문장섭 교수
Jangseop Moon
서울대학교 · 의학
연구실 소개
문장섭 교수의 연구실은 신경과학과 임상의학을 융합한 신경질환 기전 및 치료 전략 연구를 중심으로, 알츠하이머병의 조기 진단 생물학적 표지자 탐색, 약물유도 피부반응의 유전적 기반 규명, 그리고 간질의 약물내성 메커니즘 규명에 초점을 맞추고 있습니다. 특히 뇌유전자 발현 조절, 신경염증 반응, 유전자형과 약물 반응의 연관성 등 분자생물학적 접근을 통해 개인 맞춤형 치료 전략 개발을 추구하고 있습니다. 또한, 임상에서의 빠르고 정확한 진단 기법 개발을 위해 고감도 유전자 분석 기술을 활용한 감염성 폐렴 진단법 개발도 함께 진행하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Considering the risk of dreadful complications, which appear in an unpredictable manner, TFESI with fluoroscopic guidance should be done only with a nonparticulate steroid.
MicroRNA-206, which suppresses the expression of brain-derived neurotrophic factor, is known to be elevated in the brains of Alzheimer's disease (AD) patients. We performed intranasal biopsy of the olfactory epithelia of early dementia patients (n = 24) and cognitively healthy controls (n = 9). Patients with significant depression (n = 8) were analyzed separately, as their cognitive impairments were thought to be caused by their depression. Real-time PCR was performed on the biopsied tissues. Th
The OI symptoms, but not the maximal HR increment, are significantly correlated with depression and diminished QOL in patients with excessive OT. Therefore, pervasive history taking is important when encountering patients with excessive OT.
The use of lamotrigine (LTG) can be limited by the occurrence of cutaneous adverse drug reactions (cADRs) that range from maculopapular eruption (MPE) to the more severe Stevens-Johnson syndrome and toxic epidermal necrolysis. A few human leukocyte antigen (HLA)-related genetic risk factors for carbamazepine-induced cADR have been identified. However, the HLA-related genetic risk factors associated with LTG-induced cADR are not yet well known. We performed HLA genotyping in 50 Korean patients wi
This is the first study to identify a pharmacoresistant subgroup, resistant to 2 AEDs, in the pilocarpine-induced epilepsy model. We hypothesize that modulation of the identified miRNAs may play a key role in developing pharmacoresistance and behavioral alterations in the MDR group.
We used deep sequencing of the 16S rRNA gene from sputum to identify Haemophilus influenza in a patient with community-acquired pneumonia. This method may be more effective than conventional diagnostic tests in pneumonia patients because of its speed and sensitivity.
Summary Objective Oxcarbazepine ( OXC ) is a widely used antiepileptic drug for the treatment of partial seizures that was developed through structural variation of carbamazepine. Although OXC has a lower risk of cutaneous adverse drug reactions ( cADR s) than carbamazepine, cADR s ranging from maculopapular eruption ( MPE ) to the more severe Stevens‐Johnson syndrome and toxic epidermal necrolysis still limit the use of OXC in some patients. A few human leukocyte antigen ( HLA )–related genetic
Emerging Microbes & Infections (2017) 6, e94; doi:10.1038/emi.2017.81; published online 1 November 2017
Diabetic foot infections (DFIs) cause substantial morbidity and mortality. The mainstay of the treatment is empiric antibiotics and surgical debridement in severe cases. In this study, we performed nanopore 16S rDNA sequencing from the debridement specimens of DFIs. Fifty-four surgical debridement specimens obtained from 45 patients with medically intractable DFI were included. The 16S rDNA PCR was performed on each specimen, and Nanopore sequencing was performed for up to 3 h. The reads were al
Moon, Jangsup MD, PhD; Choi, Sun-Hye DVM, PhD; Shim, Ji-Young BSc; Park, Hyun-Jung BSc; Oh, Min-Jung BSc; Kim, Manho MD, PhD; Nah, Seung-Yeol DVM, PhDAuthor Information
Our data demonstrates the potential of amplicon nanopore sequencing using aqueous humor to enable rapid, sensitive and less invasive microbial diagnosis of endophthalmitis.
CSF nanopore 16S sequencing was more effective than conventional CSF culture studies in postoperative bacterial meningitis and may contribute to evidence-based decisions for antibiotic maintenance and discontinuation.
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