-
1
-
-
0000995321
-
Glycogen Storage Disease Type II: Acid alpha-Glucosidase (Acid Maltase) Deficiency
-
In:, McGraw-Hill
-
Hirschhorn R, Reuser AJ (2000) Glycogen Storage Disease Type II: Acid alpha-Glucosidase (Acid Maltase) Deficiency. In: The Metabolic and Molecular Basis of Inherited Disease McGraw-Hill. pp 3389-3420.
-
(2000)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 3389-3420
-
-
Hirschhorn, R.1
Reuser, A.J.2
-
2
-
-
33646830132
-
A retrospective, multinational, multicenter study on the natural history of infantileonset Pompe disease
-
Kishnani PS, Hwu WL, Mandel H, Nicolino M, Yong F, et al. (2006) A retrospective, multinational, multicenter study on the natural history of infantileonset Pompe disease. J Pediatr 148: 671-676.
-
(2006)
J Pediatr
, vol.148
, pp. 671-676
-
-
Kishnani, P.S.1
Hwu, W.L.2
Mandel, H.3
Nicolino, M.4
Yong, F.5
-
3
-
-
23944445667
-
The natural course of non-classic Pompe's disease; a review of 225 published cases
-
Winkel LP, Hagemans ML, Van Doorn PA, Loonen MC, Hop WJ, et al. (2005) The natural course of non-classic Pompe's disease; a review of 225 published cases. J Neurol 252: 875-884.
-
(2005)
J Neurol
, vol.252
, pp. 875-884
-
-
Winkel, L.P.1
Hagemans, M.L.2
Van Doorn, P.A.3
Loonen, M.C.4
Hop, W.J.5
-
4
-
-
0042131675
-
The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature
-
Van den Hout HM, Hop W, van Diggelen OP, Smeitink JA, Smit GP, et al. (2003) The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature. Pediatrics 112: 332-340.
-
(2003)
Pediatrics
, vol.112
, pp. 332-340
-
-
van den Hout, H.M.1
Hop, W.2
van Diggelen, O.P.3
Smeitink, J.A.4
Smit, G.P.5
-
5
-
-
33846033132
-
Recombinant human acid [alpha]-glucosidase: Major clinical benefits in infantile-onset Pompe disease
-
Kishnani PS, Corzo D, Nicolino M, Byrne B, Mandel H, et al. (2007) Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease. Neurology 68: 99-109.
-
(2007)
Neurology
, vol.68
, pp. 99-109
-
-
Kishnani, P.S.1
Corzo, D.2
Nicolino, M.3
Byrne, B.4
Mandel, H.5
-
6
-
-
63449127241
-
Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease
-
Nicolino M, Byrne B, Wraith JE, Leslie N, Mandel H, et al. (2009) Clinical outcomes after long-term treatment with alglucosidase alfa in infants and children with advanced Pompe disease. Genet Med 11: 210-219.
-
(2009)
Genet Med
, vol.11
, pp. 210-219
-
-
Nicolino, M.1
Byrne, B.2
Wraith, J.E.3
Leslie, N.4
Mandel, H.5
-
7
-
-
74849085443
-
Enzyme replacement therapy with alglucosidase alfa in 44 patients with lateonset glycogen storage disease type 2: 12-month results of an observational clinical trial
-
Strothotte S, Strigl-Pill N, Grunert B, Kornblum C, Eger K, et al. (2009) Enzyme replacement therapy with alglucosidase alfa in 44 patients with lateonset glycogen storage disease type 2: 12-month results of an observational clinical trial. J Neurol 257: 91-97.
-
(2009)
J Neurol
, vol.257
, pp. 91-97
-
-
Strothotte, S.1
Strigl-Pill, N.2
Grunert, B.3
Kornblum, C.4
Eger, K.5
-
8
-
-
77950963839
-
A randomized study of alglucosidase alfa in late-onset Pompe's disease
-
Van der Ploeg AT, Clemens PR, Corzo D, Escolar DM, Florence J, et al. (2010) A randomized study of alglucosidase alfa in late-onset Pompe's disease. N Engl J Med 362: 1396-1406.
-
(2010)
N Engl J Med
, vol.362
, pp. 1396-1406
-
-
van der Ploeg, A.T.1
Clemens, P.R.2
Corzo, D.3
Escolar, D.M.4
Florence, J.5
-
9
-
-
72549095406
-
Regulation Mechanisms and Signaling Pathways of Autophagy
-
He C, Klionsky DJ (2009) Regulation Mechanisms and Signaling Pathways of Autophagy. Annu Rev Genet 43: 67-93.
-
(2009)
Annu Rev Genet
, vol.43
, pp. 67-93
-
-
He, C.1
Klionsky, D.J.2
-
10
-
-
39849109338
-
Autophagy fights disease through cellular self-digestion
-
Mizushima N, Levine B, Cuervo AM, Klionsky DJ (2008) Autophagy fights disease through cellular self-digestion. Nature 451: 1069-1075.
-
(2008)
Nature
, vol.451
, pp. 1069-1075
-
-
Mizushima, N.1
Levine, B.2
Cuervo, A.M.3
Klionsky, D.J.4
-
12
-
-
58149468046
-
When more is less: Excess and deficiency of autophagy coexist in skeletal muscle in Pompe disease
-
Raben N, Baum R, Schreiner C, Takikita S, Mizushima N, et al. (2009) When more is less: excess and deficiency of autophagy coexist in skeletal muscle in Pompe disease. Autophagy 5: 111-113.
-
(2009)
Autophagy
, vol.5
, pp. 111-113
-
-
Raben, N.1
Baum, R.2
Schreiner, C.3
Takikita, S.4
Mizushima, N.5
-
13
-
-
34548621869
-
Deconstructing Pompe disease by analyzing single muscle fibers
-
Raben N, Takikita S, Pittis MG, Bembi B, Marie SKN, et al. (2007) Deconstructing Pompe disease by analyzing single muscle fibers. Autophagy 3: 546-552.
-
(2007)
Autophagy
, vol.3
, pp. 546-552
-
-
Raben, N.1
Takikita, S.2
Pittis, M.G.3
Bembi, B.4
Marie, S.K.N.5
-
14
-
-
33751211826
-
Characterization of pre-and post-treatment pathology after enzyme replacement therapy for pompe disease
-
Thurberg BL, Lynch MC, Vaccaro C, Afonso K, Tsai AC, et al. (2006) Characterization of pre-and post-treatment pathology after enzyme replacement therapy for pompe disease. Lab Invest 86: 1208-1220.
-
(2006)
Lab Invest
, vol.86
, pp. 1208-1220
-
-
Thurberg, B.L.1
Lynch, M.C.2
Vaccaro, C.3
Afonso, K.4
Tsai, A.C.5
-
15
-
-
33644660537
-
PGC-1 coactivators: Inducible regulators of energy metabolism in health and disease
-
Finck BN, Kelly DP (2006) PGC-1 coactivators: inducible regulators of energy metabolism in health and disease. J Clin Invest 116: 615-622.
-
(2006)
J Clin Invest
, vol.116
, pp. 615-622
-
-
Finck, B.N.1
Kelly, D.P.2
-
16
-
-
33845596500
-
Peroxisome proliferator-activated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism
-
Handschin C, Spiegelman BM (2006) Peroxisome proliferator-activated receptor gamma coactivator 1 coactivators, energy homeostasis, and metabolism. Endocr Rev 27: 728-735.
-
(2006)
Endocr Rev
, vol.27
, pp. 728-735
-
-
Handschin, C.1
Spiegelman, B.M.2
-
17
-
-
56049107038
-
PGC-1 coactivators and skeletal muscle adaptations in health and disease
-
Arany Z (2008) PGC-1 coactivators and skeletal muscle adaptations in health and disease. Curr Opin Genet Dev 18: 426-434.
-
(2008)
Curr Opin Genet Dev
, vol.18
, pp. 426-434
-
-
Arany, Z.1
-
18
-
-
0037102256
-
Transcriptional coactivator PGC-1 alpha drives the formation of slow-twitch muscle fibres
-
Lin J, Wu H, Tarr PT, Zhang CY, Wu Z, et al. (2002) Transcriptional coactivator PGC-1 alpha drives the formation of slow-twitch muscle fibres. Nature 418: 797-801.
-
(2002)
Nature
, vol.418
, pp. 797-801
-
-
Lin, J.1
Wu, H.2
Tarr, P.T.3
Zhang, C.Y.4
Wu, Z.5
-
19
-
-
77953495952
-
PGC-1{alpha} or PGC-1{beta} (peroxisome proliferator-activated receptor {gamma} coactivator 1{alpha} or 1{beta}) overexpression inhibits muscle protein degradation, induction of ubiquitin ligases, and disuse atrophy
-
Brault JJ, Jespersen JG, Goldberg AL (2010) PGC-1{alpha} or PGC-1{beta} (peroxisome proliferator-activated receptor {gamma} coactivator 1{alpha} or 1{beta}) overexpression inhibits muscle protein degradation, induction of ubiquitin ligases, and disuse atrophy. J Biol Chem 285: 19460-19471.
-
(2010)
J Biol Chem
, vol.285
, pp. 19460-19471
-
-
Brault, J.J.1
Jespersen, J.G.2
Goldberg, A.L.3
-
20
-
-
73949099327
-
Increased muscle PGC-1alpha expression protects from sarcopenia and metabolic disease during aging
-
Wenz T, Rossi SG, Rotundo RL, Spiegelman BM, Moraes CT (2009) Increased muscle PGC-1alpha expression protects from sarcopenia and metabolic disease during aging. Proc Natl Acad Sci U S A 106: 20405-20410.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 20405-20410
-
-
Wenz, T.1
Rossi, S.G.2
Rotundo, R.L.3
Spiegelman, B.M.4
Moraes, C.T.5
-
21
-
-
33750825245
-
PGC-1alpha protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophyspecific gene transcription
-
Sandri M, Lin J, Handschin C, Yang W, Arany ZP, et al. (2006) PGC-1alpha protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophyspecific gene transcription. Proc Natl Acad Sci U S A 103: 16260-16265.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 16260-16265
-
-
Sandri, M.1
Lin, J.2
Handschin, C.3
Yang, W.4
Arany, Z.P.5
-
22
-
-
57049094929
-
Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease
-
Raben N, Hill V, Shea L, Takikita S, Baum R, et al. (2008) Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease. Hum Mol Genet 17: 3897-3908.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3897-3908
-
-
Raben, N.1
Hill, V.2
Shea, L.3
Takikita, S.4
Baum, R.5
-
23
-
-
35648937073
-
Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1alpha musclespecific knock-out animals
-
Handschin C, Chin S, Li P, Liu F, Maratos-Flier E, et al. (2007) Skeletal muscle fiber-type switching, exercise intolerance, and myopathy in PGC-1alpha musclespecific knock-out animals. J Biol Chem 282: 30014-30021.
-
(2007)
J Biol Chem
, vol.282
, pp. 30014-30021
-
-
Handschin, C.1
Chin, S.2
Li, P.3
Liu, F.4
Maratos-Flier, E.5
-
24
-
-
37849042536
-
A rational mechanism for combination treatment of Huntington's disease using lithium and rapamycin
-
Sarkar S, Krishna G, Imarisio S, Saiki S, O'Kane CJ, Rubinsztein DC (2008) A rational mechanism for combination treatment of Huntington's disease using lithium and rapamycin. Hum Mol Genet 17: 170-178.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 170-178
-
-
Sarkar, S.1
Krishna, G.2
Imarisio, S.3
Saiki, S.4
O'Kane, C.J.5
Rubinsztein, D.C.6
-
25
-
-
78649288882
-
Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder-murine Pompe disease
-
in press
-
Raben N, Schreiner C, Baum R, Takikita S, Xu S, et al. (2010) Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder-murine Pompe disease. Autophagy 6: in press.
-
(2010)
Autophagy
, pp. 6
-
-
Raben, N.1
Schreiner, C.2
Baum, R.3
Takikita, S.4
Xu, S.5
-
26
-
-
19944383100
-
Replacing acid alpha-glucosidase in Pompe disease: Recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers
-
Raben N, Fukuda T, Gilbert AL, de Jong D, Thurberg BL, et al. (2005) Replacing acid alpha-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers. Mol Ther 11: 48-56.
-
(2005)
Mol Ther
, vol.11
, pp. 48-56
-
-
Raben, N.1
Fukuda, T.2
Gilbert, A.L.3
de Jong, D.4
Thurberg, B.L.5
-
27
-
-
33751014016
-
Autophagy and mistargeting of therapeutic enzyme in skeletal muscle in Pompe disease
-
Fukuda T, Ahearn M, Roberts A, Mattaliano RJ, Zaal K, et al. (2006) Autophagy and mistargeting of therapeutic enzyme in skeletal muscle in Pompe disease. Mol Ther 14: 831-839.
-
(2006)
Mol Ther
, vol.14
, pp. 831-839
-
-
Fukuda, T.1
Ahearn, M.2
Roberts, A.3
Mattaliano, R.J.4
Zaal, K.5
-
28
-
-
78649333177
-
Differences in the predominance of lysosomal and autophagic pathologies between infants and adults with Pompe disease: Implications for therapy
-
in press
-
Raben N, Ralston E, Chien YH, Baum R, Schreiner C, et al. (2010) Differences in the predominance of lysosomal and autophagic pathologies between infants and adults with Pompe disease: implications for therapy. Mol Genet Metab 6: in press.
-
(2010)
Mol Genet Metab
, pp. 6
-
-
Raben, N.1
Ralston, E.2
Chien, Y.H.3
Baum, R.4
Schreiner, C.5
-
29
-
-
77952409809
-
Mitochondrial dysfunction and oxidative stress mediate the physiological impairment induced by the disruption of autophagy
-
Wu JJ, Quijano C, Chen E, Liu H, Cao L, et al. (2009) Mitochondrial dysfunction and oxidative stress mediate the physiological impairment induced by the disruption of autophagy. Aging (Albany NY) 1: 425-437.
-
(2009)
Aging (Albany NY)
, vol.1
, pp. 425-437
-
-
Wu, J.J.1
Quijano, C.2
Chen, E.3
Liu, H.4
Cao, L.5
-
30
-
-
70449927247
-
Autophagy is required to maintain muscle mass
-
Masiero E, Agatea L, Mammucari C, Blaauw B, Loro E, et al. (2009) Autophagy is required to maintain muscle mass. Cell Metab 10: 507-515.
-
(2009)
Cell Metab
, vol.10
, pp. 507-515
-
-
Masiero, E.1
Agatea, L.2
Mammucari, C.3
Blaauw, B.4
Loro, E.5
-
31
-
-
77953531909
-
Autophagy inhibition induces atrophy and myopathy in adult skeletal muscles
-
Masiero E, Sandri M (2010) Autophagy inhibition induces atrophy and myopathy in adult skeletal muscles. Autophagy 6: 307-309.
-
(2010)
Autophagy
, vol.6
, pp. 307-309
-
-
Masiero, E.1
Sandri, M.2
-
32
-
-
34548264161
-
Activity-dependent signaling pathways controlling muscle diversity and plasticity
-
Schiaffino S, Sandri M, Murgia M (2007) Activity-dependent signaling pathways controlling muscle diversity and plasticity. Physiology (Bethesda) 22: 269-278.
-
(2007)
Physiology (Bethesda)
, vol.22
, pp. 269-278
-
-
Schiaffino, S.1
Sandri, M.2
Murgia, M.3
-
33
-
-
34347272966
-
Overexpression of peroxisome proliferator-activated receptor gamma coactivator-1alpha leads to muscle atrophy with depletion of ATP
-
Miura S, Tomitsuka E, Kamei Y, Yamazaki T, Kai Y, et al. (2006) Overexpression of peroxisome proliferator-activated receptor gamma coactivator-1alpha leads to muscle atrophy with depletion of ATP. Am J Pathol 169: 1129-1139.
-
(2006)
Am J Pathol
, vol.169
, pp. 1129-1139
-
-
Miura, S.1
Tomitsuka, E.2
Kamei, Y.3
Yamazaki, T.4
Kai, Y.5
-
34
-
-
0042232026
-
Overexpression of peroxisome proliferator-activated receptor gamma coactivator-1alpha down-regulates GLUT4 mRNA in skeletal muscles
-
Miura S, Kai Y, Ono M, Ezaki O (2003) Overexpression of peroxisome proliferator-activated receptor gamma coactivator-1alpha down-regulates GLUT4 mRNA in skeletal muscles. J Biol Chem 278: 31385-31390.
-
(2003)
J Biol Chem
, vol.278
, pp. 31385-31390
-
-
Miura, S.1
Kai, Y.2
Ono, M.3
Ezaki, O.4
-
35
-
-
58149401189
-
Paradoxical effects of increased expression of PGC-1alpha on muscle mitochondrial function and insulin-stimulated muscle glucose metabolism
-
Choi CS, Befroy DE, Codella R, Kim S, Reznick RM, et al. (2008) Paradoxical effects of increased expression of PGC-1alpha on muscle mitochondrial function and insulin-stimulated muscle glucose metabolism. Proc Natl Acad Sci U S A 105: 19926-19931.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 19926-19931
-
-
Choi, C.S.1
Befroy, D.E.2
Codella, R.3
Kim, S.4
Reznick, R.M.5
-
36
-
-
0035957375
-
Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1
-
Michael LF, Wu Z, Cheatham RB, Puigserver P, Adelmant G, et al. (2001) Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1. Proc Natl Acad Sci U S A 98: 3820-3825.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 3820-3825
-
-
Michael, L.F.1
Wu, Z.2
Cheatham, R.B.3
Puigserver, P.4
Adelmant, G.5
-
37
-
-
37549025047
-
A role for the transcriptional coactivator PGC-1alpha in muscle refueling
-
Wende AR, Schaeffer PJ, Parker GJ, Zechner C, Han DH, et al. (2007) A role for the transcriptional coactivator PGC-1alpha in muscle refueling. J Biol Chem 282: 36642-36651.
-
(2007)
J Biol Chem
, vol.282
, pp. 36642-36651
-
-
Wende, A.R.1
Schaeffer, P.J.2
Parker, G.J.3
Zechner, C.4
Han, D.H.5
-
38
-
-
34447284284
-
Differential muscular glycogen clearance after enzyme replacement therapy in a mouse model of Pompe disease
-
Hawes ML, Kennedy W, O'Callaghan MW, Thurberg BL (2007) Differential muscular glycogen clearance after enzyme replacement therapy in a mouse model of Pompe disease. Mol Genet Metab 91: 343-351.
-
(2007)
Mol Genet Metab
, vol.91
, pp. 343-351
-
-
Hawes, M.L.1
Kennedy, W.2
O'Callaghan, M.W.3
Thurberg, B.L.4
-
40
-
-
21644475161
-
Glycogen autophagy in the liver and heart of newborn rats. The effects of glucagon, adrenalin or rapamycin
-
Kondomerkos DJ, Kalamidas SA, Kotoulas OB, Hann AC (2005) Glycogen autophagy in the liver and heart of newborn rats. The effects of glucagon, adrenalin or rapamycin. Histol Histopathol 20: 689-696.
-
(2005)
Histol Histopathol
, vol.20
, pp. 689-696
-
-
Kondomerkos, D.J.1
Kalamidas, S.A.2
Kotoulas, O.B.3
Hann, A.C.4
-
41
-
-
0015251008
-
Autophagic degradation of glycogen in skeletal muscles of the newborn rat
-
Schiaffino S, Hanzlikova V (1972) Autophagic degradation of glycogen in skeletal muscles of the newborn rat. J Cell Biol 52: 41-51.
-
(1972)
J Cell Biol
, vol.52
, pp. 41-51
-
-
Schiaffino, S.1
Hanzlikova, V.2
-
42
-
-
48249111779
-
The role of autophagy in neonatal tissues: Just a response to amino acid starvation?
-
Schiaffino S, Mammucari C, Sandri M (2008) The role of autophagy in neonatal tissues: just a response to amino acid starvation? Autophagy 4.
-
(2008)
Autophagy
, pp. 4
-
-
Schiaffino, S.1
Mammucari, C.2
Sandri, M.3
-
43
-
-
39149102870
-
Stimulation of mitochondrial biogenesis and autophagy by lipopolysaccharide in the neonatal rat cardiomyocyte protects against programmed cell death
-
Hickson-Bick DL, Jones C, Buja LM (2008) Stimulation of mitochondrial biogenesis and autophagy by lipopolysaccharide in the neonatal rat cardiomyocyte protects against programmed cell death. J Mol Cell Cardiol 44: 411-418.
-
(2008)
J Mol Cell Cardiol
, vol.44
, pp. 411-418
-
-
Hickson-Bick, D.L.1
Jones, C.2
Buja, L.M.3
-
44
-
-
70349298359
-
PPARgamma activation induces autophagy in breast cancer cells
-
Zhou J, Zhang W, Liang B, Casimiro MC, Whitaker-Menezes D, et al. (2009) PPARgamma activation induces autophagy in breast cancer cells. Int J Biochem Cell Biol 41: 2334-2342.
-
(2009)
Int J Biochem Cell Biol
, vol.41
, pp. 2334-2342
-
-
Zhou, J.1
Zhang, W.2
Liang, B.3
Casimiro, M.C.4
Whitaker-Menezes, D.5
-
45
-
-
77953139736
-
Fighting disease by selective autophagy of aggregate-prone proteins
-
Knaevelsrud H, Simonsen A (2010) Fighting disease by selective autophagy of aggregate-prone proteins. FEBS Lett 584: 2635-2645.
-
(2010)
FEBS Lett
, vol.584
, pp. 2635-2645
-
-
Knaevelsrud, H.1
Simonsen, A.2
-
46
-
-
42949083922
-
Modest PGC-1alpha overexpression in muscle in vivo is sufficient to increase insulin sensitivity and palmitate oxidation in subsarcolemmal, not intermyofibrillar, mitochondria
-
Benton CR, Nickerson JG, Lally J, Han XX, Holloway GP, et al. (2008) Modest PGC-1alpha overexpression in muscle in vivo is sufficient to increase insulin sensitivity and palmitate oxidation in subsarcolemmal, not intermyofibrillar, mitochondria. J Biol Chem 283: 4228-4240.
-
(2008)
J Biol Chem
, vol.283
, pp. 4228-4240
-
-
Benton, C.R.1
Nickerson, J.G.2
Lally, J.3
Han, X.X.4
Holloway, G.P.5
-
47
-
-
33644654397
-
Endurance training increases skeletal muscle LKB1 and PGC-1alpha protein abundance: Effects of time and intensity
-
Taylor EB, Lamb JD, Hurst RW, Chesser DG, Ellingson WJ, et al. (2005) Endurance training increases skeletal muscle LKB1 and PGC-1alpha protein abundance: effects of time and intensity. Am J Physiol Endocrinol Metab 289: E960-E968.
-
(2005)
Am J Physiol Endocrinol Metab
, vol.289
-
-
Taylor, E.B.1
Lamb, J.D.2
Hurst, R.W.3
Chesser, D.G.4
Ellingson, W.J.5
-
48
-
-
71549165765
-
A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance
-
Van Rooij E, Quiat D, Johnson BA, Sutherland LB, Qi X, et al. (2009) A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance. Dev Cell 17: 662-673.
-
(2009)
Dev Cell
, vol.17
, pp. 662-673
-
-
Van Rooij, E.1
Quiat, D.2
Johnson, B.A.3
Sutherland, L.B.4
Qi, X.5
-
49
-
-
14444274334
-
Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II
-
Raben N, Nagaraju K, Lee E, Kessler P, Byrne B, et al. (1998) Targeted disruption of the acid alpha-glucosidase gene in mice causes an illness with critical features of both infantile and adult human glycogen storage disease type II. J Biol Chem 273: 19086-19092.
-
(1998)
J Biol Chem
, vol.273
, pp. 19086-19092
-
-
Raben, N.1
Nagaraju, K.2
Lee, E.3
Kessler, P.4
Byrne, B.5
-
50
-
-
23644435652
-
Carbohydrate-remodeled acid alpha-glucosidase with higher affinity for the cation-independent mannose 6-phosphate receptor demonstrates improved delivery to muscles of Pompe mice
-
Zhu Y, Li X, McVie-Wylie A, Jiang C, Thurberg BL, et al. (2005) Carbohydrate-remodeled acid alpha-glucosidase with higher affinity for the cation-independent mannose 6-phosphate receptor demonstrates improved delivery to muscles of Pompe mice. Biochem J.
-
(2005)
Biochem J.
-
-
Zhu, Y.1
Li, X.2
McVie-Wylie, A.3
Jiang, C.4
Thurberg, B.L.5
-
51
-
-
59649104665
-
Monitoring autophagy in lysosomal storage disorders
-
Raben N, Shea L, Hill V, Plotz P (2009) Monitoring autophagy in lysosomal storage disorders. Methods Enzymol 453: 417-449.
-
(2009)
Methods Enzymol
, vol.453
, pp. 417-449
-
-
Raben, N.1
Shea, L.2
Hill, V.3
Plotz, P.4
-
52
-
-
0028101953
-
Improved method for post-embedding cytochemistry using reduced osmium and LR white resin
-
Tamaki H, Yamashina S (1994) Improved method for post-embedding cytochemistry using reduced osmium and LR white resin. J Histochem Cytochem 42: 1285-1293.
-
(1994)
J Histochem Cytochem
, vol.42
, pp. 1285-1293
-
-
Tamaki, H.1
Yamashina, S.2
-
53
-
-
57049089893
-
Modulation of glycogen synthesis by RNA interference: Towards a new therapeutic approach for glycogenosis type II
-
Douillard-Guilloux G, Raben N, Takikita S, Batista L, Caillaud C, Richard E (2008) Modulation of glycogen synthesis by RNA interference: towards a new therapeutic approach for glycogenosis type II. Hum Mol Genet 17: 3876-3886.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3876-3886
-
-
Douillard-Guilloux, G.1
Raben, N.2
Takikita, S.3
Batista, L.4
Caillaud, C.5
Richard, E.6
-
54
-
-
65949114863
-
Preclinical drug trials in the mdx mouse: Assessment of reliable and sensitive outcome measures
-
Spurney CF, Gordish-Dressman H, Guerron AD, Sali A, Pandey GS, Rawat R, et al. (2009) Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures. Muscle Nerve 39: 591-602.
-
(2009)
Muscle Nerve
, vol.39
, pp. 591-602
-
-
Spurney, C.F.1
Gordish-Dressman, H.2
Guerron, A.D.3
Sali, A.4
Pandey, G.S.5
Rawat, R.6
-
55
-
-
3242888703
-
LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation
-
Kabeya Y, Mizushima N, Yamamoto A, Oshitani-Okamoto S, Ohsumi Y, Yoshimori T (2004) LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation. J Cell Sci 117: 2805-2812.
-
(2004)
J Cell Sci
, vol.117
, pp. 2805-2812
-
-
Kabeya, Y.1
Mizushima, N.2
Yamamoto, A.3
Oshitani-Okamoto, S.4
Ohsumi, Y.5
Yoshimori, T.6
-
56
-
-
0035032723
-
Beclin-phosphatidylinositol 3-kinase complex functions at the trans-Golgi network
-
Kihara A, Kabeya Y, Ohsumi Y, Yoshimori T (2001) Beclin-phosphatidylinositol 3-kinase complex functions at the trans-Golgi network. EMBO Rep 2: 330-335.
-
(2001)
EMBO Rep
, vol.2
, pp. 330-335
-
-
Kihara, A.1
Kabeya, Y.2
Ohsumi, Y.3
Yoshimori, T.4
-
57
-
-
68149147330
-
BNIP3 subfamily BH3-only proteins: Mitochondrial stress sensors in normal and pathological functions
-
Chinnadurai G, Vijayalingam S, Gibson SB (2008) BNIP3 subfamily BH3-only proteins: mitochondrial stress sensors in normal and pathological functions. Oncogene 27(Suppl 1): S114-S127.
-
(2008)
Oncogene
, vol.27
, Issue.SUPPL 1
-
-
Chinnadurai, G.1
Vijayalingam, S.2
Gibson, S.B.3
-
58
-
-
0035109715
-
Golgi complex, endoplasmic reticulum exit sites, and microtubules in skeletal muscle fibers are organized by patterned activity
-
Ralston E, Ploug T, Kalhovde J, Lomo T (2001) Golgi complex, endoplasmic reticulum exit sites, and microtubules in skeletal muscle fibers are organized by patterned activity. J Neurosci 21: 875-883.
-
(2001)
J Neurosci
, vol.21
, pp. 875-883
-
-
Ralston, E.1
Ploug, T.2
Kalhovde, J.3
Lomo, T.4
|