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The language used by COPS for specification of code generators.

["Metalanguages of the Compiler Production System COPS", J. Borowiec, in GI Fachgesprach "Compiler-Compiler", ed W. Henhapl, Tech Hochs Darmstadt 1978, pp. 122-159].



a river in Riazan’ Oblast, RSFSR, a left tributary of the Oka. It is 167 km long and drains an area of 5,520 sq km. The Pra is fed primarily by snow. It has a mean flow rate of 25 cu m per sec and a maximum flow rate of approximately 600 cu m per sec. The river freezes at the end of November, and the ice breaks up in April. Timber is floated on the Pra. The Oka Preserve is located in the lower reaches.

References in periodicals archive ?
As can be expected, these genes can be assigned to different functional groups such as cell death regulators (CASP2, ING2, MDM4, NAIP), transcriptional and translational regulation (DEPDC1, GABPB1, LHFPL2, NFIB, P0LR3C, RPL34, RPS3A, RPS21, RPS25, TFDP2, TRIM24, ZBTB1, ZBTB38, ZFP112), oxidative stress response (SPATS2L, GSTT2B, NQO1), DNA maintenance and processing (BAHCC1, FANCA, H1ST1H3G, IK, KDM4C, MCM7, PRB3, RNASEH2B, SNRPE, TFDP2), blood coagulation (FGA, MATR3, PROCR, P1K3CG), signal transduction (ANXA2, ARHGAP19, C7orf47, CCDC50, DTX3, FHL2, P1K3CG, RALB, T1CAM2), cytoskeletal components (BCL7A, DYNC1LI2, SEPT10, SEPT11), transport functions (ABCC1, FXYD2, S100A6, SCNN1G, XP05), or others (ADAM22, ALDH3A2, FAM161A, HDDC2, HLA-F).
In the instance of background staining, S100A6 can be a good substitute, although weak nuclear and cytoplasmic staining for S100A6 can be seen in normal/reactive pancreatic ducts.
The researchers then narrowed the molecules down to two proteins, S100A6 and S1009, which are most likely to appear in samples from patients with cancer but are absent from the other samples.
Finally, by altering the expression of genes including JUNB, S100A6, CTGF, SMA and collagen genes, FG-4539 pretreatment resulted in attenuation, more rapid resolution, or delayed induction of these markers of kidney damage and fibrosis.
8E-9 CACNB1, ALPL, CDH1, ITGA3, SERPINB10, TAF4B, ABCB10, IRF8 Cell proliferation ATF3, MK167, S100A6, FTH1, DHCR7 2.