2014 | | Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome. | 손영배, 정선용 |
2020 | | Identification of Korean cancer survivors' unmet needs and desired psychosocial assistance: A focus group study | 전미선 |
2011 | | Identification of major rice allergen and their clinical significance in children | 이수영 |
1997 | | Identification of N(G)-methylarginine residues in human heterogeneous RNP protein A1: Phe/Gly-Gly-Gly-Arg-Gly-Gly-Gly/Phe is a preferred recognition motif. | 백운기 |
2020 | | Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults | 조남한 |
2017 | | Identification of novel OCT4 genetic variant associated with the risk of chronic hepatitis B in a Korean population | 조성원 |
2012 | | Identification of novel peptides that stimulate human neutrophils | 박준성 |
2018 | | Identification of novel susceptibility loci associated with hepatitis B surface antigen seroclearance in chronic hepatitis B | 우현구 |
2016 | | Identification of NUCKS1 as a putative oncogene and immunodiagnostic marker of hepatocellular carcinoma | 김봉완, 김순선, 김영배, 왕희정, 정재연, 조성원 |
2011 | | Identification of oxidized serum albumin in the cerebrospinal fluid of ischaemic stroke patients. | 신동훈, 주인수, 허균 |
2011 | | Identification of P2Y12 single-nucleotide polymorphisms and their influences on the variation in ADP-induced platelet aggregation. | 조두연 |
2017 | | Identification of phenotypic clusters of nonsteroidal anti-inflammatory drugs exacerbated respiratory disease | 김승현, 박해심, 반가영, 신유섭, 예영민 |
2001 | | Identification of protein kinase C isoforms involved in interferon-gamma-induced expression of inducible nitric oxide synthase in murine BV2 microglia. | 조은혜, 주일로 |
1998 | | Identification of protein-arginine N-methyltransferase as 10-formyltetrahydrofolate dehydrogenase. | 백운기 |
2004 | | Identification of proximal left anterior descending artery stenosis with thallium-201 defect patterns in patients with angina pectoris. | 윤준기 |
2020 | | Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing | 금창대, 노정기, 이해상, 정선용, 정재연, 황진순 |
2011 | | Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia. | 김옥화 |
2009 | | Identification of the amino acid sequence motif of alpha-synuclein responsible for macrophage activation. | 박상면 |
2000 | | Identification of the human homologue of mouse KIF4, a kinesin superfamily motor protein. | 김완기, 이영미 |
2004 | | Identification of the Major Allergen in the Shrimp (Metapenaeus Joynen): Effects of Heating and Digestive Enzymes | 김현아, 남동호, 서창희, 최정희 |