Min Goo Lee

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 24

Top Topics

Intellectual Disability

Top Venues

Experimental & molecular medicine

American journal of medical genetics. Part A

Clinical genetics

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Jihoon G Yoon, Dong Geon Jang, Sung-Gyu Cho, Chaeyoung Lee, Shin Hye Noh, Soo Kyung Seo, Jung Woo Yu, Hyeon Woo Chung, KyeoRe Han, Soon Sung Kwon, Dai Hoon Han, Jaeseong Oh, In-Jin Jang, Sang-Hoon Kim, Young-Koo Jee, Hyun Lee, Dong Won Park, Tae-Hyung Kim, Ho Joo Yoon, Chul Hoon Kim, Jae Myun Lee, Sang-Heon Kim, Min Goo Lee
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Experimental & molecular medicine 56 (3) (2024)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Syndromic craniosynostosis caused by a novel missense variant in MAP4K4: Expanding the genotype-phenotype relationship in RASopathies. Clinical genetics 106 (2) (2024)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Syndromic craniosynostosis caused by a novel missense variant in MAP4K4: Expanding the genotype-phenotype relationship in RASopathies. Clinical genetics 106 (2) (2024)
Jihoon G Yoon, Dong Geon Jang, Sung-Gyu Cho, Chaeyoung Lee, Shin Hye Noh, Soo Kyung Seo, Jung Woo Yu, Hyeon Woo Chung, KyeoRe Han, Soon Sung Kwon, Dai Hoon Han, Jaeseong Oh, In-Jin Jang, Sang-Hoon Kim, Young-Koo Jee, Hyun Lee, Dong Won Park, Tae-Hyung Kim, Ho Joo Yoon, Chul Hoon Kim, Jae Myun Lee, Sang-Heon Kim, Min Goo Lee
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Experimental & molecular medicine 56 (3) (2024)
Jihoon G Yoon, Dong Geon Jang, Sung-Gyu Cho, Chaeyoung Lee, Shin Hye Noh, Soo Kyung Seo, Jung Woo Yu, Hyeon Woo Chung, KyeoRe Han, Soon Sung Kwon, Dai Hoon Han, Jaeseong Oh, In-Jin Jang, Sang-Hoon Kim, Young-Koo Jee, Hyun Lee, Dong Won Park, Tae-Hyung Kim, Ho Joo Yoon, Chul Hoon Kim, Jae Myun Lee, Sang-Heon Kim, Min Goo Lee
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Experimental & molecular medicine 56 (3) (2024)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Syndromic craniosynostosis caused by a novel missense variant in MAP4K4: Expanding the genotype-phenotype relationship in RASopathies. Clinical genetics (2024)
Jihoon G Yoon, Dong Geon Jang, Sung-Gyu Cho, Chaeyoung Lee, Shin Hye Noh, Soo Kyung Seo, Jung Woo Yu, Hyeon Woo Chung, KyeoRe Han, Soon Sung Kwon, Dai Hoon Han, Jaeseong Oh, In-Jin Jang, Sang-Hoon Kim, Young-Koo Jee, Hyun Lee, Dong Won Park, Tae-Hyung Kim, Ho Joo Yoon, Chul Hoon Kim, Jae Myun Lee, Sang-Heon Kim, Min Goo Lee
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Experimental & molecular medicine (2024)
Jihoon G Yoon, Dong Geon Jang, Sung-Gyu Cho, Chaeyoung Lee, Shin Hye Noh, Soo Kyung Seo, Jung Woo Yu, Hyeon Woo Chung, KyeoRe Han, Soon Sung Kwon, Dai Hoon Han, Jaeseong Oh, In-Jin Jang, Sang-Hoon Kim, Young-Koo Jee, Hyun Lee, Dong Won Park, Tae-Hyung Kim, Ho Joo Yoon, Chul Hoon Kim, Jae Myun Lee, Sang-Heon Kim, Min Goo Lee
Synergistic toxicity with copper contributes to NAT2-associated isoniazid toxicity. Experimental & molecular medicine 56 (3) (2024)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Multi-locus pathogenic variation identified in a patient with craniosynostosis. American journal of medical genetics. Part A 194 (5) (2023)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Multi-locus pathogenic variation identified in a patient with craniosynostosis. American journal of medical genetics. Part A 194 (5) (2023)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Multi-locus pathogenic variation identified in a patient with craniosynostosis. American journal of medical genetics. Part A (2023)
Jihoon G Yoon, Jung Woo Yu, Kyu Won Shim, Yong Oock Kim, Min Goo Lee
Multi-locus pathogenic variation identified in a patient with craniosynostosis. American journal of medical genetics. Part A 194 (5) (2023)
Hak Park, Soo Kyung Seo, Ju-Ri Sim, Su Jin Hwang, Ye Jin Kim, Dong Hoon Shin, Dong Geon Jang, Shin Hye Noh, Pil-Gu Park, Si Hwan Ko, Mi Hwa Shin, Jae Young Choi, Yukishige Ito, Chung-Min Kang, Jae-Myun Lee, Min Goo Lee
TMED3 Complex Mediates ER Stress-Associated Secretion of CFTR, Pendrin, and SARS-CoV-2 Spike. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 9 (24) (2022)
Jung Woo Han, Woon Heo, Donghyuk Lee, Choeun Kang, Hye-Yeon Kim, Ikhyun Jun, Insuk So, Hyuk Hur, Min Goo Lee, Minkyu Jung, Joo Young Kim
Plasma Membrane Localized GCaMP-MS4A12 by Orai1 Co-Expression Shows Thapsigargin- and Ca2+-Dependent Fluorescence Increases. Molecules and cells 44 (4) (2021)
Dong Hoon Shin, Minjae Kim, Yonjung Kim, Ikhyun Jun, Jinsei Jung, Joo Hyun Nam, Mary Hongying Cheng, Min Goo Lee
Bicarbonate permeation through anion channels: its role in health and disease. Pflugers Archiv : European journal of physiology 472 (8) (2020)
Young Hun Kim, Man Sup Kwak, Bin Lee, Jae Min Shin, Sowon Aum, In Ho Park, Min Goo Lee, Jeon-Soo Shin
Secretory autophagy machinery and vesicular trafficking are involved in HMGB1 secretion. Autophagy 17 (9) (2020)
Jiyoon Kim, Hyeyon Kim, Shin Hye Noh, Dong Geon Jang, Shi-Young Park, Dongkook Min, Hyunki Kim, Hee-Seok Kweon, Hoguen Kim, Sowon Aum, Sookyung Seo, Cheol Soo Choi, Hail Kim, Jae Woo Kim, Seok Jun Moon, Heon Yung Gee, Min Goo Lee
Grasp55-/- mice display impaired fat absorption and resistance to high-fat diet-induced obesity. Nature communications 11 (1) (2020)
Hak Park, Dong Hoon Shin, Ju-Ri Sim, Sowon Aum, Min Goo Lee
IRE1α kinase-mediated unconventional protein secretion rescues misfolded CFTR and pendrin. Science advances 6 (8) (2020)
Mengnan Li, Shin-Ya Nishio, Chie Naruse, Meghan Riddell, Sabrina Sapski, Tatsuya Katsuno, Takao Hikita, Fatemeh Mizapourshafiyi, Fiona M Smith, Leanne T Cooper, Min Goo Lee, Masahide Asano, Thomas Boettger, Marcus Krueger, Astrid Wietelmann, Johannes Graumann, Bryan W Day, Andrew W Boyd, Stefan Offermanns, Shin-Ichiro Kitajiri, Shin-Ichi Usami, Masanori Nakayama
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome. Nature communications 11 (1) (2020)
John Hoon Rim, Joon Suk Lee, Jinsei Jung, Ji-Hyun Lee, Seung-Tae Lee, Jong Rak Choi, Jae Young Choi, Min Goo Lee, Heon Yung Gee
Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency. Scientific reports 9 (1) (2019)
Jinsei Jung, Haiyue Lin, Young Ik Koh, Kunhi Ryu, Joon Suk Lee, John Hoon Rim, Hye Ji Choi, Hak Joon Lee, Hye-Youn Kim, Seyoung Yu, Hyunsoo Jin, Ji-Hyun Lee, Min Goo Lee, Wan Namkung, Jae Young Choi, Heon Yung Gee
Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment. Experimental & molecular medicine 51 (8) (2019)
Haiyue Lin, Ikhyun Jun, Joo Han Woo, Min Goo Lee, Sung Joon Kim, Joo Hyun Nam
Temperature-dependent increase in the calcium sensitivity and acceleration of activation of ANO6 chloride channel variants. Scientific reports 9 (1) (2019)
Jiyoon Kim, Heon Yung Gee, Min Goo Lee
Unconventional protein secretion - new insights into the pathogenesis and therapeutic targets of human diseases. Journal of cell science 131 (12) (2018)
Dong Hoon Shin, Jinsei Jung, Young Ik Koh, John Hoon Rim, Joon Suk Lee, Hye Ji Choi, Sun Young Joo, Seyoung Yu, Do Hyeon Cha, Seung Yeon Lee, Ji Hyun Lee, Min Goo Lee, Jae Young Choi, Heon Yung Gee
A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Human mutation 40 (3) (2018)