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1 ups of children for abnormalities in the IGF-IR gene.
2 T antigen to transform MEFs with deleted IGF-IR genes.
3 nate the effects of the class II and class I Ir genes.
4 hat the TCR locus can be an Immune response (Ir) gene.
5 e 1 insulin-like growth factor receptor (IGF-IR) genes.
6 ivo expression of heritable inverted-repeat (IR) genes.
7 reported immune-responsive regulation of IGF-IR genes adds to an emerging body of evidence that suppo
10 s including exon 11 of the Insulin Receptor (IR) gene and exon 5 of the cardiac Troponin T (cTNT) gen
11 e insulin-like growth factor I receptor (IGF-IR) genes) and R508 cells (derived from R- and with 15 x
12 inhibit transcription elongation of the IGF-IR gene, and emphasize the efficacy of triplex-mediated
17 ition to the effects of the classic class II Ir gene, class I (D, L) or nonclassical class I (Qa-2) m
19 ructure of insulin to study the mechanism of Ir gene control in H-2b mice, which respond to beef insu
21 ith endothelial-specific inactivation of the IR gene (EndoIRKO), we find that in response to systemic
23 e a novel mechanism of autoregulation of IGF-IR gene expression by cellular IGF-IR, which is seemingl
25 ossible mechanisms by which p53 may regulate IR gene expression, we show that p53 can repress the IR
27 Insulin-like growth factor-I receptor (IGF-IR) gene expression is regulated by various stimuli, inc
28 ase domains from six distinct members of the IR gene family were obtained, and sequence comparisons r
29 e conclude that there are at least two human Ir genes, HLA-DRB1*01 and HLA-DRB1*03, that confer a hig
31 We also examined the regulation of each IGF-IR gene in fish challenged by bacterial and viral infect
33 nt was revealed by genetic disruption of the IR gene in the oncogene-expressing pancreatic beta cells
34 prominently express two Ionotropic Receptor (IR) genes, IR76b and IR25a, and we show that both these
40 cells with a targeted disruption of the IGF-IR genes, R- cells, are refractory to transformation by
44 ental transcriptional regulation of each IGF-IR gene, revealing tight co-expression between the IGF-I
47 ote for point mutations in exon 2 of the IGF-IR gene that altered the amino acid sequence to Arg108Gl
49 demonstrated that Vbeta8.1 functioned as an Ir gene that was indispensable for immune reactivity aga
50 otential for effects of the immune response (Ir) gene that could complicate a peptide-based vaccine.
51 define 14 genes [immune response deficient (ird) genes] that have distinct roles in the immune respo
52 F and IGF-I have differential effects on IGF-IR gene transcription, with the IGF-I response region as
55 to H-Y are controlled by MHC class I and II Ir genes, which-respectively, restrict CD8 and CD4 T cel
56 lower synonymous rates consistent with other IR genes, while genes moved from the IR into the SC exhi
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