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Figure S1: Reproducibility of the Ni/CeSm5Cu experimental results: (a) Glycerol conversion into gaseous products, (b) H2 yield (c) H2 selectivity, (d) CO2 selectivity, (e) CO selectivity, (f) CH4 selectivity., Peer reviewed

[Introduction]: In monoclonal B cell lymphocytosis (MBL) and chronic lymphocytic leukemia (CLL), the expansion of malignant B cells disrupts the normal homeostasis and interactions between B cells and T cells, leading to immune dysregulation. CD20+ T cells are a subpopulation of T cells that appear to be involved in autoimmune diseases and cancer., [Methods]: Here, we quantified and phenotypically characterized CD20+ T cells from MBL subjects and CLL patients using flow cytometry and correlated our findings with the B-cell receptor mutational status and other features of the disease., [Results and discussion]: CD20+ T cells were more represented within the CD8+ T cell compartment and they showed a predominant memory Tc1 phenotype. CD20+ T cells were less represented in MBL and CLL patients vs healthy controls, particularly among those with unmutated IGVH gene. The expansion of malignant B cells was accompanied by phenotypic and functional changes in CD20+ T cells, including an increase in follicular helper CD4+ CD20+ T cells and CD20+ Tc1 cells, in addition to the expansion of the TCR Vβ 5.1 in CD4+ CD20+ T cells in CLL., Peer reviewed

[Introduction]: In monoclonal B cell lymphocytosis (MBL) and chronic lymphocytic leukemia (CLL), the expansion of malignant B cells disrupts the normal homeostasis and interactions between B cells and T cells, leading to immune dysregulation. CD20+ T cells are a subpopulation of T cells that appear to be involved in autoimmune diseases and cancer., [Methods]: Here, we quantified and phenotypically characterized CD20+ T cells from MBL subjects and CLL patients using flow cytometry and correlated our findings with the B-cell receptor mutational status and other features of the disease., [Results and discussion]: CD20+ T cells were more represented within the CD8+ T cell compartment and they showed a predominant memory Tc1 phenotype. CD20+ T cells were less represented in MBL and CLL patients vs healthy controls, particularly among those with unmutated IGVH gene. The expansion of malignant B cells was accompanied by phenotypic and functional changes in CD20+ T cells, including an increase in follicular helper CD4+ CD20+ T cells and CD20+ Tc1 cells, in addition to the expansion of the TCR Vβ 5.1 in CD4+ CD20+ T cells in CLL., Peer reviewed

Information such as spin density plots, overlap integral values, selected structural parameters corresponding to each J values, dinuclear models for each J values, simulated magnetic susceptibility vs temperature data of 2 etc., Peer reviewed

Characterization of MIL-101(Cr) NPs (XRD), additional SEM images of the surface of a LS-MIL-101(Cr) film over a cross-linked asymmetric polyimide (P84) support (LS-P84), surface pressure versus area per mg of MOF isotherm; and characterization of the LS-TFN membrane (STEM images and EDS analysis)., Peer reviewed

15 pages, 3 tables, 7 figures, Supplementary Information for the article https://doi.org/10.1002/cssc.202301671, A. Biocarbon derived from fish waste preparation.-- B. Glycogen-based carbon characterization.-- C. Morphological characterization.-- D. Electrochemical characterization (3-electrode setup).-- E. Solid-state supercapacitor prototype assembly (Full cell setup).-- F. TiO2 samples characterization.-- G. TiO2-C composite samples characterization.-- H. References, Peer reviewed

Supplementary Material 2., Peer reviewed

Additional experimental results are available. Structural analysis ((S1) TEM, size distribution, (S2) STEM-HAADF, STEM-EELS, powder XRD patterns, and (S3) Mössbauer of CoFe carbide MNPs). (S4) Magnetic properties of a powder of CoFe carbide MNPs measured at different temperature without magnetic field and under 5 T at 2 K. (S5) Magnetic properties of a powder of CoFe carbide MNPs measured at 2 and 300 K. Study of MNPs concentration and withdrawal speed of the substrate including respectively optical (S6.a and S9.a left) and SEM (S7 and S9.a right) characterizations taken after the deposition at different concentration. (S8 and S10) AFM measurements performed at different MNP concentrations and withdrawal speed. (S12) Optical images taken after the substrates were immersed in suspensions of OA and HDA dissolved in THF as well as pure THF. (S13) High resolution SEM image located between two consecutive stripes when a large excess of HDA (1 equiv) was added to the suspension. (S14) Evolution against the time of the contact angle of cleaned substrates stored in glovebox., Peer reviewed

Raw data of manuscript "Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes", This dataset includes the raw data from the manuscript “Dynamics of interaction and internalisation of the antifungal protein PeAfpA into Penicillium digitatum morphotypes”. This data comprises Excel sheets used to generate all the plots and graphs of the article (.xlsx files), 16-bit, 8-bit and RGB confocal microscopy images (.tif files), statistical analyses (.pzfx and .txt files) and “Readme” files (.txt files) to specificy experimental conditions for data collection and software-specific requirements to visualise each file., This work was supported by grant PID2021-125858OB-I00, and the Severo Ochoa Excellence Program CEX2021-001189-S, funded by MCIN/AEI/ 10.13039/501100011033 and by “ERDF, a way of making Europe”. M.G.L. and C.R.P. were recipients of predoctoral grants FPU19/02066 and ACIF/2021/364 funded by MCIN/AEI/10.13039/501100011033 and by ESF-Investing in Your future and by ”Conselleria d’Educació (Generalitat Valenciana, Comunitat Valenciana, Spain), respectively. M.G.L. international exchange was supported by EST23/00233 grant (funded by MCIN/AEI/10.13039/ 501100011033 and by ESF-Investing in Your future) and SEG10314 EMBO Scientific Exchange Grant. S.G. holds a Juan de la Cierva Incorporación grant (IJC2020-042749-I) from the Spanish Ministerio de Ciencia e Innovación, funded by the European Union, NextGenerationEU PRTR. Work undertaken with EMB and DDT was funded by the Medical Research Council Centre for Medical Mycology at the University of Exeter (MR/N006364/2 and MR/V033417/1), that forms part of the National Institute for Health and Care Research (NIHR) Exeter Biomedical Research Centre (BRC), and the BBSRC project grant BB/V017004/1 to EMB., dor (dc.descripction.sponsorship): With funding from the Spanish government through the ‘Severo Ochoa Centre of Excellence’ accreditation (CEX2021-001189-S), Figure 1_data: Antifungal activity of the antifungal proteins PeAfpA and PdAfpB against Penicillium digitatum conidia. -- Figure 2_data ROS production in Penicilliumn digitatum germlings, induced by the treatment with antifungal proteins (PeAfpA or PdAfpB).-- Figure 3_data Evaluation of the interaction of PeAfpA and PdAfpB with P. digitaum conidia. Panels show confocal microscopy images of P. digitatum conidia after 15 min or 90 min of treatment with 8 µg/mL PeAfpA (A, B), or after 90 min of treatment with 8 µg/mL PdAfpB (C).-- Figure 4_data Comparison of the PeAfpA interaction with conidia of P. digitatum wild-type strain CECT 20796 (WT) and the KO mutant strains ΔpksP and Δarp2. -- Figure 5_data BODIPY-PeAfpA internalisation dynamics in P. digitatum hyphae in low-dose conditions (2 µg/mL).-- Figure 6_data PeAfpA internalises through hyphal tips and provokes vacuolisation and hyphal burst. Raw images used for each panel are provided.-- Figure 7_data: PeAfpA co-localises with CFW in the fungal cell wall. Raw images used for each panel are provided.-- Figure 8_data: PeAfpA internalisation in fungal hyphae is energy-dependent but not an endocytic process. Raw images used for each panel are provided.-- Supplementary Figure 1_data: Antifungal activity of BODIPY-labelled and -unlabelled antifungal proteins (PeAfpA and PdAfpB) against Penicillium digitatum conidia. Raw OD600 measurements are provided in two separated Excel files. -- Supplementary Figure 2_data: Raw data for the amino acid alignment of the Aspergillus fumigatus RodA protein and the orthologous protein from Penicillium digitatum. Raw pictures for panel B are provided.-- Supplementary Figure 3_data: Raw OD measurements for the dose response curves of P. digitatum CECT 20796 and deletion mutant strains (ΔpksP and Δarp2) treated with PeAfpA and PdAfpB. -- Supplementary Figure 4_data: Evaluation of the colocalization of PeAfpA and CFW in P. digitatum hyphae. Rae images for each panel are provided, as well as raw pixel intensity data.-- Supplementary Figure 5_data: Raw images from insets shown in Figure 5., Peer reviewed

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