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KA-2 Structural Analysis Based on Measurements of Slight Cation Displacements from High Resolution STEM Images 基于高分辨率STEM图像微小阳离子位移测量的KA-2结构分析
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz044
S. Kobayashi
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引用次数: 0
SM-6 Thorough quantification of micrograph by AI and advanced mathematics SM-6通过人工智能和高等数学对显微照片进行彻底量化
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz059
Y. Adachi, T. Ogawa, Zhi‐Lei Wang, Kohei Enya, Fumito Ajioka
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引用次数: 0
SB-5 Abstraction of Pathological Information and Integration of Cancer Genome Information SB-5肿瘤病理信息提取与基因组信息整合
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz051
S. Ishikawa
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引用次数: 0
SS1-4 3D reconstruction of intracytoplasmic membrane structure of methane-oxidizing bacteria by electron microscopy imaging SS1-4甲烷氧化菌胞质内膜结构的电镜成像三维重建
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz065
K. Uematsu, Chong Chen, H. Hirayama
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引用次数: 0
PM-01 Exothermic behavior and microstructures of the LiNi1/3Mn1/3Co1/3O2 positive electrode layer for all-solid-state lithium batteries. 全固态锂电池正极层LiNi1/3Mn1/3Co1/3O2的放热行为和微观结构
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz101
H. Tsukasaki, Tomoki Uchiyama, K. Yamamoto, Misae Otoyama, H. Kowada, Atsuki Atarashi, S. Mori, Y. Uchimoto, A. Hayashi, M. Tatsumisago
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引用次数: 0
PB-15 Morphological Analysis of Reticular Dermis of Human Keloid Tissue 人瘢痕疙瘩组织网状真皮PB-15形态学分析
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz072
S. Ichinose, Chiemi Kaku, R. Ogawa
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引用次数: 0
PB-10 High-pressure freezing method can be replaced by sandwich freezing method !?: electron microscopy of human tissues and cultured cells PB-10高压冷冻法可以用三明治冷冻法代替!?:人体组织和培养细胞的电子显微镜
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz085
M. Yamaguchi, S. Wakabayashi, Y. Nakamura, H. Matsue, T. Hirao, Shigeki Aoki, H. Yamada, Nobuya Mamizu, H. Furukawa, H. Chibana
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引用次数: 0
PM-18 Technology for fundamentally improving an extremely low-quality video signal used for fine focusing and astigmatism correction in scanning electron microscopy PM-18从根本上改善扫描电子显微镜中用于精细聚焦和散光校正的极低质量视频信号的技术
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-11-01 DOI: 10.1093/jmicro/dfz106
Sadao Yamazaki, Kazuhiko Suzuki, E. Oho
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引用次数: 0
Para-crystalline membrane structures resembling prolamellar bodies in the invasion zones of indeterminate root nodules of Vicia faba L. 蚕豆(Vicia faba L.)不确定根瘤侵入区中类似前釉层体的准结晶膜结构。
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-10-09 DOI: 10.1093/jmicro/dfz027
F. Sharmin, K. Atsuzawa, Stephan Jung, S. Schubert, Y. Kaneko
Novel para-crystalline structures resembling prolamellar bodies in etioplasts were found in the invasion zones of indeterminate root nodules of Vicia faba, which possess persistent meristems and exhibit sequential developmental stages. The para-crystalline structures existed in most cells in the area of the invasion zone and a hexagonal arrangement of tubular membranes was recognized. Extensive membranes, apparently procured from the structures, were often in contact with the bacteria in young infected cells. We propose that the para-crystalline structures serve as a reservoir of membranes for the formation of the numerous symbiosomes that propagate and fill the infected cells, and suggest naming them pro-symbiosome membrane bodies.
在蚕豆(Vicia faba)不确定根瘤的侵袭区发现了类似于原生质体中前釉体的新型准结晶结构,这些根瘤具有持久的分生组织,并表现出连续的发育阶段。在入侵区的大多数细胞中都存在准结晶结构,并发现管状膜呈六边形排列。广泛的膜,显然是从结构中获得的,经常与年轻感染细胞中的细菌接触。我们提出,准结晶结构是形成大量共生体的膜库,这些共生体繁殖并填充受感染的细胞,并建议将其命名为亲共生体膜体。
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引用次数: 0
Efficient fluorescence recovery using antifade reagents in correlative light and electron microscopy. 在相关光学和电子显微镜中使用抗褪色试剂进行有效的荧光回收。
IF 1.8 4区 工程技术 Q3 MICROSCOPY Pub Date : 2019-10-09 DOI: 10.1093/jmicro/dfz029
K. Toyooka, Naeko Shinozaki‐Narikawa
Correlative light and electron microscopy (CLEM) enables ultrastructural-level analysis of fluorescence-labeled proteins by combining images obtained from both fluorescence and electron microscopies. A technical challenge with the CLEM method is the effective detection of fluorescence from samples embedded in resins, which generally cause fluorescence decay. To overcome this issue, we developed a method for fluorescence recovery of green fluorescent protein (GFP) in resin-embedded semi-thin sections using commercially available antifade reagents. By applying this method, we successfully obtained CLEM images using field-emission scanning electron microscopy with moderately enhanced GFP signals, demonstrating the efficacy of this simple fluorescence recovery method.
相关光电子显微镜(CLEM)通过结合从荧光显微镜和电子显微镜获得的图像,使荧光标记蛋白的超微结构水平分析成为可能。CLEM方法的一个技术挑战是有效检测树脂中样品的荧光,这通常会导致荧光衰减。为了克服这个问题,我们开发了一种利用市售抗褪色试剂在树脂包埋的半薄切片中荧光恢复绿色荧光蛋白(GFP)的方法。通过应用该方法,我们成功地使用场发射扫描电镜获得了具有中等增强GFP信号的CLEM图像,证明了这种简单的荧光恢复方法的有效性。
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引用次数: 3
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