Phenotypic Variability in PRKCD: a Review of the Literature-Reference-Cited by-同舟云学术

Phenotypic Variability in PRKCD: a Review of the Literature

Published:2023-10-05 Issue:8 Volume:43 Page:1692-1705
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Jefferson Lucy^ORCID,Ramanan Athimalaipet Vaidyanathan^ORCID,Jolles Stephen^ORCID,Bernatoniene Jolanta,Mathieu Anne-Laure^ORCID,Belot Alexandre^ORCID,Roderick Marion Ruth^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

https://link.springer.com/content/pdf/10.1007/s10875-023-01579-4.pdf

Reference34 articles.

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2. Salzer E, Santos-Valente E, Klaver S, Ban SA, Emminger W, Prengemann NK, et al. B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ. Blood. 2013;121(16):3112–6.

3. Kuehn HS, Niemela JE, Rangel-Santos A, Zhang M, Pittaluga S, Stoddard JL, et al. Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humans. Blood. 2013;121(16):3117–25.

4. Huppi K, Siwarski D, Goodnight J, Mischak H. Assignment of the protein kinase C delta polypeptide gene (PRKCD) to human chromosome 3 and mouse chromosome 14. Genomics. 1994;19(1):161–2.

5. Duquesnes N, Lezoualc’h F, Crozatier B. PKC-delta and PKC-epsilon: foes of the same family or strangers? J Mol Cell Cardiol. 2011;51(5):665–73.

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