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In the current molecular classification, Group 3 tumors are associated with anaplastic histology, MYC amplification, metastatic phenotype, and dismal prognosis.
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The first widely adopted molecular classification of rice groups was based on isozyme analysis (Glaszmann, 1987), in which six varietal groups were identified.
According to molecular classification, BCs were grouped into at least four "intrinsic" subtypes: two ER-positive luminal-like subtypes and two ER-negative subtypes, HER2 overexpressing (HER2 positive nonluminal) and triple negative (TN).
Hierarchical clustering analysis excluding EEF1G, H2AFZ and BZRP resulted in clusters identical to that using the original nine genes, suggesting that these three genes do not contribute to the molecular classification of three groups, but may be involved in the common pathophysiology of gastric tumours probably reflecting accelerated cell division or metabolism.
Molecular classification into the two groups was validated by the findings of increased hepatic population of lymphocyte subsets or tissue accumulation of matrix substrates.
New technologies including next-generation sequencing have enabled more detailed analysis of urothelial carcinoma, and several groups have proposed molecular classification systems based on these data, although consensus is elusive.
Unsupervised molecular classification identified three major and robust groups of breast cancers that differ in the expression of several hundred to a few thousand genes.
Investigating the HA Score in the eight groups of the molecular classification of MM (Zhan et al, 2006), HA Score was significantly higher in the proliferation subgroup (P<0.001) associated with a poor prognosis and significantly lower in the CD2 subgroup (P<0.001) (Zhan et al, 2006).
In the Ambler molecular classification, β-lactamases are separated into four groups, A through D (Table 3).
These four clinical subsets correspond closely (≥80% concordance) to groups defined by various molecular classification methods that rely on gene expression analysis or immunohistochemistry.
A similar prevalence pattern with a still significantly low incidence of luminal tumors (p = < 0.001 ) was obtained when molecular classification was attempted using other criteria previously described by several groups [ 17, 18, 20].
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