Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Man-Jin Kim"'
Autor:
Tae Woog Kang, Juhee Han, Sin Lee, In-Jun Hwang, Su-Ji Jeon, Jong-Min Ju, Man-Jin Kim, Jin-Kyoung Yang, Byoengsun Jun, Chi Ho Lee, Sang Uck Lee, Jong-Ho Kim
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
The detection of pathogenic microorganisms is key consideration for safety across a wide range of fields. Here, the authors report on the simultaneous exfoliation and functionalisation of transition metal dichalcogenides with dextran for antibody-fre
Externí odkaz:
https://doaj.org/article/c534ccc83a72422baadf8aa514351eba
Autor:
Man Jin Kim, Jee-Soo Lee, Seung Won Chae, Sung Im Cho, Jangsup Moon, Jung Min Ko, Jong-Hee Chae, Moon-Woo Seong
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Ectodermal dysplasia (ED) is a rare genetic disorder that affects structures derived from the ectodermal germ layer. Results In this study, we analyzed the genetic profiles of 27 Korean patients with ED. Whole exome sequencing (WE
Externí odkaz:
https://doaj.org/article/5e5555b0c8b14cfdaa0a6b8cee224017
Autor:
Cho-Rong Lee, Man Jin Kim, Sang-Heon Park, Sheehyun Kim, Soo Yeon Kim, Seong-Joon Koh, Seungbok Lee, Murim Choi, Jong Hee Chae, Sung-Gyoo Park, Jangsup Moon
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Fever of unknown origin (FUO) remains a formidable diagnostic challenge in the field of medicine. Numerous studies suggest an association between FUO and genetic factors, including chromosomal abnormalities. Here, we report a female patient
Externí odkaz:
https://doaj.org/article/05c5e1ddf60c4ff29bb3d01d15d9bbe1
Autor:
Jin Gyu Lim, Jae Sung Ko, Jung Min Ko, Hyun Young Kim, Man Jin Kim, Moon Woo Seong, Young Hun Choi, Gyeong Hoon Kang, Jaemoon Koh, Jin Soo Moon
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Chronic enteropathy associated with SLCO2A1 gene (CEAS) is a unique type of inflammatory bowel disease. CEAS is monogenic disease and is thought to develop from childhood, but studies on pediatric CEAS are scarce. We analyzed char
Externí odkaz:
https://doaj.org/article/518ea443ccee481782bfb784e1c26644
Autor:
Yuna Lee, Seunghyun Lee, Saebeom Hur, Yun Soo Jeong, Dong In Suh, Jangsup Moon, Man Jin Kim, Young Hun Choi, Jung-Eun Cheon
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background To describe the radiological features of Gorham–Stout disease (GSD) as evaluated using plain radiography and dynamic contrast-enhanced magnetic resonance lymphangiography (DCMRL) imaging techniques. Methods Clinical and conventi
Externí odkaz:
https://doaj.org/article/6fdd1346398f43ed935bc9cc9ebeab24
Autor:
Sungyoung Lee, Choong-Hyun Sun, Heejun Jang, Daeyoon Kim, Sung-Soo Yoon, Youngil Koh, Seung Chan Na, Sung Im Cho, Man Jin Kim, Moon-Woo Seong, Ja Min Byun, Hongseok Yun
Publikováno v:
BMC Bioinformatics, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Internal tandem duplication (ITD) of the FMS-like tyrosine kinase (FLT3) gene is associated with poor clinical outcomes in patients with acute myeloid leukemia. Although recent methods for detecting FLT3-ITD from next-generation sequencing (
Externí odkaz:
https://doaj.org/article/01948a745111426e87c311a85c08aba0
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract The electrospray process has been extensively applied in various fields, including energy, display, sensor, and biomedical engineering owing to its ability to generate of functional micro/nanoparticles. Although the mode of the electrospray
Externí odkaz:
https://doaj.org/article/2c0dd95ab42040afb5120e175918da3c
Autor:
Young Jun Ko, Soo Yeon Kim, Seungbok Lee, Jihoon G. Yoon, Man Jin Kim, Hyeji Jun, Hunmin Kim, Jong-Hee Chae, Ki Joong Kim, Kwangsoo Kim, Byung Chan Lim
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectiveAlthough pediatric epilepsy is an independent disease entity, it is often observed in pediatric neurodevelopmental disorders (NDDs) as a major or minor clinical feature, which might provide diagnostic clues. This study aimed to identify the
Externí odkaz:
https://doaj.org/article/dd4443ebdc9d4b459b9c674f5d475a7a
Autor:
Soo Hyun Seo, Seungjun Lee, Joseph Kyu-hyung Park, Eun Joo Yang, Boram Kim, Jee-Soo Lee, Man Jin Kim, Sung Sup Park, Moon-Woo Seong, Sun-Young Nam, Chan-Yeong Heo, Yujin Myung
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-6 (2022)
Abstract Lymphedema is a progressive disease caused by lymphatic flow blockage in the lymphatic pathway. Primary (hereditary) lymphedema is caused by genetic mutations without secondary causes. We performed clinical profiling on Korean primary lymphe
Externí odkaz:
https://doaj.org/article/2e3c70fbe60043bfa46ded07849076dc
Autor:
Seung Hoon Lee, Seung Han Shin, Jung Min Ko, Boram Kim, Hyeon Sae Oh, Man Jin Kim, Seul Gi Park, Ee-Kyung Kim, Han-Suk Kim
Publikováno v:
Neonatal Medicine, Vol 29, Iss 3, Pp 112-116 (2022)
Schaaf-Yang syndrome (SYS) is a rare genomic imprinting disorder caused by truncating mutations in the paternally derived MAGE family member L2 (MAGEL2) allele. It is also responsible for Prader-Willi syndrome, characterized by neonatal hypotonia, de
Externí odkaz:
https://doaj.org/article/de4e4bed93c04833b55a4930bdab3326