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Items: 1 to 50 of 71

1.

Calpain Activation Is the Major Cause of Cell Death in Photoreceptors Expressing a Rhodopsin Misfolding Mutation.

Comitato A, Schiroli D, Montanari M, Marigo V.

Mol Neurobiol. 2019 Aug 10. doi: 10.1007/s12035-019-01723-5. [Epub ahead of print]

PMID:
31401765
2.

Cellular mechanisms of hereditary photoreceptor degeneration - Focus on cGMP.

Power M, Das S, Schütze K, Marigo V, Ekström P, Paquet-Durand F.

Prog Retin Eye Res. 2019 Jul 30:100772. doi: 10.1016/j.preteyeres.2019.07.005. [Epub ahead of print] Review.

PMID:
31374251
3.

Drug delivery to retinal photoreceptors.

Himawan E, Ekström P, Buzgo M, Gaillard P, Stefánsson E, Marigo V, Loftsson T, Paquet-Durand F.

Drug Discov Today. 2019 Aug;24(8):1637-1643. doi: 10.1016/j.drudis.2019.03.004. Epub 2019 Mar 13. Review.

4.

CRISPR/Cas9 Gene Editing In Vitro and in Retinal Cells In Vivo.

Benati D, Marigo V, Recchia A.

Methods Mol Biol. 2019;1834:59-74. doi: 10.1007/978-1-4939-8669-9_4.

PMID:
30324436
5.

A Small Chaperone Improves Folding and Routing of Rhodopsin Mutants Linked to Inherited Blindness.

Behnen P, Felline A, Comitato A, Di Salvo MT, Raimondi F, Gulati S, Kahremany S, Palczewski K, Marigo V, Fanelli F.

iScience. 2018 Jun 29;4:1-19. doi: 10.1016/j.isci.2018.05.001. Epub 2018 May 5.

6.

Pigment epithelium-derived factor hinders photoreceptor cell death by reducing intracellular calcium in the degenerating retina.

Comitato A, Subramanian P, Turchiano G, Montanari M, Becerra SP, Marigo V.

Cell Death Dis. 2018 May 1;9(5):560. doi: 10.1038/s41419-018-0613-y.

7.

Primary Rod and Cone Degeneration Is Prevented by HDAC Inhibition.

Trifunović D, Petridou E, Comitato A, Marigo V, Ueffing M, Paquet-Durand F.

Adv Exp Med Biol. 2018;1074:367-373. doi: 10.1007/978-3-319-75402-4_45.

PMID:
29721965
8.

Combination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration.

Vighi E, Trifunović D, Veiga-Crespo P, Rentsch A, Hoffmann D, Sahaboglu A, Strasser T, Kulkarni M, Bertolotti E, van den Heuvel A, Peters T, Reijerkerk A, Euler T, Ueffing M, Schwede F, Genieser HG, Gaillard P, Marigo V, Ekström P, Paquet-Durand F.

Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):E2997-E3006. doi: 10.1073/pnas.1718792115. Epub 2018 Mar 12.

9.

New cGMP analogues restrain proliferation and migration of melanoma cells.

Vighi E, Rentsch A, Henning P, Comitato A, Hoffmann D, Bertinetti D, Bertolotti E, Schwede F, Herberg FW, Genieser HG, Marigo V.

Oncotarget. 2017 Dec 25;9(4):5301-5320. doi: 10.18632/oncotarget.23685. eCollection 2018 Jan 12.

10.

New dimeric cGMP analogues reduce proliferation in three colon cancer cell lines.

Hoffmann D, Rentsch A, Vighi E, Bertolotti E, Comitato A, Schwede F, Genieser HG, Marigo V.

Eur J Med Chem. 2017 Dec 1;141:61-72. doi: 10.1016/j.ejmech.2017.09.053. Epub 2017 Sep 27.

PMID:
29028532
11.

The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells.

Palmisano I, Bagnato P, Palmigiano A, Innamorati G, Rotondo G, Altimare D, Venturi C, Sviderskaya EV, Piccirillo R, Coppola M, Marigo V, Incerti B, Ballabio A, Surace EM, Tacchetti C, Bennett DC, Schiaffino MV.

Hum Mol Genet. 2017 Aug 1;26(15):3028-3029. doi: 10.1093/hmg/ddx131. No abstract available.

12.

HDAC inhibition in the cpfl1 mouse protects degenerating cone photoreceptors in vivo.

Trifunović D, Arango-Gonzalez B, Comitato A, Barth M, Del Amo EM, Kulkarni M, Sahaboglu A, Hauck SM, Urtti A, Arsenijevic Y, Ueffing M, Marigo V, Paquet-Durand F.

Hum Mol Genet. 2016 Oct 15;25(20):4462-4472. doi: 10.1093/hmg/ddw275.

PMID:
28172811
13.

Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing.

Bernardis I, Chiesi L, Tenedini E, Artuso L, Percesepe A, Artusi V, Simone ML, Manfredini R, Camparini M, Rinaldi C, Ciardella A, Graziano C, Balducci N, Tranchina A, Cavallini GM, Pietrangelo A, Marigo V, Tagliafico E.

Biomed Res Int. 2016;2016:6341870. doi: 10.1155/2016/6341870. Epub 2016 Dec 29.

14.

In vivo Editing of the Human Mutant Rhodopsin Gene by Electroporation of Plasmid-based CRISPR/Cas9 in the Mouse Retina.

Latella MC, Di Salvo MT, Cocchiarella F, Benati D, Grisendi G, Comitato A, Marigo V, Recchia A.

Mol Ther Nucleic Acids. 2016 Nov 22;5(11):e389. doi: 10.1038/mtna.2016.92.

15.

Dominant and recessive mutations in rhodopsin activate different cell death pathways.

Comitato A, Di Salvo MT, Turchiano G, Montanari M, Sakami S, Palczewski K, Marigo V.

Hum Mol Genet. 2016 Jul 1;25(13):2801-2812. Epub 2016 May 5.

PMID:
27149983
16.

Small Retinoprotective Peptides Reveal a Receptor-binding Region on Pigment Epithelium-derived Factor.

Kenealey J, Subramanian P, Comitato A, Bullock J, Keehan L, Polato F, Hoover D, Marigo V, Becerra SP.

J Biol Chem. 2015 Oct 16;290(42):25241-53. doi: 10.1074/jbc.M115.645846. Epub 2015 Aug 24.

17.

Stem cells as source for retinal pigment epithelium transplantation.

Bertolotti E, Neri A, Camparini M, Macaluso C, Marigo V.

Prog Retin Eye Res. 2014 Sep;42:130-44. doi: 10.1016/j.preteyeres.2014.06.002. Epub 2014 Jun 13. Review.

PMID:
24933042
18.

Activation of Bax in three models of retinitis pigmentosa.

Comitato A, Sanges D, Rossi A, Humphries MM, Marigo V.

Invest Ophthalmol Vis Sci. 2014 May 13;55(6):3555-62. doi: 10.1167/iovs.14-13917.

PMID:
24825107
19.

Melanoregulin, product of the dsu locus, links the BLOC-pathway and OA1 in organelle biogenesis.

Rachel RA, Nagashima K, O'Sullivan TN, Frost LS, Stefano FP, Marigo V, Boesze-Battaglia K.

PLoS One. 2012;7(9):e42446. doi: 10.1371/journal.pone.0042446. Epub 2012 Sep 11.

20.

Functional and molecular characterization of rod-like cells from retinal stem cells derived from the adult ciliary epithelium.

Demontis GC, Aruta C, Comitato A, De Marzo A, Marigo V.

PLoS One. 2012;7(3):e33338. doi: 10.1371/journal.pone.0033338. Epub 2012 Mar 14. Erratum in: PLoS One. 2012;7(8): doi/10.1371/annotation/ca21f359-8e8e-4c3d-8308-e0f20fc446bb.

21.

Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa.

Mussolino C, Sanges D, Marrocco E, Bonetti C, Di Vicino U, Marigo V, Auricchio A, Meroni G, Surace EM.

EMBO Mol Med. 2011 Mar;3(3):118-28. doi: 10.1002/emmm.201000119. Epub 2011 Jan 26.

22.

In vitro differentiation of retinal pigment epithelium from adult retinal stem cells.

Aruta C, Giordano F, De Marzo A, Comitato A, Raposo G, Nandrot EF, Marigo V.

Pigment Cell Melanoma Res. 2011 Feb;24(1):233-40. doi: 10.1111/j.1755-148X.2010.00793.x. Epub 2010 Nov 10.

PMID:
21232026
23.

Photoreceptor rescue and toxicity induced by different calpain inhibitors.

Paquet-Durand F, Sanges D, McCall J, Silva J, van Veen T, Marigo V, Ekström P.

J Neurochem. 2010 Nov;115(4):930-40. doi: 10.1111/j.1471-4159.2010.06983.x. Epub 2010 Sep 28.

24.

PEDF promotes retinal neurosphere formation and expansion in vitro.

De Marzo A, Aruta C, Marigo V.

Adv Exp Med Biol. 2010;664:621-30. doi: 10.1007/978-1-4419-1399-9_71.

PMID:
20238066
25.

Transient receptor potential melastatin type 7 channel is critical for the survival of bone marrow derived mesenchymal stem cells.

Cheng H, Feng JM, Figueiredo ML, Zhang H, Nelson PL, Marigo V, Beck A.

Stem Cells Dev. 2010 Sep;19(9):1393-403. doi: 10.1089/scd.2009.0262.

26.

The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition.

Giordano F, Bonetti C, Surace EM, Marigo V, Raposo G.

Hum Mol Genet. 2009 Dec 1;18(23):4530-45. doi: 10.1093/hmg/ddp415. Epub 2009 Aug 28.

PMID:
19717472
27.

TRPM4 impacts on Ca2+ signals during agonist-induced insulin secretion in pancreatic beta-cells.

Marigo V, Courville K, Hsu WH, Feng JM, Cheng H.

Mol Cell Endocrinol. 2009 Feb 27;299(2):194-203. doi: 10.1016/j.mce.2008.11.011. Epub 2008 Nov 21.

PMID:
19063936
28.

The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells.

Palmisano I, Bagnato P, Palmigiano A, Innamorati G, Rotondo G, Altimare D, Venturi C, Sviderskaya EV, Piccirillo R, Coppola M, Marigo V, Incerti B, Ballabio A, Surace EM, Tacchetti C, Bennett DC, Schiaffino MV.

Hum Mol Genet. 2008 Nov 15;17(22):3487-501. doi: 10.1093/hmg/ddn241. Epub 2008 Aug 12. Erratum in: Hum Mol Genet. 2017 Aug 1;26(15):3028-3029.

29.

Stem cells as prospective therapeutic tools for retinal degeneration.

Marigo V.

Arch Soc Esp Oftalmol. 2008 Jul;83(7):397-400. English, Spanish. No abstract available.

30.

A high-resolution RNA expression atlas of retinitis pigmentosa genes in human and mouse retinas.

Trifunovic D, Karali M, Camposampiero D, Ponzin D, Banfi S, Marigo V.

Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2330-6. doi: 10.1167/iovs.07-1513. Epub 2008 Feb 15.

PMID:
18281612
31.
32.

Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy.

Chakarova CF, Papaioannou MG, Khanna H, Lopez I, Waseem N, Shah A, Theis T, Friedman J, Maubaret C, Bujakowska K, Veraitch B, Abd El-Aziz MM, Prescott de Q, Parapuram SK, Bickmore WA, Munro PM, Gal A, Hamel CP, Marigo V, Ponting CP, Wissinger B, Zrenner E, Matter K, Swaroop A, Koenekoop RK, Bhattacharya SS.

Am J Hum Genet. 2007 Nov;81(5):1098-103. Epub 2007 Sep 26.

33.

Novel adeno-associated virus serotypes efficiently transduce murine photoreceptors.

Allocca M, Mussolino C, Garcia-Hoyos M, Sanges D, Iodice C, Petrillo M, Vandenberghe LH, Wilson JM, Marigo V, Surace EM, Auricchio A.

J Virol. 2007 Oct;81(20):11372-80. Epub 2007 Aug 15.

34.

Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells.

Comitato A, Spampanato C, Chakarova C, Sanges D, Bhattacharya SS, Marigo V.

Hum Mol Genet. 2007 Jul 15;16(14):1699-707. Epub 2007 May 20.

PMID:
17517693
35.
36.

Identification and characterization of microRNAs expressed in the mouse eye.

Karali M, Peluso I, Marigo V, Banfi S.

Invest Ophthalmol Vis Sci. 2007 Feb;48(2):509-15.

PMID:
17251443
37.

Apoptosis in retinal degeneration involves cross-talk between apoptosis-inducing factor (AIF) and caspase-12 and is blocked by calpain inhibitors.

Sanges D, Comitato A, Tammaro R, Marigo V.

Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17366-71. Epub 2006 Nov 6.

39.

Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotides.

Vetrini F, Tammaro R, Bondanza S, Surace EM, Auricchio A, De Luca M, Ballabio A, Marigo V.

Hum Mutat. 2006 May;27(5):420-6.

PMID:
16550551
40.

The ocular albinism type 1 (OA1) gene controls melanosome maturation and size.

Cortese K, Giordano F, Surace EM, Venturi C, Ballabio A, Tacchetti C, Marigo V.

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4358-64.

PMID:
16303920
41.

Molecular characterization of a t(2;6) balanced translocation that is associated with a complex phenotype and leads to truncation of the TCBA1 gene.

Bocciardi R, Giorda R, Marigo V, Zordan P, Montanaro D, Gimelli S, Seri M, Lerone M, Ravazzolo R, Gimelli G.

Hum Mutat. 2005 Nov;26(5):426-36.

PMID:
16145689
42.

Amelioration of both functional and morphological abnormalities in the retina of a mouse model of ocular albinism following AAV-mediated gene transfer.

Surace EM, Domenici L, Cortese K, Cotugno G, Di Vicino U, Venturi C, Cellerino A, Marigo V, Tacchetti C, Ballabio A, Auricchio A.

Mol Ther. 2005 Oct;12(4):652-8.

43.

The amino acid transporter asc-1 is not involved in cystinuria.

Pineda M, Font M, Bassi MT, Manzoni M, Borsani G, Marigo V, Fernández E, Río RM, Purroy J, Zorzano A, Nunes V, Palacín M.

Kidney Int. 2004 Oct;66(4):1453-64.

44.

URB expression in human bone marrow stromal cells and during mouse development.

Liu Y, Monticone M, Tonachini L, Mastrogiacomo M, Marigo V, Cancedda R, Castagnola P.

Biochem Biophys Res Commun. 2004 Sep 17;322(2):497-507.

PMID:
15325258
45.

The microphthalmia transcription factor (Mitf) controls expression of the ocular albinism type 1 gene: link between melanin synthesis and melanosome biogenesis.

Vetrini F, Auricchio A, Du J, Angeletti B, Fisher DE, Ballabio A, Marigo V.

Mol Cell Biol. 2004 Aug;24(15):6550-9.

46.

Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains.

Marigo V, Nigro A, Pecci A, Montanaro D, Di Stazio M, Balduini CL, Savoia A.

Genomics. 2004 Jun;83(6):1125-33.

PMID:
15177565
47.

An expression atlas of connexin genes in the mouse.

Buniello A, Montanaro D, Volinia S, Gasparini P, Marigo V.

Genomics. 2004 May;83(5):812-20.

PMID:
15081111
48.

An in vivo doxycycline-controlled expression system for functional studies of the retina.

Angeletti B, Löster J, Auricchio A, Gekeler F, Shinoda K, Ballabio A, Graw J, Marigo V.

Invest Ophthalmol Vis Sci. 2003 Feb;44(2):755-60.

PMID:
12556410
49.

Human chromosome 21 gene expression atlas in the mouse.

Reymond A, Marigo V, Yaylaoglu MB, Leoni A, Ucla C, Scamuffa N, Caccioppoli C, Dermitzakis ET, Lyle R, Banfi S, Eichele G, Antonarakis SE, Ballabio A.

Nature. 2002 Dec 5;420(6915):582-6.

PMID:
12466854
50.

Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4B.

Bolino A, Marigo V, Ferrera F, Loader J, Romio L, Leoni A, Di Duca M, Cinti R, Cecchi C, Feltri ML, Wrabetz L, Ravazzolo R, Monaco AP.

Gene. 2002 Jan 23;283(1-2):17-26.

PMID:
11867209

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