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Using a different molecular approach, Irie and Sehara-Fujisawa (2007) also provide evidence for the vertebrate phylotypic stage.
These findings are different from what has been previously reported in a study using a different molecular method of analysis (fluorescent in situ hybridization), which reported, "the absence of a correlation between the bacterial species Staphylococcus aureus and Pseudomonas aeruginosa detected in wound by culture and what is in fact present" [ 5].
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Thus, credibility is lent to the phylogeny estimates presented here, despite their low support levels, by the fact that very similar relationships among lepidopteran superfamilies are emerging from an independent molecular study using a different but comparable gene sample, and a larger taxon sample (M. Mutanen, L. Kaila, N. Wahlberg, personal communication).
Directly analyzing gene expression in bladder biopsies allows us to use a different approach for the molecular characterization of IC.
Many biologists that analyze the evolution of development or "evo-devo" use a different set of molecular and morphological investigative techniques to uncover robust and important developmental constraints (see, e.g., Müller and Newman 2003, Kirschner and Gerhart 2005).
One study using the read-pair method reported 241 SVs over 8 kb in a sampled genome [ 7], while another using the same approach but with a different molecular construct reported 422 and 753 SVs over 3 kb in two tested genomes [ 4].
Phylogenetic analysis by using two different molecular markers showed that this new cyanobacterium belongs to a cluster of the genus Nostoc, with the closest relative of Nostoc muscorum.
The 3D matrices were evaluated for in vitro release using two different molecular weight model compounds, bovine serum albumin (66 kDa) and FITC Inulin (3.9 kDa).
Loading efficiency was investigated using two different molecular weights of PAGS.
We have therefore carried out a systematic analysis of canonical Wnt signaling in embryos and cells that are mutant for four different IFT proteins, using four different molecular assays.
Several methods of detecting PRRSV RNA and PRRSV antibodies (Ab), using both different molecular diagnostic methods and serological techniques, were developed [ 1- 3].
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