subject specific binary t1 brain mask image Search Results


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Thermo Fisher rnase t1
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Seikagaku corporation rnase t 1
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Synaptic Systems brain specific homeobox pou protein 3a
<t>BRN-3A-labeled</t> RGCs in flat-mounted retinas. Retinas treated with PGRN-NSCs ( a – d ) or control-NSCs ( e – h ) 14 ( a , e ), 28 ( b , f ), 56 ( c , g ), and 112 ( d , h ) days after an intraorbital optic nerve crush. PGRN-treated retinas contained significantly higher numbers of surviving RGCs than control retinas at all post-lesion time points. Abbreviations: BRN-3A, <t>brain-specific</t> <t>homeobox/POU</t> domain protein 3A; DAPI, 4′,6-di-amidino-2-phenylindole; dpl, days post lesion; NSCs, neural stem cells; PGRN, progranulin; RGCs, retinal ganglion cells. Scale bar: 50 μm.
Brain Specific Homeobox Pou Protein 3a, supplied by Synaptic Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bruker Corporation t 1
MRI <t>T</t> <t>1</t> and T 2 relaxation times as a function of the Fe concentration for DMSA coated magnetite nanoparticle suspensions obtained by microwave (MW) and thermal decomposition (TD) using different solvents.
T 1, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson troponin t
MRI <t>T</t> <t>1</t> and T 2 relaxation times as a function of the Fe concentration for DMSA coated magnetite nanoparticle suspensions obtained by microwave (MW) and thermal decomposition (TD) using different solvents.
Troponin T, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Promega rnase a-rnase t 1
MRI <t>T</t> <t>1</t> and T 2 relaxation times as a function of the Fe concentration for DMSA coated magnetite nanoparticle suspensions obtained by microwave (MW) and thermal decomposition (TD) using different solvents.
Rnase A Rnase T 1, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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t 1  (ATCC)
95
ATCC t 1
HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, <t>T-1,</t> and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.
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Binax Inc binax t1
HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, <t>T-1,</t> and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.
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Tembec Inc tembec t2
HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, <t>T-1,</t> and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.
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Merck KGaA troponin t abs1675
HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, <t>T-1,</t> and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.
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AnMo Electronics dinolite_notilt_ eo _t1
Pairwise analysis of landmark datasets comparing Procrustes ANOVA residual R 2 percentages (ProcANOVA R 2 [%]) and repeatability among datasets, absolute differences among comparisons in cross‐validated linear discriminant analysis predicted group membership error (PGM Error Change [%]), and differences among comparisons in the percent of predicted group membership changes among individual Project 23 fossils of unknown species affinity (Fossil PGM Change [%])
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Image Search Results


BRN-3A-labeled RGCs in flat-mounted retinas. Retinas treated with PGRN-NSCs ( a – d ) or control-NSCs ( e – h ) 14 ( a , e ), 28 ( b , f ), 56 ( c , g ), and 112 ( d , h ) days after an intraorbital optic nerve crush. PGRN-treated retinas contained significantly higher numbers of surviving RGCs than control retinas at all post-lesion time points. Abbreviations: BRN-3A, brain-specific homeobox/POU domain protein 3A; DAPI, 4′,6-di-amidino-2-phenylindole; dpl, days post lesion; NSCs, neural stem cells; PGRN, progranulin; RGCs, retinal ganglion cells. Scale bar: 50 μm.

Journal: Cells

Article Title: Progranulin Is a Survival Factor for Axotomized Retinal Ganglion Cells in Adult Mice

doi: 10.3390/cells15110988

Figure Lengend Snippet: BRN-3A-labeled RGCs in flat-mounted retinas. Retinas treated with PGRN-NSCs ( a – d ) or control-NSCs ( e – h ) 14 ( a , e ), 28 ( b , f ), 56 ( c , g ), and 112 ( d , h ) days after an intraorbital optic nerve crush. PGRN-treated retinas contained significantly higher numbers of surviving RGCs than control retinas at all post-lesion time points. Abbreviations: BRN-3A, brain-specific homeobox/POU domain protein 3A; DAPI, 4′,6-di-amidino-2-phenylindole; dpl, days post lesion; NSCs, neural stem cells; PGRN, progranulin; RGCs, retinal ganglion cells. Scale bar: 50 μm.

Article Snippet: To visualize the surviving RGCs, retinal flatmounts were incubated overnight with rabbit antibodies directed against brain-specific homeobox/POU protein 3A (BRN-3A; 1:1000; Synaptic Systems, Göttingen, Germany), followed by Cy3-conjugated donkey anti-rabbit secondary antibodies (1:200; Dianova) and DAPI.

Techniques: Labeling, Control

MRI T 1 and T 2 relaxation times as a function of the Fe concentration for DMSA coated magnetite nanoparticle suspensions obtained by microwave (MW) and thermal decomposition (TD) using different solvents.

Journal: Contrast Media & Molecular Imaging

Article Title: Key Parameters on the Microwave Assisted Synthesis of Magnetic Nanoparticles for MRI Contrast Agents

doi: 10.1155/2017/8902424

Figure Lengend Snippet: MRI T 1 and T 2 relaxation times as a function of the Fe concentration for DMSA coated magnetite nanoparticle suspensions obtained by microwave (MW) and thermal decomposition (TD) using different solvents.

Article Snippet: Finally, MRI relaxometric properties were investigated by measuring the longitudinal ( T 1 ) (sequence t1_ir_mb) and transversal ( T 2 ) (sequence t2_ir_mb) protons relaxation times at different dilutions between 0 and 0.07 mM of Fe in a MINISPEC MQ60 (Bruker) at 37°C and a magnetic field of 1.5 T. The sequences used are original from Bruker.

Techniques: Concentration Assay

HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, T-1, and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.

Journal:

Article Title: Heteroduplex Panel Analysis, a Novel Method for Genetic Identification of Aspergillus Section Flavi Strains

doi: 10.1128/AEM.67.9.4084-4090.2001

Figure Lengend Snippet: HPA panels of Aspergillus Section Flavi strains obtained by using ITS-region DNAs amplified by PCR. The left panels of reference strains P-39-1, IFO4082, A0754, and ATCC 15546 are the standard panels of F-1, P-1, T-1, and N-1, respectively. On the right are the test panels of 20 strains that are indicated above the panels. F-2, N-2, N-3, and TN-1 are additional new panels of heteroduplex types. Heteroduplex bands in lanes f, p, t, and n were formed with reference strains of A. flavus, A. parasiticus, A. tamarii, and A. nomius, respectively.

Article Snippet: Except for type TN-1, intraspecific diversity (1 to 3 bp) did not display any heteroduplex bands with mobility shifts (lane f of F-2 and lanes n of N-2 to N-3 in Fig. ), while other interspecific heteroduplexes (lanes p, t, and n of F-2 and lanes f, p, and t of N-2 and N-3 in Fig. ) displayed mobility shifts apparently different from those of the corresponding standard panels. table ft1 table-wrap mode="anchored" t5 TABLE 3 caption a7 Type a Nucleotide diversity (no. of bases) from: F-1 (595) b F-2 (594) P-1 (595) T-1 (598) N-1 (598) N-2 (598) N-3 (598) TN-1 (597) F-1 0 F-2 1 0 P-1 8 9 0 T-1 13 14 9 0 N-1 20 21 14 13 0 N-2 19 20 13 12 2 0 N-3 19 20 13 12 1 3 0 TN-1 14 15 8 5 8 8 7 0 Open in a separate window a F-1, A. flavus P-39-1 and A. oryzae IFO 30113; F-2, A. oryzae IFO 5375; P-1, A. parasiticus IFO 4082 and A. sojae IFO 4200; T-1, A. tamarii A0754; N-1, A. nomius ATCC 15546; N-2, A. nomius NRRL 6552; N-3, A. nomius IMI 358751; TN-1, A. nomius IMI 358749. b The numbers within parentheses indicate the sizes (base pairs) of ITS region DNAs amplified by PCR.

Techniques: Amplification

Nucleotide sequence alignments for ITS1 (A) and ITS2 (B) of rRNA genes from Aspergillus Section Flavi strains. F-1, A. flavus P-39-1; F-2, A. oryzae IFO 5375; P-1, A. parasiticus IFO 4082; T-1, A. tamarii A0754; N-1, A. nomius ATCC 15546; N-2, A. nomius NRRL 6552; N-3, A. nomius IMI 358751; TN-1, A. nomius IMI 358749. Dots indicate identity to the sequence of F-1. Dashes indicate alignment gaps (insertion or deletion differences). Boxes A to E indicate variable regions.

Journal:

Article Title: Heteroduplex Panel Analysis, a Novel Method for Genetic Identification of Aspergillus Section Flavi Strains

doi: 10.1128/AEM.67.9.4084-4090.2001

Figure Lengend Snippet: Nucleotide sequence alignments for ITS1 (A) and ITS2 (B) of rRNA genes from Aspergillus Section Flavi strains. F-1, A. flavus P-39-1; F-2, A. oryzae IFO 5375; P-1, A. parasiticus IFO 4082; T-1, A. tamarii A0754; N-1, A. nomius ATCC 15546; N-2, A. nomius NRRL 6552; N-3, A. nomius IMI 358751; TN-1, A. nomius IMI 358749. Dots indicate identity to the sequence of F-1. Dashes indicate alignment gaps (insertion or deletion differences). Boxes A to E indicate variable regions.

Article Snippet: Except for type TN-1, intraspecific diversity (1 to 3 bp) did not display any heteroduplex bands with mobility shifts (lane f of F-2 and lanes n of N-2 to N-3 in Fig. ), while other interspecific heteroduplexes (lanes p, t, and n of F-2 and lanes f, p, and t of N-2 and N-3 in Fig. ) displayed mobility shifts apparently different from those of the corresponding standard panels. table ft1 table-wrap mode="anchored" t5 TABLE 3 caption a7 Type a Nucleotide diversity (no. of bases) from: F-1 (595) b F-2 (594) P-1 (595) T-1 (598) N-1 (598) N-2 (598) N-3 (598) TN-1 (597) F-1 0 F-2 1 0 P-1 8 9 0 T-1 13 14 9 0 N-1 20 21 14 13 0 N-2 19 20 13 12 2 0 N-3 19 20 13 12 1 3 0 TN-1 14 15 8 5 8 8 7 0 Open in a separate window a F-1, A. flavus P-39-1 and A. oryzae IFO 30113; F-2, A. oryzae IFO 5375; P-1, A. parasiticus IFO 4082 and A. sojae IFO 4200; T-1, A. tamarii A0754; N-1, A. nomius ATCC 15546; N-2, A. nomius NRRL 6552; N-3, A. nomius IMI 358751; TN-1, A. nomius IMI 358749. b The numbers within parentheses indicate the sizes (base pairs) of ITS region DNAs amplified by PCR.

Techniques: Sequencing

Pairwise analysis of landmark datasets comparing Procrustes ANOVA residual R 2 percentages (ProcANOVA R 2 [%]) and repeatability among datasets, absolute differences among comparisons in cross‐validated linear discriminant analysis predicted group membership error (PGM Error Change [%]), and differences among comparisons in the percent of predicted group membership changes among individual Project 23 fossils of unknown species affinity (Fossil PGM Change [%])

Journal: Ecology and Evolution

Article Title: Are geometric morphometric analyses replicable? Evaluating landmark measurement error and its impact on extant and fossil Microtus classification

doi: 10.1002/ece3.6063

Figure Lengend Snippet: Pairwise analysis of landmark datasets comparing Procrustes ANOVA residual R 2 percentages (ProcANOVA R 2 [%]) and repeatability among datasets, absolute differences among comparisons in cross‐validated linear discriminant analysis predicted group membership error (PGM Error Change [%]), and differences among comparisons in the percent of predicted group membership changes among individual Project 23 fossils of unknown species affinity (Fossil PGM Change [%])

Article Snippet: Dinolite_NoTilt_ EO _T1–Dinolite_NoTilt_ NO _T1 , Interobserver , 0.21 , 31.01 , 20.6 , 32.3.

Techniques: Imaging