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Showing results 60 to 70 of 70

Pub YearTitleAuthor(s)
2013NF1 deficiency causes Bcl-xL upregulation in Schwann cells derived from neurofibromatosis type 1-associated malignant peripheral nerve sheath tumors.김영배, 손영배, 임현이, 정선용, 진현석, 한재호
2018Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population조남한
1999Participation of the melanocortin-1 receptor in the UV control of pigmentation.임성빈
2005Polymorphisms of high-affinity IgE receptor and histamine-related genes in patients with ASA-induced urticaria/angioedema.김승현, 남동호, 박해심, 서창희
2015Replication of genome wide association studies on hepatocellular carcinoma susceptibility loci of STAT4 and HLA-DQ in a Korean population.정재연, 조성원
2021Somatic uniparental disomy mitigates the most damaging EFL1 allele combination in Shwachman-Diamond syndrome손영배
2010The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome.고정민
2005The human leucocyte antigen-DRB1*1302-DQB1*0609-DPB1*0201 haplotype may be a strong genetic marker for aspirin-induced urticaria.김승현, 남동호, 박해심, 서창희
2013Ticlopidine with Ginkgo Biloba extract: a feasible combination for patients with acute cerebral ischemia.이진수, 임영애, 주인수, 홍지만
2015Tolerance to acetic acid is improved by mutations of the TATA-binding protein gene.김완기
2003VIM- and IMP-type metallo-beta-lactamase-producing Pseudomonas spp. and Acinetobacter spp. in Korean hospitals.이위교
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