Author

D. Maric

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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Immunology· 3 Biochemistry· 2 Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 6 Research Focus:cell type annotation· 3 Research Focus:differential expression· 3 Research Focus:host-pathogen & immune response· 3 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:metabolism & bioenergetics· 2 Organism:mouse· 2

Frequent Co-Authors

T. J. Hope· 3 shared B. S. Mallon· 2 shared K. G. Chen· 2 shared K. Park· 2 shared M. McRaven· 2 shared N. Greco· 2 shared P. G. Robey· 2 shared R. S. Veazey· 2 shared

Activity by Year

2021-2024 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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3 shared papersImmunology

T. J. Hope

Mutual co-authors in cluster

Author profile →

7 papers

Recent·Most cited

Endogenously produced hydrogen cyanide serves as a novel mammalian gasotransmitter

K. Zuhra, M. Petrosino, L. Janickova, T. Vignane, J. Petric, M. Khalaf, T. Philipp, S. Ravani, A. Anand, V. Martins, S. Santos, A. Kieronska-Rudek, T. Majtan, L. Filgueira, D. Maric, , C. Szabo

This study identifies endogenous hydrogen cyanide as a novel gasotransmitter in mammals, showing it regulates mitochondrial function and cell metabolism at optimal levels.

bioRxiv · Jun 3, 2024 · PreprintBiochemistry

Metabolic Quadrivalency in RSeT Human Embryonic Stem Cells

K. G. Chen, K. Park, D. Maric, K. R. Johnson, P. G. Robey, B. S. Mallon

This study identifies a unique metabolic state in RSeT human embryonic stem cells characterized by quadrivalency, linking it to growth independence from oxygen and resistance to naive reprogramming.

bioRxiv · Feb 21, 2024 · PreprintBiochemistry

Resistance to Naive and Formative Pluripotency Conversion in RSeT Human Embryonic Stem Cells

K. G. Chen, K. J. Johnson, K. Park, D. Maric, F. Yang, W. F. Liu, Y. C. Fann, B. S. Mallon, P. G. Robey

This study characterizes a new pluripotent state in RSeT hESCs, showing resistance to naive and formative conversion and distinct transcriptomic and signaling features.

bioRxiv · Feb 16, 2024 · PreprintCell Biology

Single-cell multiomic analysis reveals the involvement of Type I interferon-responsive CD8+ T cells in amyloid beta-associated memory loss

N. Fernando, J. Gopalakrishnan, A. Behensky, L. Reich, C. Liu, V. Bass, M. Bono, W. Montgomery, R. De Pace, M. Mattapallil, V. Nagarajan, S. Brooks, D. Maric, R. Caspi, D. McGavern, H.-Y. Shih

This study identifies a unique CD8+ T cell population in AD mouse brains that contributes to amyloid beta-associated memory loss and shows that reducing these cells improves memory and reduces plaque formation.

bioRxiv · Mar 18, 2023 · PreprintImmunology

Temporal and spatial characterization of HIV/SIV infection at anorectal mucosa using rhesus macaque rectal challenge model

T. J. Hope, D. Maric, L. Corbin, N. Greco, R. Lorenzo-Redondo, M. McRaven, R. S. Veazey

The study investigates HIV/SIV infection in rhesus macaques, identifying early infected cell types and tissue-specific changes in the anorectal mucosa.

bioRxiv · Feb 22, 2023 · PreprintImmunology

Simultaneous in vivo Pharmacokinetics and Pharmacodynamics of TDF Intravaginal Ring during High-dose Vaginal SHIV Challenge in Pigtail Macaques

K. Klotnik Halavaty, A. Ott, D. Maric, J. Su, E. Matias, E. J. Allen, A. Martin, L. E. Pereira, F. Deyounks, J. Smith, P. F. Kiser, T. J. Hope

This study examines TFV distribution and protection efficacy of a TDF IVR in macaques during high-dose SIV challenge, finding uneven TFV distribution and incomplete protection.

bioRxiv · Jun 29, 2021 · PreprintPharmacology & Toxicology

Th17 T cells and immature dendritic cells are the preferential initial targets after rectal challenge with an SIV-based replication-defective dual-reporter vector

T. J. Hope, D. Maric, W. A. Grimm, N. Greco, M. McRaven, A. J. Fought, R. S. Veazey

This study identifies Th17 T cells and immature dendritic cells as the primary initial targets of HIV/SIV rectal transmission using a dual-reporter vector in rhesus macaques.

bioRxiv · Apr 27, 2021Immunology