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PMID |
Sentence |
1 |
7578887
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The percentage of CD4+PBL was higher in NOD/Smrf females than males, was intermediate in [NOD X NON] F1 mice and approximated a 1:1 distribution in F1 mice backcrossed to either NOD or NON parental strains, suggesting primary control of the phenotype by an incompletely dominant gene, but not excluding additional effects by other genes.
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2 |
7578887
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We term this primary gene Tlf(T lymphocyte frequency) because it also influenced the percentage of CD8+ T cells, although to lesser extent and independently from the MHC previously shown to lower the CD8+ T cell fraction in NON mice.
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3 |
7578887
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Dihydrotestosterone simultaneously lowered CD4+ PBL levels and prevented diabetes in NOD females while, in vitro, it had a differential effect on Con A elicited cytokines, increasing IL-2 22% and decreasing IL-4 39% (p < 0.0001).
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4 |
9001194
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TLF (d < 1.210 kg/L) shown to be free of plasma T4 transport proteins (TBG, TTR, HSA) was equilibrated with 0.3 nM 125I-labeled T4, T3 or reverse T3 (rT3) and chromatographed on Sepharose CL-6B.
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5 |
9754812
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Candidate genes for Tlf are Ets1 and Fli1, proximally and Igif distally.
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6 |
14726532
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The general transcription factor TFIID sets the mRNA start site and consists of TATA-binding protein and associated factors (TAF(II)s), some of which are also present in SPT-ADA-GCN5 (SAGA)-related complexes.
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7 |
14726532
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In yeast, results of multiple studies indicate that TFIID-specific TAF(II)s are not required for the transcription of most genes, implying that intact TFIID may have a surprisingly specialized role in transcription.
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8 |
14726532
|
Previously, we investigated functions of four shared TFIID/SAGA TAF(II)s in Caenorhabditis elegans.
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9 |
14726532
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Whereas TAF-4 was required for essentially all embryonic transcription, TAF-5, TAF-9, and TAF-10 were dispensable at multiple developmental and other metazoan-specific promoters.
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10 |
14726532
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Here we show evidence that in C. elegans embryos transcription of most genes requires TFIID-specific TAF-1.
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11 |
14726532
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TAF-2, which binds core promoters with TAF-1, appears to be required for a similarly substantial proportion of transcription.
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12 |
14726532
|
C. elegans TAF-1 overlaps functionally with the coactivator p300/CBP (CBP-1), and at some genes it is required along with the TBP-like protein TLF(TRF2).
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13 |
14726532
|
We conclude that during C. elegans embryogenesis TAF-1 and TFIID have broad roles in transcription and development and that TFIID and TLF may act together at certain promoters.
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14 |
14726532
|
The general transcription factor TFIID sets the mRNA start site and consists of TATA-binding protein and associated factors (TAF(II)s), some of which are also present in SPT-ADA-GCN5 (SAGA)-related complexes.
|
15 |
14726532
|
In yeast, results of multiple studies indicate that TFIID-specific TAF(II)s are not required for the transcription of most genes, implying that intact TFIID may have a surprisingly specialized role in transcription.
|
16 |
14726532
|
Previously, we investigated functions of four shared TFIID/SAGA TAF(II)s in Caenorhabditis elegans.
|
17 |
14726532
|
Whereas TAF-4 was required for essentially all embryonic transcription, TAF-5, TAF-9, and TAF-10 were dispensable at multiple developmental and other metazoan-specific promoters.
|
18 |
14726532
|
Here we show evidence that in C. elegans embryos transcription of most genes requires TFIID-specific TAF-1.
|
19 |
14726532
|
TAF-2, which binds core promoters with TAF-1, appears to be required for a similarly substantial proportion of transcription.
|
20 |
14726532
|
C. elegans TAF-1 overlaps functionally with the coactivator p300/CBP (CBP-1), and at some genes it is required along with the TBP-like protein TLF(TRF2).
|
21 |
14726532
|
We conclude that during C. elegans embryogenesis TAF-1 and TFIID have broad roles in transcription and development and that TFIID and TLF may act together at certain promoters.
|