Fang Cai

Streptozotocin-induced diabetes reduces retrograde axonal transport in the afferent and efferent vagus nerve.

Streptozotocin-induced diabetes and the neurochemistry of vagal afferent neurons.

Abnormal PI3 kinase/Akt signal pathway in vagal afferent neurons and vagus nerve of streptozotocin-diabetic rats.

Analysis of a repressor region in the human neuropeptide Y gene that binds Oct-1 and Pbx-1 in GT1-7 neurons.

Expression of circadian rhythm genes in gonadotropin-releasing hormone-secreting GT1-7 neurons.

Generation of a phenotypic array of hypothalamic neuronal cell models to study complex neuroendocrine disorders.

Alpha-lipoic acid treatment prevents the diabetes-induced attenuation of the afferent limb of the baroreceptor reflex in rats.

Uptake of botulinum neurotoxin into cultured neurons.

Day/night rhythms in gene expression of the normal murine heart.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.

A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family.

The combination of suicide gene therapy and radiation enhances the killing of nasopharyngeal carcinoma xenographs.

A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinoma.

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.

Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.

[Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].

Identification of the alternative promoters of the KChIP4 subfamily.

Research on screening and identification of proteins interacting with ataxin-3.

[Effect of IP3 on BK channels of porcine coronary artery smooth muscle cells].

Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families.

Cx31 is assembled and trafficked to cell surface by ER-Golgi pathway and degraded by proteasomal or lysosomal pathways.

[Stable suppression of beta-catenin expression in prostate cancer cell line by retrovirus mediated RNAi].

Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells.

Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.

Molecular analysis of SLC26A4 gene in a Chinese deafness family.

Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.

[Mutation analysis of PINK1 gene in Chinese patients with autosomal recessive early-onset parkinsonism type 6].

[Prenatal diagnosis of prelingual deafness by determination of SLC26A4 gene mutation].

[Mutation analysis of small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease].

[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR].

Anorexigenic hormones leptin, insulin, and alpha-melanocyte-stimulating hormone directly induce neurotensin (NT) gene expression in novel NT-expressing cell models.

[The characteristics of gene mutations in Chinese patients with Charcot-Marie-Tooth disease].

Carbohydrate mimicry of Campylobacter jejuni lipooligosaccharide is critical for the induction of anti-GM1 antibody and neuropathy.

[Genetic linkage analysis in localizing a gene of autosomal dominant familial dilated cardiomyopathy with conduction defect].

[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.

A father and son with mental retardation, a characteristic face, inv(12), and insertion trisomy 12p12.3-p11.2.

[Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].

[Effects of tetramethylpyrazine on large-conductance Ca(2+)-activated potassium channels in porcine coronary artery smooth muscle cells.].

Mapping and identification of disease responsible genes based on genetic resource reservation and bioinformatics approach.

[Identification and clone of human Alzheimer's disease related gene nicastrin promoter].

The sialic acid residue is a crucial component of C. jejuni lipooligosaccharide ganglioside mimicry in the induction Guillain-Barré syndrome.

Coordinate regulation of neuropeptide Y and agouti-related peptide gene expression by estrogen depends on the ratio of estrogen receptor (ER) alpha to ERbeta in clonal hypothalamic neurons.

[Construction of the eukaryotic expression vector of MJD1 and its expression in SH-SY5Y cells].

Essential role of Pten in body size determination and pancreatic beta-cell homeostasis in vivo.

[Exon rearrangement analysis of parkin gene in patients with isolated early-onset parkinsonism using semi-quantitative PCR].

Comparison of extracellular and intracellular potency of botulinum neurotoxins.

[Functional interaction of the C-terminal of Nogo protein with connexin 26 and the expression of Nogo's mRNA in the murine inner ear].

Ubiquitin-proteasome pathway mediates degradation of APH-1.

Leptin signaling in neurotensin neurons involves STAT, MAP kinases ERK1/2, and p38 through c-Fos and ATF1.

Hypoxia facilitates Alzheimer's disease pathogenesis by up-regulating BACE1 gene expression.

Characteristic of spontaneous transient outward potassium currents in vascular smooth muscle cells of porcine coronary artery.

Degradation of nicastrin involves both proteasome and lysosome.

Glucose regulates AMP-activated protein kinase activity and gene expression in clonal, hypothalamic neurons expressing proopiomelanocortin: additive effects of leptin or insulin.

[Azoospermia factor microdeletion on Y chromosome in patients with idiopathic azoospermia or severe oligozoospermia].

[Identification of the origin of marker chromosome by comparative genomic hybridization].

Role of calcium mobilization in the regulation of spontaneous transient outward currents in porcine coronary artery myocytes.

SP1 regulates a human SNAP-25 gene expression.

Efficient protein expression from the endogenous RNA polymerase I promoter using a human ribosomal DNA targeting vector.

Oncogenicity of DNA in vivo: tumor induction with expression plasmids for activated H-ras and c-myc.

[UTP regulates spontaneous transient outward currents in porcine coronary artery smooth muscle cells through PLC-IP(3) signaling pathway.].

East learns from West: Asiatic honeybees can understand dance language of European honeybees.

Estrogen facilitates both phosphatidylinositol 3-kinase/Akt and ERK1/2 mitogen-activated protein kinase membrane signaling required for long-term neuropeptide Y transcriptional regulation in clonal, immortalized neurons.

Activation of high conductance Ca(2+)-activated K(+) channels by sodium tanshinoneII-A sulfonate (DS-201) in porcine coronary artery smooth muscle cells.

Valproic acid inhibits Abeta production, neuritic plaque formation, and behavioral deficits in Alzheimer's disease mouse models.

Structure of SF-1 bound by different phospholipids: evidence for regulatory ligands.

Intestinal trefoil factor maybe useful in prophylaxis of acute graft-versus-host disease.

[Identification and analysis of genuine and false Flos Rosae Rugosae by FTIR and 2D correlation IR spectroscopy].

Tumors induced in mice by direct inoculation of plasmid DNA expressing both activated H-ras and c-myc.

BACE1 gene promoter single-nucleotide polymorphisms in Alzheimer's disease.

NF-κB signaling inhibits ubiquitin carboxyl-terminal hydrolase L1 gene expression.

Increased NF-κB signalling up-regulates BACE1 expression and its therapeutic potential in Alzheimer's disease.

Transcriptional Regulation of TMP21 by NFAT.

Small molecule agonists of the orphan nuclear receptors steroidogenic factor-1 (SF-1, NR5A1) and liver receptor homologue-1 (LRH-1, NR5A2).

Relationship between the GTPase, metal-binding, and dimerization activities of E. coli HypB.

Formalin-inactivated vaccine provokes cross-protective immunity in a mouse model of human enterovirus 71 infection.

Eliminating SF-1 (NR5A1) sumoylation in vivo results in ectopic hedgehog signaling and disruption of endocrine development.

Control of BACE1 degradation and APP processing by ubiquitin carboxyl-terminal hydrolase L1.

Role of polyunsaturated fatty acids and lipid peroxidation on colorectal cancer risk and treatments.

低氧调节的 ATP13A2 (PARK9) 基因转录。

Combination of fucoxanthin and conjugated linoleic acid attenuates body weight gain and improves lipid metabolism in high-fat diet-induced obese rats.