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

Molecular genetics of renal diseases.

Internal medicine (Tokyo, Japan) - 1 Feb 1997

Saito A, Yamazaki H, Nakagawa Y, Arakawa M

Abstract excerpt

Recent progress in molecular genetics has strongly influenced nephrology. Gene mutations have been identified which cause various monogenic hereditary renal diseases including Alport syndrome, autosomal dominant polycystic kidney disease, and tubular transporter disorders. The data obtained will be useful not only to develop new methods of diagnosis and treatment of such particular diseases but also to expand the...

Read the complete abstract on PubMed

Topics

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

Share to Diabetic Nephropathies
Share to Glomerulonephritis
Share to Kidney Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney Tubules

Share to Mutation

Share to Nephritis, Hereditary

Share to Polycystic Kidney Diseases

Source

Identifiers

PMID: 9099587
DOI: 10.2169/internalmedicine.36.81

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

Molecular genetics of renal diseases.PMID 9099587Read ↗

Overview: the genetics of renal disease.Semantic proximity Read ↗

Genetics and CKD.Semantic proximity Read ↗

Unravelling the genetic basis of renal diseases; from single gene to multifactorial disorders.Semantic proximity Read ↗

Hereditary kidney diseases: highlighting the importance of classical Mendelian phenotypes.Semantic proximity Read ↗

Recent Advances in Elucidating the Mechanism Underlying Proteinuric Kidney Disease/Nephrotic Syndrome: Lessons From Knockout/Transgenic Mouse ModelsSemantic proximity Read ↗

Genetics of kidney disease.Semantic proximity Read ↗

Molecular genetics of hereditary nephritis.Semantic proximity Read ↗

Inherited renal diseases.Semantic proximity Read ↗

[Molecular genetics in nephrology. Genetic kidney diseases provide clues for understanding the pathogenesis of proteinuria].Semantic proximity Read ↗

Genetics in kidney disease in 2013: Susceptibility genes for renal and urological disorders.Semantic proximity Read ↗

Genetics and kidney dysfunction.Semantic proximity Read ↗

The genetic basis of human glomerular disease.Semantic proximity Read ↗

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