Pages that link to "Q28363814"

The following pages link to Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. (Q28363814):

Displaying 44 items.

• Methods for high-density admixture mapping of disease genes (Q22337164) (← links)
• The prion protein gene in humans revisited: lessons from a worldwide resequencing study (Q24537613) (← links)
• Transmissible Spongiform Encephalopathies Affecting Humans (Q24549130) (← links)
• A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea (Q24642582) (← links)
• An overview of human prion diseases (Q27007967) (← links)
• The prion gene is associated with human long-term memory (Q28259028) (← links)
• Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP (Q28943533) (← links)
• Analyses of the survival time and the influencing factors of chinese patients with prion diseases based on the surveillance data from 2008-2011. (Q30625752) (← links)
• The expanding universe of prion diseases (Q33239695) (← links)
• No temporal trends in the prevalence of atypical scrapie in British sheep, 2002-2006 (Q33326750) (← links)
• Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease (Q33329713) (← links)
• Genomic and post-genomic analyses of human prion diseases (Q33347355) (← links)
• Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia (Q33427673) (← links)
• Two adjacent nuclear factor-binding domains activate expression from the human PRNP promoter (Q33501379) (← links)
• PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism (Q33520832) (← links)
• Genetic studies in human prion diseases. (Q33627593) (← links)
• Kuru in the 21st century--an acquired human prion disease with very long incubation periods (Q33997105) (← links)
• Analyses of the mitochondrial mutations in the Chinese patients with sporadic Creutzfeldt-Jakob disease (Q34705051) (← links)
• Molecular neurology of prion disease (Q35488760) (← links)
• Molecular and clinical classification of human prion disease (Q35549016) (← links)
• Genome wide association studies and prion disease (Q35578768) (← links)
• An overview of transmissible spongiform encephalopathies (Q36177322) (← links)
• Antiprion activity of cholesterol esterification modulators: a comparative study using ex vivo sheep fibroblasts and lymphocytes and mouse neuroblastoma cell lines. (Q36295466) (← links)
• Prion disease genetics (Q36359872) (← links)
• Genotype patterns and characteristics of PRNP in the Korean population (Q36719058) (← links)
• Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series (Q36944491) (← links)
• Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study (Q37097991) (← links)
• The prion protein M129V polymorphism: longevity and cognitive impairment among Polish centenarians (Q37197684) (← links)
• Spatial clusters of Creutzfeldt-Jakob disease mortality in Japan between 1995 and 2004. (Q37466852) (← links)
• Polymorphism at 129 dictates metastable conformations of the human prion protein N-terminal β-sheet. (Q37725033) (← links)
• Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob disease (Q39331213) (← links)
• Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study (Q43145870) (← links)
• Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation (Q43444644) (← links)
• Molecular classification of sporadic Creutzfeldt-Jakob disease. (Q44451927) (← links)
• The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population (Q46911435) (← links)
• Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease (Q47199656) (← links)
• Linkage disequilibrium across six prion gene regions spanning 20 kbp in U.S. sheep. (Q48083595) (← links)
• A polymorphism in the YWHAH gene encoding 14-3-3 eta that is not associated with sporadic Creutzfeldt-Jakob disease (CJD). (Q49074496) (← links)
• Polymorphism at 3′ UTR +28 of the prion-like protein gene is associated with sporadic Creutzfeldt–Jakob disease (Q59294063) (← links)
• Retrospective sequence analysis of the human PRNP gene from the formaldehyde-fixed paraffin-embedded tissues: report of two cases of Creutzfeldt-Jakob disease (Q80208609) (← links)
• Polymorphisms of the PRNP gene in Chinese populations and the identification of a novel insertion mutation (Q80363678) (← links)
• Are further genetic factors associated with the risk of developing variant Creutzfeldt-Jakob disease? (Q82961955) (← links)
• A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes (Q84522846) (← links)
• Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study (Q99573881) (← links)