Advanced search    

Search: authors:"Xiaofeng Hu"

5 papers found.
Use AND, OR, NOT, +word, -word, "long phrase", (parentheses) to fine-tune your search.

Association of the angiotensinogen M235T polymorphism with recurrence after catheter ablation of acquired atrial fibrillation

predisposition.7–10 Percutaneous *Qunshan Wang and Xiaofeng Hu contributed equally to the study. radiofrequency catheter ablation (CA) is widely accepted as an effective treatment for AF and is currently

A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population

Background Recent research has implicated that mutations in the neurexin-1 (NRXN1) gene on chromosome 2p16.3 might play a role in schizophrenia, autism, and nicotine dependence. In order to explore the association of NRXN1 polymorphisms with schizophrenia, we made a case-control association study in Chinese Han population. Methods We examined six tag single nucleotide...

Higher Isolation of NDM-1 Producing Acinetobacter baumannii from the Sewage of the Hospitals in Beijing

Multidrug resistant microbes present in the environment are a potential public health risk. In this study, we investigate the presence of New Delhi metallo-β-lactamase 1 (NDM-1) producing bacteria in the 99 water samples in Beijing City, including river water, treated drinking water, raw water samples from the pools and sewage from 4 comprehensive hospitals. For the blaNDM-1...

ABCC6 and pseudoxanthoma elasticum

Arthur A. B. Bergen . Astrid S. Plomp . Xiaofeng Hu . Paulus T. V. M. de Jong . Theo G. M. F. Gorgels 0 1 0 P. T. V. M. de Jong Department of Epidemiology and Biostatistics , ErasmusMC, Rotterdam

Disruption of Abcc6 in the mouse: novel insight in the pathogenesis of pseudoxanthoma elasticum

Pseudoxanthoma elasticum (PXE) is a heritable disorder of connective tissue, affecting mainly skin, eye and the cardiovascular system. PXE is characterized by dystrophic mineralization of elastic fibres. The condition is caused by loss of function mutations in ABCC6. We generated Abcc6 deficient mice (Abcc6−/−) by conventional gene targeting. As shown by light and electron...