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Dive into the research topics where Hae-Joon Park is active.

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Featured researches published by Hae-Joon Park.


Helicobacter | 1999

Oral Immunization with Helicobacter pylori‐Loaded Poly( d, l‐Lactide‐Co‐Glycolide) Nanoparticles

Seong-Youl Kim; Hyun-Joo Doh; Myoung Ho Jang; Young-Ju Ha; Soo-Il Chung; Hae-Joon Park

Helicobacter pylori is a major cause of chronic antral gastritis and peptic ulcer diseases. Many researchers have examined the possibility of immunologically‐mediated prevention of H. pylori infection using an oral vaccine. The purpose of this study is to investigate whether mucosal and systemic immune responses are induced by oral immunization with H. pylori lysate‐loaded poly( d, l‐lactide‐coglycolide)[PLG] nanoparticles, and if so, how the distribution of serum IgG subclasses are produced.


Acta Tropica | 2011

A novel real-time PCR assay for the detection of Plasmodium falciparum and Plasmodium vivax malaria in low parasitized individuals.

Seung-Young Hwang; So-Hee Kim; Ga-Young Lee; Vu Thi Thu Hang; Chisook Moon; Jeong Hwan Shin; Wan-Lim Koo; Seong-Youl Kim; Hae-Joon Park; Han-Oh Park; Weon-Gyu Kho

The rapid, accurate diagnosis of Plasmodium spp. is essential for the effective control of malaria, especially in asymptomatic infections. In this study, we developed a sensitive, genus-specific, real-time quantitative PCR assay. It was compared with the microscopic examination of Giemsa-stained blood smears and two different molecular diagnostic techniques: nested PCR and multiplex PCR. For the effective quantitative detection of malaria parasites, all reagents were designed with a lyophilized format in one tube. Plasmodium was detected successfully in all 112 clinically suspected malaria patients, including 32 individuals with low parasitemia (1-100 parasites/μl). The sensitivity threshold was 0.2 parasites/μl and no PCR-positive reaction occurred when malaria parasites were not present. This may be a useful method for detecting malaria parasites in endemic areas.


Archive | 2004

Primer and probe for detection of sars coronavirus, kit comprising the primer and/or the probe, and detection method thereof

Hae-Joon Park; Young-Ju Ha; Meehyein Kim


Archive | 2008

Dried composition for hot-start PCR with long-term stability

Seong-Youl Kim; Hyun Bae Kim; Hae-Joon Park; Han Oh Park


Virus Research | 2006

Structural requirements for assembly and homotypic interactions of the hepatitis C virus core protein

Meehyein Kim; Young-Ju Ha; Hae-Joon Park


Archive | 2010

APPARATUS FOR INTEGRATED REAL-TIME NUCLEIC ACID ANALYSIS, AND METHOD FOR DETECTING A TARGET NUCLEIC ACID USING SAME

Yu-Jeong Kim; Wan-Lim Koo; Jong-Hoon Kim; Dae-jin Jang; Jin-Cheol Seo; Seong-Youl Kim; Hae-Joon Park; Han Oh Park


Archive | 2002

DNA and peptides of a diabetes-specific endogenous retrovirus

Ji-won Yoon; Hee-sook Jun; Hae-Joon Park; Jong Seong Ahn; Young-Ju Ha; Soo-Il Chung


Journal of Applied Biological Chemistry | 2006

A Rapid PCR-based Assay for Detecting Hepatitis B Viral DNA Using GenSpector TMC-1000

Bum Huh; Young-Ju Ha; Jae-Tak Oh; Eun-Ha Park; Jin-Su Park; Hae-Joon Park


한국생물공학회 학술대회 | 2008

A DNA Extraction Technique Using Single Buffer System, AccuPrep® -Quick DNA Kit

Moon-Ja Park; Jong-Hoon Kim; Hae-Joon Park; Han-Oh Park


한국생물공학회 학술대회 | 2008

Performance Evaluation of Fully Automated Nucleic Acid Extraction System, ExiPrep TM 16

Young-Joo Na; Jong-Hoon Kim; Hae-Joon Park; Han-Oh Park

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Seong-Youl Kim

University of Mississippi Medical Center

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Han Oh Park

Korea Research Institute of Bioscience and Biotechnology

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Ing K. Ho

University of Mississippi Medical Center

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Nuannoi Chudapongse

University of Mississippi Medical Center

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Sangmin Lee

United States Department of Veterans Affairs

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