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The aim of the study was to establish an experimental workflow allowing reliable molecular single cell analysis in a clinical setting within an acceptable time frame.
Our combined functional and molecular single cell analysis strongly suggests that the long D2l splice variant alone can build functional D2-autoreceptors in SN DA neurons.
Therefore, we correlated the GII with three different types of molecular single cell analyses to assess its diagnostic utility, including (i) gene-specific point mutation analysis (PIK3CA mutations in exon 9 and exon 20), (ii) gene-specific quantification of copy number (ERBB2 (HER2) amplification) and (iii) genome-wide array CGH (aCGH).
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Until now, several methods were employed to fabricate CuInSe2, such as sputtering [5], evaporation [6], electrodeposition [7, 8], and pyrolysis of molecular single-source precursors [9].
However, none of these in silico methods are applicable in the case of molecular single-electron transistors (SET) with incoherent electron transport [15].
For the validation set of 225 molecular single-crystal structures, the average r.m.s.
TiNi serves as a molecular single-source precursor for both NiO x, which acts as the electrocatalyst, and TiO2, which stabilizes the WO3 semiconductor.
Here we report the low-pressure chemical vapor deposition (LPCVD) of single-phase, crystalline TiSe2 thin films onto SiO2 and TiN substrates using the molecular single-source precursor [TiCl4(Se n Bu2)2] (1).
Here, we used molecular (single-nucleotide polymorphism) data to estimate the genetic correlation between height and general intelligence (g) in 6,815 unrelated subjects (median age 57, IQR 49 63) from the Generation Scotland: Scottish Family Health Study cohort.
The film is prepared by the simple drop casting of the molecular single-source precursor, [{Ti2 OEt 9(NiCl)}2] (TiNipre), onto the p-Si surface at room temperature, followed by cathodic in situ activation to form the catalytically active TiNi film (TiNicat).
Since PS1 dimers have been previously reported, [22]-[24] we tested how much of the FRET signal is contributed by inter-molecular (PS1 dimers) versus intra-molecular (single PS1 molecule) interaction.
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