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Peter J. McKinnon

Researcher at St. Jude Children's Research Hospital

Publications -  122
Citations -  12718

Peter J. McKinnon is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: DNA repair & DNA damage. The author has an hindex of 55, co-authored 117 publications receiving 11630 citations. Previous affiliations of Peter J. McKinnon include American Association For Cancer Research & University of Sydney.

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Puma is an essential mediator of p53-dependent and -independent apoptotic pathways

TL;DR: It is reported that Puma is essential for hematopoietic cell death triggered by ionizing radiation, deregulated c-Myc expression, and cytokine withdrawal, and required for IR-induced death throughout the developing nervous system and accounts for nearly all of the apoptotic activity attributed to p53 under these conditions.
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Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development

TL;DR: It is demonstrated that regionalization of the vertebrate forebrain involves repression of Wnt1 expression by Six3 within the anterior neuroectoderm, and this results support the hypothesis that a Wnt signal gradient specifies posterior fates in the anterior neural plate.
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Phosphorylation of SMC1 is a critical downstream event in the ATM-NBS1-BRCA1 pathway.

TL;DR: It is suggested that many of the abnormal stress responses seen in cells lacking ATM, NBS1, or BRCA1 result from a failure of ATM migration to sites of DNA breaks and a resultant lack of SMC1 phosphorylation.
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Requirement for Atm in Ionizing Radiation-Induced Cell Death in the Developing Central Nervous System

TL;DR: In wild-type, but not Atm-/- mice, up-regulation of p53 coincided with cell death, suggesting that Atn-dependent apoptosis in the CNS is mediated by p53, and p53 null mice showed a similar lack of radiation-induced cell death in the developing nervous system.