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Giuseppe Macino

Researcher at Sapienza University of Rome

Publications -  122
Citations -  17574

Giuseppe Macino is an academic researcher from Sapienza University of Rome. The author has contributed to research in topics: Neurospora crassa & Gene. The author has an hindex of 55, co-authored 122 publications receiving 16847 citations. Previous affiliations of Giuseppe Macino include Policlinico Umberto I & Columbia University.

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A mammalian microRNA expression atlas based on small RNA library sequencing.

TL;DR: A relatively small set of miRNAs, many of which are ubiquitously expressed, account for most of the differences in miRNA profiles between cell lineages and tissues.
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The genome sequence of the filamentous fungus Neurospora crassa

James E. Galagan, +77 more
- 24 Apr 2003 - 
TL;DR: A high-quality draft sequence of the N. crassa genome is reported, suggesting that RIP has had a profound impact on genome evolution, greatly slowing the creation of new genes through genomic duplication and resulting in a genome with an unusually low proportion of closely related genes.
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Quelling: transient inactivation of gene expression in Neurospora crassa by transformation with homologous sequences

TL;DR: The phenotypic reversion is characterized by a progressive release of the transcriptional inhibition and seems to correlate with a reduction of the number of the ectopic integrated sequences, which indicates that quelling appears to be monodirectional, as, once relieved, it cannot take place again, despite the continuing presence of some of theectopic sequences in the genome.
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Gene silencing in Neurospora crassa requires a protein homologous to RNA-dependent RNA polymerase.

TL;DR: The cloning of qde-1, the first cellular component of the gene-silencing mechanism to be isolated, defines a new gene family conserved among different species including plants, animals and fungi, which is similar to an RNA-dependent RNA polymerase found in the tomato.
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Cell-type-specific signatures of microRNAs on target mRNA expression

TL;DR: The hypothesis that miRNA expression broadly contributes to tissue specificity of mRNA expression in many human tissues is supported.