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Sony multiscan 17seii color monitor
Multiscan 17seii Color Monitor, supplied by Sony, 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/graphical+visualisations/multiscan+17seii+monitor/pmc02896204-55-15-14
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multiscan 17seii color monitor - by Bioz Stars, 2026-10
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Article Title: Perceptual efficiency and the inversion effect for faces, words and houses.
Article Snippet: Stimuli were presented on a SONY Trinitron 17-inch monitor (model Multiscan17seII) with a Cambridge Research Systems (CRS) VSG 2/3 graphics card.

Article Title: An exploratory factor analysis of visual performance in a large population.
Article Snippet: The stimuli were presented on a Trinitron Multiscan17seII CRT monitor (Sony, Tokyo, Japan), and the image was reflected in a mirror to give a total view- ing distance of 7.3 m. Responses were gathered using a CT3 response box.

Article Title: Optical coherence tomography in acute optic neuritis: A population-based study.
Article Snippet: 1Institutes of Regional Health Research and Molecular Medicine, University of Southern Denmark, Odense, Denmark 2OPEN, Odense Patient data Explorative Network, Odense University Hospital, Odense, Denmark 3Department of Neurology, Slagelse Hospital, Slagelse, Denmark 4Department of Neurology, Lillebaelt Hospital, Vejle, Denmark 5Department of Ophthalmology, Odense University Hospital, Odense, Denmark 6NeuroCure Clinical Research Center, Charité Universitätsmedizin Berlin, Berlin, Germany 7Freie Universität Berlin, Berlin, Germany 8Humboldt-Universität zu Berlin, Berlin, Germany 9Berlin Institute of Health, Berlin, Germany 10Department of Clinical Research, University of Southern Denmark, Odense, Denmark 11Department of Ophthalmology, Lillebaelt Hospital, Vejle, Denmark 12Max Delbrueck Center for Molecular Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany 13Department of Neurology, University of California Irvine, Irvine, CA, USA

Article Title: Link Between Facial Identity and Expression Abilities Suggestive of Origins of Face Impairments in Autism: Support for the Social-Motivation Hypothesis.
Article Snippet: Individuals with autism spectrum disorder (ASD) often have difficulties with processing identity and expression in faces.. This is at odds with influential models of face processing that propose separate neural pathways for the identity and expression domains.. The social-motivation hypothesis of ASD posits a lack of visual experience with faces as the root cause of face impairments in autism.

Article Title: Qualitatively similar processing for own- and other-race faces: Evidence from efficiency and equivalent input noise.
Article Snippet: We utilized a computer equipped with a Cambridge Research Systems (CRS) VSG 2/3 graphics card and a SONY Trinitron 17 in. monitor (model Multiscan17seII).

Article Title: Information Transmission Rates of Cat Retinal Ganglion Cells
Article Snippet: The receptive field was then projected via an adjustable mirror onto a video display (Multiscan 17se, Sony) running at a frame rate of 150 Hz.

Article Title: Lateralized Effects in Troxler Fading and Parvo and Magnocellular Processing Tasks after Localized 1Hz rTMS
Article Snippet: All programs were created using the Visual Stimulus Generator (VSG2/4F; Cambridge Research Systems) and the stimuli were delivered on a Sony Trinitron (Multiscan 17seII) color monitor.



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Active site of K69A T. brucei ODC in complex with DFMO. The figure was drawn based on the data of reference 7 using the RasMol 2.6 Molecular Graphics Visualisation tool (Glaxo Wellcome Research & Development Co., Stevenage, Herts., United Kingdom). In reference 7, the N terminus of recombinant T. brucei ODC corresponds to the 21st residue of intact ODC (Fig. ​(Fig.3).3). Residues (V62, T63, P64, D72, and T359) which correspond to the residues mutated in this study and were identified as functionally important for substrate specificity in S. ruminantium LDC are purple and violet. The atoms of PLP are yellow, the atoms of DFMO are green, A69 and C360 are orange, and Y389 and F397, which cradle the aliphatic portion of DFMO, are brown. R277, D332, and D361 are also shown, and nitrogen and oxygen atoms of these residues are blue and red, respectively. The asterisked residues belong to the other subunit of the dimer.
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Active site of K69A T. brucei ODC in complex with DFMO. The figure was drawn based on the data of reference 7 using the RasMol 2.6 Molecular Graphics Visualisation tool (Glaxo Wellcome Research & Development Co., Stevenage, Herts., United Kingdom). In reference 7, the N terminus of recombinant T. brucei ODC corresponds to the 21st residue of intact ODC (Fig. ​(Fig.3).3). Residues (V62, T63, P64, D72, and T359) which correspond to the residues mutated in this study and were identified as functionally important for substrate specificity in S. ruminantium LDC are purple and violet. The atoms of PLP are yellow, the atoms of DFMO are green, A69 and C360 are orange, and Y389 and F397, which cradle the aliphatic portion of DFMO, are brown. R277, D332, and D361 are also shown, and nitrogen and oxygen atoms of these residues are blue and red, respectively. The asterisked residues belong to the other subunit of the dimer.

Journal:

Article Title: Gene Cloning and Molecular Characterization of Lysine Decarboxylase from Selenomonas ruminantium Delineate Its Evolutionary Relationship to Ornithine Decarboxylases from Eukaryotes

doi:

Figure Lengend Snippet: Active site of K69A T. brucei ODC in complex with DFMO. The figure was drawn based on the data of reference 7 using the RasMol 2.6 Molecular Graphics Visualisation tool (Glaxo Wellcome Research & Development Co., Stevenage, Herts., United Kingdom). In reference 7, the N terminus of recombinant T. brucei ODC corresponds to the 21st residue of intact ODC (Fig. ​(Fig.3).3). Residues (V62, T63, P64, D72, and T359) which correspond to the residues mutated in this study and were identified as functionally important for substrate specificity in S. ruminantium LDC are purple and violet. The atoms of PLP are yellow, the atoms of DFMO are green, A69 and C360 are orange, and Y389 and F397, which cradle the aliphatic portion of DFMO, are brown. R277, D332, and D361 are also shown, and nitrogen and oxygen atoms of these residues are blue and red, respectively. The asterisked residues belong to the other subunit of the dimer.

Article Snippet: The figure was drawn based on the data of reference 7 using the RasMol 2.6 Molecular Graphics Visualisation tool (Glaxo Wellcome Research & Development Co., Stevenage, Herts., United Kingdom).

Techniques: Recombinant