Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature-Reference-Cited by-同舟云学术

Diversity in Serine/Threonine Protein Kinase-4 Deficiency and Review of the Literature

Published:2021-10 Issue:10 Volume:9 Page:3752-3766.e4
ISSN:2213-2198
Container-title:The Journal of Allergy and Clinical Immunology: In Practice
language:en
Short-container-title:The Journal of Allergy and Clinical Immunology: In Practice

Author:

Cagdas Deniz^ORCID,Halacli Sevil Oskay,Tan Cagman,Esenboga Saliha,Karaatmaca Betül,Cetinkaya Pınar Gur,Balcı-Hayta Burcu,Ayhan Arzu,Uner Aysegul,Orhan Diclehan,Boztug Kaan,Ozen Seza,Topaloglu Rezan,Sanal Ozden,Tezcan Ilhan

Funder

TÜBİTAK

Publisher

Elsevier BV

Subject

Immunology and Allergy

Reference51 articles.

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2. Cloning and characterization of a member of the MST subfamily of Ste20-like kinases;Creasy;Gene,1995

3. MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival;Nehme;Blood,2012

4. Inherited MST1 deficiency underlies susceptibility to EV-HPV infections;Crequer;PLoS One,2012

5. The phenotype of human STK4 deficiency;Abdollahpour;Blood,2012

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1. Inhibiting endothelial cell Mst1 attenuates acute lung injury in mice;JCI Insight;2024-09-10

2. Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency;Viruses;2024-09-05

3. Epidermodysplasia Verruciformis and Vδ2 γδ T-cell Expansion in STK4 Deficiency;Journal of Clinical Immunology;2024-08-07

4. The Hippo kinases control inflammatory Hippo signaling and restrict bacterial infection in phagocytes;mBio;2024-05-08

5. A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report;Frontiers in Immunology;2024-02-01