Mitochondrial encephalomyopathies are a group of multisystemic disorders that caused by Mitochondrial DNA or nuclear mutations to result in disturbance of mitochondrial Structures and function, which involve central nervous system and muscle mainly.

Clinical,imaging and pathological features of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(report of 1 case)

Analysis of two mitochondrial encephalomyopathy cases on clinical、image and pathology

Prokaryotic expression and reactogenicity of nonstructural protein 2C of porcine encephalomyocarditis virus;

Objective To explore if cDNAs of two subunits, p40 and p35 of interleukin 12 ligated by internal ribosome entry site(IRES)of encephalomyocarditis virus(EMCV)can be expressed efficiently under the control of one promoter and processed into heterodimer p70.

Expression and antigenicity of the epitope of VP1 gene of encephalomyocarditis virus(EMCV)in E.coli;

For production of encephalomyocarditis virus(EMCV) structural proteins in adenovirus vector and their application as a vaccine,two recombinant replication-defective human adenovirus serotype 5 vectors containing EMCV capsid P1,and P12A plus viral 3C protease coding regions were constructed(de-signated Ad-P1 and Ad-P12A3C respectively).

A pair of primers was designed according to the sequence of the VP1 gene of porcine encephalomyocarditis virus(EMCV) and a recombinant plasmid containing the target gene was constructed as a standard control.