Published in Nature on April 02, 1971
Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature (1961) 6.36
Neuronal migration, with special reference to developing human brain: a review. Brain Res (1973) 4.49
Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat. Hum Mol Genet (2000) 4.42
Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy. J Comp Neurol (1979) 3.86
Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha -subunit. Proc Natl Acad Sci U S A (2000) 3.72
Morphological, physiological, and biochemical changes in rhodopsin knockout mice. Proc Natl Acad Sci U S A (1999) 3.71
Differential effect of the rd mutation on rods and cones in the mouse retina. Invest Ophthalmol Vis Sci (1978) 3.30
Engraftable human neural stem cells respond to developmental cues, replace neurons, and express foreign genes. Nat Biotechnol (1998) 3.28
Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus. Proc Natl Acad Sci U S A (1997) 3.16
Rod outer segment disk shedding in rat retina: relationship to cyclic lighting. Science (1976) 3.04
Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa. Nat Med (1998) 2.66
Photoreceptor degeneration in inherited retinal dystrophy delayed by basic fibroblast growth factor. Nature (1990) 2.61
Inherited retinal dystrophy: primary defect in pigment epithelium determined with experimental rat chimeras. Science (1976) 2.59
Increased susceptibility to light damage in an arrestin knockout mouse model of Oguchi disease (stationary night blindness) Invest Ophthalmol Vis Sci (1999) 2.53
Rods and cones in the mouse retina. II. Autoradiographic analysis of cell generation using tritiated thymidine. J Comp Neurol (1979) 2.35
Expression of a myelin basic protein gene in transgenic shiverer mice: correction of the dysmyelinating phenotype. Cell (1987) 2.29
Purkinje cell degeneration, a new neurological mutation in the mouse. Proc Natl Acad Sci U S A (1976) 2.14
Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk. Proc Natl Acad Sci U S A (2001) 1.91
Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans. J Comp Neurol (1970) 1.85
Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice. J Comp Neurol (1973) 1.83
Chondrodysplasia and neurological abnormalities in ATF-2-deficient mice. Nature (1996) 1.82
Climate change and the integrity of science. Science (2010) 1.80
Basic fibroblast growth factor and local injury protect photoreceptors from light damage in the rat. J Neurosci (1992) 1.80
Influence of eye pigmentation and light deprivation on inherited retinal dystrophy in the rat. Exp Eye Res (1975) 1.77
Genetic regulation of light damage to photoreceptors. Invest Ophthalmol Vis Sci (1987) 1.76
A naturally occurring mouse model of X-linked congenital stationary night blindness. Invest Ophthalmol Vis Sci (1998) 1.76
Kinetics of rod outer segment renewal in the developing mouse retina. J Cell Biol (1973) 1.75
Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis. J Comp Neurol (1973) 1.74
The retrograde intraaxonal transport of horseradish peroxidase in the chick visual system: a light and electron microscopic study. J Comp Neurol (1974) 1.74
Injury-induced upregulation of bFGF and CNTF mRNAS in the rat retina. J Neurosci (1995) 1.67
Retrograde axonal transport in the central nervous system. Science (1972) 1.67
Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice. J Comp Neurol (1973) 1.65
Weaver mutant mouse cerebellum: defective neuronal migration secondary to abnormality of Bergmann glia. Proc Natl Acad Sci U S A (1973) 1.61
C57BL-6J mice with inherited retinal degeneration. Arch Ophthalmol (1974) 1.61
Direct spread of reovirus from the intestinal lumen to the central nervous system through vagal autonomic nerve fibers. Proc Natl Acad Sci U S A (1991) 1.60
Characterization of rhodopsin mis-sorting and constitutive activation in a transgenic rat model of retinitis pigmentosa. Invest Ophthalmol Vis Sci (2000) 1.60
Myelin deficient mice: expression of myelin basic protein and generation of mice with varying levels of myelin. Cell (1987) 1.55
Trembler mouse carries a point mutation in a myelin gene. Nature (1992) 1.51
Prostaglandin E2 induces vascular endothelial growth factor and basic fibroblast growth factor mRNA expression in cultured rat Müller cells. Invest Ophthalmol Vis Sci (1998) 1.44
Growth and development of the mouse retinal pigment epithelium. I. Cell and tissue morphometrics and topography of mitotic activity. Dev Biol (1987) 1.42
Magnetic resonance imaging and micro-computed tomography combined atlas of developing and adult mouse brains for stereotaxic surgery. Neuroscience (2009) 1.39
Computer-aided three-dimensional reconstruction and quantitative analysis of cells from serial electron microscopic montages of foetal monkey brain. Nature (1974) 1.39
Abnormal spermiogenesis in quaking, a myelin-deficient mutant mouse. Biol Reprod (1971) 1.38
Light and inherited retinal degeneration. Br J Ophthalmol (2006) 1.37
A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. Proc Natl Acad Sci U S A (1992) 1.36
Circadian nature of rod outer segment disc shedding in the rat. Invest Ophthalmol Vis Sci (1980) 1.36
Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering. Science (1979) 1.34
Role of neurotrophin receptor TrkB in the maturation of rod photoreceptors and establishment of synaptic transmission to the inner retina. J Neurosci (1999) 1.34
New mutant mouse with communicating hydrocephalus and secondary aqueductal stenosis. Acta Neuropathol (1972) 1.32
Segregation of human neural stem cells in the developing primate forebrain. Science (2001) 1.29
PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect. Proc Natl Acad Sci U S A (1993) 1.29
Spare the rod and spoil the eye. Br J Ophthalmol (2005) 1.28
Protection of the rat retina from ischemic injury by brain-derived neurotrophic factor, ciliary neurotrophic factor, and basic fibroblast growth factor. Invest Ophthalmol Vis Sci (1994) 1.25
Supravital DNA synthesis in the developing human and mouse brain. J Neuropathol Exp Neurol (1968) 1.24
Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats. Vision Res (2001) 1.23
Analysis of neurological mutants with inherited retinal degeneration. Friedenwald lecture. Invest Ophthalmol Vis Sci (1981) 1.22
Histogenesis of mouse cerebellum in microwell cultures. Cell reaggregation and migration, fiber and synapse formation. J Cell Biol (1977) 1.22
bcl-2 overexpression reduces apoptotic photoreceptor cell death in three different retinal degenerations. Proc Natl Acad Sci U S A (1996) 1.21
Rod outer segment disc shedding in relation to cyclic lighting. Exp Eye Res (1976) 1.21
Role of the pigment epithelium in inherited retinal degeneration analyzed with experimental mouse chimeras. Exp Eye Res (1976) 1.13
Differentiation of engrafted multipotent neural progenitors towards replacement of missing granule neurons in meander tail cerebellum may help determine the locus of mutant gene action. Development (1997) 1.13
Increased rate of peripheral nerve regeneration using bioresorbable nerve guides and a laminin-containing gel. Exp Neurol (1985) 1.12
Fine mapping of a putative rd cDNA and its co-segregation with rd expression. Invest Ophthalmol Vis Sci (1990) 1.10
Growth and development of the mouse retinal pigment epithelium. II. Cell patterning in experimental chimaeras and mosaics. Dev Biol (1987) 1.10
Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis. J Comp Neurol (1982) 1.08
An anti-angiogenic state in mice and humans with retinal photoreceptor cell degeneration. Proc Natl Acad Sci U S A (2001) 1.07
Congenic strains of RCS rats with inherited retinal dystrophy. J Hered (1975) 1.07
Histochemical characterization of lectin binding in mouse cerebellum. Neuroscience (1979) 1.06
Electron microscopic analysis of postnatal histogenesis in the cerebellar cortex of staggerer mutant mice. J Comp Neurol (1978) 1.05
Morphometric analysis of normal, mutant, and transgenic CNS: correlation of myelin basic protein expression to myelinogenesis. J Neurochem (1992) 1.04
Strain differences in sensitivity to light-induced photoreceptor degeneration in albino mice. Curr Eye Res (1987) 1.04
A mechanism for the guidance and topographic patterning of retinal ganglion cell axons. J Comp Neurol (1980) 1.03
Genetic control of retinal ganglion cell projections. J Comp Neurol (1978) 1.03
Rhodopsin content and rod outer segment length in albino rat eyes: modification by dark adaptation. Exp Eye Res (1978) 1.03
Telencephalic origin of pulvinar neurons in the fetal human brain. Z Anat Entwicklungsgesch (1969) 1.02
Retrohippocampal, hippocampal and related structures of the forebrain in the reeler mutant mouse. J Comp Neurol (1973) 1.02
Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol (1983) 1.01
Neurotrophin receptor TrkB activation is not required for the postnatal survival of retinal ganglion cells in vivo. Exp Neurol (2001) 1.01
Cell reassociation behavior and lectin-induced agglutination of embryonic mouse cells from different brain regions. Exp Cell Res (1978) 1.00
Photoreceptor-pigment epithelial cell relationships in rats with inherited retinal degeneration. Radioautographic and electron microscope evidence for a dual source of extra lamellar material. J Cell Biol (1972) 1.00
Retrograde intraaxonal transport of horseradish peroxidase in retinal ganglion cells of the chick. Brain Res (1975) 0.99
Pink-eyed dilution (p) gene in rodents: increased pigmentation in tissue culture. Dev Biol (1965) 0.98
Myotonia, a new inherited muscle disease in mice. J Neurosci (1982) 0.98
Light-evoked changes in the interphotoreceptor matrix. Science (1990) 0.97
Photoreceptor characteristics in congenic strains of RCS rats. Invest Ophthalmol Vis Sci (1981) 0.97
Benzo(a)pyrene and X-rays induce reversions of the pink-eyed unstable mutation in the retinal pigment epithelium of mice. Mutat Res (2000) 0.97
Degeneration of thalamic neurons in "Purkinje cell degeneration" mutant mice. I. Distribution of neuron loss. J Comp Neurol (1985) 0.96
Inherited muscle and nerve diseases in mice: a tabulation with commentary. Ann N Y Acad Sci (1979) 0.95
Outer segment disc shedding and phagocytosis in the outer retina. Trans Ophthalmol Soc U K (1983) 0.95
The interphotoreceptor matrix in rats with inherited retinal dystrophy. Invest Ophthalmol Vis Sci (1981) 0.95
Localization of theta alloantigens in mouse brain by immunofluroescence and cytotoxic inhibition. Brain Res (1971) 0.95
Human trophoblast cells express CD4 and are permissive for productive infection with HIV-1. Clin Exp Immunol (1992) 0.95
Serial section radioautography of the inner ear. Histological technique. Arch Otolaryngol (1967) 0.94
A reproductive endocrine profile in the diabetes (db) mutant mouse. Biol Reprod (1979) 0.94
Matrix metalloproteinase-2 and tissue inhibitor of metalloproteinase-1 in the retinal pigment epithelium and interphotoreceptor matrix: vectorial secretion and regulation. Exp Eye Res (1997) 0.94
Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographic analysis. J Comp Neurol (1982) 0.94