Author

Daniëlle Peterse

Boston Children's HospitalORCID 0000-0002-8514-2248Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

Alejandra VerhasseliD· 1 shared Amelie Fassbender· 1 shared Anne E. Lindholm· 1 shared Anne‐Sophie Van RompuyiD· 1 shared Arne Vanhie· 1 shared Ashish Kumar JainiD· 1 shared Dorien F. OiD· 1 shared Fernanda Soares Rasquel-OliveiraiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCell Biology

Alejandra VerhasselORCID

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2 papers

Recent·Most cited

Investigating endometriosis development and endometriosis-related pain over time and in relation to estrogen in a laparoscopic mouse model

Daniëlle Peterse, Alejandra Verhassel, Amelie Fassbender, Dorien F. O, Arne Vanhie, Anne‐Sophie Van Rompuy, Philippa T. K. Saunders, Joris Vriens, Thomas M. D’Hooghe

This study investigates endometriosis development and associated pain in a mouse model, examining the effects of estrogen on lesion progression over time.

bioRxiv · Mar 28, 2024 · PreprintCell Biology

Nociceptor to macrophage communication through CGRP/RAMP1 signaling drives endometriosis-associated pain and lesion growth

Victor Fattori, Tiago H. Zaninelli, Fernanda Soares Rasquel-Oliveira, Olivia K. Heintz, Ashish Kumar Jain, Liang Sun, Maya L. Seshan, Daniëlle Peterse, Anne E. Lindholm, Raymond M. Anchan, Waldiceu Aparecido Verri Jr, Michael S. Rogers

This study identifies CGRP/RAMP1 signaling as a driver of endometriosis pain and lesion growth, showing that blocking this pathway reduces pain and lesion size in mice.

bioRxiv · Aug 28, 2023 · PreprintNeuroscience