Association of single-nucleotide polymorphism in the FKBP5 gene with response to steroids in pediatric patients with primary nephrotic syndrome .

doi:10.5414/CN109126

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Association of single-nucleotide polymorphism in the FKBP5 gene with response to steroids in pediatric patients with primary nephrotic syndrome .

Clinical nephrology - 1 Dec 2017

Du Ni, Yang Fang, Li Liangzhi, Liu Xiaoxiao, Sun Liangzhong, Zhang Sui, He Xianhong, Tang Yuewu, Shi Jihong, Liu Chunqiu, Zhang Xianxiang

Abstract excerpt

AIM: This study aimed to assess the association of single-nucleotide polymorphism (SNP) of FKBP5 with response to steroids in children with primary nephrotic syndrome (NS). MATERIALS AND METHODS: A total of 66 primary NS patients (cases) and 68 healthy individuals (controls) were enrolled in this study. The FKBP5 polymorphism rs4713916 (T/C) was analyzed by polymerase chain reaction (PCR) and sequencing after...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Genotype

Share to Glucocorticoids

Share to Infant

Share to Nephrotic Syndrome

Share to Polymorphism, Single Nucleotide

Share to Tacrolimus Binding Proteins

Source

Open in PubMed

Identifiers

PMID: 28992850
DOI: 10.5414/CN109126

Genes

FKBP5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of single-nucleotide polymorphism in the FKBP5 gene with response to steroids in pediatric patients with primary nephrotic syndrome .PMID 28992850Read ↗

Molecular genetic analysis of Steroid Resistant Nephrotic Syndrome: Detection of a novel mutationSemantic proximity Read ↗

Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.Semantic proximity Read ↗

Association of HLA-DQA1 gene polymorphisms with the risk of children primary nephrotic syndrome in Chinese population.Semantic proximity Read ↗

Association of ACTN4 Gene Mutation with Primary Nephrotic Syndrome in Children in Guangxi Autonomous Region, China.Semantic proximity Read ↗

Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndrome.Semantic proximity Read ↗

Causal and Putative Pathogenic Mutations Identified in 38.6% of Children with Primary SRNS in South AfricaSemantic proximity Read ↗

FCGR2A single nucleotide polymorphism confers susceptibility to childhood-onset idiopathic nephrotic syndrome.Semantic proximity Read ↗

Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian children.Semantic proximity Read ↗

NR3C1 gene polymorphisms are associated with steroid resistance in patients with primary nephrotic syndrome.Semantic proximity Read ↗

Analysis of the association of NPHS2 and ACTN4 genes polymorphism with nephrotic syndrome in Egyptian childrenSemantic proximity Read ↗

Relationship between TIM-3 gene polymorphisms and steroid-resistant primary nephrotic syndrome in children.Semantic proximity Read ↗

Characterization of NPHS2 gene polymorphisms associated to steroid resistance nephrotic syndrome in Indian children.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.