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

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.

Neuron - 18 Nov 2004

Paisán-Ruíz Coro, Jain Shushant, Evans E Whitney, Gilks William P, Simón Javier, van der Brug Marcel, López de Munain Adolfo, Aparicio Silvia, Gil Angel Martínez, Khan Naheed, Johnson Janel, Martinez Javier Ruiz, Nicholl David, Martí Carrera Itxaso, Pena Amets Saénz, de Silva Rohan, Lees Andrew, Martí-Massó José Félix, Pérez-Tur Jordi, Wood Nick W, Singleton Andrew B

Abstract excerpt

Parkinson's disease (PD; OMIM #168600) is the second most common neurodegenerative disorder in the Western world and presents as a progressive movement disorder. The hallmark pathological features of PD are loss of dopaminergic neurons from the substantia nigra and neuronal intracellular Lewy bod...

Read the complete abstract on PubMed

Topics

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

Share to Blotting, Northern
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cloning, Molecular

Share to Leucine-Rich Repeat Serine-Threonine Protein Kinase-2

Share to Nerve Tissue Proteins

Share to Parkinson Disease

Share to Protein Kinases

Share to Protein Serine-Threonine Kinases

Source

Identifiers

PMID: 15541308
DOI: 10.1016/j.neuron.2004.10.023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15541308-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.PMID 15541308Read ↗

Familial Parkinson's disease: Clinical and genetic analysis of four Basque familiesSemantic proximity Read ↗

PARK6 is a common cause of familial parkinsonism.Semantic proximity Read ↗

Systematic mutational analysis of FBXO7 in a Parkinson's disease population from southern Spain.Semantic proximity Read ↗

A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family.Semantic proximity Read ↗

Parkinson's Disease in Saudi Patients: A Genetic Study.Semantic proximity Read ↗

Fine mapping and resequencing of the PARK16 locus in Parkinson's disease.Semantic proximity Read ↗

The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing IntervalSemantic proximity Read ↗

Porcine DJ-1: cloning of PARK7 cDNA, sequence comparison, expression analysis and chromosomal localization.Semantic proximity Read ↗

DJ-1 linked parkinsonism (PARK7) is associated with Lewy body pathology.Semantic proximity Read ↗

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.Semantic proximity Read ↗

Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease.Semantic proximity Read ↗

A new F-box protein 7 gene mutation causing typical Parkinson's disease.Semantic proximity Read ↗

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