Reduction in mRNA Expression of the Neutrophil Chemoattract Factor CXCL1 in <i>Pseudomonas aeruginosa</i> Treated Barth Syndrome B Lymphoblasts

Barth Syndrome (BTHS) is a rare X-linked genetic disease caused by a mutation in the <i>TAFAZZIN</i> gene, which codes for the protein tafazzin involved in cardiolipin remodeling. Approximately 70% of patients with BTHS exhibit severe infections due to neutropenia. However, neutrophils from BTHS pat...

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Bibliografische gegevens

Hoofdauteurs:	Hana M. Zegallai, Kangmin Duan, Grant M. Hatch
Formaat:	Artigo
Taal:	Inglês
Gepubliceerd in:	MDPI AG 2023-05-01
Reeks:	Biology
Onderwerpen:	Barth Syndrome X-linked genetic disease human B lymphoblasts <i>TAFAZZIN</i> cardiolipin chemokine (C-X-C motif) ligand 1
Online toegang:	https://www.mdpi.com/2079-7737/12/5/730
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