Search PubMed⌕ Search

PubMed · 15192519

[Basic principles of diffusion tensor MR tractography].

Abstract

Diffusion tensor MR tractography allows in vivo depiction of anatomical bundles composing the white matter of the brain and of spinal cord. Diffusion MRI uses the effects of heterogeneous water molecule movement to determine for each pixel the main axis and magnitude of local anisotropy. Tractography exploits these data to reconstruct the tridimensional geometry of the bundles providing neurologists with precise information about white matter tract architecture involvement by various pathologies. In this paper, the basic principles of molecular diffusion and the subsequent diffusion tensor that describes its geometrical and quantitative characteristics will be reviewed, in particular within bundles of white matter. Then main principles of diffusion tensor MR imaging and tractography will be presented.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

C Habas. 2004. [Basic principles of diffusion tensor MR tractography].. https://doi.org/10.1016/s0221-0363(04)97579-8

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Hydrodynamic narrowing of tubes extruded from cells.

We discuss the pulling force f required to extrude a lipid tube from a living cell as a function of the extrusion velocity L. The main feature is membrane friction on the cytoskeleton. As recently observed for neutrophils, the tether force exhibits a "shear thinning" response over a large range of pulling velocities, which was previously interpreted by assuming viscoelastic flows of the sliding membrane. Here, we propose an alternative explanation based on purely Newtonian flow: The diameter of the tether decreases concomitantly with the increase of the membrane tension in the lipid tube. The pulling force is found to vary as L(1/3), which is consistent with reported experimental data for various types of cells.

Biophysical Phenomena↗

Size distribution of pressure-decomposed casein micelles studied by dynamic light scattering and AFM.

Reversible and irreversible states of pressure-dissociated casein micelles were studied by in situ light scattering techniques and ex situ atomic force microscopy. AFM experiments performed at ambient pressure reveal heterogeneities across the micelle, suggesting a sub-structure on a 20 nm scale. At pressures between 50 and 250 MPa, the native micelles disintegrate into small fragments on the scale of the observed sub-structure. At pressures above 300 MPa the micelles fully decompose into their monomeric constituents. After pressure release two discrete populations of casein aggregates are observed, depending on the applied initial pressure: Between 160 and 240 MPa stable micelles with diameters near 100 nm without detectable sub-structures are formed. Casein micelles exposed to pressures above 280 MPa re-associate at ambient pressure yielding mini-micelles with diameters near 25 nm. The implications concerning structural models are discussed.

Biophysical Phenomena↗