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Records of patients who had colonized or infected with Staphylococcus strains with decreased susceptibility to glycopeptides were reviewed and data related to the patients age, gender, ward, underlying disease, specimen, duration of hospitalization and previous treatment with glycopeptides were evaluated.
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The past year has also seen a transition from experiments involving a small number of conditions, with an emphasis on the specific genes induced or repressed, to experiments involving hundreds of conditions in which patterns of global gene expression are used to classify disease specimens and discover gene functions and drug targets.
In contrast, CDI could clearly distinguish between prion disease and non-prion disease specimens after pretreament of the homogenates with 2.5 μg/ml PK.
Thirty disease specimens were grade 3 macroscopically of which 26 were also grade 3 and 1 was grade 2 on histology.
For his doctoral work, he is developing novel bioinformatics approaches to identify various kinds of molecular signatures from genomic information of human disease specimens (e.g. tumor biopsies).
Two (6.7%) of the 30 extragenital Bowen's disease specimens were positive for types 16 and 33 of mucosal high-risk HPV, respectively.
In addition, we analyzed two benign fibrocystic disease specimens and in both cases we saw no methylation of the CpG island and DSC3 gene expression in one of two specimens analyzed.
The sample was subsequently given to the Center of Excellence in Viral Hepatitis, Faculty of Medicine, Chulalongkorn University, for molecular diagnosis and then stored at –70°C, where specific precautions implemented for handling highly infectious disease specimens such as H5N1 influenza virus were observed.
In the absence of PK digestion, CDI is ineffective at discriminating between prion disease and non-prion disease specimens: using the mean D-N value for non-CJD cases plus 3 s.d. as a cut-off value (158 μg PrP per gram brain) only sCJD VV2 subtype, vCJD and GSS (type 1 PrPres) give values above this cut-off.
The HERV-W env sequence encoding the surface unit-transmembrane region (650bp) was amplified (Figure 5Ai), cloned (≥11 per specimen) from the fetal and adult brain (non-disease) specimens and subsequently aligned (Figure 5Aii).
6-keto-PGF1 alpha and thromboxane B2 were determined by radioimmunoassay in 37 extracts of breast carcinomata, 8 fibroadenomata, 12 sclerocystic-disease specimens and 51 normal breast tissues.
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