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CHEBI ID

CHEBI:15354 (2)
CHEBI:15756 (2)
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CHEBI:16704 (2)
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CHEBI:7916 (2)

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(+/-)12(13)-DiHOME (1)
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IsPrivate

False (1)

Modelling Approach

Ordinary differential equation model (1)

Study type

Transcription profiling by array (38)
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Lab affiliation

1. Barts Cancer Institute Queen Mary, University of London John Vane Science Centre, Charterhouse Square, London EC1M 6BQ 2. Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas (CSIC), Granada, 18016, Spain (2)
1. Barts Cancer Institute, Queen Mary University of London; Charterhouse Square, London EC1M 6BQ, UK. 2. Instituto de Parasitología y Biomedicina “López-Neyra” (IPBLN-CSIC); E-18016 Granada, Spain. (1)
Centre for Cancer Genomics and Computational Biology, Barts Cancer Institute, Queen Mary University of London. EC1M6BQ, London, UK (1)

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Helin-Human-HH9si

Gene expression in HeLa cells was monitored after interference for HectH9

ORGANISM(S): Homo sapiens

2005-10-17 | E-MEXP-408 | biostudies-arrayexpress

H2A.Z (pht1) ChIP-seq data in 968, Y0036, and swc5-del strains

After finding a QTL hotspot in a fission yeast cross of strains 968xY0036 that was apparently driven by frame shift mutation in swc5 (swc5-fs), we have determined the genome-wide occupancy of the histone variant H2AZ (PhT1). Indeed swc5 has been shown to affect H2AZ occupancy. To test the impact of ...

ORGANISM(S): Schizosaccharomyces pombe

2014-12-04 | E-MTAB-2650 | biostudies-arrayexpress

Rituximab extended schedule or re-treatment trial for low-tumor burden follicular lymphoma: eastern cooperative oncology group protocol e4402.

Not available

S-EPMC4171355 | biostudies-literature

EpiMethylTag: simultaneous detection of ATAC-seq or ChIP-seq signals with DNA methylation.

Not available

S-EPMC6868874 | biostudies-literature

Phase IB Study of Selinexor, a First-in-Class Inhibitor of Nuclear Export, in Patients With Advanced Refractory Bone or Soft Tissue Sarcoma.

Not available

S-EPMC5321073 | biostudies-literature

Nascent Induced Pluripotent Stem Cells Efficiently Generate Entirely iPSC-Derived Mice while Expressing Differentiation-Associated Genes.