Miao Sun

Construction and Expression of hTNFalpha-hTGF3 Fused Gene.

Identifying novel transcripts and novel genes in the human genome by using novel SAGE tags.

Determination of the energetics governing the regulatory step in growth hormone-induced receptor homodimerization.

[Analysis on genetic polymorphism of 14 short tandem repeat loci on chromosome 7p14-15 and 12q13 in Chinese north Hans].

SAGE is far more sensitive than EST for detecting low-abundance transcripts.

[Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].

Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria.

Dissecting the binding energy epitope of a high-affinity variant of human growth hormone: cooperative and additive effects from combining mutations from independently selected phage display mutagenesis libraries.

Homology modeling and molecular dynamics study of GSK3/SHAGGY-like kinase.

Over 20% of human transcripts might form sense-antisense pairs.

[A de nono I462S mutation in the KRT6A gene is associated with pachyonychia congenita type I].

Homology modeling and S(N)2 displacement reaction of fluoroacetate dehalogenase from Burkholderia sp. FA1.

Molecular simulation studies of a selenium-containing scFv catalytic antibody that mimics glutathione peroxidase.

[HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].

Human antisense genes have unusually short introns: evidence for selection for rapid transcription.

Homology modeling and PAPS ligand (cofactor) binding study of bovine phenol sulfotransferase.

Homology modeling and docking study of cyclin-dependent kinase (CDK) 10.

Genome-wide analysis of coordinate expression and evolution of human cis-encoded sense-antisense transcripts.

Homology modeling and substrate binding study of Nudix hydrolase Ndx1 from Thermos thermophilus HB8.

The small introns of antisense genes are better explained by selection for rapid transcription than by "genomic design".

Evidence for a preferential targeting of 3'-UTRs by cis-encoded natural antisense transcripts.

Gene expression profiles in acute myeloid leukemia with common translocations using SAGE.

Mutational screening of FGFR1, CER1, and CDON in a large cohort of trigonocephalic patients.

The molecular mechanism of interaction between sushi peptide and Pseudomonas endotoxin.

Evidence for variation in abundance of antisense transcripts between multicellular animals but no relationship between antisense transcriptionand organismic complexity.

Molecular mechanisms that govern the specificity of Sushi peptides for Gram-negative bacterial membrane lipids.

MicroRNA and cancer: Current status and prospective.

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.

Substitution effect on the geometry and electronic structure of the ferrocene.

MicroRNA expression signatures accurately discriminate acute lymphoblastic leukemia from acute myeloid leukemia.

Novel point mutations in GDF5 associated with two distinct limb malformations in Chinese: brachydactyly type C and proximal symphalangism.

Thioredoxin-like 6 protects retinal cell line from photooxidative damage by upregulating NF-kappaB activity.

Theoretical study on the reaction of SiH(CH(3))(3) with SiH(3) radical.

Distinct microRNA expression profiles in acute myeloid leukemia with common translocations.

[Rapid detection of common ATP7B mutations in Wilson disease by high resolution melting analysis].

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.

Consistent deregulation of gene expression between human and murine MLL rearrangement leukemias.

A ZRS duplication causes syndactyly type IV with tibial hypoplasia.

NiO-polyoxometalate nanocomposites as efficient catalysts for the oxidative dehydrogenation of propane and isobutane.

A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family.

Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.

Theoretical study and rate constants calculation for the reactions of SiH3 radical with SiH3CH3 and SiH2(CH3)2.

[Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].

Inhalative formaldehyde exposure enhances aggressive behavior and disturbs monoamines in frontal cortex synaptosome of male rats.

[Treating high angle bimaxillary protrusion with three kinds of extraction method: a clinical study].

[Identification of a novel TP53 germline mutation in one child with adrenocortical carcinoma].

[The effect of Nifedipine and mechanical strain on matrix metalloproteinase expression in human periodontal ligament fibroblast].

[Mutation analysis of a Uighur family with epidermolytic palmoplantar keratoderma].

Copper downregulates neprilysin activity through modulation of neprilysin degradation.

Aberrant overexpression and function of the miR-17-92 cluster in MLL-rearranged acute leukemia.

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.

Magnesium modulates amyloid-beta protein precursor trafficking and processing.

Polyoxometalate-supported Pd nanoparticles as efficient catalysts for the direct synthesis of hydrogen peroxide in the absence of acid or halide promoters.

[Immunophenotypic analysis of Philadelphia chromosome positive acute lymphoblastic leukaemia in adults].

Theoretical studies on the reactions CH3SCH3 with OH, CF3, and CH3 radicals.

[Bag3 gene expression in chronic lymphocytic leukemia and its association with patients' prognosis].

Gamma-secretase gene mutations in familial acne inversa.

Expression and functional characterization of a recombinant targeted toxin with an uPA cleavable linker in Pichia pastoris.

Multiple sequence-specific DNA-binding proteins mediate estrogen receptor signaling through a tethering pathway.

X-linked congenital hypertrichosis syndrome is associated with interchromosomal insertions mediated by a human-specific palindrome near SOX3.

Induced crystallization of single-chain polyethylene on a graphite surface: molecular dynamics simulation.

Formononetin Protects Neurons Against Hypoxia-Induced Cytotoxicity Through Upregulation of ADAM10 and sAβPPα

Effects of potassium ion channels in term pregnant myometrium.

Epitope mapping of a monoclonal antibody against the Gp85 of avian leukosis virus subgroup J.

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

Xylocoside G reduces amyloid-β induced neurotoxicity by inhibiting NF-κB signaling pathway in neuronal cells.

Estrogen regulates JNK1 genomic localization to control gene expression and cell growth in breast cancer cells.

p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

[Protective effects and mechanisms of OSR on primary cultured hippocampus neurons subjected to anoxic injury in neonatal rat].

Acute promyelocytic leukemia with a STAT5b-RARα fusion transcript defined by array-CGH, FISH, and RT-PCR.

Maternal androgen excess reduces placental and fetal weights, increases placental steroidogenesis, and leads to long-term health effects in their female offspring.

Acoustic vibration sensor based on nonadiabatic tapered fibers.

Continuous administration of a P450 aromatase inhibitor induces polycystic ovary syndrome with a metabolic and endocrine phenotype in female rats at adult age.

A unique aliphatic tertiary amine chromophore: fluorescence, polymer structure, and application in cell imaging.

Methane reacts with heteropolyacids chemisorbed on silica to produce acetic acid under soft conditions.

Identification of a 24-gene prognostic signature that improves the European LeukemiaNet risk classification of acute myeloid leukemia: an international collaborative study.

[Role of chemokine receptor 2 in renal damage induced by deoxycorticosterone acetate-salt hypertension].

Comment on 'response to "comment on 'levels of soluble endothelial selectin in umbilical cord serum are influenced by gestational age and histological chorioamnionitis, but not by pre-eclampsia' " '.

Bactericidal effects of hematoporphyrin monomethyl ether-mediated photosensitization against pathogenic communities from supragingival plaque.

Loss of Ahi1 affects early development by impairing BM88/Cend1-mediated neuronal differentiation.

Resveratrol is not as effective as physical exercise for improving reproductive and metabolic functions in rats with dihydrotestosterone-induced polycystic ovary syndrome.

HMGA2/TET1/HOXA9 signaling pathway regulates breast cancer growth and metastasis.

Absence of EZH2 Gene Mutation in Chronic Myeloid Leukemia Patients in Blast Crisis.

TET1 plays an essential oncogenic role in MLL-rearranged leukemia.

Homocysteine restricts copper availability leading to suppression of cytochrome C oxidase activity in phenylephrine-treated cardiomyocytes.

Minireview: Long noncoding RNAs: new "links" between gene expression and cellular outcomes in endocrinology.

Mapping ERβ genomic binding sites reveals unique genomic features and identifies EBF1 as an ERβ interactor.

Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family.

A 3D QSAR study of betulinic acid derivatives as anti-tumor agents using topomer CoMFA: model building studies and experimental verification.