The Mechanism of the NLRP3 Inflammasome Activation and Pathogenic Implication in the Pathogenesis of Gout

김성규

대한류마티스학회지

2022 .07

NLRP3 인플라마좀 경로를 통한 치조골 소실

송주한 ,  김옥수 ,  박석균 외 1명

대한구강해부학회지

2021 .12

Novel Germline Mutations of BRCA1 and BRCA2 in Korean Familial Breast Cancer Patients

김희남 ,  신민호 ,  이란 외 2명

전남의대학술지

2019 .01

The First Korean Case of De Novo Proximal 4p Deletion Syndrome in a Child With Developmental Delay

Soyoung Pa ,  k ,  Byung Ryul Jeon 외 3명

Annals of Laboratory Medicine

2020 .01

The R278I Mutation of PSEN1 in the Familial Alzheimer Disease

Jong Hun Kim ,  Seong Hye Choi ,  Jun Hong Lee

Dementia and Neurocognitive Disorders(대한치매학회지)

2020 .01

Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan

Muhammad Usman Rashid ,  Faiz Ali Khan ,  Noo 외 3명

Cancer Research and Treatment

2019 .01

The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome

Ma ,  cin R. Lene ,  Ani 외 13명

Cancer Research and Treatment

2017 .01

NLRP3 Exacerbate NETosis-Associated Neuroinflammation in an LPS-Induced Inflamed Brain

Da Jeong Byun ,  Jaeho Lee ,  Je-Wook Yu 외 1명

Immune Network

2023 .06

Familial Pancreatic Cancer and the Future of Directed Screening

Sa ,  a Welinsky ,  Aimee L. Lucas

Gut and Liver

2017 .01

The NLRP3 inflammasome is inhibited in natural products, protecting against acute gout

Hyeonjin Kim ,  Soohyun Jeong ,  Gabsik Yang

한국실험동물학회 학술발표대회 논문집

2022 .07

Korean Red Ginseng, a regulator of NLRP3 inflammasome, in the COVID-19 pandemic

Eui-Man Jung ,  Geun-Shik Lee

Journal of Ginseng Research

2022 .05

Hb-M Hyde Park: a rare cause of cyanosis arising from a de novo mutation

Loveena Rastogi ,  Sabina Lange ,  Nita Radhak 외 3명

Blood Research

2020 .01

Primary Familial Brain Calcification With XPR1 Mutation Presenting With Cognitive Dysfunction

Sojung Yoon ,  Seok Jong Chung ,  Yun Joong Kim

Journal of Clinical Neurology

2024 .03

The First Case of a Korean Patient with a Mutation-Confirmed Tumor Necrosis Factor Receptor-Associated Periodic Syndrome

안종균 ,  이석진 ,  백지연 외 1명

Yonsei Medical Journal

2024 .04

De novo mutations in COL4A5 identified by whole exome sequencing in 2 girls with Alport syndrome in Korea

Han ,  Kyoung Hee ,  Pa 외 4명

Clinical and Experimental Pediatrics

2019 .01

A Korean Case of De Novo 18q Deletion Syndrome With a Large Atrial Septal Defect and Cyanosis

김영진 ,  박태성 ,  한미영 외 2명

Annals of Laboratory Medicine

2015 .01

The First Case of an Infant with Familial A20 Haploinsufficiency in Korea

Kim Hye-Young ,  Song Ji Yeon ,  Kim Woo-Il 외 5명

Journal of Korean Medical Science

2020 .01

A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations

한지연 ,  김수연 ,  천정은 외 3명

Journal of Clinical Neurology

2020 .01

Familial Creutzfeldt-Jakob Disease with M232R Mutation Progressed Slowly like Alzheimer’s Disease

이슬기 ,  배희원 ,  양영순

Dementia and Neurocognitive Disorders(대한치매학회지)

2017 .01

Nonsaponin fractions of Korean Red Ginseng extracts prime activation of NLRP3 inflammasome

Byung-Cheol Han ,  Huijeong Ahn ,  Jiseon Lee 외 6명

Journal of Ginseng Research

2017 .10