Motor areas in the frontal lobe of the primate.

By R. Dum, Peter Strick. Physiology and Behavior, 2002

659 citations recorded by the source corpus.

Subfields: Cognitive Neuroscience, Neurology

View Paper: https://www.semanticscholar.org/paper/c996284d12d68c8a046df5d555da269dd90b3b76

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Citations in the corpus

Human volition: towards a neuroscience of will (2008, background): “However, many of these show similar preferences for voluntary and stimulus-driven actions, suggesting that there is a fundamental distinction in the cortical organization of actio”
Conjoint activity of anterior insular and anterior cingulate cortex: awareness and response (2010, neutral): “The three main cingulate regions are then further subdivided as follows: anterior cingulate is divided into subgenual (sACC) and pregenual (pACC) areas, mid-cingulate into anterior (aMCC) and posterior (pMCC) areas, and posterior cingulate into dorsal (dPCC) and ventral (vPCC) areas (see Fig.”
Dynamic causal modeling of cortical activity from the acute to the chronic stage after stroke (2011, positive): “The premotor cortex within the interhemispheric fissure hosts the supplementary motor area (SMA, macaque area F3), which is engaged in the initiation of movements and sequential movements (Dum and Strick, 2002; Jenkins et al., 2000; Passingham, 1997).”
Emergence of Functional Hierarchy in a Multiple Timescale Neural Network Model: A Humanoid Robot Experiment (2008, background): “Unlike hierarchical connections from the SMA to the PM, and from the PM to the MI, these motor cortices are bidirectionally connected to each other, the majority of them moreover projecting directly to the spinal cord [53,62].”
Modulating cortical connectivity in stroke patients by rTMS assessed with fMRI and dynamic causal modeling (2010, positive): “Studies in both humans and monkeys suggest that the ventral premotor cortex (PMC) is involved in the planning and execution of hand movements (Dum and Strick, 2002; for a review see Schubotz and von Cramon, 2003), while the SMA seems to be more engaged in the temporal organization of movements (Jenk”
Commentary: Cortical activity in the null space: permitting preparation without movement (2017, background): “asked how it was possible that M1 and PMd, known to project to the spinal cord and to each other (Dum and Strick, 2002), modulated their activity in in a timeand direction-dependent manner during the delay but did not induce EMG responses.”
Activation likelihood estimation meta-analysis of motor-related neural activity after stroke (2012, background): “SMA and lateral premotor areas, including vPMC and dPMC, have projections to M1 as well as to the CST and are involved in movement preparation (Dum and Strick, 2002).”
The primate basal ganglia: parallel and integrative networks. (2003, background): “…to be defined by their physiology and connectivity (Kunishio and Haber, 1994; Lu et al., 1994; Dum and Strick, 1996; Matelli and Luppino, 1996; Picard and Strick, 1996; Tanji and Mushiake, 1996; Strick et al., 1998; Schieber, 1999a; Schieber, 1999b; Kakei et al., 2001; Dum and Strick, 2002).”
Biological pattern generation: the cellular and computational logic of networks in motion. (2006, background): “Only a small population of corticospinal cells project monosynaptically to motoneurons in the cervical spinal cord and are thus linked to speciﬁc sets of muscles (Dum and Strick, 2002), the large majority instead targets spinal interneurons.”