28 results match your criteria: "Korea Centers for Diseases Control and Prevention[Affiliation]"
J Comp Pathol
November 2014
Department of Veterinary Pathology, College of Veterinary Medicine, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 151-742, Republic of Korea. Electronic address:
The aim of this study was to compare the virulence of type 1 and type 2 porcine reproductive and respiratory syndrome virus (PRRSV) as assessed by the level of viral replication, viral distribution and apoptosis in stillborn fetuses and live-born piglets from infected pregnant gilts. Type 1 or type 2 PRRSV was given intranasally to pregnant gilts at 3 weeks before the expected date of parturition. Regardless of virus genotype, PRRSV-infected gilts farrowed between 102 and 109 days of gestation, while control uninfected gilts carried the pregnancy to term and farrowed at 114-115 days of gestation.
View Article and Find Full Text PDFBMC Infect Dis
January 2014
Division of AIDS, Center for Immunology and Pathology, Korea Centers for Diseases Control and Prevention, Osong Health Technology Adminstration Complex, 187 Osongsaengmyeong2(i)-ro, Cheongwon-gun, Chungcheongbukdo 363-951, Korea.
Background: This study aimed to identify the characteristics of HIV and herpes simplex virus (HSV)-2 seroprevalence in male patients with anal disease.
Methods: HIV seroprevalence was estimated for different age groups of male patients with anal disease who were treated at Songdo colorectal hospital in Korea between 2001 and 2011. HIV seroprevalence of patients with anal disease was compared with that of patients with nonanal disease for each year from 2007 to 2011.
Osong Public Health Res Perspect
April 2013
Division of Malaria and Parasitic Diseases, Korea National Institute of Health, Osong, Korea. ; Division of Epidemic Intelligence Service, Korea Centers for Diseases Control and Prevention, Osong, Korea.
Objectives: To identify the pathogen of the diarrhea outbreak in a village in Jeollabuk province in Korea in April 2010.
Methods: DNA extraction was performed from the 120 L of collected water, which was centrifuged at 10,000 x g for 30 min. PCR reactions were conducted in a total of 25 ul, which included PCR premix (GenDEPOT, Barker, TX, USA), 2 ul (∼100 ng) of extracted DNA, and 10 pmol of each primer.