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Tian-Biao Zhou, Gregor P.C. Drummen, Zong-Pei Jiang & Hong-Yan Li. (2015) Methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism and diabetic nephropathy susceptibility in patients with type 2 diabetes mellitus. Renal Failure 37:8, pages 1247-1259.
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Weiqiang Zhong, Tian-Biao Zhou & Zongpei Jiang. (2015) Association of endothelial nitric oxide synthase gene polymorphism with the risk of Henoch-Schönlein purpura/Henoch-Schönlein purpura nephritis. Renal Failure 37:3, pages 372-376.
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Danhua Lin, Shuguang Li, Haishan Xu, Hong Chen & Zhiyong Dong. (2015) Association of uteroglobin G38A gene polymorphism with IgA nephropathy risk: an updated meta-analysis. Journal of Receptors and Signal Transduction 35:2, pages 115-121.
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Ozturk Ozdemir, Mansur Kayatas, Selma Cetinkaya, Malik Ejder Yildirim, Fatma Silan, Hande Kucuk Kurtulgan, Binnur Koksal, Mine Urfali & Ferhan Candan. (2015) Bcıı—RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis. Renal Failure 37:2, pages 292-296.
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Tian-Biao Zhou, Zong-Pei Jiang, Meng-Jun Liang & Ya-Juan Huang. (2015) Relationship between MCP-1 promoter -2518 A/G gene polymorphism (rs1024611) and systemic lupus erythematosus/lupus nephritis. Journal of Receptors and Signal Transduction 35:1, pages 85-93.
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Tian-Biao Zhou & Zong-Pei Jiang. (2015) Association between plasminogen activator inhibitor-1 4G/5G gene polymorphism and immunoglobulin A nephropathy susceptibility. Journal of Receptors and Signal Transduction 35:1, pages 63-66.
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Zhu Yun, Yang Yu-Ping, Tong Zong-Wu, Sun Yang, Yang Fang & Sun Fang. (2014) Association of endothelial nitric oxide synthase gene polymorphisms with end-stage renal disease: a systematic review and meta-analysis. Renal Failure 36:6, pages 987-993.
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Jie Zhang, Yan Xiao, Xian-Wen Zhang, Zhi-Qing Gao & Jing-Hui Han. (2014) Relationship between methylenetetrahydrofolate reductase (MTHFR) A1298C gene polymorphism and type 2 diabetic nephropathy risk: a meta-analysis. Renal Failure 36:6, pages 974-978.
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Tian-Biao Zhou, Xue-Feng Guo & Sheng-Sheng Yin. (2014) Association of peroxisome proliferator-activated receptor γ Pro12Ala gene polymorphism with type 2 diabetic nephropathy risk in Caucasian population. Journal of Receptors and Signal Transduction 34:3, pages 180-184.
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Tian-Biao Zhou, Xue-Feng Guo & Sheng-Sheng Yin. (2014) Association of T869, C509T, G915C gene polymorphism of transforming growth factor-β1 with IgA nephropathy risk. Renal Failure 36:5, pages 823-828.
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Guohui Liu, Tian-Biao Zhou, Zongpei Jiang, Dongwen Zheng, Fei Yuan, Yi Li, Haoqiang Hu & Zijun Chen. (2014) Relationship between PPARγ Pro12Ala gene polymorphism and type 2 diabetic nephropathy risk in Asian population: results from a meta-analysis. Journal of Receptors and Signal Transduction 34:2, pages 131-136.
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Jianbo Liang, Zebin Wang, Guohui Liu, Junlin Zhan, Liping Jiang & Zongpei Jiang. (2014) Association of dialysate calcium concentration with fetuin a level and carotid intima-media thickness in peritoneal dialysis patients. Renal Failure 36:1, pages 65-68.
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Articles from other publishers (14)
İlhan Kılıç, Orkide Palabıyık, İlhan Kurultak, Tammam Sipahi & Sedat Üstündağ. (2022) The role of eNOS gene polymorphisms on contrast induced nephropathy development in chronic kidney disease patients. Therapeutic Apheresis and Dialysis 27:2, pages 240-245.
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Ryan J. Adam, Adaysha C. Williams & Alison J. Kriegel. (2022) Comparison of the surgical resection and infarct 5/6 nephrectomy rat models of chronic kidney disease. American Journal of Physiology-Renal Physiology 322:6, pages F639-F654.
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A. Parker Ruhl, Neal Jeffries, Yu Yang, Rakhi P. Naik, Amit Patki, Lydia H. Pecker, Bryan T. Mott, Neil A. Zakai, Cheryl A. Winkler, Jeffrey B. Kopp, Leslie A. Lange, Marguerite R. Irvin, Orlando M. Gutierrez, Mary Cushman & Hans C. Ackerman. (2022) Alpha Globin Gene Copy Number Is Associated with Prevalent Chronic Kidney Disease and Incident End-Stage Kidney Disease among Black Americans. Journal of the American Society of Nephrology 33:1, pages 213-224.
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О. А. Svitich, А. V. Kudryavtseva, Е. S. Slyusareva, Е. О. Kravtsova, Е. А. Meremianina, Е. P. Bystritskaya, V. V. Sobolev, А. I. Ryabtsev, А. B. Potapova & V. V. Zverev. (2021) Association of the NOS3 Gene Polymorphisms with the Risk of Atopic Dermatitis in Children. Bulletin of Experimental Biology and Medicine 170:6, pages 787-790.
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Yuji Oe, Shohei Mitsui, Emiko Sato, Naoko Shibata, Kiyomi Kisu, Akiyo Sekimoto, Mariko Miyazaki, Hiroshi Sato, Sadayoshi Ito & Nobuyuki Takahashi. (2021) Lack of Endothelial Nitric Oxide Synthase Accelerates Ectopic Calcification in Uremic Mice Fed an Adenine and High Phosphorus Diet. The American Journal of Pathology 191:2, pages 283-293.
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R. Ivanochko, O. Abrahamovych & I. Kravchuk. (2020) Features of the Functional State of the L-arginine / NO-synthase / Arginase System and Oxidative Processes in Patients with end-stage Renal Disease due to Chronic Glomerulonephritis Before and After a Hemodialysis Session. Lviv clinical bulletin 3:31, pages 37-45.
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Atma Gunawan, Jonny Karunia Fajar, Fredo Tamara, Aditya Indra Mahendra, Muhammad Ilmawan, Yeni Purnamasari, Dessy Aprilia Kartini, Eden Suryoiman Winoto, Efriko Septananda Saifillah, Dewi Sri Wulandari, Pratista Adi Krisna, Ema Dianita Mayasari, Tri Wahyudi Iman Dantara, Ramadi Satryo Wicaksono & Djoko Wahono Soeatmadji. (2021) Nitride oxide synthase 3 and klotho gene polymorphisms in the pathogenesis of chronic kidney disease and age-related cognitive impairment: a systematic review and meta-analysis. F1000Research 9, pages 252.
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Atma Gunawan, Jonny Karunia Fajar, Fredo Tamara, Aditya Indra Mahendra, Muhammad Ilmawan, Yeni Purnamasari, Dessy Aprilia Kartini, Eden Suryoiman Winoto, Efriko Septananda Saifillah, Dewi Sri Wulandari, Pratista Adi Krisna, Ema Dianita Mayasari, Tri Wahyudi Iman Dantara, Ramadi Satryo Wicaksono & Djoko Wahono Soeatmadji. (2020) Nitride oxide synthase 3 and klotho gene polymorphisms in the pathogenesis of chronic kidney disease and age-related cognitive impairment: a systematic review and meta-analysis. F1000Research 9, pages 252.
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Wesen Adel Mehdi, Atheer Awad Mehde, Faridah Yusof, Raha Ahmed Raus, Ali Khudhair Resen & Hamid Ghazali. (2019) The endothelial nitric oxide synthase gene G894T, glutathione S-transferase (GSTM1 and GSTT1) polymorphisms as a risk factor in the patient with nephrolithiasis. International Journal of Biological Macromolecules 140, pages 719-726.
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Alejandro Marín Medina, Eduardo Esteban Zubero, Moisés Alejandro Alatorre Jiménez, Sara Anabel Alonso Barragan, Carlos Arturo López García, José Juan Gómez Ramos, Juan Francisco Santoscoy Gutierrez & Zurisadai González Castillo. (2018) NOS3 Polymorphisms and Chronic Kidney Disease. Brazilian Journal of Nephrology 40:3, pages 273-277.
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Jie Gao, Meng Wang, Linting Wei, Dan Niu, Jiali Wei, Yan Ou, Tianbo Jin, Qiaoling Yu, Xinghan Liu, Tian Tian, Cong Dai, Rongguo Fu & Li Wang. (2017) The Endothelial Nitric Oxide Synthase Gene Polymorphism is Associated with the Susceptibility to Immunoglobulin a Nephropathy in Chinese Population. Kidney and Blood Pressure Research 42:3, pages 608-616.
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Syed Kashif Nawaz, Asima Rani, Memoona Yousaf, Aasma Noreen & Muhammad Arshad. (2014) Genetic etiology of coronary artery disease considering NOS 3 gene variant rs1799983. Vascular 23:3, pages 270-276.
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Tian-Biao Zhou, Zong-Pei Jiang, Jia-Fan Zhou & Ning Su. (2014) Relationship between chemokine receptor 5 Δ32/W gene polymorphism and lupus nephritis. Human Immunology 75:9, pages 968-972.
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Tian-Biao Zhou, Zong-Pei Jiang, Yuan-Han Qin & Gregor PC Drummen. (2014) Association of transforming growth factor-β1 T869C gene polymorphism with diabetic nephropathy risk. Nephrology 19:2, pages 107-115.
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