Intracellular delivery of purine nucleoside phosphorylase (PNP) fused to protein transduction domain corrects PNP deficiency in vitro (Q24300640)

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0070970

Purine nucleoside phosphorylase

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Ana Toro

1

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Melissa Paiva

2

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Cameron Ackerley

3

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Eyal Grunebaum

Reduced thymic output, increased spontaneous apoptosis and oligoclonal B cells in polyethylene glycol-adenosine deaminase-treated patients

4

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language of work or name

English

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publication date

April 2006

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published in

Cellular Immunology

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volume

240

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page(s)

107-15

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issue

2

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cites work

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Adenosine deaminase and purine nucleoside phosphorylase deficiencies: evaluation of therapeutic interventions in eight patients

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Tat peptide-mediated cellular delivery: back to basics

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Involvement of astrocytes in purine-mediated reparative processes in the brain

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A novel TAT-mitochondrial signal sequence fusion protein is processed, stays in mitochondria, and crosses the placenta

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Ability of the Tat basic domain and VP22 to mediate cell binding, but not membrane translocation of the diphtheria toxin A-fragment

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Two novel mutations in a purine nucleoside phosphorylase (PNP)-deficient patient

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Transducible TAT-HA fusogenic peptide enhances escape of TAT-fusion proteins after lipid raft macropinocytosis.

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Purine nucleoside phosphorylase deficiency: improved metabolic and immunologic function with erythrocyte transfusions

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The use of enzyme therapy to regulate the metabolic and phenotypic consequences of adenosine deaminase deficiency in mice. Differential impact on pulmonary and immunologic abnormalities

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The C Terminus of HIV-1 Tat Modulates the Extent of CD178-mediated Apoptosis of T Cells

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Novel mutations and hot-spots in patients with purine nucleoside phosphorylase deficiency

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A technique for ultracryotomy of cell suspensions and tissues

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Purine nucleoside phosphorylase is associated with centrioles and basal bodies

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Mitochondrial basis for immune deficiency. Evidence from purine nucleoside phosphorylase-deficient mice

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Immunoglobulin replacement treatment by rapid subcutaneous infusion

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Control of hyperuricemia in subjects with refractory gout, and induction of antibody against poly(ethylene glycol) (PEG), in a phase I trial of subcutaneous PEGylated urate oxidase

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