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Institution

Sungkyunkwan University

EducationSeoul, South Korea
About: Sungkyunkwan University is a education organization based out in Seoul, South Korea. It is known for research contribution in the topics: Thin film & Graphene. The organization has 28229 authors who have published 56428 publications receiving 1352733 citations. The organization is also known as: 성균관대학교.


Papers
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Journal ArticleDOI
TL;DR: These isolates are highly resistant to major antimicrobial agents, which could limit the therapeutic options in the clinical practice and significantly increases the likelihood of pneumonia-related mortality.
Abstract: Rationale: Hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) remain important causes of morbidity and mortality. Increasing antimicrobial resistance has aroused the concern of the failure of antibiotic treatment.Objectives: To determine the distribution of the bacterial isolates of HAP and VAP, their antimicrobial resistance patterns, and impact of discordant antibiotic therapy on clinical outcome in Asian countriesMethods: A prospective surveillance study was conducted in 73 hospitals in 10 Asian countries from 2008–2009. A total of 2,554 cases with HAP or VAP in adults were enrolled and 2,445 bacterial isolates were collected from 1,897 cases. Clinical characteristics and antimicrobial resistance profiles were analyzed.Measurement and Main Results: Major bacterial isolates from HAP and VAP cases in Asian countries were Acinetobacter spp., Pseudomonas aeruginosa, Staphylococcus aureus, and Klebsiella pneumoniae. Imipenem resistance rates of Acinetobacter and P. aeruginosa were 6...

272 citations

Journal ArticleDOI
TL;DR: Mapping the number of independent imports of the staphylococcal cassette chromosome methicillin-resistance island shows that import has occurred on at least 23 occasions within this single sequence type and that the progeny of such recombinant strains usually are distributed locally rather than globally.
Abstract: A small number of clonal lineages dominates the global population structure of methicillin-resistant Staphylococcus aureus (MRSA), resulting in the concept that MRSA has emerged on a few occasions after penicillinase-stable β-lactam antibiotics were introduced to clinical practice, followed by intercontinental spread of individual clones. We investigated the evolutionary history of an MRSA clone (ST5) by mutation discovery at 108 loci (46 kb) within a global collection of 135 isolates. The SNPs that were ascertained define a radial phylogenetic structure within ST5 consisting of at least 5 chains of mutational steps that define geographically associated clades. These clades are not concordant with previously described groupings based on staphylococcal protein A gene (spa) typing. By mapping the number of independent imports of the staphylococcal cassette chromosome methicillin-resistance island, we also show that import has occurred on at least 23 occasions within this single sequence type and that the progeny of such recombinant strains usually are distributed locally rather than globally. These results provide strong evidence that geographical spread of MRSA over long distances and across cultural borders is a rare event compared with the frequency with which the staphylococcal cassette chromosome island has been imported.

271 citations

Journal ArticleDOI
TL;DR: It is shown that RAD18 promotes homologous recombination in a manner strictly dependent on its ability to be recruited to sites of DNA breaks and that this recruitment relies on a well-defined DNA damage signalling pathway mediated by another E3 ligase, RNF8.
Abstract: To maintain genome stability, cells respond to DNA damage by activating signalling pathways that govern cell-cycle checkpoints and initiate DNA repair. Cell-cycle checkpoint controls should connect with DNA repair processes, however, exactly how such coordination occurs in vivo is largely unknown. Here we describe a new role for the E3 ligase RAD18 as the integral component in translating the damage response signal to orchestrate homologous recombination repair (HRR). We show that RAD18 promotes homologous recombination in a manner strictly dependent on its ability to be recruited to sites of DNA breaks and that this recruitment relies on a well-defined DNA damage signalling pathway mediated by another E3 ligase, RNF8. We further demonstrate that RAD18 functions as an adaptor to facilitate homologous recombination through direct interaction with the recombinase RAD51C. Together, our data uncovers RAD18 as a key factor that orchestrates HRR through surveillance of the DNA damage signal.

270 citations

Journal ArticleDOI
TL;DR: The results demonstrate that the proposed integrated CAD system, through all stages of detection, segmentation, and classification, outperforms the latest conventional deep learning methodologies.

270 citations


Authors

Showing all 28506 results

NameH-indexPapersCitations
Michael Grätzel2481423303599
Hyun-Chul Kim1764076183227
Yongsun Kim1562588145619
David J. Mooney15669594172
Jongmin Lee1502257134772
Byung-Sik Hong1461557105696
Inkyu Park1441767109433
Y. Choi141163198709
Kazunori Kataoka13890870412
E. J. Corey136137784110
Pasi A. Jänne13668589488
Suyong Choi135149597053
Intae Yu134137289870
Tae Jeong Kim132142093959
Anders Hagfeldt12960079912
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023103
2022588
20214,342
20204,248
20194,124
20183,826