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Difference between Git and Mercurial
What is the main difference between Git and Mercurial?
Git is distributed.
Mercurial is centralized.
Git’s main differentiating feature is that it is distributed. It supports distributed operation, commits, branches, and merging, along with a lot of other things. It’s big.
With Mercurial, you have a single repository, and it’s easy to clone it so you can all work on it. It can work with branches and merges if you want, but that’s optional.
A systematic approach to false positive diagnosis of prostate cancer using the TRUS guided extraperitoneal template prostate biopsy: the use of a 0.5/1.5 mm core biopsy protocol.
To investigate the feasibility and accuracy of a system for false positive diagnosis of prostate cancer using the transrectal ultrasound (TRUS) guided extraperitoneal template prostate biopsy (TEPB), employing a 0.5/1.5 mm core biopsy protocol. From March 2004 to September 2005, a total of 90 consecutive patients underwent TRUS guided TEPB. Each patient had at least two 12 cores biopsies performed. The first 12 cores included six needles containing 0.5 mm core biopsies and the remaining six biopsy cores were 1.5 mm core biopsies. A total of 104 prostatic zones (PZs) were taken into consideration. Biopsy cores and PZs were assigned a score between 1 and 3, where 1 = No abnormality, 2 = Benign, 3 = Malignant. The accuracy rate, sensitivity and specificity of the system were calculated. A total of 96.2% (97/101) of cancer cases were detected, with a sensitivity of 72.6% (74/101), a specificity of 96.9% (96/100) and an overall accuracy of 77.2% (89/113). The optimal cut-off for detecting significant cancerous lesions was >1.5, and the area under the curve (AUC) was 0.893. A total of 23 (22.1%) benign lesions were histologically diagnosed
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Sphingolipid metabolism has been implicated in the pathogenesis of malaria infection, and the pathogenesis of the malaria parasite Plasmodium falciparum is a particularly interesting subject. In this report, we identified a sphinganine/sphingosine kinase gene, designated as SPHK (Sphinganine/sphingosine kinase) in P. falciparum, by sequence analysis of the genomic DNA. The level of the mRNA in the asexual erythrocytic stage of the parasite was increased depending on the differentiation of the parasite, confirming the presence of SPHK activity in the malaria parasite. Yeast complementation studies showed that the recombinant SPHK protein expressed in S. cerevisiae was able to transform sphinganine into sphingosine. Sphingosine kinase activity was inhibited by sphingosine and it was activated by sphingosine-1-phosphate. High concentrations of dic