The mesencephalic locomotor region recruits V2a reticulospinal neurons to drive forward locomotion in larval zebrafish.

The mesencephalic locomotor region (MLR) is a brain stem area whose stimulation triggers graded forward locomotion. How MLR neurons recruit downstream vsx2 (V2a) reticulospinal neurons (RSNs) is poorly understood. Here, to overcome this challenge, we uncovered the locus of MLR in transparent larval zebrafish and show that the MLR locus is distinct from the nucleus of the medial longitudinal fasciculus.

When makes you unique: Temporality of the human brain fingerprint.

The extraction of “fingerprints” from human brain connectivity data has become a new frontier in neuroscience. However, the time scales of human brain identifiability are still largely unexplored. We here investigate the dynamics of brain fingerprints along two complementary axes: (i) What is the optimal time scale at which brain fingerprints integrate information and (ii) when best identification happens.

Large-scale functional network dynamics in human callosal agenesis: Increased subcortical involvement and preserved laterality.

In the human brain, the corpus callosum is the major white-matter commissural tract enabling the transmission of sensory-motor, and higher level cognitive information between homotopic regions of the two cerebral hemispheres. Despite developmental absence (i.e.

Altered anterior default mode network dynamics in progressive multiple sclerosis.

Background: Modifications in brain function remain relatively unexplored in progressive multiple sclerosis (PMS), despite their potential to provide new insights into the pathophysiology of the disease at this stage.

Objectives: To characterize the dynamics of functional networks at rest in patients with PMS, and the relation with clinical disability.

Methods: Thirty-two patients with PMS underwent clinical and cognitive assessment.

Deconvolution of Sustained Neural Activity From Large-Scale Calcium Imaging Data.

Recent technological advances in light-sheet microscopy make it possible to perform whole-brain functional imaging at the cellular level with the use of Ca indicators. The outstanding spatial extent and resolution of this type of data open unique opportunities for understanding the complex organization of neuronal circuits across the brain. However, the analysis of this data remains challenging because the observed variations in fluorescence are, in fact, noisy indirect measures of the neuronal activity.