Author

M. Tremblay

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 1 Immunology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:host-pathogen & immune response· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

A. Bergeron· 1 shared A. Kumar· 1 shared A. Schmidt· 1 shared B. Boivin· 1 shared B. G. Allen· 1 shared C. F. Rose· 1 shared D. P. Labbe· 1 shared E. Cassol· 1 shared

Activity by Year

2019-2019 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperCell Biology

A. Bergeron

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Protein Tyrosine Phosphatase 1B Regulates MicroRNA-208b-Argonaute 2 Association and Thyroid Hormone Responsiveness in Cardiac Hypertrophy

G. Coulis, Y. Shi, D. P. Labbe, A. Bergeron, F. Sahmi, V. Vinette, G. Karsenty, B. G. Allen, M. Tremblay, J.-C. Tardif, B. Boivin

This study shows that PTP1B inactivation disrupts miR-208b-Argonaute 2 interaction, leading to increased THRAP1 expression and thyroid hormone-induced cardiac hypertrophy.

bioRxiv · Sep 10, 2019 · PreprintCell Biology

An investigation of PS-b-PEO polymersomes for the oral treatment and diagnosis of hyperammonemia

S. Matoori, Y. Bao, A. Schmidt, E. J. Fischer, R. Ochoa-Sanchez, M. Tremblay, M. Oliveira, C. F. Rose, J.-C. Leroux

This paper investigates polymersomes for oral treatment and diagnosis of hyperammonemia, finding they do not reduce ammonia levels in rats but can detect ammonia via pH changes.

bioRxiv · May 8, 2019Pharmacology & Toxicology

Inhibitor of apoptosis, IAP, genes play a critical role in the survival of HIV-infected macrophages

A. Kumar, R. E. H. Caballero, S. X. M. Dong, N. Gajanayaka, H. Ali, E. Cassol, W. Cameron, R. Korneluk, M. Tremblay, J. Angel

This study shows that SMAC-mimetics induce apoptosis in HIV-infected macrophages by targeting IAPs, suggesting IAP modulation as a strategy for eliminating viral reservoirs.

bioRxiv · Feb 6, 2019 · PreprintImmunology