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functional magnetic resonance imaging fmri data  (Bruker Corporation)


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    Bruker Corporation functional magnetic resonance imaging fmri data
    (A) Computer-aided design schematic of the cranial window and optic fiber installation. (B) Image of a chronic cranial window installed on a mouse. (C) Coronal (left) and sagittal (right) view of a <t>structural</t> <t>magnetic</t> resonance image (MRI) with a cranial window and optic fiber implanted in the right primary motor cortex (M1). (D) Representative histological image of endogenous ChR2-YFP expression in layer V of M1. (E) Power Doppler image depicting the coronal field of view at bregma +0 mm. (F) Experimental timeline for fUSI, <t>fMRI,</t> and electrophysiological recordings in response to optogenetic stimulations. (G) Average fMRI (pre-cranial window; top, purple) and fUSI (bottom, green) time series from the bilateral primary motor cortex (M1) and striatum during right M1 stimulation at 10 Hz. Data are presented as mean (color) ± SEM (shaded region). Increasing darkness of the lines represents increasing stimulation intensities. The blue vertical bars indicate stimulation periods.
    Functional Magnetic Resonance Imaging Fmri Data, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 98/100, based on 3007 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/functional+magnetic+resonance+imaging+fmri+data/pmc09584544-250-0-10
    Average 98 stars, based on 3007 article reviews
    functional magnetic resonance imaging fmri data - by Bioz Stars, 2026-09
    98/100 stars

    Images

    1) Product Images from "High-sensitivity detection of optogenetically-induced neural activity with functional ultrasound imaging"

    Article Title: High-sensitivity detection of optogenetically-induced neural activity with functional ultrasound imaging

    Journal: NeuroImage

    doi: 10.1016/j.neuroimage.2021.118434

    (A) Computer-aided design schematic of the cranial window and optic fiber installation. (B) Image of a chronic cranial window installed on a mouse. (C) Coronal (left) and sagittal (right) view of a structural magnetic resonance image (MRI) with a cranial window and optic fiber implanted in the right primary motor cortex (M1). (D) Representative histological image of endogenous ChR2-YFP expression in layer V of M1. (E) Power Doppler image depicting the coronal field of view at bregma +0 mm. (F) Experimental timeline for fUSI, fMRI, and electrophysiological recordings in response to optogenetic stimulations. (G) Average fMRI (pre-cranial window; top, purple) and fUSI (bottom, green) time series from the bilateral primary motor cortex (M1) and striatum during right M1 stimulation at 10 Hz. Data are presented as mean (color) ± SEM (shaded region). Increasing darkness of the lines represents increasing stimulation intensities. The blue vertical bars indicate stimulation periods.
    Figure Legend Snippet: (A) Computer-aided design schematic of the cranial window and optic fiber installation. (B) Image of a chronic cranial window installed on a mouse. (C) Coronal (left) and sagittal (right) view of a structural magnetic resonance image (MRI) with a cranial window and optic fiber implanted in the right primary motor cortex (M1). (D) Representative histological image of endogenous ChR2-YFP expression in layer V of M1. (E) Power Doppler image depicting the coronal field of view at bregma +0 mm. (F) Experimental timeline for fUSI, fMRI, and electrophysiological recordings in response to optogenetic stimulations. (G) Average fMRI (pre-cranial window; top, purple) and fUSI (bottom, green) time series from the bilateral primary motor cortex (M1) and striatum during right M1 stimulation at 10 Hz. Data are presented as mean (color) ± SEM (shaded region). Increasing darkness of the lines represents increasing stimulation intensities. The blue vertical bars indicate stimulation periods.

    Techniques Used: Expressing

    Related Articles

    Functional Assay:

    Article Title: High-sensitivity detection of optogenetically-induced neural activity with functional ultrasound imaging
    Article Snippet: .. Functional magnetic resonance imaging (fMRI) data was acquired with a Bruker BioSpec 70/30 USR small animal MR system (Bruker BioSpin MRI, Ettlingen, Germany) operating at 300MHz (7T). .. Animals were initially anesthetized with 3–4% isoflurane (Sigma-Aldrich, St. Louis, MO, USA) in 100% O2 and secured in a MRI-compatible cradle.

    Magnetic Resonance Imaging:

    Article Title: High-sensitivity detection of optogenetically-induced neural activity with functional ultrasound imaging
    Article Snippet: .. Functional magnetic resonance imaging (fMRI) data was acquired with a Bruker BioSpec 70/30 USR small animal MR system (Bruker BioSpin MRI, Ettlingen, Germany) operating at 300MHz (7T). .. Animals were initially anesthetized with 3–4% isoflurane (Sigma-Aldrich, St. Louis, MO, USA) in 100% O2 and secured in a MRI-compatible cradle.



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    Image Search Results


    (A) Computer-aided design schematic of the cranial window and optic fiber installation. (B) Image of a chronic cranial window installed on a mouse. (C) Coronal (left) and sagittal (right) view of a structural magnetic resonance image (MRI) with a cranial window and optic fiber implanted in the right primary motor cortex (M1). (D) Representative histological image of endogenous ChR2-YFP expression in layer V of M1. (E) Power Doppler image depicting the coronal field of view at bregma +0 mm. (F) Experimental timeline for fUSI, fMRI, and electrophysiological recordings in response to optogenetic stimulations. (G) Average fMRI (pre-cranial window; top, purple) and fUSI (bottom, green) time series from the bilateral primary motor cortex (M1) and striatum during right M1 stimulation at 10 Hz. Data are presented as mean (color) ± SEM (shaded region). Increasing darkness of the lines represents increasing stimulation intensities. The blue vertical bars indicate stimulation periods.

    Journal: NeuroImage

    Article Title: High-sensitivity detection of optogenetically-induced neural activity with functional ultrasound imaging

    doi: 10.1016/j.neuroimage.2021.118434

    Figure Lengend Snippet: (A) Computer-aided design schematic of the cranial window and optic fiber installation. (B) Image of a chronic cranial window installed on a mouse. (C) Coronal (left) and sagittal (right) view of a structural magnetic resonance image (MRI) with a cranial window and optic fiber implanted in the right primary motor cortex (M1). (D) Representative histological image of endogenous ChR2-YFP expression in layer V of M1. (E) Power Doppler image depicting the coronal field of view at bregma +0 mm. (F) Experimental timeline for fUSI, fMRI, and electrophysiological recordings in response to optogenetic stimulations. (G) Average fMRI (pre-cranial window; top, purple) and fUSI (bottom, green) time series from the bilateral primary motor cortex (M1) and striatum during right M1 stimulation at 10 Hz. Data are presented as mean (color) ± SEM (shaded region). Increasing darkness of the lines represents increasing stimulation intensities. The blue vertical bars indicate stimulation periods.

    Article Snippet: Functional magnetic resonance imaging (fMRI) data was acquired with a Bruker BioSpec 70/30 USR small animal MR system (Bruker BioSpin MRI, Ettlingen, Germany) operating at 300MHz (7T).

    Techniques: Expressing