Results 171 to 180 of about 2,907,863 (245)

Case reports in the past, present and future

open access: yesEuropean Journal of Case Reports in Internal Medicine
John G. Kellett
doaj   +1 more source

Diversity Presents in Issue Two

open access: yesJACC: Case Reports, 2019
Julia Grapsa, MD, PhD
doaj   +1 more source

Finding novel vulnerabilities of hypomorphic BRCA1 alleles

open access: yesMolecular Oncology, EarlyView.
Synthetic lethality screens performed to identify novel vulnerabilities often model complete gene loss, thereby overlooking patient‐derived hypomorphic mutations. In this study, we have performed genome‐wide CRISPR screens on BRCA1 hypomorphic mutations, showing BRCA1I26A behaves like wild‐type, while BRCA1R1699Q mimics deficiency. Furthermore, we have
Anne Schreuder   +10 more
wiley   +1 more source

Vision for JACC: Case Reports

open access: yesJACC: Case Reports, 2019
Julia Grapsa, MD, PhD
doaj   +1 more source

MITF maintains genome stability in nonmelanocyte lineages

open access: yesMolecular Oncology, EarlyView.
MITF is essential for melanocyte survival and acts as an oncogene in 10%–20% of melanomas. We show that MITF depletion causes genome instability in nonmelanocytic cells, leading to LATS2‐mediated P53 activation, cell cycle arrest, and apoptosis. This study highlights the role of MITF as a genome maintenance factor beyond the melanocyte lineage. Created
Drifa H. Gudmundsdottir   +13 more
wiley   +1 more source

Voices in Cardiology

open access: yesJACC: Case Reports, 2019
Julia Grapsa, MD, PhD
doaj   +1 more source

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