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Most tissues tested, including spinal cord, skeletal muscle, spleen, thymus, heart, lungs, liver, and oesophagus, were negative for LacZ expression.
This is unusual since previous studies showed that heterozygous mice have normal serum concentrations of CSF-1 and normal populations of macrophages in most tissues tested [57].
Stfa2l1 expression was weak or undetectable in most tissues tested, with the notable exception of the fetal liver, bone marrow, and spleen which presented high expression levels (Figure S1 and 2B).
Genes from the PIN1 and PIN3 groups were differentially expressed in all or most tissues tested.
Intriguingly, the expression pattern of the two genes was highly concordant in most tissues tested, suggesting common regulatory transcriptional mechanisms.
SCBV promoters from several isolates of the virus have been tested in transgenic plants and shown to be highly expressed in most tissues tested [ 21, 22, 36].
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Prdm14 is normally expressed at low levels in most control tissues tested but is massively upregulated in all Evi32 tumors.
The result revealed a single, 2.4-Kb mRNA in most human tissues tested, with highest levels in the heart (Fig. 5A).
LCP1 is also expressed in most other tissues tested (with the possible exception of muscle) and thus has a more widespread pattern of expression than previously found for the Tox gene.
Previous work on human AIM2 found expression predominantly in spleen, with detectable mRNA in small intestine and peripheral blood but levels below detection in most other tissues tested [ 25].
In contrast to this, its expression was strongly down-regulated in most neoplastic cells or tissues tested.
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