Mara Doimo
发表
M. Andréasson,
Sjoerd Wanrooij,
Valentin L'Hôte,
2022,
Chemical science.
G. Basso,
E. Trevisson,
L. Salviati,
2013,
Human mutation.
E. Trevisson,
L. Salviati,
M. A. Desbats,
2015,
Journal of Inherited Metabolic Disease.
V. Pertegato,
S. Dimauro,
E. Schon,
2012,
Orphanet Journal of Rare Diseases.
C. Angelini,
P. Navas,
E. Trevisson,
2015,
European Journal of Human Genetics.
P. Navas,
G. Basso,
E. Trevisson,
2016,
Human molecular genetics.
E. Trevisson,
L. Salviati,
M. A. Desbats,
2014,
Molecular Syndromology.
V. Pertegato,
P. Navas,
G. Basso,
2009,
The Journal of Biological Chemistry.
P. Navas,
M. Bergdoll,
F. Hildebrandt,
2014,
Biochimica et biophysica acta.
P. Navas,
M. Bergdoll,
F. Hildebrandt,
2013
.
L. Salviati,
M. A. Desbats,
I. Bellezza,
2018,
Biochimica et biophysica acta. Molecular basis of disease.
V. Pertegato,
S. Dimauro,
P. Navas,
2012,
Journal of Medical Genetics.
E. Trevisson,
L. Salviati,
Mara Doimo,
2014
.
A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriL
M. Zeviani,
A. Reyes,
M. Falkenberg,
2018,
Nucleic acids research.
E. Bertini,
V. Petruzzella,
R. Carrozzo,
2013,
Journal of Inherited Metabolic Disease.
P. Navas,
E. Trevisson,
A. Casarín,
2014,
Biochimica et biophysica acta.
P. Navas,
E. Trevisson,
A. Casarín,
2014
.
G. Basso,
E. Trevisson,
L. Salviati,
2018,
Biochimica et biophysica acta. Bioenergetics.
K. Chand,
M. Hedenström,
Rajendra Kumar,
2020,
Journal of the American Chemical Society.
Sjoerd Wanrooij,
A. Pfeiffer,
Paulina H. Wanrooij,
2020
.
V. Pertegato,
Y. Raphael,
H. Prokisch,
2011,
The Journal of clinical investigation.
E. Trevisson,
L. Salviati,
A. Burlina,
2012,
Journal of Inherited Metabolic Disease.
Marcela Dávila López,
J. Pohjoismäki,
S. Goffart,
2022,
bioRxiv.
R. Tenconi,
E. Trevisson,
M. Clementi,
2009,
American journal of medical genetics. Part A.
V. Pertegato,
P. Navas,
G. Basso,
2008,
Biochemical and biophysical research communications.
E. Bertini,
R. Carrozzo,
E. Lamantea,
2017,
Orphanet Journal of Rare Diseases.
L. Blanco,
Sjoerd Wanrooij,
Kazutoshi Kasho,
2020,
bioRxiv.
P. Navas,
E. Trevisson,
L. Salviati,
1993
.
P. Navas,
F. Hildebrandt,
S. Ashraf,
2017,
Human mutation.