GSM5179116[Accession] - GEO DataSets - NCBI

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Items: 3

Select item 2001691561.

Persistent Variations of Blood DNA Methylation Associated with Treatment Exposures and Risk for Cardiometabolic Outcomes in Childhood Cancer Survivors

(Submitter supplied) Background: It is well-established that cancer treatment substantially increases risk of long-term adverse health outcomes among childhood cancer survivors. However, there is limited research on the underlying mechanisms. To elucidate the pathophysiology and a possible causal pathway from treatment exposures to cardiometabolic conditions, we conducted epigenome-wide association studies (EWAS) to identify DNA methylation (DNAm) sites associated with cancer treatment exposures and examined whether treatment-associated DNAm sites mediate associations between specific treatments and cardiometabolic conditions. more...

Organism:: Homo sapiens

Type:: Methylation profiling by genome tiling array

Platform:: GPL23976
2052 Samples

Download data: IDAT, TXT

Series

Accession:: GSE169156

ID:: 200169156

PubMed Full text in PMC Similar studies

Select item 1000239762.

Illumina Infinium HumanMethylation850 BeadChip

(Submitter supplied) See manufacturer's website

Organism:: Homo sapiens

281 Series
1 Related Platform
16960 Samples

Platform

Accession:: GPL23976

ID:: 100023976

Select item 3051791163.

genomic DNA derived from blood samples from survivor of childhood cancer [SJALL044972_G1]

Organism:: Homo sapiens

Source name:: peripheral blood mononuclear cells

Platform:: GPL23976
Series:: GSE169156

Download data: IDAT

Sample

Accession:: GSM5179116

ID:: 305179116

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GSM5179116[Accession] (3)
GEO DataSets
Aspergillus udagawae strain SFC20230725-M381 beta-tubulin (BenA) gene, partial c...
Aspergillus udagawae strain SFC20230725-M381 beta-tubulin (BenA) gene, partial cds
gi|2697035613|gb|OR394845.1|

Nucleotide
Aspergillus udagawae KW2237 CaM gene for calmodulin, partial sequence
Aspergillus udagawae KW2237 CaM gene for calmodulin, partial sequence
gi|2625187051|dbj|LC710185.1|

Nucleotide
txid9894[Organism] (432)
SRA
Leukoencephalopathy, progressive, infantile-onset, with or without deafness
Leukoencephalopathy, progressive, infantile-onset, with or without deafness

MedGen

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