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Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-ox...

Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-ox...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A759254671

Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-oxidation deficiencies

About this item

Full title

Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-oxidation deficiencies

Publisher

Public Library of Science

Journal title

PloS one, 2023-08, Vol.18 (8), p.e0289285

Language

English

Formats

Publication information

Publisher

Public Library of Science

More information

Scope and Contents

Contents

Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal disease of hematopoietic cells with a variable clinical spectrum characterized by intravascular hemolysis, high risk of thrombosis, and cytopenias. To understand the biochemical shifts underlying PNH, this study aimed to search for the dysfunctional pathways involved in PNH physiopathology by co...

Alternative Titles

Full title

Biochemical phenotyping of paroxysmal nocturnal hemoglobinuria reveals solute carriers and [beta]-oxidation deficiencies

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A759254671

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A759254671

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0289285

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