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Image Search Results
Journal: Blood Neoplasia
Article Title: Microenvironmentally derived fatty acid–binding proteins 4 and 5 are novel therapeutic vulnerabilities in multiple myeloma
doi: 10.1016/j.bneo.2026.100229
Figure Lengend Snippet: DIO exacerbates phenotypic differences between WT and Fabp4/5 dKO mice. Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10), ultrafocus dual-energy X-ray absorptiometry-Faxitron quantification of total weight (B) and fat weight (C) over the course of HFD administration before tumor cell injection (WT M, n = 9-10; Fabp4/5 dKO M, n = 10; WT F, n = 9-10; Fabp4/5 dKO , n = 10). Glucose levels assessed during glucose (D) and insulin (E) tolerance testing in WT (n = 10) and Fabp4/5 dKO mice (n = 10); statistical analysis performed using 2-way analysis of variance (ANOVA) and Tukey multiple comparisons tests. AUC for glucose tolerance testing (D) and insulin tolerance testing (E); statistical significance was determined using 2-way ANOVA with Tukey multiple comparison tests for panels B-C, whereas unpaired t tests were used for panels D-E (WT, n = 10; Fabp4/5 dKO , n = 10). AUC, area under the curve; min, minute.
Article Snippet: Mouse weights over time (A; WT male, n = 9-10; Fabp4/5 dKO male, n = 9-10; WT female, n = 8-10; Fabp4/5 dKO female, n = 10),
Techniques: Injection, Comparison
Journal: PLoS ONE
Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions
doi: 10.1371/journal.pone.0163958
Figure Lengend Snippet: A, B : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from five male healthy donors, (H1 to H5) (A), and five females (H6 to H10) (B) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration was evaluated by the displayed linear regression. C, D : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (C) and HK cleavage (D), measured as in panel A. densito: densitometry in 10 7 arbitrary units; NS: non-significant; ****: p <10 −4 (Mann-Whitney-Wilcoxon test).
Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and
Techniques: Purification, Clinical Proteomics, SDS Page, Concentration Assay, MANN-WHITNEY
Journal: PLoS ONE
Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions
doi: 10.1371/journal.pone.0163958
Figure Lengend Snippet: A : Purified human HK (20, 40, 80, and 110ng) and 0.5μL of plasma from nC1Inh-AE male patients (M1 to M5) were subjected to SDS-PAGE. The signal of HK native chain (N-HK), light chain (LC-HK), and cleaved light chain (cLC-HK) were quantified by densitometry and N-HK concentration by the displayed linear regression. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of plasma concentration of N-HK (B) and HK cleavage (C), measured as in panel A, compared to the healthy cohort studied in . D, E, F : as in A, B, C, concerning female patients (W1 to W5). densito: densitometry in 10 7 arbitrary units; ****: p <10 −4 (Mann-Whitney-Wilcoxon test); nC1Inh-AE: angioedema with normal C1 inhibitor.
Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and
Techniques: Purification, Clinical Proteomics, SDS Page, Concentration Assay, MANN-WHITNEY
Journal: PLoS ONE
Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions
doi: 10.1371/journal.pone.0163958
Figure Lengend Snippet: High-molecular-weight kininogen (HK) molecular pattern of plasma samples from healthy women taking or not estrogen/progestin combination (OP; Healthy+OP, n = 32; Healthy-OP, n = 30) and from nC1Inh-AE patients taking OP and ≥2 months after OP withdrawal (nC1INh-AE+/-OP, n = 13). A : Analysis of plasma samples (0.5μL/lane) from six patients (O1–O6) and the corresponding figures. N-HK concentration of P1 and P2 was evaluated by the displayed linear regression, kinin-forming activity was determined as in , pathological values were labelled in bold fonts. B, C : Box-plot displaying 5–95% range ( italic fonts), median ( bold fonts), and interquartile values of the plasma concentration of N-HK (B) and cleaved HK species (C), measured as in panel A. D, E : Details of the paired samples of panel B and C respectively analysed using the Wilcoxon matched-pairs signed rank test. densito: densitometry in 10 7 arbitrary units; NS : non-significant; *: p <0.05; **: p <0.01; ***: p <0.001; ****: p <10 −4 (non-parametric tests); N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively; nC1Inh-AE: angioedema with normal C1 inhibitor.
Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and
Techniques: High Molecular Weight, Clinical Proteomics, Concentration Assay, Activity Assay
Journal: PLoS ONE
Article Title: Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions
doi: 10.1371/journal.pone.0163958
Figure Lengend Snippet: A : High-molecular-weight kininogen (HK) molecular pattern of plasma samples (0.5μL/lane) from two nC1Inh-AE patients (W6, M6) less than 24h after the onset of an AE attack (Att) and at least two weeks after remission (Rem), analysed as in . B : Same as for A, with plasma samples from three patients (K1–K3) with ACEi-AE and low kinin catabolism (L-Cat) and three patients (M7–M9) with nC1Inh-AE and normal kinin catabolism (N-Cat). N-HK concentrations were evaluated by the displayed linear regressions, kinin-forming activity was determined as in , pathological values were labelled in bold font. densito: densitometry in 10 7 arbitrary units; N-HK, LC-HK, cLC-HK: native chain, light chain, cleaved light chain of HK respectively.
Article Snippet: Using enhanced chemiluminescence (Clarity Western ECL TM substrate, Biorad, Hercules, USA) and
Techniques: High Molecular Weight, Clinical Proteomics, Activity Assay