BRANCACCIO, ANDREA
BRANCACCIO, ANDREA
Istituto di Scienze e Tecnologie Chimiche "Giulio Natta" - SCITEC
Determination of Agrin and Related Proteins Levels as a Function of Age in Human Hearts
2022 Skeffington, Kl; Jones, Fp; Suleiman, Ms; Caputo, M; Brancaccio, A; Bigotti, Mg
High degree of conservation of the enzymes synthesizing the laminin-binding glycoepitope of alpha-dystroglycan
2021 Bigotti, Mg; Brancaccio, A
Agrin-Mediated Cardiac Regeneration: Some Open Questions
2020 Bigotti, Mg; Skeffington, Kl; Jones, Fp; Caputo, M; Brancaccio, A
Loss of dystroglycan drives cellular senescence via defective mitosis-mediated genomic instability
2020 JimenezGutierrez G.E.; MondragonGonzalez R.; SotoPonce L.A.; GomezMonsivais W.L.; GarciaAguirre I.; PachecoRivera R.A.; SuarezSanchez R.; Brancaccio A.; Magana J.J.; Perlingeiro R.C.R.; Cisneros B.
The molecular basis and biologic significance of the ?-dystroglycan-emerin interaction
2020 Gomezmonsivais, Wl; Monterrubioledezma, F; Huertacantillo, J; Mondragongonzalez, R; Alamilloiniesta, A; Garciaaguirre, I; Azuaramedina, Pm; Arguellogarcia, R; Riveramonroy, Je; Holaska, Jm; Hernandezmendez, Jme; Garrido, E; Magana, Jj; Winder, Sj; Brancaccio, A; Martinezvieyra, I; Navarrogarcia, F; Cisneros, B
A molecular overview of the primary dystroglycanopathies
2019 Brancaccio, Andrea; Brancaccio, Andrea
Analysis of alpha-Dystroglycan/LG Domain Binding Modes: Investigating Protein Motifs That Regulate the Affinity of Isolated LG Domains
2019 E Dempsey, Christopher; Giulia Bigotti, Maria; C Adams, Josephine; Brancaccio, Andrea
A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein.
2018 Signorino, Giulia; Covaceuszach, Sonia; Bozzi, Manuela; Hubner, Wolfgang; Monkemoller, Viola; Konarev Petr, V; Cassetta, Alberto; Brancaccio, Andrea; Sciandra, Francesca
A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein
2018 Signorino, G; Covaceuszach, S; Bozzi, M; Hübner, W; Mönkemöller, V; Konarev, Pv; Cassetta, A; Brancaccio, A; Sciandra, F
Intraring allostery controls the function and assembly of a hetero-oligomeric class II chaperonin.
2018 Shoemark, Dk; Sessions, Rb; Brancaccio, A; Bigotti, Mg
The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site
2018 Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M.
The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site
2018 Gioia, M; Fasciglione, Gf; Sbardella, D; Sciandra, F; Casella, M; Camerini, S; Crescenzi, M; Gori, A; Tarantino, U; Cozza, P; Brancaccio, A; Coletta, M; Bozzi, M
?-Dystroglycan hypoglycosylation affects cell migration by influencing ?-dystroglycan membrane clustering and filopodia length: A musticale confocal microscopi analysis
2017 Palmieri, V; Bozzi, M; Signorino, G; Papi, M; De Spirito, M; Brancaccio, A; Maulucci, G; Sciandra, F
An evaluation of the evolution of the gene structure of dystroglycan.
2017 Brancaccio, Andrea; Adams Josephine, C
Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene
2017 Sciandra, F; Scicchitano, Bm; Signorino, G; Bigotti, Mg; Tavazzi, B; Lombardi, F; Bozzi, M; Sica, G; Giardina, B; Blaess, S; Brancaccio, A
Structural flexibility of human alpha-dystroglycan
2017 Covaceuszach, Sonia; Bozzi, Manuela; Bigotti Maria, Giulia; Sciandra, Francesca; Konarev Petr, Valeryevich; Brancaccio, Andrea; Cassetta, Alberto
The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of ?-dystroglycan
2017 Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A
Internal (His)(6)-tagging delivers a fully functional hetero-oligomeric class II chaperonin in high yield
2016 Paul, Danielle M.; Beuron, Fabienne; Sessions, Richard B.; Brancaccio, Andrea; Bigotti, Maria Giulia
Quantification, 2DE analysis and identification of enriched glycosylated proteins from mouse muscles: Difficulties and alternatives
2016 Menegoci Eugenio Patricia de, Fatima; Assuncao Nilson, Antonio; Sciandra, Francesca; Aquino, Adriano; Brancaccio, Andrea; Carrilho, Emanuel
A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core portein in some, but not all, dystroglycanopathy patients
2015 L Humphrey, E; Lacey, E; Le, Lt; Feng, L; Sciandra, F; Morris, Cr; Hewitt, Je; Holt, I; Brancaccio, A; Barresi, R; A Sewry, C; Brown, Sc; Morris, Ge
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Determination of Agrin and Related Proteins Levels as a Function of Age in Human Hearts | 1-gen-2022 | Skeffington, Kl; Jones, Fp; Suleiman, Ms; Caputo, M; Brancaccio, A; Bigotti, Mg | |
| High degree of conservation of the enzymes synthesizing the laminin-binding glycoepitope of alpha-dystroglycan | 1-gen-2021 | Bigotti, Mg; Brancaccio, A | |
| Agrin-Mediated Cardiac Regeneration: Some Open Questions | 1-gen-2020 | Bigotti, Mg; Skeffington, Kl; Jones, Fp; Caputo, M; Brancaccio, A | |
| Loss of dystroglycan drives cellular senescence via defective mitosis-mediated genomic instability | 1-gen-2020 | JimenezGutierrez G.E.; MondragonGonzalez R.; SotoPonce L.A.; GomezMonsivais W.L.; GarciaAguirre I.; PachecoRivera R.A.; SuarezSanchez R.; Brancaccio A.; Magana J.J.; Perlingeiro R.C.R.; Cisneros B. | |
| The molecular basis and biologic significance of the ?-dystroglycan-emerin interaction | 1-gen-2020 | Gomezmonsivais, Wl; Monterrubioledezma, F; Huertacantillo, J; Mondragongonzalez, R; Alamilloiniesta, A; Garciaaguirre, I; Azuaramedina, Pm; Arguellogarcia, R; Riveramonroy, Je; Holaska, Jm; Hernandezmendez, Jme; Garrido, E; Magana, Jj; Winder, Sj; Brancaccio, A; Martinezvieyra, I; Navarrogarcia, F; Cisneros, B | |
| A molecular overview of the primary dystroglycanopathies | 1-gen-2019 | Brancaccio, Andrea; Brancaccio, Andrea | |
| Analysis of alpha-Dystroglycan/LG Domain Binding Modes: Investigating Protein Motifs That Regulate the Affinity of Isolated LG Domains | 1-gen-2019 | E Dempsey, Christopher; Giulia Bigotti, Maria; C Adams, Josephine; Brancaccio, Andrea | |
| A dystroglycan mutation (p.Cys667Phe) associated to muscle-eye-brain disease with multicystic leucodystrophy results in ER-retention of the mutant protein. | 1-gen-2018 | Signorino, Giulia; Covaceuszach, Sonia; Bozzi, Manuela; Hubner, Wolfgang; Monkemoller, Viola; Konarev Petr, V; Cassetta, Alberto; Brancaccio, Andrea; Sciandra, Francesca | |
| A dystroglycan mutation (p.Cys66uPhe) associated to muscle-eye-brain disease with multicystic leukodystrophy results in ER-retention of the mutant protein | 1-gen-2018 | Signorino, G; Covaceuszach, S; Bozzi, M; Hübner, W; Mönkemöller, V; Konarev, Pv; Cassetta, A; Brancaccio, A; Sciandra, F | |
| Intraring allostery controls the function and assembly of a hetero-oligomeric class II chaperonin. | 1-gen-2018 | Shoemark, Dk; Sessions, Rb; Brancaccio, A; Bigotti, Mg | |
| The enzymatic processing of ?-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site | 1-gen-2018 | Gioia M.; Fasciglione G.F.; Sbardella D.; Sciandra F.; Casella M.; Camerini S.; Crescenzi M.; Gori A.; Tarantino U.; Cozza P.; Brancaccio A.; Coletta M.; Bozzi M. | |
| The enzymatic processing of ?-dystroglycan by MMP-2 is controller by two anchoring sites distinct from the active site | 1-gen-2018 | Gioia, M; Fasciglione, Gf; Sbardella, D; Sciandra, F; Casella, M; Camerini, S; Crescenzi, M; Gori, A; Tarantino, U; Cozza, P; Brancaccio, A; Coletta, M; Bozzi, M | |
| ?-Dystroglycan hypoglycosylation affects cell migration by influencing ?-dystroglycan membrane clustering and filopodia length: A musticale confocal microscopi analysis | 1-gen-2017 | Palmieri, V; Bozzi, M; Signorino, G; Papi, M; De Spirito, M; Brancaccio, A; Maulucci, G; Sciandra, F | |
| An evaluation of the evolution of the gene structure of dystroglycan. | 1-gen-2017 | Brancaccio, Andrea; Adams Josephine, C | |
| Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene | 1-gen-2017 | Sciandra, F; Scicchitano, Bm; Signorino, G; Bigotti, Mg; Tavazzi, B; Lombardi, F; Bozzi, M; Sica, G; Giardina, B; Blaess, S; Brancaccio, A | |
| Structural flexibility of human alpha-dystroglycan | 1-gen-2017 | Covaceuszach, Sonia; Bozzi, Manuela; Bigotti Maria, Giulia; Sciandra, Francesca; Konarev Petr, Valeryevich; Brancaccio, Andrea; Cassetta, Alberto | |
| The effect of the pathological V72I, D109N and T190M missense mutations on the molecular structure of ?-dystroglycan | 1-gen-2017 | Covaceuszach, S; Bozzi, M; Bigotti, Mg; Sciandra, F; Konarev, Pv; Brancaccio, A; Cassetta, A | |
| Internal (His)(6)-tagging delivers a fully functional hetero-oligomeric class II chaperonin in high yield | 1-gen-2016 | Paul, Danielle M.; Beuron, Fabienne; Sessions, Richard B.; Brancaccio, Andrea; Bigotti, Maria Giulia | |
| Quantification, 2DE analysis and identification of enriched glycosylated proteins from mouse muscles: Difficulties and alternatives | 1-gen-2016 | Menegoci Eugenio Patricia de, Fatima; Assuncao Nilson, Antonio; Sciandra, Francesca; Aquino, Adriano; Brancaccio, Andrea; Carrilho, Emanuel | |
| A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core portein in some, but not all, dystroglycanopathy patients | 1-gen-2015 | L Humphrey, E; Lacey, E; Le, Lt; Feng, L; Sciandra, F; Morris, Cr; Hewitt, Je; Holt, I; Brancaccio, A; Barresi, R; A Sewry, C; Brown, Sc; Morris, Ge |