User profiles for Christopher C. Oakes
Christopher OakesAssistant Professor, Division of Hematology, Departments of Internal Medicine and … Verified email at osumc.edu Cited by 5675 |
DNA methylation dynamics during B cell maturation underlie a continuum of disease phenotypes in chronic lymphocytic leukemia
Charting differences between tumors and normal tissue is a mainstay of cancer research.
However, clonal tumor expansion from complex normal tissue architectures potentially …
However, clonal tumor expansion from complex normal tissue architectures potentially …
DNMT and HDAC inhibitors induce cryptic transcription start sites encoded in long terminal repeats
Several mechanisms of action have been proposed for DNA methyltransferase and histone
deacetylase inhibitors (DNMTi and HDACi), primarily based on candidate-gene approaches. …
deacetylase inhibitors (DNMTi and HDACi), primarily based on candidate-gene approaches. …
Aging results in hypermethylation of ribosomal DNA in sperm and liver of male rats
There is a concern that increased paternal age may be associated with altered fertility and an
increased incidence of birth defects in man. In previous studies of aged male rats, we have …
increased incidence of birth defects in man. In previous studies of aged male rats, we have …
Evolution of DNA methylation is linked to genetic aberrations in chronic lymphocytic leukemia
Although clonal selection by genetic driver aberrations in cancer is well documented, the
ability of epigenetic alterations to promote tumor evolution is undefined. We used 450k arrays …
ability of epigenetic alterations to promote tumor evolution is undefined. We used 450k arrays …
[HTML][HTML] Drug-perturbation-based stratification of blood cancer
…, M Słabicki, A Mock, CC Oakes… - The Journal of …, 2018 - Am Soc Clin Investig
As new generations of targeted therapies emerge and tumor genome sequencing discovers
increasingly comprehensive mutation repertoires, the functional relationships of mutations …
increasingly comprehensive mutation repertoires, the functional relationships of mutations …
BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence
Prostate cancer is driven by a combination of genetic and/or epigenetic alterations. Epigenetic
alterations are frequently observed in all human cancers, yet how aberrant epigenetic …
alterations are frequently observed in all human cancers, yet how aberrant epigenetic …
[HTML][HTML] Quantitative DNA methylation analysis identifies a single CpG dinucleotide important for ZAP-70 expression and predictive of prognosis in chronic lymphocytic …
Purpose Increased ZAP-70 expression predicts poor prognosis in chronic lymphocytic
leukemia (CLL). Current methods for accurately measuring ZAP-70 expression are problematic, …
leukemia (CLL). Current methods for accurately measuring ZAP-70 expression are problematic, …
High-content screening identifies kinase inhibitors that overcome venetoclax resistance in activated CLL cells
…, Y Shi, S Hariharan, CC Oakes… - Blood, The Journal …, 2016 - ashpublications.org
Novel agents such as the Bcl-2 inhibitor venetoclax (ABT-199) are changing treatment paradigms
for chronic lymphocytic leukemia (CLL) but important problems remain. Although some …
for chronic lymphocytic leukemia (CLL) but important problems remain. Although some …
[HTML][HTML] Outcome prediction by the 2022 European LeukemiaNet genetic-risk classification for adults with acute myeloid leukemia: an Alliance study
Recently, the European LeukemiaNet (ELN) revised its genetic-risk classification of acute
myeloid leukemia (AML). We categorized 1637 adults with AML treated with cytarabine/…
myeloid leukemia (AML). We categorized 1637 adults with AML treated with cytarabine/…
Genomic analysis of hairy cell leukemia identifies novel recurrent genetic alterations
Classical hairy cell leukemia (cHCL) is characterized by a near 100% frequency of the
BRAFV600E mutation, whereas ∼30% of variant HCLs (vHCLs) have MAP2K1 mutations. …
BRAFV600E mutation, whereas ∼30% of variant HCLs (vHCLs) have MAP2K1 mutations. …