GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population
暂无分享,去创建一个
P. Deyn | C. Broeckhoven | S. Engelborghs | J. Theuns | P. Cras | B. Pickut | K. Peeters | D. Crosiers | P. Pals | E. Corsmit | Bram Meeus | Maria Mattheijssens | Karen Nuytemans
[1] Jeremy R. B. Newman,et al. Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease , 2009, Movement disorders : official journal of the Movement Disorder Society.
[2] A. Singleton,et al. Lack of replication of association between GIGYF2 variants and Parkinson disease. , 2008, Human molecular genetics.
[3] A. Singleton,et al. Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls. , 2008, Human molecular genetics.
[4] C. van Broeckhoven,et al. Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease , 2008, Human mutation.
[5] C. Lautier,et al. Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease. , 2008, American journal of human genetics.
[6] Jan Gründemann,et al. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase , 2006, Nature Genetics.
[7] M. Farrer. Genetics of Parkinson disease: paradigm shifts and future prospects , 2006, Nature Reviews Genetics.
[8] J. Schulz,et al. Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease. , 2005, Human molecular genetics.
[9] Modesto Orozco,et al. PMUT: a web-based tool for the annotation of pathological mutations on proteins , 2005, Bioinform..
[10] C. van Broeckhoven,et al. novoSNP, a novel computational tool for sequence variation discovery. , 2005, Genome research.
[11] Andrew Lees,et al. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease , 2004, Neuron.
[12] R. Nussbaum,et al. Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 , 2004, Science.
[13] D. Goldstein,et al. UCHL1 is a Parkinson's disease susceptibility gene. , 2004 .
[14] F. Giorgino,et al. Two Novel Proteins That Are Linked to Insulin-like Growth Factor (IGF-I) Receptors by the Grb10 Adapter and Modulate IGF-I Signaling* , 2003, Journal of Biological Chemistry.
[15] C. Broeckhoven,et al. Evaluation of breast cancer risk assessment packages in the family history evaluation and screening programme , 2003, Journal of medical genetics.
[16] Steven Henikoff,et al. SIFT: predicting amino acid changes that affect protein function , 2003, Nucleic Acids Res..
[17] D. Hernandez,et al. Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease. , 2003, Human molecular genetics.
[18] L. Seeberger,et al. Significant linkage of Parkinson disease to chromosome 2q36-37. , 2003, American journal of human genetics.
[19] P. Cras,et al. Case–control study of environmental risk factors for Parkinson's disease in Belgium , 2002, European Journal of Epidemiology.
[20] Patrizia Rizzu,et al. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism , 2002, Science.
[21] T. Foroud,et al. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. , 2002, American journal of human genetics.
[22] M. Farrer,et al. Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease. , 1999, Neuroreport.
[23] S. Minoshima,et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism , 1998, Nature.
[24] J Q Trojanowski,et al. Aggregation of alpha-synuclein in Lewy bodies of sporadic Parkinson's disease and dementia with Lewy bodies. , 1998, The American journal of pathology.
[25] Robert L. Nussbaum,et al. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease , 1997 .
[26] M. Farrer,et al. Reported mutations in GIGYF2 are not a common cause of Parkinson's disease. , 2009, Movement disorders : official journal of the Movement Disorder Society.
[27] Hong Jiang,et al. Mutations in NR4A2 associated with familial Parkinson disease , 2003, Nature Genetics.
[28] A. Hofman,et al. Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group. , 2000, Neurology.