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David T. Breault

Researcher at Boston Children's Hospital

Publications -  117
Citations -  5335

David T. Breault is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Stem cell & Biology. The author has an hindex of 30, co-authored 92 publications receiving 4040 citations. Previous affiliations of David T. Breault include University of Connecticut Health Center & Harvard University.

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Telomerase Reverse Transcriptase Expression in Mouse Endometrium During Reepithelialization and Regeneration in a Menses-Like Model

TL;DR: This study investigates the expression pattern of a green fluorescent protein (GFP) reporter for mTert promoter activity (mTert-GFP), which may play a role in immune cell regulated repair in endometrial regeneration following a menses-like event.
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Factors regulating quiescent stem cells: insights from the intestine and other self-renewing tissues.

TL;DR: The regulatory mechanisms underlying the quiescent state include factors essential for cell cycle control, stress response and survival pathways, developmental signalling pathways, and post-transcriptional modulation as discussed by the authors, and these regulatory mechanisms citing observations from the intestine and other self-renewing tissues.
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Tacrolimus-binding protein FKBP8 directs myosin light chain kinase-dependent barrier regulation and is a potential therapeutic target in Crohn’s disease

TL;DR: Binding to FKBP8, which can be blocked by tacrolimus, is required for MLCK1 recruitment to intercellular junctions and downstream events leading to immune-mediated barrier loss.
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Sex Differences in Adrenal Bmal1 Deletion–Induced Augmentation of Glucocorticoid Responses to Stress and ACTH in Mice

TL;DR: Gene analysis showed increased expression of adrenal genes in female SCC-KO mice involved in cell cycle control, cell adhesion-extracellular matrix interaction and ligand receptor activity that could promote steroid production.
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International workshop: radiation effects on mutation in somatic and germline stem cells.

TL;DR: Stem cells and their niche have become much better characterized in recent years, and their radiation response can be elucidated in detail in experimental systems to help underpin both protection and therapeutic recommendations established from human epidemiological evidence.