Ernesto Di Mauro
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Ernesto Di Mauro has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
Rodolfo Negri
3 shared publicationsGiovanna Costanzo
Fondazione ‘Istituto Pasteur, Fondazione Cenci Bolognetti’ c/o Dipartimento di Genetica e Biologia Molecolare, Università La Sapienza, P. le Aldo Moro, 5 00185 Roma, Italy
2 shared publicationsRaffaele Saladino
2 shared publicationsLucia DI Marcotullio
Dipartimento di Genetica e Biologia Molecolare, Università La Sapienza, P. le Aldo Moro, 5 00185 Roma, Italy
1 shared publicationMemmo Buttinelli
Fondazione ‘Istituto Pasteur, Fondazione Cenci Bolognetti’ c/o Dipartimento di Genetica e Biologia Molecolare, Università La Sapienza, P. le Aldo Moro, 5 00185 Roma, Italy
1 shared publicationPietro Tagliatesta
1 shared publication
Latest Publications
- 1 September 1998
- Published by Elsevier in Journal of Molecular Biology
- Vol. 282 (1) , 43-57
Manganese water-soluble porphyrin senses DNA conformation
- 1 September 1998
- Published by Elsevier in Journal of Molecular Biology
- Vol. 282 (1) , 43-57
Manganese water-soluble porphyrin senses DNA conformation
- Open Access
- 1 July 1998
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 333 (1) , 65-69
Changing nucleosome positions in vivo through modification of the DNA rotational information
The effects of the rotational information of DNA in determining the in vivolocalization of nucleosomal core particles (ncps) have been studied in the Saccharomyces cerevisiae5 S rRNA repeat gene. The distribution of the phased series of flexibility signals present in this DNA has been altered by inserting in its centre a 25 bp tract. The effects of such alteration on the in vivodistribution of the helically phased, alternatively located ncps have been determined relative to a reference 21 bp insertion mutant. The results show that the answers provided in vitroand in vivoby the yeast 5 S rRNA gene sequence to specific modifications of the DNA rotational frame are similar, thus pointing to the relevance of DNA rotational information in vivo.
- 1 July 1998
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 333 (1) , 65-69
Open AccessChanging nucleosome positions in vivo through modification of the DNA rotational information
The effects of the rotational information of DNA in determining the in vivolocalization of nucleosomal core particles (ncps) have been studied in the Saccharomyces cerevisiae5 S rRNA repeat gene. The distribution of the phased series of flexibility signals present in this DNA has been altered by inserting in its centre a 25 bp tract. The effects of such alteration on the in vivodistribution of the helically phased, alternatively located ncps have been determined relative to a reference 21 bp insertion mutant. The results show that the answers provided in vitroand in vivoby the yeast 5 S rRNA gene sequence to specific modifications of the DNA rotational frame are similar, thus pointing to the relevance of DNA rotational information in vivo.
- Open Access
- 1 November 1996
- Published by Taylor & Francis in BioTechniques
- Vol. 21 (5) , 910-917
One-Step, One-Lane Chemical DNA Sequencing by N -Methylformamide in the Presence of Metal Ions
We report on a chemical method that allows DNA sequencing by a single reaction. It is based on treatment of 5′-end-labeled DNA with N-methylformamide in the presence of manganese. This method allows the manipulation of samples to be kept to a minimum and consists of a single chemical step that requires about 30 minutes to complete base degradation, phosphodiester bond cleavage and denaturation. Examples of one-treatment, one-lane DNA sequencing of both radioactively and fluorescently 5′-end-labeled DNAs are reported.
- 1 November 1996
- Published by Taylor & Francis in BioTechniques
- Vol. 21 (5) , 910-917
Open AccessOne-Step, One-Lane Chemical DNA Sequencing by N -Methylformamide in the Presence of Metal Ions
We report on a chemical method that allows DNA sequencing by a single reaction. It is based on treatment of 5′-end-labeled DNA with N-methylformamide in the presence of manganese. This method allows the manipulation of samples to be kept to a minimum and consists of a single chemical step that requires about 30 minutes to complete base degradation, phosphodiester bond cleavage and denaturation. Examples of one-treatment, one-lane DNA sequencing of both radioactively and fluorescently 5′-end-labeled DNAs are reported.