Sara Trimidal
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View article: Itaconate promotes the differentiation of murine stress erythroid progenitors by increasing Nrf2 activity
Itaconate promotes the differentiation of murine stress erythroid progenitors by increasing Nrf2 activity Open
View article: Itaconate promotes the differentiation of murine stress erythroid progenitors by increasing Nrf2 activity
Itaconate promotes the differentiation of murine stress erythroid progenitors by increasing Nrf2 activity Open
Steady state erythropoiesis produces new erythrocytes at a constant rate to replace senescent erythrocytes removed in the spleen and liver. Inflammation caused by infection or tissue damage skews bone marrow hematopoiesis, increasing myelo…
View article: Nitric oxide regulates metabolism in murine stress erythroid progenitors to promote recovery during inflammatory anemia
Nitric oxide regulates metabolism in murine stress erythroid progenitors to promote recovery during inflammatory anemia Open
Inflammation skews bone marrow hematopoiesis increasing the production of myeloid effector cells at the expense of steady-state erythropoiesis. A compensatory stress erythropoiesis response is induced to maintain homeostasis until inflamma…
View article: XRCC4 and MRE11 Roles and Transcriptional Response to Repair of TALEN-Induced Double-Strand DNA Breaks
XRCC4 and MRE11 Roles and Transcriptional Response to Repair of TALEN-Induced Double-Strand DNA Breaks Open
Double-strand breaks (DSB) are one of the most lethal forms of DNA damage that, if left unrepaired, can lead to genomic instability, cellular transformation, and cell death. In this work, we examined how repair of transcription activator-l…
View article: Robust Transcriptional Regulatory Response Upon Blocking NHEJ
Robust Transcriptional Regulatory Response Upon Blocking NHEJ Open
Double strand breaks are one of the most lethal forms of DNA lesions that, if left unrepaired can lead to genomic instability, cellular transformation, and cell death. However, cells have two main machineries namely error prone Non homolog…
View article: BioEssays 12/2019
BioEssays 12/2019 Open
Gene editing with engineered nucleases introduce double-strand breaks that are repaired by error-prone nonhomologous end-joining (NHEJ). In article number 1900126, Sara G. Trimidal et al. propose that the length and type or resulting indel…
View article: Can Designer Indels Be Tailored by Gene Editing?
Can Designer Indels Be Tailored by Gene Editing? Open
Genome editing with engineered nucleases (GEENs) introduce site‐specific DNA double‐strand breaks (DSBs) and repairs DSBs via nonhomologous end‐joining (NHEJ) pathways that eventually create indels (insertions/deletions) in a genome. Wheth…