Relation between single nucleotide polymorphism rs3738423 (C>T) of NPHS2 gene and some biochemical parameters in pediatrics nephrotic syndrome patients by Nga Van Vu, Long Doan Dinh, Dem Van Pham, Nhung Hong Thi Pham, Quy Van Dam, Huong Quynh Thi Nguyen, Thinh Huy Tran, Thom Thi Vu

Subjects: “…NPHS2…”
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Evaluation of NPHS2 gene polymorphism (R229Q) in chronic kidney disease patients by Ahmed Mohamed rashid, Rania Elsayed sheir, Thoraya Mohamed Ahmed, Hanan Mohamed Farhan

Subjects: “…chronic kidney disease ˗ nphs2 gene polymorphism…”
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Familial Focal Segmental Glomerulosclerosis With Late-Onset Presentation and R229Q/R291W Podocin Mutations by Michelle T. P. Riguetti, Patrícia Varela, Danilo E. Fernandes, M. Goretti Polito, Fernanda M. Casimiro, João B. Pesquero, Gianna Mastroianni-Kirsztajn

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Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome by Manal Micheal Thomas, Mohamed S. Abdel-Hamid, Nermine Nabil Mahfouz, Emad Emil Ghobrial

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Heterozygous expression of Cre recombinase in podocytes has no impact on the anti‐glomerular basement membrane glomerulonephritis model in C57BL/6J mice by Cyril Mousseaux, Tiffany Migeon, Perrine Frère, Marie Christine Verpont, Elisabeth Lutete, Claire Navarro, Liliane Louedec, Juliette Hadchouel

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Urinary podocyte markers in diabetic kidney disease by Chuanlei Li, Cheuk-Chun Szeto

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Genotyping Rs2274625 Marker in NPHS2 Gene Associated with Nephrotic Syndrome in Isfahan Population by L Esmaili Chamgordani, A Jazayeri, S Vallian Borujeni

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Non-collagen genes role in digenic Alport syndrome by S. Daga, C. Fallerini, S. Furini, C. Pecoraro, F. Scolari, F. Ariani, M. Bruttini, M. A. Mencarelli, F. Mari, A. Renieri, A. M. Pinto

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Familial steroid-sensitive idiopathic nephrotic syndrome: seven cases from three families in China by Yonghui Xia, Jianhua Mao, Xia Jin, Wenjing Wang, Lizhong Du, Aimin Liu

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NPHS2 gene mutation, atopy, and gender as risk factors for steroid-resistant nephrotic syndrome in Indonesians by Dedi Rachmadi, Danny Hilmanto, Ponpon Ijradinata, Abdurahman Sukadi

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Comparing NPHS2 and WT1 Mutations in Children with Nephrotic Syndrome by Alaleh Gheissari, Mona Ziaei, Ali Reza Merrikhi

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Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome by Aiysha Abid, Saba Shahid, Madiha Shakoor, Ali A. Lanewala, Seema Hashmi, Shagufta Khaliq

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Nephrin and podocin mRNA detection in urine sediment of dogs with chronic kidney disease: preliminary observations by Souza Camilla de, Coelho Mariana, Antonelo Daniel Silva, Passarelli Danielle, Rochetti Arina Lázaro, Fukumasu Heidge, Leite-Dellova Deise Carla Almeida

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Case Report: The Monogenic Familial Steroid-Resistant Nephrotic Syndrome Caused by a Novel Missense Mutation of NPHS2 Gene A593C in a Chinese Family by Ling Bai, Jing Zhuang, Changrong Zhang, Chen Lu, Xuefei Tian, Hong Jiang

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Prevalence of NPHS2 gene R229Q polymorphism in Bangladeshi children with nephrotic syndrome by Sharmin Sultana Jyoti, Farhana Islam, Ishrat Islam Shrabonee, Taposhi Nahid Sultana, Nusrat Islam Chaity, Noor Ahmed Nahid, Md Reazul Islam, Md Saiful Islam, Mohd Nazmul Hasan Apu

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CASE OF NON-SEVERE CONGENITAL NEPHROTIC SYNDROME by I. S. Kostushina, T. V. Margieva, T. N. Gusarova, G. T. Yakhyaeva, L. S. Namazova-Baranova, A. A. Pushkov, K. V. Savost'yanov

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The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated w... by Dana Thomasová, Michaela Zelinová, Malgorzata Libik, Jan Geryk, Pavel Votýpka, Silvie Rajnochová Bloudíčková, Karel Krejčí, Jana Reiterová, Eva Jančová, Jana Machová, Jana Machová, Martina Kollárová, Ivan Rychík, Martin Havrda, Miroslava Horáčková, Martina Putzová, Martina Putzová, Roman Šafránek, Marek Kollár, Milan Macek

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Mutasi Gen NPHS2 (412C→T, 419delG) dan Manifestasi Klinis Sindrom Nefrotik Resisten Steroid Anak Indonesia by Dedi Rachmadi, Dany Hilmanto, Ponpon Idjradinata, Abdurahman Sukadi

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Association Between NPHS2 p.R229Q and Focal Segmental Glomerular Sclerosis/Steroid-Resistant Nephrotic Syndrome by Qiongxiu Zhou, Qiongxiu Zhou, Qinjie Weng, Xiaoyan Zhang, Yunzi Liu, Jun Tong, Xu Hao, Hao Shi, Pingyan Shen, Hong Ren, Jingyuan Xie, Nan Chen

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The Role of p.Ser1105Ser (in <i>NPHS1</i> Gene) and p.Arg548Leu (in <i>PLCE1</i> Gene) with Disease Status of Vietnamese Patients with Congenital Nephrotic Syndrome: Benign or Path... by Nguyen Thi Kim Lien, Pham Van Dem, Nguyen Thu Huong, Tran Minh Dien, Ta Thi Thu Thuy, Nguyen Van Tung, Nguyen Huy Hoang, Nguyen Thi Quynh Huong

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