Roy V. Sillitoe

Whole-mount immunohistochemistry: a high-throughput screen for patterning defects in the mouse cerebellum.

Compartmentation of the rabbit cerebellar cortex.

Patterned Purkinje cell degeneration in mouse models of Niemann-Pick type C disease.

Topographical anatomy of the cerebellum in the guinea pig, Cavia porcellus.

Antigenic compartmentation of the cat cerebellar cortex.

Abnormal dysbindin expression in cerebellar mossy fiber synapses in the mdx mouse model of Duchenne muscular dystrophy.

Zebrin II compartmentation of the cerebellum in a basal insectivore, the Madagascan hedgehog tenrec Echinops telfairi.

Antigenic compartmentation of the primate and tree shrew cerebellum: a common topography of zebrin II in Macaca mulatta and Tupaia belangeri.

Abnormal HNK-1 expression in the cerebellum of an N-CAM null mouse.

Schizophrenia genetics: dysbindin under the microscope.

Conservation of the architecture of the anterior lobe vermis of the cerebellum across mammalian species.

SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA.

Morphology, molecular codes, and circuitry produce the three-dimensional complexity of the cerebellum.

Desire, disease, and the origins of the dopaminergic system.

Golgi cell dendrites are restricted by Purkinje cell stripe boundaries in the adult mouse cerebellar cortex.

Engrailed homeobox genes determine the organization of Purkinje cell sagittal stripe gene expression in the adult cerebellum.

Neurofilament heavy chain expression reveals a unique parasagittal stripe topography in the mouse cerebellum.

Engrailed homeobox genes regulate establishment of the cerebellar afferent circuit map.

Fluorescence mapping of afferent topography in three dimensions.

Patterned expression of a cocaine- and amphetamine-regulated transcript peptide reveals complex circuit topography in the rodent cerebellar cortex.

Parasagittal compartmentation of cerebellar mossy fibers as revealed by the patterned expression of vesicular glutamate transporters VGLUT1 and VGLUT2.

Cerebellar zones: history, development, and function.

X-linked Angelman-like syndrome caused by Slc9a6 knockout in mice exhibits evidence of endosomal-lysosomal dysfunction.