Author

H. True

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· 2 Biochemistry· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

B. M. Doratt· 2 shared C. C. Weihl· 2 shared I. Messaoudi· 2 shared M. Rincon· 2 shared N. E. Marshall· 2 shared A. Bhadra· 1 shared A. K. Bhadra· 1 shared A. R. Findlay· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

B. M. Doratt

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Mild/Asymptomatic Maternal SARS-CoV-2 Infection Leads to Immune Paralysis in Fetal Circulation and Immune Dysregulation in Fetal-Placental Tissues

B. M. Doratt, S. Sureshchandra, H. True, M. Rincon, N. E. Marshall, I. Messaoudi

This study examines the effects of mild maternal SARS-CoV-2 infection on fetal immune responses, finding altered inflammatory mediators and immune cell activation in cord blood and placental tissues.

bioRxiv · May 10, 2023 · PreprintImmunology

SARS-CoV-2 Vaccine Booster Elicits Robust Prolonged Maternal Antibody Responses and Passive Transfer Via The Placenta And Breastmilk

N. E. Marshall, M. B. Blanton, B. M. Doratt, D. C. Malherbe, M. Rincon, H. True, T. McDonald, C. Beauregard, R. Adatorwovor, I. Messaoudi

This study evaluates maternal SARS-CoV-2 vaccine antibody responses in circulation and breastmilk, showing that boosters increase antibody levels for passive transfer to newborns.

bioRxiv · Nov 29, 2022 · PreprintImmunology

Myopathy mutations in DNAJB6 slow conformer specific substrate processing that is rescued by NEF modulation

A. K. Bhadra, M. J. Rau, J. A. Daw, J. A. J. Fitzpatrick, C. C. Weihl, H. True

This study identifies how LGMDD1 mutations in DNAJB6 disrupt chaperone function and shows that modulating NEF can rescue substrate processing defects.

bioRxiv · Dec 22, 2021 · PreprintBiochemistry

Inhibition of DNAJ-HSP70 interaction improves strength in muscular dystrophy

R. Bengoechea, A. R. Findlay, A. Bhadra, H. Shao, K. Stein, S. K. Pittman, J. Daw, J. Gestwicki, H. True, C. C. Weihl

This study shows that inhibiting DNAJ-HSP70 interaction improves muscle strength in LGMD1D by re-mobilizing HSP70 and correcting myopathology.

bioRxiv · Jan 3, 2020Cell Biology