2015
DOI: 10.1016/j.cortex.2015.01.009
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Target sites for transcallosal fibers in human visual cortex – A combined diffusion and polarized light imaging study

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Cited by 37 publications
(42 citation statements)
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References 87 publications
(127 reference statements)
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“…A model focused on the contribution of the constituent physiological characteristics of white matter would be ideal for future applications of the watershed model, e.g. to test the complementary roles of axonal structure vs. myelin fraction (Caspers et al, 2015, Seehaus et al, 2015). Because our model does not make specific predictions for specific cellular constituents (e.g., water fraction, axonal diameter, myelin density), we favour the use of a simple tensor measure of diffusion organisation, fractional anisotropy (FA).…”
Section: Methods and Experimental Proceduresmentioning
confidence: 99%
“…A model focused on the contribution of the constituent physiological characteristics of white matter would be ideal for future applications of the watershed model, e.g. to test the complementary roles of axonal structure vs. myelin fraction (Caspers et al, 2015, Seehaus et al, 2015). Because our model does not make specific predictions for specific cellular constituents (e.g., water fraction, axonal diameter, myelin density), we favour the use of a simple tensor measure of diffusion organisation, fractional anisotropy (FA).…”
Section: Methods and Experimental Proceduresmentioning
confidence: 99%
“…The results greatly benefit from the application of automated high-throughput microscopy instruments, such as knife-edge scanning microscopy, 40 micro-optical sectioning tomography, 41 or light-sheet fluorescence microscopy 42 in Figure 4B,C,D, D being an enlarged view of the border region in C; the color wheel in C also applies to D). 24 while V1 and V2 can be separated in all modalities, note the particular change in fiber architecture at the border region, already visible in the myeloarchitectonic stain as the fringe area (Randsaum, Rs) and the border tuft (Grenzbüschel, Gb), but even better delineated with the transcallosal fiber bundle entering the border tuft and reaching layers I and II, as revealed by 3D-PLI combination with high-end labeling and tissue preparation techniques. 34,35,43 The combination of imaging during or before sectioning provides nearly distortion-free datasets.…”
Section: The Challenges Of Human Brain Microscopymentioning
confidence: 91%
“…23 Determining the exact target sites of fiber bundles as they leave the white matter and enter the cortex is difficult, and requires high-angular resolution diffusion imaging protocols. 24 Considering theories on cortical folding and connectivity, it is of particular interest to understand which sites of the cortex (i.e. gyri or sulci) are connected to which other sites.…”
Section: Current Frontiers In Diffusion Imagingmentioning
confidence: 99%
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“…3D-PLI utilizes the birefringence of myelinated and to a minor extent also unmyelinated axons in histological sections to contrast fibers with nerve cell bodies or glial cells and to determine their spatial courses in a form of 3D fiber orientation vectors. Apparently, 3D-PLI images disclose an intriguing fiber architecture, which integrates classic myeloarchitecture [6] with tissue anisotropy as revealed by diffusion magnetic resonance imaging on a microscopic level [3,5,7,8]. 3D-PLI has an obvious important bridging function between the macroscopic and the microscopic world of fiber architecture, i.e., between fiber pathways and single fibers.…”
Section: D Polarized Light Imaging In a Nutshellmentioning
confidence: 99%