Browsing by Keyword : Phenotype

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Showing results 61 to 120 of 127

Pub YearTitleAuthor(s)
2017Identification and Functional Characterization of ST3GAL5 and ST8SIA1 Variants in Patients with Thyroid-Associated Ophthalmopathy국경훈
2010Identification of a cholangiocarcinoma-like gene expression trait in hepatocellular carcinoma.우현구
2011Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.김현주, 정선용
2013Identification of asthma clusters in two independent Korean adult asthma cohorts.남동호
2018Identification of five novel genetic loci related to facial morphology by genome-wide association studies조남한
2017Identification of phenotypic clusters of nonsteroidal anti-inflammatory drugs exacerbated respiratory disease김승현, 박해심, 반가영, 신유섭, 예영민
2005Immortalized human microglial cell line: phenotypic expression.김승업
2010Immunoglobulin G subclass deficiency is the major phenotype of primary immunodeficiency in a Korean adult cohort.김정은, 김주희, 남동호, 박해심, 예영민, 최길순
2022Immunologic Basis of Type 2 Biologics for Severe Asthma박해심, 최영우
2014Impact of enzyme replacement therapy on linear growth in Korean patients with mucopolysaccharidosis type II (Hunter syndrome).손영배
2016Impact of the beta-1 adrenergic receptor polymorphism on tolerability and efficacy of bisoprolol therapy in Korean heart failure patients: association between beta adrenergic receptor polymorphism and bisoprolol therapy in heart failure (ABBA) study신준한
2013Implications of time-series gene expression profiles of replicative senescence.김유선, 변해옥, 우현구, 윤계순
2024Inflamed immune phenotype predicts favorable clinical outcomes of immune checkpoint inhibitor therapy across multiple cancer types김석휘
2010Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome.고정민
2003Intercellular adhesion molecule-1 polymorphisms in Korean patients with Behcet s disease.이성낙, 이은소
2012Interleukin-1ß and interleukin-1 receptor accessory protein gene polymorphisms are associated with persistent hepatitis B virus infection김순선, 정재연, 조성원
2017Intratumor stromal proportion predicts aggressive phenotype of gastric signet ring cell carcinomas김영배, 손상용, 이다근, 한상욱, 허훈
2010IS6110-restriction fragment length polymorphism and spoligotyping analysis of Mycobacterium tuberculosis clinical isolates for investigating epidemiologic distribution in Korea.이위교
2011Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits조남한
2014Letter to the editor. Two major phenotypes of sulfite hypersensitivity: asthma and urticaria.박해심, 반가영, 예영민, 유혜수
1998Low dose poly I:C prevents diabetes in the diabetes prone BB rat.윤지원
2011Low-intensity ultrasound increased colony forming unit-fibroblasts of mesenchymal stem cells during primary culture.민병현
2019Metabolic features and regulation in cell senescence권소미, 윤계순, 이영경, 홍선미
2016MicroRNA-155 regulates the Th17 immune response by targeting Ets-1 in Behcet's disease박선, 이은소
2004Microsatellite instability and expression of hMLH1 and hMSH2 proteins in ovarian endometrioid cancer.장기홍
2007Mitochondrial fission and fusion mediators, hFis1 and OPA1, modulate cellular senescence.김수정, 정선용, 조혜성
2005Molecular characterization of vancomycin-resistant Enterococcus faecium isolates from Korea.이위교
2014Molecular epidemiology of vancomycin-resistant enterococci isolated from non-tertiary-care and tertiary-care hospitals in Korea.이위교
2012Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism김현주, 정선용
2018Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics장정훈, 정연훈
2017Mutations acquired by hepatocellular carcinoma recurrence give rise to an aggressive phenotype권소미, 왕희정, 우현구
2004Neurogenin1 is sufficient to induce neuronal differentiation of embryonal carcinoma P19 cells in the absence of retinoic acid.김승업, 서해영, 이영돈
2019New phenotypes in hypersensitivity reactions to nonsteroidal anti-inflammatory drugs박해심, 신유섭, 이영수
2010Non-synonymous single-nucleotide polymorphisms associated with blood pressure and hypertension.진현석
2010Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family.김옥화
2015On the Estimation of Heritability with Family-Based and Population-Based Samples.조남한
2013Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patients.김옥화
2020Osteopontin contributes to late-onset asthma phenotypes in adult asthma patients김승현, 박해심
2014Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.김옥화
2012PAPSS2 mutations cause autosomal recessive brachyolmia김옥화
2010Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.고정민, 배기수
2011Pulmonary manifestations in Proteus syndrome: pulmonary varicosities and bullous lung disease.김옥화
2004Reduction in glycopeptide resistance in vancomycin-resistant enterococci as a result of vanA cluster rearrangements.이위교, 임영애, 조성란, 허지영
2014Risk factors for asthma-related healthcare use: longitudinal analysis using the NHI claims database in a Korean asthma cohort.남동호
2016Risk of the Development of Diabetes and Cardiovascular Disease in Metabolically Healthy Obese People: The Korean Genome and Epidemiology Study조남한
2018Role of clusterin/progranulin in toluene diisocyanate-induced occupational asthma김승현, 박해심, 신유섭, 예영민
2022Serum Amyloid A1: A Biomarker for Neutrophilic Airway Inflammation in Adult Asthmatic Patients박해심, 신유섭, 최영우
2016Shifting p53-induced senescence to cell death by TIS21(/BTG2/Pc3) gene through posttranslational modification of p53 protein유민숙, 임인경
2014Similar clinical characteristics of familial and sporadic inflammatory bowel disease in South Korea.정숙희
2014Single nucleotide polymorphisms associated with abnormal coronary microvascular function.최병주
2003Sonic hedgehog and FGF8 collaborate to induce dopaminergic phenotypes in the Nurr1-overexpressing neural stem cell.김승업, 이명애, 이용범
2005Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.정윤석
2019T helper 1 and 2 stimuli induce distinct phenotypes in gingival fibroblasts지숙
1998The cDNA cloning and ontogeny of mouse alpha-synuclein.곽병주, 조은혜
2023The First Korean Family of Spinocerebellar Ataxia 21 (ATX-TMEM240) with Facial Dystonic Phenotype박동규, 윤정한
2014The role of classical and alternative macrophages in the immunopathogenesis of herpes simplex virus-induced inflammation in a mouse model.손성향
2014The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype.김승현, 박해심, 예영민
2017The Ubiquitin-like with PHD and Ring Finger Domains 1 (UHRF1)/DNA Methyltransferase 1 (DNMT1) Axis Is a Primary Regulator of Cell Senescence우현구, 윤계순, 이영경
2005Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.김대중, 이관우
2017TIS21(/BTG2) inhibits doxorubicin-induced stress fiber-vimentin networks via Nox4-ROS-ABI2-DRF-linked signal cascade유민숙, 임인경
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