Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Steven E. Pierce"'
Publikováno v:
iScience, Vol 27, Iss 2, Pp 108921- (2024)
Summary: Genome-wide association studies have identified thousands of single nucleotide polymorphisms that associate with increased risk for Parkinson’s disease (PD), but the functions of most of them are unknown. Using assay for transposase-access
Externí odkaz:
https://doaj.org/article/fd12b32ddd524e3fb696dafe15536816
Publikováno v:
Neurobiology of Disease, Vol 114, Iss , Pp 53-64 (2018)
In genome-wide association studies of complex diseases, many risk polymorphisms are found to lie in non-coding DNA and likely confer risk through allele-dependent differences in gene regulatory elements. However, because distal regulatory elements ca
Externí odkaz:
https://doaj.org/article/6a2cfec1199e409b94f45885fbc4ba2d
Publikováno v:
Human Molecular Genetics. 32:1-14
One of the most significant risk variants for Parkinson’s disease (PD), rs356182, is located at the PD-associated locus near the alpha-synuclein (α-syn) encoding gene, SNCA. SNCA-proximal variants, including rs356182, are thought to function in PD
Autor:
Stacey L Thomas, Ting-Hai Xu, Brittany L Carpenter, Steven E Pierce, Bradley M Dickson, Minmin Liu, Gangning Liang, Peter A Jones
Publikováno v:
Nucleic Acids Research.
CpG methylation generally occurs on both DNA strands and is essential for mammalian development and differentiation. Until recently, hemimethylation, in which only one strand is methylated, was considered to be simply a transitory state generated dur
Autor:
Edwin J C van der Schans, Steven E. Pierce, Jordan Prahl, Trevor A. Tyson, Alix Booms, Gerhard A. Coetzee
Publikováno v:
npj Parkinson's Disease, Vol 6, Iss 1, Pp 1-5 (2020)
NPJ Parkinson's Disease
NPJ Parkinson's Disease
Genetic risk for complex diseases very rarely reflects only Mendelian-inherited phenotypes where single-gene mutations can be followed in families by linkage analysis. More commonly, a large set of low-penetrance, small effect-size variants combine t
Publikováno v:
Molecular and cellular neurosciences. 119
As researchers grapple with the mechanisms and implications of alpha-synuclein (α-syn) in neuropathology, it is often forgotten that the function(s) of α-syn in healthy cells remain largely elusive. Previous work has relied on observing α-syn loca
SUMMARYOne of the most significant Parkinson’s disease (PD) risk variants, rs356182, is located at the PD-associated locus near the alpha-synuclein encoding gene, SNCA. SNCA-proximal variants, including rs356182, are thought to function in PD via a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa172e5fb06d8fac01cc8a045f104292
https://doi.org/10.1101/2021.07.06.451330
https://doi.org/10.1101/2021.07.06.451330
Genome-wide association studies (GWAS) have uncovered thousands of single nucleotide polymorphisms (SNPs) that are associated with Parkinson’s disease (PD) risk. The functions of most of these SNPs, including the cell type they influence, and how t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f66e5dfbc4566bcb5686ad07ad938e3f
https://doi.org/10.1101/2020.08.17.254276
https://doi.org/10.1101/2020.08.17.254276
Autor:
Steven E. Pierce, Gerhard A. Coetzee
Publikováno v:
Journal of Parkinson's Disease. 8:13-15
Genome-wide association studies of Parkinson's disease have revealed polymorphic variants associated with closely mapped genes of interest. We propose here that those genes may only represent the tip of an iceberg of regulatory effects and do not nec
Autor:
Emily Schulz, Lena Brundin, Martha L. Escobar Galvis, Nolwen L. Rey, Trevor A. Tyson, Zachary Madaj, Patrik Brundin, Sonia George, Corinne Esquibel, Steven E. Pierce, Amanda R. Burmeister, Jennifer A. Steiner, Lindsay Meyerdirk
Publikováno v:
Molecular Neurodegeneration
Molecular Neurodegeneration, BioMed Central, 2019, 14, pp.34. ⟨10.1186/s13024-019-0335-3⟩
Molecular Neurodegeneration, 2019, 14, pp.34. ⟨10.1186/s13024-019-0335-3⟩
Molecular Neurodegeneration, Vol 14, Iss 1, Pp 1-22 (2019)
Molecular Neurodegeneration, BioMed Central, 2019, 14, pp.34. ⟨10.1186/s13024-019-0335-3⟩
Molecular Neurodegeneration, 2019, 14, pp.34. ⟨10.1186/s13024-019-0335-3⟩
Molecular Neurodegeneration, Vol 14, Iss 1, Pp 1-22 (2019)
Background Cell-to-cell propagation of α-synuclein (α-syn) aggregates is thought to contribute to the pathogenesis of Parkinson’s disease (PD) and underlie the spread of α-syn neuropathology. Increased pro-inflammatory cytokine levels and activa