Searching journal content for articles similar to Rao et al. 21 (9): 1404.

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  1. ...talk between GR and ESR1, as well as ESR1 and AR, has been well characterized in breast cancer (Swinstead et al. 2018; Hickey et al. 2021; Paakinaho and Palvimo 2021; Prekovic et al. 2023). Notably, direct cross talk is not limited to steroid receptors alone; other TFs like FOXA1, NF-kB, and CREB have...
  2. ...(also known as A20). However, our studies lacked sufficient temporal resolution to determine whether GR-mediated repression is affected solely as a secondary consequence of inductive gene regulation, including targets of GR-RELA cooperation such as TNFAIP3, or whether primary repression of NF-kB...
  3. ...high pool mostly contained cell types from the neuronal lineage (Fig. 4B, left), confirming previous findings on the essential role of RFX in sensory neuron differentiation (Swoboda et al. 2000). Despite the fact that the NF-kB and NFAT motifs are associated to two related families of Rel Homology...
  4. .... 2002). The major transactivating subunit of NFκB is v-rel avian reticuloendotheliosis viral oncogene homolog A (RELA; also known as p65), which, following inflammatory activation, translocates to the nucleus and binds DNA as a heterodimer with the mature product of NFKB1 (p50) to GGGRNYYYCC response...
  5. ...transcription factors such as NFKB, AP-1, and NFAT respond to T-cell receptor (TCR) signaling that occurs universally during differentiation for all Th lineages (Isakov and Altman 2002). These transcription factors 3Present address: The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University...
  6. ...TP53, CDKN2A (also known as P16), or CDKN1A (also known as P21) was observed (Fig. 6F). Similarly, no increase in phosphorylation of RELA, the subunit of NFKB normally associated with activation of the secretome genes, was observed, whereas HMGA1 expression was increased as reported previously (Fig...
  7. ...in multicellular organisms (e.g., Odomet al. 2004; Carroll et al. 2005; Cao et al. 2010). The second, gene-centered (DNA-to-protein) methods for the identification of TF–target gene interactions start with a regulatory genomic DNA sequence and identify the repertoire of TFs with which this sequence can interact...
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