Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients-Reference-Cited by-同舟云学术

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Defective glycosylation leads to defective gp130-dependent STAT3 signaling in PGM3-deficient patients

Published:2019-04 Issue:4 Volume:143 Page:1638-1640.e2
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Ben-Ali Meriem,Ben-Khemis Leila,Mekki Najla,Yaakoubi Roukaya,Ouni Rym,Benabdessalem Chaouki,Ben-Mustapha Imen,Barbouche Mohamed-Ridha

Funder

Tunisian Ministry of Higher Education and Research

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference9 articles.

1. Agm1/Pgm3-mediated sugar nucleotide synthesis is essential for hematopoiesis and development;Greig;Mol Cell Biol,2007

2. Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairment;Zhang;J Allergy Clin Immunol,2014

3. PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia;Stray-Pedersen;Am J Hum Genet,2014

4. Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels;Sassi;J Allergy Clin Immunol,2014

5. A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patients;Ben-Khemis;Mol Immunol,2017

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5. The Human GP130 Cytokine Receptor and Its Expression—an Atlas and Functional Taxonomy of Genetic Variants;Journal of Clinical Immunology;2023-12-22

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