Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Jiwon Yun"'
Autor:
Chae-eun Lee, Yoonsik Park, Hyunjae Park, Kiwoong Kwak, Hyeonmin Lee, Jiwon Yun, Donghyun Lee, Jung Hun Lee, Sang Hee Lee, Lin-Woo Kang
Publikováno v:
Emerging Microbes and Infections, Vol 13, Iss 1 (2024)
The extensive use of β-lactam antibiotics has led to significant resistance, primarily due to hydrolysis by β-lactamases. OXA class D β-lactamases can hydrolyze a wide range of β-lactam antibiotics, rendering many treatments ineffective. We inves
Externí odkaz:
https://doaj.org/article/d43e621b6bc84737bf304796e602aaa5
Publikováno v:
Humanities & Social Sciences Communications, Vol 10, Iss 1, Pp 1-13 (2023)
Abstract Forced alignment is a speech technique that can automatically align audio files with transcripts. With the help of forced alignment tools, annotating audio files and creating annotated speech databases have become much more accessible and ef
Externí odkaz:
https://doaj.org/article/3504ca6d654b4be4a5038111997eda28
Autor:
Sooyong Park, Jiwon Yun, Sung Yoon Choi, Dajeong Jeong, Ja-Yoon Gu, Jee-Soo Lee, Moon-Woo Seong, Yoon Hwan Chang, Hongseok Yun, Hyun Kyung Kim
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract T-cell large granular lymphocyte leukemia (T-LGL) is often accompanied by pure red cell aplasia (PRCA). A high depth of next generation sequencing (NGS) was used for detection of the mutational profiles in T-LGL alone (n = 25) and T-LGL comb
Externí odkaz:
https://doaj.org/article/dc7b5f12be3242faa05ab92d5a305285
Autor:
Jiwon Yun, Hyojin Song, Sung-Min Kim, Soonok Kim, Seok Ryun Kwon, Young Eun Lee, Dajeong Jeong, Jae Hyeon Park, Sunghoon Kwon, Hongseok Yun, Dong Soon Lee
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-19 (2023)
Abstract Background Therapy-related myeloid neoplasm (T-MN) rarely occurs among cancer survivors, and was characterized by poor prognosis. T-MN has germline predisposition in a considerable proportion. Here, clinical characteristics and germline/soma
Externí odkaz:
https://doaj.org/article/5a187ce8c60e4562b61c9aecaca68297
Autor:
Sooyong Park, Jiwon Yun, Sung Yoon Choi, Dajeong Jeong, Ja-Yoon Gu, Jee-Soo Lee, Moon-Woo Seong, Yoon Hwan Chang, Hongseok Yun, Hyun Kyung Kim
Publikováno v:
HemaSphere, Vol 7, p e3469528 (2023)
Externí odkaz:
https://doaj.org/article/6c3f08f1a34149c79341b221df00b519
Autor:
Dajeong Jeong, Sung-Min Kim, Byung Joo Min, Ju Han Kim, Young Seok Ju, Yong-Oon Ahn, Jiwon Yun, Young Eun Lee, Seok Ryun Kwon, Jae Hyeon Park, Jong Hyun Yoon, Dong Soon Lee
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Congenital neutropenia (CN) is a hematological disease heterogeneous in its genetic, phenotypic and histologic aspects. We aimed to identify the genetic etiology of Korean CN patients in the context of bone marrow (BM) histology and clinical
Externí odkaz:
https://doaj.org/article/8c1ba510314242138632d50b3ffb8e79
Autor:
Kyunghoon Jung, M. H. Abobeih, Jiwon Yun, Gyeonghun Kim, Hyunseok Oh, Ang Henry, T. H. Taminiau, Dohun Kim
Publikováno v:
npj Quantum Information, Vol 7, Iss 1, Pp 1-9 (2021)
Abstract The detection of nuclear spins using individual electron spins has enabled diverse opportunities in quantum sensing and quantum information processing. Proof-of-principle experiments have demonstrated atomic-scale imaging of nuclear-spin sam
Externí odkaz:
https://doaj.org/article/aae3cb9c096d4172ab8a755f13be46a2
Autor:
Sung‐Min Kim, Naery Euphrasia Yang, Dajeong Jeong, Jiwon Yun, Sohee Ryu, Sung‐Soo Yoon, Yong‐Oon Ahn, Dong Soon Lee
Publikováno v:
eJHaem, Vol 1, Iss 2, Pp 563-566 (2020)
Abstract Next‐generation flow (NGF) has detected minimal residual disease (MRD) in numerous myeloma patients who achieve a complete response (CR). However, when MRD is not detected via NGF in non‐CR patients, its clinical meaning is uncertain. He
Externí odkaz:
https://doaj.org/article/ba25d9fdf7404a0d90e74ced08857d6a
Autor:
Seok Ryun Kwon, Man Jin Kim, Young-Eun Lee, Jiwon Yun, Da-Jeong Jeong, Jae Hyeon Park, Sunghoon Kwon, Dong Soon Lee
Publikováno v:
PLoS ONE, Vol 17, Iss 12, p e0271624 (2022)
Hereditary thrombocytopenia is a heterogeneous group of congenital disorders with a wide range of symptoms depending on the severity of platelet dysfunction or thrombocytopenia. Because of its clinical phenotypes and the bone marrow morphology associ
Externí odkaz:
https://doaj.org/article/cf660de900d24fafa761c5dc3216d9be
Autor:
Dajeong Jeong, Sung-Min Kim, Byung Joo Min, Ju Han Kim, Young Seok Ju, Yong-Oon Ahn, Jiwon Yun, Young Eun Lee, Seok Ryun Kwon, Jae Hyeon Park, Jong Hyun Yoon, Dong Soon Lee
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/1e0c010e421e458e9607f6edbdbe5366