Marigo V - Search Results

1

Structural aspects of rod opsin and their implication in genetic diseases.

Fanelli F, Felline A, Marigo V. Fanelli F, et al. Among authors: marigo v. Pflugers Arch. 2021 Sep;473(9):1339-1359. doi: 10.1007/s00424-021-02546-x. Epub 2021 Mar 16. Pflugers Arch. 2021. PMID: 33728518 Review.

2

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. Behnen P, et al. Among authors: marigo v. iScience. 2018 Jun 29;4:1-19. doi: 10.1016/j.isci.2018.05.001. Epub 2018 May 5. iScience. 2018. PMID: 30240733 Free PMC article.

3

Differential Contribution of Calcium-Activated Proteases and ER-Stress in Three Mouse Models of Retinitis Pigmentosa Expressing P23H Mutant RHO.

Comitato A, Schiroli D, La Marca C, Marigo V. Comitato A, et al. Among authors: marigo v. Adv Exp Med Biol. 2019;1185:311-316. doi: 10.1007/978-3-030-27378-1_51. Adv Exp Med Biol. 2019. PMID: 31884630

4

New In Vitro Cellular Model for Molecular Studies of Retinitis Pigmentosa.

Huang L, Kutluer M, Adani E, Comitato A, Marigo V. Huang L, et al. Among authors: marigo v. Int J Mol Sci. 2021 Jun 16;22(12):6440. doi: 10.3390/ijms22126440. Int J Mol Sci. 2021. PMID: 34208617 Free PMC article.

5

Conformational insights into the C-terminal mutations of human rhodopsin in retinitispigmentosa.

Picarazzi F, Manetti F, Marigo V, Mori M. Picarazzi F, et al. Among authors: marigo v. J Mol Graph Model. 2022 Jan;110:108076. doi: 10.1016/j.jmgm.2021.108076. Epub 2021 Nov 11. J Mol Graph Model. 2022. PMID: 34798368

6

Structure network-based landscape of rhodopsin misfolding by mutations and algorithmic prediction of small chaperone action.

Felline A, Schiroli D, Comitato A, Marigo V, Fanelli F. Felline A, et al. Among authors: marigo v. Comput Struct Biotechnol J. 2021 Nov 2;19:6020-6038. doi: 10.1016/j.csbj.2021.10.040. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 34849206 Free PMC article.

7

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. Comitato A, et al. Among authors: marigo v. Hum Mol Genet. 2016 Jul 1;25(13):2801-2812. doi: 10.1093/hmg/ddw137. Epub 2016 May 5. Hum Mol Genet. 2016. PMID: 27149983 Free article.

8

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. Bernardis I, et al. Among authors: marigo v. Biomed Res Int. 2016;2016:6341870. doi: 10.1155/2016/6341870. Epub 2016 Dec 29. Biomed Res Int. 2016. PMID: 28127548 Free PMC article.

9

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

Comitato A, Schiroli D, Montanari M, Marigo V. Comitato A, et al. Among authors: marigo v. Mol Neurobiol. 2020 Feb;57(2):589-599. doi: 10.1007/s12035-019-01723-5. Epub 2019 Aug 10. Mol Neurobiol. 2020. PMID: 31401765

10

New Improved cGMP Analogues to Target Rod Photoreceptor Degeneration.

Pérez O, Stanzani A, Huang L, Schipper N, Loftsson T, Bollmark M, Marigo V. Pérez O, et al. Among authors: marigo v. J Med Chem. 2024 May 23;67(10):8396-8405. doi: 10.1021/acs.jmedchem.4c00586. Epub 2024 Apr 30. J Med Chem. 2024. PMID: 38688030

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