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

PAX2 Gene Mutation in Pediatric Renal Disorders-A Narrative Review.

International journal of molecular sciences - 13 Aug 2023

Muntean Carmen, Chirtes Camelia, Baczoni Balazs, Banescu Claudia

Abstract excerpt

The PAX2 gene is a transcription factor that is essential for the development of the urinary system among other transcription factors. The role of PAX2 is highlighted from the seventh week of gestation, when it is involved in development processes and the emergence of nephrons and collecting tubes. Being an important factor in renal development, mutations of this gene can produce severe alterations in the...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Kidney
Share to Kidney Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Nephrons

Share to PAX2 Transcription Factor

Share to Renal Insufficiency

Share to Transcription Factors

Source

Open in PubMed Open full text

Identifiers

PMID: 37628926
DOI: 10.3390/ijms241612737
PMCID: PMC10454596

Provenance

PubMed metadata and Literature Corpus relationships.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PAX2 Gene Mutation in Pediatric Renal Disorders-A Narrative Review.PMID 37628926Read ↗

The role of PAX2 in normal and abnormal development of the urinary tract.Semantic proximity Read ↗

Pax2 in the development of renal and urinary tract diseases.Semantic proximity Read ↗

PAX2 in human kidney malformations and diseaseSemantic proximity Read ↗

Congenital anomalies of the kidney and urinary tractSemantic proximity Read ↗

PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomaliesSemantic proximity Read ↗

New PAX2 Mutation Associated with Polycystic Kidney Disease: A Case ReportSemantic proximity Read ↗

Renal-coloboma syndrome: a multi-system developmental disorder caused by PAX2 mutations.Semantic proximity Read ↗

Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)Semantic proximity Read ↗

Congenital anomalies of the kidney and urinary tract: An embryogenetic reviewSemantic proximity Read ↗

Pathophysiology of Congenital Anomalies of the Kidney and Urinary Tract: A Comprehensive Review.Semantic proximity Read ↗

Mutation of PAX2 in two siblings with renal-coloboma syndrome.Semantic proximity Read ↗

PAX genes in development and disease: the role of PAX2 in urogenital tract development.Semantic proximity Read ↗

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