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We subsequently identified several families of anticocaine catalytic antibodies and found that the most potent antibody possessed sufficient activity to block cocaine-induced reinforcement, organ dysfunction and sudden death in rodent models of addiction, toxicity and overdose, respectively.
We subsequently identified the gene for HHT 1 as endoglin (McAllister et al., 1994b) — a transforming growth factor- OOTGF-OO) binding protein ofactor- OOTGF-OOlls.
In our laboratory, we subsequently identified a second missense mutations in tie-2 which causes FVM, and have shown that both known mutations constitutively activate the receptor (Calvert et al., 1999).
We subsequently identified the gene for HHT 1 as endoglin (McAllister et al., 1994b), a transforming growth factor-ÿ TGF-ÿÿ) binding protein ofactor-ÿ TGF-ÿÿells, and the HHT 2 locus as the activin-like kinase receptor, ALK-1, which has sequence homology to type I TGfactor-ÿ TGF-ÿÿ(Johnson et al., 1996).
As a representation of common group versus group differential gene expression analysis we subsequently identified differentially expressed probes between histological grade 1 (n = 9) and histological grade 3 (n = 16) tumors (see Table 1) for both FFPE and FF paired samples using SAM (Significance Analysis of Microarray) [29].
In light of the fact that DOC is known to regulate genes via nuclear receptors [31], we subsequently identified genes showing whole brain expression that correlated (Pearson's r) with basal cortical DOC levels across BXD strains, using existing microarray data within GeneNetwork (Table S6).
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2011, doi 10.1093/gbe/evr100 Among the 3151 Chromera EST-contigs that we recently published (Woehle et al. 2011; Genome Biol. Evol. 3 1220 1230) we have subsequently identified 113 sequences having very high nucleotide sequence identity (≥90%) to some higher eukaryote accessions, mainly Hordeum or Triticum, at the NCBI nucleotide database.
AntiSMASH did not reveal any putative natural product gene clusters, but we did find a gene cluster potentially encoding the biosynthesis of a lasso-peptide, which we have subsequently identified and characterised (manuscript in preparation).
We have subsequently identified the homologous human MATER gene and protein[ 26] In ongoing work we are evaluating the value of MATER antibodies as a marker for autoimmune ovarian failure in women.
We thus subsequently identified the major unexplored themes and present an organized, systematic research program for a more holistic and quantifiable understanding of the interaction between social behavior and underground spaces.
We have subsequently identified this protein as a surface-expressed form of the cytoskeletal protein vimentin.
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