The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis.
By Markus Landthaler, A. Yalçin, Thomas Tuschl. Current Biology, 2004
925 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/647074e79f7df3ceb352f779128fd1f4b62cbd42
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In Cancer Research
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- Richard I. Gregory
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In Molecular Biology
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Citations in the corpus
- Perspective: machines for RNAi. (2005, background): “GENES & DEVELOPMENT 521 Landthaler et al. 2004), but Drosha and Pasha are believed to function in the nucleus, whereas miRNA loading into RISC is thought to be cytoplasmic.”
- A human snoRNA with microRNA-like functions. (2008, methodology): “(C) FH-DGCR8 or untreated cells were immunoprecipitated using anti-FLAG antibodies.”
- Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex. (2006, background): “Drosha and its cofactor, DGCR8 (Gregory et al., 2004; Han et al., 2004; Landthaler et al., 2004) (known as Pasha in D.”
- The role of PACT in the RNA silencing pathway (2006, background): “…Molecular Biology Organization |All Rights Reserved 0261-4189/06 www.embojournal.org The EMBO Journal VOL 25 | NO 3 | 2006 &2006 European Molecular Biology Organization EMBO THE JOURNAL 522 pri-miRNAs into pre-miRNAs (Denli et al, 2004; Gregory et al, 2004; Han et al, 2004; Landthaler et al, 2004).”
- TUT4 in concert with Lin28 suppresses microRNA biogenesis through pre-microRNA uridylation. (2009, background): “, 2003) and its cofactor DGCR8/Pasha (Denli et al., 2004; Gregory et al., 2004; Han et al., 2004; Landthaler et al., 2004).”
- Processing of intronic microRNAs (2007, background): “Drosha functions as a complex called ‘Microprocessor’ that also contains a double-stranded RNAbinding protein, DGCR8 (also known as Pasha in flies and nematodes) (Denli et al, 2004; Gregory et al, 2004; Han et al, 2004; Landthaler et al, 2004).”
- MicroRNAs in development and disease. (2011, background): “The pri-miRNA is cleaved in the nucleus at the base of the stem-loop structure by the RNAse III enzyme Drosha (344) and its partner DGCR8/Pasha (139, 216, 229, 330) (FIGURE 1), which have been shown to require an intact secondary structure of the pri-miRNA for efficient processing (230).”