about
The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosisAbcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient miceMechanistic insights into PTS2-mediated peroxisomal protein import: the co-receptor PEX5L drastically increases the interaction strength between the cargo protein and the receptor PEX7Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes.Ether lipid deficiency does not cause neutropenia or leukopenia in mice and men.
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-1257-4522
@en
name
Christoph Wiesinger
@ast
Christoph Wiesinger
@en
Christoph Wiesinger
@es
Christoph Wiesinger
@nl
type
label
Christoph Wiesinger
@ast
Christoph Wiesinger
@en
Christoph Wiesinger
@es
Christoph Wiesinger
@nl
prefLabel
Christoph Wiesinger
@ast
Christoph Wiesinger
@en
Christoph Wiesinger
@es
Christoph Wiesinger
@nl
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P1153
55778454500
P31
P496
0000-0003-1257-4522