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

Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene.

Kidney international - 1 Nov 2001

Yazaki M, Liepnieks J J, Yamashita T, Guenther B, Skinner M, Benson M D

Abstract excerpt

BACKGROUND: Although apolipoprotein A-II (apoA-II) associated amyloidosis has been described in the senescent accelerated mouse (SAM) model of aging, so far there has been no report of human apoA-II amyloidosis except for a recent report of renal amyloidosis resulting from a stop-codon to glycine mutation of apoA-II. The mechanisms of amyloid formation in human apoA-II amyloidosis are not clear. METHODS: A...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Amyloidosis
Share to Apolipoprotein A-II

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Base Sequence

Share to Codon, Terminator

Share to Kidney Diseases

Share to Molecular Sequence Data

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 11703582
DOI: 10.1046/j.1523-1755.2001.00024.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Renal amyloidosis caused by a novel stop-codon mutation in the apolipoprotein A-II gene.PMID 11703582Read ↗

Hereditary systemic amyloidosis associated with a new apolipoprotein AII stop codon mutation Stop78Arg.Semantic proximity Read ↗

A new human hereditary amyloidosis: the result of a stop-codon mutation in the apolipoprotein AII gene.Semantic proximity Read ↗

Accelerated APOA-II senile amyloidosis in a <i>PAI-1</i> (plasminogen activator inhibitor 1) knock-out modelSemantic proximity Read ↗

Renal apolipoprotein A-I amyloidosis associated with a novel mutant Leu64Pro.Semantic proximity Read ↗

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.Semantic proximity Read ↗

Wild type ApoA-II gene does not rescue senescence-accelerated mouse (SAMP1) from short life span and accelerated mortality.Semantic proximity Read ↗

Accelerated senile amyloidosis induced by amyloidogenic Apoa-II gene shortens the life span of mice but does not accelerate the rate of senescence.Semantic proximity Read ↗

Divergent renal localization patterns of heterozygote-derived two distinct AA amyloids in a catSemantic proximity Read ↗

Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I.Semantic proximity Read ↗

Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain.Semantic proximity Read ↗

Clinical and pathologic characteristics of hereditary apolipoprotein A-I amyloidosis in Ireland.Semantic proximity Read ↗

Hereditary renal amyloidosis with a novel variant fibrinogen.Semantic proximity Read ↗

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