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Recent advances in the research on mechanisms underlying podocyte-specific gene mutation-related steroid-resistant nephrotic syndrome / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics ; (12): 99-following 102, 2014.
Article in Chinese | WPRIM | ID: wpr-269530
ABSTRACT
Steroid-resistant nephrotic syndrome poses a significant clinical challenge. Its pathogenesis has not been fully elucidated. In recent years, numerous studies have shown that podocyte-specific gene mutations may play important roles in the development of steroid-resistant nephrotic syndrome. Among the identified genes mutated in podocytes include NPHS2, NPHS1, WT1, TRPC6, MDR1, PLCE1, LMX1B, and LAMB2. This review aims to summarize the characteristics of these mutated genes in podocytes. The putative role for these podocyte-specific mutated genes in the pathogenesis, diagnosis, treatment and prognosis of steroid-resistant nephrotic syndrome is also discussed.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Transcription Factors / Genes, Wilms Tumor / ATP Binding Cassette Transporter, Subfamily B, Member 1 / ATP Binding Cassette Transporter, Subfamily B / Intracellular Signaling Peptides and Proteins / Podocytes / TRPC Cation Channels / LIM-Homeodomain Proteins / TRPC6 Cation Channel / Genetics Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Transcription Factors / Genes, Wilms Tumor / ATP Binding Cassette Transporter, Subfamily B, Member 1 / ATP Binding Cassette Transporter, Subfamily B / Intracellular Signaling Peptides and Proteins / Podocytes / TRPC Cation Channels / LIM-Homeodomain Proteins / TRPC6 Cation Channel / Genetics Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Chinese Journal of Contemporary Pediatrics Year: 2014 Type: Article