Searching journal content for articles similar to Bashford-Rogers et al. 23 (11): 1874.

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  1. ...with deep sequencing (ChIP-seq) with DHT-only treatment or AR ChIP-seq with Dex-only treatment. ChIP-seq analyses indicated that DexDHT treatment substantially increased GR chromatin occupancy, whereas AR binding remained unchanged (Fig. 1A,B; Supplemental Table S1). Because AR-binding sites (ARBs) in VCa...
  2. ...(TEC) is essential for generating a diverse T cell antigen receptor repertoire tolerant to self-antigens, and thus for avoiding autoimmunity. Nevertheless, the extent and nature of this unusual expression program within TEC populations and single cells are unknown. Using deep transcriptome sequencing...
  3. ...in human individuals (in naive B cell repertoires), we computed the normalized JSD on a cohort of 99 unrelated individuals from the HUMAN3 data set (see Methods, “Experimental immunoglobulin sequencing data”) (Fig. 3A; Gidoni et al. 2019). Analogously to the HUMAN1 and the HUMAN2 data sets (Fig. 2), we...
  4. ...-specific manner makes them critical components of gene regulatory networks (Shlyueva et al. 2014). Although enhancer–reporter assays (Banerji et al. 1981) and comparative genomics (Pennacchio et al. 2006) enabled initial discoveries, enhancers are usually mapped within nucleosome-free open chromatin regions...
  5. ...is generated by a genetic network of cell-autonomous transcription–translation feedback loops (TTFLs) driven by the activators circadian locomotor output cycles kaput (CLOCK) and basic helix-loop-helix ARNT like 1 (BMAL1) and the repressors period (PER) and cryptochrome (CRY) (Takahashi et al. 2008...
  6. ...patients remains hidden for lack of a population-wide role (Garraway and Lander 2013; Chang et al. 2016). The sequencing of diverse types of somatic tumor tissue from a large number of patients by The Cancer Genome Atlas (TCGA) (The Cancer Genome Atlas Research Network 2008; The Cancer Genome Atlas...
  7. ...by deep DNA sequencing. Antibodies (Dolfini et al. 2009)were validated by Western blot and IP-WB, showing that NF-YA and NF-YB are specifically recognized (Supplemental Fig. 1A,B). Immunoprecipitated DNA was validated on known NF-Y targets (Supplemental Fig. 1C,D) and the reproducibility between...
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