-15

5. Polimorfismo rs5370 del gen de la endotelina-1 en el síndrome nefrótico primario: estudio de casos y controles;Anales de Pediatría;2021-12

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