Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene family
about
Novel alternatively spliced isoforms of the neurofibromatosis type 2 tumor suppressor are targeted to the nucleus and cytoplasmic granulesSpectrin and ankyrin-based pathways: metazoan inventions for integrating cells into tissuesCytoskeletal protein 4.1G binds to the third intracellular loop of the A1 adenosine receptor and inhibits receptor actionA nonerythroid isoform of protein 4.1R interacts with components of the contractile apparatus in skeletal myofibersA nonerythroid isoform of protein 4.1R interacts with the nuclear mitotic apparatus (NuMA) proteinPIKE GTPase signaling and functionThe prototypical 4.1R-10-kDa domain and the 4.1g-10-kDa paralog mediate fodrin-actin complex formationThe LFA-1-associated molecule PTA-1 (CD226) on T cells forms a dynamic molecular complex with protein 4.1G and human discs largeEssential function of protein 4.1G in targeting of membrane protein palmitoylated 6 into Schmidt-Lanterman incisures in myelinated nervesMitotic regulation of protein 4.1R involves phosphorylation by cdc2 kinaseProtein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities.Lack of protein 4.1G causes altered expression and localization of the cell adhesion molecule nectin-like 4 in testis and can cause male infertility.Similarities and differences in the structure and function of 4.1G and 4.1R135, two protein 4.1 paralogues expressed in erythroid cells.Protein 4.1R links E-cadherin/beta-catenin complex to the cytoskeleton through its direct interaction with beta-catenin and modulates adherens junction integrity.Topographical significance of membrane skeletal component protein 4.1 B in mammalian organs.The membrane-cytoskeletal protein 4.1N is involved in the process of cell adhesion, migration and invasion of breast cancer cellsEvolving concepts in the pathogenesis of hairy-cell leukaemia.Downregulation of protein 4.1R, a mature centriole protein, disrupts centrosomes, alters cell cycle progression, and perturbs mitotic spindles and anaphase.Protein 4.1G Regulates Cell Adhesion, Spreading, and Migration of Mouse Embryonic Fibroblasts through the β1 Integrin Pathway.Kainate receptor post-translational modifications differentially regulate association with 4.1N to control activity-dependent receptor endocytosisThe N-terminal 209-aa domain of high molecular-weight 4.1R isoforms abrogates 4.1R targeting to the nucleus.Impaired intestinal calcium absorption in protein 4.1R-deficient mice due to altered expression of plasma membrane calcium ATPase 1b (PMCA1b).Deciphering the nuclear import pathway for the cytoskeletal red cell protein 4.1R.Cytoskeletal protein 4.1R negatively regulates T-cell activation by inhibiting the phosphorylation of LATAlternatively spliced exon 5 of the FERM domain of protein 4.1R encodes a novel binding site for erythrocyte p55 and is critical for membrane targeting in epithelial cells.Interaction of 4.1G and cGMP-gated channels in rod photoreceptor outer segments.Inhibition of protein 4.1 R and NuMA interaction by mutagenization of their binding-sites abrogates nuclear localization of 4.1 R.Histochemistry and cell biology: the annual review 2010.Insights into the Function of the Unstructured N-Terminal Domain of Proteins 4.1R and 4.1G in Erythropoiesis.Involvement of membrane skeletal molecules in the Schmidt-Lanterman incisure in Schwann cells.Comprehensive characterization of protein 4.1 expression in epithelium of large intestine.4.1G promotes arborization and tight junction formation of oligodendrocyte cell line OLN-93.Increase in cell-surface localization of parathyroid hormone receptor by cytoskeletal protein 4.1G.Molecular and functional characterization of protein 4.1B, a novel member of the protein 4.1 family with high level, focal expression in brain.A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane.Lipid rafts establish calcium waves in hepatocytes.Two distinct domains of protein 4.1 critical for assembly of functional nuclei in vitro.Two protein 4.1 domains essential for mitotic spindle and aster microtubule dynamics and organization in vitro.Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing.Alternative polyadenylation in a family of paralogous EPB41 genes generates protein 4.1 diversity.
P2860
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P2860
Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene family
description
1998 nî lūn-bûn
@nan
1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@ast
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en-gb
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@nl
type
label
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@ast
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en-gb
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@nl
prefLabel
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@ast
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
@en-gb
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
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P2093
P356
P1433
P1476
Cloning and characterization o ...... rotein 4.1 (EPB41) gene family
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P2093
P304
P356
10.1006/GENO.1998.5265
P407
P577
1998-04-15T00:00:00Z