-
2
-
-
0033814140
-
Molecular basis of muscular dystrophies
-
R.D. Cohn, and K.P. Campbell Molecular basis of muscular dystrophies Muscle Nerve 23 2000 1456 1471
-
(2000)
Muscle Nerve
, vol.23
, pp. 1456-1471
-
-
Cohn, R.D.1
Campbell, K.P.2
-
3
-
-
0023821420
-
Ultrastructu4re of type VI collagen in human skin and cartilage suggests an anchoring function for this filamentous network
-
DOI 10.1083/jcb.107.5.1995
-
D.R. Keene, E. Engvall, and R.W. Glanville Ultrastructure of type VI collagen in human skin and cartilage suggests an anchoring function for this filamentous network J. Cell Biol. 107 1988 1995 2006 (Pubitemid 18263557)
-
(1988)
Journal of Cell Biology
, vol.107
, Issue.5
, pp. 1995-2006
-
-
Keene, D.R.1
Engvall, E.2
Glanville, R.W.3
-
4
-
-
0017259099
-
Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees
-
J. Bethlem, and G.K. Wijngaarden Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees Brain 99 1976 91 100
-
(1976)
Brain
, vol.99
, pp. 91-100
-
-
Bethlem, J.1
Wijngaarden, G.K.2
-
5
-
-
0035912809
-
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
-
DOI 10.1073/pnas.121027598
-
O. Camacho Vanegas, E. Bertini, R.Z. Zhang, S. Petrini, C. Minosse, P. Sabatelli, B. Giusti, M.L. Chu, and G. Pepe Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI Proc. Natl. Acad. Sci. USA 98 2001 7516 7521 (Pubitemid 32567980)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.13
, pp. 7516-7521
-
-
Vanegas, O.C.1
Bertini, E.2
Zhang, R.-Z.3
Petrini, S.4
Minosse, C.5
Sabatelli, P.6
Giusti, B.7
Chu, M.-L.8
Pepe, G.9
-
6
-
-
84863877497
-
ColVI myopathies: Where do we stand, where do we go?
-
V. Allamand, L. Brinas, P. Richard, T. Stojkovic, S. Quijano-Roy, and G. Bonne ColVI myopathies: where do we stand, where do we go? Skelet. Muscle 1 2011 30
-
(2011)
Skelet. Muscle
, vol.1
, pp. 30
-
-
Allamand, V.1
Brinas, L.2
Richard, P.3
Stojkovic, T.4
Quijano-Roy, S.5
Bonne, G.6
-
7
-
-
10744233522
-
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
-
DOI 10.1038/ng1270
-
W.A. Irwin, N. Bergamin, P. Sabatelli, C. Reggiani, A. Megighian, L. Merlini, P. Braghetta, M. Columbaro, D. Volpin, G.M. Bressan, P. Bernardi, and P. Bonaldo Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency Nat. Genet. 35 2003 367 371 (Pubitemid 37486921)
-
(2003)
Nature Genetics
, vol.35
, Issue.4
, pp. 367-371
-
-
Irwin, W.A.1
Bergamin, N.2
Sabatelli, P.3
Reggiani, C.4
Megighian, A.5
Merlini, L.6
Braghetta, P.7
Columbaro, M.8
Volpin, D.9
Bressan, G.M.10
Bernardi, P.11
Bonaldo, P.12
-
8
-
-
41849118741
-
Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy
-
DOI 10.1038/nm1736, PII NM1736
-
D.P. Millay, M.A. Sargent, H. Osinska, C.P. Baines, E.R. Barton, G. Vuagniaux, H.L. Sweeney, J. Robbins, and J.D. Molkentin Genetic and pharmacologic inhibition of mitochondrial-dependent necrosis attenuates muscular dystrophy Nat. Med. 14 2008 442 447 (Pubitemid 351499389)
-
(2008)
Nature Medicine
, vol.14
, Issue.4
, pp. 442-447
-
-
Millay, D.P.1
Sargent, M.A.2
Osinska, H.3
Baines, C.P.4
Barton, E.R.5
Vuagniaux, G.6
Sweeney, H.L.7
Robbins, J.8
Molkentin, J.D.9
-
9
-
-
65549087972
-
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice
-
E. Palma, T. Tiepolo, A. Angelin, P. Sabatelli, N.M. Maraldi, E. Basso, M.A. Forte, P. Bernardi, and P. Bonaldo Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice Hum. Mol. Genet. 18 2009 2024 2031
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2024-2031
-
-
Palma, E.1
Tiepolo, T.2
Angelin, A.3
Sabatelli, P.4
Maraldi, N.M.5
Basso, E.6
Forte, M.A.7
Bernardi, P.8
Bonaldo, P.9
-
10
-
-
0036838245
-
Oxidative stress and the pathogenesis of muscular dystrophies
-
T.A. Rando Oxidative stress and the pathogenesis of muscular dystrophies Am. J. Phys. Med. Rehabil. 81 2002 S175 S186
-
(2002)
Am. J. Phys. Med. Rehabil.
, vol.81
-
-
Rando, T.A.1
-
11
-
-
77957870248
-
Oxidative stress by monoamine oxidases is causally involved in myofiber damage in muscular dystrophy
-
S. Menazza, B. Blaauw, T. Tiepolo, L. Toniolo, P. Braghetta, B. Spolaore, C. Reggiani, F. Di Lisa, P. Bonaldo, and M. Canton Oxidative stress by monoamine oxidases is causally involved in myofiber damage in muscular dystrophy Hum. Mol. Genet. 19 2010 4207 4215
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 4207-4215
-
-
Menazza, S.1
Blaauw, B.2
Tiepolo, T.3
Toniolo, L.4
Braghetta, P.5
Spolaore, B.6
Reggiani, C.7
Di Lisa, F.8
Bonaldo, P.9
Canton, M.10
-
12
-
-
84882600223
-
Oxidative stress and pathology in muscular dystrophies: Focus on protein thiol oxidation and dysferlinopathies
-
J.R. Terrill, H.G. Radley-Crabb, T. Iwasaki, F.A. Lemckert, P.G. Arthur, and M.D. Grounds Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies FEBS J. 280 2013 4149 4164
-
(2013)
FEBS J.
, vol.280
, pp. 4149-4164
-
-
Terrill, J.R.1
Radley-Crabb, H.G.2
Iwasaki, T.3
Lemckert, F.A.4
Arthur, P.G.5
Grounds, M.D.6
-
13
-
-
0030890145
-
Oxidative damage to muscle protein in Duchenne muscular dystrophy
-
J.W. Haycock, S. MacNeil, P. Jones, J.B. Harris, and D. Mantle Oxidative damage to muscle protein in Duchenne muscular dystrophy Neuroreport 8 1996 357 361 (Pubitemid 126785588)
-
(1996)
NeuroReport
, vol.8
, Issue.1
, pp. 357-361
-
-
Haycock, J.W.1
Mac Neil, S.2
Jones, P.3
Harris, J.B.4
Mantle, D.5
-
14
-
-
33644854044
-
Green tea extract and its major polyphenol (-)-epigallocatechin gallate improve muscle function in a mouse model for Duchenne muscular dystrophy
-
O.M. Dorchies, S. Wagner, O. Vuadens, K. Waldhauser, T.M. Buetler, P. Kucera, and U.T. Ruegg Green tea extract and its major polyphenol (-)-epigallocatechin gallate improve muscle function in a mouse model for Duchenne muscular dystrophy Am. J. Physiol. Cell Physiol. 290 2006 C616 C625
-
(2006)
Am. J. Physiol. Cell Physiol.
, vol.290
-
-
Dorchies, O.M.1
Wagner, S.2
Vuadens, O.3
Waldhauser, K.4
Buetler, T.M.5
Kucera, P.6
Ruegg, U.T.7
-
15
-
-
45549084494
-
N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice
-
DOI 10.1113/jphysiol.2007.148338
-
N.P. Whitehead, C. Pham, O.L. Gervasio, and D.G. Allen N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice J. Physiol. 586 2008 2003 2014 (Pubitemid 351997524)
-
(2008)
Journal of Physiology
, vol.586
, Issue.7
, pp. 2003-2014
-
-
Whitehead, N.P.1
Pham, C.2
Gervasio, O.L.3
Allen, D.G.4
-
16
-
-
33645307953
-
The therapeutic potential of monoamine oxidase inhibitors
-
M.B. Youdim, D. Edmondson, and K.F. Tipton The therapeutic potential of monoamine oxidase inhibitors Nat. Rev. Neurosci. 7 2006 295 309
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 295-309
-
-
Youdim, M.B.1
Edmondson, D.2
Tipton, K.F.3
-
17
-
-
0018689023
-
The pattern of urinary catecholamines and their metabolites in Duchenne myopathy, in relation to disease evolution
-
Y. Dalmaz, L. Peyrin, J.C. Mamelle, D. Tuil, R. Gilly, and J.F. Cier The pattern of urinary catecholamines and their metabolites in Duchenne myopathy, in relation to disease evolution J. Neural Transm. 46 1979 17 34 (Pubitemid 10224593)
-
(1979)
Journal of Neural Transmission - General Section
, vol.46
, Issue.1
, pp. 17-34
-
-
Dalmaz, Y.1
Peyrin, L.2
Mamelle, J.C.3
-
18
-
-
0015988713
-
Proximal myopathy induced by 5-HT-imipramine simulates Duchenne dystrophy
-
J.M. Parker, and J.R. Mendell Proximal myopathy induced by 5-HT-imipramine simulates Duchenne dystrophy Nature 247 1974 103 104
-
(1974)
Nature
, vol.247
, pp. 103-104
-
-
Parker, J.M.1
Mendell, J.R.2
-
19
-
-
0037377592
-
Age-dependent increase in hydrogen peroxide production by cardiac monoamine oxidase A in rats
-
A. Maurel, C. Hernandez, O. Kunduzova, G. Bompart, C. Cambon, A. Parini, and B. Frances Age-dependent increase in hydrogen peroxide production by cardiac monoamine oxidase A in rats Am. J. Physiol. Heart Circ. Physiol 284 2003 H1460 H1467
-
(2003)
Am. J. Physiol. Heart Circ. Physiol
, vol.284
-
-
Maurel, A.1
Hernandez, C.2
Kunduzova, O.3
Bompart, G.4
Cambon, C.5
Parini, A.6
Frances, B.7
-
20
-
-
33644874936
-
Oxidative stress by monoamine oxidase mediates receptor-independent cardiomyocyte apoptosis by serotonin and postischemic myocardial injury
-
DOI 10.1161/CIRCULATIONAHA.104.528133, PII 0000301720051122000015
-
P. Bianchi, O. Kunduzova, E. Masini, C. Cambon, D. Bani, L. Raimondi, M.H. Seguelas, S. Nistri, W. Colucci, N. Leducq, and A. Parini Oxidative stress by monoamine oxidase mediates receptor-independent cardiomyocyte apoptosis by serotonin and postischemic myocardial injury Circulation 112 2005 3297 3305 (Pubitemid 43739375)
-
(2005)
Circulation
, vol.112
, Issue.21
, pp. 3297-3305
-
-
Bianchi, P.1
Kunduzova, O.2
Masini, E.3
Cambon, C.4
Bani, D.5
Raimondi, L.6
Seguelas, M.-H.7
Nistri, S.8
Colucci, W.9
Leducq, N.10
Parini, A.11
-
21
-
-
84870544267
-
P53-PGC-1alpha pathway mediates oxidative mitochondrial damage and cardiomyocyte necrosis induced by monoamine oxidase-A upregulation: Role in chronic left ventricular dysfunction in mice
-
C. Villeneuve, C. Guilbeau-Frugier, P. Sicard, O. Lairez, C. Ordener, T. Duparc, D. De Paulis, B. Couderc, O. Spreux-Varoquaux, F. Tortosa, A. Garnier, C. Knauf, P. Valet, E. Borchi, C. Nediani, A. Gharib, M. Ovize, M.B. Delisle, A. Parini, and J. Mialet-Perez p53-PGC-1alpha pathway mediates oxidative mitochondrial damage and cardiomyocyte necrosis induced by monoamine oxidase-A upregulation: role in chronic left ventricular dysfunction in mice Antioxid. Redox Signal. 18 2013 5 18
-
(2013)
Antioxid. Redox Signal.
, vol.18
, pp. 5-18
-
-
Villeneuve, C.1
Guilbeau-Frugier, C.2
Sicard, P.3
Lairez, O.4
Ordener, C.5
Duparc, T.6
De Paulis, D.7
Couderc, B.8
Spreux-Varoquaux, O.9
Tortosa, F.10
Garnier, A.11
Knauf, C.12
Valet, P.13
Borchi, E.14
Nediani, C.15
Gharib, A.16
Ovize, M.17
Delisle, M.B.18
Parini, A.19
Mialet-Perez, J.20
more..
-
22
-
-
23444436335
-
Monoamine oxidase-A is a major target gene for glucocorticoids in human skeletal muscle cells
-
DOI 10.1096/fj.04-3660fje
-
I. Manoli, H. Le, S. Alesci, K.K. McFann, Y.A. Su, T. Kino, G.P. Chrousos, and M.R. Blackman Monoamine oxidase-A is a major target gene for glucocorticoids in human skeletal muscle cells FASEB J. 19 2005 1359 1361 (Pubitemid 41113749)
-
(2005)
FASEB Journal
, vol.19
, Issue.10
, pp. 1359-1361
-
-
Manoli, I.1
Le, H.2
Alesci, S.3
McFann, K.K.4
Su, Y.A.5
Kino, T.6
Chrousos, G.P.7
Blackman, M.R.8
-
23
-
-
80051673220
-
Transcriptional regulation and multiple functions of MAO genes
-
J.C. Shih, J.B. Wu, and K. Chen Transcriptional regulation and multiple functions of MAO genes J. Neural Transm. 118 2011 979 986
-
(2011)
J. Neural Transm.
, vol.118
, pp. 979-986
-
-
Shih, J.C.1
Wu, J.B.2
Chen, K.3
-
24
-
-
0036895072
-
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC International Workshop, 23-24 November 2001, Naarden, NLD
-
DOI 10.1016/S0960-8966(02)00139-6, PII S0960896602001396
-
G. Pepe, E. Bertini, P. Bonaldo, K. Bushby, B. Giusti, M. de Visser, P. Guicheney, G. Lattanzi, L. Merlini, F. Muntoni, I. Nishino, I. Nonaka, R.B. Yaou, P. Sabatelli, C. Sewry, H. Topaloglu, and A. van der Kooi Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23-24 November 2001, Naarden, The Netherlands Neuromuscul. Disord. 12 2002 984 993 (Pubitemid 35408680)
-
(2002)
Neuromuscular Disorders
, vol.12
, Issue.10
, pp. 984-993
-
-
Pepe, G.1
Bertini, E.2
Bonaldo, P.3
Bushby, K.4
Giusti, B.5
De Visser, M.6
Guicheney, P.7
Lattanzi, G.8
Merlini, L.9
Muntoni, F.10
Nishino, I.11
Nonaka, I.12
Yaou, R.B.13
Sabatelli, P.14
Sewry, C.15
Topaloglu, H.16
Van Der Kooi, A.17
-
25
-
-
0347722754
-
Effects on collagen VI mRNA stability and microfibrillar assembly of three COL6A2 mutations in two families with Ullrich congenital muscular dystrophy
-
DOI 10.1074/jbc.M207696200
-
R.Z. Zhang, P. Sabatelli, T.C. Pan, S. Squarzoni, E. Mattioli, E. Bertini, G. Pepe, and M.L. Chu Effects on collagen VI mRNA stability and microfibrillar assembly of three COL6A2 mutations in two families with Ullrich congenital muscular dystrophy J. Biol. Chem. 277 2002 43557 43564 (Pubitemid 36157768)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.46
, pp. 43557-43564
-
-
Zhang, R.-Z.1
Sabatelli, P.2
Pan, T.-C.3
Squarzoni, S.4
Mattioli, E.5
Bertini, E.6
Pepe, G.7
Chu, M.-L.8
-
26
-
-
13444293092
-
Automated genomic sequence analysis of the three collagen VI genes: Applications to Ullrich congenital muscular dystrophy and Bethlem myopathy
-
DOI 10.1136/jmg.2004.023754
-
A.K. Lampe, D.M. Dunn, A.C. von Niederhausern, C. Hamil, A. Aoyagi, S.H. Laval, S.K. Marie, M.L. Chu, K. Swoboda, F. Muntoni, C.G. Bonnemann, K.M. Flanigan, K.M. Bushby, and R.B. Weiss Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy J. Med. Genet. 42 2005 108 120 (Pubitemid 40204364)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.2
, pp. 108-120
-
-
Lampe, A.K.1
Dunn, D.M.2
Von Niederhausern, A.C.3
Hamil, C.4
Aoyagi, A.5
Laval, S.H.6
Marie, S.K.7
Chu, M.-L.8
Swoboda, K.9
Muntoni, F.10
Bonnemann, C.G.11
Flanigan, K.M.12
Bushby, K.M.D.13
Weiss, R.B.14
-
27
-
-
33846477445
-
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
-
DOI 10.1073/pnas.0610270104
-
A. Angelin, T. Tiepolo, P. Sabatelli, P. Grumati, N. Bergamin, C. Golfieri, E. Mattioli, F. Gualandi, A. Ferlini, L. Merlini, N.M. Maraldi, P. Bonaldo, and P. Bernardi Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins Proc. Natl. Acad. Sci. USA 104 2007 991 996 (Pubitemid 46154724)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.3
, pp. 991-996
-
-
Angelin, A.1
Tiepolo, T.2
Sabatelli, P.3
Grumati, P.4
Bergamin, N.5
Golfieri, C.6
Mattioli, E.7
Gualandi, F.8
Ferlini, A.9
Merlini, L.10
Maraldi, N.M.11
Bonaldo, P.12
Bernardi, P.13
-
28
-
-
66749094790
-
Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophy
-
E. Martoni, A. Urciuolo, P. Sabatelli, M. Fabris, M. Bovolenta, M. Neri, P. Grumati, A. D'Amico, M. Pane, E. Mercuri, E. Bertini, L. Merlini, P. Bonaldo, A. Ferlini, and F. Gualandi Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophy Hum. Mutat. 30 2009 E662 E672
-
(2009)
Hum. Mutat.
, vol.30
-
-
Martoni, E.1
Urciuolo, A.2
Sabatelli, P.3
Fabris, M.4
Bovolenta, M.5
Neri, M.6
Grumati, P.7
D'Amico, A.8
Pane, M.9
Mercuri, E.10
Bertini, E.11
Merlini, L.12
Bonaldo, P.13
Ferlini, A.14
Gualandi, F.15
-
29
-
-
20144368040
-
Lamin A N-terminal phosphorylation is associated with myoblast activation: Impairment in Emery-Dreifuss muscular dystrophy
-
DOI 10.1136/jmg.2004.026112
-
V. Cenni, P. Sabatelli, E. Mattioli, S. Marmiroli, C. Capanni, A. Ognibene, S. Squarzoni, N.M. Maraldi, G. Bonne, M. Columbaro, L. Merlini, G. Lattanzi, and A. Lamin N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy J. Med. Genet. 42 2005 214 220 (Pubitemid 40380301)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.3
, pp. 214-220
-
-
Cenni, V.1
Sabatelli, P.2
Mattioli, E.3
Marmiroli, S.4
Capanni, C.5
Ognibene, A.6
Squarzoni, S.7
Maraldi, N.M.8
Bonne, G.9
Columbaro, M.10
Merlini, L.11
Lattanzi, G.12
-
30
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
M.W. Pfaffl A new mathematical model for relative quantification in real-time RT-PCR Nucleic Acids Res. 29 2001 e45
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 45
-
-
Pfaffl, M.W.1
-
31
-
-
0036581160
-
Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
-
M.W. Pfaffl, G.W. Horgan, and L. Dempfle Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR Nucleic Acids Res. 30 2002 e36
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 36
-
-
Pfaffl, M.W.1
Horgan, G.W.2
Dempfle, L.3
-
32
-
-
0030051609
-
Interactions of cyclophilin with the mitochondrial inner membrane and regulation of the permeability transition pore, a cyclosporin A-sensitive channel
-
DOI 10.1074/jbc.271.4.2185
-
A. Nicolli, E. Basso, V. Petronilli, R.M. Wenger, and P. Bernardi Interactions of cyclophilin with the mitochondrial inner membrane and regulation of the permeability transition pore, and cyclosporin A-sensitive channel J. Biol. Chem. 271 1996 2185 2192 (Pubitemid 26047809)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.4
, pp. 2185-2192
-
-
Nicolli, A.1
Basso, E.2
Petronilli, V.3
Wenger, R.M.4
Bernardi, P.5
-
33
-
-
0346154812
-
Monoamine Oxidase (MAO) in Human Peripheral Tissues
-
DOI 10.1016/S0161-813X(03)00094-9
-
E. Billett Monoamine oxidase (MAO) in human peripheral tissues NeuroToxicology 25 2004 139 148 (Pubitemid 38044175)
-
(2004)
NeuroToxicology
, vol.25
, Issue.1-2
, pp. 139-148
-
-
Billett, E.E.1
-
34
-
-
42449109035
-
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
-
DOI 10.1073/pnas.0800962105
-
L. Merlini, A. Angelin, T. Tiepolo, P. Braghetta, P. Sabatelli, A. Zamparelli, A. Ferlini, N.M. Maraldi, P. Bonaldo, and P. Bernardi Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies Proc. Natl. Acad. Sci. USA 105 2008 5225 5229 (Pubitemid 351738538)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.13
, pp. 5225-5229
-
-
Merlini, L.1
Angelin, A.2
Tiepolo, T.3
Braghetta, P.4
Sabatelli, P.5
Zamparelli, A.6
Ferlini, A.7
Maraldi, N.M.8
Bonaldo, P.9
Bernardi, P.10
-
35
-
-
0037014635
-
PUVA-induced apoptosis involves mitochondrial dysfunction caused by the opening of the permeability transition pore
-
DOI 10.1016/S0014-5793(02)02926-5, PII S0014579302029265
-
M. Canton, S. Caffieri, F. Dall'Acqua, and F. Di Lisa PUVA-induced apoptosis involves mitochondrial dysfunction caused by the opening of the permeability transition pore FEBS Lett. 522 2002 168 172 (Pubitemid 34722518)
-
(2002)
FEBS Letters
, vol.522
, Issue.1-3
, pp. 168-172
-
-
Canton, M.1
Caffieri, S.2
Dall'Acqua, F.3
Di Lisa, F.4
-
36
-
-
46349109604
-
Altered threshold of the mitochondrial permeability transition pore in Ullrich congenital muscular dystrophy
-
A. Angelin, P. Bonaldo, and P. Bernardi Altered threshold of the mitochondrial permeability transition pore in Ullrich congenital muscular dystrophy Biochim. Biophys. Acta 1777 2008 893 896
-
(2008)
Biochim. Biophys. Acta
, vol.1777
, pp. 893-896
-
-
Angelin, A.1
Bonaldo, P.2
Bernardi, P.3
-
37
-
-
84898670714
-
Monoamine oxidase is a major determinant of redox balance in human atrial myocardium and is associated with postoperative atrial fibrillation
-
E.J. Anderson, J.T. Efird, S.W. Davies, W.T. O'Neal, T.M. Darden, K.A. Thayne, L.A. Katunga, L.C. Kindell, T.B. Ferguson, C.A. Anderson, W.R. Chitwood, T.C. Koutlas, J.M. Williams, E. Rodriguez, and A.P. Kypson Monoamine oxidase is a major determinant of redox balance in human atrial myocardium and is associated with postoperative atrial fibrillation J. Am. Heart Assoc. 3 2014 e000713
-
(2014)
J. Am. Heart Assoc.
, vol.3
, pp. 000713
-
-
Anderson, E.J.1
Efird, J.T.2
Davies, S.W.3
O'Neal, W.T.4
Darden, T.M.5
Thayne, K.A.6
Katunga, L.A.7
Kindell, L.C.8
Ferguson, T.B.9
Anderson, C.A.10
Chitwood, W.R.11
Koutlas, T.C.12
Williams, J.M.13
Rodriguez, E.14
Kypson, A.P.15
-
38
-
-
0013899347
-
Catecholamine distribution in mice afflicted with muscular dystrophy
-
P. Gordon, and R.M. Dowben Catecholamine distribution in mice afflicted with muscular dystrophy Am. J. Physiol. 210 1966 728 732
-
(1966)
Am. J. Physiol.
, vol.210
, pp. 728-732
-
-
Gordon, P.1
Dowben, R.M.2
-
39
-
-
0015800032
-
Abnormal intrafibrillar monoamines in sex-linked muscular dystrophy
-
T.L. Wright, J.A. O'Neill, and W.H. Olson Abnormal intrafibrillar monoamines in sex-linked muscular dystrophy Neurology 23 1973 510 517
-
(1973)
Neurology
, vol.23
, pp. 510-517
-
-
Wright, T.L.1
O'Neill, J.A.2
Olson, W.H.3
-
40
-
-
84891823906
-
Monoamine oxidase B prompts mitochondrial and cardiac dysfunction in pressure overloaded hearts
-
N. Kaludercic, A. Carpi, T. Nagayama, V. Sivakumaran, G. Zhu, E.W. Lai, D. Bedja, A. De Mario, K. Chen, K.L. Gabrielson, M.L. Lindsey, K. Pacak, E. Takimoto, J.C. Shih, D.A. Kass, F. Di Lisa, and N. Paolocci Monoamine oxidase B prompts mitochondrial and cardiac dysfunction in pressure overloaded hearts Antioxid. Redox Signal. 20 2014 267 280
-
(2014)
Antioxid. Redox Signal.
, vol.20
, pp. 267-280
-
-
Kaludercic, N.1
Carpi, A.2
Nagayama, T.3
Sivakumaran, V.4
Zhu, G.5
Lai, E.W.6
Bedja, D.7
De Mario, A.8
Chen, K.9
Gabrielson, K.L.10
Lindsey, M.L.11
Pacak, K.12
Takimoto, E.13
Shih, J.C.14
Kass, D.A.15
Di Lisa, F.16
Paolocci, N.17
-
41
-
-
84880253528
-
Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex i
-
E.T. Chouchani, C. Methner, S.M. Nadtochiy, A. Logan, V.R. Pell, S. Ding, A.M. James, H.M. Cocheme, J. Reinhold, K.S. Lilley, L. Partridge, I.M. Fearnley, A.J. Robinson, R.C. Hartley, R.A. Smith, T. Krieg, P.S. Brookes, and M.P. Murphy Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex I Nat. Med 19 2013 753 759
-
(2013)
Nat. Med
, vol.19
, pp. 753-759
-
-
Chouchani, E.T.1
Methner, C.2
Nadtochiy, S.M.3
Logan, A.4
Pell, V.R.5
Ding, S.6
James, A.M.7
Cocheme, H.M.8
Reinhold, J.9
Lilley, K.S.10
Partridge, L.11
Fearnley, I.M.12
Robinson, A.J.13
Hartley, R.C.14
Smith, R.A.15
Krieg, T.16
Brookes, P.S.17
Murphy, M.P.18
-
42
-
-
81155123702
-
Cysteine 203 of cyclophilin D is critical for cyclophilin D activation of the mitochondrial permeability transition pore
-
T.T. Nguyen, M.V. Stevens, M. Kohr, C. Steenbergen, M.N. Sack, and E. Murphy Cysteine 203 of cyclophilin D is critical for cyclophilin D activation of the mitochondrial permeability transition pore J. Biol. Chem. 286 2011 40184 40192
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 40184-40192
-
-
Nguyen, T.T.1
Stevens, M.V.2
Kohr, M.3
Steenbergen, C.4
Sack, M.N.5
Murphy, E.6
-
44
-
-
84876031864
-
Dimers of mitochondrial ATP synthase form the permeability transition pore
-
V. Giorgio, S. von Stockum, M. Antoniel, A. Fabbro, F. Fogolari, M. Forte, G.D. Glick, V. Petronilli, M. Zoratti, I. Szabo, G. Lippe, and P. Bernardi Dimers of mitochondrial ATP synthase form the permeability transition pore Proc. Natl. Acad. Sci. USA 110 2013 5887 5892
-
(2013)
Proc. Natl. Acad. Sci. USA
, vol.110
, pp. 5887-5892
-
-
Giorgio, V.1
Von Stockum, S.2
Antoniel, M.3
Fabbro, A.4
Fogolari, F.5
Forte, M.6
Glick, G.D.7
Petronilli, V.8
Zoratti, M.9
Szabo, I.10
Lippe, G.11
Bernardi, P.12
-
45
-
-
21244446551
-
Properties of the permeability transition pore in mitochondria devoid of cyclophilin D
-
DOI 10.1074/jbc.C500089200
-
E. Basso, L. Fante, J. Fowlkes, V. Petronilli, M.A. Forte, and P. Bernardi Properties of the permeability transition pore in mitochondria devoid of cyclophilin D J. Biol. Chem. 280 2005 18558 18561 (Pubitemid 41379552)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.19
, pp. 18558-18561
-
-
Basso, E.1
Fante, L.2
Fowlkes, J.3
Petronilli, V.4
Forte, M.A.5
Bernardi, P.6
-
46
-
-
77957842939
-
Cyclophilin D controls mitochondrial pore-dependent Ca(2+) exchange, metabolic flexibility, and propensity for heart failure in mice
-
J.W. Elrod, R. Wong, S. Mishra, R.J. Vagnozzi, B. Sakthievel, S.A. Goonasekera, J. Karch, S. Gabel, J. Farber, T. Force, J.H. Brown, E. Murphy, and J.D. Molkentin Cyclophilin D controls mitochondrial pore-dependent Ca(2+) exchange, metabolic flexibility, and propensity for heart failure in mice J. Clin. Invest. 120 2010 3680 3687
-
(2010)
J. Clin. Invest.
, vol.120
, pp. 3680-3687
-
-
Elrod, J.W.1
Wong, R.2
Mishra, S.3
Vagnozzi, R.J.4
Sakthievel, B.5
Goonasekera, S.A.6
Karch, J.7
Gabel, S.8
Farber, J.9
Force, T.10
Brown, J.H.11
Murphy, E.12
Molkentin, J.D.13
-
47
-
-
84855323182
-
Cyclosporine A in Ullrich congenital muscular dystrophy: Long-term results
-
L. Merlini, P. Sabatelli, A. Armaroli, S. Gnudi, A. Angelin, P. Grumati, M.E. Michelini, A. Franchella, F. Gualandi, E. Bertini, N.M. Maraldi, A. Ferlini, P. Bonaldo, and P. Bernardi Cyclosporine A in Ullrich congenital muscular dystrophy: long-term results Oxid. Med. Cell Longev 2011 2011 139194
-
(2011)
Oxid. Med. Cell Longev
, vol.2011
, pp. 139194
-
-
Merlini, L.1
Sabatelli, P.2
Armaroli, A.3
Gnudi, S.4
Angelin, A.5
Grumati, P.6
Michelini, M.E.7
Franchella, A.8
Gualandi, F.9
Bertini, E.10
Maraldi, N.M.11
Ferlini, A.12
Bonaldo, P.13
Bernardi, P.14
-
48
-
-
34147152905
-
The role of free radicals in the pathophysiology of muscular dystrophy
-
DOI 10.1152/japplphysiol.01145.2006
-
J.G. Tidball, and M. Wehling-Henricks The role of free radicals in the pathophysiology of muscular dystrophy J. Appl. Physiol. 102 2007 1677 1686 (Pubitemid 46571068)
-
(2007)
Journal of Applied Physiology
, vol.102
, Issue.4
, pp. 1677-1686
-
-
Tidball, J.G.1
Wehling-Henricks, M.2
-
49
-
-
0029194750
-
The definition and measurement of antioxidants in biological systems
-
B. Halliwell, and J.M. Gutteridge The definition and measurement of antioxidants in biological systems Free Radic. Biol. Med. 18 1995 125 126
-
(1995)
Free Radic. Biol. Med.
, vol.18
, pp. 125-126
-
-
Halliwell, B.1
Gutteridge, J.M.2
-
50
-
-
84858625921
-
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies
-
P. Sabatelli, E. Palma, A. Angelin, S. Squarzoni, A. Urciuolo, C. Pellegrini, T. Tiepolo, P. Bonaldo, F. Gualandi, L. Merlini, P. Bernardi, and N.M. Maraldi Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies J. Cell Physiol. 227 2012 2927 2935
-
(2012)
J. Cell Physiol.
, vol.227
, pp. 2927-2935
-
-
Sabatelli, P.1
Palma, E.2
Angelin, A.3
Squarzoni, S.4
Urciuolo, A.5
Pellegrini, C.6
Tiepolo, T.7
Bonaldo, P.8
Gualandi, F.9
Merlini, L.10
Bernardi, P.11
Maraldi, N.M.12
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