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Pubblicazioni antecedenti il 2004
Reliable Resequencing Identifies Mitochondrial Mutations Using
the mitoSEQr™ System
(Innovations 2008; 8:6-8)
Applied Biosystems – Customer Profile
Reliable Resequencing of Human Mitochondrial Genome to Identify
Mutations Linked to Mitochondrial Related Diseases
(Applied Biosystems; Application Note 2008)
Proceedings:
LANG M, PRADELLA L.M, TURCHETTI D, GASPARRE G. (2011). A BHD
patient with parotid gland oncocytoma with neither folliculin LOH
nor mtDNA mutations. In: 3rd Birt-Hogg-Dubé Symposium. Maastricht,
NL
PRADELLA L.M, LANG M, GASPARRE G., SERI M, TURCHETTI D (2011).
Recurrence of pancreatic cancer in a family with Birt-Hogg-Dubè
Syndrome (BHD). In: 3rd Birt-Hogg-Dubé Symposium. Maastricht,
NL
CAPRISTO M, GASPARRE G., KURELAC I, NICOLETTI G, LOLLINI PL,
RUGOLO M, PORCELLI AM (2010). Homoplasmic shift of ND1 mutation
reduces tumor growth in immunodeficient mice. In: GIBB. Bertinoro
di Romagna, 2010
PRADELLA LM, MARIANI E, GASPARRE G., AMATO L, LANZONI A, ISHIOKA
C, SAIJO K, ROSSI G, ROMEO G, TURCHETTI D (2010). A novel missense
mutation in the PTEN gene in a patient with multiple melanoma and
features of Cowden Syndrome. In: American Society of Human
Genetics. Washington DC, 2010
F.M. CALABRESE, M. LANG, D.SIMONE, G. MINECCIA, R. PIREDDA,
GASPARRE G., M. ATTIMONELLI (2010). Inter and intra species
comparative analyses of RHNumtS sequences. In: BITS. Bari, 2010
D. SIMONE, F.M. CALABRESE, G. MINECCIA, M. LANG, GASPARRE G., M.
ATTIMONELLI (2010). The human NumtS revised compilation, RHNumtS.2:
custom tracks, polymorphisms and validation by amplification and
sequencing. In: BITS. Bari, 2010
KURELAC I, PORCELLI AM, CAPRISTO M, ZUNTINI R, BARTOLETTI-STELLA
A, NICOLETTI G, NANNI P, DE GIOVANNI C, LOLLINI PL, ROMEO G,
GASPARRE G. (2010). Homoplasmic shift of ND1 mutation reduces tumor
growth in immunodeficient mice. In: ESHG. Goteborg, June 2010
TURCHETTI D, PRADELLA LM, ZUNTINI R, NERI I, MISCIALI C,
GASPARRE G., ROMEO G (2010). Decreased expression of PTEN
transcript level in a Cowden Syndrome patient without detectable
PTEN mutations. In: ESHG. Goteborg, June 2010
PRADELLA LM, AMATO L, MINIERI V, TURINETTO V, GIACHINO C,
ZUNTINI R, GASPARRE G., ROMEO G, TURCHETTI D (2010). A missense
mutation of the NBS1 gene in a patient with familial early-onset
breast cancer. In: ESHG. Goteborg, June 2010
KURELAC I, LANG M, ZUNTINI R, GASPARRE G., ROMEO G (2009).
Experimental and critical assessment of six methodological
approaches to quantify heteroplasmy of mitochondrial mutations. In:
European Human Genetics Conference. Vienna, 2009
RUGOLO M, GHELLI A, IOMMARINI L, MARIANI E, HOQUE M, GASPARRE
G., PORCELLI AM (2008). Bcl-2 antioxidant function in cells with
defective respiratory complex I. In: 53rd National Meeting of the
Italian Society of Biochemistry and Molecular Biology (SIB).
Riccione, 2008
M. LANG, GASPARRE G., L. IOMMARINI, A.M. PORCELLI ET AL (2008).
An inherited mitochondrial DNA disruptive mutation shifts to
homoplasmy in oncocytic tumor cells. In: American Society of Human
Genetics. Philadelphia, 2008
GASPARRE G., L. IOMMARINI, A.M. PORCELLI ET AL (2008). An
inherited mitochondrial DNA disruptive mutation shifts to
homoplasmy in oncocytic tumor cells. In: Euromit. Stoccolma,
2008
GASPARRE G., PENNISI LF, IOMMARINI L, PORCELLI AM, LANG M, FERRI
GG, KURELAC I, GHELLI A, BONORA E, CECCARELLI C, RUGOLO M, SALFI N,
ROMEO G, CARELLI V (2008). An inherited mitochondrial DNA
disruptive mutation preferentially selected in oncocytic tumor
cells. In: European Human Genetics Conference. Barcelona, 2008
PORCELLI AM, GHELLI A, MARIANI E, HOQUE M, GASPARRE G., ZANNA C,
RUGOLO M (2008). Actin cleavage in cells with defective respiratory
complex I is inhibited by Bcl-2 through an antioxidant function.
In: GIBB. Bari, 2008
GASPARRE G., A.M. PORCELLI, E. BONORA, L. F. PENNISI, M. TOLLER,
L. IOMMARINI, A. GHELLI, C. BETTS, V. CARELLI, M. RUGOLO, G.
TALLINI, G. ROMEO (2007). Disruptive mitochondrial DNA mutations in
complex I subunits are markers of oncocytic phenotype in thyroid
tumors. In: European Society Human Genetics. Nizza, FR, 2007
GASPARRE G., L. F. PENNISI, E. BONORA L. IOMMARINI, V. CARELLI,
G. TALLINI, G. ROMEO (2006). Mutazioni del mtDNA nell'oncocitoma
tiroideo ed in tumori non oncocitici: uno studio completo di
correlazione clinico-molecolare (Oral communication). In: Società
Italiana Genetica Umana. Venezia, 2006
GASPARRE G., E. BONORA, A. PORCELLI, A. BIONDI, A. GHELLI, V.
CARELLI, A. BARACCA, G. TALLINI, G. LENAZ, M. RUGOLO, G. ROMEO
(2006). Defective oxidative phosphorylation in thyroid oncocytic
carcinoma is associated with pathogenic mitochondrial DNA mutations
affecting complexes I and III (Oral communication). In: 2nd Milan
Thyroid Cancer Conference. Milano, 2006
E. BONORA, A. PORCELLI, GASPARRE G., A. BIONDI, A. GHELLI, G.
LENAZ, M. RUGOLO, G. ROMEO (2006). Defective oxidative
phosphorylation in thyroid oncocytic carcinoma is associated with
pathogenic mitochondrial DNA mutations affecting complexes I and
III. In: International Congress of Human Genetics. Brisbane,
2006
E. BONORA, C. EVANGELISTI, GASPARRE G., G. ROMEO (2006).
Familial Thyroid Tumors: mutation analysis of candidate genes
mapping to chromosome 19p13.2 genes and their relevance for the
oncocytic phenotype. In: International Congress of Human Genetics.
Brisbane, 2006
E. BONORA, GASPARRE G., A. PORCELLI, A. BIONDI, A. GHELLI, V.
CARELLI, A. BARACCA, G. TALLINI, G. LENAZ, M. RUGOLO, G. ROMEO
(2006). Mutation in the mitochondrial genome and their functional
relevance in thyroid oncocytoma. In: American Association for
Cancer Research. Washington, 2006
GASPARRE G., E. BONORA, F. SEBASTIANI, G. TALLINI, C. GODINOT,
O. HES, G. ROMEO (2006). Familial and sporadic Thyroid Tumors: new
variants identified in nuclear and mtDNA-encoded genes and their
relevance for the oxyphilic phenotype. In: American Association for
Cancer Research. Washington, 2006
GASPARRE G., E. BONORA, A. PORCELLI, A. BIONDI, A. GHELLI, V.
CARELLI, A. BARACCA, G. TALLINI, A. MARTINUZZI, G. LENAZ, M.
RUGOLO, G. ROMEO (2006). Defective oxidative phosphorylation in
thyroid oncocytoma is associated with pathogenic mitochondrial DNA
mutations affecting complexes I and III (Oral communication). In:
European Society of Human Genetics. Amsterdam, 2006
GASPARRE G., A. PORCELLI, L. F. PENNISI, E. BONORA, A. BIONDI,
A. GHELLI, V. CARELLI, L. IOMMARINI, A. BARACCA, G. TALLINI, G.
LENAZ, M. RUGOLO, G. ROMEO (2006). Pathogenic mitochondrial DNA
mutations in OXPHOS complexes and biochemical defective phenotype
in thyroid oncocytoma: unravelling the molecular mechanisms. In:
Sixth ESH: Mechanisms of cell death and disease: advances in
therapeutic intervention and drug development. Cascais, Portugal,
2006
GASPARRE G., E BONORA, A PORCELLI, A GHELLI, L IOMMARINI, A
BIONDI, G LENAZ, M RUGOLO, G. ROMEO (2005). Difetti nella
fosforilazione ossidativa nei tumori ossifilici della tiroide
correlano con nuove mutazioni in geni mitocondriali per subunità
della catena respiratoria. In: Società Italiana Genetica Umana.
Cagliari, 2005
BIONDI A, STANKOV K, GASPARRE G., FALASCA A, ROMEO G, LENAZ G
(2005). Mitochondrial activities of a cell line derived from
thyroid Hürthle cell tumors. In: GIBB, 2005
A. PORCELLI, GASPARRE G., E. BONORA, A. GHELLI, L. IOMMARINI, A.
BIONDI, A. BARACCA, M. RUGOLO, G. LENAZ, G. ROMEO (2005). Novel
mutations in mitochondrial respiratory complexes and their
functional relevance in thyroid oncocytoma. In: International
Conference on Mitochondria, from Molecular Insight to Physiology
and Pathology. Bari, 2005
GASPARRE G., BUDNICK K, MOFFATT T, FOTHERINGHAM J, MAYNE M (2003).
Microarray analysis of T-cells infected with HHV-6A (U1102) shows
inhibition of cell division and apoptosis and enhancement of cell
adhesion. In: 5th International Symposium of Neurovirology.
Baltimore. MD, USA, 2003
