Yumei Li

The mitotic spindle is required for loading of the DASH complex onto the kinetochore.

The DASH complex component Ask1 is a cell cycle-regulated Cdk substrate in Saccharomyces cerevisiae.

Genetic analysis of the kinetochore DASH complex reveals an antagonistic relationship with the ras/protein kinase A pathway and a novel subunit required for Ask1 association.

Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless.

Controlled strain on a double-templated textured polymer film: a new approach to patterned surfaces with bravais lattices and chains.

A novel beta-galactosidase capable of glycosyl transfer from Enterobacter agglomerans B1.

Comparative analysis of prophage-like elements in Helicobacter sp. genomes.

An entropy-based index for fine-scale mapping of QTL.

An entropy-based index for fine-scale mapping of disease genes.

The application of the entropy-based statistic for genomic association study of QTL.

20-Hydroxyeicosatetraenoic acid inhibits the apoptotic responses in pulmonary artery smooth muscle cells.

[RAPD genetic analysis on etiological factor of mink self-biting disease].

Purification and characterization of a novel beta-galactosidase with transglycosylation activity from Bacillus megaterium 2-37-4-1.

Mutation survey of known LCA genes and loci in the Saudi Arabian population.

15-HETE suppresses K(+) channel activity and inhibits apoptosis in pulmonary artery smooth muscle cells.

Role of protein kinase C in 15-HETE-induced hypoxic pulmonary vasoconstriction.

Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.

Earliest domestication of common millet (Panicum miliaceum) in East Asia extended to 10,000 years ago.

High-throughput multiplex sequencing to discover copy number variants in Drosophila.

Cell surface engineering of a beta-galactosidase for galactooligosaccharide synthesis.

Lipopolysaccharide "two-hit" induced refractory hypoxemia acute respiratory distress model in rats.

Prokaryotic diversity in continuous cropping and rotational cropping soybean soil.

Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing.

Genome-wide reinforcement of cohesin binding at pre-existing cohesin sites in response to ionizing radiation in human cells.

DNA demethylase activity maintains intestinal cells in an undifferentiated state following loss of APC.

The Drosophila melanogaster transcriptome by paired-end RNA sequencing.

Human telomeric proteins occupy selective interstitial sites.

4-[3,5-Bis(ethoxy-carbon-yl)-2,6-dimethyl-4-pyrid-yl]pyridinium nitrate.

Diethyl 2,6-dimethyl-4-(4-pyrid-yl)-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.

Hypothyroidism caused by phenobarbital affects patterns of estrous cyclicity in rats.

Analysis of flavonoids by capillary zone electrophoresis with electrokinetic supercharging.

[Effectiveness of microsurgical repair of flexor tendon rupture by non-knot Kessler suture method in anastomotic stoma].

Exome capture sequencing identifies a novel mutation in BBS4.

Synthesis of galactooligosaccharides by CBD fusion β-galactosidase immobilized on cellulose.

Enhanced anti-tumor and anti-angiogenic effects of metronomic cyclophosphamide combined with Endostar in a xenograft model of human lung cancer.

Transient receptor potential canonical 3 (TRPC3) is required for IgG immune complex-induced excitation of the rat dorsal root ganglion neurons.

Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration.

Tanshinone IIA improves miR-133 expression through MAPK ERK1/2 pathway in hypoxic cardiac myocytes.

Effects of irradiation on osteoblast-like cells on different titanium surfaces in vitro.

Osthole relaxes pulmonary arteries through endothelial phosphatidylinositol 3-kinase/Akt-eNOS-NO signaling pathway in rats.

Two methods for full-length RNA sequencing for low quantities of cells and single cells.

Optimization of fermentation conditions and properties of an exopolysaccharide from Klebsiella sp. H-207 and application in adsorption of hexavalent chromium.

Idiopathic orbital inflammation syndrome with retro-orbital involvement: a retrospective study of eight patients.

Anaplastic astrocytoma masquerading as hemorrhagic stroke.

Proteomic-based analysis for identification of proteins involved in 5-fluorouracil resistance in hepatocellular carcinoma.

mRNA profiles of cytokine receptors in unstimulated peripheral blood mononuclear cells from patients with chronic idiopathic urticaria.

Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa.

Cloning and characterization of new transcript variants of insulin-like growth factor-I in Sika deer (Cervus elaphus).

miR-129-2 suppresses proliferation and migration of esophageal carcinoma cells through downregulation of SOX4 expression.

optix functions as a link between the retinal determination network and the dpp pathway to control morphogenetic furrow progression in Drosophila.

Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing.

Sex identification of dog by PCR based on the differences in the AMELX and AMELY genes.

An intronic miRNA regulates expression of the human endothelial nitric oxide synthase gene and proliferation of endothelial cells by a mechanism related to the transcription factor SP-1.

15-LO/15-HETE mediated vascular adventitia fibrosis via p38 MAPK-dependent TGF-β.

PBK/TOPK expression in non-small-cell lung cancer: its correlation and prognostic significance with Ki67 and p53 expression.

Epidermal growth factor receptor (EGFR) signaling regulates epiphyseal cartilage development through β-catenin-dependent and -independent pathways.

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements.

Regulation of EMT by Notch signaling pathway in tumor progression.

Loss of has-miR-337-3p expression is associated with lymph node metastasis of human gastric cancer.

Differential expression of the melanocortin-4 receptor in male and female C57BL/6J mice.

Expression of Tiam1 predicts lymph node metastasis and poor survival of lung adenocarcinoma patients.

Application of next-generation sequencing to identify genes and mutations causing autosomal dominant retinitis pigmentosa (adRP).

Production, purification, and antibiofilm activity of a novel exopolysaccharide from Arthrobacter sp. B4.

Tanshinone IIA promotes pulmonary artery smooth muscle cell apoptosis in vitro by inhibiting the JAK2/STAT3 signaling pathway.

The incidence of inflammatory bowel disease in Northern China: a prospective population-based study.

miR-21 inhibitor suppresses proliferation and migration of nasopharyngeal carcinoma cells through down-regulation of BCL2 expression.

Cellular FLICE-like inhibitory protein protects against cardiac hypertrophy by blocking ASK1/p38 signaling in mice.

Characterization and flocculation mechanism of an alkali-activated polysaccharide flocculant from Arthrobacter sp. B4.

Interventions for the treatment of stretch marks: a systematic review.

[Effects of irradiation on proliferation and differentiation of MC3T3-E1 osteoblastic cells in vitro].

Large-scale identification of chemically induced mutations in Drosophila melanogaster.

A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa.

MicroRNA-21 inhibits platelet-derived growth factor-induced human aortic vascular smooth muscle cell proliferation and migration through targeting activator protein-1.

Activation of miR-21 by STAT3 induces proliferation and suppresses apoptosis in nasopharyngeal carcinoma by targeting PTEN gene.

Prognostic role of SPARC expression in gastric cancer: a meta-analysis.

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina.

PBK/TOPK expression correlates with mutant p53 and affects patients' prognosis and cell proliferation and viability in lung adenocarcinoma.

Next-generation sequencing-based molecular diagnosis of 82 retinitis pigmentosa probands from Northern Ireland.

Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions.

A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.

Combining serum and urine biomarkers in the early diagnosis of mild cognitive impairment that evolves into Alzheimer's disease in patients with the apolipoprotein E ϵ4 genotype.

STAT3-mediated MMP-2 expression is required for 15-HETE-induced vascular adventitial fibroblast migration.

CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes.

The PDGF-D/miR-106a/Twist1 pathway orchestrates epithelial-mesenchymal transition in gemcitabine resistance hepatoma cells.

Suppression of endothelial nitric oxide synthase expression and endothelial cell proliferation by an intronic 27-ntmiRNA and it's a novel link to AP-1.

Roles of miRNA-24 in regulating endothelial nitric oxide synthase expression and vascular endothelial cell proliferation.

MiRNA profile of osteosarcoma with CD117 and stro-1 expression: miR-1247 functions as an onco-miRNA by targeting MAP3K9.

Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming.

Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort.

ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement.

Reduced EGFR signaling enhances cartilage destruction in a mouse osteoarthritis model.

Emergence, Retention and Selection: A Trilogy of Origination for Functional De Novo Proteins from Ancestral LncRNAs in Primates.

Erratum: CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes.

Chromium (VI) detoxification by oxidation and flocculation of exopolysaccharides from Arthrobacter sp. B4.

Mutations in human IFT140 cause non-syndromic retinal degeneration.

The complete sequence of mitochondrial genome of Siberian accentor (Prunella montanella).

Complete mitochondrial genome sequence of Chestnut-flanked white-eye (Zosterops erythropleurus).

Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.

Identification and characterization of the cDNA sequence encoding amelogenin in rabbit (Oryctolagus cuniculus).

How users adopt healthcare information: An empirical study of an online Q&A community.

Randomized controlled trial comparing letrozole with laparoscopic ovarian drilling in women with clomiphene citrate-resistant polycystic ovary syndrome.

ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa.

TGF-β1/FGF-2 signaling mediates the 15-HETE-induced differentiation of adventitial fibroblasts into myofibroblasts.

Testing association and maternally mediated genetic effects with the principal component analysis in case-parents studies.

Threshold Dependence of Deep- and Near-subwavelength Ripples Formation on Natural MoS2 Induced by Femtosecond Laser.

MiR-130a-3p regulates cell migration and invasion via inhibition of Smad4 in gemcitabine resistant hepatoma cells.

Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1.

Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity.

Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa.

Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes.

Production and optimization of curdlan produced by Pseudomonas sp. QL212.

Melittin inhibits tumor angiogenesis modulated by endothelial progenitor cells associated with the SDF-1α/CXCR4 signaling pathway in a UMR-106 osteosarcoma xenograft mouse model.

MicroRNA-145 regulates platelet-derived growth factor-induced human aortic vascular smooth muscle cell proliferation and migration by targeting CD40.

Nutlin-3 reverses the epithelial-mesenchymal transition in gemcitabine-resistant hepatocellular carcinoma cells.

Draft Genome Sequence of Paenibacillus polymyxa KF-1, an Excellent Producer of Microbicides.

CCL21/CCR7 Axis Contributed to CD133+ Pancreatic Cancer Stem-Like Cell Metastasis via EMT and Erk/NF-κB Pathway.

Extracellular Release and Signaling by Heat Shock Protein 27: Role in Modifying Vascular Inflammation.

Tanshinone IIA inhibits apoptosis in the myocardium by inducing microRNA-152-3p expression and thereby downregulating PTEN.

Overexpression of myosin VI regulates gastric cancer cell progression.

Next-generation sequencing-based molecular diagnosis of 35 Hispanic retinitis pigmentosa probands.

CEP78 is mutated in a distinct type of Usher syndrome.

Tetramethylpyrazine and Astragaloside IV Synergistically Ameliorate Left Ventricular Remodeling and Preserve Cardiac Function in a Rat Myocardial Infarction Model.

Galectin-3 contributes to vascular fibrosis in monocrotaline-induced pulmonary arterial hypertension rat model.

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa.

Spliceosomal protein eftud2 mutation leads to p53-dependent apoptosis in zebrafish neural progenitors.

Directed functional connectivity of posterior cingulate cortex and whole brain in Alzheimer's disease and mild cognitive impairment.

[Influence of chromosomal polymorphisms on the clinical outcome of patients undergoing in vitro fertilization embryo transfer].

Cinepazide Maleate Improves Cognitive Function and Protects Hippocampal Neurons in Diabetic Rats with Chronic Cerebral Hypoperfusion.

Single-cell analysis of differences in transcriptomic profiles of oocytes and cumulus cells at GV, MI, MII stages from PCOS patients.

Enhanced adhesion and proliferation of human umbilical vein endothelial cells on conductive PANI-PCL fiber scaffold by electrical stimulation.

The Role of Autophagy in the Correlation Between Neuron Damage and Cognitive Impairment in Rat Chronic Cerebral Hypoperfusion.

Programmed cell death 1 correlates with the occurrence and development of MG63 osteosarcoma.

[Imiquimod combined with dendritic cell vaccine decreases Treg proportion and enhances anti-tumor responses in mice bearing melanoma].

Biosynthesis of poly (3-hydroxybutyrate-co-3-hydroxyvalerate) by bacterial community from propylene oxide saponification wastewater residual sludge.

Erratum to: the Role of Autophagy in the Correlation Between Neuron Damage and Cognitive Impairment in Rat Chronic Cerebral Hypoperfusion.

Over-expression of Thrombospondin 4 correlates with loss of miR-142 and contributes to migration and vascular invasion of advanced hepatocellular carcinoma.

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.

Third-generation Dual-source CT for Head and Neck CT Angiography with 70 kV Tube Voltage and 20-25 ml Contrast Medium in Patients With Body Weight Lower than 75 kg.

Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies.

Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells.

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.

High-sensitivity neuroimaging biomarkers for the identification of amnestic mild cognitive impairment based on resting-state fMRI and a triple network model.

REEP6 Deficiency Leads to Retinal Degeneration through Disruption of ER Homeostasis and Protein Trafficking.

Characterization of S-adenosylhomocysteine/Methylthioadenosine nucleosidase on secretion of AI-2 and biofilm formation of Escherichia coli.

Divergent Requirements for EZH1 in Heart Development Versus Regeneration.

Evaluation of Absolute Serum Creatinine Changes in Staging of Cirrhosis-Induced Acute Renal Injury and its Association with Long-term Outcomes.

A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States.

Inhibitory effect of trans-caryophyllene (TC) on leukocyte-endothelial attachment.

Benign ependymoma with extensive intracranial and spinal cerebrospinal fluid dissemination: case report and literature review.

Chitosan surface modified electrospun poly(ε-caprolactone)/carbon nanotube composite fibers with enhanced mechanical, cell proliferation and antibacterial properties.

Functionalized magnetic iron oxide/polyacrylonitrile composite electrospun fibers as effective chromium (VI) adsorbents for water purification.

Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants amongst exon-captured variants of uncertain significance.

The phenotypic variability of HK1-associated retinal dystrophy.