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  1. Tremblin, Pascal ; Phillips, Mark ; et al.
    2023
    unknown
  2. Sallehuddin Md Yusof
    2021
    Konferenz
  3. Αγγελιδάκη, Παρασκευή
    2022
    Online Hochschulschrift
  4. Richard C. Lavin (11198639) ; Calvin Johnson (3440432) ; et al.
    2021
    Bild
  5. Mudgil, P ; Al Dhaheri, MKO ; et al.
    2023
    Online academicJournal
  6. Stojanov, Ana
    In: International Journal of Educational Technology in Higher Education, 2023
    Online academicJournal
  7. Nishiyama, Shogo ; Tamura, Motohide ; et al.
    2009
    academicJournal
  8. Thomas Kisby (10751512) ; Irene de Lázaro (276398) ; et al.
    2021
    unknown
  9. Thomas Kisby (10751512) ; Irene de Lázaro (276398) ; et al.
    2021
    unknown
  10. Thomas Kisby (10751512) ; Irene de Lázaro (276398) ; et al.
    2021
    unknown
  11. The Pennsylvania State University CiteSeerX Archives
    In: http://arxiv.org/pdf/astro-ph/0307032v1.pdf, 2008
    Online academicJournal
  12. Figure 3. Exogenous autoinducers drive V. cholerae aggregation and HapR is required. ; Quantitation of aggregate volume fraction at 22 h for the ΔvpsL HCD QS-locked (HCD-locked), ΔvpsL LCD QS-locked (LCD-locked), CAI-1-responsive (± CAI-1), and AI-2-responsive (± AI-2 and boric acid) V. cholerae strains (A). Autoinducers or solvent controls were added at the time of inoculation. Concentrations used: CAI-1: 5 μM, AI-2: 1 μM, and boric acid: 100 μM. (B) Quantitation of aggregate volume fraction (black bars) and bioluminescence (gray bars) at 22 h for the CAI-1-responsive strain to which CAI-1 was added at T = 0 h and from 3 to 8 h at 1 h intervals. Also shown is bioluminescence quantified in a CAI-1-responsive strain harboring the cosmid pBB1 which carries the luxCDABE genes. RLU denotes relative lights units, defined as counts/min mL−1 per OD600. In A and B aggregate volume fraction was quantified in a strain harboring mKO constitutively expressed from the chromosome; quantitation of mean ± standard deviation (SD) (N=3 biological replicates). Representative cross-sections of the ΔvpsL HCD-locked (C), ΔvpsL ΔaphA HCD-locked (D), ΔvpsL ΔhapR HCD-locked (E), ΔvpsL ΔaphA ΔhapR HCD-locked (F), ΔvpsL LCD-locked (G), ΔvpsL ΔaphA LCD-locked (H), ΔvpsL ΔhapR LCD-locked (I), and ΔvpsL ΔaphA ΔhapR LCD-locked (J) V. cholerae strains following 22 h of growth. (C–J) Magnification: 10X; scale bar: 250 μm. All strains harbor mKO constitutively expressed from the chromosome. (K) Quantitation of aggregate volume fraction for samples in C–J. Shown are mean ± SD (N=3 biological replicates). The ΔvpsL ΔaphA LCD-locked strain appears to exhibit modest aggregation (H), possibly due to AphA repression of hapR transcription (Rutherford et al., 2011), but the level of aggregation is below the detection threshold employed in the segmenting analysis (K).
    2019
    unknown
  13. Ghinassi, F. ; Lic, J. ; et al.
    In: http://arxiv.org/pdf/astro-ph/0202483v1.pdf, 2002
    Online academicJournal
  14. Ghinassi, F. ; Licandro, J. ; et al.
    2002
    academicJournal
  15. Halaczkiewicz, Marta
    In: All Graduate Theses and Dissertations, 2022
    Online academicJournal
  16. Wong, MK ; Connie, T ; et al.
    2022
    Online academicJournal
  17. 2018
    unknown
  18. Figure 2. Rod signaling influences TH-positive cell number and dopamine levels through ipRGC-independent pathways. ; (A) Diagram depicting potential pathways by which light information could reach DACs (1. Via melanopsin signals relayed by ipRGCs, (2. Via rod signals relayed to DACs, (3. Via cone signals relayed to DACs, or (4. Via rod, cone, and/or melanopsin signals through ipRGC-dependent pathways. Dashed arrows represent indirect influence through multicellular circuits while solid arrows represent direct synaptic connectivity between subtypes. (B) Diagram depicting signaling pathways disrupted in MKO, RKO, CKO, and DTA mouse lines. Dashed arrows represent indirect influence through multicellular circuits while solid arrows represent direct synaptic connectivity between subtypes. (C–D) TH+ cell number and DA levels in Control (black circles, n = 9), MKO (blue circles, n = 6), RKO (red circles, n = 8), and CKO (green circles, n = 9) retinas from adult littermates. (E–F) TH+ cell number (n = 8 Control, n = 6 DTA) and DA levels (n = 6 Control, n = 6 DTA) in Control (black circles) and DTA (gray circles) retinas from adult littermates. (G) TH+ cell anatomy in WT and DTA adult retinal sections. We observed no morphological differences between TH+ cells in these two mouse lines. DA: dopamine, DAC: dopaminergic amacrine cell, MKO: animals lacking melanopsin phototransduction, RKO: animals lacking rod signaling, CKO: animals lacking cone signaling, DTA: animals where ipRGCs are ablated through expression of diphtheria toxin. Scale bar in (G) is 50 μm. *p < 0.05, bars on plots represent mean.
    2018
    unknown
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