1
Here, we report the development of a panel of human GPIHBP1- specific mAbs.
2
Directional transport of specific mRNAs is of primary biological relevance.
3
Depleting LT-alpha- specific mAb inhibited T cell-mediated models of delayed-type hypersensitivity and experimental autoimmune encephalomyelitis.
4
This apparently coordinated accumulation of specific mRNAs results from increased transcription of the relevant genes.
5
How these RNA structures mediate eIF3 recruitment to affect translation of specific mRNAs remains unclear.
6
Serial Southern hybridization in this study confirmed the specific mRNA expression corresponding to each enzyme.
7
As expected, specific mRNA levels correlated with the intensity of lacZ expression for each variant.
8
They bind to the 3'-untranslated region of specific mRNAs and inhibit translation or promote mRNA degradation.
9
Freshly isolated lymphocytes were analyzed by flow cytometry using a panel of V gene subset- specific mAbs.
10
The same method could also be applied to other RNA-binding proteins interacting with specific mRNAs or miRNAs.
11
Two alternative promoters underlie the transcription of two classes of HOX-5.1- specific mRNAs.
12
MicroRNAs are small noncoding RNAs that regulate gene expression by targeting specific mRNAs for degradation or translation inhibition.
13
Accumulating evidence suggests that changes of the protein synthesis machinery alter translation of specific mRNAs and participate in malignant transformation.
14
Tryptophan-activated TRAP negatively regulates expression by binding to specific mRNA sequences and either promoting transcription termination or blocking translation initiation.
15
The examination of YY1- specific mRNA expression demonstrated at least six mRNA isoforms ubiquitously expressed in normal human adult and fetal tissues.
16
One stable clone decreased the efflux of rapidly labeled RNA and of one specific mRNA (ovalbumin) from isolated nuclei.
