EDITORIAL
Published on 14 Aug 2023
Editorial: Deciphering the etiology of rare genetic disorders associated with protein phosphatases
doi 10.3389/fcell.2023.1241606
- 892 views
- Frontiers in Cell and Developmental Biology
- Molecular and Cellular Pathology
- Research Topics
- Deciphering the Etiology of Rare Genetic Disorders Associated with Protein Phosphatases
Deciphering the Etiology of Rare Genetic Disorders Associated with Protein Phosphatases
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Articles
ORIGINAL RESEARCH
Published on 12 Jun 2023
Quantum-based modeling implies that bidentate Arg89-substrate binding enhances serine/threonine protein phosphatase-2A(PPP2R5D/PPP2R1A/PPP2CA)-mediated dephosphorylation
doi 10.3389/fcell.2023.1141804
- 1,434 views
- 1 citation
ORIGINAL RESEARCH
Published on 28 Mar 2023
A retrospective analysis of phosphatase catalytic subunit gene variants in patients with rare disorders identifies novel candidate neurodevelopmental disease genes
doi 10.3389/fcell.2023.1107930
- 2,902 views
- 2 citations
REVIEW
Published on 23 Jan 2023
Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty?
doi 10.3389/fcell.2022.1051311
- 5,855 views
- 1 citation
ORIGINAL RESEARCH
Published on 30 Nov 2022
Clinical and molecular characteristics of a novel rare de novo variant in PPP2CA in a patient with a developmental disorder, autism, and epilepsy
doi 10.3389/fcell.2022.1059938
- 2,642 views
- 1 citation
REVIEW
Published on 04 Nov 2022
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
doi 10.3389/fcell.2022.1046415
- 3,361 views
- 6 citations
REVIEW
Published on 13 Oct 2022
The role of serine/threonine phosphatases in human development: Evidence from congenital disorders
doi 10.3389/fcell.2022.1030119
- 4,758 views
- 8 citations
Published in
Frontiers in Cell and Developmental Biology
Molecular and Cellular Pathology
Cellular Biochemistry
Participating Journals
Frontiers in Molecular Biosciences
- 3.9 impact factor
- 7.2 citescore