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
Zhongguo dangdai erke zazhi
; Zhongguo dangdai erke zazhi;(12): 99-following 102, 2014.
Article
in Zh
| WPRIM
| ID: wpr-269530
Responsible library:
WPRO
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.
Full text:
1
Index:
WPRIM
Main subject:
Transcription Factors
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Genes, Wilms Tumor
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ATP Binding Cassette Transporter, Subfamily B, Member 1
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ATP Binding Cassette Transporter, Subfamily B
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Intracellular Signaling Peptides and Proteins
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Podocytes
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TRPC Cation Channels
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LIM-Homeodomain Proteins
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TRPC6 Cation Channel
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Genetics
Type of study:
Prognostic_studies
Limits:
Humans
Language:
Zh
Journal:
Zhongguo dangdai erke zazhi
Year:
2014
Type:
Article