Discover Community Create You

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

Article

Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.

Journal of nephrology - 1 Aug 2020

Basit Sulman, Al-Edressi Howaida Mohammed, Sairafi Mona Hamza, Hashmi Jamil Amjad, Alharby Essa, Safar Ramzia, Ramzan Khushnooda

Abstract excerpt

BACKGROUND: Individuals with proteinuria in association with hypoalbuminemia, edema, and hyperlipidemia are considered as having nephrotic syndrome (NS). NS is the most common kidney disease seen in the paediatric age group. NS is usually classified into steroid resistant nephrotic syndrome (SRNS) and steroid sensitive nephrotic syndrome (SSNS). More than 58 genes have been identified as a monogenic cause of...

Read the complete abstract on PubMed

Topics

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

Share to Centromere
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-Binding Proteins

Share to Homozygote

Share to Nephrotic Syndrome

Share to Phenotype

Share to Steroids

Source

Identifiers

PMID: 31912435
DOI: 10.1007/s40620-019-00692-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.PMID 31912435Read ↗

Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An UpdateSemantic proximity Read ↗

Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndromeSemantic proximity Read ↗

Multi-population genome-wide association study implicates both immune and non-immune factors in the etiology of pediatric steroid sensitive nephrotic syndromeSemantic proximity Read ↗

Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent ApproachesSemantic proximity Read ↗

Identification of monogenic variants in steroid-resistant and steroid-sensitive nephrotic syndrome.Semantic proximity Read ↗

A multicenter study investigating the genetic analysis of childhood steroid-resistant nephrotic syndrome: Variants in COL4A5 may not be coincidental.Semantic proximity Read ↗

HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.Semantic proximity Read ↗

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.Semantic proximity Read ↗

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

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

Genetic basis of adult-onset nephrotic syndrome and focal segmental glomerulosclerosis.Semantic proximity Read ↗

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.Semantic proximity Read ↗

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