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A family with NKX2.5 gene mutations presenting as familial atrial septal defect and atrioventricular block: A case report
Journal of genetic medicine
2018 .01
CRISPR/Cas9-mediated knockout of NKX3.1 leads to adenoma and hyperplasia in prostate of C57BL/6 mice
한국실험동물학회 학술발표대회 논문집
2019 .01
Developmental defect of prostate in CRISPR/cas9-mediated C57BL/6-NKX3.1 knockout mice
한국실험동물학회 학술발표대회 논문집
2018 .01
Loss of glutathione peroxidase 3 induces ROS and contributed to prostatic hyperplasia in Nkx3.1 knockout mice
한국실험동물학회 학술발표대회 논문집
2020 .02
Adenoma and hyperplasia abundantly developed in the prostate of CRISPR/cas9-mediated C57BL/6-NKX3.1 knockout mice
한국실험동물학회 학술발표대회 논문집
2018 .07
Comprehensive analysis and report of immune infiltration based on clinical big data of NKX3.2 in hepatocelluar carcinoma
대한체질인류학회 학술대회 연제 초록
2023 .05
Globus Pallidus Interna Deep Brain Stimulation for Chorea-Acanthocytosis
대한신경외과학회지
2015 .01
Nkx-2.5 Regulates MDR1 Expression via Its Upstream Promoter in Breast Cancer Cells
Journal of Korean Medical Science
2019 .01
Chorea in Sporadic Creutzfeldt-Jakob disease
Journal Of Movement Disorders
2018 .01
소뇌경색의 후유증으로 발생한 지연성 혈관 무도병 증례 보고 : 협진 치험 1례
대한한방내과학회지
2016 .01
Chorea as a Presentation of SARS-CoV-2 Encephalitis: A Clinical Case Report
Journal Of Movement Disorders
2021 .09
억간산이 유효했던 지연성 Chorea Hyperglycemia Basal Ganglia Syndrome 환자 1례
대한한방내과학회지
2020 .01
Hereditary cancer panel and clinical application
대한외과학회 학술대회 초록집
2016 .11
Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test
Cancer Research and Treatment
2020 .01
비케톤성 당뇨병으로 유발된 고혈당성 무도증의 한 · 양방 복합치료 증례보고
대한한의학회지
2016 .09
Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan
Cancer Research and Treatment
2019 .01
Characteristics of South Korean Patients with Hereditary Transthyretin Amyloidosis
Journal of Clinical Neurology
2018 .01
The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network
Yonsei Medical Journal
2022 .08
Genetic Mutation Analysis Can Supplement Clinically Confirmed Hereditary Hemorrhagic Telangiectasia Populations
Clinical and Experimental Otorhinolaryngology
2019 .01
Clinicopathological Features and Type of Surgery for Lynch Syndrome: Changes during the Past Two Decades
Cancer Research and Treatment
2016 .01
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