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Items: 1 to 50 of 206

1.

Potential role of Anitschkow cells in cardiovascular disease in human and veterinary medicine: A review of the literature.

Colombino E, Biasato I, Biasibetti E, Sereno A, Chiappino L, Evangelista R, Cenacchi G, Guarda F, Capucchio MT.

Anat Histol Embryol. 2019 May;48(3):201-206. doi: 10.1111/ahe.12433. Epub 2019 Feb 17. Review.

PMID:
30772944
2.

The use of an acellular matrix derived from human dermis for the treatment of full-thickness skin wounds.

Bondioli E, Purpura V, Orlandi C, Carboni A, Minghetti P, Cenacchi G, De Luca G, Capirossi D, Nigrisoli E, Melandri D.

Cell Tissue Bank. 2019 Jun;20(2):183-192. doi: 10.1007/s10561-019-09755-w. Epub 2019 Feb 14.

PMID:
30767153
3.

The clinical spectrum of CASQ1-related myopathy.

Semplicini C, Bertolin C, Bello L, Pantic B, Guidolin F, Vianello S, Catapano F, Colombo I, Moggio M, Gavassini BF, Cenacchi G, Papa V, Previtero M, Calore C, Sorarù G, Minervini G, Tosatto SCE, Stramare R, Pegoraro E.

Neurology. 2018 Oct 23;91(17):e1629-e1641. doi: 10.1212/WNL.0000000000006387. Epub 2018 Sep 26.

4.

Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts.

Milev MP, Graziano C, Karall D, Kuper WFE, Al-Deri N, Cordelli DM, Haack TB, Danhauser K, Iuso A, Palombo F, Pippucci T, Prokisch H, Saint-Dic D, Seri M, Stanga D, Cenacchi G, van Gassen KLI, Zschocke J, Fauth C, Mayr JA, Sacher M, van Hasselt PM.

J Med Genet. 2018 Nov;55(11):753-764. doi: 10.1136/jmedgenet-2018-105441. Epub 2018 Aug 17.

PMID:
30120216
5.

A Rare Case of Systemic AL Amyloidosis with Muscle Involvement: A Misleading Diagnosis.

Accardi F, Papa V, Capozzi AR, Capello GL, Verga L, Mancini C, Martella E, Costa R, Notarfranchi L, Dalla Palma B, Aversa F, Pietrini V, Cenacchi G, Giuliani N.

Case Rep Hematol. 2018 Jan 31;2018:9840405. doi: 10.1155/2018/9840405. eCollection 2018.

6.

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy.

Caporali L, Iommarini L, La Morgia C, Olivieri A, Achilli A, Maresca A, Valentino ML, Capristo M, Tagliavini F, Del Dotto V, Zanna C, Liguori R, Barboni P, Carbonelli M, Cocetta V, Montopoli M, Martinuzzi A, Cenacchi G, De Michele G, Testa F, Nesti A, Simonelli F, Porcelli AM, Torroni A, Carelli V.

PLoS Genet. 2018 Feb 14;14(2):e1007210. doi: 10.1371/journal.pgen.1007210. eCollection 2018 Feb.

7.

Spontaneously occurring intramural coronary arteriosclerosis in regularly slaughtered veal calves and beef cattle: a screening study about prevalence and histopathological features.

Biasato I, Biasibetti E, Biagini D, Bruatto G, Cenacchi G, Guarda F, Capucchio MT.

J Vet Cardiol. 2018 Feb;20(1):55-63. doi: 10.1016/j.jvc.2017.12.001. Epub 2018 Jan 20.

PMID:
29371083
8.

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy.

Gramegna LL, Pisano A, Testa C, Manners DN, D'Angelo R, Boschetti E, Giancola F, Pironi L, Caporali L, Capristo M, Valentino ML, Plazzi G, Casali C, Dotti MT, Cenacchi G, Hirano M, Giordano C, Parchi P, Rinaldi R, De Giorgio R, Lodi R, Carelli V, Tonon C.

AJNR Am J Neuroradiol. 2018 Mar;39(3):427-434. doi: 10.3174/ajnr.A5507. Epub 2018 Jan 18.

9.

Subpopulations of dermal skin fibroblasts secrete distinct extracellular matrix: implications for using skin substitutes in the clinic.

Ghetti M, Topouzi H, Theocharidis G, Papa V, Williams G, Bondioli E, Cenacchi G, Connelly JT, Higgins CA.

Br J Dermatol. 2018 Aug;179(2):381-393. doi: 10.1111/bjd.16255. Epub 2018 May 16.

10.

Corrigendum to "A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy" [J. Neurol. Sci. 381C (2017) 209-212].

Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G.

J Neurol Sci. 2018 Feb 15;385:238. doi: 10.1016/j.jns.2017.12.002. Epub 2017 Dec 15. No abstract available.

PMID:
29254810
11.

Histological and ultrastructural evaluation of human decellularized matrix as a hernia repair device.

Ghetti M, Papa V, Deluca G, Purpura V, Ruscelli P, Melandri D, Capirossi D, Nigrisoli E, Minghetti P, Bondioli E, Cenacchi G.

Ultrastruct Pathol. 2018 Jan-Feb;42(1):32-38. doi: 10.1080/01913123.2017.1365788. Epub 2017 Dec 1.

PMID:
29192810
12.

A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy.

Iannello G, Graziano C, Cenacchi G, Cordelli DM, Zuntini R, Papa V, Magistà AM, Gagliardi M, Procopio R, Quattrone A, Annesi G.

J Neurol Sci. 2017 Oct 15;381:209-212. doi: 10.1016/j.jns.2017.08.3260. Epub 2017 Sep 1. Erratum in: J Neurol Sci. 2017 Dec 15;:.

PMID:
28991683
13.

Decellularized human dermal matrix produced by a skin bank A new treatment for abdominal wall defects.

Ghetti M, Bondioli E, Purpura V, Cenacchi G, Ruscelli P, Melandri D.

Ann Ital Chir. 2017;5:443-448.

PMID:
28874630
14.

Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function.

Morelli FF, Verbeek DS, Bertacchini J, Vinet J, Mediani L, Marmiroli S, Cenacchi G, Nasi M, De Biasi S, Brunsting JF, Lammerding J, Pegoraro E, Angelini C, Tupler R, Alberti S, Carra S.

Cell Rep. 2017 Aug 29;20(9):2100-2115. doi: 10.1016/j.celrep.2017.08.018.

15.

Different renal phenotypes in related adult males with Fabry disease with the same classic genotype.

Mignani R, Moschella M, Cenacchi G, Donati I, Flachi M, Grimaldi D, Cerretani D, Giovanni P, Montevecchi M, Rigotti A, Ravasio A.

Mol Genet Genomic Med. 2017 May 8;5(4):438-442. doi: 10.1002/mgg3.292. eCollection 2017 Jul.

16.

Functional expression of calcium-permeable canonical transient receptor potential 4-containing channels promotes migration of medulloblastoma cells.

Wei WC, Huang WC, Lin YP, Becker EBE, Ansorge O, Flockerzi V, Conti D, Cenacchi G, Glitsch MD.

J Physiol. 2017 Aug 15;595(16):5525-5544. doi: 10.1113/JP274659. Epub 2017 Jul 20.

17.

Activity of synthetic peptides against Chlamydia.

Donati M, Cenacchi G, Biondi R, Papa V, Borel N, Vecchio Nepita E, Magnino S, Pasquinelli G, Levi A, Franco OL.

Biopolymers. 2017 Nov;108(6). doi: 10.1002/bip.23032.

18.

In vitro activity of a partially purified and characterized bark extract of Castanea sativa Mill. (ENC®) against Chlamydia spp.

Papa V, Ginocchietti L, Budriesi R, Micucci M, Costa R, Biondi R, Cevenini R, Chiarini A, Aldini R, Donati M, Pollini GM, Cenacchi G.

Ultrastruct Pathol. 2017 Mar-Apr;41(2):147-153. doi: 10.1080/01913123.2016.1275909. Epub 2017 Feb 8.

PMID:
28277149
19.

Building blocks of the GIPU, Italian Group of Ultrastructural Pathology.

Papa V, Costa R, Cenacchi G.

Pathologica. 2016 Jun;108(2):45-47.

PMID:
28195249
20.

Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy.

De Giorgio R, Pironi L, Rinaldi R, Boschetti E, Caporali L, Capristo M, Casali C, Cenacchi G, Contin M, D'Angelo R, D'Errico A, Gramegna LL, Lodi R, Maresca A, Mohamed S, Morelli MC, Papa V, Tonon C, Tugnoli V, Carelli V, D'Alessandro R, Pinna AD.

Ann Neurol. 2016 Sep;80(3):448-55. doi: 10.1002/ana.24724. Epub 2016 Aug 4.

PMID:
27421916
21.

Magnetic Labelling of Mesenchymal Stem Cells with Iron-Doped Hydroxyapatite Nanoparticles as Tool for Cell Therapy.

Panseri S, Montesi M, Iafisco M, Adamiano A, Ghetti M, Cenacchi G, Tampieri A.

J Biomed Nanotechnol. 2016 May;12(5):909-21.

PMID:
27305814
22.

Lipolysis and lipophagy in lipid storage myopathies.

Angelini C, Nascimbeni AC, Cenacchi G, Tasca E.

Biochim Biophys Acta. 2016 Jul;1862(7):1367-73. doi: 10.1016/j.bbadis.2016.04.008. Epub 2016 Apr 13.

23.

Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.

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.

Eur J Hum Genet. 2016 May;24(5):780. doi: 10.1038/ejhg.2016.12. No abstract available.

24.

ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy.

D'Angelo R, Rinaldi R, Carelli V, Boschetti E, Caporali L, Capristo M, Casali C, Cenacchi G, Gramegna LL, Lodi R, Pinna AD, Pironi L, Stanzani M, Tonon C, D'Alessandro R, De Giorgio R.

Neurol Sci. 2016 Jul;37(7):1149-51. doi: 10.1007/s10072-016-2552-7. Epub 2016 Mar 23.

PMID:
27007276
25.

Juvenile dermatomyositis: A report of three cases.

Papa V, Romanin B, Bergamaschi R, Cordelli DM, Costa R, De Giorgi LB, Cenacchi G.

Ultrastruct Pathol. 2016;40(2):83-5. doi: 10.3109/01913123.2016.1141823. Epub 2016 Feb 17.

PMID:
26886841
26.

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation.

Jansen JC, Timal S, van Scherpenzeel M, Michelakakis H, Vicogne D, Ashikov A, Moraitou M, Hoischen A, Huijben K, Steenbergen G, van den Boogert MA, Porta F, Calvo PL, Mavrikou M, Cenacchi G, van den Bogaart G, Salomon J, Holleboom AG, Rodenburg RJ, Drenth JP, Huynen MA, Wevers RA, Morava E, Foulquier F, Veltman JA, Lefeber DJ.

Am J Hum Genet. 2016 Feb 4;98(2):322-30. doi: 10.1016/j.ajhg.2015.12.011. Epub 2016 Jan 28.

27.

Proteomic analysis of extracellular vesicles from medullospheres reveals a role for iron in the cancer progression of medulloblastoma.

Bisaro B, Mandili G, Poli A, Piolatto A, Papa V, Novelli F, Cenacchi G, Forni M, Zanini C.

Mol Cell Ther. 2015 Oct 13;3:8. doi: 10.1186/s40591-015-0045-3. eCollection 2015.

28.

Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.

Pippucci T, Maresca A, Magini P, Cenacchi G, Donadio V, Palombo F, Papa V, Incensi A, Gasparre G, Valentino ML, Preziuso C, Pisano A, Ragno M, Liguori R, Giordano C, Tonon C, Lodi R, Parmeggiani A, Carelli V, Seri M.

EMBO Mol Med. 2015 Jun;7(6):848-58. doi: 10.15252/emmm.201404399.

29.

XAV939-mediated ARTD activity inhibition in human MB cell lines.

Renna C, Salaroli R, Cocchi C, Cenacchi G.

PLoS One. 2015 Apr 2;10(4):e0124149. doi: 10.1371/journal.pone.0124149. eCollection 2015.

30.

Clinical and ultrastructural spectrum of diffuse lung disease associated with surfactant protein C mutations.

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.

Eur J Hum Genet. 2015 Aug;23(8):1033-41. doi: 10.1038/ejhg.2015.45. Epub 2015 Mar 18. Erratum in: Eur J Hum Genet. 2016 May;24(5):780. Ullman, Nicola [corrected to Ullmann, Nicola].

31.

Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure.

Desbats MA, Vetro A, Limongelli I, Lunardi G, Casarin A, Doimo M, Spinazzi M, Angelini C, Cenacchi G, Burlina A, Rodriguez Hernandez MA, Chiandetti L, Clementi M, Trevisson E, Navas P, Zuffardi O, Salviati L.

Eur J Hum Genet. 2015 Sep;23(9):1254-8. doi: 10.1038/ejhg.2014.277. Epub 2015 Jan 7.

32.

The effects of palladium nanoparticles on the renal function of female Wistar rats.

Fontana L, Leso V, Marinaccio A, Cenacchi G, Papa V, Leopold K, Schindl R, Bocca B, Alimonti A, Iavicoli I.

Nanotoxicology. 2015;9(7):843-51. doi: 10.3109/17435390.2014.980759. Epub 2015 Sep 4.

PMID:
25405262
33.

Wnt activation affects proliferation, invasiveness and radiosensitivity in medulloblastoma.

Salaroli R, Ronchi A, Buttarelli FR, Cortesi F, Marchese V, Della Bella E, Renna C, Baldi C, Giangaspero F, Cenacchi G.

J Neurooncol. 2015 Jan;121(1):119-27. doi: 10.1007/s11060-014-1621-0. Epub 2014 Sep 28.

PMID:
25261924
34.

Sclerosing paraganglioma of the carotid body: a potential pitfall of malignancy.

Santi R, Franchi A, Saladino V, Trovati M, Cenacchi G, Squadrelli-Saraceno M, Nesi G.

Head Neck Pathol. 2015 Jun;9(2):300-4. doi: 10.1007/s12105-014-0569-x. Epub 2014 Sep 7.

35.

A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates.

Rossi D, Vezzani B, Galli L, Paolini C, Toniolo L, Pierantozzi E, Spinozzi S, Barone V, Pegoraro E, Bello L, Cenacchi G, Vattemi G, Tomelleri G, Ricci G, Siciliano G, Protasi F, Reggiani C, Sorrentino V.

Hum Mutat. 2014 Oct;35(10):1163-70. doi: 10.1002/humu.22631. Epub 2014 Sep 10.

36.

Skeletal muscle satellite cells in amyotrophic lateral sclerosis.

Scaramozza A, Marchese V, Papa V, Salaroli R, Sorarù G, Angelini C, Cenacchi G.

Ultrastruct Pathol. 2014 Oct;38(5):295-302. doi: 10.3109/01913123.2014.937842. Epub 2014 Jul 31.

PMID:
25079897
37.

Familial polyglucosan body myopathy with unusual phenotype.

Fanin M, Nascimbeni AC, Savarese M, Papa V, Cenacchi G, Nigro V, Angelini C.

Neuropathol Appl Neurobiol. 2015 Apr;41(3):385-90. doi: 10.1111/nan.12171. No abstract available.

PMID:
25041762
38.

Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathy.

Boschetti E, D'Alessandro R, Bianco F, Carelli V, Cenacchi G, Pinna AD, Del Gaudio M, Rinaldi R, Stanghellini V, Pironi L, Rhoden K, Tugnoli V, Casali C, De Giorgio R.

PLoS One. 2014 May 6;9(5):e96692. doi: 10.1371/journal.pone.0096692. eCollection 2014. Erratum in: PLoS One. 2014;9(10):e110583.

39.

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.

Magini P, Pippucci T, Tsai IC, Coppola S, Stellacci E, Bartoletti-Stella A, Turchetti D, Graziano C, Cenacchi G, Neri I, Cordelli DM, Marchiani V, Bergamaschi R, Gasparre G, Neri G, Mazzanti L, Patrizi A, Franzoni E, Romeo G, Bordo D, Tartaglia M, Katsanis N, Seri M.

Hum Mol Genet. 2014 Jul 1;23(13):3607-17. doi: 10.1093/hmg/ddu070. Epub 2014 Feb 19.

PMID:
24556213
40.

Sleep and cardiovascular phenotype in middle-aged hypocretin-deficient narcoleptic mice.

Silvani A, Bastianini S, Berteotti C, Cenacchi G, Leone O, Lo Martire V, Papa V, Zoccoli G.

J Sleep Res. 2014 Feb;23(1):98-106. doi: 10.1111/jsr.12081. Epub 2013 Aug 29.

41.

Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α.

Bartoletti-Stella A, Mariani E, Kurelac I, Maresca A, Caratozzolo MF, Iommarini L, Carelli V, Eusebi LH, Guido A, Cenacchi G, Fuccio L, Rugolo M, Tullo A, Porcelli AM, Gasparre G.

Cell Death Dis. 2013 Jun 13;4:e663. doi: 10.1038/cddis.2013.187.

42.

Medullospheres from DAOY, UW228 and ONS-76 cells: increased stem cell population and proteomic modifications.

Zanini C, Ercole E, Mandili G, Salaroli R, Poli A, Renna C, Papa V, Cenacchi G, Forni M.

PLoS One. 2013 May 24;8(5):e63748. doi: 10.1371/journal.pone.0063748. Print 2013.

43.

Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophy.

Malena A, Pennuto M, Tezze C, Querin G, D'Ascenzo C, Silani V, Cenacchi G, Scaramozza A, Romito S, Morandi L, Pegoraro E, Russell AP, Sorarù G, Vergani L.

Acta Neuropathol. 2013 Jul;126(1):109-21. doi: 10.1007/s00401-013-1122-9. Epub 2013 May 4.

PMID:
23644820
44.

CD99 suppresses osteosarcoma cell migration through inhibition of ROCK2 activity.

Zucchini C, Manara MC, Pinca RS, De Sanctis P, Guerzoni C, Sciandra M, Lollini PL, Cenacchi G, Picci P, Valvassori L, Scotlandi K.

Oncogene. 2014 Apr 10;33(15):1912-21. doi: 10.1038/onc.2013.152. Epub 2013 May 6.

PMID:
23644663
45.

Response of human chondrocytes and mesenchymal stromal cells to a decellularized human dermis.

Giavaresi G, Bondioli E, Melandri D, Giardino R, Tschon M, Torricelli P, Cenacchi G, Rotini R, Castagna A, Veronesi F, Pagani S, Fini M.

BMC Musculoskelet Disord. 2013 Jan 7;14:12. doi: 10.1186/1471-2474-14-12.

46.

Ultrastructural changes in LGMD1F.

Cenacchi G, Peterle E, Fanin M, Papa V, Salaroli R, Angelini C.

Neuropathology. 2013 Jun;33(3):276-80. doi: 10.1111/neup.12003. Epub 2012 Dec 21.

PMID:
23279333
47.

Somatic complex I disruptive mitochondrial DNA mutations are modifiers of tumorigenesis that correlate with low genomic instability in pituitary adenomas.

Kurelac I, MacKay A, Lambros MB, Di Cesare E, Cenacchi G, Ceccarelli C, Morra I, Melcarne A, Morandi L, Calabrese FM, Attimonelli M, Tallini G, Reis-Filho JS, Gasparre G.

Hum Mol Genet. 2013 Jan 15;22(2):226-38. doi: 10.1093/hmg/dds422. Epub 2012 Oct 9.

PMID:
23049073
48.

The empowerment of translational research: lessons from laminopathies.

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.

Orphanet J Rare Dis. 2012 Jun 12;7:37.

49.

Development and evaluation of a decellularized membrane from human dermis.

Bondioli E, Fini M, Veronesi F, Giavaresi G, Tschon M, Cenacchi G, Cerasoli S, Giardino R, Melandri D.

J Tissue Eng Regen Med. 2014 Apr;8(4):325-36. doi: 10.1002/term.1530. Epub 2012 Jun 11.

PMID:
22689414
50.

Differentiation of mesenchymal stem cells derived from pancreatic islets and bone marrow into islet-like cell phenotype.

Zanini C, Bruno S, Mandili G, Baci D, Cerutti F, Cenacchi G, Izzi L, Camussi G, Forni M.

PLoS One. 2011;6(12):e28175. doi: 10.1371/journal.pone.0028175. Epub 2011 Dec 16.

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