Author

Thierry Capiod

Hôpital Necker-Enfants MaladesORCID 0000-0002-8448-7041Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Cancer Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Aasta Kelly· 1 shared Alistair R. R. ForrestiD· 1 shared Anna ViholaiD· 1 shared Anne‐Sophie ArmandiD· 1 shared Ashirwad MerveiD· 1 shared Bjarne UddiD· 1 shared Chiara L FollandiD· 1 shared Coline Lefèvre· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Aasta Kelly

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

In vitro neuroendocrine differentiation of BPH-1 cells under beta2 adrenergic receptor stimulation

Natascha Pigat, Laura Nalleli Garrido Castillo, Coline Lefèvre, Manon Baurès, Vincent Goffin, Julien Anract, Anne‐Sophie Armand, Thierry Capiod

This study shows that beta2 adrenergic receptor stimulation increases neuroendocrine differentiation and reduces proliferation in BPH-1 cells, suggesting a link between adrenergic signaling and benign prostatic hyperplasia.

bioRxiv · Dec 4, 2024 · PreprintCancer Biology

Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis

Macarena Cabrera‐Serrano, Laure Caccavelli, Marco Savarese, Anna Vihola, Manu E. Jokela, Mridul Johari, Thierry Capiod, Marine Madrange, Enrico Bugiardini, Stefen Brady, Rosaline C. M. Quinlivan, Ashirwad Merve, R. Scalco, David Hilton‐Jones, Henry Houlden, , Gianina Ravenscroft

The paper identifies biallelic loss-of-function OBSCN variants in six patients with severe, recurrent rhabdomyolysis and shows reduced OBSCN expression and impaired SR Ca2+ handling in patient muscle.

Brain · Dec 23, 2021Peer-reviewedGenetics