3d design program inventor 2022 Search Results


102-3d  (cell applications inc)
93
cell applications inc 102-3d
102 3d, supplied by cell applications inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/pmc06615970-18-0-4?v=cell+applications+inc
Average 93 stars, based on 1 article reviews
102-3d - by Bioz Stars, 2026-07
93/100 stars
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3d surface rendering reconstructions  (Oxford Instruments)
99
Oxford Instruments 3d surface rendering reconstructions
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
3d Surface Rendering Reconstructions, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/bio_rxiv__2022__08__10__503440-77-34-38?v=Oxford+Instruments
Average 99 stars, based on 1 article reviews
3d surface rendering reconstructions - by Bioz Stars, 2026-07
99/100 stars
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cad software (2022 sp2.0 professional version  (SolidWorks Corp)
90
SolidWorks Corp cad software (2022 sp2.0 professional version
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Cad Software (2022 Sp2.0 Professional Version, supplied by SolidWorks Corp, 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/3d+design+program+inventor+2022/pm37893266-4-8-7?v=SolidWorks+Corp
Average 90 stars, based on 1 article reviews
cad software (2022 sp2.0 professional version - by Bioz Stars, 2026-07
90/100 stars
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metrology grade 3d analysis software program  (Geomagic Inc)
86
Geomagic Inc metrology grade 3d analysis software program
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Metrology Grade 3d Analysis Software Program, supplied by Geomagic Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/pm42276901-76-17-22?v=Geomagic+Inc
Average 86 stars, based on 1 article reviews
metrology grade 3d analysis software program - by Bioz Stars, 2026-07
86/100 stars
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3d infomax  (InfoMax Inc)
90
InfoMax Inc 3d infomax
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
3d Infomax, supplied by InfoMax Inc, 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/3d+design+program+inventor+2022/pm37491407-345-12-16?v=InfoMax+Inc
Average 90 stars, based on 1 article reviews
3d infomax - by Bioz Stars, 2026-07
90/100 stars
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workbench 2022 r1  (ANSYS inc)
90
ANSYS inc workbench 2022 r1
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Workbench 2022 R1, supplied by ANSYS inc, 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/3d+design+program+inventor+2022/pm36297897-94-17-16?v=ANSYS+inc
Average 90 stars, based on 1 article reviews
workbench 2022 r1 - by Bioz Stars, 2026-07
90/100 stars
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control x 2022 3d superimposition software  (Geomagic Inc)
86
Geomagic Inc control x 2022 3d superimposition software
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Control X 2022 3d Superimposition Software, supplied by Geomagic Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/pmc12375729-290-35-34?v=Geomagic+Inc
Average 86 stars, based on 1 article reviews
control x 2022 3d superimposition software - by Bioz Stars, 2026-07
86/100 stars
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full-wave 3d finite element method simulator ansys hfss 2022 r1  (ANSYS inc)
90
ANSYS inc full-wave 3d finite element method simulator ansys hfss 2022 r1
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Full Wave 3d Finite Element Method Simulator Ansys Hfss 2022 R1, supplied by ANSYS inc, 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/3d+design+program+inventor+2022/pmc09515602-98-11-18?v=ANSYS+inc
Average 90 stars, based on 1 article reviews
full-wave 3d finite element method simulator ansys hfss 2022 r1 - by Bioz Stars, 2026-07
90/100 stars
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magnetic milliplex map antibody-conjugated beads  (Merck KGaA)
90
Merck KGaA magnetic milliplex map antibody-conjugated beads
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Magnetic Milliplex Map Antibody Conjugated Beads, supplied by Merck KGaA, 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/3d+design+program+inventor+2022/pm36429120-101-27-39?v=Merck+KGaA
Average 90 stars, based on 1 article reviews
magnetic milliplex map antibody-conjugated beads - by Bioz Stars, 2026-07
90/100 stars
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3d cad software solid edge 2022  (Siemens AG)
90
Siemens AG 3d cad software solid edge 2022
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
3d Cad Software Solid Edge 2022, supplied by Siemens 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/3d+design+program+inventor+2022/10__1016_slash_j__nucengdes__2024__113389-130-6-12?v=Siemens+AG
Average 90 stars, based on 1 article reviews
3d cad software solid edge 2022 - by Bioz Stars, 2026-07
90/100 stars
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fem software package named abaqus 2022 version  (Abaqus Inc)
86
Abaqus Inc fem software package named abaqus 2022 version
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Fem Software Package Named Abaqus 2022 Version, supplied by Abaqus Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/pm40634508-112-2-6?v=Abaqus+Inc
Average 86 stars, based on 1 article reviews
fem software package named abaqus 2022 version - by Bioz Stars, 2026-07
86/100 stars
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nanoject ii  (Drummond Scientific)
86
Drummond Scientific nanoject ii
NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in <t>3D</t> <t>surface-reconstruction</t> of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain
Nanoject Ii, supplied by Drummond Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3d+design+program+inventor+2022/pm36178731-71-49-51?v=Drummond+Scientific
Average 86 stars, based on 1 article reviews
nanoject ii - by Bioz Stars, 2026-07
86/100 stars
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NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in 3D surface-reconstruction of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain

Journal: bioRxiv

Article Title: Cortical distribution of neurofilaments associates with pathological hallmarks and MRI measures of atrophy and diffusivity in Parkinson’s disease

doi: 10.1101/2022.08.10.503440

Figure Lengend Snippet: NfL accumulation and fragmentation, and loss of neurofilament colocalization in PD and PDD/DLB. Maximum projections (z-stacks n=6 μm) of fluorescence stainings of NfL (red) and p-NfM/H (green) together with DAPI (blue) in the parahippocampal gyrus of a representative control ( left , control number 10 in Supplementary Table 1, online resource 1), PD ( middle , PD number 3 in Supplementary Table 1, online resource 1) and PDD/DLB ( right , here a DLB donor, PDD/DLB number 12 in Supplementary Table 1, online resource 1) are shown. a , b , and c show the difference in NfL staining pattern in control, PD and PDD/DLB, respectively. NfL was markedly accumulated in neuronal somas and proximal axons in PDD/DLB cases, reflecting the higher NfL immunoreactivity described quantitatively in . High NfL immunoreactivity was found in neuronal somas showing neurodegenerative morphological features, such as c neurons with nuclear fragmentation and swelling (*), and d corkscrew (**) and ballooned (***) appearances (panel d shows a zoom-in 3D surface-reconstruction of neurodegenerative neurons). Moreover, c NfL accumulation was also identified in a proximal axon showing fragmentation (arrow), closely tighten by a glial cell (#); e shows the zoom-in 3D surface-reconstruction of the white square in c , showing axonal fragmented morphology (arrow) and a glial cell wrapping the degenerating axon (#). f , g and h show the colocalization (yellow) of NfL and p-NfM/H in control, PD and PDD/DLB, respectively, which was reduced in PD and PDD/DLB. Moreover, accumulation and fragmentation of NfL staining patterns were observed in several axons, where g NfL seemed to fragment within a p-NfM/H axon in PD (dashed arrow) and h axonal swellings intermitted axonal fragmentations in PDD/DLB (arrows). i shows the zoom-in 3D surface-reconstruction of the white square in h , clearly showing fragmentation of the NfL positive axon (arrows). Legend: DLB: Dementia with Lewy Bodies; NfL: neurofilament light chain; PD: Parkinson’s disease; PDD: Parkinson’s disease dementia; p-NfM/H: phosphorylated neurofilament medium and heavy chain

Article Snippet: After scanning, the images were deconvoluted using CMLE algorithms in Huygens Professional (Scientific Volume imaging; Huygens, The Netherlands; https://svi.nl/Huygens-Professional ), and their maximum projections (ImageJ Fiji, National Institute of Health USA; https://imagej.nih.gov/ij/ ) or 3D surface rendering reconstructions (Imaris, Oxford instruments 2022: https://imaris.oxinst.com/ ) were used to represent graphically the structures of interests and their morphologies.

Techniques: Fluorescence, Control, Staining