14390 results for ""Pennsylvania+German"+ACS+study+'Socius'+open+access"

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• Nasal brushes analysis

  scRNA-seq samples from healthy and asthma donors part 1.

  Study EGAS00001006657

• ORIENT study

  scRNAseq dataset containing 5 healthy donors and 4 asthmatic donors.

  Dataset EGAD00001009687

• IRF5 HL RNASeq dataset

  bam files associated with the study EGAS00001001205

  Dataset EGAD00001001417

• Pipeline study - RNAseq dataset

  Fernandez-Cuesta et al., RNAseq data Pipline

  Dataset EGAD00001000746

• Reference epigenome OB56_N_PreA_WGBS data generated from KEP study

  A OB56_N_PreA_WGBS paired end data for Preadipocytes(fat)

  Dataset EGAD00001003479

• Melanoma multi site metastases

  These are caveman, pindel, battenberg and brass calls for index patients' metastatic melanoma genomes within this study.

  Dataset EGAD00001005483

• PTA_thyroid__RNA_

  Exploring the somatic mutations in single cells derived from the thyroid

  Study EGAS00001007946

• PTA__thyroid_

  Investigation into thyroid pathologies utilising single cell/nuclei genome sequencing.

  Study EGAS00001007833

• Whole exome sequencing of soft tissue sarcoma

  We characterized genomic alterations of soft tissue sarcoma.

  Study EGAS50000001673

• Offspring Sex Impacts DNA Methylation and Gene Expression in Placentae from Women with Diabetes during Pregnancy

  Exposure to diabetes in utero is known to increase the offspring's likelihood of developing metabolic disease in adulthood, but the mechanisms involved are unknown. It has been proposed that early exposure to hyperglycemia and elevated insulin levels may lead to malprogramming of the fetus leading to the subsequent development of diabetes and obesity. Epigenetic modifications of the genome including DNA methylation, provide a plausible mechanism that allows for permanent propagation of gene activity states from one generation of cells to the next. The placenta, a fetal tissue easily accessible for study, is a complex organ that is essential in regulating fetal growth. The changes in placental nutrient transport associated with diabetes during pregnancy (DDP) have significant effects on the developing fetus, indicating that the placenta plays a critical role in fetal programming. The aim of our study was to investigate whether exposure to DDP alters genome-wide DNA methylation in the placenta obtained from term pregnancies resulting in differentially methylated loci of metabolically relevant genes and downstream changes in RNA and protein expression.

  Study phs001535