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1 d, placebo-controlled, phase 3 trial between Oct 6, 2009, and Jan 26, 2012, at 119 centres in 29 coun
2 ha3 gene promoter is activated by SCIP/Tst-1/Oct-6, a POU domain transcription factor proposed to be
3                                   Tst-1/SCIP/Oct-6, a POU domain transcription factor, is transiently
4                                              Oct-6, a POU-III domain transcription factor, is express
5 iting NF-kappaB also prevented activation of Oct-6, a transcription factor induced by axonal contact
6                    They fail to downregulate Oct-6 and arrest at the premyelinating stage.
7 e in the cAMP-regulated transcription factor Oct-6 and expression of myelin basic protein.
8 otype of Schwann cells, including SCIP/tst-1/Oct-6 and Krox-20, both of which are required for the no
9  promoter in 293 cells, and YY1, Sp1, Oct-1, Oct-6, C/EBP, and c-Jun transcription factors seem to be
10 lliger oxidation (1R, 5S)-3-oxabicyclo[3.3.0]oct-6-en-2-one and (1S, 5R)-2-oxabicyclo[3.3.0]oct-6-en-
11 selective oxidation of an 8-oxabicyclo[3.2.1]oct-6-en-3-one cycloadduct by means of the Moriarty meth
12 t-6-en-2-one and (1S, 5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one were detected.
13                                Bicyclo[3.2.1]oct-6-en-8-ylidene (1) can assume either the conformatio
14 m the LacZ gene seems to parallel Tst-1/SCIP/Oct-6 expression from the endogenous tst-1/scip/oct-6 ge
15      Western blot analysis was used to study Oct-6 expression in the frontal and temporal cortex in t
16                              The presence of Oct-6 expression in the schizophrenic subjects but not i
17     Immunohistochemistry was used to examine Oct-6 expression in the temporal lobe in postmortem tiss
18 -6 mice, in which one copy of the tst-1/scip/oct-6 gene has been replaced with the LacZ gene.
19 -6 expression from the endogenous tst-1/scip/oct-6 gene in developing and regenerating sciatic nerves
20 /oct-6-null mice, indicating that Tst-1/SCIP/Oct-6 has a critical role in promyelinating Schwann cell
21                   In schizophrenic subjects, Oct-6 immunoreactivity was found in a subset of cells in
22                                    Extensive Oct-6 immunoreactivity was present in the temporal lobe
23       This study evaluated the expression of Oct-6 in schizophrenia, a disorder that has been linked
24 tern blot analysis confirmed the presence of Oct-6 in the frontal and temporal cortex in schizophreni
25                                  Pou3f1/SCIP/Oct-6 is a POU-domain transcription factor that is an im
26 in transcription factor pou3f1 (Tst-1, SCIP, Oct-6) is required for the normal differentiation of mye
27 not in the comparison subjects suggests that Oct-6 may provide a marker for the neuropathology associ
28 a-gal) expression in heterozygous tst-1/scip/oct-6 mice, in which one copy of the tst-1/scip/oct-6 ge
29  which development is arrested in tst-1/scip/oct-6-null mice, indicating that Tst-1/SCIP/Oct-6 has a
30                                In tst-1/scip/oct-6-null sciatic nerves, Schwann cells are transiently
31 f beta-gal, a surrogate marker of Tst-1/SCIP/Oct-6, peaks at the same stage of Schwann cell developme
32                        Deletion of the Tst-1/Oct-6/SCIP gene produces a severe defect in peripheral m
33    The POU domain transcription factor Tst-1/Oct-6/SCIP is expressed transiently during myelination,
34 n and migration of specific neurons in Tst-1/Oct-6/SCIP mutant homozygotes is associated with a fatal
35  genes appears to be unaffected by the Tst-1/Oct-6/SCIP mutation, demonstrating that multiple, indepe
36 i (Skn-1a/i/Epoc/Oct-11) and Testes-1 (Tst-1/Oct-6/SCIP) in epidermis where proliferating basal kerat
37                                              Oct-6 staining was predominantly localized in the cytopl
38  the proximal rGnRH promoter containing SCIP/Oct-6/Tst-1 binding sites.
39                           Activation of SCIP/Oct-6/Tst-1 expression in terminally differentiated GnRH
40                         Coexpression of SCIP/Oct-6/Tst-1 in neuronal cells inhibited rat GnRH (rGnRH)
41 n-protein interactions are required for SCIP/Oct-6/Tst-1 modulation of GnRH gene expression.
42 ivity was suggested by the detection of SCIP/Oct-6/Tst-1 mRNA in a subset of GnRH neurons in the hypo
43 ion assays demonstrated the presence of SCIP/Oct-6/Tst-1 mRNA in the GnRH-producing neuronal cell lin
44 UP-TFI acts as an upstream regulator of SCIP/Oct-6/Tst-1, a transcription factor involved in axon mye
45 opment, is regulated by the POU protein SCIP/Oct-6/Tst-1.
46 ermine when Schwann cells express Tst-1/SCIP/Oct-6, we examined beta-galactosidase (beta-gal) express
47 hyl-but-2-enyl)-oxiranyl ]-1-oxa-spiro [2.5] oct-6-yl ester (PPI-2458), in a rat model of peptidoglyc

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