PEX19

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PEX19

A gene on chromosome 1q23.2 that encodes a peroxin involved in early peroxisomal biogenesis, which acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins.
  
Molecular pathology
PEX19 mutations cause peroxisome biogenesis spectrum disorder, complementation type 14 and a clinical form of Zellweger syndrome.
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75 billion PXF facility and USD400 million PXF facility) and 31 December 2020 (for tranche B under the USD4.
In addition, we compared KBG with PXF, which has been generally considered to have some efficacy on RBC deformability.
4 yrs) were treated with 100 mg of PXF three times daily for 4 weeks (PXF group).
Comparisons of the laboratory data between the non-"oketsu" subgroup and "oketsu" subgroup in the KBG and PXF groups were performed with the use of the Mann-Whitney test.
The PXF group was also divided into two subgroups, the non-"oketsu" group (PXF-NO, n = 6, 68.
On the other hand, there was no significant change in "oketsu" score in the PXF group.
On the other hand, there was no significant change of RBC filtration time in the PXF group.
On the other hand, there was no significant change in intracellular ATP content in the PXF group.
It was reported that PXF improved RBC deformability by increasing the ATP content in RBC (Stefanovich, 1975; Palek, et al.