
Moesin - Wikipedia
Moesin (for membrane-organizing extension spike protein) is a member of the ERM protein family which includes ezrin and radixin. ERM proteins appear to function as cross-linkers between plasma membranes and actin -based cytoskeletons .
Activation of Moesin, a Protein That Links Actin Cytoskeleton to …
To elucidate the structural basis of possible mechanisms, we generated informative moesin mutations and tested three attributes: membrane localization of the expressed moesin, moesin binding to PIP2, and PIP2-induced release of moesin autoinhibition.
MSN Gene - GeneCards | MOES Protein | MOES Antibody
2025年3月30日 · MSN (Moesin) is a Protein Coding gene. Diseases associated with MSN include Immunodeficiency 50 and Verrucous Carcinoma. Among its related pathways are Sensory processing of sound and Interleukin-12 family signaling. Gene Ontology (GO) annotations related to this gene include protein kinase binding and actin binding.
Moesin, an Ezrin/Radixin/Moesin Family Member, Regulates …
Background and aims: Moesin, an ezrin/radixin/moesin family member, is involved in the regulation of cell adhesion, polarity, and migration by cross-linking between the actin cytoskeleton and plasma membrane.
Moesin is an effector of tau-induced actin overstabilization, cell ...
Moesin, an EMT driver, is elevated in cells harboring disease-associated phosphotau, over-stabilized actin, and ectopic cell cycle activation. We further find that genetic manipulation of Moesin mediates tau-induced neurodegeneration. Taken together, our study identifies novel parallels between tauopathy and cancer.
Moesin, an ERM family member, regulates hepatic fibrosis
Moesin, an ezrin-radixin-moesin (ERM) family member, is involved in the regulation of cell adhesion, polarity and migration by cross-linking between the actin cytoskeleton and plasma membrane. The primary effector cell in hepatic fibrosis is the ...
Actin dynamics in the regulation of endothelial barrier functions …
Moesin. Moesin is an ABP involved in paracellular gap formation but also in wound healing by inducing cell migration in HUVEC . Proteomic analysis of HUVEC after stimulation with LPS for 24 h revealed that moesin was secreted into supernatants . Notably, moesin levels also increased in a time-dependent fashion in sera of mice with lethal sepsis ...
Moesin deficiency | Immune Deficiency Foundation
Moesin deficiency is an X-linked immunodeficiency associated with lymphopenia, neutropenia, and recurrent bacterial infections. Prolonged or severe varicella virus infections have been described in several affected individuals.
Moesin - an overview | ScienceDirect Topics
Moesin is a cytoskeletal protein that belongs to the ezrin-radixin-moesin family. It is primarily expressed in lymphocytes and is involved in maintaining cell shape. Mutations in the moesin gene can cause Moesin Deficiency, a combined immunodeficiency disorder characterized by T cell lymphopenia, hypogammaglobulinemia, antibody deficiency, and ...
The ERM protein moesin regulates natural killer cell ... - PubMed
2021年11月21日 · Moesin is a member of the ezrin-radixin-moesin (ERM) family of proteins that link plasma membrane proteins with actin filaments in the cell cortex. Hemizygous mutations in the X-linked moesin gene are associated with primary immunodeficiency with T and B cell lymphopenia, which also affects natural …