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Welcome to the Forscher Lab Publications
Page! Below you will find the publications of the Forscher Lab and
collaborators. Each reference has a link to the NCBI PubMed
reference report. Medeiros
NA, Burnette DT, Forscher P. Myosin II functions in actin-bundle turnover in
neuronal growth cones. Suter DM, Schaefer AW, Forscher P. Microtubule dynamics are necessary for SRC
family kinase-dependent growth cone steering. Zhang XF, Schaefer AW, Burnette DT, Schoonderwoert VT, Forscher P. Rho-dependent contractile responses in the
neuronal growth cone are independent of classical peripheral retrograde actin
flow. Rodriguez OC, Schaefer AW, Mandato CA, Forscher P, Bement WM, Waterman-Storer CM. Conserved microtubule-actin interactions in
cell movement and morphogenesis. Nakhost A, Kabir N, Forscher P, Sossin WS. Protein kinase C isoforms are translocated to
microtubules in neurons. Filopodia and actin arcs guide
the assembly and transport of two populations of microtubules with unique
dynamic parameters in neuronal growth cones Transmission of growth cone
traction force through apCAM-cytoskeletal linkages is regulated by Src family
tyrosine kinase activity. Protein kinase C activation
promotes microtubule advance in neuronal growth cones by increasing average
microtubule growth lifetimes. Substrate-cytoskeletal coupling
as a mechanism for the regulation of growth cone motility and guidance. Localization of unconventional
myosins V and VI in neuronal growth cones. A diffusion barrier maintains
distribution of membrane proteins in polarized neurons. Binding of protein kinase C
isoforms to actin in Aplysia. The Ig superfamily cell adhesion
molecule, apCAM, mediates growth cone steering by substrate-cytoskeletal
coupling. An emerging link between
cytoskeletal dynamics and cell adhesion molecules in growth cone guidance. Myosin drives retrograde F-actin
flow in neuronal growth cones. An Aplysia cell adhesion molecule
associated with site-directed actin filament assembly in neuronal growth
cones. Myosin drives retrograde F-actin
flow in neuronal growth cones. In vitro motility of
immunoadsorbed brain myosin-V using a Limulus acrosomal process and optical
tweezer-based assay. Growth cone advance is inversely
proportional to retrograde F-actin flow. Cytoskeletal reorganization
underlying growth cone motility. Cyclic AMP modulates fast axonal
transport in Aplysia bag cell neurons by increasing the probability of single
organelle movement. Brain myosin-V is a two-headed
unconventional myosin with motor activity. In vitro motilities of the
unconventional myosins, brush border myosin-I, and chick brain myosin-V
exhibit assay-dependent differences in velocity. Calcium-calmodulin
and regulation of brush border myosin-I MgATPase
and mechanochemistry. A motility in the eukaryotic
flagellum unrelated to flagellar beating. Cytoskeletal remodeling during growth
cone-target interactions. A novel cytoskeletal structure involved
in purse string wound closure and cell polarity maintenance. Novel form of growth cone
motility involving site-directed actin filament assembly. Calcium and polyphosphoinositide
control of cytoskeletal dynamics. Actions of cytochalasins on the
organization of actin filaments and microtubules in a neuronal growth cone. Cyclic AMP induces changes in
distribution and transport of organelles within growth cones of Aplysia bag
cell neurons. Noradrenaline
modulates calcium channels in avian dorsal root ganglion cells through tight
receptor-channel coupling. Modulation of calcium channels by
norepinephrine in internally dialyzed avian sensory
neurons. |
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