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 mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis

5 Jan 2006

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cellular transport and secretion
Share to Lysosomal Storage Disorders Research
Share to Neurological diseases and metabolism

Source

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

Identifiers

PMID: 16386934
DOI: 10.1016/j.ymgme.2005.11.005

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.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosisPMID 16386934Read ↗

The canine CTSD gene as a candidate for late-onset neuronal ceroid lipofuscinosis.Semantic proximity Read ↗

Identification of a Mutation Causing Mucopolysaccharidosis Type IIIA in New Zealand Huntaway DogsSemantic proximity Read ↗

Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies.Semantic proximity Read ↗

Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosisSemantic proximity Read ↗

Mutations of CTSK result in pycnodysostosis via a reduction in cathepsin K protein.Semantic proximity Read ↗

Molecular analysis of a novel cathepsin K gene mutation in a Chinese child with pycnodysostosis.Semantic proximity Read ↗

Mutation analysis of cathepsin C gene in a Chinese patient with pre-pubertal periodontitis.Semantic proximity Read ↗

Cathepsin D deficiency causes juvenile-onset ataxia and distinctive muscle pathologySemantic proximity Read ↗

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