Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain.

PubWeight™: 0.94‹?› | Rank: Top 15%

🔗 View Article (PMC 3590453)

Published in Neuroimage on February 16, 2011

Authors

Jon O Cleary1, Frances K Wiseman, Francesca C Norris, Anthony N Price, Mankin Choy, Victor L J Tybulewicz, Roger J Ordidge, Sebastian Brandner, Elizabeth M C Fisher, Mark F Lythgoe

Author Affiliations

1: Centre for Advanced Biomedical Imaging, Department of Medicine and Institute of Child Health, University College London, London, UK.

Articles cited by this

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science (2005) 3.61

A three-dimensional digital atlas database of the adult C57BL/6J mouse brain by magnetic resonance microscopy. Neuroscience (2005) 3.41

Morphologic phenotyping with MR microscopy: the visible mouse. Radiology (2002) 3.24

Aldehyde fixative solutions alter the water relaxation and diffusion properties of nervous tissue. Magn Reson Med (2009) 2.21

High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice. Neuroimage (2008) 2.08

Statistical diffusion tensor histology reveals regional dysmyelination effects in the shiverer mouse mutant. Neuroimage (2005) 1.86

Morphometric analysis of the C57BL/6J mouse brain. Neuroimage (2007) 1.75

Voxel-based morphometry in the R6/2 transgenic mouse reveals differences between genotypes not seen with manual 2D morphometry. Neurobiol Dis (2008) 1.73

Postmortem MR imaging of formalin-fixed human brain. Neuroimage (2004) 1.65

Magnetic resonance microscopy of the C57BL mouse brain. Neuroimage (2000) 1.56

The olfactory granule cell: from classical enigma to central role in olfactory processing. Brain Res Rev (2007) 1.55

Automated deformation analysis in the YAC128 Huntington disease mouse model. Neuroimage (2007) 1.54

Magnetic resonance histology for morphologic phenotyping. J Magn Reson Imaging (2002) 1.49

Measurements of T1 and T2 over time in formalin-fixed human whole-brain specimens. Acta Radiol (1992) 1.49

p73 regulates neurodegeneration and phospho-tau accumulation during aging and Alzheimer's disease. Neuron (2008) 1.42

Enhanced T2 contrast for MR histology of the mouse brain. Magn Reson Med (2006) 1.41

Postmortem MRI of human brain hemispheres: T2 relaxation times during formaldehyde fixation. Magn Reson Med (2009) 1.33

Staining methods for magnetic resonance microscopy of the rat fetus. J Magn Reson Imaging (2007) 1.32

How simple is the organization of the olfactory glomerulus?: the heterogeneity of so-called periglomerular cells. Neurosci Res (1998) 1.31

Neuroanatomical phenotypes in the reeler mouse. Neuroimage (2006) 1.26

Optimising imaging parameters for post mortem MR imaging of the human brain. Acta Radiol (1999) 1.26

Contrast manipulation and artifact assessment of 2D and 3D RARE sequences. Magn Reson Imaging (1990) 1.25

Magnetic resonance virtual histology for embryos: 3D atlases for automated high-throughput phenotyping. Neuroimage (2010) 1.24

Structural insights from high-resolution diffusion tensor imaging and tractography of the isolated rat hippocampus. Neuroimage (2006) 1.23

Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging. Neuroimage (2010) 1.14

The reaction of formaldehyde with proteins; cross-linking between amino and primary amide or guanidyl groups. J Am Chem Soc (1948) 1.08

The morphology of the granule cells of the olfactory bulb. J Cell Sci (1970) 1.08

Use of magnetic resonance imaging for anatomical phenotyping of the R6/2 mouse model of Huntington's disease. Neurobiol Dis (2008) 1.06

Manipulation of tissue contrast using contrast agents for enhanced MR microscopy in ex vivo mouse brain. Neuroimage (2009) 0.99

Reversible and irreversible effects of chemical fixation on the NMR properties of single cells. Magn Reson Med (2006) 0.94

MRI of cellular layers in mouse brain in vivo. Neuroimage (2009) 0.91

A quantitative-genetic analysis of hippocampal variation in the mouse. J Neurogenet (1986) 0.90

Cardiac phenotyping in ex vivo murine embryos using microMRI. NMR Biomed (2009) 0.88

Enhanced delineation of white matter structures of the fixed mouse brain using Gd-DTPA in microscopic MRI. NMR Biomed (2009) 0.87

Changes in T1 and T2 observed in brain magnetic resonance imaging with delivery of high concentrations of oxygen. J Comput Assist Tomogr (2007) 0.85

Timm's sulfide silver reaction for zinc during experimental anterograde degeneration of hippocampal mossy fibers. J Comp Neurol (1971) 0.85

T2 relaxation values in the developing preterm brain. AJNR Am J Neuroradiol (2003) 0.85

Articles by these authors

De novo cardiomyocytes from within the activated adult heart after injury. Nature (2011) 5.17

A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet (2009) 5.01

Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis. Science (2003) 4.57

Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science (2003) 4.40

Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease. J Cell Biol (2007) 4.30

The SYK tyrosine kinase: a crucial player in diverse biological functions. Nat Rev Immunol (2010) 4.26

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nat Genet (2005) 4.21

Species-specific transcription in mice carrying human chromosome 21. Science (2008) 4.03

An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science (2005) 3.61

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics. Science (2003) 3.59

Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report. Lancet (2006) 3.12

In vivo imaging of glucose uptake and metabolism in tumors. Nat Med (2013) 3.01

A novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2. Blood (2005) 2.90

Human prion protein with valine 129 prevents expression of variant CJD phenotype. Science (2004) 2.82

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey. BMJ (2013) 2.74

Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice. Neuron (2007) 2.58

CD19 is essential for B cell activation by promoting B cell receptor-antigen microcluster formation in response to membrane-bound ligand. Nat Immunol (2007) 2.51

Critical roles for Rac1 and Rac2 GTPases in B cell development and signaling. Science (2003) 2.46

Genetic analysis of the cytoplasmic dynein subunit families. PLoS Genet (2006) 2.35

Monoclonal antibodies inhibit prion replication and delay the development of prion disease. Nature (2003) 2.31

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathol (2010) 2.30

Syk, c-Src, the alphavbeta3 integrin, and ITAM immunoreceptors, in concert, regulate osteoclastic bone resorption. J Cell Biol (2007) 2.27

Fbw7 controls neural stem cell differentiation and progenitor apoptosis via Notch and c-Jun. Nat Neurosci (2010) 2.23

Requirement of Rac1 and Rac2 expression by mature dendritic cells for T cell priming. Science (2004) 2.20

The origins and uses of mouse outbred stocks. Nat Genet (2005) 2.19

Neuroprotective role of the Reaper-related serine protease HtrA2/Omi revealed by targeted deletion in mice. Mol Cell Biol (2004) 2.15

Validation study of the accuracy of echocardiographic measurements of systemic blood flow volume in newborn infants. J Am Soc Echocardiogr (2013) 2.11

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. PLoS Genet (2007) 2.09

C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes. Sci Rep (2012) 2.09

Rac1 is essential for platelet lamellipodia formation and aggregate stability under flow. J Biol Chem (2005) 2.07

The BAFF receptor transduces survival signals by co-opting the B cell receptor signaling pathway. Immunity (2013) 2.02

A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice. J Cell Biol (2005) 2.01

ERM proteins regulate cytoskeleton relaxation promoting T cell-APC conjugation. Nat Immunol (2004) 1.99

Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion protein. Lancet (2004) 1.96

Magnetic tagging increases delivery of circulating progenitors in vascular injury. JACC Cardiovasc Interv (2009) 1.94

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain (2013) 1.93

NKG2D triggers cytotoxicity in mouse NK cells lacking DAP12 or Syk family kinases. Nat Immunol (2003) 1.89

Vav1 transduces TCR signals required for LFA-1 function and cell polarization at the immunological synapse. Eur J Immunol (2003) 1.88

Post-mortem examination of human fetuses: a comparison of whole-body high-field MRI at 9.4 T with conventional MRI and invasive autopsy. Lancet (2009) 1.86

Down syndrome--recent progress and future prospects. Hum Mol Genet (2009) 1.85

Requirement for Rac1 in a K-ras induced lung cancer in the mouse. Cancer Res (2007) 1.80

Compartment models of the diffusion MR signal in brain white matter: a taxonomy and comparison. Neuroimage (2011) 1.79

Vav1 transduces T cell receptor signals to the activation of phospholipase C-gamma1 via phosphoinositide 3-kinase-dependent and -independent pathways. J Exp Med (2002) 1.78

Beta1 integrin activates Rac1 in Schwann cells to generate radial lamellae during axonal sorting and myelination. J Cell Biol (2007) 1.77

Suburothelial myofibroblasts in the human overactive bladder and the effect of botulinum neurotoxin type A treatment. Eur Urol (2008) 1.73

Single treatment with RNAi against prion protein rescues early neuronal dysfunction and prolongs survival in mice with prion disease. Proc Natl Acad Sci U S A (2008) 1.71

Cytoplasmic dynein nomenclature. J Cell Biol (2005) 1.71

Neonatal hepatic steatosis by disruption of the adenosine kinase gene. Proc Natl Acad Sci U S A (2002) 1.70

Tumour angiogenesis is reduced in the Tc1 mouse model of Down's syndrome. Nature (2010) 1.70

Combinations of genetic mutations in the adult neural stem cell compartment determine brain tumour phenotypes. EMBO J (2009) 1.66

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proc Natl Acad Sci U S A (2009) 1.66

PTEN is essential for cell migration but not for fate determination and tumourigenesis in the cerebellum. Development (2002) 1.64

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations. Mov Disord (2010) 1.56

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes. PLoS Genet (2013) 1.50

Acupuncture needling sensation: the neural correlates of deqi using fMRI. Brain Res (2009) 1.49

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors. Brain (2011) 1.45

DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. Am J Hum Genet (2008) 1.45

TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander. Mamm Genome (2008) 1.44

Activation of the small GTPase Rac2 via the B cell receptor regulates B cell adhesion and immunological-synapse formation. Immunity (2008) 1.43

Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosis. J Biol Chem (2005) 1.42

Magnetic resonance imaging of mesenchymal stem cells homing to pulmonary metastases using biocompatible magnetic nanoparticles. Cancer Res (2009) 1.42

Vav1 transduces T cell receptor signals to the activation of the Ras/ERK pathway via LAT, Sos, and RasGRP1. J Biol Chem (2004) 1.42

High field (9.4 Tesla) magnetic resonance imaging of cortical grey matter lesions in multiple sclerosis. Brain (2010) 1.42

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathol (2013) 1.41

Atypical scrapie prions from sheep and lack of disease in transgenic mice overexpressing human prion protein. Emerg Infect Dis (2013) 1.38

Kuru prions and sporadic Creutzfeldt-Jakob disease prions have equivalent transmission properties in transgenic and wild-type mice. Proc Natl Acad Sci U S A (2008) 1.37

Unexpected requirement for ZAP-70 in pre-B cell development and allelic exclusion. Immunity (2003) 1.36

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations. Hum Mol Genet (2010) 1.35

A critical role for Syk protein tyrosine kinase in Fc receptor-mediated antigen presentation and induction of dendritic cell maturation. J Immunol (2003) 1.34

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein. Brain (2006) 1.34

Wnt signalling inhibits neural differentiation of embryonic stem cells by controlling bone morphogenetic protein expression. Mol Cell Neurosci (2003) 1.32

Mitochondria and quality control defects in a mouse model of Gaucher disease--links to Parkinson's disease. Cell Metab (2013) 1.32

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice. Neurogenetics (2002) 1.31

High-resolution fast spin echo imaging of the human brain at 4.7 T: implementation and sequence characteristics. Magn Reson Med (2004) 1.30

CLEC-2 and Syk in the megakaryocytic/platelet lineage are essential for development. Blood (2011) 1.30

Natural cytotoxicity uncoupled from the Syk and ZAP-70 intracellular kinases. Nat Immunol (2002) 1.29

Brain imaging of acupuncture: comparing superficial with deep needling. Neurosci Lett (2008) 1.28

Down syndrome: searching for the genetic culprits. Dis Model Mech (2011) 1.28

Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis. PLoS One (2010) 1.25

Magnetic resonance virtual histology for embryos: 3D atlases for automated high-throughput phenotyping. Neuroimage (2010) 1.24

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice. J Gen Virol (2004) 1.23

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Dis Model Mech (2009) 1.22