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May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.. Zusätzlich bieten wir Ihnen MTSS1 Antikörper (72) und viele weitere Produktgruppen zu diesem Protein an.
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Human MTSS1 Protein expressed in Escherichia coli (E. coli) - ABIN2005419
Glassmann, Molly, Surchev, Nazwar, Holst, Hartmann, Baader, Oberdick, Pietsch, Schilling: Developmental expression and differentiation-related neuron-specific splicing of metastasis suppressor 1 (Mtss1) in normal and transformed cerebellar cells. in BMC developmental biology 2008
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Overexpression of MTSS1 reduced BUCC cell proliferation, cell-cycle progression and colony formation, but had no influence on BUCC cell apoptosis.
in contrast to MIM, which is a prototype of I-BAR proteins and does not contain an SH3 domain, IRTKS (zeige BAIAP2L1 Proteine) promoted serum-induced cell migration along with enhanced phosphorylation of mitogen activated kinases Erk1/2 and p38 (zeige CRK Proteine)
this study shows a previously unknown property of MIM that establishes the linkage of protein ubiquitylation with Rab (zeige HRB Proteine)-guided trafficking of CXCR4 (zeige CXCR4 Proteine) in endocytic vesicles
MTSS1 suppressed H1299 cell migration and invasion, and its expression level can be used as a new independent factor for determining the prognosis of non-small cell lung cancer.
MTSS1 is a new authentic target of miR (zeige MLXIP Proteine)-96 in prostate carcinoma.
Down-regulation of MTSS1 expression is associated with lymph node metastasis in Pancreatic Cancer.
Low expression of Mtss1 is associated with Chronic myeloid leukemia (zeige BCL11A Proteine).
MTSS1 plays an essential inhibitory role in the development and progression of ovarian cancers
human breast tumors data sets the MTSS1/p63 (zeige RPE65 Proteine) co-expression is a negative prognostic factor on patient survival, suggesting that the MTSS1/p63 (zeige RPE65 Proteine) axis might be functionally important to regulate breast tumor progression
our findings suggest that MTSS1 might have a context-dependent function and could act as a tumor suppressor, which is pharmacologically targetable in AML (zeige RUNX1 Proteine) patients.
Identify the inverse-BAR (I-BAR) protein MIM/MTSS1 as a nucleator of dendritic spines. MIM accumulated to future spine initiation sites in a PIP2-dependent manner and deformed the plasma membrane outward into a proto-protrusion via its I-BAR domain.
The data demonstrated for the first time an important role for missing-in-metastasis protein in B-cell development. There was a predisposition of missing-in-metastasis-null mice to develop diffuse large B lymphomas.
MTSS1 might be involved in shaping neuronal membranes in vivo.
endogenous MIM protein regulates globally the cell architecture and endocytosis that ultimately influence a variety of cellular behaviors, including cell polarity, motility, receptor signaling and membrane ruffling
MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epithelia.
Results suggest that MIM promotes ciliogenesis by antagonizing Src (zeige SRC Proteine)-dependent phosphorylation of Cortactin (zeige CTTN Proteine) and describe a mechanism linking regulation of the actin cytoskeleton with ciliogenesis and Shh (zeige SHH Proteine) signaling during tissue regeneration.
tissue-specific regulator of cytoskeletal dynamics that interacts with ATP-actin monomers through its C-terminal WH2 domain
Hedgehog (zeige SHH Proteine)-responsive gene MIM cooperates with receptor protein tyrosine phosphatase (zeige PTPRT Proteine)-delta (zeige PTPRD Proteine) to induce cytoskeletal remodeling.
Mtss1 represents a novel signaling pathway from PDGF (zeige PDGFA Proteine) receptor to the actin cytoskeleton via Src (zeige SRC Proteine)-related kinases.
The crystal structures of MIM's IMD and that of its WH2 bound to actin was determined.
morphogenetic pathway involving Daam1 (zeige DAAM1 Proteine) and MIM that transduces non-canonical Wnt (zeige WNT2 Proteine) signaling for the cytoskeletal changes and membrane dynamics required for vertebrate neural tube closure
May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.
metastasis suppressor 1
, metastasis suppressor protein 1
, metastasis suppressor protein 1-like
, metastasis suppressor YGL-1
, missing in metastasis protein
, actin monomer-binding protein