Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.
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Summary
It is concluded that on chromosome 1 a second locus, PARK7, involved in autosomal recessive, early-onset parkinsonism is identified.
- Type
- article
- Published
- 2001-09-01
- Cited by
- 403
- References
- 17
- Access
- Open access
- OpenAlex
- https://openalex.org/W2134412560
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:13567511
Keywords
Genetics, Locus (genetics), Biology, Parkinsonism, Haplotype
References
- Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.
- Recent Developments in Parkinson's Disease
- The ubiquitin pathway in Parkinson's disease
- Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
- Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
- A susceptibility locus for Parkinson's disease maps to chromosome 2p13
- Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children.
- Parkinsonism
- Pitfalls in homozygosity mapping.
- A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
- A simple salting out procedure for extracting DNA from human nucleated cells.
- Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?
- A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor.
- Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
- Association between early-onset Parkinson's disease and mutations in the parkin gene.
- Unified Parkinson's Disease Rating Scale
Cited by
- Loss of DJ-1 impairs antioxidant response by altered glutamine and serine metabolism.
- Genetic Forms of Parkinson's Disease
- A genetic-epidemiologic study of Alzheimer’s disease
- Terapia celular y aplicación de células madre en la enfermedad de Parkinson (Revisión)
- Genetic studies of LRRK2 and PINK1 in Parkinson's disease
- Biomarkers of neurodegenerative disorders: How good are they?
- Genetic Characterisation of Neurodegenerative disorders
- DOXORUBICIN-INDUCED, TNF-α-MEDIATED BRAIN OXIDATIVE STRESS, NEUROCHEMICAL ALTERATIONS, AND COGNITIVE DECLINE: INSIGHTS INTO MECHANISMS OF CHEMOTHERAPY INDUCED COGNITIVE IMPAIRMENT AND ITS PREVENTION
- LRRK2 genetics and expression in the Parkinsonian brain
- Splicing: is there an alternative contribution to Parkinson’s disease?
- Familial parkinsonism [Parkinson's disease and early onset parkinsonism]: a genetic, clinical study and 18F-dopa pet study.
- Identifying Genetic Causes of Parkinson’s Disease in Norway
- Signal Transduction Pathways Modulated by the PD-causative Gene LRRK2
- The mechanism of trichloroethylene neurotoxicity and its relation to Parkinsonism
- Recherche des facteurs génétiques à l’origine de la maladie de Parkinson dans la population canadienne-française du Québec
- Proteomic analysis of cellular models of neurodegeneration and mitochondrial dysfunction
- [Genetic factors associated with dementia in Parkinson's disease (PD)].
- RETRACTED: Genetic Susceptibility Model of Parkinson’s Disease Resulting from Exposure of DJ-1 Deficient Mice to MPTP: Evaluation of Neuroprotection by Ubisol-Q10
- Genetics in Parkinson's disease
- Tea and Parkinson's disease: Constituents of tea synergize with antiparkinsonian drugs to provide better therapeutic benefits.
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