Published in J AAPOS on February 01, 2011
Integrative annotation of 21,037 human genes validated by full-length cDNA clones. PLoS Biol (2004) 7.17
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Role of TBX1 in human del22q11.2 syndrome. Lancet (2003) 4.45
Identification of eight members of the Argonaute family in the human genome. Genomics (2003) 3.55
Retracted Crucial role of interleukin-7 in T helper type 17 survival and expansion in autoimmune disease. Nat Med (2010) 2.43
The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts. Nucleic Acids Res (2007) 2.07
The human ribosomal protein genes: sequencing and comparative analysis of 73 genes. Genome Res (2002) 2.03
Three cases of corneal melting after instillation of a new nonsteroidal anti-inflammatory drug. Cornea (2006) 1.94
DNA sequence and analysis of human chromosome 8. Nature (2006) 1.91
Recommendations of the 2006 Human Variome Project meeting. Nat Genet (2007) 1.90
Molecular cloning and expression analysis of a novel gene DGCR8 located in the DiGeorge syndrome chromosomal region. Biochem Biophys Res Commun (2003) 1.77
Overview of the ID, EPI and REL tasks of BioNLP Shared Task 2011. BMC Bioinformatics (2012) 1.62
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Nucleolar localization of DGCR8 and identification of eleven DGCR8-associated proteins. Exp Cell Res (2007) 1.60
Magnetic resonance imaging of the medial rectus muscle of patients with consecutive exotropia after medial rectus muscle recession. Ophthalmology (2010) 1.60
Leucine deprivation increases hepatic insulin sensitivity via GCN2/mTOR/S6K1 and AMPK pathways. Diabetes (2011) 1.55
Composition, sources, and potential toxicological significance of PAHs in the surface sediments of the Meiliang Bay, Taihu Lake, China. Environ Int (2005) 1.51
Urinary beta 2-microglobulin in premature infants with chorioamnionitis and chronic lung disease. J Pediatr (2003) 1.44
Two-step transplantation for primary hyperoxaluria: a winning strategy to prevent progression of systemic oxalosis in early onset renal insufficiency cases. Pediatr Transplant (2014) 1.40
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Circadian regulation of intracellular G-protein signalling mediates intercellular synchrony and rhythmicity in the suprachiasmatic nucleus. Nat Commun (2011) 1.34
Variants in optineurin gene and their association with tumor necrosis factor-alpha polymorphisms in Japanese patients with glaucoma. Invest Ophthalmol Vis Sci (2004) 1.28
Loss of stereopsis with optic chiasmal lesions and stereoscopic tests as a differential test. Ophthalmology (2002) 1.23
Clinical features of congenital retinal folds. Am J Ophthalmol (2011) 1.20
Leucine deprivation decreases fat mass by stimulation of lipolysis in white adipose tissue and upregulation of uncoupling protein 1 (UCP1) in brown adipose tissue. Diabetes (2009) 1.20
Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population. PLoS One (2012) 1.17
Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Hum Mol Genet (2003) 1.17
Residues and source identification of persistent organic pollutants in farmland soils irrigated by effluents from biological treatment plants. Environ Int (2005) 1.12
A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1. Biochem Biophys Res Commun (2003) 1.12
Scleral window surgery and topical mitomycin C for nanophthalmic uveal effusion complicated by renal failure: case report. Graefes Arch Clin Exp Ophthalmol (2006) 1.11
Identification of three novel proteins (SGSM1, 2, 3) which modulate small G protein (RAP and RAB)-mediated signaling pathway. Genomics (2007) 1.09
Choroidal neovascularization in a child following laser pointer-induced macular injury. Jpn J Ophthalmol (2010) 1.09
Rice SPK, a calmodulin-like domain protein kinase, is required for storage product accumulation during seed development: phosphorylation of sucrose synthase is a possible factor. Plant Cell (2002) 1.07
Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype. J Clin Endocrinol Metab (2009) 1.05
SNPs and interaction analyses of noelin 2, myocilin, and optineurin genes in Japanese patients with open-angle glaucoma. Invest Ophthalmol Vis Sci (2006) 1.05
Human sclera maintains common characteristics with cartilage throughout evolution. PLoS One (2008) 1.02
Protective effects of EGCg or GCg, a green tea catechin epimer, against postischemic myocardial dysfunction in guinea-pig hearts. Life Sci (2006) 1.00
Leucine deprivation stimulates fat loss via increasing CRH expression in the hypothalamus and activating the sympathetic nervous system. Mol Endocrinol (2011) 0.99
Distribution and effects of nonsense polymorphisms in human genes. PLoS One (2008) 0.99
Chronic angle closure glaucoma secondary to frail zonular fibres and spherophakia. Acta Ophthalmol Scand (2003) 0.98
The enhancement effect of gold nanoparticles in drug delivery and as biomarkers of drug-resistant cancer cells. ChemMedChem (2007) 0.98
Superior segmental optic hypoplasia found in Tajimi Eye Health Care Project participants. Jpn J Ophthalmol (2004) 0.98
PKD2 and PKD3 promote prostate cancer cell invasion by modulating NF-κB- and HDAC1-mediated expression and activation of uPA. J Cell Sci (2012) 0.98
Stress-activated protein kinase MKK7 regulates axon elongation in the developing cerebral cortex. J Neurosci (2011) 0.97
A novel missense mutation (Leu46Val) of PAX6 found in an autistic patient. Neurosci Lett (2009) 0.96
Association between glaucoma and gene polymorphism of endothelin type A receptor. Mol Vis (2005) 0.96
Identification and characterization of a novel gene family YPEL in a wide spectrum of eukaryotic species. Gene (2004) 0.96
Vascular abnormalities in aggressive posterior retinopathy of prematurity detected by fluorescein angiography. Ophthalmology (2009) 0.95
Antioxidant constituents in distillation residue of Awamori spirits. J Agric Food Chem (2007) 0.95
Macular carotenoid levels of normal subjects and age-related maculopathy patients in a Japanese population. Ophthalmology (2008) 0.94
Novel mutations in the OPA1 gene and associated clinical features in Japanese patients with optic atrophy. Ophthalmology (2006) 0.92
Effects of the serotonin and noradrenaline reuptake inhibitor (SNRI) milnacipran on marble burying behavior in mice. Biol Pharm Bull (2007) 0.92
Evaluation of Surgical Strategy Based on the Intraoperative Superior Oblique Tendon Traction Test. PLoS One (2016) 0.91
Enhanced S-cone syndrome with subfoveal neovascularization. Am J Ophthalmol (2002) 0.90
Maternal ghrelin plays an important role in rat fetal development during pregnancy. Endocrinology (2005) 0.90
Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations. J Hum Genet (2011) 0.90
YPEL5 protein of the YPEL gene family is involved in the cell cycle progression by interacting with two distinct proteins RanBPM and RanBP10. Genomics (2010) 0.89
Elevated transcription factor specificity protein 1 in autistic brains alters the expression of autism candidate genes. Biol Psychiatry (2011) 0.89
Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity. Mol Vis (2010) 0.89
Paraoxonase 1 gene polymorphisms influence clinical features of open-angle glaucoma. Graefes Arch Clin Exp Ophthalmol (2006) 0.89
Detection of cytotoxic anti-LEDGF autoantibodies in atopic dermatitis. Autoimmunity (2002) 0.89
Mouse strain differences in immobility and sensitivity to fluvoxamine and desipramine in the forced swimming test: analysis of serotonin and noradrenaline transporter binding. Eur J Pharmacol (2008) 0.88
p38 Mitogen-activated protein kinase controls a switch between cardiomyocyte and neuronal commitment of murine embryonic stem cells by activating myocyte enhancer factor 2C-dependent bone morphogenetic protein 2 transcription. Stem Cells Dev (2010) 0.88
NodMutDB: a database for genes and mutants involved in symbiosis. Bioinformatics (2005) 0.87
Analysis of eighteen deletion breakpoints in the parkin gene. Biochem Biophys Res Commun (2009) 0.86
Initial characterization of an uromodulin-like 1 gene on human chromosome 21q22.3. Biochem Biophys Res Commun (2004) 0.86
Establishment and characterization of pleomorphic adenoma cell systems: an in-vitro demonstration of carcinomas arising secondarily from adenomas in the salivary gland. BMC Cancer (2009) 0.86
Interarm interaction of DNA cruciform forming at a short inverted repeat sequence. Biophys J (2003) 0.86
Improvement of skeletal lesions in mice with mucopolysaccharidosis type VII by neonatal adenoviral gene transfer. Mol Ther (2003) 0.86
Development of a premacular vitreous pocket. JAMA Ophthalmol (2013) 0.86
Congenital rotated macula with good vision and binocular function. Jpn J Ophthalmol (2009) 0.86
Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1. J Hum Genet (2010) 0.85
A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3. Genomics (2004) 0.85
Polymorphism of beta-adrenergic receptors and susceptibility to open-angle glaucoma. Mol Vis (2006) 0.85
Combination treatment of human pancreatic cancer xenograft models with the epidermal growth factor receptor tyrosine kinase inhibitor erlotinib and oncolytic herpes simplex virus HF10. Ann Surg Oncol (2013) 0.85
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes. J Hum Genet (2010) 0.85
Stress induces mitochondria-mediated apoptosis independent of SAPK/JNK activation in embryonic stem cells. J Biol Chem (2003) 0.85
Early detection of thinning of retinal nerve fiber layer in glaucomatous eyes by optical coherence tomography 3000: analysis of retinal nerve fiber layer corresponding to the preserved hemivisual field. Ophthalmic Res (2005) 0.85
Clinical features of anterior segment dysgenesis associated with congenital corneal opacities. Cornea (2012) 0.85
Central corneal thickness in Japanese children. Jpn J Ophthalmol (2009) 0.84
Outcome of early surgery for bilateral congenital cataracts in eyes with microcornea. Am J Ophthalmol (2007) 0.84
Risk factors for recurrent fibrovascular proliferation in aggressive posterior retinopathy of prematurity after early vitreous surgery. Am J Ophthalmol (2010) 0.84
ATF4 deficiency protects mice from high-carbohydrate-diet-induced liver steatosis. Biochem J (2011) 0.84
Encapsulation of basic fibroblast growth factor by polyelectrolyte multilayer microcapsules and its controlled release for enhancing cell proliferation. Biomacromolecules (2012) 0.84
Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa. Ophthalmic Genet (2008) 0.83
Effect of early vitreous surgery for aggressive posterior retinopathy of prematurity detected by fundus fluorescein angiography. Ophthalmology (2009) 0.83