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Investigation of the human single nucleotide polymorphism in Graves disease

ABSTRACT: An investigation of the relationship between a subset of human single nucleotide polymorphism and Graves' disease

INSTRUMENT(S): -

ORGANISM(S): Homo Sapiens

SUBMITTER: The Core Laboratory in Medical Center of Clinical Research

PROVIDER: PRJEB48200 | EVA | 2022-09-01

REPOSITORIES: EVA

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			Action	DRS
	chr20-44500-44900kb-2.vcf.gz	Vcf
	chr20-44500-44900kb-2.vcf.gz.csi	Vcf
	chr20-44500-44900kb-2.vcf.gz.tbi	Vcf

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GSTM3 single nucleotide polymorphism (rs7483) associated with peripheral BMC expression in Alzheimer disease

Project description:Comparisons between the sample groups (normal elderly control (NEC) and Alzheimer disease (AD)) allowed the identification of genes with disease expression patterns associated with the glutathione S-transferase M3 single nucleotide polymorphism rs7483. Keywords: biological repeat Peripheral blood mononuclear cells (BMC) were obtained from normal elderly control (NEC) and Alzheimer disease (AD) subjects. Targets from biological replicates of NEC (n=18) and AD (n=16) were generated and the expression profiles were determined using the NIA Human MGC cDNA microarray.

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