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All paraffin-embedded tumours were reviewed by an independent pathologist to ensure the validity of the specimen and define the most appropriate tumour area for microdissection.
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This increase in cases enabled us to collect blood specimens from patients shortly after clinical onset of disease, characterize these specimens, and define a new PUUV clade (North East Hesse, clade 4).
To ensure that the copy number of nuclear DNA is sufficient for amplifying nuclear Neandertal DNA and to monitor potential nuclear DNA contamination we additionally amplified a control position on the Y-chromosome, which was previously described as ancestral in both specimens and defines the deepest clade in the human Y-chromosome tree (Y2 in [ 24]).
With heterogeneity of the specimen and a defined trauma mechanism fractures became comparable.
There is now an International Barcode of Life project, which has collected more than one million specimens and has defined the DNA bar codes for more than 95,732 species.
Chemotherapy effects were determined employing operative specimens and we defined pCR as invasive nest disappearance based only on the primary breast tumour, i.e. without lymph node evaluation.
Chemotherapy effects were determined employing operative specimens and we defined pathological complete response (pCR) as invasive nest disappearance, based only on the primary breast tumour.
For each of slides, 200 nuclei of cells were evaluated independently by two observers and the cut-off values for each probe were determined from three FFPE tonsil specimens and were defined as the mean copy number in tonsil plus three standard deviations for FFPE specimens.
To address this fundamental question, we first performed cancer stem cell marker profile analysis using human breast cancer cell lines and specimens to further define and characterize different stem cell populations by flow cytometry, along with in vitro and in vivo assays to verify the stem cell properties of different cell isolates.
Additionally a tripod of three ultrasound markers was attached to each bone and anatomic landmarks were identified on the specimen to define kinematic pattern in relation to the coordinate system of each bone.
Non-linear finite element analyses for 3-D models of plane-sided SE(B) and PCVN specimens define the relationship between ˜σw and J from which the variation of fracture toughness across different crack configurations is predicted.
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