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  High-resolution 3D MRI of mouse brain reveals small cerebral structures in vivo

Natt, O., Watanabe, T., Boretius, S., Radulovic, J., Frahm, J., & Michaelis, T. (2002). High-resolution 3D MRI of mouse brain reveals small cerebral structures in vivo. Journal of Neuroscience Methods, 120(2), 203-209. Retrieved from http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T04-46YV98M-C-G&_cdi=4852&_user=38661&_pii=S016502700200211X&_orig=search&_coverDate=10%2F30%2F2002&_sk=998799997&view=c&wchp=dGLbVlz-zSkzk&md5=0b87492f0f770a07ebb3747a8f5cbd79&ie=/sdarticle.pdf.

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 Creators:
Natt, O.1, Author           
Watanabe, T.1, Author           
Boretius, S.1, Author           
Radulovic, J., Author
Frahm, J.1, Author           
Michaelis, T.1, Author           
Affiliations:
1Biomedical NMR Research GmbH, MPI for biophysical chemistry, Max Planck Society, ou_578634              

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Free keywords: MRI; MR microscopy; mouse brain; mouse strain; manganese; contrast; neuroaxonal tracing; phenotyping
 Abstract: This work demonstrates technical approaches to high-quality magnetic resonance imaging (MRI) of small structures of the mouse brain in vivo. It turns out that excellent soft-tissue contrast requires the reduction of partial volume effects by using 3D MRI at high (isotropic) resolution with linear voxel dimensions of about 100-150 mum. The long T-2* relaxation times at relatively low magnetic fields (2.35 T) offer the benefit of a small receiver bandwidth (increased signal-to-noise) at a moderate echo time which together with the small voxel size avoids visual susceptibility artifacts. For measuring times of 1-1.5 h both * relaxation times at relatively low magnetic fields (2.35 T) offer the benefit of a small receiver bandwidth (increased signal-to-noise) at a moderate echo time which together with the small voxel size avoids visual susceptibility artifacts. For measuring times of 1-1.5 h both T-1-weighted (FLASH) and T-2-weighted (Fast Spin-Echo) 3D MRI acquisitions exhibit detailed anatomical insights in accordance with histological sections from a mouse brain atlas. Preliminary applications address the identification of neuroanatomical variations in different mouse strains and the use of Mn2+ as a T-1 contrast agent for neuroaxonal tracing of fiber tracts within the mouse visual pathway. (C) 2002 Elsevier Science B.V. All rights reserved.

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Language(s): eng - English
 Dates: 2002-10-30
 Publication Status: Issued
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 Rev. Type: Peer
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Title: Journal of Neuroscience Methods
  Alternative Title : J. Neurosci. Methods
Source Genre: Journal
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Pages: - Volume / Issue: 120 (2) Sequence Number: - Start / End Page: 203 - 209 Identifier: -