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Curriculum Vitae
INFORMAZIONI PERSONALI
Stefania Petrini
Stefania Petrini
Via Cremuzio Cordo 43, 00136 Roma
+39-3391458551
[email protected]
Data di nascita 20/11/1964
Nazionalità Italiana
POSIZIONE RICOPERTA
Responsabile del Servizio di Microscopia Laser Confocale
ESPERIENZA
PROFESSIONALE
2007-presente
Responsabile della Core Facility di Microscopia Laser Confocale, Laboratori di
Ricerca dell’Ospedale Pediatrico Bambino Gesu’ (OPBG) di Roma
2007-2005
Contratto di ricerca (Post Doctoral Fellowship) nell’ambito del “Research Fellows
Programme”, presso i Laboratori di Ricerca dell’OPBG di Roma.
Supervisore: Dott. Enrico Bertini
2005-2003
Contratto di ricerca (Post Doctoral Fellowship) in: “Autosomal dominant myopathies
in the general population: clinical-molecular innovative protocols and pathogenetic
mechanisms”. Resp: Dott. Enrico Bertini
2003-2000
Contratto di ricerca della Comunità Europea (Titolo del progetto: “Genetic
resolution of Myopathies: European Cluster”) svolto presso l’Unità di Medicina
Molecolare e Neuromuscolare, dell’OPBG di Roma. Resp: Dott. Enrico Bertini
1998-1998
Contratto di ricerca presso la Sezione di Neurofisiopatologia degli Istituti Ortopedici
Rizzoli (Bologna) nell’ambito del progetto “Genetica delle malattie
neuromuscolari” (Resp.le: Dott. Luciano Merlini) in collaborazione con il
Laboratorio di Biologia Cellulare e Microscopia Elettronica (Direttore: Prof. Nadir
M. Maraldi; Istituto di Ricerca “Codivilla Putti”, II.OO.RR.).
ISTRUZIONE E
FORMAZIONE
2010
Conseguimento del Titolo della Scuola di Specializzazione in “Patologia
Clinica, Indirizzo Tecnico” (direttore Prof. G. Isacchi), presso l’Universita’
degli Studi di Tor Vergata. AA. 2006-20110. Tesi discussa il 24/11/2010 con
voti 50/50 con lode
1995
Conseguimento del titolo di Dottorato di Ricerca in Biologia Animale (AA 1992-1995).
Dip.to di Biologia Evoluzionistica e Sperimentale, Università degli Studi Bologna. Tesi
discussa presso l'Università degli Studi di Milano (il 24/10/1995).
1991
Laurea in Scienze Biologiche (AA. 1984-1990) conseguita presso l'Università degli
Studi di Bologna (11/03/1991). Punteggio di laurea: 110 su 110
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Curriculum Vitae
COMPETENZE PERSONALI
CAMPI DI INTERESSE
Lingua madre
Altre lingue
Inglese
Competenze comunicative
Competenze organizzative e
gestionali
Competenze professionali
Competenze informatiche
Patente di guida
Stefania Petrini
Microscopia Laser Confocale; Microscopia ottica a campo chiaro e a fluorescenza;
Microscopia a microdissezione; Microscopia Elettronica a Trasmissione.
Analisi di immagine quantitativa e Citometria. Scanner Digitale automatizzato.
Biologia cellulare, Istologia, Citologia, Immunoistochimica, Immunocitochimica,
Morfologia, Analisi Ultrastrutturale, Malattie neuromuscolari e malattie rare.
Italiano
COMPRENSIONE
PRODUZIONE
SCRITTA
PARLATO
Ascolto
Lettura
Interazione
Produzione orale
buono
buono
buono
buono
buono
buone competenze comunicative in ambito biomedico, acquisite nel corso degli studi
universitari e degli anni di attività lavorativa presso centri, istituti di ricerca e università
buone competenze organizzative acquisite nel corso dell’attività di ricerca e come
responsabile del servizio di ricerca di Microscopia Laser Confocale
ottima conoscenza delle tecniche di colorazione per l’Istologia, l’Istoenzimatica,
l’Istochimica, delle tecniche di Immunocitochimica e Immunoistochimica
(immunoperossidasi, immunofosfatasi alcalina, immunofluorescenza) e di
allestimento di preparati per l’esame ultrastrutturale e immunocitochimico
buona padronanza degli strumenti Microsoft Office, di software di acquisizione e/o di
analisi di immagine (LAS X, IAS, FV1000, IMARIS; Metamorph, ImageJ, Adobe Photoshop)
Patente di guida B
Pubblicazioni
(Allegato 1)
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Curriculum Vitae
Capitoli di libri
Stefania Petrini
Petrini S., D’Oria V., Piemonte F. (2015) “Intracellular distribution of glutathionylated
proteins in cultured dermal fibroblasts by immunofluorescence”. Methods in Molecular
Biology, 1208:395-408.
Petrini S, D’Amico A, Rizza T, Coccetti M, Carrozzo R, Gualandi F, Bertini E.
(2010). “Two and three dimensional imaging in confocal laser scanning microscopy application for collagen VI defect studies”. In: Microscopy: Science, Technology,
Applications and Education", Microscopy Book Series, Vol. 4, pp 649-657, published
by Formatex Research Center, Zurbaran, Badajoz, Spain (Editors Antonio MéndezVilas and Jesús Díaz Álvarez).
Petrini S, Piemonte F, Passarelli C, Bertini E (2010). “Epifluorescence, confocal
laser microscopy and colocalization analyses in the study of protein glutathionylation
in primary cultured fibroblasts and in their in situ extracted matrix”. In: Microscopy:
Science, Technology, Applications and Education", Microscopy Book Series, Vol. 4,
pp 641-648, published by Formatex Research Center, Zurbaran, Badajoz, Spain
(Editors Antonio Méndez-Vilas and Jesús Díaz Álvarez).
F. Marinelli, F. Bersani, S. Santi, M. Riccio, S. Petrini, A. Valmori, N.M. Maraldi.
(1999). “Intramembrane Proteins Clustering Induced by 50 Hz Pulsed Magnetic
Fields is Reverted to a Random Distribution in the Absence of the Field Exposure”.
In book: Electricity and Magnetism in Biology and Medicine, pp.573-576.
Partecipazione a progetti di
ricerca e network
2014-2016. Referente nello studio Istologico/morfometrico nel trial di fase II
DSC/11/2357/43: “A two part study to assess the safety and tolerability,
pharmacokinetics, and effects on histology and different clinical parameters of
Givinostat in ambulant children with Duchenne Muscular Dystrophy”. Coordinatore:
Dr. Enrico Bertini.
2014-2009 Grants of Cystinosis Research Network and Cystinosis Research
Foundation (F. Emma).
2013. Ricerca Finalizzata: “Inducible pluripotent stem (iPS) cell-derived human
astrocytes as a new disease model to shed light into the molecular pathogenesis of
megalencephalic leukoencephalopathy with subcortical cysts (MLC)”. Grant to Dr.
Enrico Bertini and Dr. Claudia Compagnucci, GR-2013-02355882)
2011. Italian Ministry for University and Research, FIRB project n.RBNE01JJ45_005).
2010. Telethon Foundation-Italy “Transglutaminase 2 in insulin secretion:
mitochondrial substrates and the role of 37 kD isoform“, (grant no GGP09147 to
Ornella Massa)
2010. Ministero Italiano della Salute: grant GR-2010-2309463 “ Role of riboflavin
transporters in motor neurone diseases: genetic analysis of the Brown Vialetto Van
Laere and Fazio Londe syndromes and development of potential treatment strategies
for motor neurone diseases”. (Dr. Enrico Bertini).
2009. Membro del Network Italiano delle Laminopatie.
2009. European Leukodystrophy Association (ELA) Research Foundation:
“Development of trafficking based therapeutic strategies to restore MLC1 membrane
protein expression in MLC affected patients”, grant ELA 2009-002C5A to Elena
Ambrosini e Fabrizio De Benedetti).
2009-2007. Italian Telethon Project "Collagen VI myopathies: from mouse theraphy to
human trials" (grant n. GGP04113 and 1201, Dr. Enrico Bertini);
2005-2003. Ministero Italiano della Salute: “Autosomal dominant myopathies in the
general population: clinical-molecular innovative protocols and pathogenetic
mechanisms” (project n. 83/2001; Dr. Enrico. Bertini);
2003-2000. European Community project: "Genetic resolution of Myopathies:
European Cluster” (“Myo-cluster” project: QLG1-199-00870, Dr. Enrico Bertini).
2000-2003. Italian Telethon Project "Collagen VI myopathies: from mouse theraphy to
human trials" (grant n. GGP04113 and 120; Dr. Enrico Bertini);
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Curriculum Vitae
Partecipazione a
Congressi e Worhshops
Stefania Petrini
Congresso Nazionale AIM (Associazione Italiana di Miologia) Lecce 8-11 giugno 2016.
D’Amico A., Fattori F., Gualandi F.,Tasca G., Petrini S., D’Oria V., Catteruccia M., Niceta
M., Tartaglia M., Ferlini A., Bertini E. “De novo dominant mosaic mutations in collagen 6
genes: uncommon cause of Bethlem and Ullrich myopathies that may be missed by
sanger sequencing”. Poster presentation.
Nikon Practical Workshop. IHC Digital Image Analysis. Roma, 5 Maggio 2016.
S. Petrini. “Acquisizione di immagini a fuorescenza con scanner Hamamatsu”.
Complesso Ospedaliero San Giovanni Addolorata, Roma.
15th International congress of the WMS. Kumamoto, 13-16 October, 2010.
A. D’Amico, S. Petrini, F. Fattori, M. Verardo, R. Boldrini, F. Renaldo, V. Nigro, E. Bertini.
“Clinical, histological and molecular genetic features of a congenital severe infantile
rimmed vacuolar myopathy”. Conference paper in Neuromuscular Disorders October
2010
14th International congress of the WMS. Geneva 9-12 september 2009.
S. Petrini. P. Sabatelli, A. d’Amico, F. Gualandi, P. Braghetta, M. Coccetti, T. Rizza, R.
Carrozzo, G. Pepe, P. Bonaldo, A. Ferlini, L. Merlini, E. Bertini. “Abnormal elastin
deposits and altered organization of elastic fibers in collagen VI related disorders”.
Conference Paper in Neuromuscular Disorders Oct 2009.
13th International congress of the WMS. Newcastle upon Tyne, UK, 29 Sept-2
October 2008
M. Mirabella, R. Charlton, E.M. Valente, S. Petrini, A. d’Amico, M. Roberts, E. Ricci, F.
De Benedett. “Partial caveolin 3 deficiency in acquired rippling muscle disease”.
Conference Paper in Neuromuscular Disorders October 2008
International Society for Hearth Research (ISHR) World Congress:
Electrophysiology from bench to bedside. Bologna 22-25 June 2007.
S. Marston, E. Bertini, A. Porfirio, C. Graziano, S. Petrini, A. D'Amico, F.M. Santorelli, G.
Pacileo, C. Sewry. “Fatal hypertrophic cardiomyopathy and nemaline myopathy
associated with ACTA1 K336E mutation”. Conference Paper in Journal of Molecular
and Cellular Cardiology 42(6):S73. June 2007.
12th International Congress of the World-Muscle-Society. Taormina, Italy, 17-20
October 2007.
d’Amico, S. Petrini, C. Bruno, R. Boldrini, M. Scarpelli, E. Bertini. “Clinical heterogeneity
of autophagic vacuolar myopathies”. Conference Paper in Neuromusc. Disorders Oct
2007.
11th International Congress of the World-Muscle-Society. Bruges, Belgium 4-7
October 2006.
S. Petrini, A. d’Amico, P. Sale, L. Lucarini, P. Sabatelli, B. Giusti,M. Verardo, R.
Carrozzo, E. Mattioli,M. Scarpelli,M.L. Chu, G. Pepe, M.A.Russo, E. Bertini. “Confocal
imaging and electron microscopy analysis to identify secondary collagen VI defects”.
Conference Paper in Neuromuscular Disorders Oct 2006.
11th International Congress of the World-Muscle-Society. Bruges, Belgium 4-7
October 2006.
P. Sabatelli, Y. Zou, S. Squarzoni, C. Bonneman, L. Merlini, G. Pepe, B. Giusti, S.
Petrini, E. Bertini, D. Sudano, M.L. Chu, N.M. Maraldi. “Effect on collagen VI extracellular
assembly of COL6A1 and COL6A2 C-terminal mutations in Ullrich congenital muscular
dystrophy”. Conference Paper in Neur. Disorders Oct 2006.
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Curriculum Vitae
Stefania Petrini
26th International Congress of the International-Academy-of-Pathology.
Montreal, 16-21 September 2006. P. Francalanci, F. Zara, C. Bruno, L. Ballerini, S.
Petrini, M. Verardo, F. Callea, E. Bertini. “Danon disease: A very unsual cause of
hypertrophic cardiomyopathy. Pathological features and molecular analyses on
explanted heart”. Conference Paper in Modern Pathology, Sept. 2006
10th International Congress of the World-Muscle-Society. Iguassu Falls, Brazil,
28 September-1 October 2005.
D'Amico, S Benedetti, S. Petrini, R Boldrini, M. Ferrari, I Menditto, L Salvato, L
Golfarb, E. Bertini. “Heterozygous de novo missense mutation in lamin A/C gene
presenting as early onset myofibrillar myopathy”. Conference Paper in Neuromusc.
Disorders Oct. 2005
10th International Congress of the World-Muscle-Society. Iguassu Falls, Brazil,
28 September-1 October 2005.
E. Bertini, B Porfirio, C. Graziano, S. Petrini, A. D'Amico, A. Tessa, G Pacileo, C
Sewry, JJ Feng, S. Marston. “A mutant actin (Lys336Glu) in a patient with nemaline
myopathy and hypertrophic cardiomyopathy”. Conference Paper in Neuromusc.
Disorders Oct. 2005
9th International Congress of the World-Muscle-Society. Gotenborg, Sweden, 1-4
September 2004.
E. Bertini, M Bado, P. Broda, D. Cassandrini, C. Dionisi-Vici, L. Ballerini, S. Petrini, R
Boldrini , A. D'Amico, C. Minetti, FM Santorelli, C. Bruno. “Unusual phenotype in a
patient with infantile onset Danon disease”. Conference Paper in Neur.Disor. Sept.
2004
Dati personali
Autorizzo il trattamento dei miei dati personali ai sensi del Decreto Legislativo 30 giugno 2003,
n. 196 "Codice in materia di protezione dei dati personali”.
Roma, li 01/12/2016
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Curriculum Vitae
Stefania Petrini
Allegato 1
Pubblicazioni (ultimi 5 anni)
1: Compagnucci C, Piermarini E, Sferra A, Borghi R, Niceforo A, Petrini S, Piemonte F, Bertini E. Cytoskeletal dynamics during in vitro
neurogenesis of induced pluripotent stem cells (iPSCs). Mol Cell Neurosci. 2016 Dec;77:113-124.
2: Taranta A, Bellomo F, Petrini S, Polishchuk E, De Leo E, Rega LR, Pastore A, Polishchuk R, De Matteis MA, Emma F. CystinosinLKG rescues cystine accumulation and decreases apoptosis rate in cystinotic proximal tubular epithelial cells. Pediatr Res. 2016 Oct 19.
3: Bettica P, Petrini S, D'Oria V, D'Amico A, Catteruccia M, Pane M, Sivo S, Magri F, Brajkovic S, Messina S, Vita GL, Gatti B,
Moggio M, Puri PL, Rocchetti M, De Nicolao G, Vita G, Comi GP, Bertini E, Mercuri E. Histological effects of givinostat in boys with
Duchenne muscular dystrophy. Neuromuscul Disord. 2016 Oct;26(10):643-649.
4: Piermarini E, Cartelli D, Pastore A, Tozzi G, Compagnucci C, Giorda E, D'Amico J, Petrini S, Bertini E, Cappelletti G, Piemonte F.
Frataxin silencing alters microtubule stability in motor neurons: implications for Friedreich's ataxia. Hum Mol Genet. 2016 Aug 11. pii:
ddw260.
5: Bellomo F, Taranta A, Petrini S, Venditti R, Rocchetti MT, Rega LR, Corallini S, Gesualdo L, De Matteis MA, Emma F. CarboxylTerminal SSLKG Motif of the Human Cystinosin-LKG Plays an Important Role in Plasma Membrane Sorting. PLoS One. 2016 May
5;11(5):e0154805
6: Lanciotti A, Brignone MS, Visentin S, De Nuccio C, Catacuzzeno L, Mallozzi C, Petrini S, Caramia M, Veroni C, Minnone G,
Bernardo A, Franciolini F, Pessia M, Bertini E, Petrucci TC, Ambrosini E. Megalencephalic leukoencephalopathy with subcortical cysts
protein-1 regulates epidermal growth factor receptor signaling in astrocytes. Hum Mol Genet. 2016 Apr 15;25(8):1543-58.
7: Panera N, Gnani D, Piermarini E, Petrini S, Bertini E, Nobili V, Pastore A, Piemonte F, Alisi A. High concentrations of H2O2 trigger
hypertrophic cascade and phosphatase and tensin homologue (PTEN) glutathionylation in H9c2 cardiomyocytes. Exp Mol Pathol. 2016
Feb;100(1):199-206.
8: Ceccarelli S, Panera N, Mina M, Gnani D, De Stefanis C, Crudele A, Rychlicki C, Petrini S, Bruscalupi G, Agostinelli L, Stronati L,
Cucchiara S, Musso G, Furlanello C, Svegliati-Baroni G, Nobili V, Alisi A. LPS-induced TNF-α factor mediates pro-inflammatory and
pro-fibrogenic pattern in non-alcoholic fatty liver disease. Oncotarget. 2015 Dec 8;6(39):41434-52.
9: Peverelli L, Testolin S, Villa L, D'Amico A, Petrini S, Favero C, Magri F, Morandi L, Mora M, Mongini T, Bertini E, Sciacco M,
Comi GP, Moggio M. Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophy. Neurology. 2015
Nov 24;85(21):1886-93
10: Compagnucci C, Petrini S, Higuraschi N, Trivisano M, Specchio N, Hirose S, Bertini E, Terracciano A. Characterizing PCDH19 in
human induced pluripotent stem cells (iPSCs) and iPSC-derived developing neurons: emerging role of a protein involved in controlling
polarity during neurogenesis. Oncotarget. 2015 Sep 29;6(29):26804-13.
11: Peca D, Boldrini R, Johannson J, Shieh JT, Citti A, Petrini S, Salerno T, Cazzato S, Testa R, Messina F, Onofri A, Cenacchi G,
Westermark P, Ullmann N, Cogo P, Cutrera R, Danhaive O. Clinical and ultrastructural spectrum of diffuse
lung disease associated with surfactant protein C mutations. Eur J Hum Genet. 2015 Aug;23(8):1033-41.
12: Cifaldi L, Romania P, Falco M, Lorenzi S, Meazza R, Petrini S, Andreani M, Pende D, Locatelli F, Fruci D. ERAP1 regulates natural
killer cell function by controlling the engagement of inhibitory receptors. Cancer Res. 2015 Mar
1;75(5):824-34.
13: Masotti A, Celluzzi A, Petrini S, Bertini E, Zanni G, Compagnucci C. Aged iPSCs display an uncommon mitochondrial appearance
and fail to undergo in vitro neurogenesis. Aging (Albany NY). 2014 Dec;6(12):1094-108.
14: Compagnucci C, Barresi S, Petrini S, Bertini E, Zanni G. Rho-kinase signaling controls nucleocytoplasmic shuttling of class IIa
histone deacetylase (HDAC7) and transcriptional activation of orphan nuclear receptor NR4A1. Biochem Biophys Res Commun. 2015
Apr 3;459(2):179-83.
15: Colucci M, Stöckmann H, Butera A, Masotti A, Baldassarre A, Giorda E, Petrini S, Rudd PM, Sitia R, Emma F, Vivarelli M.
Sialylation of N-linked glycans influences the immunomodulatory effects of IgM on T cells. J Immunol. 2015 Jan 1;194(1):151-7
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Curriculum Vitae
Stefania Petrini
16: Petrini S, D'Oria V, Piemonte F. Intracellular distribution of glutathionylated proteins in cultured dermal fibroblasts by
immunofluorescence. Methods Mol Biol. 2015;1208:395-408.
17: Prencipe G, Minnone G, Strippoli R, De Pasquale L, Petrini S, Caiello I, Manni L, De Benedetti F, Bracci-Laudiero L. Nerve growth
factor downregulates inflammatory response in human monocytes through TrkA. J Immunol. 2014 Apr 1;192(7):3345-54.
18: Hedberg C, Niceta M, Fattori F, Lindvall B, Ciolfi A, D'Amico A, Tasca G, Petrini S, Tulinius M, Tartaglia M, Oldfors A, Bertini E.
Childhood onset tubular aggregate myopathy associated with de novo STIM1 mutations. J Neurol. 2014
May;261(5):870-6.
19: Brignone MS, Lanciotti A, Visentin S, De Nuccio C, Molinari P, Camerini S, Diociaiuti M, Petrini S, Minnone G, Crescenzi M,
Laudiero LB, Bertini E, Petrucci TC, Ambrosini E. Megalencephalic leukoencephalopathy with subcortical cysts protein-1 modulates
endosomal pH and protein trafficking in astrocytes: relevance to MLC disease pathogenesis. Neurobiol Dis. 2014 Jun;66:1-18.
20: Prencipe G, Caiello I, Cherqui S, Whisenant T, Petrini S, Emma F, De Benedetti F. Inflammasome activation by cystine crystals:
implications for the pathogenesis of cystinosis. J Am Soc Nephrol. 2014 Jun;25(6):1163-9.
21: Sileno S, D'Oria V, Stucchi R, Alessio M, Petrini S, Bonetto V, Maechler P, Bertuzzi F, Grasso V, Paolella K, Barbetti F, Massa O.
A possible role of transglutaminase 2 in the nucleus of INS-1E and of cells of human pancreatic islets. J Proteomics. 2014 Jan 16;96:31427.
22: Citti A, Peca D, Petrini S, Cutrera R, Biban P, Haass C, Boldrini R, Danhaive O. Ultrastructural characterization of genetic diffuse
lung diseases in infants and children: a cohort study and review. Ultrastruct Pathol. 2013
Oct;37(5):356-65.
23: Petrini S, Minnone G, Coccetti M, Frank C, Aiello C, Cutarelli A, Ambrosini E, Lanciotti A, Brignone MS, D'Oria V, Strippoli R, De
Benedetti F, Bertini E, Bracci-Laudiero L. Monocytes and macrophages as biomarkers for the diagnosis of megalencephalic
leukoencephalopathy with subcortical cysts. Mol Cell Neurosci. 2013 Sep;56:307-21
24: Alisi A, Ceccarelli S, Panera N, Prono F, Petrini S, De Stefanis C, Pezzullo M, Tozzi A, Villani A, Bedogni G, Nobili V. Association
between Serum Atypical Fibroblast Growth Factors 21 and 19 and Pediatric Nonalcoholic Fatty Liver Disease. PLoS One. 2013 Jun
26;8(6):e67160
25: Martoni E, Petrini S, Trabanelli C, Sabatelli P, Urciuolo A, Selvatici R, D'Amico A, Falzarano S, Bertini E, Bonaldo P, Ferlini A,
Gualandi F. Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1
gene C-terminal domain: a case report. BMC Med Genet. 2013 Jun 5;14:59.
26: D'Oria V, Petrini S, Travaglini L, Priori C, Piermarini E, Petrillo S, Carletti B, Bertini E, Piemonte F. Frataxin deficiency leads to
reduced expression and impaired translocation of NF-E2-related factor (Nrf2) in cultured motor neurons. Int J Mol Sci. 2013 Apr
10;14(4):7853-65
27: Budoni M, Fierabracci A, Luciano R, Petrini S, Di Ciommo V, Muraca M. The immunosuppressive effect of mesenchymal stromal
cells on B lymphocytes is mediated by membrane vesicles. Cell Transplant. 2013;22(2):369-79.
28: Martinelli D, Travaglini L, Drouin CA, Ceballos-Picot I, Rizza T, Bertini E, Carrozzo R, Petrini S, de Lonlay P, El Hachem M,
Hubert L, Montpetit A, Torre G, Dionisi-Vici C. MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate
therapy. Brain. 2013 Mar;136(Pt 3):872-81.
29: Ciccolella M, Corti S, Catteruccia M, Petrini S, Tozzi G, Rizza T, Carrozzo R, Nizzardo M, Bordoni A, Ronchi D, D'Amico A, Rizzo
C, Comi GP, Bertini E. Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutations. J Med
Genet. 2013 Feb;50(2):104-7.
30: Alisi A, Arciello M, Petrini S, Conti B, Missale G, Balsano C. Focal adhesion kinase (FAK) mediates the induction of pro-oncogenic
and fibrogenic phenotypes in hepatitis C virus (HCV)-infected cells. PLoS One. 2012;7(8):e44147.
31: Benedetti S, Bernasconi P, Bertini E, Biagini E, Boriani G, Capanni C, Carboni N, Cenacchi G, Columbaro M, D'Adamo M, D'Amico
A, D'Apice MR, Fontana M, Gambineri A, Lattanzi G, Liguori R, Maraldi NM, Mazzanti L, Mercuri E, Mongini T, Morandi LO, Neri I,
Nigro G, Novelli G, Ortolani M, Pasquali R, Pini A Petrini S, Politano L, Previtali S, Pucci L, Rapezzi C, Ricci G, Rodolico C, Sbraccia
P, Scarano E, Siciliano G, Squarzoni S, Toscano A, Vercelli L, Ziacchi M. The empowerment of translational research: lessons from
laminopathies. Orphanet J Rare Dis. 2012 Jun 12;7:37.
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Stefania Petrini
32: Petrini S, Passarelli C, Pastore A, Tozzi G, Coccetti M, Colucci M, Bianchi M, Carrozzo R, Bertini E, Piemonte F. Protein
glutathionylation in cellular compartments: a constitutive redox signal. Redox Rep. 2012;17(2):63-71.
33: Taranta A, Petrini S, Citti A, Boldrini R, Corallini S, Bellomo F, Levtchenko E, Emma F. Distribution of cystinosin-LKG in human
tissues. Histochem Cell Biol. 2012 Aug;138(2):351-63.
34: Bertini E, D'Amico A, Gualandi F, Petrini S. Congenital muscular dystrophies: a brief review. Semin Pediatr Neurol. 2011
Dec;18(4):277-88. Review.
35: Peca D, Petrini S, Tzialla C, Boldrini R, Morini F, Stronati M, Carnielli VP, Cogo PE, Danhaive O. Altered surfactant homeostasis
and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect. Respir Res. 2011 Aug 25;12:115.
36: Alisi A, Bruscalupi G, Pastore A, Petrini S, Panera N, Massimi M, Tozzi G, Leoni S, Piemonte F, Nobili V. Redox homeostasis and
posttranslational modifications/activity of phosphatase and tensin homolog in hepatocytes from rats with diet-induced hepatosteatosis. J
Nutr Biochem. 2012 Feb;23(2):169-78.
37: Lo HP, Bertini E, Mirabella M, Domazetovska A, Dale RC, Petrini S, D'Amico A, Valente EM, Barresi R, Roberts M, Tozzi G, Tasca
G, Cooper ST, Straub V, North KN. Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia
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