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Tafazzin regulates neutrophil maturation and inflammatory response

Abstract Barth syndrome (BTHS) is a rare genetic disease caused by mutations in the TAFAZZIN gene. It is characterized by neutropenia, cardiomyopathy and skeletal myopathy. Neutropenia in BTHS is associated with life-threatening infections, yet there is little understanding of the molecular and phys...

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Gardado en:
Principais autores: Przemysław Zakrzewski, Christopher M Rice, Kathryn Fleming, Drinalda Cela, Sarah J Groves, Fernando M Ponce-Garcia, Willem Gibbs, Kiran Roberts, Tobias Pike, Douglas Strathdee, Eve Anderson, Angela H Nobbs, Ashley M Toye, Colin Steward, Borko Amulic
Formato: Artigo
Idioma:Inglês
Publicado: Springer Nature 2025-02-01
Series:EMBO Reports
Assuntos:
Mitochondria
Neutrophil
Neutropenia
Inflammation
Tafazzin
Acceso en liña:https://doi.org/10.1038/s44319-025-00393-w
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