Showing items 1 - 17 of 17

Your selections:

Alteration of DNA Methylation and Epigenetic Scores Associated with Features of Schizophrenia and Common Variant Genetic Risk

HLA-DRB1*15:01 and the MERTK Gene Interact to Selectively Influence the Profile of MERTK-Expressing Monocytes in Both Health and MS

Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing

DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes

Evaluation of Cell-Specific Epigenetic Age Acceleration in People With Multiple Sclerosis

Interferon beta treatment is a potent and targeted epigenetic modifier in multiple sclerosis

p53 Dysregulation in Breast Cancer: Insights on Mutations in the TP53 Network and p53 Isoform Expression

Parity is associated with long-term differences in DNA methylation at genes related to neural plasticity in multiple sclerosis

Whole-blood methylation signatures are associated with and accurately classify multiple sclerosis disease severity

Epigenome-wide association studies: current knowledge, strategies and recommendations

Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes

Epigenetic differences at the HTR2A locus in progressive multiple sclerosis patients

Identification of new causative genes in inherited colorectal cancer

Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome

TAPES: A tool for assessment and prioritisation in exome studies

Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

  • 1
  • Disclaimer
  • Privacy
  • Copyright
  • Contact
  • Deposit