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Brainlab AG elements fibertracking software
Elements Fibertracking Software, supplied by Brainlab AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/elements+software/elements+fibertracking+software/pm40072663-3-12-26
Average 90 stars, based on 1 article reviews
elements fibertracking software - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Quantitative evaluation of neuroradiological and morphometric alteration of inferior Fronto-Occipital Fascicle across different brain tumor histotype: an Italian multicentric study.
Article Snippet: IFOF reconstructions were calculated for both hemispheres for each patient diagnosed with Glioblastoma (GBM), Low Grade Glioma (LGG), Brain Metastasis and Meningioma using Elements Fibertracking software (Brainlab AG).

Article Title: Function-guided differences of arcuate fascicle and inferior fronto-occipital fascicle tractography as diagnostic indicators for surgical risk stratification
Article Snippet: Additionally, each of the reconstructed tracts was defined as an object within the Brainlab Elements Fibertracking module (Brainlab AG, Germany) which allowed to derive the volume of each tract and the complete reconstruction of the left-hemispheric language network in cm 3 .

Article Title: Letter to the Editor: Application of a Human Stereotactic System for Image-Guided Deep Brain Stimulation Neurosurgery in a Swine Model.
Article Snippet: 116 117 Jo urn al Pr e-p roo f 118 Fig. 1 | Application of a human frame-based stereotactic system for image-guided DBS 119 surgery in a swine model. (A) 3D rendering of the skull-mounted anchor “key.” (B-D) 120 Isometric, anterior, and lateral views showing the unmodified human stereotactic frame attached 121 to the key. (E) Direct targeting of the nucleus accumbens (NAcc, blue) and ventral tegmental 122 area (VTA, pink). (F) Mesolimbic pathway tractography confirms accuracy of direct targeting, as 123 projection fibers from the VTA to NAcc are traversed by the planned targets/trajectories 124 (generated using Elements Fibertracking v2.0, Brainlab AG, Munich, Germany).

Article Title: THE 2023 AAPM ANNUAL MEETING PROGRAM.
Article Snippet: Fibers were calculated using Elements Fibertracking software (Brainlab AG, Germany) with a fractional anisotropy (FA) of 20, maximum angulation of 20° and a minimum length of 80 mm.

Article Title: Neuroradiological Evaluation of Anatomo-Morphometric Arcuate Fascicle Modifications According to Different Brain Tumor Histotypes: An Italian Multicentric Study.
Article Snippet: Preoperative fiber tractography of the AF was performed using Elements Fibertracking and SmartBrush V. 2.0 (Brainlab AG) by neurosurgeons with proved neuro-oncological expertise.

Article Title: Brainshift correction using navigated intraoperative ultrasound informs intraoperative decision-making during glioma surgery.
Article Snippet: Tractography (Elements Fibertracking, Brainlab AG, Germany) and semi-automated outlining of the tumor volume and other objects (Elements SmartBrush, Brainlab AG, Germany) was done.

Software:

Article Title: Time-synchronized deep brain stimulation optimization
Article Snippet: .. Subsequently, tractographic fibre reconstruction is performed in step S2.4 using e.g. the “Fibertracking Element” software module provided by Brainlab AG. ..



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Nikon nikon nis elements software
A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon <t>NIS</t> <t>Elements</t> <t>software.</t> All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Biofilm

Article Title: Inactivation of Cysteine Synthase CysK-A enhances flocculation, biofilm formation, and sensitivity to oxidative stress in Azospirillum brasilense Sp7

doi: 10.1016/j.bioflm.2025.100335

Figure Lengend Snippet: A. brasilense AR mutant exhibits elevated levels of intracellular c-di-GMP. Colony morphology of wild-type A. brasilense Sp7 ( A ) and the AR mutant ( B ) expressing a c-di-GMP biosensor (pFY4535). Cultures were grown for five days at 30 °C on Nfb∗ agar supplemented with KNO 3 . The intracellular c-di-GMP concentration is proportional to the expression of TurboRFP (red), resulting in a red colony color. The AR mutant's more intense coloration indicates higher c-di-GMP accumulation than in the WT. Representative fluorescence microscopy of individual WT and AR mutant cells. Images were captured on a Nikon Eclipse TE2000-U microscope using the following excitation/emission wavelengths: 489/519 nm for AmCyan (green) and 553/574 nm for TurboRFP (red). Gray images are intensity surface plots corresponding to the fluorescence emitted by TurboRFP. Images were processed using Nikon NIS Elements software. All images shown are representative of three independent experiments. Scale bars, 10 mm (colonies); 10 μm (individual cells). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: Obtained images were processed and analyzed using Nikon NIS Elements software.

Techniques: Mutagenesis, Expressing, Concentration Assay, Fluorescence, Microscopy, Software