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Thioflavin T fluorescence and atomic force microscopy studies support the notion that the structural transition is associated with cross-β-intermolecular aggregation and formation of non-fibrillar oligomers.
In pig and human pancreas, immunofluorescence and confocal microscopy studies support the expression of CCKR-1 in glucagon secreting cells only [ 33].
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Microscopy studies were supported by a Wellcome Trust grant to the MBB/BMS Light Microscopy Facility (GR077544AIA).
Irregular crack fronts and unbroken ligaments left on the fracture surfaces seen in complementary microscopy studies seem to support this approach.
Microscopy studies have tended to support the role of some sort of axial determinants of mitotic chromosome structure [ 44 47].
Transmission electron microscopy studies show that for supported MoS2, prepared using atmospheric pressure gas-phase sulphidation, particle size decreases upon exposure to ambient air for 24 h, whereas after 1 month of air exposure the number of slabs remaining has decreased significantly.
The importance of the steric contribution of the agarose support in IEX was further supported by confocal microscopy studies in Daniels et al. FCS and blip analysis were used to quantify the diffusion dynamics and affinity, respectively, of alpha-lactalbumin at glass, agarose, and penta-argininamide functionalized agarose interfaces.
Kinetic evidence and microscopy studies in erythroid cells have provided support for the 'kiss and run' hypothesis, which postulates the direct delivery of Tf-derived iron to mitochondria through a transient contact with the endosome [ 43].
This concept was supported by electron microscopy studies.
A direct role for VPS4 in membrane scission during retrovirus budding was also supported by light microscopy studies that tracked HIV-1 recruitment of ESCRTs over time to the plasma membrane of live cells.
This imperfect arrangement of nearly parallel crystals has been supported by SAXS and transmission electron microscopy studies (Burger et al. 2008).
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