Published in Biol Reprod on August 01, 1971
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Identification and cloning of a protein kinase-encoding mouse gene, Plk, related to the polo gene of Drosophila. Proc Natl Acad Sci U S A (1993) 1.96
A novel mammalian protein kinase gene (mak) is highly expressed in testicular germ cells at and after meiosis. Mol Cell Biol (1990) 1.46
Differential expression of the mouse homeobox-containing gene Hox-1.4 during male germ cell differentiation and embryonic development. Proc Natl Acad Sci U S A (1987) 1.17
Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant. Proc Natl Acad Sci U S A (2004) 1.13
Expression of cellular protooncogenes in the mouse male germ line: a distinctive 2.4-kilobase pim-1 transcript is expressed in haploid postmeiotic cells. Proc Natl Acad Sci U S A (1988) 1.07
Regulation of the synthesis of lactate dehydrogenase-X during spermatogenesis in the mouse. J Cell Biol (1981) 0.99
Production of fertile offspring from genetically infertile male mice. Proc Natl Acad Sci U S A (2004) 0.99
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The proximal end of mouse chromosome 17: new molecular markers identify a deletion associated with quakingviable. Genetics (1992) 0.94
MNS1 is essential for spermiogenesis and motile ciliary functions in mice. PLoS Genet (2012) 0.93
Expression of the proopiomelanocortin gene is developmentally regulated and affected by germ cells in the male mouse reproductive system. Proc Natl Acad Sci U S A (1987) 0.93
courtless, the Drosophila UBC7 homolog, is involved in male courtship behavior and spermatogenesis. Genetics (2000) 0.90
Male-enhanced antigen gene is phylogenetically conserved and expressed at late stages of spermatogenesis. Proc Natl Acad Sci U S A (1989) 0.82
Behavioral analysis of Drosophila mutants displaying abnormal male courtship. Invert Neurosci (1998) 0.79
A MEIG1/PACRG complex in the manchette is essential for building the sperm flagella. Development (2015) 0.78
Reproductive and neurological Quaking(viable) phenotypes in a severe combined immune deficient mouse background. Immunogenetics (2005) 0.75
Animal models of physiologic markers of male reproduction: genetically defined infertile mice. Environ Health Perspect (1987) 0.75
Dissecting the structural basis of MEIG1 interaction with PACRG. Sci Rep (2016) 0.75
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
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
Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets. Proc Natl Acad Sci U S A (1976) 2.59
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
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
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
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
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
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
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
Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering. Science (1979) 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
Supravital DNA synthesis in the developing human and mouse brain. J Neuropathol Exp Neurol (1968) 1.24
Histogenesis of mouse cerebellum in microwell cultures. Cell reaggregation and migration, fiber and synapse formation. J Cell Biol (1977) 1.22
Inherited primary hypothyroidism in mice. Science (1981) 1.17
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
Growth and development of the mouse retinal pigment epithelium. II. Cell patterning in experimental chimaeras and mosaics. Dev Biol (1987) 1.10
Artificial insemination of dystrophic mice with mixtures of spermatozoa. Nature (1965) 1.10
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
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
Retrohippocampal, hippocampal and related structures of the forebrain in the reeler mutant mouse. J Comp Neurol (1973) 1.02
Telencephalic origin of pulvinar neurons in the fetal human brain. Z Anat Entwicklungsgesch (1969) 1.02
Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination. J Neuropathol Exp Neurol (1983) 1.01
Muscular dystrophy in the mouse caused by an allele at the dy-locus. Life Sci (1970) 1.00
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
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
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
Localization of theta alloantigens in mouse brain by immunofluroescence and cytotoxic inhibition. Brain Res (1971) 0.95
A reproductive endocrine profile in the diabetes (db) mutant mouse. Biol Reprod (1979) 0.94
Serial section radioautography of the inner ear. Histological technique. Arch Otolaryngol (1967) 0.94
Shiverer gene maps near the distal end of chromosome 18 in the house mouse. Cytogenet Cell Genet (1985) 0.93
Peripheral nerve regeneration with entubulation repair: comparison of biodegradeable nerve guides versus polyethylene tubes and the effects of a laminin-containing gel. Exp Neurol (1987) 0.92
Cell patterning in vertebrate development: models and model systems. Curr Top Dev Biol (1987) 0.92
Concentrations of glutamic acid in cerebellar cortex and deep nuclei of normal mice and Weaver, Staggerer and nervous mutants. Brain Res (1978) 0.91
Hearing and vision in neurological mutant mice: a method for their evaluation. Exp Neurol (1966) 0.90
Report on a maternity unit. The first thousand confinements. Practitioner (1966) 0.90
Persistent hypersynchronization of neocortical neurons in the mocha mutant of mouse. J Neurogenet (1989) 0.90
A multimodal system for reconstruction and quantification of neurologic structures. Anal Quant Cytol Histol (1986) 0.90
Chromosome 19 of the house mouse. J Hered (1975) 0.90
Myelin deficient (shimld) mutant allele: morphological comparison with shiverer (shi) allele on a B6C3 mouse stock. Brain Res (1985) 0.89
Vibrator (vb): a spinocerebellar system degeneration with autosomal recessive inheritance in mice. Brain Res (1982) 0.89
Psychotic disorder caused by a general medical condition, with delusions. Secondary "organic" delusional syndromes. Psychiatr Clin North Am (1995) 0.89
Nerve regeneration through synthetic biodegradable nerve guides: regulation by the target organ. Plast Reconstr Surg (1984) 0.88
Plant lectins detect age and region specific differences in cell surface carbohydrates and cell reassociation behavior of embryonic mouse cerebellar cells. J Supramol Struct (1977) 0.88
Autoradiographic studies on lipid synthesis in the mouse brain during postnatal development. J Neurochem (1965) 0.87
Pathology of the spongiform encephalopathy in the Gray tremor mutant mouse. J Neuropathol Exp Neurol (1986) 0.86
The murine mutation trembler-J: proof of semidominant expression by use of the linked vestigial tail marker. J Neurogenet (1983) 0.86
Transmissible spongiform encephalopathy in the gray tremor mutant mouse. Proc Natl Acad Sci U S A (1985) 0.85
An in vivo model to quantify motor and sensory peripheral nerve regeneration using bioresorbable nerve guide tubes. Brain Res (1985) 0.85
Subcommissural organ and adjacent ependyma: autoradiographic study of their origin in the mouse brain. Am J Anat (1968) 0.85
Neurological Mutants of the Mouse. Science (1965) 0.85
Cribriform degeneration (cri): a new recessive neurological mutation in the mouse. Science (1972) 0.85
Susceptibility of proliferating cells to benzo[a]pyrene-induced homologous recombination in mice. Carcinogenesis (2001) 0.85
Complications following surgery for cancer of the larynx and hypopharynx. Cancer (1977) 0.84
Liposarcoma of the larynx: a multicentric or a metastatic malignancy. Laryngoscope (1977) 0.84
Intracellular injection of lucifer yellow into lightly fixed cerebellar neurons. Neurosci Lett (1986) 0.83
The mouse mutation claw paw: forelimb deformity and delayed myelination throughout the peripheral nervous system. J Hered (1991) 0.83
Long lives for homozygous trembler mutant mice despite virtual absence of peripheral nerve myelin. Science (1988) 0.83
The hybrid reeler mouse. J Hered (1973) 0.83
X-ray diffraction study of myelin structure in immature and mutant mice. Biochim Biophys Acta (1976) 0.83
Cultures of shiverer mutant cerebellum injected with normal oligodendrocytes make both normal and shiverer myelin. Proc Natl Acad Sci U S A (1984) 0.83
Paranodal dysmyelination and increase in tetrodotoxin binding sites in the sciatic nerve of the motor end-plate disease (med/med) mouse during postnatal development. Dev Biol (1984) 0.82
Discrimination of light intensity by rats with inherited retinal degeneration: a behavioral and cytological study. Vision Res (1974) 0.82
Neuronal differentiation in cultures of weaver (wv) mutant mouse cerebellum. J Supramol Struct Cell Biochem (1981) 0.82
Distribution of H-2 alloantigen in adult and developing mouse brain. Brain Res (1973) 0.82
Purkinje cells and granule cells in the cerebellum of the Stumbler mutant mouse. Brain Res (1981) 0.82
p21 controls patterning but not homologous recombination in RPE development. DNA Repair (Amst) (2005) 0.82
Nerve regeneration through biodegradable polyester tubes. Exp Neurol (1985) 0.81
Cross-linked collagen surface for cell culture that is stable, uniform, and optically superior to conventional surfaces. In Vitro Cell Dev Biol (1985) 0.81
Phagosome number and distribution in retinal pigment epithelial cells of vitiligo mutant mice. Exp Eye Res (1996) 0.81
Control of direction of growth during the elongation of neurites. Exp Neurol (1975) 0.81
Neurochemical and morphological consequences of axon terminal degeneration in cerebellar deep nuclei of mice with inherited Purkinje cell degeneration. Brain Res (1979) 0.81
Uptake and transport of lectins from the cerebrospinal fluid by cells of the immature mouse brain. Acta Histochem (1984) 0.80