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479 Treffer

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  1. Detailansicht für Treffer 1 öffnen
    Plasma antibody neutralization of HIV-1 pseudovirus infection of TZM-bl cells.
    Fangping Cai (8129868) ; Wei-Hung Chen (693540) ; et al.
    2021
    academicJournal
    Wie komme ich dran?
  2. Detailansicht für Treffer 2 öffnen
    Cytotoxic analysis of the novel isoflavones, their anti-HIV activity and the time-of-addition studies to quantify the entry inhibiting capabilities of the isoflavones, all in TZM-bl cell
    Raubenheimer, Steven
    2023
    unknown
    Wie komme ich dran?
  3. Detailansicht für Treffer 3 öffnen
    Cytotoxic analysis of the novel isoflavones, their anti-HIV activity and the time-of-addition studies to quantify the entry inhibiting capabilities of the isoflavones, all in TZM-bl cell
    Raubenheimer, Steven
    2023
    unknown
    Wie komme ich dran?
  4. Detailansicht für Treffer 4 öffnen
    Tic Ve Zrc İlaveli Tzm Kompozitlerinin Spark Plazma Sinterleme (sps) Yöntemi İle Üretimi Ve Karakterizasyonu ; Production And Characterization Of Tzm Based Tic Or Zrc Reinforced Composites Prepared By Spark Plasma Sintering (sps)
    Tüzemen, Cansinem ; Göller, Gültekin ; et al.
    2016
    Online Hochschulschrift
    Zugriff:
    Volltext
    Wie komme ich dran?
  5. Detailansicht für Treffer 5 öffnen
    Tzm Alaşımının Spark Plazma Sinterleme (sps) Yöntemi İle Üretimi Ve Karakterizasyonu ; Production And Characterization Of Tzm Alloys Prepared By Spark Plazma Sintering (sps)
    Danışman, Can Burak ; Göller, Gültekin ; et al.
    2016
    Online Hochschulschrift
    Zugriff:
    Volltext
    Wie komme ich dran?
  6. Detailansicht für Treffer 6 öffnen
    Texture evolution during hot deformation of Moly-TZM
    Chaudhuri, A ; Behera, A N ; et al.
    In: IOP Conference Series: Materials Science and Engineering ; volume 82, page 012088 ; ISSN 1757-899X, 2015
    Online academicJournal
    Zugriff:
    Volltext
    Wie komme ich dran?
  7. Detailansicht für Treffer 7 öffnen
    kppw99/tzMon: 1st release for TZMon
    Sanghoon Jeon (Kevin)
    2021
    Online Elektronische Ressource
    Wie komme ich dran?
  8. Detailansicht für Treffer 8 öffnen
    Welding of TZM molybdenum alloy
    Hanks, G.S.
    2021
    unknown
    Wie komme ich dran?
  9. Detailansicht für Treffer 9 öffnen
    Neutralization of 3 HIV-1 strains (as assessed by TZM-bl HIV neutralization assay) and HSV-2 (as assessed by HSV-2 Plaque Reduction Neutralization assay) by CVLs before and at various time points following MB66 Active and Placebo film insertion in Segment B.
    Joseph A. Politch (10090370) ; Susan Cu-Uvin (320337) ; et al.
    2021
    Bild
    Wie komme ich dran?
  10. Detailansicht für Treffer 10 öffnen
    Neutralization of 3 HIV-1 strains (as assessed by TZM-bl HIV neutralization assay) and HSV-2 (as assessed by HSV-2 Plaque Reduction Neutralization assay) by CVLs before and after MB66 film insertion in Segment A.
    Joseph A. Politch (10090370) ; Susan Cu-Uvin (320337) ; et al.
    2021
    Bild
    Wie komme ich dran?
  11. Detailansicht für Treffer 11 öffnen
    Development of Hydrogen Permeation Barrier and Matrix Interaction Protection Coatings for TZM Enclosure of Hydride Moderators
    Bhattacharya, Sumit ; Miao, Yinbin ; et al.
    2023
    unknown
    Wie komme ich dran?
  12. Detailansicht für Treffer 12 öffnen
    Corrosion characteristics of Mo and TZM alloy for plasma facing components in molten lithium at 623 K
    Meng, X. C. ; Li, L. ; et al.
    2023
    unknown
    Wie komme ich dran?
  13. Detailansicht für Treffer 13 öffnen
    Evolution in microstructure and hardness of Titanium–Zirconium–Molybdenum (TZM) alloy after depth marker implantation for erosion diagnostic in fusion devices
    Waseem, Owais Ahmed ; Woller, Kevin Benjamin
    2023
    unknown
    Wie komme ich dran?
  14. Detailansicht für Treffer 14 öffnen
    Thermal stability of oxidized ultrathin Li films on TZM for plasma facing components
    Fasoranti, O. ; Ostrowski, E. T. ; et al.
    2023
    unknown
    Wie komme ich dran?
  15. Detailansicht für Treffer 15 öffnen
    High temperature deformation behavior of the molybdenum alloy TZM
    Mrotzek, T ; Martin, U ; et al.
    In: Journal of Physics: Conference Series ; volume 240, page 012079 ; ISSN 1742-6596, 2010
    Online academicJournal
    Zugriff:
    Volltext
    Wie komme ich dran?
  16. Detailansicht für Treffer 16 öffnen
    Figure 9. Deletion of the KH-like domain or mutations in the NYN domain in KHNYN prevent reconstitution of CpG-dependent inhibition of HIV-1 infectious virus production in KHNYN CRISPR cells. ; (A–B) HeLa KHNYN-G1 CRISPR clone B cells were transfected with 500 ng pHIV-1 or pHIV-1EnvCpG86-561 and 500 ng of pGFP-FLAG or 31.25 ng, 62.5 ng, 125 ng, 250 ng or 500 ng of pKHNYN-1-CRG1-FLAG or pKHNYN-2-CRG1-FLAG plus the amount of pGFP-FLAG required to make 500 ng total. Culture supernatants from the cells were used to infect TZM-bl reporter cells (A). Each point shows the average value of three independent experiments normalized to the value obtained for HeLa Control CRISPR cells co-transfected with pHIV-1 and pGFP. Data are represented as mean ± SD. Gag expression in the media as well as Gag, Hsp90, Env, Actin, KHNYN-FLAG and GFP-FLAG expression in the cell lysates was detected using quantitative immunoblotting (B). (C–D) HeLa KHNYN-G1 CRISPR clone B cells were transfected with 500 ng pHIV-1 or pHIV-1EnvCpG86-561, 468.75 ng of pGFP-FLAG and 31.25 ng of pKHNYN-1-CRG1-FLAG expressing either wild-type or mutant proteins. Culture supernatants from the cells were used to infect TZM-bl reporter cells (C). Each point shows the average value of seven independent experiments normalized to the value obtained for HeLa Control CRISPR cells co-transfected with pHIV-1 and pGFP. Data are represented as mean ± SD. *p
    2019
    unknown
    Wie komme ich dran?
  17. Detailansicht für Treffer 17 öffnen
    Figure 1. TRIM28 suppresses HIV-1 expression and contributes to HIV-1 latency. ; (A) A siRNA library targeting 182 human genes was transfected into TZM-bl cell line, respectively. Three distinct siRNAs targeting each gene were transfected as a mixture. Forty-eight hours post-transfection, cells were harvested and the activity of luciferase from cell lysates was measured. Fold changes were calculated for each gene compared to negative control siRNA (siNC). (B–C) shRNA constructs were packaged into recombinant lentiviruses and infected J-Lat 10.6. The reactivation efficiency was measured by the GFP-positive percentage which was shown in the top right corner. SAHA and JQ-1 were used as positive controls. (D) Eight ChIP-qPCR primers targeting HIV-1 reporter provirus were designed. G5: Cellular DNA and viral 5’LTR junction; A: Nucleosome 0 assembly site; B: Nucleosome-free region; C: Nucleosome one assembly site; V5: Viral 5’LTR and gag leader sequence junction; L: Luciferase region; V3: Viral poly purine tract and 3’LTR junction; G3: Viral 3’LTR and cellular DNA junction. (E) ChIP assay with antibody against TRIM28 was performed in TZM-bl cell line. All the ChIP-qPCR DNA signals were normalized to siNC IgG of G5. (F–J) ChIP assays with antibodies against H3K9me2, H3K9me3, H3K4me3, H3K9Acetyl and H3K27me3 were performed in TZM-bl cell lines. Data represents mean ±SEM in triplicates. p-Values were calculated by Student’s t-test. *p
    2019
    unknown
    Wie komme ich dran?
  18. Detailansicht für Treffer 18 öffnen
    Figure 8—figure supplement 1. The distribution and GO analysis of increased accessible regions upon TRIM28 depletion. ; (A–B) The distribution of increased accessible regions upon TRIM28 knockout in J-Lat 10.6 (A) and TRIM28 knockdown in TZM-bl (B). (C–D) GO analyses which included biological process analysis, cellular component analysis and molecular function analysis were used to classify genes with increased accessible regions upon TRIM28 knockout in J-Lat 10.6 (C) and TRIM28 knockdown in TZM-bl (D).
    2019
    unknown
    Wie komme ich dran?
  20. Detailansicht für Treffer 20 öffnen
    Figure 8. CDK9 function is reduced when SUMOylated by TRIM28. ; (A–B) TRIM28-defective (sgTRIM28) J-Lat 10.6 cell line was generated by CRISPR-CAS9 technique. ATAC-Seq was conducted with sgNT and sgTRIM28 J-Lat 10.6 cell lines, as well as siNC and siTRIM28 TZM-bl cell lines. The tag reads of the HIV-1 pseudotyped virus/minigenome 5’LTR integration sites were counted and normalized to the total mapped reads, and represented as relative tag density. The highest tag density was set as 100. Figures showed 2 kb range centered the 5’LTR integration sites. (C–D) ChIP assays with antibodies against CDK9 and Ser2 Pho-Pol II were performed in TZM-bl cell lines which were treated with siNC, siSUMO4 and siTRIM28, respectively. (E) Cyclin T1 or GFP was co-overexpressed with CDK9 in the absence or presence of SUMO4, UBC9 and TRIM28. Cyclin T1 and GFP were IP followed by IB. (F) Fold change of kinase activity when CDK9 was SUMOylated. Data represents mean ±SEM in triplicates. p-Values were calculated by Student’s t-test. *p
    2019
    unknown
    Wie komme ich dran?
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