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Changes in descending motor pathway connectivity after corticospinal tract lesion in macaque monkey

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Multi-segmental innervation of single pontine reticulospinal axons in the cervico-thoracic region of the cat: Anterograde PHA-L tracing study

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Morphology of single pontine reticulospinal axons in the lumbar enlargement of the cat: A study using the anterograde tracer PHA-L

inferredcites →https://doi.org/10.1002/ana.410040308openalex-snapshot

A Behavioral analysis of complete unilateral section of the pyramidal tract at the medullary level in macaca mulatta

inferredcites →https://doi.org/10.1002/cne.21438openalex-snapshot

Localization of arm representation in the cerebral peduncle of the non‐human primate

inferredcites →https://doi.org/10.1002/cne.21940openalex-snapshot

Extensive spinal decussation and bilateral termination of cervical corticospinal projections in rhesus monkeys

inferredcites →https://doi.org/10.1002/cphy.cp010213openalex-snapshot

Anatomy of the Descending Pathways

inferredcites →https://doi.org/10.1006/nimg.1996.0036openalex-snapshot

A Stereotaxic Template Atlas of the Macaque Brain for Digital Imaging and Quantitative Neuroanatomy

inferredcites →https://doi.org/10.1007/bf00231167openalex-snapshot

Reorganisation of descending motor pathways in patients after hemispherectomy and severe hemispheric lesions demonstrated by magnetic brain stimulation

inferredcites →https://doi.org/10.1007/bf00236284openalex-snapshot

Integration in descending motor pathways controlling the forelimb in the cat

inferredcites →https://doi.org/10.1007/bf00237170openalex-snapshot

Effects of unilateral and bilateral pyramidotomy on a conditioned rapid precision grip in monkeys (Macaca fascicularis)

inferredcites →https://doi.org/10.1007/bf00237494openalex-snapshot

Integration in descending motor pathways controlling the forelimb in the cat

inferredcites →https://doi.org/10.1007/bf00238019openalex-snapshot

Patterns of projection and branching of reticulospinal neurons

inferredcites →https://doi.org/10.1007/s00221-006-0374-1openalex-snapshot

Bilateral actions of the reticulospinal tract on arm and shoulder muscles in the monkey: stimulus triggered averaging

inferredcites →https://doi.org/10.1016/0006-8993(72)90770-6openalex-snapshot

Unilateral pyramidotomy in monkeys: Effect on force and speed of a conditioned precision grip

inferredcites →https://doi.org/10.1016/0013-4694(82)90003-7openalex-snapshot

Recovery of function following unilateral lesions of the bulbar pyramid in the monkey

inferredcites →https://doi.org/10.1016/j.neuroscience.2010.10.007openalex-snapshot

Quantitative inter-segmental and inter-laminar comparison of corticospinal projections from the forelimb area of the primary motor cortex of macaque monkeys

inferredcites →https://doi.org/10.1038/nn.2691openalex-snapshot

Extensive spontaneous plasticity of corticospinal projections after primate spinal cord injury

inferredcites →https://doi.org/10.1038/nn1195openalex-snapshot

The injured spinal cord spontaneously forms a new intraspinal circuit in adult rats

inferredcites →https://doi.org/10.1073/pnas.0602933103openalex-snapshot

Muscle representation in the macaque motor cortex: An anatomical perspective

inferredcites →https://doi.org/10.1093/brain/118.2.495openalex-snapshot

Abnormal muscle coactivation patterns during isometric torque generation at the elbow and shoulder in hemiparetic subjects

inferredcites →https://doi.org/10.1093/brain/120.9.1579openalex-snapshot

Reorganization of motor output in the non-affected hemisphere after stroke

inferredcites →https://doi.org/10.1093/brain/63.1.36openalex-snapshot

PYRAMIDAL LESION IN THE MONKEY

inferredcites →https://doi.org/10.1093/brain/74.4.443openalex-snapshot

THE RESTORATION OF MOTOR FUNCTION FOLLOWING HEMIPLEGIA IN MAN

inferredcites →https://doi.org/10.1093/brain/78.2.248openalex-snapshot

LONG DESCENDING TRACTS IN MAN

inferredcites →https://doi.org/10.1093/brain/91.1.1openalex-snapshot

THE FUNCTIONAL ORGANIZATION OF THE MOTOR SYSTEM IN THE MONKEY

inferredcites →https://doi.org/10.1093/brain/91.1.15openalex-snapshot

THE FUNCTIONAL ORGANIZATION OF THE MOTOR SYSTEM IN THE MONKEY

inferredcites →https://doi.org/10.1093/brain/awg088openalex-snapshot

Changes in propriospinally mediated excitation of upper limb motoneurons in stroke patients

inferredcites →https://doi.org/10.1093/brain/awg145openalex-snapshot

Neural correlates of outcome after stroke: a cross‐sectional fMRI study

inferredcites →https://doi.org/10.1093/brain/awg245openalex-snapshot

Neural correlates of motor recovery after stroke: a longitudinal fMRI study

inferredcites →https://doi.org/10.1097/00001756-200112210-00005openalex-snapshot

Sequential activation brain mapping after subcortical stroke: changes in hemispheric balance and recovery

inferredcites →https://doi.org/10.1111/j.1469-7793.1998.191bi.xopenalex-snapshot

Does a C3‐C4 propriospinal system transmit corticospinal excitation in the primate? An investigation in the macaque monkey

inferredcites →https://doi.org/10.1113/expphysiol.1993.sp003686openalex-snapshot

The G. L. Brown Prize Lecture. Cortical control of the primate hand

inferredcites →https://doi.org/10.1113/jphysiol.1970.sp009091openalex-snapshot

Early facilitation at corticomotoneuronal synapses

inferredcites →https://doi.org/10.1113/jphysiol.1991.sp018464openalex-snapshot

Pattern of cutaneous inhibition of the propriospinal‐like excitation to human upper limb motoneurones.

inferredcites →https://doi.org/10.1113/jphysiol.2003.048009openalex-snapshot

Both dorsal horn and lamina VIII interneurones contribute to crossed reflexes from feline group II muscle afferents

inferredcites →https://doi.org/10.1113/jphysiol.2011.215160openalex-snapshot

The primate reticulospinal tract, hand function and functional recovery

inferredcites →https://doi.org/10.1126/science.1147243openalex-snapshot

Time-Dependent Central Compensatory Mechanisms of Finger Dexterity After Spinal Cord Injury

inferredcites →https://doi.org/10.1152/jn.00342.2004openalex-snapshot

Dexterous Finger Movements in Primate Without Monosynaptic Corticomotoneuronal Excitation

inferredcites →https://doi.org/10.1152/jn.00342.2006openalex-snapshot

Descending Signals From the Pontomedullary Reticular Formation Are Bilateral, Asymmetric, and Gated During Reaching Movements in the Cat

inferredcites →https://doi.org/10.1152/jn.1991.66.6.1965openalex-snapshot

Facilitation and suppression of wrist and digit muscles from single rubromotoneuronal cells in the awake monkey

inferredcites →https://doi.org/10.1152/jn.1999.82.6.3580openalex-snapshot

Disynaptic Pyramidal Excitation in Forelimb Motoneurons Mediated Via C 3 –C 4 Propriospinal Neurons in the Macaca fuscata

inferredcites →https://doi.org/10.1152/jn.2000.83.5.3147openalex-snapshot

Plasticity in the Distribution of the Red Nucleus Output to Forearm Muscles After Unilateral Lesions of the Pyramidal Tract

inferredcites →https://doi.org/10.1152/jn.2001.86.4.1573openalex-snapshot

Investigation Into Non-Monosynaptic Corticospinal Excitation of Macaque Upper Limb Single Motor Units

inferredcites →https://doi.org/10.1161/01.str.0000165922.96430.d0openalex-snapshot

Active Finger Extension Predicts Outcomes After Constraint-Induced Movement Therapy for Individuals With Hemiparesis After Stroke

inferredcites →https://doi.org/10.1161/01.str.28.12.2518openalex-snapshot

A Functional MRI Study of Subjects Recovered From Hemiparetic Stroke

inferredcites →https://doi.org/10.1161/01.str.31.3.656openalex-snapshot

Evolution of Cortical Activation During Recovery From Corticospinal Tract Infarction

inferredcites →https://doi.org/10.1161/01.str.31.6.1360openalex-snapshot

Chronic Motor Dysfunction After Stroke

inferredcites →https://doi.org/10.1177/1073858408331375openalex-snapshot

Compensatory Changes at the Cerebral Cortical Level after Spinal Cord Injury

inferredcites →https://doi.org/10.1371/journal.pone.0014430openalex-snapshot

Carbocyanine Dye Usage in Demarcating Boundaries of the Aged Human Red Nucleus

inferredcites →https://doi.org/10.1523/jneurosci.0040-07.2007openalex-snapshot

Bilateral Spike-Triggered Average Effects in Arm and Shoulder Muscles from the Monkey Pontomedullary Reticular Formation

inferredcites →https://doi.org/10.1523/jneurosci.0257-11.2011openalex-snapshot

Lack of Evidence for Direct Corticospinal Contributions to Control of the Ipsilateral Forelimb in Monkey

inferredcites →https://doi.org/10.1523/jneurosci.3720-08.2009openalex-snapshot

Direct and Indirect Connections with Upper Limb Motoneurons from the Primate Reticulospinal Tract

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Terminal distribution of the corticospinal projection from the hand/arm region of the primary motor cortex to the cervical enlargement in rhesus monkey

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Frontal and frontoparietal injury differentially affect the ipsilateral corticospinal projection from the nonlesioned hemisphere in monkey ( Macaca mulatta )

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Long-term forced-use therapy after sensorimotor cortex lesions restores contralesional hand function and promotes its preference in Macaca mulatta

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Changes in the location of cortico-muscular coherence following stroke

inferred← citeshttps://doi.org/10.1016/j.nicl.2013.12.003openalex-snapshot

Motor recovery and microstructural change in rubro-spinal tract in subcortical stroke

inferred← citeshttps://doi.org/10.1016/j.nicl.2017.04.016openalex-snapshot

Synergistic but independent: The role of corticospinal and alternate motor fibers for residual motor output after stroke

inferred← citeshttps://doi.org/10.1016/j.nicl.2017.05.026openalex-snapshot

Relationship between brainstem neurodegeneration and clinical impairment in traumatic spinal cord injury

inferred← citeshttps://doi.org/10.1016/j.nicl.2017.07.024openalex-snapshot

Time-dependent functional role of the contralesional motor cortex after stroke

inferred← citeshttps://doi.org/10.1016/j.nicl.2023.103398openalex-snapshot

Force oscillations underlying precision grip in humans with lesioned corticospinal tracts

inferred← citeshttps://doi.org/10.1016/j.physbeh.2025.115147openalex-snapshot

Differential changes in spinal motor neurons innervating paretic upper limb flexors and extensors after stroke

inferred← citeshttps://doi.org/10.1016/j.pmrj.2015.10.009openalex-snapshot

Mirror Movements After Stroke Suggest Facilitation From Nonprimary Motor Cortex: A Case Presentation

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2016.04.005openalex-snapshot

White matter injury in ischemic stroke

inferred← citeshttps://doi.org/10.1016/s1474-4422(13)70264-3openalex-snapshot

Connectivity-based approaches in stroke and recovery of function

inferred← citeshttps://doi.org/10.1016/s1474-4422(14)70144-9openalex-snapshot

Restoring function after spinal cord injury: towards clinical translation of experimental strategies

inferred← citeshttps://doi.org/10.1017/9781108917339.016openalex-snapshot

Degenerative Cervical Myelopathy

inferred← citeshttps://doi.org/10.1038/s41593-018-0093-5openalex-snapshot

Cortico–reticulo–spinal circuit reorganization enables functional recovery after severe spinal cord contusion

inferred← citeshttps://doi.org/10.1038/s41593-022-01196-1openalex-snapshot

Natural and targeted circuit reorganization after spinal cord injury

inferred← citeshttps://doi.org/10.1038/s41598-019-48164-7openalex-snapshot

The cortico-rubral and cerebello-rubral pathways are topographically organized within the human red nucleus

inferred← citeshttps://doi.org/10.1038/s41598-020-70805-5openalex-snapshot

Extrapyramidal plasticity predicts recovery after spinal cord injury

inferred← citeshttps://doi.org/10.1038/s41598-020-72887-7openalex-snapshot

Dissociated leg muscle atrophy in amyotrophic lateral sclerosis/motor neuron disease: the ‘split-leg’ sign

inferred← citeshttps://doi.org/10.1038/s41598-021-91605-5openalex-snapshot

Measurement of stretch-evoked brainstem function using fMRI

inferred← citeshttps://doi.org/10.1038/s41598-023-33493-5openalex-snapshot

Startle-triggered responses indicate reticulospinal drive is larger for voluntary shoulder versus finger movements

inferred← citeshttps://doi.org/10.1038/s42003-025-08734-0openalex-snapshot

AAV9-mediated KCC2 upregulation enhances functional recovery following cervical spinal cord injury

inferred← citeshttps://doi.org/10.1038/sc.2014.136openalex-snapshot

rTMS modulates reciprocal inhibition in patients with traumatic spinal cord injury

inferred← citeshttps://doi.org/10.1073/pnas.1610787114openalex-snapshot

Contribution of propriospinal neurons to recovery of hand dexterity after corticospinal tract lesions in monkeys

inferred← citeshttps://doi.org/10.1073/pnas.2008597118openalex-snapshot

Serial sarcomere number is substantially decreased within the paretic biceps brachii in individuals with chronic hemiparetic stroke

inferred← citeshttps://doi.org/10.1080/00222895.2016.1191416openalex-snapshot

Effects of Sensory Deficit on Phalanx Force Deviation During Power Grip Post Stroke

inferred← citeshttps://doi.org/10.1080/01616412.2020.1866354openalex-snapshot

Split phenomenon of antagonistic muscle groups in amyotrophic lateral sclerosis: relative preservation of flexor muscles

inferred← citeshttps://doi.org/10.1080/08990220.2018.1500363openalex-snapshot

Stroke rehabilitation and research: consideration of the role of the cortico-reticulospinal system

inferred← citeshttps://doi.org/10.1080/10749357.2020.1846932openalex-snapshot

Asymmetric atrophy of the multifidus in persons with hemiplegic presentation post-stroke

inferred← citeshttps://doi.org/10.1080/17590914.2024.2440299openalex-snapshot

Neurons Are Not All the Same: Diversity in Neuronal Populations and Their Intrinsic Responses to Spinal Cord Injury

inferred← citeshttps://doi.org/10.1080/21646821.2021.1991716openalex-snapshot

Postoperative Focal Lower Extremity Supplementary Motor Area Syndrome: Case Report and Review of the Literature

inferred← citeshttps://doi.org/10.1088/1741-2552/ad8961openalex-snapshot

An ANN models cortical-subcortical interaction during post-stroke recovery of finger dexterity

inferred← citeshttps://doi.org/10.1088/1741-2560/13/4/046009openalex-snapshot

Adaptive neuron-to-EMG decoder training for FES neuroprostheses

inferred← citeshttps://doi.org/10.1089/neu.2016.4565openalex-snapshot

Supraspinal Control Predicts Locomotor Function and Forecasts Responsiveness to Training after Spinal Cord Injury

inferred← citeshttps://doi.org/10.1089/neu.2022.0145openalex-snapshot

A Novel Method to Classify Cervical Incomplete Spinal Cord Injury Based on Potential for Recovery: A Group-Based Trajectory Analysis

inferred← citeshttps://doi.org/10.1093/brain/awu038openalex-snapshot

Altering spinal cord excitability enables voluntary movements after chronic complete paralysis in humans

inferred← citeshttps://doi.org/10.1093/brain/awx384openalex-snapshot

Evidence for a subcortical origin of mirror movements after stroke: a longitudinal study

inferred← citeshttps://doi.org/10.1097/phm.0000000000001558openalex-snapshot

The Essentials of Brain Anatomy for Physiatrists

inferred← citeshttps://doi.org/10.1097/wco.0000000000000749openalex-snapshot

Alternative routes for recovery of hand functions after corticospinal tract injury in primates and rodents

inferred← citeshttps://doi.org/10.1101/129510openalex-snapshot

Finger recruitment patterns during mirror movements suggest two systems for hand recovery after stroke

inferred← citeshttps://doi.org/10.1101/2020.03.12.989525openalex-snapshot

Serial sarcomere number is substantially decreased within the paretic biceps brachii in individuals with chronic hemiparetic stroke

inferred← citeshttps://doi.org/10.1101/2021.06.22.449412openalex-snapshot

Computational neural network provides naturalistic solution for recovery of finger dexterity after stroke

inferred← citeshttps://doi.org/10.1101/2021.10.05.21264572openalex-snapshot

Paretic upper extremity strength at acute rehabilitation evaluation predicts motor function outcome after stroke

inferred← citeshttps://doi.org/10.1101/2022.06.07.495015openalex-snapshot

Generalization reveals asymmetric and history-dependent control networks for multi-finger dexterous movements

inferred← citeshttps://doi.org/10.1101/2022.12.03.518692openalex-snapshot

The kinematics of 3D arm movements in sub-acute stroke: impaired inter-joint coordination caused by both weakness and flexor synergy intrusion

inferred← citeshttps://doi.org/10.1101/2023.08.29.555444openalex-snapshot

Loss of finger control complexity and intrusion of flexor biases are dissociable in finger individuation impairment after stroke

inferred← citeshttps://doi.org/10.1101/2023.10.27.563544openalex-snapshot

Activity in the reticulospinal tract scales with handgrip force in humans

inferred← citeshttps://doi.org/10.1101/2024.04.04.588112openalex-snapshot

Corticospinal and corticoreticulospinal projections benefit motor behaviors in chronic stroke

inferred← citeshttps://doi.org/10.1101/2024.06.28.601213openalex-snapshot

Self-organizing recruitment of compensatory areas maximizes residual motor performance post-stroke

inferred← citeshttps://doi.org/10.1101/2025.08.06.668715openalex-snapshot

Arm Control and its Recovery after Selective Lesions of Sensorimotor Cortex and the Red Nucleus: A Kinematic Study in Non-Human Primates

inferred← citeshttps://doi.org/10.1101/2025.10.31.685962openalex-snapshot

Absence of cortical reorganization following an internal capsule stroke in rodents

inferred← citeshttps://doi.org/10.1101/570796openalex-snapshot

Modulation of Rapid Visual Responses during Reaching by Multimodal Stimuli

inferred← citeshttps://doi.org/10.1101/582692openalex-snapshot

StretchfMRI: a new technique to quantify the contribution of the reticular formation to long-latency responses via fMRI

inferred← citeshttps://doi.org/10.1101/681320openalex-snapshot

No evidence for motor recovery-related cortical reorganization after stroke using resting-state fMRI

inferred← citeshttps://doi.org/10.1109/embc.2019.8857014openalex-snapshot

Experimentally Modifiable Parameters and Their Relation to the Tonic Vibration Reflex in Chronic Hemiparetic Stroke

inferred← citeshttps://doi.org/10.1109/embc53108.2024.10781597openalex-snapshot

Perturbation-induced electromyographic activity is predictive of flexion synergy expression and a sensitive measure of post-stroke motor impairment

inferred← citeshttps://doi.org/10.1109/icorr.2017.8009468openalex-snapshot

Training wrist extensor function and detecting unwanted movement strategies in an EMG-controlled visuomotor task

inferred← citeshttps://doi.org/10.1109/icorr.2019.8779451openalex-snapshot

StretchfMRI: a novel technique to quantify the contribution of the reticular formation to long-latency responses via fMRI

inferred← citeshttps://doi.org/10.1111/apha.12153openalex-snapshot

Human spinal cord injury: motor unit properties and behaviour

inferred← citeshttps://doi.org/10.1111/ejn.12623openalex-snapshot

Facilitation of ipsilateral actions of corticospinal tract neurons on feline motoneurons by transcranial direct current stimulation

inferred← citeshttps://doi.org/10.1111/ejn.13576openalex-snapshot

Corticobulbar projections from distinct motor cortical areas to the reticular formation in macaque monkeys

inferred← citeshttps://doi.org/10.1111/ejn.13670openalex-snapshot

Highlights from the 2017 meeting of the Society for Neural Control of Movement (Dublin, Ireland)

inferred← citeshttps://doi.org/10.1111/ejn.14074openalex-snapshot

Changes of motor corticobulbar projections following different lesion types affecting the central nervous system in adult macaque monkeys

inferred← citeshttps://doi.org/10.1111/ncn3.12818openalex-snapshot

Pattern of paresis in amyotrophic lateral sclerosis: A cohort study

inferred← citeshttps://doi.org/10.1111/nyas.12054openalex-snapshot

Glutamatergic reticulospinal neurons in the mouse: developmental origins, axon projections, and functional connectivity

inferred← citeshttps://doi.org/10.1113/ep088629openalex-snapshot

Task‐specific strength increases after lower‐limb compound resistance training occurred in the absence of corticospinal changes in vastus lateralis

inferred← citeshttps://doi.org/10.1113/ep092134openalex-snapshot

Preserved force control by the digits via minimal sparing of cortico‐spinal connectivity after stroke

inferred← citeshttps://doi.org/10.1113/ep092763openalex-snapshot

Mapping reticulospinal drive across various muscles of the upper and lower extremities

inferred← citeshttps://doi.org/10.1113/ep093536openalex-snapshot

Breathing‐driven modulation of reticulospinal tract activity

inferred← citeshttps://doi.org/10.1113/jp270184openalex-snapshot

Learning from the other limb's experience: sharing the ‘trained’ M1 representation of the motor sequence knowledge

inferred← citeshttps://doi.org/10.1113/jp273679openalex-snapshot

Cortical and reticular contributions to human precision and power grip

inferred← citeshttps://doi.org/10.1113/jp274968openalex-snapshot

Progressive recruitment of contralesional cortico‐reticulospinal pathways drives motor impairment post stroke

inferred← citeshttps://doi.org/10.1113/jp277462openalex-snapshot

A hierarchy of corticospinal plasticity in human hand and forearm muscles

inferred← citeshttps://doi.org/10.1113/jp277940openalex-snapshot

Disparity among muscles: different levels of plasticity of cortical representation of different muscles revealed by transcranial magnetic stimulation

inferred← citeshttps://doi.org/10.1113/jp279377openalex-snapshot

Limited capacity for ipsilateral secondary motor areas to support hand function post‐stroke

inferred← citeshttps://doi.org/10.1113/jp279794openalex-snapshot

Induction of plasticity in the human motor system by motor imagery and transcranial magnetic stimulation

inferred← citeshttps://doi.org/10.1113/jp281681openalex-snapshot

Corticoreticulospinal tract neurophysiology in an arm and hand muscle in healthy and stroke subjects

inferred← citeshttps://doi.org/10.1113/jp285510openalex-snapshot

Enhanced inhibitory input to triceps brachii in humans with spinal cord injury

inferred← citeshttps://doi.org/10.1113/jp285563openalex-snapshot

Adaptation in the spinal cord after stroke: Implications for restoring cortical control over the final common pathway

inferred← citeshttps://doi.org/10.1113/jp290565openalex-snapshot

Impact of the brainstem in normal and impaired human movement control

inferred← citeshttps://doi.org/10.1113/jphysiol.2011.225169openalex-snapshot

Cells in the monkey ponto‐medullary reticular formation modulate their activity with slow finger movements

inferred← citeshttps://doi.org/10.1113/jphysiol.2011.226209openalex-snapshot

Reticular formation responses to magnetic brain stimulation of primary motor cortex

inferred← citeshttps://doi.org/10.1123/mc.2014-0055openalex-snapshot

Neural Control of Hand Movements

inferred← citeshttps://doi.org/10.1126/scitranslmed.aac5811openalex-snapshot

Pronounced species divergence in corticospinal tract reorganization and functional recovery after lateralized spinal cord injury favors primates

inferred← citeshttps://doi.org/10.1136/jnnp-2023-331996openalex-snapshot

The relationship between corticospinal excitability and structural integrity in stroke patients

inferred← citeshttps://doi.org/10.1152/japplphysiol.00264.2021openalex-snapshot

Does the reticulospinal tract mediate adaptation to resistance training in humans?

inferred← citeshttps://doi.org/10.1152/japplphysiol.01122.2025openalex-snapshot

Intra- and intersession reliability of ipsilateral motor pathway excitability measurements in male and female adults

inferred← citeshttps://doi.org/10.1152/jn.00067.2024openalex-snapshot

Evidence of the existence of multiple modules for the stroke-caused flexion synergy from Fugl-Meyer assessment scores

inferred← citeshttps://doi.org/10.1152/jn.00115.2022openalex-snapshot

Startling stimuli increase maximal motor unit discharge rate and rate of force development in humans

inferred← citeshttps://doi.org/10.1152/jn.00123.2017openalex-snapshot

Separable systems for recovery of finger strength and control after stroke

inferred← citeshttps://doi.org/10.1152/jn.00148.2021openalex-snapshot

No evidence for motor-recovery-related cortical connectivity changes after stroke using resting-state fMRI

inferred← citeshttps://doi.org/10.1152/jn.00153.2023openalex-snapshot

Different descending pathways mediate early and late portions of lower limb responses to transcranial magnetic stimulation

inferred← citeshttps://doi.org/10.1152/jn.00158.2019openalex-snapshot

Multimodal stimuli modulate rapid visual responses during reaching

inferred← citeshttps://doi.org/10.1152/jn.00185.2018openalex-snapshot

Hyperexcitability of brain stem pathways in cerebral palsy

inferred← citeshttps://doi.org/10.1152/jn.00188.2014openalex-snapshot

Differential modulation of descending signals from the reticulospinal system during reaching and locomotion

inferred← citeshttps://doi.org/10.1152/jn.00269.2016openalex-snapshot

Neural coupling between homologous muscles during bimanual tasks: effects of visual and somatosensory feedback

inferred← citeshttps://doi.org/10.1152/jn.00282.2019openalex-snapshot

Rapid crossed responses in an intrinsic hand muscle during perturbed bimanual movements

inferred← citeshttps://doi.org/10.1152/jn.00301.2024openalex-snapshot

Corticospinal and corticoreticulospinal projections have discrete but complementary roles in chronic motor behaviors after stroke

inferred← citeshttps://doi.org/10.1152/jn.00347.2019openalex-snapshot

The mammalian spinal commissural system: properties and functions

inferred← citeshttps://doi.org/10.1152/jn.00391.2019openalex-snapshot

Modulatory effects of the supplementary motor area on primary motor cortex outputs

inferred← citeshttps://doi.org/10.1152/jn.00407.2023openalex-snapshot

Activity in the pontine reticular nuclei scales with handgrip force in humans

inferred← citeshttps://doi.org/10.1152/jn.00447.2021openalex-snapshot

Dissociation between abnormal motor synergies and impaired reaching dexterity after stroke

inferred← citeshttps://doi.org/10.1152/jn.00672.2017openalex-snapshot

Different contributions of primary motor cortex, reticular formation, and spinal cord to fractionated muscle activation

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