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«PARK2

Below is an extended PARK2 research listing. Click here to return to the gene page.

Recent Publications on :

Mapping preclinical compensation in Parkinson's disease: An imaging genomics approach.
Mutations in the Parkin (PARK2) and PINK1 gene (PARK 6) can cause...
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31st October, 2009
Department of Neurology, Donders Institute for Brain, Cognition and
Prevalence and clinical features of LRRK2 mutations in patients with Parkinson's disease in southern Spain.
BACKGROUND AND PURPOSE: Mutations in leucine-rich repeat kinase 2 (LRRK2)...
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20th October, 2009
Laboratorio de Investigaciones Biomedicas,, Servicio de Neurologia,
Genome wide DNA-profiling of HIV-related B-cell lymphomas.
Summary Non-Hodgkin lymphomas (NHL) represent a frequent complication of...
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17th October, 2009
Division of Haematology, Department of Clinical and Experimental Medicine
Loss of parkin or PINK1 function increases Drp1-dependent mitochondrial fragmentation.
Loss-of-function mutations in the parkin gene (PARK2) and PINK1 gene...
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7th October, 2009
Neurobiochemistry, Deutsches Zentrum fur Neurodegenerative Erkrankungen
Expression changes of dopaminergic system-related genes in PC12 cells induced by manganese, silver, or copper nanoparticles.
Nanoparticles have received a great deal of attention for producing new...
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29th September, 2009
Neurochemistry Laboratory, Division of Neurotoxicology, National Center
Rapamycin activation of 4E-BP prevents parkinsonian dopaminergic neuron loss.
Mutations in PINK1 and PARK2 cause autosomal recessive parkinsonism, a...
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24th September, 2009
Medical Research Council Centre for Developmental and Biomedical Genetics,
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
The relative contribution of simple mutations and copy number variations...
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24th September, 2009
Neurodegenerative Brain Diseases Group, Department of Molecular Genetics,
Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses.
BACKGROUND: Purely epistatic multi-locus interactions cannot generally be...
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19th September, 2009
Department of Electrical Engineering, Faculty of Engineering, King
Are genetic and sporadic Parkinson's disease patients equally susceptible to develop dementia?
The occurrence of dementia in genetic Parkinson's disease is...
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11th September, 2009
Department of Neurology, The Sagol Neuroscience Center, Sheba Medical
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia.
Dopa-responsive dystonia is a childhood-onset dystonic disorder,...
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10th September, 2009
AP-HP, Departement de Genetique et Cytogenetique, Groupe Hospitalier Pitie
Hereditary parkinsonism: Parkinson disease look-alikes-An algorithm for clinicians to "PARK" genes and beyond.
In the past decade, a number of genetic causes of parkinsonism have been...
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8th September, 2009
Department of Neurology, University of Lubeck, Lubeck, Germany.
Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India.
Among several etiological factors, PARK2 mutations are the most common...
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8th September, 2009
Departments of Neurology, Post Graduate Institute of Medical Education and
Evidence for the presence of full-length PARK2 mRNA and Parkin protein in human blood.
Research on Parkinson's disease fails to pinpoint a single gene or a gene...
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26th August, 2009
Kocaeli University, Department
Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease.
OBJECTIVE: Mutations in the PARK2 (Parkin) gene result in an early-onset...
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25th July, 2009
Department of Neurology, Faculty of Heath Science, Medical University of
High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
Glioblastoma multiforme (GBM) is an extremely malignant brain tumor. To...
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24th June, 2009
Division of Hematology and Oncology, Cedars-Sinai Medical Center,

 

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