Published in Vision Res on January 30, 2007
Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. J Clin Invest (2010) 2.13
Retinal ganglion cells survive and maintain normal dendritic morphology in a mouse model of inherited photoreceptor degeneration. J Neurosci (2008) 1.89
Long-term retinal function and structure rescue using capsid mutant AAV8 vector in the rd10 mouse, a model of recessive retinitis pigmentosa. Mol Ther (2010) 1.75
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation. Invest Ophthalmol Vis Sci (2008) 1.68
Identification of molecular markers of bipolar cells in the murine retina. J Comp Neurol (2008) 1.68
Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomography. Invest Ophthalmol Vis Sci (2012) 1.27
Mouse model resources for vision research. J Ophthalmol (2010) 1.26
Differential loss and preservation of glutamate receptor function in bipolar cells in the rd10 mouse model of retinitis pigmentosa. Eur J Neurosci (2009) 1.23
Functional rescue of degenerating photoreceptors in mice homozygous for a hypomorphic cGMP phosphodiesterase 6 b allele (Pde6bH620Q). Invest Ophthalmol Vis Sci (2008) 1.22
New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene. Hum Mol Genet (2008) 1.19
Progression of neuronal and synaptic remodeling in the rd10 mouse model of retinitis pigmentosa. J Comp Neurol (2010) 1.15
Overexpression of SOD in retina: need for increase in H2O2-detoxifying enzyme in same cellular compartment. Free Radic Biol Med (2011) 1.14
Naturally occurring animal models with outer retina phenotypes. Vision Res (2009) 1.14
Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesterase. Am J Hum Genet (2010) 1.13
TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice. Invest Ophthalmol Vis Sci (2012) 1.09
Self-complementary AAV5 vector facilitates quicker transgene expression in photoreceptor and retinal pigment epithelial cells of normal mouse. Exp Eye Res (2010) 1.07
Intrinsic bursting of AII amacrine cells underlies oscillations in the rd1 mouse retina. J Neurophysiol (2014) 1.06
Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration. EMBO Mol Med (2015) 1.06
Tauroursodeoxycholic acid preservation of photoreceptor structure and function in the rd10 mouse through postnatal day 30. Invest Ophthalmol Vis Sci (2008) 1.05
NRF2 promotes neuronal survival in neurodegeneration and acute nerve damage. J Clin Invest (2015) 1.05
shRNA knockdown of guanylate cyclase 2e or cyclic nucleotide gated channel alpha 1 increases photoreceptor survival in a cGMP phosphodiesterase mouse model of retinitis pigmentosa. J Cell Mol Med (2011) 1.02
Lentivirus-mediated expression of cDNA and shRNA slows degeneration in retinitis pigmentosa. Exp Biol Med (Maywood) (2011) 1.02
Early synaptic defects in tulp1-/- mice. Invest Ophthalmol Vis Sci (2009) 1.02
Inhibition of ceramide biosynthesis preserves photoreceptor structure and function in a mouse model of retinitis pigmentosa. Proc Natl Acad Sci U S A (2010) 1.02
Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy. Mol Ther (2012) 1.00
Analysis of the RPE sheet in the rd10 retinal degeneration model. Adv Exp Med Biol (2012) 0.98
Single-stranded oligonucleotide-mediated in vivo gene repair in the rd1 retina. Mol Vis (2007) 0.95
Bile acids in treatment of ocular disease. J Ocul Biol Dis Infor (2009) 0.94
Cone degeneration following rod ablation in a reversible model of retinal degeneration. Invest Ophthalmol Vis Sci (2011) 0.94
Neuronal remodeling in retinal circuit assembly, disassembly, and reassembly. Trends Neurosci (2014) 0.92
Layer-specific blood-flow MRI of retinitis pigmentosa in RCS rats. Exp Eye Res (2012) 0.92
Spontaneous Oscillatory Rhythm in Retinal Activities of Two Retinal Degeneration (rd1 and rd10) Mice. Korean J Physiol Pharmacol (2011) 0.91
Constituents of bile, bilirubin and TUDCA, protect against oxidative stress-induced retinal degeneration. J Neurochem (2010) 0.91
Blood flow and anatomical MRI in a mouse model of retinitis pigmentosa. Magn Reson Med (2012) 0.89
Intrinsically photosensitive retinal ganglion cells are resistant to N-methyl-D-aspartic acid excitotoxicity. Mol Vis (2012) 0.88
Non-contact measurement of linear external dimensions of the mouse eye. J Neurosci Methods (2010) 0.88
Insights into the role of RD3 in guanylate cyclase trafficking, photoreceptor degeneration, and Leber congenital amaurosis. Front Mol Neurosci (2014) 0.88
Retinal degeneration increases susceptibility to myopia in mice. Mol Vis (2013) 0.87
Aberrant activity in retinal degeneration impairs central visual processing and relies on Cx36-containing gap junctions. Exp Eye Res (2015) 0.86
Dominant cone-rod dystrophy: a mouse model generated by gene targeting of the GCAP1/Guca1a gene. PLoS One (2011) 0.85
Review: the history and role of naturally occurring mouse models with Pde6b mutations. Mol Vis (2013) 0.85
Neuroprotective Effects of Voluntary Exercise in an Inherited Retinal Degeneration Mouse Model. Invest Ophthalmol Vis Sci (2015) 0.84
AAV-mediated gene therapy in mouse models of recessive retinal degeneration. Curr Mol Med (2012) 0.84
CX3CL1 (fractalkine) protein expression in normal and degenerating mouse retina: in vivo studies. PLoS One (2014) 0.84
Function of human pluripotent stem cell-derived photoreceptor progenitors in blind mice. Sci Rep (2016) 0.84
Activation of the molecular chaperone, sigma 1 receptor, preserves cone function in a murine model of inherited retinal degeneration. Proc Natl Acad Sci U S A (2016) 0.84
Caspase inhibition with XIAP as an adjunct to AAV vector gene-replacement therapy: improving efficacy and prolonging the treatment window. PLoS One (2012) 0.83
PGC-1α determines light damage susceptibility of the murine retina. PLoS One (2012) 0.83
The role of mislocalized phototransduction in photoreceptor cell death of retinitis pigmentosa. PLoS One (2012) 0.83
Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors. Mol Vis (2011) 0.83
Overexpressed or intraperitoneally injected human transferrin prevents photoreceptor degeneration in rd10 mice. Mol Vis (2010) 0.83
Cone phosphodiesterase-6α' restores rod function and confers distinct physiological properties in the rod phosphodiesterase-6β-deficient rd10 mouse. J Neurosci (2013) 0.82
Neuoroprotective efficacies by KUS121, a VCP modulator, on animal models of retinal degeneration. Sci Rep (2016) 0.82
Dark-rearing the rd10 mouse: implications for therapy. Adv Exp Med Biol (2012) 0.81
Complementation test of Rpe65 knockout and tvrm148. Invest Ophthalmol Vis Sci (2013) 0.81
The Rpe65 rd12 allele exerts a semidominant negative effect on vision in mice. Invest Ophthalmol Vis Sci (2014) 0.81
Functional principal component analysis reveals discriminating categories of retinal pigment epithelial morphology in mice. Invest Ophthalmol Vis Sci (2013) 0.81
Mouse models for studies of retinal degeneration and diseases. Methods Mol Biol (2013) 0.81
The effects of iodoacetic acid on the mouse retina. Graefes Arch Clin Exp Ophthalmol (2014) 0.80
Electrophysiological and Histologic Evaluation of the Time Course of Retinal Degeneration in the rd10 Mouse Model of Retinitis Pigmentosa. Korean J Physiol Pharmacol (2013) 0.80
Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice. Mol Vis (2015) 0.79
A profile of transcriptomic changes in the rd10 mouse model of retinitis pigmentosa. Mol Vis (2014) 0.79
The synthetic progestin norgestrel acts to increase LIF levels in the rd10 mouse model of retinitis pigmentosa. Mol Vis (2016) 0.79
Correlations between ERG, OCT, and Anatomical Findings in the rd10 Mouse. J Ophthalmol (2014) 0.79
Changes in morphology and visual function over time in mouse models of retinal degeneration: an SD-OCT, histology, and electroretinography study. Jpn J Ophthalmol (2016) 0.79
Photoreceptor protection via blockade of BET epigenetic readers in a murine model of inherited retinal degeneration. J Neuroinflammation (2017) 0.79
Degeneration modulates retinal response to transient exogenous oxidative injury. PLoS One (2014) 0.78
Evaluation of micro Electroretinograms Recorded with Multiple Electrode Array to Assess Focal Retinal Function. Sci Rep (2016) 0.77
Changes in ganglion cell physiology during retinal degeneration influence excitability by prosthetic electrodes. J Neural Eng (2016) 0.77
Progesterone Attenuates Microglial-Driven Retinal Degeneration and Stimulates Protective Fractalkine-CX3CR1 Signaling. PLoS One (2016) 0.77
Oxidative stress retards vascular development before neural degeneration occurs in retinal degeneration rd1 mice. Graefes Arch Clin Exp Ophthalmol (2013) 0.77
Genetically modified neural stem cells for a local and sustained delivery of neuroprotective factors to the dystrophic mouse retina. Stem Cells Transl Med (2013) 0.77
Tamoxifen Provides Structural and Functional Rescue in Murine Models of Photoreceptor Degeneration. J Neurosci (2017) 0.76
Adalimumab Reduces Photoreceptor Cell Death in A Mouse Model of Retinal Degeneration. Sci Rep (2015) 0.76
Atypical retinal degeneration 3 in mice is caused by defective PDE6B pre-mRNA splicing. Vision Res (2012) 0.76
Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ. Invest Ophthalmol Vis Sci (2016) 0.76
Photoreceptor degeneration by intravitreal injection of N-methyl-N-nitrosourea (MNU) in rabbits: a pilot study. Graefes Arch Clin Exp Ophthalmol (2016) 0.75
Advances in Gene Therapy for Diseases of the Eye. Hum Gene Ther (2016) 0.75
Alterations in Kainate Receptor and TRPM1 Localization in Bipolar Cells after Retinal Photoreceptor Degeneration. Front Cell Neurosci (2015) 0.75
Carnosic acid slows photoreceptor degeneration in the Pde6b(rd10) mouse model of retinitis pigmentosa. Sci Rep (2016) 0.75
Reduced phosphoCREB in Müller glia during retinal degeneration in rd10 mice. Mol Vis (2017) 0.75
Different effects of valproic acid on photoreceptor loss in Rd1 and Rd10 retinal degeneration mice. Mol Vis (2014) 0.75
MUTYH promotes oxidative microglial activation and inherited retinal degeneration. JCI Insight (2016) 0.75
Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice. Nat Commun (2017) 0.75
A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function. J Neurophysiol (2017) 0.75
p75(NTR) antagonists attenuate photoreceptor cell loss in murine models of retinitis pigmentosa. Cell Death Dis (2017) 0.75
Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa. Front Neurosci (2017) 0.75
Role of the sigma-1 receptor chaperone in rod and cone photoreceptor degenerations in a mouse model of retinitis pigmentosa. Mol Neurodegener (2017) 0.75
Assessment of Safety and Functional Efficacy of Stem Cell-Based Therapeutic Approaches Using Retinal Degenerative Animal Models. Stem Cells Int (2017) 0.75
Retinal degeneration mutants in the mouse. Vision Res (2002) 4.93
Cyclic GMP-activated conductance of retinal photoreceptor cells. Annu Rev Neurosci (1989) 4.22
The Inheritance of a Retinal Abnormality in White Mice. Proc Natl Acad Sci U S A (1924) 4.16
Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse. Proc Natl Acad Sci U S A (1991) 3.77
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nat Genet (1993) 3.49
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa. Proc Natl Acad Sci U S A (1995) 2.41
Cyclic guanosine monophosphate: elevation in degenerating photoreceptor cells of the C3H mouse retina. Science (1974) 2.34
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes. Mol Vis (1999) 2.04
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. Proc Natl Acad Sci U S A (1993) 1.95
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene. Hum Mol Genet (2003) 1.83
Multiple cyclic nucleotide phosphodiesterases. Mol Pharmacol (1994) 1.80
PCR-amplification of simple sequence repeat variants from pooled DNA samples for rapidly mapping new mutations of the mouse. Genomics (1994) 1.73
C57BL-6J mice with inherited retinal degeneration. Arch Ophthalmol (1974) 1.61
Enzymic basis for cyclic GMP accumulation in degenerative photoreceptor cells of mouse retina. J Cyclic Nucleotide Res (1976) 1.56
Retinal degeneration in the mouse is rodless retina. J Hered (1966) 1.50
Genotype-phenotype correlation of mouse pde6b mutations. Invest Ophthalmol Vis Sci (2005) 1.31
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
NIH Swiss and Black Swiss mice have retinal degeneration and performance deficits in cognitive tests. Comp Med (2005) 1.15
FVB.129P2-Pde6b(+) Tyr(c-ch)/Ant, a sighted variant of the FVB/N mouse strain suitable for behavioral analysis. Genes Brain Behav (2006) 1.08
The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse. The Mouse Genome Database Group. Nucleic Acids Res (2000) 20.44
The virulence plasmid of Yersinia, an antihost genome. Microbiol Mol Biol Rev (1998) 5.78
Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice. Nat Genet (1997) 5.13
A mouse model for Down syndrome exhibits learning and behaviour deficits. Nat Genet (1995) 4.95
Retinal degeneration mutants in the mouse. Vision Res (2002) 4.93
Two Cases of Thromboembolic Disease Associated with Oral Contraceptives. Br Med J (1962) 4.49
The Mouse Genome Database (MGD): genetic and genomic information about the laboratory mouse. The Mouse Genome Database Group. Nucleic Acids Res (1999) 4.39
The Mouse Genome Database (MGD). A comprehensive public resource of genetic, phenotypic and genomic data. The Mouse Genome Informatics Group. Nucleic Acids Res (1997) 4.31
Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci U S A (1991) 4.10
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8. Genomics (1991) 3.93
Essential iris atrophy, pigment dispersion, and glaucoma in DBA/2J mice. Invest Ophthalmol Vis Sci (1998) 3.61
In vivo 13 carbon metabolic imaging at 3T with hyperpolarized 13C-1-pyruvate. Magn Reson Med (2007) 3.58
Modification in the xylose absorption test as an index of intestinal function. Gut (1967) 3.47
Low molecular weight versus standard heparin for prevention of venous thromboembolism after major abdominal surgery. The Thromboprophylaxis Collaborative Group. Lancet (1993) 3.41
Separation of transfer ribonucleic acid by sepharose chromatography using reverse salt gradients. Proc Natl Acad Sci U S A (1975) 3.23
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Hum Mutat (2001) 3.07
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Genet (2000) 2.85
Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene. Am J Hum Genet (2001) 2.80
Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nat Genet (1996) 2.75
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12). Nat Genet (1999) 2.75
Rules and guidelines for mouse gene nomenclature: a condensed version. International Committee on Standardized Genetic Nomenclature for Mice. Genomics (1997) 2.65
Myelinated retinal nerve fibers. Am J Ophthalmol (1981) 2.45
Mutations in MKKS cause Bardet-Biedl syndrome. Nat Genet (2000) 2.45
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. Am J Hum Genet (2001) 2.43
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage. Genes Dev (1994) 2.41
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice. Nat Genet (1999) 2.30
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. Am J Hum Genet (1998) 2.29
The Mouse Genome Database (MGD): a community resource. Status and enhancements. The Mouse Genome Informatics Group. Nucleic Acids Res (1998) 2.20
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa. Nat Genet (1999) 2.13
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency. J Clin Invest (1989) 2.09
Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Mol Genet Metab (2000) 2.07
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta. Proc Natl Acad Sci U S A (1993) 2.07
Molecular analysis of reverse mutations from nonagouti (a) to black-and-tan (a(t)) and white-bellied agouti (Aw) reveals alternative forms of agouti transcripts. Genes Dev (1994) 2.07
Gene sharing by delta-crystallin and argininosuccinate lyase. Proc Natl Acad Sci U S A (1988) 2.07
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes. Mol Vis (1999) 2.04
The fatty liver dystrophy (fld) mutation. A new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activities. J Biol Chem (1989) 1.91
An analysis of allelic variation in the ABCA4 gene. Invest Ophthalmol Vis Sci (2001) 1.90
Informatics for mouse genetics and genome mapping. Methods (1998) 1.89
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. Proc Natl Acad Sci U S A (2000) 1.88
Total parenteral nutrition at home for 23 months, without complication, and with good rehabilitation. A study of technical and metabolic features. Gastroenterology (1973) 1.87
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness. Am J Hum Genet (2002) 1.86
Sinusoidal lining cell damage: the critical injury in cold preservation of liver allografts in the rat. Transplantation (1988) 1.78
TyeA, a protein involved in control of Yop release and in translocation of Yersinia Yop effectors. EMBO J (1998) 1.78
Ribavirin inhibits viral-induced macrophage production of TNF, IL-1, the procoagulant fgl2 prothrombinase and preserves Th1 cytokine production but inhibits Th2 cytokine response. J Immunol (1998) 1.77
Imaging considerations for in vivo 13C metabolic mapping using hyperpolarized 13C-pyruvate. Magn Reson Med (2009) 1.72
Classification of congenital and early onset retinitis pigmentosa. Arch Ophthalmol (1985) 1.67
Albumin, fibrinogen and transferrin synthesis in isolated rat hepatocyte suspensions. A model for the study of plasma protein synthesis. Biochem J (1975) 1.66
Ia-positive dendritic cells form a tightly meshed network within the human airway epithelium. Clin Exp Allergy (1989) 1.64
Targeted inactivation of sister of P-glycoprotein gene (spgp) in mice results in nonprogressive but persistent intrahepatic cholestasis. Proc Natl Acad Sci U S A (2001) 1.63
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens. Invest Ophthalmol Vis Sci (2000) 1.61
Optimization of fast spiral chemical shift imaging using least squares reconstruction: application for hyperpolarized (13)C metabolic imaging. Magn Reson Med (2007) 1.61
Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. Invest Ophthalmol Vis Sci (1995) 1.56
Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene. Hum Mol Genet (2000) 1.55
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice. Proc Natl Acad Sci U S A (2000) 1.54
Ts65Dn -- localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome. Cytogenet Cell Genet (2001) 1.52
Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older. Ophthalmology (1999) 1.51
The evolutionary history of the extinct ratite moa and New Zealand Neogene paleogeography. Proc Natl Acad Sci U S A (2009) 1.50
Two simple programs for the analysis of data from enzyme-linked immunosorbent (ELISA) assays on a programmable desk-top calculator. Anal Biochem (1981) 1.49
X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11. Am J Hum Genet (1995) 1.49
Measuring disability in stroke: relationship between the modified Rankin scale and the Barthel index. J Neurol (2007) 1.48
Genetic heterogeneity among blue-cone monochromats. Am J Hum Genet (1993) 1.47
Ultrastructural hepatocellular alterations induced by in vivo fructose infusion. Lab Invest (1970) 1.46
Clinical spectrum of the Budd-Chiari syndrome and its surgical management. Am J Surg (1975) 1.42
Menkes disease. New ocular and electroretinographic findings. Ophthalmology (1998) 1.42
The mouse mutation severe combined immune deficiency (scid) is on chromosome 16. Immunogenetics (1989) 1.41
Automated single-voxel proton MRS: technical development and multisite verification. Magn Reson Med (1994) 1.41
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals. Genome Res (2000) 1.40
Ultrastructure of bile canaliculi, with special reference to the surface coat and the pericanalicular web. Lab Invest (1974) 1.39
Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa. Genomics (1995) 1.38
Obstetricians' and gynecologists' beliefs and preferred modes of treatment for women diagnosed with premenstrual symptoms. Womens Health Issues (1992) 1.38
Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures. Epilepsy Res (1990) 1.37
Mouse models of ocular diseases. Vis Neurosci (2005) 1.37
Lymphocyte targeting of the central nervous system: a review of afferent and efferent CNS-immune pathways. Brain Pathol (1996) 1.36
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. Hum Mol Genet (1999) 1.35
A new variant of Ehlers-Danlos syndrome: an autosomal dominant disorder of fragile skin, abnormal scarring, and generalized periodontitis. Birth Defects Orig Artic Ser (1977) 1.33
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. Proc Natl Acad Sci U S A (1995) 1.33
Synaptonemal complex analysis of mouse chromosomal rearrangements. IV. Synapsis and synaptic adjustment in two paracentric inversions. Chromosoma (1982) 1.32
Contractility of bile canaliculi: implications for liver function. Science (1981) 1.31
Incidence of leukaemia in young people in the vicinity of Hinkley Point nuclear power station, 1959-86. BMJ (1989) 1.29
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I. Am J Hum Genet (2000) 1.29
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. Am J Hum Genet (2000) 1.28
Telangiectasia and optic atrophy in cone-rod degenerations. Arch Ophthalmol (1981) 1.28