WAVE2- and microtubule-dependent formation of long protrusions and invasion of cancer cells cultured on three-dimensional extracellular matrices.
about
Invasion of breast cancer cells into collagen matrix requires TGF-α and Cdc42 signalingThe interplay between the proteolytic, invasive, and adhesive domains of invadopodia and their roles in cancer invasionHeading off with the herd: how cancer cells might maneuver supernumerary centrosomes for directional migrationA novel 3D fibril force assay implicates src in tumor cell force generation in collagen networksComparative mechanisms of cancer cell migration through 3D matrix and physiological microtracksMechanical interplay between invadopodia and the nucleus in cultured cancer cellsA microfluidic coculture and multiphoton FAD analysis assay provides insight into the influence of the bone microenvironment on prostate cancer cellsActin, microtubules, and vimentin intermediate filaments cooperate for elongation of invadopodiaClinicopathological significance of the microRNA-146a/WASP-family verprolin-homologous protein-2 axis in gastric cancerImportance of RhoGTPases in formation, characteristics, and functions of invadosomes.Epithelial-mesenchymal transition stimulates human cancer cells to extend microtubule-based invasive protrusions and suppresses cell growth in collagen gel.Mechanobiology of tumor invasion: engineering meets oncology.Normal mammary epithelial cells promote carcinoma basement membrane invasion by inducing microtubule-rich protrusions.Invasive cells in animals and plants: searching for LECA machineries in later eukaryotic lifeDigging a little deeper: the stages of invadopodium formation and maturation.WAVE2 Protein Complex Coupled to Membrane and Microtubules.CLASP1 regulates endothelial cell branching morphology and directed migration.Mesenchymal Cell Invasion Requires Cooperative Regulation of Persistent Microtubule Growth by SLAIN2 and CLASP1.
P2860
Q24317376-655D82D5-CA69-4623-A5CA-B7A894543759Q27003744-02A18934-A4FB-4B72-96A3-6A3667512C7AQ27004734-F5679EB6-7D2C-4758-A4C2-0B8029F20B91Q27335593-04260E3C-205A-4C0B-80C0-03FD1105AC32Q30627878-40770CE2-DBA3-4BD5-B307-42D9BCCD2145Q30633015-EFF70735-F059-425E-B560-B7DE981DE668Q33830268-FC88DF6B-D71C-4FDF-9421-56C1058D6334Q33840016-3941C280-FABD-435B-A04F-E1743DD2D628Q33873278-F09D70DD-0635-4C1E-81DF-42A4A3BE058AQ33968821-CBF93F7D-6549-4A19-97BC-B4A914F5E1D1Q34541763-23016C8A-209F-4F48-95EF-CAB6F6E49D60Q35877893-5EB6ABF6-CC83-456D-9779-5000F0CA1049Q36544928-23DD0F90-80E0-48CC-932D-58764401B4D9Q36874387-62586611-0682-4CAE-8716-BD6E5ED84FA7Q38239028-668CE873-DC1F-4E22-9E03-3B4494943C33Q40793196-6A220E8E-9C54-43DD-B319-E9A704681061Q43660809-BF770C24-2C91-4948-9804-3ADB1B5889E7Q46816570-1D3DCB7A-26E2-42B5-BCC5-26A0FE4524CB
P2860
WAVE2- and microtubule-dependent formation of long protrusions and invasion of cancer cells cultured on three-dimensional extracellular matrices.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@en
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@nl
type
label
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@en
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@nl
prefLabel
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@en
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@nl
P2860
P1433
P1476
WAVE2- and microtubule-depende ...... sional extracellular matrices.
@en
P2093
Kazuhide Takahashi
Keiji Kikuchi
P2860
P304
P356
10.1111/J.1349-7006.2008.00927.X
P577
2008-09-15T00:00:00Z