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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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Corticotropin-releasing hormone deficiency increases allergen-induced airway inflammation in a mouse model of asthma

TL;DR: It is concluded that CRH deficiency disrupts endogenous glucocorticoid production and enhances allergen-induced airway inflammation and lung mechanical dysfunction in mice, which could increase asthma severity in human subjects.
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The Circadian Clock Gene BMAL1 Coordinates Intestinal Regeneration.

TL;DR: The results show that a circadian rhythm in inflammation and regeneration occurs during the gastrointestinal syndrome, and the study and treatment of radiation-induced illnesses, and other gastrointestinal illnesses, should consider 24-hour timing in physiology and pathology.
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Angiotensin II induces coordinated calcium bursts in aldosterone-producing adrenal rosettes.

TL;DR: It is demonstrated that within the rosette, angiotensin II evokes periodic Ca v 3-dependent calcium events that form bursts that are stereotypic in form that define the calcium burst as the fundamental unit of zG layer activity evoked by angiotENSin II and highlight a novel role for the ro sette as a facilitator of cell communication.
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Characterization and Fate of Telomerase-expressing Epithelia during Kidney Repair

TL;DR: The data suggest that cells expressing telomerase reverse transcriptase are not a progenitor-cell population, and they do not play a direct role in kidney repair.
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Primary Human Colonic Mucosal Barrier Crosstalk with Super Oxygen-Sensitive Faecalibacterium prausnitzii in Continuous Culture

TL;DR: This work investigated the effects of an abundant super oxygen-sensitive commensal anaerobe, Faecalibacterium prausnitzii, on a primary human mucosal barrier using a Gut-MIcrobiome (GuMI) physiome platform and identified elevated differentiation and hypoxia-responsive genes and pathways in the platform.