ANGELIN, ALESSIA

ANGELIN, ALESSIA  

Dipartimento di Medicina Sperimentale  

Mostra records
Risultati 1 - 20 di 35 (tempo di esecuzione: 0.021 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-2023 Advances and prospects for the Human BioMolecular Atlas Program (HuBMAP) Jain, S; Pei, L; Spraggins, Jm; Angelo, M; Carson, Jp; Gehlenborg, N; Ginty, F; Gonçalves, Jp; Hagood, Js; Hickey, Jw; Kelleher, Nl; Laurent, Lc; Lin, S; Lin, Y; Liu, H; Naba, A; Nakayasu, Es; Qian, Wj; Radtke, A; Robson, P; Stockwell, Br; Van de Plas, R; Vlachos, Is; Zhou, M; Ahn, Kj; Allen, J; Anderson, Dm; Anderton, Cr; Curcio, C; Angelin, A; Arvanitis, C; Atta, L; Awosika-Olumo, D; Bahmani, A; Bai, H; Balderrama, K; Balzano, L; Bandyopadhyay, G; Bandyopadhyay, S; Bar-Joseph, Z; Barnhart, K; Barwinska, D; Becich, M; Becker, L; Becker, W; Bedi, K; Bendall, S; Benninger, K; Betancur, D; Bettinger, K; Billings, S; Blood, P; Bolin, D; Border, S; Bosse, M; Bramer, L; Brewer, M; Brusko, M; Bueckle, A; Burke, K; Burnum-Johnson, K; Butcher, E; Butterworth, E; Cai, L; Calandrelli, R; Caldwell, M; Campbell-Thompson, M; Cao, D; Cao-Berg, I; Caprioli, R; Caraccio, C; Caron, A; Carroll, M; Chadwick, C; Chen, A; Chen, D; Chen, F; Chen, H; Chen, J; Chen, L; Chen, L; Chiacchia, K; Cho, S; Chou, P; Choy, L; Cisar, C; Clair, G; Clarke, L; Clouthier, Ka; Colley, Me; Conlon, K; Conroy, J; Contrepois, K; Corbett, A; Corwin, A; Cotter, D; Courtois, E; Cruz, A; Csonka, C; Czupil, K Articolo su rivista
1-gen-2008 Altered threshold of the mitochondrial permeability transition pore in Ullrich congenital muscular dystrophy Angelin, A; Bonaldo, P; Bernardi, P Articolo su rivista
11-giu-2004 Arachidonic acid released by phospholipase A2 activation triggers Ca2+-dependent apoptosis through the mitochondrial pathway Penzo, D; Petronilli, V; Angelin, A; Cusan, C; Colonna, R; Scorrano, L; Pagano, F; Prato, M; Di Lisa, F; Bernardi, P Articolo su rivista
31-ott-2010 Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration Grumati, P; Coletto, L; Sabatelli, P; Cescon, M; Angelin, A; Bertaggia, E; Blaauw, B; Urciuolo, A; Tiepolo, T; Merlini, L; Maraldi, Nm; Bernardi, P; Sandri, M; Bonaldo, P Articolo su rivista
1-gen-2020 Collagen VI Deficiency Results in Structural Abnormalities in the Mouse Lung Mereness, Ja; Bhattacharya, S; Ren, Y; Wang, Q; Anderson, Cs; Donlon, K; Dylag, Am; Haak, J; Angelin, A; Bonaldo, P; Mariani, Tj Articolo su rivista
1-gen-2023 Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts Guarnieri, Jw; Dybas, Jm; Fazelinia, H; Kim, Ms; Frere, J; Zhang, Y; Albrecht, Ys; Murdock, Dg; Angelin, A; Singh, Ln; Weiss, Sl; Best, Sm; Lott, Mt; Zhang, S; Cope, H; Zaksas, V; Saravia-Butler, A; Meydan, C; Foox, J; Mozsary, C; Bram, Y; Kidane, Y; Priebe, W; Emmett, Mr; Meller, R; Demharter, S; Stentoft-Hansen, V; Salvatore, M; Galeano, D; Enguita, Fj; Grabham, P; Trovao, Ns; Singh, U; Haltom, J; Heise, Mt; Moorman, Nj; Baxter, Vk; Madden, Ea; Taft-Benz, Sa; Anderson, Ej; Sanders, Wa; Dickmander, Rj; Baylin, Sb; Wurtele, Es; Moraes-Vieira, Pm; Taylor, D; Mason, Ce; Schisler, Jc; Schwartz, Re; Beheshti, A; Wallace, Dc Articolo su rivista
1-mar-2024 Correction to: Advances and prospects for the Human BioMolecular Atlas Program (HuBMAP) (Nature Cell Biology, (2023), 25, 8, (1089-1100), 10.1038/s41556-023-01194-w) Jain, S; Pei, L; Spraggins, Jm; Angelo, M; Carson, Jp; Gehlenborg, N; Ginty, F; Gonçalves, Jp; Hagood, Js; Hickey, Jw; Kelleher, Nl; Laurent, Lc; Lin, S; Lin, Y; Liu, H; Naba, A; Nakayasu, Es; Qian, Wj; Radtke, A; Robson, P; Stockwell, Br; Van de Plas, R; Vlachos, Is; Zhou, M; Börner, K; Snyder, Mp; Ahn, Kj; Allen, J; Anderson, Dm; Anderton, Cr; Curcio, C; Angelin, A; Arvanitis, C; Atta, L; Awosika-Olumo, D; Bahmani, A; Bai, H; Balderrama, K; Balzano, L; Bandyopadhyay, G; Bandyopadhyay, S; Bar-Joseph, Z; Barnhart, K; Barwinska, D; Becich, M; Becker, L; Becker, W; Bedi, K; Bendall, S; Benninger, K; Betancur, D; Bettinger, K; Billings, S; Blood, P; Bolin, D; Border, S; Bosse, M; Bramer, L; Brewer, M; Brusko, M; Bueckle, A; Burke, K; Burnum-Johnson, K; Butcher, E; Butterworth, E; Cai, L; Calandrelli, R; Caldwell, M; Campbell-Thompson, M; Cao, D; Cao-Berg, I; Caprioli, R; Caraccio, C; Caron, A; Carroll, M; Chadwick, C; Chen, A; Chen, D; Chen, F; Chen, H; Chen, J; Chen, L; Chen, L; Chiacchia, K; Cho, S; Chou, P; Choy, L; Cisar, C; Clair, G; Clarke, L; Clouthier, Ka; Colley, Me; Conlon, K; Conroy, J; Contrepois, K; Corbett, A; Corwin, A; Cotter, D; Courtois, E; Cruz, A Articolo su rivista
1-lug-2012 Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies Sabatelli, P; Palma, E; Angelin, A; Squarzoni, S; Urciuolo, A; Pellegrini, C; Tiepolo, T; Bonaldo, P; Gualandi, F; Merlini, L; Bernardi, P; Maraldi, N Articolo su rivista
14-lug-2023 Cyclin-dependent kinases regulate the adult nervous system via the one-carbon-metabolism Angelin, A Articolo su rivista
1-gen-2008 Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies Merlini, L; Angelin, A; Tiepolo, T; Braghetta, P; Sabatelli, P; Zamparelli, A; Ferlini, A; Maraldi, Nm; Bonaldo, P; Bernardi, P Articolo su rivista
17-ott-2011 Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results Merlini, L; Sabatelli, P; Armaroli, A; Gnudi, S; Angelin, A; Grumati, P; Michelini, Me; Franchella, A; Gualandi, F; Bertini, E; Maraldi, Nm; Ferlini, A; Bonaldo, P; Bernardi, P Articolo su rivista
1-ago-2016 Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction Kokoszka, Je; Waymire, Kg; Flierl, A; Sweeney, Km; Angelin, A; Macgregor, Gr; Wallace, Dc Articolo su rivista
1-gen-2015 Erratum: Landscape of the mitochondrial Hsp90 metabolome in tumours (Nature Communications (2013) 4 (2139) DOI:10.1038/ncomms3139) Chae, Yc; Angelin, A; Lisanti, S; Kossenkov, Av; Speicher, Kd; Wang, H; Powers, Jf; Tischler, As; Pacak, K; Fliedner, S; Michalek, Rd; Karoly, Ed; Wallace, Dc; Languino, Lr; Speicher, Dw; Altieri, Dc Articolo su rivista
13-feb-2015 Essential role of mitochondrial energy metabolism in Foxp3+ T-regulatory cell function and allograft survival Beier, Uh; Angelin, A; Akimova, T; Wang, L; Liu, Y; Xiao, H; Koike, Ma; Hancock, Sa; Bhatti, Tr; Han, R; Jiao, J; Veasey, Sc; Sims, Ca; Baur, Ja; Wallace, Dc; Hancock, Ww Articolo su rivista
6-giu-2017 Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments Angelin, A; Gil-de-Gómez, L; Dahiya, S; Jiao, J; Guo, L; Levine, Mh; Wang, Z; Quinn, Wj; Kopinski, Pk; Wang, L; Akimova, T; Liu, Y; Bhatti, Tr; Han, R; Laskin, Bl; Baur, Ja; Blair, Ia; Wallace, Dc; Hancock, Ww; Beier, Uh Articolo su rivista
1-gen-2009 Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice Palma, E; Tiepolo, T; Angelin, A; Sabatelli, P; Maraldi, N; Basso, E; Forte, M; Bernardip, P; Bonaldo, P Articolo su rivista
1-dic-2014 Genetic analysis of dTSPO, an outer mitochondrial membrane protein, reveals its functions in apoptosis, longevity, and Aβ42-induced neurodegeneration Lin, R; Angelin, A; Da Settimo, F; Martini, C; Taliani, S; Zhu, S; Wallace, Dc Articolo su rivista
1-gen-2019 H+ transport is an integral function of the mitochondrial ADP/ATP carrier Bertholet, Am; Chouchani, Et; Kazak, L; Angelin, A; Fedorenko, A; Long, Jz; Vidoni, S; Garrity, R; Cho, J; Terada, N; Wallace, Dc; Spiegelman, Bm; Kirichok, Y Articolo su rivista
16-gen-2020 HDAC10 deletion promotes Foxp3+ T-regulatory cell function Dahiya, S; Beier, Uh; Wang, L; Han, R; Jiao, J; Akimova, T; Angelin, A; Wallace, Dc; Hancock, Ww Articolo su rivista
15-dic-2020 Lactate Limits T Cell Proliferation via the NAD(H) Redox State Quinn, Wj; Jiao, J; Teslaa, T; Stadanlick, J; Wang, Z; Wang, L; Akimova, T; Angelin, A; Schäfer, Pm; Cully, Md; Perry, C; Kopinski, Pk; Guo, L; Blair, Ia; Ghanem, Lr; Leibowitz, Ms; Hancock, Ww; Moon, Ek; Levine, Mh; Eruslanov, Eb; Wallace, Dc; Baur, Ja; Beier, Uh Articolo su rivista