Zobrazeno 1 - 10
of 22
pro vyhledávání: '"James F. Simpson"'
Publikováno v:
Genes. 13(9)
Elucidating the actions of genetic polymorphisms associated with the risk of Alzheimer's disease (AD) may provide novel insights into underlying mechanisms. Two polymorphisms have implicated
An Alternatively Spliced TREM2 Isoform Lacking the Ligand Binding Domain is Expressed in Human Brain
Autor:
Benjamin C. Shaw, Henry C. Snider, Andrew K. Turner, Diana J. Zajac, James F. Simpson, Steven Estus
Publikováno v:
J Alzheimers Dis
Background: Genetic variants in TREM2 are strongly associated with Alzheimer’s disease (AD) risk but alternative splicing in TREM2 transcripts has not been comprehensively described. Objective: Recognizing that alternative splice variants can resul
Publikováno v:
Genes
Volume 12
Issue 7
Genes, Vol 12, Iss 1008, p 1008 (2021)
Volume 12
Issue 7
Genes, Vol 12, Iss 1008, p 1008 (2021)
Genome-wide association studies (GWAS) have identified immune-related genes as risk factors for Alzheimer’s disease (AD), including TREM2 and CD33, frequently passing a stringent false-discovery rate. These genes either encode or signal through imm
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e33923 (2012)
The minor allele of rs11136000 within CLU is strongly associated with reduced Alzheimer's disease (AD) risk. The mechanism underlying this association is unclear. Here, we report that CLU1 and CLU2 are the two primary CLU isoforms in human brain; CLU
Externí odkaz:
https://doaj.org/article/99ee7dac0e6d4d618827f496ed6cc3a5
Autor:
Paul K. Crane, Christopher Medway, Shobha Potluri, Joe Chiles, James F. Simpson, Shubhabrata Mukherjee, Ying Liang, Christian M. Paumi, Dianna S. Howard, Steven G. Younkin, David W. Fardo, Steven Estus, Hualin S. Xi, Manasi Malik
Publikováno v:
Human Molecular Genetics. 24:3557-3570
The CD33 single-nucleotide polymorphism (SNP) rs3865444 has been associated with the risk of Alzheimer's disease (AD). Rs3865444 is in linkage disequilibrium with rs12459419 which has been associated with efficacy of an acute myeloid leukemia (AML) c
Publikováno v:
Journal of Alzheimer's disease : JAD. 59(2)
Both common and rare polymorphisms within ABCA7 have been associated with Alzheimer’s disease (AD). In particular, the rare AD associated polymorphism rs200538373 was associated with altered ABCA7 exon 41 splicing and an AD risk odds ratio of ~1.9.
Autor:
Crisley de Camargo, Mercival R. Francisco, James F. Simpson, Luís Fábio Silveira, Paulo V. Davanço, Mariellen C. Costa, Natasha M. Laganaro, Paulo R. R. Oliveira, Roberto M. A. Azeredo
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 1, p e0169636 (2017)
PLoS ONE, Vol 12, Iss 1, p e0169636 (2017)
The conservation of many endangered taxa relies on hybrid identification, and when hybrids become morphologically indistinguishable from the parental species, the use of molecular markers can assign individual admixture levels. Here, we present the p
Publikováno v:
Journal of Neurochemistry. 115:614-624
As low-density lipoprotein receptor (LDLR) contributes to cholesterol and amyloid beta homeostasis, insights into LDLR regulation may facilitate our understanding of cardiovascular disease and Alzheimer's disease. Previously, we identified LDLR isofo
Autor:
James F. Simpson, Mathew J. Thayer, Olga N. Ponomoreva, Robert W. Burman, Phillip A. Yates, Mitchell S. Turker
Publikováno v:
Molecular and Cellular Biology. 23:4461-4470
Mouse Aprt constructs that are highly susceptible to DNA methylation-associated inactivation in embryonal carcinoma cells were transfected into differentiated cells, where they were expressed. Construct silencing was induced by either whole-cell fusi
Autor:
C. Jeffrey Woodbury, James F. Simpson, H. Richard Koerber, John N. Burkett, Melissa Zwick, Brian M. Davis, Kathryn M. Albers
Publikováno v:
The Journal of Neuroscience. 22:4057-4065
Most, if not all, nociceptor sensory neurons are dependent on nerve growth factor (NGF) during early embryonic development. A large subpopulation of these sensory neurons loses NGF dependency between embryonic day 16 and postnatal day 14 and become r