Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Jong-Ha Yoo"'
Autor:
Hee-Jin Kim, Duk-Kyung Kim, Ki-Young Yoo, Chur-Woo You, Jong-Ha Yoo, Ki-O Lee, In-Ae Park, Hae-Sun Choung, Hee-Jung Kim, Min-Jung Song, Sun-Hee Kim
Publikováno v:
Haematologica, Vol 97, Iss 2 (2012)
Background The recent advent of genome-wide molecular platforms has facilitated our understanding of the human genome and disease, particularly copy number aberrations. We performed genome-wide single nucleotide polymorphism-array in hereditary coagu
Externí odkaz:
https://doaj.org/article/9711dbfa605c412b9f7475abe04c831b
Publikováno v:
Clinical & Experimental Pediatrics; Nov2023, Vol. 66 Issue 11, p493-500, 8p
Autor:
Jong-Ha Yoo1 jhyoo92@nhimc.or.kr, Jee-Hyoung Yoo2 jhlovys@nhimc.or.kr, Yoon-Jung Choi3 chris316@nhimc.or.kr, Jung-Gu Kang4 kangski@nhimc.or.kr, Young-Kyu Sun1 labsun@nhimc.or.kr, Chang-Seok Ki5 changski@skku.edu, Kyung-A Lee6 KAL1119@yuhs.ac, Jong-Rak Choi6 cjr0606@yuhs.ac
Publikováno v:
BMC Medical Genetics. 2008, Vol. 9, Special section p1-5. 5p. 1 Color Photograph, 1 Diagram, 1 Graph.
Publikováno v:
Microbiology and Immunology. 56:372-377
We prepared mAb specific to the H1N1 2009 virus (H1N1 2009) to facilitate development of an RDT with enhanced sensitivity and specificity. Among these antibodies, we identified two clones—hybridomas 1H7E1 and 3A3H7—that specifically bound to H1N1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1a6ca5becacc0a36c67f70d12684e34
https://doi.org/10.1111/j.1348-0421.2012.00455.x
https://doi.org/10.1111/j.1348-0421.2012.00455.x
Publikováno v:
Gene. 499:339-342
Birt-Hogg-Dubé syndrome (BHDS) is an autosomal dominant disease presenting with skin fibrofolliculomas, pulmonary cysts, primary spontaneous pneumothorax (PSP), and renal cancer. It is caused by germline mutations in the FLCN gene, which encodes fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35bb5df953d1930ae09570420d559a69
https://doi.org/10.1016/j.gene.2012.03.037
https://doi.org/10.1016/j.gene.2012.03.037
Autor:
Young Kyu Sun, Jong Ha Yoo, Jong Rak Choi, Jaewoo Song, Tae Sung Park, Kyung A. Lee, Young Ah Kim
Publikováno v:
The American Journal of Tropical Medicine and Hygiene. 82:412-414
Recently, the XE-2100 hematology analyzer was investigated in a rather small patient group; pseudoeosinophilia or abnormal white blood cell (WBC) scattergrams reported by this instrument were considered as significantly valuable diagnostic parameters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daa2cf85c8cf8ef5f9e212b1253a9690
https://doi.org/10.4269/ajtmh.2010.09-0560
https://doi.org/10.4269/ajtmh.2010.09-0560
Publikováno v:
Annals of clinical and laboratory science. 43(3)
Trichothiodystrophy (TTD) is a rare, autosomal recessive, multisystem disorder characterized by sulfur-deficient brittle hair, growth and mental retardation, and ichthyosis. TTD is caused primarily by mutations in the xeroderma pigmentosum group D (X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5cbe161c327cf32ef295ae9aa687c48a
https://pubmed.ncbi.nlm.nih.gov/23884229
https://pubmed.ncbi.nlm.nih.gov/23884229
Publikováno v:
Microbiology and immunology. 56(6)
We prepared mAb specific to the H1N1 2009 virus (H1N1 2009) to facilitate development of an RDT with enhanced sensitivity and specificity. Among these antibodies, we identified two clones--hybridomas 1H7E1 and 3A3H7-that specifically bound to H1N1 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::936df1350b6402efd46859a513193671
https://pubmed.ncbi.nlm.nih.gov/22686191
https://pubmed.ncbi.nlm.nih.gov/22686191
Autor:
Seung Jun, Choi, Eun-Young, Lee, Hee-Jin, Kim, Kyung-A, Lee, Jaewoo, Song, Jong-Rak, Choi, Jong-Ha, Yoo
Publikováno v:
Annals of clinical and laboratory science. 42(1)
We describe a case of a c.4825GA (p.Gly1609Arg [Gly846Arg]) missense mutation in the gene encoding von Willebrand factor (vWF) in a Korean patient with von Willebrand disease (vWD) type 2A. The proband is a 37-year-old female who suffers from dysmeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d669b2b8cb286d067a6a4f812a4bc7c9
https://pubmed.ncbi.nlm.nih.gov/22371917
https://pubmed.ncbi.nlm.nih.gov/22371917
Publikováno v:
Annals of clinical and laboratory science. 41(4)
Hereditary protein S (PS) deficiency (Gene ID: 5627; MIM # 176880) is a notable risk factor for recurrent venous thrombosis, inherited as an autosomal-dominant trait, either homozygous or heterozygous. It may be caused by point mutations in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e77e68e9ddbeb74bc0bf57182ba17b2
https://pubmed.ncbi.nlm.nih.gov/22166512
https://pubmed.ncbi.nlm.nih.gov/22166512