3 Nuclear(3 핵)란 무엇입니까?
3 Nuclear 3 핵 - RESULTS: SHetA2 induced p53 nuclear and mitochondrial accumulation in ovarian cancer cell lines, but not in hFTSECs. [1] To understand how South Florida functions as a barrier for blacknose shark, a highly migratory species that has genetically diverged Atlantic and Gulf populations, patterns of genetic variation were assessed in 212 individuals sampled from the Atlantic, eastern Gulf, and Florida Keys at 2213 nuclear-encoded SNP-containing loci. [2]결과: SHetA2는 난소암 세포주에서 p53 핵 및 미토콘드리아 축적을 유도했지만 hFTSEC에서는 그렇지 않았습니다. [1] 남부 플로리다가 대서양과 걸프만 개체군을 유전적으로 갈라진 고도로 이동하는 종인 흑코상어의 장벽으로 기능하는 방법을 이해하기 위해 2213 핵-에서 대서양, 동부 걸프 및 플로리다 사주에서 표본 추출한 212명의 개체에서 유전적 변이 패턴을 평가했습니다. 인코딩된 SNP 함유 유전자좌. [2]
proton nuclear magnetic 양성자 핵자기
Characterization of the synthesized vinylic glycomonomers was carried out using elemental analysis, fourier transform infrared (FT-IR), Carbon-13 nuclear magnetic resonance (13C NMR) and proton nuclear magnetic resonance (1H NMR) spectroscopy. [1] The structures of the compounds were confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), and High Resolution Mass Spectrometry (HRMS) analyses. [2] Their structures were determined on the basis of proton nuclear magnetic resonance and carbon-13 nuclear magnetic resonance spectroscopy. [3] Their chemical structures were confirmed by proton nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, mass spectrometry, and infrared. [4] Characterization methods which were used to determine the structure of these compounds are Fourier Transform Infrared (FTIR), Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), and Ultraviolet Visible (UV Vis) spectroscopies and elemental analysis. [5] A novel palmitic imidazoline compound, N-(2-(2-pentadecyl-4,5-dihydro-1H-imidazol-1-yl)ethyl)palmitamide (NIMP) has been successfully synthesized and characterized with Fourier transform spectroscopy (FTIR), Proton nuclear magnetic resonance (1H NMR), and Carbon-13 nuclear magnetic resonance (13C NMR). [6] The structure of synthesized compounds has been confirmed by FT-IR spectroscopy, proton nuclear magnetic resonance (H-NMR) spectroscopy and carbon 13 nuclear magnetic resonance (C-NMR) spectroscopy the final synthesized compounds were also screened for their antibacterial and antifungal activity. [7] The structures of the compounds were confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR) and High Resolution Mass Spectrometry (HRMS) analyses. [8] It was then crystallized in methanol and characterized using various spectroscopic techniques such as Fourier transform infra-red spectroscopy (FTIR), ultra-violet visible spectroscopy (UV-vis), proton nuclear magnetic resonance (1H-NMR), X-ray photoelectron spectroscopy (XPS), and carbon-13 nuclear magnetic resonance (13C-NMR). [9] A product was isolated from the dichloromethane/methanol (2%) fraction and the structure was determined on the basis of spectroscopic data; Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), Heteronuclear Multiple Bond Correlation (HMBC), H-correlation spectroscopy (H-COSY), attached proton test (APT), heteronuclear multiple quantum coherence (HSQC). [10] A series of aromatic diimide and monoimide compounds condensed with p-phenylamino(phenyl)amine were synthesized and confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), Fourier Transform Infrared Spectroscopy (FT-IR), Elemental Analysis (EA), and High Resolution Mass Spectroscopy (HRMS). [11]합성된 비닐 글리코단량체의 특성화는 원소 분석, 푸리에 변환 적외선(FT-IR), 탄소-13 핵 자기 공명(13C NMR) 및 양성자 핵 자기 공명(1H NMR) 분광법을 사용하여 수행되었습니다. [1] 화합물의 구조는 양성자 핵 자기 공명(1H NMR), 탄소-13 핵 자기 공명(13C NMR) 및 고분해능 질량 분석(HRMS) 분석에 의해 확인되었습니다. [2] nan [3] nan [4] nan [5] nan [6] nan [7] nan [8] nan [9] nan [10] nan [11]
transform infrared spectroscopy 적외선 분광법 변환
Physicochemical properties were evaluated by attenuated total reflection–Fourier transform infrared spectroscopy (ATR-FTIR), carbon-13 nuclear magnetic resonance (13C NMR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) method and stereoscopic microscopy. [1] The characterization of the mucilage of Dillenia indica was done using Fourier transform infrared spectroscopy (FTIR) and solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C NMR), and the signals obtained indicated the presence of polysaccharides, which are responsible for enhancing the CF process. [2] Thin layer chromatography, melting points, Fourier transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (H-NMR) and carbon-13 nuclear magnetic resonance (C-NMR) techniques confirmed formation of the prepared compounds. [3] X-ray diffraction, Fourier-transform infrared spectroscopy, and solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance analysis revealed that HTP mainly interrupted unstable chemical bonds (acetyl groups, glycosidic bonds, and ether linkage in lignin) and changed the biomass crystallinity. [4] Carbon-13 nuclear magnetic resonance and Fourier transform infrared spectroscopy suggested a highly substituted xylan structure for QSG. [5] The structure of the product was characterized by Fourier transform infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance (H NMR) and carbon-13 nuclear magnetic resonance (C NMR). [6] The synthesized copolymer was characterized using Fourier transform infrared spectroscopy (FT-IR), carbon-13 nuclear magnetic resonance spectroscopy, and differential scanning calorimetry. [7] The depolymerized products showed significant reduction in molecular weight and improvement in solubility in an 80% ethanol-water (v/v) solution owing to the cleavage of ether linkages; this was confirmed by gel permeation chromatography (GPC), fourier transform-infrared spectroscopy (FT-IR), pyrolysis-gas chromatography/ mass spectrometer (Py-GC/MS), carbon-13 nuclear magnetic resonance spectrometry (13C NMR), and heteronculear single quantum coherence nuclear magnetic resonance spectrometry (HSQC NMR) analyses. [8]물리화학적 특성은 감쇠 전반사-푸리에 변환 적외선 분광법(ATR-FTIR), 탄소-13 핵 자기 공명(13C NMR), 열중량 분석(TGA), 주사 전자 현미경(SEM), Brunauer-Emmett-Teller(BET)에 의해 평가되었습니다. ) 방법 및 입체 현미경. [1] Dillenia indica 점액의 특성화는 푸리에 변환 적외선 분광법(FTIR) 및 고체 교차 편광 마법각 회전 탄소-13 핵 자기 공명(CP/MAS 13C NMR)을 사용하여 수행되었으며, 얻은 신호는 다음의 존재를 나타냅니다. CF 과정을 강화하는 책임이 있는 다당류. [2] nan [3] nan [4] nan [5] nan [6] nan [7] nan [8]
nuclear magnetic resonance 핵자기공명
The structures of the synthesized compounds were characterized by Fourier transform infrared (FT-IR), hydrogen-1 nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, and elemental analysis. [1] The derivatives were characterized via nuclear magnetic resonance hydrogen spectroscopy (1H-NMR), carbon-13 nuclear magnetic resonance spectroscopy (13C-NMR), and electrospray ionization high resolution mass spectrometry (ESI-HRMS). [2] Periodic weak measurements of just a few carbon-13 nuclear spins in diamond demonstrate sensitive, high-resolution nuclear magnetic resonance spectroscopy at the molecular level. [3] A series of novel linear and V-shaped carbazole-based molecules functionalized by cyano acceptors and diversified donors (carbazole, diphenylamino, dimethylamino, methoxy, and ferrocene) were synthesized and characterized by hydrogen-1 nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, Fourier transform infrared spectroscopy, and high-resolution mass spectrometry. [4]합성된 화합물의 구조는 푸리에 변환 적외선(FT-IR), 수소-1 핵 자기 공명, 탄소-13 핵 자기 공명 및 원소 분석에 의해 특성화되었습니다. [1] 유도체는 핵 자기 공명 수소 분광법(1H-NMR), 탄소-13 핵 자기 공명 분광법(13C-NMR) 및 전자분무 이온화 고분해능 질량 분석법(ESI-HRMS)을 통해 특성화되었습니다. [2] nan [3] nan [4]
state cross polarization 상태 교차 편광
The structure of coal samples was characterized by solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C NMR) and Fourier transform infrared spectrometer (FTIR). [1] The structural features and pyrolysis characteristics of Shendong demineralized coal (DC) and its ethanol swelling coal (EDSC) were investigated by Fourier transform infrared (FTIR), solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C-NMR), thermo-gravimeter-Fourier transform infrared (TG-FTIR) spectroscopy, the self-made steel retort assay, and pyrolysis gas chromatography-mass spectrometer (Py-GC/MS). [2]석탄 샘플의 구조는 고체 상태 교차 편광 마법각 회전 탄소-13 핵 자기 공명(CP/MAS 13C NMR) 및 푸리에 변환 적외선 분광기(FTIR)로 특성화되었습니다. [1] Shendong 탈염탄(DC) 및 에탄올 팽창탄(EDSC)의 구조적 특징 및 열분해 특성은 푸리에 변환 적외선(FTIR), 고체 교차 편광 마법각 회전 탄소-13 핵자기 공명(CP/MAS)에 의해 조사되었습니다. 13C-NMR), 열중량계-푸리에 변환 적외선(TG-FTIR) 분광법, 자체 제작된 강철 레토르트 분석 및 열분해 가스 크로마토그래피-질량 분석계(Py-GC/MS). [2]
magnetic resonance spectroscopy 자기 공명 분광법
Carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) facilitated the probable identification of these ambers as ‘Class Ib' (sensu Anderson et al. [1] Before and after demethylation, the eucalyptus pyrolysis oil was analyzed by carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) and matrix-assisted laser desorption ionization-time of flight (MALDI-TOF). [2]탄소-13 핵자기 공명 분광법(13C NMR)은 이러한 호박을 'Class Ib'로 식별하는 데 도움이 되었습니다(sensu Anderson et al. [1] 탈메틸화 전후에 유칼립투스 열분해 오일을 탄소-13 핵자기 공명 분광법(13C NMR) 및 매트릭스 보조 레이저 탈착 이온화 비행 시간(MALDI-TOF)으로 분석했습니다. [2]
cross polarization magic 교차 편광 마법
The novel modified Schiff base nanoparticles resulted from the crosslinking of FMPC with chitosan were confirmed by cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance spectroscopy. [1]FMPC와 키토산의 가교로 인한 새로운 변형 쉬프 베이스 나노입자는 교차 편광 매직 앵글 스피닝 탄소-13 핵 자기 공명 분광법에 의해 확인되었습니다. [1]
Grade 3 Nuclear 3급 원자력
Patients and Methods: The present study was performed on 30 eyes of 30 individuals preoperative assessed by pentacam to detect grade 3 nuclear cataract to be selected in our study, then corneal endothelium assessed by specular microscopy to evaluate the corneal endothelium to be reference and to be compared to 1st and 3 rd month. [1] Presenting visual acuity (PVA) was 20/200, and a grade 3 nuclear cataract was noted. [2]대상 및 방법: 본 연구는 수술 전 30명 30안 30안을 대상으로 pentacam으로 평가하여 본 연구에서 선별할 3등급 핵백내장을 진단한 후, 각막내피를 경면현미경으로 평가하여 참고 및 참고할 각막내피를 평가하였다. 1개월과 3개월에 비해 [1] 제시시력(PVA)은 20/200이었고 3등급 핵백내장이 관찰되었다. [2]
3 nuclear magnetic 3 핵자기
The interaction between the hemicellulose and ILs was evaluated using carbon-13 nuclear magnetic resonance. [1] Characterization of the synthesized vinylic glycomonomers was carried out using elemental analysis, fourier transform infrared (FT-IR), Carbon-13 nuclear magnetic resonance (13C NMR) and proton nuclear magnetic resonance (1H NMR) spectroscopy. [2] The novel modified Schiff base nanoparticles resulted from the crosslinking of FMPC with chitosan were confirmed by cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance spectroscopy. [3] Physicochemical properties were evaluated by attenuated total reflection–Fourier transform infrared spectroscopy (ATR-FTIR), carbon-13 nuclear magnetic resonance (13C NMR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) method and stereoscopic microscopy. [4] The structures of the compounds were confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), and High Resolution Mass Spectrometry (HRMS) analyses. [5] Their structures were determined on the basis of proton nuclear magnetic resonance and carbon-13 nuclear magnetic resonance spectroscopy. [6] The structures of the bis-azo dyes were identified by Fourier transform infrared, proton and carbon 13 nuclear magnetic resonance data. [7] The structure of coal samples was characterized by solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C NMR) and Fourier transform infrared spectrometer (FTIR). [8] Their chemical structures were confirmed by proton nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, mass spectrometry, and infrared. [9] The characterization of the mucilage of Dillenia indica was done using Fourier transform infrared spectroscopy (FTIR) and solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C NMR), and the signals obtained indicated the presence of polysaccharides, which are responsible for enhancing the CF process. [10] Characterization methods which were used to determine the structure of these compounds are Fourier Transform Infrared (FTIR), Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), and Ultraviolet Visible (UV Vis) spectroscopies and elemental analysis. [11] The structural features and pyrolysis characteristics of Shendong demineralized coal (DC) and its ethanol swelling coal (EDSC) were investigated by Fourier transform infrared (FTIR), solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance (CP/MAS 13C-NMR), thermo-gravimeter-Fourier transform infrared (TG-FTIR) spectroscopy, the self-made steel retort assay, and pyrolysis gas chromatography-mass spectrometer (Py-GC/MS). [12] In this study, the supramolecular structure before and after pretreatment was characterized using solid-state carbon-13 nuclear magnetic resonance (C-13 NMR), and the findings related to the swelling of dissolving pulp and cotton were quantified with a fiber analyzer. [13] Thin layer chromatography, melting points, Fourier transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (H-NMR) and carbon-13 nuclear magnetic resonance (C-NMR) techniques confirmed formation of the prepared compounds. [14] X-ray diffraction, Fourier-transform infrared spectroscopy, and solid-state cross-polarization magic angle spinning carbon-13 nuclear magnetic resonance analysis revealed that HTP mainly interrupted unstable chemical bonds (acetyl groups, glycosidic bonds, and ether linkage in lignin) and changed the biomass crystallinity. [15] 75 MMA/MAA molar ratio determined by carbon-13 nuclear magnetic resonance. [16] The structures of the synthesized compounds were characterized by Fourier transform infrared (FT-IR), hydrogen-1 nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, and elemental analysis. [17] Carbon-13 nuclear magnetic resonance and Fourier transform infrared spectroscopy suggested a highly substituted xylan structure for QSG. [18] The branch degree, sequence structure, molecular weight, and molecular weight distribution of the copolymer products were determined by Fourier transform infrared spectroscopy(FTIR), carbon-13 nuclear magnetic resonance(13C NMR) spectrometry and gel permeation chromatography(GPC). [19] Herein, it is presented a methodology for the characterization of organosulfur compounds in asphalt cement (AC) samples employing solid-phase extraction (SPE) associated with methylation reactions and positive-ion mode electrospray Fourier transform ion cyclotron resonance mass spectrometry (ESI(+)FT-ICR MS) and carbon-13 nuclear magnetic resonance (13C NMR) spectroscopy. [20] The structure of the product was characterized by Fourier transform infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance (H NMR) and carbon-13 nuclear magnetic resonance (C NMR). [21] The derivatives were characterized via nuclear magnetic resonance hydrogen spectroscopy (1H-NMR), carbon-13 nuclear magnetic resonance spectroscopy (13C-NMR), and electrospray ionization high resolution mass spectrometry (ESI-HRMS). [22] The chemical structures of this study were confirmed by spectral instrumentation; infrared, differential scanning calorimeter thermal analyzer, proton and carbon-13 nuclear magnetic resonance. [23] Correlation between strength in an external magnetic field and spectral width of solid-state sulfur-33 nuclear magnetic resonance (NMR) spectra in an organosulfur compound, whose quadrupolar coupli. [24] Compounds synthesized were characterized by Fourier-transform infrared, H-1, P-31, and C-13 nuclear magnetic resonance spectroscopic methods, which confirmed the coordination of ylide to the metal center through the ylidic carbon atom. [25] Carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) facilitated the probable identification of these ambers as ‘Class Ib' (sensu Anderson et al. [26] The branch degree, sequence structure, molecular weight, and molecular weight distribution of the copolymer products were determined by Fourier transform infrared spectroscopy(FTIR), carbon-13 nuclear magnetic resonance(13C NMR) spectrometry and gel permeation chromatography(GPC). [27] Cellulose bearing pendant Schiff base with heterocyclic chelating groups (CMC-Bz) was synthesized, which were fully characterized using various instrumental techniques such as solid state carbon-13 nuclear magnetic resonance (13C-NMR), Fourier transform infrared (FTIR), scanning electron microscope (SEM) and energy dispersive X-ray analysis (EDX) spectra. [28] The synthesized copolymer was characterized using Fourier transform infrared spectroscopy (FT-IR), carbon-13 nuclear magnetic resonance spectroscopy, and differential scanning calorimetry. [29] A novel palmitic imidazoline compound, N-(2-(2-pentadecyl-4,5-dihydro-1H-imidazol-1-yl)ethyl)palmitamide (NIMP) has been successfully synthesized and characterized with Fourier transform spectroscopy (FTIR), Proton nuclear magnetic resonance (1H NMR), and Carbon-13 nuclear magnetic resonance (13C NMR). [30] The structure of synthesized compounds has been confirmed by FT-IR spectroscopy, proton nuclear magnetic resonance (H-NMR) spectroscopy and carbon 13 nuclear magnetic resonance (C-NMR) spectroscopy the final synthesized compounds were also screened for their antibacterial and antifungal activity. [31] The structures of the compounds were confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR) and High Resolution Mass Spectrometry (HRMS) analyses. [32] A series of novel linear and V-shaped carbazole-based molecules functionalized by cyano acceptors and diversified donors (carbazole, diphenylamino, dimethylamino, methoxy, and ferrocene) were synthesized and characterized by hydrogen-1 nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, Fourier transform infrared spectroscopy, and high-resolution mass spectrometry. [33] The structures of the prepared products were deduced from their Fourier-transform infrared, elemental analysis and proton and carbon-13 nuclear magnetic resonance spectral data. [34] The nematic order in the melt of both model compounds at elevated temperature is monitored with X-ray Diffraction (XRD) and C-13 Nuclear Magnetic Resonance (13C NMR). [35] Chemical modifications were investigated using quantitative analysis by carbon-13 nuclear magnetic resonance of samples taken during the synthesis. [36] It was then crystallized in methanol and characterized using various spectroscopic techniques such as Fourier transform infra-red spectroscopy (FTIR), ultra-violet visible spectroscopy (UV-vis), proton nuclear magnetic resonance (1H-NMR), X-ray photoelectron spectroscopy (XPS), and carbon-13 nuclear magnetic resonance (13C-NMR). [37] Before and after demethylation, the eucalyptus pyrolysis oil was analyzed by carbon-13 nuclear magnetic resonance spectroscopy (13C NMR) and matrix-assisted laser desorption ionization-time of flight (MALDI-TOF). [38] The depolymerized products showed significant reduction in molecular weight and improvement in solubility in an 80% ethanol-water (v/v) solution owing to the cleavage of ether linkages; this was confirmed by gel permeation chromatography (GPC), fourier transform-infrared spectroscopy (FT-IR), pyrolysis-gas chromatography/ mass spectrometer (Py-GC/MS), carbon-13 nuclear magnetic resonance spectrometry (13C NMR), and heteronculear single quantum coherence nuclear magnetic resonance spectrometry (HSQC NMR) analyses. [39] The chemical features of the nine biofilms were analyzed using elemental analysis, infrared spectroscopy, X-ray photoelectron spectroscopy, and carbon-13 nuclear magnetic resonance. [40] Carbon-13 Nuclear Magnetic Resonance (13C NMR) was used as supporting technique for analysis of the obtained polymers. [41] A product was isolated from the dichloromethane/methanol (2%) fraction and the structure was determined on the basis of spectroscopic data; Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), Heteronuclear Multiple Bond Correlation (HMBC), H-correlation spectroscopy (H-COSY), attached proton test (APT), heteronuclear multiple quantum coherence (HSQC). [42] A series of aromatic diimide and monoimide compounds condensed with p-phenylamino(phenyl)amine were synthesized and confirmed by Proton Nuclear Magnetic Resonance (1H NMR), Carbon-13 Nuclear Magnetic Resonance (13C NMR), Fourier Transform Infrared Spectroscopy (FT-IR), Elemental Analysis (EA), and High Resolution Mass Spectroscopy (HRMS). [43] Carbon-13 nuclear magnetic resonance ( 13 C NMR) spectroscopy was used for the quantitative determination of structural chemical groups and contaminants. [44] In the present study, a set of new benzamide derivatives (4a-e), which are structurally similar to paracetamol, were synthesized from thymol using a green synthetic approach and characterized by Fourier-transform infrared (FT-IR) and H-1 and C-13 nuclear magnetic resonance (NMR) spectroscopies, liquid chromatography-mass spectrometry (LC-MS), and X-ray single-crystallographic analysis for derivative 4c. [45]헤미셀룰로오스와 IL 사이의 상호 작용은 탄소-13 핵 자기 공명을 사용하여 평가되었습니다. [1] 합성된 비닐 글리코단량체의 특성화는 원소 분석, 푸리에 변환 적외선(FT-IR), 탄소-13 핵 자기 공명(13C NMR) 및 양성자 핵 자기 공명(1H NMR) 분광법을 사용하여 수행되었습니다. [2] FMPC와 키토산의 가교로 인한 새로운 변형 쉬프 베이스 나노입자는 교차 편광 매직 앵글 스피닝 탄소-13 핵 자기 공명 분광법에 의해 확인되었습니다. [3] 물리화학적 특성은 감쇠 전반사-푸리에 변환 적외선 분광법(ATR-FTIR), 탄소-13 핵 자기 공명(13C NMR), 열중량 분석(TGA), 주사 전자 현미경(SEM), Brunauer-Emmett-Teller(BET)에 의해 평가되었습니다. ) 방법 및 입체 현미경. [4] 화합물의 구조는 양성자 핵 자기 공명(1H NMR), 탄소-13 핵 자기 공명(13C NMR) 및 고분해능 질량 분석(HRMS) 분석에 의해 확인되었습니다. [5] nan [6] 비스-아조 염료의 구조는 푸리에 변환 적외선, 양성자 및 탄소 13 핵 자기 공명 데이터에 의해 확인되었습니다. [7] 석탄 샘플의 구조는 고체 상태 교차 편광 마법각 회전 탄소-13 핵 자기 공명(CP/MAS 13C NMR) 및 푸리에 변환 적외선 분광기(FTIR)로 특성화되었습니다. [8] nan [9] Dillenia indica 점액의 특성화는 푸리에 변환 적외선 분광법(FTIR) 및 고체 교차 편광 마법각 회전 탄소-13 핵 자기 공명(CP/MAS 13C NMR)을 사용하여 수행되었으며, 얻은 신호는 다음의 존재를 나타냅니다. CF 과정을 강화하는 책임이 있는 다당류. [10] nan [11] Shendong 탈염탄(DC) 및 에탄올 팽창탄(EDSC)의 구조적 특징 및 열분해 특성은 푸리에 변환 적외선(FTIR), 고체 교차 편광 마법각 회전 탄소-13 핵자기 공명(CP/MAS)에 의해 조사되었습니다. 13C-NMR), 열중량계-푸리에 변환 적외선(TG-FTIR) 분광법, 자체 제작된 강철 레토르트 분석 및 열분해 가스 크로마토그래피-질량 분석계(Py-GC/MS). [12] 본 연구에서는 고체상 탄소-13 핵자기공명(C-13 NMR)을 이용하여 전처리 전·후의 초분자 구조를 특성화하고, 용해 펄프 및 면화의 팽윤과 관련된 소견을 섬유 분석기로 정량화하였다. [13] nan [14] nan [15] 탄소-13 핵자기 공명에 의해 결정된 75 MMA/MAA 몰비. [16] 합성된 화합물의 구조는 푸리에 변환 적외선(FT-IR), 수소-1 핵 자기 공명, 탄소-13 핵 자기 공명 및 원소 분석에 의해 특성화되었습니다. [17] nan [18] 공중합체 생성물의 분지도, 서열 구조, 분자량 및 분자량 분포는 푸리에 변환 적외선 분광법(FTIR), 탄소-13 핵 자기 공명(13C NMR) 분광법 및 겔 투과 크로마토그래피(GPC)에 의해 결정되었다. [19] 여기에서는 메틸화 반응과 관련된 고체상 추출(SPE) 및 양이온 모드 전자분무 푸리에 변환 이온 사이클로트론 공명 질량 분석법(ESI(+) FT-ICR MS) 및 탄소-13 핵 자기 공명(13C NMR) 분광법. [20] nan [21] 유도체는 핵 자기 공명 수소 분광법(1H-NMR), 탄소-13 핵 자기 공명 분광법(13C-NMR) 및 전자분무 이온화 고분해능 질량 분석법(ESI-HRMS)을 통해 특성화되었습니다. [22] nan [23] nan [24] nan [25] 탄소-13 핵자기 공명 분광법(13C NMR)은 이러한 호박을 'Class Ib'로 식별하는 데 도움이 되었습니다(sensu Anderson et al. [26] nan [27] nan [28] nan [29] nan [30] nan [31] nan [32] nan [33] nan [34] nan [35] nan [36] nan [37] 탈메틸화 전후에 유칼립투스 열분해 오일을 탄소-13 핵자기 공명 분광법(13C NMR) 및 매트릭스 보조 레이저 탈착 이온화 비행 시간(MALDI-TOF)으로 분석했습니다. [38] nan [39] nan [40] nan [41] nan [42] nan [43] nan [44] nan [45]
3 nuclear translocation 3 핵 이식
IRF3 nuclear translocation during RLR signaling was impaired in Nup93-deficient RAW264. [1] Compared with naive ADSCs, BP-preconditioned ADSCs provided a significant increase of Akt and STAT3 phosphorylation, STAT3 activity, STAT3 nuclear translocation, myocardial IL-10 levels, and the percentage of M2 macrophage infiltration. [2] Moreover, MEST leads to Twist-1 induction by STAT3 activation and subsequently enables the induction of activation of the EMT program via the induction of STAT3 nuclear translocation. [3] In this study, the pro-apoptotic effect of PEDV was examined in Vero cells and we observed that PEDV infection increased MDM2 and CBP, promoted p53 phosphorylation at serine 20 and, promoted p53 nuclear translocation, leading to p53 activation in Vero cells. [4] Calenduloside E dose-dependently decreased the expression levels of iNOS and COX-2 induced by LPS, inhibited LPS-induced release of TNF-α and IL-1β, and suppressed LPS-induced JAK1-stat3 signaling pathway activation and stat3 nuclear translocation. [5] In both age groups, n‐butylidenephthalide effectively provided a significant increase of STAT3 phosphorylation, STAT3 activity, STAT3 nuclear translocation, myocardial IL‐10 levels and the percentage of M2c macrophage and a decrease of myofibroblast infiltration. [6] After poly I:C, IRF3 nuclear translocation occurred earlier (6 h) in female mice and later (14 h) in male mice. [7] We revealed that WX20120108 selectively activated Foxo3, evidenced by Foxo3 nuclear translocation in both gene modified cell line and HeLa cells, as well as the upregulated expression of Foxo3-targeted genes (Bnip3, Pik3c3, Atg5, and Atg4b), which played a key role in autophagy initiation. [8] 0) optimally enhances the tumorigenic effect of bile, by inducing activation of NF‐κB, STAT3 nuclear translocation, bcl‐2 overexpression and significant overexpression of the oncogenic mRNA phenotype, compared to weakly acidic pH (5. [9] TGF-βR1 and P-Smad2/3 expression was downregulated and Smad2/3 nuclear translocation was inhibited. [10] Importantly, change of extracellular Ca2+ in culture medium prevents LPS-induced NFATc3 nuclear translocation, up-regulation of proinflammatory cytokines and ROS production in macrophages. [11] 7c inhibited STAT3 nuclear translocation in mouse embryonic fibroblast while 7b and 7c inhibited STAT3 DNA-binding activity in the A375 cell line. [12] It reduced EZH2, DNA methyltransferase 3A（DNMT3a）, ASXL1 and downstream H3K4me3, H3K27me3 and HOXA9 expression and inhibited EZH2 and H3K27me3 nuclear translocation. [13] In an IL-1β dependent manner, albumin/R-III inhibited Smad3 nuclear translocation via TAK1-, JNK-mediated Smad3 linker phosphorylation and decreased expression of Smad3 target genes, such as α-smooth muscle actin and collagen type I. [14] The inhibition of the DNA-sensing pathway by HBV was tested using IRF3 nuclear translocation assay. [15] The reduction in AKT activity led to dephosphorylation of cytosolic TFE3 at Ser565 and promoted TFE3 nuclear translocation independently of MTORC1. [16] Fnip1 regulates TFE3 nuclear translocation and lysosome biogenesis in pre–B cells. [17] Compared with naïve hADSCs, BP-preconditioned hADSCs provided a further decrease of ROS and LVH and an increase of local hADSC engraftment, STAT3 phosphorylation, STAT3 activity, STAT3 nuclear translocation, myocardial IL-10 levels, and the percentage of M2 macrophage infiltration. [18] Abundant TUNEL-positive cells, ARHI and PIAS3 upregulation, CA125 reduction, and decreased STAT3 nuclear translocation were found in the Res-in-ethanol and, especially, the Res-in-DMSO group. [19] Furthermore, HER2/HER3 nuclear translocation mediates overexpression of cyclin D1, leading to tumor cell survival and drug resistance. [20] Moreover, there is a direct interaction between STAT3 and nAChRα1 that modulates STAT3 nuclear translocation and its binding to the Akt promoter region upon nicotine exposure. [21]RLR 신호 전달 중 IRF3 핵 전위는 Nup93-결핍 RAW264에서 손상되었습니다. [1] 순진한 ADSC와 비교하여 BP 사전 조절된 ADSC는 Akt 및 STAT3 인산화, STAT3 활성, STAT3 핵 전위, 심근 IL-10 수준 및 M2 대식세포 침윤 비율의 상당한 증가를 제공했습니다. [2] 더욱이, MEST는 STAT3 활성화에 의해 Twist-1 유도를 유도하고 후속적으로 STAT3 핵 전위의 유도를 통해 EMT 프로그램의 활성화 유도를 가능하게 한다. [3] 이 연구에서 PEDV의 pro-apoptotic 효과가 Vero 세포에서 조사되었으며 우리는 PEDV 감염이 MDM2와 CBP를 증가시키고 세린 20에서 p53 인산화를 촉진하고 p53 핵 전위를 촉진하여 Vero 세포에서 p53 활성화를 유도한다는 것을 관찰했습니다. [4] Calenduloside E는 LPS에 의해 유도된 iNOS와 COX-2의 발현 수준을 용량 의존적으로 감소시켰고, LPS에 의해 유도된 TNF-α와 IL-1β의 방출을 억제했으며, LPS에 의해 유도된 JAK1-stat3 신호 전달 경로 활성화 및 stat3 핵 전위를 억제했습니다. [5] 두 연령 그룹 모두에서 n-부틸리덴프탈라이드는 STAT3 인산화, STAT3 활성, STAT3 핵 전위, 심근 IL-10 수준 및 M2c 대식세포 비율의 상당한 증가 및 근섬유아세포 침윤 감소를 효과적으로 제공했습니다. [6] 폴리 I:C 후, IRF3 핵 전위는 암컷 마우스에서 더 일찍(6시간) 수컷 마우스에서 나중에(14시간) 발생했습니다. [7] 우리는 WX20120108이 Foxo3를 선택적으로 활성화했으며, 이는 유전자 변형된 세포주와 HeLa 세포 모두에서 Foxo3 핵 전위뿐만 아니라 Foxo3 표적 유전자(Bnip3, Pik3c3, Atg5 및 Atg4b)의 상향 조절된 발현에 의해 입증되었으며, 이는 핵심 역할을 했습니다. 자가포식 개시. [8] 0) 약산성 pH와 비교하여 NF-κB, STAT3 핵 전위, bcl-2 과발현 및 발암성 mRNA 표현형의 현저한 과발현을 유도하여 담즙의 종양 유발 효과를 최적으로 향상시킵니다(5. [9] nan [10] nan [11] nan [12] nan [13] nan [14] nan [15] nan [16] nan [17] nan [18] nan [19] nan [20] nan [21]
3 nuclear accumulation 3 핵 축적
Besides, we ascertained that GPER and FAK activation are involved in the STAT3 nuclear accumulation and gene expression changes. [1] Moreover, β‐catenin activation induced CX43 nuclear accumulation, which impeded CX43 down‐regulation induced by PDGFR inhibition, suggesting that CX43 expression is positively correlated with nuclear β‐catenin expression. [2] The presence of TP53 missense mutation, indicated by p53 nuclear accumulation using a genetically validated assay, was significantly associated with increased CD3+ T-cell density (median, 341 versus 231 CD3+ T cells/mm2; P =. [3] Loss of betaIV-spectrin function promotes STAT3 nuclear accumulation and transcriptional activity, altered gene expression and CF activation. [4] We then showed that combination treatment with Cl-amidine and docetaxel enhanced p53 nuclear accumulation, which synergistically induced cell cycle arrest and apoptosis. [5] Mechanistically, DHA decreases late, but not early, SMAD3 nuclear accumulation and inhibits p65/RelA-S536 phosphorylation, which is required for HSC survival. [6] They found that FF in high concentrations could cause significant DNA damage, double-stranded breaks, and TP53 nuclear accumulation that created an immunostaining pattern similar to that seen in p53 signature. [7]또한 GPER 및 FAK 활성화가 STAT3 핵 축적 및 유전자 발현 변화에 관여함을 확인했습니다. [1] 또한, β-카테닌 활성화는 CX43 핵 축적을 유도하여 PDGFR 억제에 의해 유도된 CX43 하향 조절을 방해하여 CX43 발현이 핵 β-카테닌 발현과 양의 상관관계가 있음을 시사합니다. [2] 유전적으로 검증된 분석을 사용하여 p53 핵 축적에 의해 표시되는 TP53 미스센스 돌연변이의 존재는 증가된 CD3+ T-세포 밀도(중앙값, 341 대 231 CD3+ T 세포/mm2, P=. [3] betaIV-spectrin 기능의 손실은 STAT3 핵 축적 및 전사 활성, 변경된 유전자 발현 및 CF 활성화를 촉진합니다. [4] 그런 다음 우리는 Cl-아미딘과 도세탁셀의 병용 치료가 p53 핵 축적을 향상시켜 상승적으로 세포 주기 정지 및 세포 사멸을 유도한다는 것을 보여주었습니다. [5] nan [6] nan [7]
3 nuclear localization 3 핵 국산화
Engineered Cas9 containing 3 nuclear localization sequences edited human hematopoietic stem and progenitor cells more efficiently and consistently than conventional Cas9 with 2 nuclear localization sequences. [1] Mechanistic studies indicated that DSS inhibited JAK2-STAT3 signaling, it reduced IDO1 expression, STAT3 phosphorylation and STAT3 nuclear localization. [2] This correlated with enhanced chondrogenesis and a reduction in the expression of markers associated with chondrocyte hypertrophy, as well as increased SMAD 2/3 nuclear localization in the encapsulated MSCs. [3] In cultured cells, brevilin A reduced cell viability, induced apoptosis, suppressed migration and invasion, decreased protein levels of phospho-JAK2 (Y1007/1008) and phospho-STAT3 (Tyr705), and restrained STAT3 nuclear localization. [4] Furthermore, sequence analysis showed that the amino acids of PCV3 nuclear localization signals were highly conserved. [5] Moreover, accumulated evidence suggests that both p53 and nuclear exporter protein, exportin 1 (XPO1), are working in reciprocal manner may lead to loss of p53 nuclear localization and enhance cancer progression through hyperactive nuclear export. [6]3개의 핵 국재화 서열을 포함하는 조작된 Cas9는 2개의 핵 국재화 서열을 포함하는 기존 Cas9보다 인간 조혈 줄기 및 전구 세포를 더 효율적이고 일관되게 편집했습니다. [1] 역학 연구에 따르면 DSS는 JAK2-STAT3 신호 전달을 억제하고 IDO1 발현, STAT3 인산화 및 STAT3 핵 국소화를 감소시켰습니다. [2] 이것은 강화된 연골 형성 및 연골 세포 비대와 관련된 마커의 발현 감소, 뿐만 아니라 캡슐화된 MSC에서 증가된 SMAD 2/3 핵 국소화와 관련이 있습니다. [3] 배양된 세포에서 브레빌린 A는 세포 생존력을 감소시키고 세포자멸사를 유도하며 이동 및 침입을 억제하고 phospho-JAK2(Y1007/1008) 및 phospho-STAT3(Tyr705)의 단백질 수준을 감소시키고 STAT3 핵 국소화를 억제했습니다. [4] 또한, 서열 분석은 PCV3 핵 국소화 신호의 아미노산이 고도로 보존되어 있음을 보여주었다. [5] 더욱이, 축적된 증거는 p53과 핵 수출 단백질인 exportin 1(XPO1)이 상호 작용하는 방식으로 p53 핵 국소화의 손실로 이어질 수 있고 과잉 핵 수출을 통해 암 진행을 향상시킬 수 있음을 시사합니다. [6]
3 nuclear microsatellite 3 핵 마이크로위성
Here, we tested the cross-amplification of 43 nuclear microsatellite markers, originally developed for other bromeliad species. [1] METHODS We evaluated 149 individuals using two plastid DNA regions (cpDNA) and 13 nuclear microsatellite markers (nuSSRs) to access the historical patterns, genetic diversity, and structure of V. [2] Molecular data from the nuclear internal transcribed spacer, six plastid markers and 13 nuclear microsatellite loci were analyzed for 240 individuals from 19 populations of this section. [3] We sequenced the complete mitochondrial genome (16,341 base pairs; n = 60 moose) and genotyped 13 nuclear microsatellites (n = 253) to evaluate genetic variation among moose samples. [4]여기에서 우리는 원래 다른 브로멜리아드 종을 위해 개발된 43개의 핵 미세위성 마커의 교차 증폭을 테스트했습니다. [1] 행동 양식 우리는 V. [2] 핵 내부 전사된 스페이서, 6개의 색소체 마커 및 13개의 핵 미세위성 유전자좌의 분자 데이터를 이 섹션의 19개 개체군에서 240명에 대해 분석했습니다. [3] nan [4]
3 nuclear family 3 핵가족
We genotyped 26 SNPs harboured in genes previously reported to be associated with ADHD and evaluated their potential association in 386 individuals belonging to 113 nuclear families from a Caribbean community in Barranquilla, Colombia, using family-based association tests. [1] We investigated the HLA haplotypes of 1017 subjects in 263 nuclear families sourced from five US clinical immunogenetics laboratories, primarily as part of the evaluation of related donor candidates for hematopoietic stem cell and solid organ transplantation. [2] Methods We investigated depression and anxiety symptoms, quantified using the Hospital and Depression Scale (HADS) in 1,375 individuals from 93 nuclear families recruited from an admixed population in Brazil. [3]우리는 이전에 ADHD와 관련이 있는 것으로 보고된 유전자에 숨겨져 있는 26개의 SNP를 유전자형으로 지정하고 가족 기반 연관 테스트를 사용하여 콜롬비아 바랑키야의 카리브해 지역 사회의 113개 핵가족에 속하는 386명의 개인에서 이들의 잠재적 연관성을 평가했습니다. [1] 우리는 주로 조혈 줄기 세포 및 고형 장기 이식에 대한 관련 기증자 후보 평가의 일환으로 5개의 미국 임상 면역 유전학 연구소에서 제공한 263개의 핵가족에서 1017명의 대상체의 HLA 일배체형을 조사했습니다. [2] nan [3]
3 nuclear expression 3 핵 표현
Pevious studies have shown that FOXA1 is a significant predictor of good outcome in breast cancer, while Nestin expression was preferentially found in triple-negative breast cancers, revealing a strong association with germline BRCA1-related breast cancer, a basal-like phenotype, stemness characteristics, high proliferation rates, p53 nuclear expression, increased rate of nodal metastases, and reduced survival (1,2,3,4). [1] Reported results show that CSE increased TLR4 and survivin, LPS binding, ERK 1/2 activation, IL‐8 release and mRNA levels but decreased SIRT1, HDAC2, HDAC3 and FoxO3 nuclear expression. [2] Moreover, the neoplastic cells reveal an aberrant p63 nuclear expression. [3]이전 연구에 따르면 FOXA1은 유방암에서 좋은 결과를 예측하는 중요한 예측 인자이며 Nestin 발현은 삼중 음성 유방암에서 우선적으로 발견되어 생식계열 BRCA1 관련 유방암, 기저 유사 표현형, 줄기 특성과 강한 연관성을 나타냅니다. , 높은 증식율, p53 핵 발현, 결절 전이율 증가 및 생존율 감소(1,2,3,4). [1] 보고된 결과에 따르면 CSE는 TLR4 및 서바이빈, LPS 결합, ERK 1/2 활성화, IL-8 방출 및 mRNA 수준을 증가시켰지만 SIRT1, HDAC2, HDAC3 및 FoxO3 핵 발현을 감소시켰다. [2] nan [3]
3 nuclear cataract 3 핵 백내장
Patients and Methods: The present study was performed on 30 eyes of 30 individuals preoperative assessed by pentacam to detect grade 3 nuclear cataract to be selected in our study, then corneal endothelium assessed by specular microscopy to evaluate the corneal endothelium to be reference and to be compared to 1st and 3 rd month. [1] Presenting visual acuity (PVA) was 20/200, and a grade 3 nuclear cataract was noted. [2]대상 및 방법: 본 연구는 수술 전 30명 30안 30안을 대상으로 pentacam으로 평가하여 본 연구에서 선별할 3등급 핵백내장을 진단한 후, 각막내피를 경면현미경으로 평가하여 참고 및 참고할 각막내피를 평가하였다. 1개월과 3개월에 비해 [1] 제시시력(PVA)은 20/200이었고 3등급 핵백내장이 관찰되었다. [2]
3 nuclear export 3 원자력 수출
Correspondingly, CAMTA3 is directly phosphorylated by two flg22-responsive mitogen-activated protein kinases (MAPKs), MPK3 and MPK6, which triggers CAMTA3 nuclear export and destabilization. [1] In the nucleus, TAZ binds to SMAD2/3 to prevent SMAD2/3 nuclear export. [2]상응하게, CAMTA3는 2개의 flg22-반응성 미토겐 활성화 단백질 키나제(MAPK), MPK3 및 MPK6에 의해 직접 인산화되어 CAMTA3 핵 수출 및 불안정화를 유발합니다. [1] 핵에서 TAZ는 SMAD2/3에 결합하여 SMAD2/3 핵 수출을 방지합니다. [2]
3 nuclear dna 3 핵 DNA
To address this knowledge gap, we collected brown bear samples from the Gobi Desert (n = 2360), Altai, Sayan, Khentii, and Ikh Khyangan mountains of Mongolia (n = 79), and Deosai National Park in the Himalayan Mountain Range of Pakistan (n = 5) and generated 927 base pairs of mitochondrial DNA (mtDNA) sequence data and genotypes at 13 nuclear DNA microsatellite loci. [1] This data set contains a description of 3 mitochondrial DNA and 93 nuclear DNA Single Nucleotide Polymorphism (SNP) loci and sequence information developed through double digest restriction-site associated DNA sequencing (ddRADseq) techniques for Greater White-Fronted Goose (Anser albifrons) that winter in California. [2]이러한 지식 격차를 해소하기 위해 우리는 몽골의 고비 사막(n = 2360), 알타이, 사얀, 켄티, 이크 캉간 산맥(n = 79), 파키스탄 히말라야 산맥의 데오사이 국립공원에서 불곰 샘플을 수집했습니다. (n = 5) 미토콘드리아 DNA(mtDNA) 서열 데이터의 927개 염기쌍과 13개의 핵 DNA 미세위성 유전자좌에서 유전자형을 생성했습니다. [1] 이 데이터 세트에는 3개의 미토콘드리아 DNA 및 93개의 핵 DNA SNP(Single Nucleotide Polymorphism) 유전자좌에 대한 설명과 그해 겨울 Greater White-Fronted Goose(Anser albifrons)에 대한 이중 소화 제한 부위 관련 DNA 시퀀싱(ddRADseq) 기술을 통해 개발된 서열 정보가 포함되어 있습니다. 캘리포니아에서. [2]
3 nuclear transport 3 원자력 운송
Further data showed that NRON overexpression suppressed, whereas NRON silencing further promoted the Ang II-induced NFATc3 nuclear transport and IL-12 expression in atrial myocytes. [1] Our findings repurpose disulfiram as a modulator of ataxin-3 nuclear transport that aggravates the pathology of SCA3, which is a new target for disulfiram. [2]추가 데이터는 NRON 과발현이 억제되는 반면, NRON 침묵은 심방 근세포에서 Ang II 유도 NFATc3 핵 수송 및 IL-12 발현을 더욱 촉진한다는 것을 보여주었습니다. [1] 우리의 연구 결과는 disulfiram의 새로운 표적인 SCA3의 병리를 악화시키는 ataxin-3 핵 수송의 조절제로 disulfiram을 용도 변경했습니다. [2]