Author

D. Laudier

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· 2 Bioengineering· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Assay:imaging· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

A. Hecht· 2 shared J. C. Iatridis· 2 shared J. Gansau· 2 shared A. Garcia-Ortiz· 1 shared A. Lai· 1 shared A. Seifert· 1 shared C. Fu· 1 shared C. Liu· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersBioengineering

A. Hecht

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Novel Approach for Refractive Index Matching in Calcified Tissues

D. Laudier, M. Mora-Antionette, A. Garcia-Ortiz, K. J. Lewis

This paper introduces a modified BABB clearing protocol to improve imaging of calcified tissues by addressing their opacity and rigidity.

bioRxiv · Jul 23, 2024 · PreprintCell Biology

TNFR1-mediated senescence and lack of TNFR2-signaling limit human intervertebral disc cell repair in back pain conditions

J. Gansau, E. Grossi, L. Rodriguez, M. Wang, D. Laudier, S. Chaudhary, A. Hecht, W. Fu, R. Sebra, C. Liu, J. C. Iatridis

This study identifies TNFR1-mediated senescence and limited TNFR2 signaling as barriers to intervertebral disc cell repair in back pain, suggesting immunomodulation as a therapeutic strategy.

bioRxiv · Feb 22, 2024 · PreprintBioengineering

Lumbar endplate microfracture injury induces Modic-like changes, intervertebral disc degeneration and spinal cord sensitization-An In Vivo Rat Model

D. Wang, A. Lai, J. Gansau, A. Seifert, J. Munitz, K. Zaheer, N. Bhadouria, Y. Lee, P. Nasser, D. Laudier, N. Holguin, A. Hecht, J. C. Iatridis

bioRxiv · Jan 27, 2023Pathology

Wnt7a Suppresses Adipogenesis of Skeletal Muscle Mesenchymal Stem Cells and Fatty Infiltration Through the Alternative Wnt-Rho-YAP/TAZ Signaling Axis

C. Fu, M. Guzman-Seda, D. Laudier, W. M. Han

This study shows Wnt7a inhibits adipogenesis of fibro-adipogenic progenitors and reduces fatty infiltration in muscle through the Wnt-Rho-YAP/TAZ signaling pathway.

bioRxiv · Jun 30, 2022Cell Biology