Additional file 9: Fig. S4. Whole-genome variation of two parental lines of QYSM. a, Density and chromosome distribution of polymorphic SNPs between Q9311B and WSSM. b, The principal component analysis. c, Phylogenetic positions of two parental lines (Q9311B and WSSM) in the neighbor-joining tree of 1,946 rice accessions from 3 K-RG, in which the known information on the clades of 3 K-RG is indicated.

Additional file 1. Fig. S1. A HDFs were treated with other HOCI probes for 10 days, and morphological changes of HDFs were observed under an inverted phase contrast microscope (Eclipse TS-100; Nikon, Tokyo). Scale bar: 20 μm.

Additional file 2: Fig S2. Construct of intermediate cloning vectors for preparing Donor DNA. (A) Fragment A cloned from BW25113-T7 was concatenated to pACYCD-Blank to assemble pACYCD-gene. (B) Reverse-PCR to constructed pACYCD-Donor. (C) The map of Donor DNA, which contains HRL and HRR.

Supplemental material, sj-tif-3-onc-10.1177_11795549221127161 for Effect of Number of Retrieved Lymph Nodes on Prognosis in FIGO Stage IA1-IIA2 Cervical Cancer Patients Treated With Primary Radical Surgery by Shan Jiang, Peng Jiang, Tingting Jiang, Yuan Tu, Jingni Zhang, Ning Li, Wei Kong, Yuzhen Huang and Rui Yuan in Clinical Medicine Insights: Oncology

Additional file 7: Figure S3. The box plot of expression data (A) before and (B) after the batch effect correction for the GSE15459. The training-validation expression set was used as reference.

Previously, we reported that the mediation of Newcastle disease virus (NDV) pathogenicity by the 524YLMY527 motif depends mainly on the regulation of F protein transport to the cell surface. The virus and host determinants that govern this intracellular trafficking remain unknown. Here, we confirmed that host adaptor protein (AP) complexes are involved in NDV infection using small interfering RNA. The transport of viral F protein to the cell surface depends on host transport proteins. We...

Supplementary Material 2

Additional file 3: Figure S3. Tissue expression of differentially expressed protein-coding genes in atm mutated flies after ionizing radiation. A Heatmap of differentially expressed genes expressed in larval tissues. B Heatmap of differentially expressed genes expressed in adult female tissues. C Heatmap of differentially expressed genes expressed in adult male tissues.

Additional file 3: Figure S3. HE (scale bar = 200 μm) and Masson (scale bar = 50 μm) staining in the rat calvarial defect model (n = 6).

Additional file 6: Figure S6. CBX and Panx 1-siRNA do not affect TGF-β mRNA expression in LPS-treated Schwann cells. A-B. Pretreatment with CBX (100 mM) for 2 h or Panx 1 siRNA for 36 h, qPCR was used to determine TGF-β mRNA expression levels in LPS-treated Schwann cells. All data are mean ± SEM. n = 4.

Additional file 1: Supplementary Figure 1. MMP-13 levels in the medium of IL-1β-induced C28/I2 cells detected by ELISA.

Additional file 1: Figure S1. The vector map of (A) wt-circ_0003570-luc, (B) mut-circ_0003570-luc; (C) wt-STARD13-luc, and (D) mut-STARD13-luc. Figure S2. Knockdown of circ_0003570 promotes proliferation, migration and invasion of MHCC-97L cells in vitro. (A) MTT assays and (B) colony formation assays showing that downregulation of circ_0003570 promoted the proliferation of MHCC-97L cells, *P < 0.05. (C) Transwell assays showed circ_0003570 knockdown reduced the migration and invasion of MHCC-97L cells. *P < 0.05. (D) Representative images...

Additional file 3: Figure S3. ShRNA Panx 1-AAV or Ctrl-AAV-labeled EGFP-positive cells have a sound co-localization with S100 β-labeled Schwann cells. Enlarged images in lower panel are from the inset boxes of upper panel. Upper panel, scale bar = 50 μm. Lower panel, scale bar = 25 μm. n = 3–4 mice/group.

Additional file 1: Figure S1. The relative abundance of P-CA regulators in DLAT wild and DLAT mutation groups is presented

Additional file 4. Intercellular communication between all celltypes

Additional file 1: Figure S1. Relationship between Sp1 and mitochondrial network. (A-B) The mitochondrial morphology of Sp1-knockout and overexpression cervical cancer cells by Tomm70A staining. (C) The proportion of globe and tube mitochondria of cervical cancer cells with treatment as indicated, detected by electron microscopy. (D) The correlation between mitochondrial dynamics-related proteins and Sp1 expression. The expression of Sp1 was positively related to Mfn1/2, Drp1, and Opa1.

Additional file 3: Figure S3. The time course for measurement of ECAR in C2C12 cells treated with or without glucosamine and/or NaB. The ECAR was measured under baseline conditions and after glucose, oligomycin and 2-Deoxy-D-glucoseinjection, as indicated by the arrowheads.Glycolysis.Glycolytic capacity. ECAR as calculated from the bioenergetic analysis. Data were normalized to protein concentration units per well prior to statistical analysis. Data are the means ± SEMs. The NaB effect was analysed by ANOVA, *p<0.05,...

Additional file 4: Figure S4. Confocal microscopy analyses in C2C12 cells with GLcN or NaB treatment.Mean fluorescence intensity of ERα.Mean fluorescence intensity of AMPK. Data are the means ± SEMs. The NaB effect was analysed by ANOVA, *p<0.05, **p<0.01, ***p<0.001.

Additional file 1: Figure S1. 1H-NMR (600 MHz) spectrum of R5H3 (A) and Stearyl-H3R5 (B).

Additional file 3: Figure S3. Viability of human skin squamous cell carcinoma (SCL-1) cells incubated for 48 h with blank cell-penetrating peptide modified transfersomes with components of soybean phospholipid and sodium cholate hydrate (STFs-CPP) and cell-penetrating peptide modified transfersomes with components of 1,2-dioleoyl-3-trimethylammonium-propane and sodium cholate hydrate (DTFs-CPP) without lycorine (LR).

Additional file 6: Figure S6. Average tumor weight of mice in each group after 14 days of treatment. *p < 0.05, **p < 0.01, and ***p < 0.001.

Additional file 4.

Additional file 6.

Additional file 5: Figure S3. Comparison of lymphocytes counts in 260 LCs and HCs. The figures show the median and quartiles. **P < 0.01.

Additional file 3: Figure S1. SARS-CoV-2 antibodies response in 40 LC patients after the second or booster dose of inactivated vaccine. Total antibodies against SARS-CoV-2. Concentrations of IgG anti-RBD antibodies. Inhibition rates of NAb against SARS-CoV-2 WT. Inhibition rates of NAb against Omicron BA.4/5.