PALB2: THE HUB OF A NETWORK OF TUMOR SUPPRESSORS INVOLVED IN DNA DAMAGE RESPONSES

por Park, Jung-Young, Zhang, Fan, Andreassen, Paul R.
Publicado 2014

MDC1 and RNF8 function in a pathway that directs BRCA1-dependent localization of PALB2 required for homologous recombination

por Zhang, Fan, Bick, Gregory, Park, Jung-Young, Andreassen, Paul R.
Publicado 2012

Identification of a novel human Rad51 variant that promotes DNA strand exchange

por Park, Jung-Young, Yoo, Han-Wook, Kim, Bok-Ryang, Park, Raekil, Choi, Sang-Yun, Kim, Youngho
Publicado 2008

Effects of a chemical chaperone on genetic mutations in α-galactosidase A in Korean patients with Fabry disease

por Park, Jung-Young, Kim, Gu-Hwan, Kim, Sung-Su, Ko, Jung Min, Lee, Jin-Joo, Yoo, Han-Wook
Publicado 2009

Proteomic analysis of sera of asymptomatic, early-stage patients with Wilson's disease

por Park, Jung-Young, Mun, Joo Hee, Lee, Beom Hee, Heo, Sun Hee, Kim, Gu-Hwan, Yoo, Han-Wook
Publicado 2009

BREAST CANCER-ASSOCIATED MISSENSE MUTANTS OF THE PALB2 WD40 DOMAIN, WHICH DIRECTLY BINDS RAD51C, RAD51 AND BRCA2, DISRUPT DNA REPAIR

por Park, Jung-Young, Singh, Thiyam R., Nassar, Nicolas, Zhang, Fan, Freund, Marcel, Hanenberg, Helmut, Meetei, Amom Ruhikanta, Andreassen, Paul R.
Publicado 2013

Prevention of Hyperuricemia by Clerodendrum trichotomum Leaf Extract in Potassium Oxonate-Induced Mice

por Jang, Mi Gyeong, Song, Hana, Kim, Ji Hye, Oh, Jung Min, Park, Jung Young, Ko, Hee Chul, Hur, Sung-Pyo, Kim, Se-Jae
Publicado en Dev Reprod (2020)

COMPLEMENTATION OF HYPERSENSITIVITY TO DNA INTERSTRAND CROSSLINKING AGENTS DEMONSTRATES THAT XRCC2 IS A FANCONI ANEMIA GENE

por Park, Jung-Young, Virts, Elizabeth L., Jankowska, Anna, Wiek, Constanze, Othman, Mohamed, Chakraborty, Sujata C., Vance, Gail H., Alkuraya, Fowzan S., Hanenberg, Helmut, Andreassen, Paul R.
Publicado en J Med Genet (2016)

The p.Ser64Leu and p.Pro104Leu missense variants of PALB2 identified in familial pancreatic cancer patients compromise the DNA damage response

por Zhang, Yue, Park, Jung-Young, Zhang, Fan, Olson, Sara H., Orlow, Irene, Li, Yirong, Kurtz, Robert C., Ladanyi, Marc, Chen, Jie, Toland, Amanda E., Zhang, Liying, Andreassen, Paul R.
Publicado en Hum Mutat (2020)

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE

por Seo, Go Hun, Kim, Taeho, Choi, In Hee, Park, Jung‐young, Lee, Jungsul, Kim, Sehwan, Won, Dhong‐gun, Oh, Arum, Lee, Yena, Choi, Jeongmin, Lee, Hajeong, Kang, Hee Gyung, Cho, Hee Yeon, Cho, Min Hyun, Kim, Yoon Jeon, Yoon, Young Hee, Eun, Baik‐Lin, Desnick, Robert J., Keum, Changwon, Lee, Beom Hee
Publicado en Clin Genet (2020)

SUN-721 Implementation of Whole Exome Sequencing for Clinical Diagnostics: A Prospective Busan Kyung-Sang Regional Co-Work Team Experience

por Lee, Jeong Eun, Chung, WooYeong, Lee, BoLyun, Ku, SooHyun, Jeon, Ga Won, Park, JiKyung, Kim, TaeHee, Eom, MiJa, Huh, YoonJung, Park, Jinse, Kwak, MinJung, Kim, JinKyung, Kang, Seok-Jin, Jang, Kyung-mi, Park, Jung-young, Seo, GoHun, Keum, Changwon, Jun, KyungRan, Oh, SeungHwan
Publicado en J Endocr Soc (2020)