Research Topics
Genomes and Genes | Lynn M BekrisSummaryAffiliation: University of Washington Country: USA Publications
| Collaborators
|
Detail Information
Publications
Chronic beryllium disease and glutathione biosynthesis genesLynn M Bekris
Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington 98195, USA
J Occup Environ Med 48:599-606. 2006..Glutamate cysteine ligase consists of a catalytic subunit (GCLC) and modifier subunit (GCLM)...
ADAM10 expression and promoter haplotype in Alzheimer's diseaseLynn M Bekris
Geriatric Research, Education, and Clinical Center GRECC, VA Puget Sound Health Care System, Seattle, WA, USA
Neurobiol Aging 33:2229.e1-2229.e9. 2012..Taken together, these findings suggest that ADAM10 expression is modulated according to a promoter haplotype that is influenced in a brain region- and cell type-specific manner...
Tau phosphorylation pathway genes and cerebrospinal fluid tau levels in Alzheimer's diseaseLynn M Bekris
Geriatric Research, Education, and Clinical Center GRECC, VA Puget Sound Health Care System, Seattle, Washington 98108, USA
Am J Med Genet B Neuropsychiatr Genet 159:874-83. 2012..These results suggest that rs7768046 and rs913275 both influence CSF tau levels in an AD-associated manner...
Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOELynn M Bekris
Geriatric Research, Education and Clinical Center, VA Puget Sound Health Care System, 1660 South Columbian Way, Seattle, WA 98108, USA
J Hum Genet 57:18-25. 2012....
Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's diseaseL M Bekris
Geriatric Research, Education and Clinical Center GRECC, VA Puget Sound Health Care System, Seattle, WA, USA
Neurobiol Aging 32:556.e13-23. 2011..These results suggest that genetic variation within ADAM10, an APP processing gene, influences CSF APPα levels in an AD specific manner...
The genetics of Parkinson diseaseLynn M Bekris
Geriatric Research, Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA 98108, USA
J Geriatr Psychiatry Neurol 23:228-42. 2010..The function of these genes and their contribution to PD pathogenesis remain to be fully elucidated. The prevalence, incidence, clinical manifestations, and genetic components of PD are discussed in this review...
APOE mRNA and protein expression in postmortem brain are modulated by an extended haplotype structureLynn M Bekris
Geriatric Research, Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, Washington 98108, USA
Am J Med Genet B Neuropsychiatr Genet 153:409-17. 2010....
Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levelsLynn M Bekris
Geriatric Research, Education, and Clinical Center GRECC, VA Puget Sound Health Care System, Seattle, WA 98108, USA
J Alzheimers Dis 13:255-66. 2008..Further investigation of the genetic influence of these loci on apoE expression levels in the central nervous system is likely to provide new insight into apoE regulation as well as AD pathogenesis...
Glutathione-s-transferase M1 and T1 polymorphisms and associations with type 1 diabetes age-at-onsetLynn M Bekris
Department of Environmental and Occupational Health Sciences, University of Washington, Box 357710, Seattle, WA 98195, USA
Autoimmunity 38:567-75. 2005..035) may be a susceptibility factor in T1D 14-20 years old. These results suggest that the GSTM1 null genotype is associated with T1D protection and T1D age-at-onset and that susceptibility to T1D may involve GST conjugation...
Targeting type 1 diabetes before and at the clinical onset of diseaseL M Bekris
Department of Medicine, University of Washington, Box 357710, Seattle, WA 206 543 0756, USA
Endocr Metab Immune Disord Drug Targets 6:103-24. 2006..It is speculated that drug targets of factors important to disease pathogenesis may provide safe and effective adductive treatment to preserve beta cell function in autoantibody positive subjects who are at maximum risk for disease...
Cerebrospinal fluid concentration of brain-derived neurotrophic factor and cognitive function in non-demented subjectsGe Li
Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, Washington, USA
PLoS ONE 4:e5424. 2009..01). CONCLUSIONS/SIGNIFICANCE: Reduced CSF BDNF was associated with age-related cognitive decline, suggesting a potential mechanism that may contribute in part to cognitive decline in older individuals...
Genetics of Alzheimer diseaseLynn M Bekris
Department of Medicine, University of Washington School of Medicine, Seattle, WA 98108, USA
J Geriatr Psychiatry Neurol 23:213-27. 2010..Identification of these genes has led to a number of animal models that have been useful to study the pathogenesis underlying AD. In this article, we provide an overview of the clinical and genetic features of AD...
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationChang En Yu
Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, 1660 S Columbian Way, Seattle, WA 98108, USA
Arch Neurol 67:161-70. 2010..However, it is unclear whether some rare FTD-related GRN variants are pathogenic and whether neurodegenerative disorders other than FTD can also be caused by GRN mutations...
Antibodies to GAD65 and peripheral nerve function in the DCCTRobert D Hoeldtke
Department of Medicine, West Virginia University, Morgantown, WV 26506 9159, USA
J Neuroimmunol 185:182-9. 2007..248+/-.03 versus .278+/-.03). Epitope analysis, based on the blocking of conformational epitopes by recombinant Fab, revealed that the binding to multiple epitopes was decreased in the patients with neuropathy...
Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in SwedenJared C Roach
Institute for Systems Biology, Seattle, WA 98103, USA
Am J Hum Genet 79:614-27. 2006..0%-31.0%) suggests that variation within ITPR3 reflects an important contribution to T1D in Sweden. Two-locus regression analysis supports an influence of ITPR3 variation on T1D that is distinct from that of any MHC class II gene...
Mutations in the TSGA14 gene in families with autism spectrum disordersO Korvatska
Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, 98195, USA
Am J Med Genet B Neuropsychiatr Genet 156:303-11. 2011..022). This is the first report of a possible link of a gene with a centrosomal function with familial autism...
Differential expression of the glutamate transporter GLT-1 in pancreasJames S Meabon
Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, Washington, USA
J Histochem Cytochem 60:139-51. 2012..Finally, glutamine synthetase was coexpressed with GLT-1 in islets, which suggests that, as with liver and brain, one possible role of GLT-1 in the pancreas is to support glutamine synthesis...
GAD65 autoantibody epitopes in adult patients with latent autoimmune diabetes following GAD65 vaccinationL M Bekris
Department of Medicine, University of Washington, Seattle, WA 98195, USA
Diabet Med 24:521-6. 2007..In this study we analysed the effect of rhGAD65 administration on the GAD65-specific autoimmune response...
Glutamate cysteine ligase catalytic subunit promoter polymorphisms and associations with type 1 diabetes age-at-onset and GAD65 autoantibody levelsL M Bekris
Department of Medicine, University of Washington, Seattle, WA 98195, USA
Exp Clin Endocrinol Diabetes 115:221-8. 2007..13-0.82). The GCLC -129 SNP and GCLC TNR appear to be in linkage disequilibrium (p-value<0.0001). These results suggest that GCLC promoter polymorphisms may influence GAD65Ab levels and may influence the age at which T1D is diagnosed...
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysisVivianna M Van Deerlin
Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, USA
Lancet Neurol 7:409-16. 2008..Our aim was to investigate whether TARDBP is a candidate disease gene for familial ALS that is not associated with mutations in superoxide dismutase 1 (SOD1)...
