R. Mark Henkelman

Why does MTR change with neuronal depolarization?

Pulse-wave velocity measured in one heartbeat using MR tagging.

Orientational diffusion reflects fiber structure within a voxel.

Multiple-mouse MRI.

Ultrasound-guided left-ventricular catheterization: a novel method of whole mouse perfusion for microimaging.

High-resolution longitudinal screening with magnetic resonance imaging in a murine brain cancer model.

MicroCT scanner performance and considerations for vascular specimen imaging.

Comprehensive transthoracic cardiac imaging in mice using ultrasound biomicroscopy with anatomical confirmation by magnetic resonance imaging.

Angiopoietin-1 causes reversible degradation of the portal microcirculation in mice: implications for treatment of liver disease.

Foxh1 is essential for development of the anterior heart field.

Multiple mouse biological loading and monitoring system for MRI.

Baf60c is essential for function of BAF chromatin remodelling complexes in heart development.

Identification of human brain tumour initiating cells.

Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development.

Imaging articular cartilage under compression--cartilage elastography.

Abnormal cardiac inflow patterns during postnatal development in a mouse model of Holt-Oram syndrome.

Neuroanatomical differences between mouse strains as shown by high-resolution 3D MRI.

T1, T2 relaxation and magnetization transfer in tissue at 3T.

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.

Correction of artefacts in optical projection tomography.

Gradient hysteresis in MRI and NMR experiments.

Magnetic resonance imaging for detection and analysis of mouse phenotypes.

Disease phenotyping: structural and functional readouts.

Anatomical phenotyping in the brain and skull of a mutant mouse by magnetic resonance imaging and computed tomography.

Retrospective gating for mouse cardiac MRI.

In vivo magnetic resonance imaging and semiautomated image analysis extend the brain phenotype for cdf/cdf mice.

Using metamaterial yokes in NMR measurements.

Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis.

High-grade glioma formation results from postnatal pten loss or mutant epidermal growth factor receptor expression in a transgenic mouse glioma model.

Hemodynamics in the mouse aortic arch as assessed by MRI, ultrasound, and numerical modeling.

Presentation of 3D isotropic imaging data for optimal viewing.

Magnetic resonance imaging with ultrashort TE (UTE) PULSE sequences: technical considerations.

Sexual dimorphism revealed in the structure of the mouse brain using three-dimensional magnetic resonance imaging.

Morphological and functional evaluation of murine heterotopic cardiac grafts using ultrasound biomicroscopy.

Mouse behavioral mutants have neuroimaging abnormalities.

4D cardiac MRI in the mouse.

MR technology for biological studies in mice.

Resolution improvement in emission optical projection tomography.

Behavioral phenotypes of Disc1 missense mutations in mice.

Noninvasive ultrasonic measurement of regional and local pulse-wave velocity in mice.

Combined magnetic resonance and bioluminescence imaging of live mice.

Automated deformation analysis in the YAC128 Huntington disease mouse model.

Optimization of the SNR-resolution tradeoff for registration of magnetic resonance images.

Tbx5-dependent pathway regulating diastolic function in congenital heart disease.

Cortical thickness measured from MRI in the YAC128 mouse model of Huntington's disease.

Longitudinal neuroanatomical changes determined by deformation-based morphometry in a mouse model of Alzheimer's disease.

Three-dimensional analysis of vascular development in the mouse embryo.

p73 regulates neurodegeneration and phospho-tau accumulation during aging and Alzheimer's disease.

Acoustic and kinetic behaviour of definity in mice exposed to high frequency ultrasound.

Trading off SNR and resolution in MR images.

GLP-1R agonist liraglutide activates cytoprotective pathways and improves outcomes after experimental myocardial infarction in mice.

Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2.

Measurement of cerebral blood volume in mouse brain regions using micro-computed tomography.

Reptilian heart development and the molecular basis of cardiac chamber evolution.

Lunatic Fringe-mediated Notch signaling is required for lung alveogenesis.

Cerebral asymmetries in 12-week-old C57Bl/6J mice measured by magnetic resonance imaging.

Genetic deletion or pharmacological inhibition of dipeptidyl peptidase-4 improves cardiovascular outcomes after myocardial infarction in mice.

Aortic regurgitation dramatically alters the distribution of atherosclerotic lesions and enhances atherogenesis in mice.

Anatomical phenotyping in a mouse model of fragile X syndrome with magnetic resonance imaging.

Hedgehog regulates distinct vascular patterning events through VEGF-dependent and -independent mechanisms.

Systems biology through mouse imaging centers: experience and new directions.

A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions.

Comparative SNR for high-throughput mouse embryo MR microscopy.

Maze training in mice induces MRI-detectable brain shape changes specific to the type of learning.

Electrical remodelling precedes heart failure in an endothelin-1-induced model of cardiomyopathy.

A mouse model of heritable cerebrovascular disease.

Correlation between local hemodynamics and lesion distribution in a novel aortic regurgitation murine model of atherosclerosis.

MRI phenotyping of genetically altered mice.

Suppressor of fused controls mid-hindbrain patterning and cerebellar morphogenesis via GLI3 repressor.

Chromatin remodelling complex dosage modulates transcription factor function in heart development.

Multiple developmental programs are altered by loss of Zic1 and Zic4 to cause Dandy-Walker malformation cerebellar pathogenesis.

Natural history of disease in the YAC128 mouse reveals a discrete signature of pathology in Huntington disease.

Semi-automatic segmentation of multiple mouse embryos in MR images.

Altered palmitoylation and neuropathological deficits in mice lacking HIP14.

Iroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje network.

Mice lacking caspase-2 are protected from behavioral changes, but not pathology, in the YAC128 model of Huntington disease.

Brain abnormalities in a Neuroligin3 R451C knockin mouse model associated with autism.

Genes into geometry: imaging for mouse development in 3D.

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.

Priming of hypoxia-inducible factor by neuronal nitric oxide synthase is essential for adaptive responses to severe anemia.

Robust method for 3D arterial spin labeling in mice.

Preparation of fixed mouse brains for MRI.