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

A fungal perspective on human inborn errors of metabolism: alkaptonuria and beyond.

Fungal genetics and biology : FG & B - 1 Oct 2001

Peñalva M A

Abstract excerpt

Crucial for the establishment and development of biochemical genetics as a self-standing discipline was Beadle and Tatum's choice of Neurospora crassa as experimental organism some 60 years ago. Although Garrod's insights on biochemical genetics and his astonishingly modern concepts of biochemical individuality and susceptibility to disease had been ignored by their contemporaries, Beadle acknowledged on several...

Read the complete abstract on PubMed

Topics

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

Share to Genes, Fungal
Share to Aspergillus nidulans
Share to Metabolism, Inborn Errors

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

Share to Models, Chemical

Share to Mutation

Share to Phenylalanine

Share to Tyrosine

Source

Identifiers

PMID: 11567547
DOI: 10.1006/fgbi.2001.1284

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

A fungal perspective on human inborn errors of metabolism: alkaptonuria and beyond.PMID 11567547Read ↗

Fungal metabolic model for human type I hereditary tyrosinaemia.Semantic proximity Read ↗

Structural and functional analysis of mutations in alkaptonuria.Semantic proximity Read ↗

Fumarase deficiency: a rare disorder on the crossroads of clinical and metabolic genetics, neurology and cancer.Semantic proximity Read ↗

Porphyria with double errors in the heme biosynthetic pathway.Semantic proximity Read ↗

Chemical individuality: concept and outlook.Semantic proximity Read ↗

Functional analysis of mutations in the human carnitine/acylcarnitine translocase in Aspergillus nidulans.Semantic proximity Read ↗

New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder.Semantic proximity Read ↗

Characterization of a Fungal Maleylacetoacetate Isomerase Gene and Identification of Its Human HomologueSemantic proximity Read ↗

Underground metabolism.Semantic proximity Read ↗

Yeast to Study Human Purine Metabolism DiseasesSemantic proximity Read ↗

Fungal metabolic model for type I 3-methylglutaconic aciduria.Semantic proximity Read ↗

Gene expression & biochemical analysis in alkaptonuria caused by a founder pathogenic variant across different age groups from India.Semantic proximity Read ↗

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