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Valeria MARIGO
Valeria MARIGO
professore di biologia molecolare, Università di Modena e Reggio Emilia
在 unimore.it 的电子邮件经过验证 - 首页
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Biochemical evidence that patched is the Hedgehog receptor
V Marigo, RA Davey, Y Zuo, JM Cunningham, CJ Tabin
Nature 384 (6605), 176-179, 1996
10821996
Sonic hedgehog differentially regulates expression ofGLIandGLI3during limb development
V Marigo, RL Johnson, A Vortkamp, CJ Tabin
Developmental biology 180 (1), 273-283, 1996
4871996
Regulation of patched by sonic hedgehog in the developing neural tube.
V Marigo, CJ Tabin
Proceedings of the National Academy of Sciences 93 (18), 9346-9351, 1996
3911996
Conservation in hedgehog signaling: induction of a chicken patched homolog by Sonic hedgehog in the developing limb
V Marigo, MP Scott, RL Johnson, LV Goodrich, CJ Tabin
Development 122 (4), 1225-1233, 1996
3591996
Novel adeno-associated virus serotypes efficiently transduce murine photoreceptors
M Allocca, C Mussolino, M Garcia-Hoyos, D Sanges, C Iodice, M Petrillo, ...
Journal of virology 81 (20), 11372-11380, 2007
3112007
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog
V Marigo, DJ Roberts, SMK Lee, O Tsukurov, T Levi, JM Gastier, ...
Genomics 28 (1), 44-51, 1995
2741995
Apoptosis in retinal degeneration involves cross-talk between apoptosis-inducing factor (AIF) and caspase-12 and is blocked by calpain inhibitors
D Sanges, A Comitato, R Tammaro, V Marigo
Proceedings of the National Academy of Sciences 103 (46), 17366-17371, 2006
2582006
Human chromosome 21 gene expression atlas in the mouse
A Reymond, V Marigo, MB Yaylaoglu, A Leoni, C Ucla, N Scamuffa, ...
Nature 420 (6915), 582-586, 2002
2482002
Identification and characterization of microRNAs expressed in the mouse eye
M Karali, I Peluso, V Marigo, S Banfi
Investigative ophthalmology & visual science 48 (2), 509-515, 2007
2412007
Emilin, a component of elastic fibers preferentially located at the elastin-microfibrils interface.
GM Bressan, D Daga-Gordini, A Colombatti, I Castellani, V Marigo, ...
The Journal of cell biology 121 (1), 201-212, 1993
2071993
In vivo editing of the human mutant rhodopsin gene by electroporation of plasmid-based CRISPR/Cas9 in the mouse retina
MC Latella, MT Di Salvo, F Cocchiarella, D Benati, G Grisendi, A Comitato, ...
Molecular Therapy-Nucleic Acids 5, 2016
1892016
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development
A Bulfone, S Martinez, V Marigo, M Campanella, A Basile, N Quaderi, ...
Mechanisms of development 84 (1-2), 133-138, 1999
1701999
Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma
AM Barbieri, V Broccoli, P Bovolenta, G Alfano, A Marchitiello, C Mocchetti, ...
Oxford University Press for The Company of Biologists Limited 129 (3), 805-813, 2002
1652002
Programmed cell death in retinal degeneration: targeting apoptosis in photoreceptors as potential therapy for retinal degeneration
V Marigo
Cell cycle 6 (6), 652-655, 2007
1432007
Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1
B Incerti, K Cortese, A Pizzigoni, EM Surace, S Varani, M Coppola, ...
Human molecular genetics 9 (19), 2781-2788, 2000
1172000
Cross-talk between two apoptotic pathways activated by endoplasmic reticulum stress: differential contribution of caspase-12 and AIF
D Sanges, V Marigo
Apoptosis 11, 1629-1641, 2006
1102006
Combination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration
E Vighi, D Trifunović, P Veiga-Crespo, A Rentsch, D Hoffmann, ...
Proceedings of the National Academy of Sciences 115 (13), E2997-E3006, 2018
1072018
Cellular mechanisms of hereditary photoreceptor degeneration–Focus on cGMP
M Power, S Das, K Schütze, V Marigo, P Ekström, F Paquet-Durand
Progress in Retinal and Eye Research 74, 100772, 2020
1022020
The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells
I Palmisano, P Bagnato, A Palmigiano, G Innamorati, G Rotondo, ...
Human molecular genetics 17 (22), 3487-3501, 2008
1002008
Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy
CF Chakarova, MG Papaioannou, H Khanna, I Lopez, N Waseem, A Shah, ...
The American Journal of Human Genetics 81 (5), 1098-1103, 2007
992007
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