Mechanical counterbalance of kinesin and dynein motors in a microtubular network regulates cell mechanics, 3D architecture, and mechanosensing.
→https://facultyopinions.com/prime/741041131 (July 13, 2022)
Microtubules tune mechanosensitive cell responses..
→ https://www.nature.com/articles/s41563-021-01108-x (Oct 18, 2021
PI4P/PS countertransport by ORP10 at ER-endosome membrane contact sites regulates endosome fission.
→ https://facultyopinions.com/prime/738870648 (Jan 03, 2022)
Phagosome resolution regenerates lysosomes and maintains the degradative capacity in phagocytes
→ https://facultyopinions.com/prime/738870648 (Aug 04, 2021)
mTORC1 activity is supported by spatial association with focal adhesions.
→ https://facultyopinions.com/prime/738870648 (Mar 26, 2021)
ER-resident oxidoreductases are glycosylated and trafficked to the cell surface to promote matrix degradation by tumour cells.
→ https://facultyopinions.com/prime/738870648 (Dec 14, 2020)
Microtubules control cellular shape and coherence in amoeboid migrating cells.
→ https://facultyopinions.com/prime/737915344 (July 27, 2020)
Mechanical regulation of glycolysis via cytoskeleton architecture.
→ https://f1000.com/prime/737356853 (Apr 07, 2020)
Physical principles of membrane shape regulation by the glycocalyx.
→ http://f1000.com/prime/735679550 (Feb 07, 2020)
RAB6 and microtubules restrict protein secretion to focal adhesions.
→ http://f1000.com/prime/735844771 (Oct 15, 2019)
Rhes travels from cell to cell and transports Huntington disease protein via TNT-like protrusion.
→ http://f1000.com/prime/735744963 (May 10, 2019)
LINC complex-Lis1 interplay controls MT1-MMP matrix digest-on-demand response for confined tumor cell migration.
→ http://f1000.com/prime/733499036 (June 22, 2018)
Integrins Form an Expanding Diffusional Barrier that Coordinates Phagocytosis.
→ http://f1000.com/prime/726076896 (Jan 29, 2016)
Repeated ER-endosome contacts promote endosome translocation and neurite outgrowth.
→ http://f1000.com/prime/725428494 (May 05, 2015)
A Trio-Rac1-Pak1 signalling axis drives invadopodia disassembly.
→ http://f1000.com/prime/718415306 (August 13, 2014)
Endosomal WASH and exocyst complexes control exocytosis of MT1-MMP at invadopodia.
→ http://f1000.com/prime/718206068 (April 08, 2014)
The formin Daam1 and fascin directly collaborate to promote filopodia formation.
→ http://f1000.com/prime/718030968 (Nov 04, 2013)
Release of cellular tension signals self-restorative ventral lamellipodia to heal barrier micro-wounds.
→ http://f1000.com/prime/718015756 (July 02, 2013)
An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2.
→ http://f1000.com/prime/717973167 (Mar 19, 2013)
Network analysis of the focal adhesion to invadopodia transition identifies a PI3K-PKCα invasive signaling axis.
→ http://f1000.com/prime/717963449 (Nov 21, 2012)
Actin network architecture can determine myosin motor activity.
→ http://f1000.com/prime/717097853 (Jun 25, 2012)
[CONFERENCE POSTER]: Cortactin controls cell motility and lamellipodial dynamics by regulating ECM secretion.
→ http://f1000.com/prime/13912959 (Jan 20, 2012)
An actin-dependent mechanism for long-range vesicle transport.
→ http://f1000.com/prime/13364977 (Dec 15, 2011)
Mechanosensitive EPLIN-dependent remodeling of adherens junctions regulates epithelial reshaping.
→ http://f1000.com/prime/12817956 (Sept 12, 2011)
Myosin IIA/IIB restrict adhesive and protrusive signaling to generate front-back polarity in migrating cells.
→ http://f1000.com/prime/10064956 (May 3, 2011)
Kinectin-mediated endoplasmic reticulum dynamics supports focal adhesion growth in the cellular lamella.
→ http://f1000.com/prime/6071962 (Nov 11, 2010)
Dissecting the molecular architecture of integrin adhesion sites by cryo-electron tomography.
→ http://f1000.com/prime/4764956 (Aug 18, 2010)