Ming Zhang

Shear stress regulates forward and reverse planar cell polarity of vascular endothelium in vivo and in vitro.

Force-induced polarized mitosis of endothelial and smooth muscle cells in arterial remodeling.

Homotypic and endothelial cell adhesions via N-cadherin determine polarity and regulate migration of vascular smooth muscle cells.

Proteome alteration of U251 human astrocytoma cell after inhibiting retinoic acid synthesis.

Role of tumour necrosis factor-alpha and other cytokines in ischemia-reperfusion-induced injury in the heart.

Mechanotransduction by endothelial cells is locally generated, direction-dependent, and ligand-specific.

Rear polarization of the microtubule-organizing center in neointimal smooth muscle cells depends on PKCα, ARPC5, and RHAMM.

Cadherins at cell-autonomous membrane contacts control macropinocytosis.

Progesterone receptor membrane component 1 is a functional part of the glucagon-like peptide-1 (GLP-1) receptor complex in pancreatic β cells.

GluA1 phosphorylation contributes to postsynaptic amplification of neuropathic pain in the insular cortex.

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.

Mutation analysis of CHCHD10 in different neurodegenerative diseases.

Drug repositioning for diabetes based on 'omics' data mining.

Characterization of Zinc Influx Transporters (ZIPs) in Pancreatic β Cells: ROLES IN REGULATING CYTOSOLIC ZINC HOMEOSTASIS AND INSULIN SECRETION.

Jump from pre-mutation to pathologic expansion in C9orf72.

The Identification of Novel Protein-Protein Interactions in Liver that Affect Glucagon Receptor Activity.

Mutation analysis of C9orf72 in patients with corticobasal syndrome.

Isoform-specific antibodies reveal distinct subcellular localizations of C9orf72 in amyotrophic lateral sclerosis.

A Novel GLP1 Receptor Interacting Protein ATP6ap2 Regulates Insulin Secretion in Pancreatic Beta Cells.

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.

Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.

A Predictive Metabolic Signature for the Transition From Gestational Diabetes Mellitus to Type 2 Diabetes.

Spinal column chordoma: prognostic significance of clinical variables and T (brachyury) gene SNP rs2305089 for local recurrence and overall survival.

Marked Differences in C9orf72 Methylation Status and Isoform Expression between C9/ALS Human Embryonic and Induced Pluripotent Stem Cells.

Drug Repositioning for Alzheimer's Disease Based on Systematic 'omics' Data Mining.

Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease.

C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism.

DNA methylation age-acceleration is associated with disease duration and age at onset in C9orf72 patients.

The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration.

Unaffected mosaiccase: RNA foci, dipeptide proteins, but upregulated C9orf72 expression.

Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy.