Compared with the results in Wilkerson et al (2010), we have clearly shown the difference between primitive and secretory subtypes regarding the similarities to the bronchial epithelial cells at different culturing days, as well as the stage of cells that needs to be targeted.
With the Luminal A subtype as reference, Cox regression analyses showed no statistically significant differences between subtypes regarding "Local recurrence" or "Invasive or general recurrence" (Table 2).
Intrinsic sub-typing of breast carcinomas based on global gene expression profiles has revealed large differences between the basal-like, ERBB2/Her2Neu and luminal subtypes regarding patterns of CNA's [ 13, 23– 25].
As shown by X-ray crystallography, only subtle structural differences between the subtypes were observed regarding the architecture of their F pockets, including the presence of distinct networks of water molecules.
There were no significant differences identified between the subtypes of male breast cancer regarding patients' race, presence of distant metastasis, and clinical stage.
Nevertheless, our preliminary findings, especially regarding brain volume differences between the subtypes of AN, provide regions of interest for future studies.
There were no significant disproportions between the two groups regarding CH subtype diagnosis (i.e., episodic and chronic diagnosis), the presence of CH in first-degree relatives and the occurrence of comorbid migraine or of a prior head injury.
We distinguished between the subtypes migraine with aura (MA) and migraine without aura (MO).
The mechanisms of action varied between the subtypes.
Additionally, no differences were observed between the different subtypes of JIA regarding the presence of MRI-based synovial hypertrophy or bone marrow changes suggestive of bone marrow oedema.
