This dataset corresponds to a PLOS ONE paper, "Fully-automated µMRI morphometric phenotyping of the Tc1 mouse model of Down syndrome".<br><br><b>Corresponding article</b>: Powell NM, Modat M, Cardoso MJ, Ma D, Holmes HE, Yu Y, et al. (2016) Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome. PLoS ONE 11(9): e0162974. doi:10.1371/journal.pone.0162974 - http://dx.doi.org/10.1371/journal.pone.0162974<br><br><b>See also:</b><br><a target="_blank">* Cohort 1: </a><a target="_blank"><br></a><a href="https://figshare.com/s/3077acc7a50b0db24774" target="_blank">https://figshare.com/s/3077acc7a50b0db24774</a> doi: <br><a target="_blank">10.6084/m9.figshare.3382693<br>* 3-brain holder for ex vivo µMRI scans: h...
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), whi...
AbstractThe Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
This dataset corresponds to a PLOS ONE paper, "Fully-automated µMRI morphometric phenotyping of the ...
We describe a fully automated pipeline for the morphometric phenotyping of mouse brains from μMRI da...
We describe a fully automated pipeline for the morphometric phenotyping of mouse brains from μMRI da...
<p><b>STEPS brain mask</b> overlaid on representative slices (a, sagittal; b—c, coronal; d, transver...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
<p><b>Multiple-subject scanning</b>: (a) 3-brain holder and syringe; (b) 3 <i>ex vivo</i> mouse brai...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
<p>Protein expression levels of 77 proteins measured in the nuclear fraction of cortex from control ...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Published along with the journal paper: Substantially thinner internal granular layer and reduced mo...
Summary: Down syndrome (DS) results from trisomy of human chromosome 21 (HSA21), and DS research has...
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), whi...
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), whi...
AbstractThe Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
This dataset corresponds to a PLOS ONE paper, "Fully-automated µMRI morphometric phenotyping of the ...
We describe a fully automated pipeline for the morphometric phenotyping of mouse brains from μMRI da...
We describe a fully automated pipeline for the morphometric phenotyping of mouse brains from μMRI da...
<p><b>STEPS brain mask</b> overlaid on representative slices (a, sagittal; b—c, coronal; d, transver...
Down syndrome, also referred to as trisomy 21, is a chromosomal abnormality in which the 21st human ...
<p><b>Multiple-subject scanning</b>: (a) 3-brain holder and syringe; (b) 3 <i>ex vivo</i> mouse brai...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
<p>Protein expression levels of 77 proteins measured in the nuclear fraction of cortex from control ...
Intellectual disabilities, hypotonia and cranio-facial dysmorphism are the cardinal characteristics ...
Published along with the journal paper: Substantially thinner internal granular layer and reduced mo...
Summary: Down syndrome (DS) results from trisomy of human chromosome 21 (HSA21), and DS research has...
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), whi...
The Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU16), whi...
AbstractThe Ts1Cje mouse model of Down syndrome (DS) has partial trisomy of mouse chromosome 16 (MMU...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...