-
1
-
-
0022496289
-
Isolation of candidate cDNAs for portions of the Duch-enne muscular dystrophy gene
-
Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM: Isolation of candidate cDNAs for portions of the Duch-enne muscular dystrophy gene. Nature 1986, 323:646-650
-
(1986)
Nature
, vol.323
, pp. 646-650
-
-
Monaco, A.P.1
Neve, R.L.2
Colletti-Feener, C.3
Bertelson, C.J.4
Kurnit, D.M.5
Kunkel, L.M.6
-
2
-
-
0023614271
-
Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
-
Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM: Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 1987, 50:509-517
-
(1987)
Cell
, vol.50
, pp. 509-517
-
-
Koenig, M.1
Hoffman, E.P.2
Bertelson, C.J.3
Monaco, A.P.4
Feener, C.5
Kunkel, L.M.6
-
3
-
-
0023614188
-
Dystrophin: The protein product of the Duchenne muscular dystrophy locus
-
Hoffman EP, Brown RH Jr, Kunkel LM: Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987, 51:919-928
-
(1987)
Cell
, vol.51
, pp. 919-928
-
-
Hoffman, E.P.1
Brown Jr, R.H.2
Kunkel, L.M.3
-
4
-
-
0024600620
-
Association of dystrophin and an integral membrane glycoprotein
-
Campbell KP, Kahl SD: Association of dystrophin and an integral membrane glycoprotein. Nature 1989, 338:259-262
-
(1989)
Nature
, vol.338
, pp. 259-262
-
-
Campbell, K.P.1
Kahl, S.D.2
-
5
-
-
0025272250
-
Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle
-
Ervasti JM, Ohlendieck K, Kahl SD, Gaver MG, Campbell KP: Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature 1990, 345:315-319
-
(1990)
Nature
, vol.345
, pp. 315-319
-
-
Ervasti, J.M.1
Ohlendieck, K.2
Kahl, S.D.3
Gaver, M.G.4
Campbell, K.P.5
-
6
-
-
0025242185
-
Glycoprotein complex anchoring dystrophin to sarcolemma
-
Yoshida M, Ozawa E: Glycoprotein complex anchoring dystrophin to sarcolemma. J Biochem (Tokyo) 1990, 108:748-752
-
(1990)
J Biochem (Tokyo)
, vol.108
, pp. 748-752
-
-
Yoshida, M.1
Ozawa, E.2
-
7
-
-
0026543686
-
Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
-
Ibraghimov-Beskrovnaya O, Ervasti JM, Leveille CJ, Slaughter CA, Sernett SW, Campbell KP: Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 1992, 355:696-702
-
(1992)
Nature
, vol.355
, pp. 696-702
-
-
Ibraghimov-Beskrovnaya, O.1
Ervasti, J.M.2
Leveille, C.J.3
Slaughter, C.A.4
Sernett, S.W.5
Campbell, K.P.6
-
8
-
-
0026328022
-
Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
-
Ohlendieck K, Campbell KP: Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice. J Cell Biol 1991, 115:1685-1694
-
(1991)
J Cell Biol
, vol.115
, pp. 1685-1694
-
-
Ohlendieck, K.1
Campbell, K.P.2
-
9
-
-
0029013870
-
SH3 domain-mediated interaction of dystroglycan and Grb2
-
Yang B, Jung D, Motto D, Meyer J, Koretzky G, Campbell KP: SH3 domain-mediated interaction of dystroglycan and Grb2. J Biol Chem 1995, 270:11711-11714
-
(1995)
J Biol Chem
, vol.270
, pp. 11711-11714
-
-
Yang, B.1
Jung, D.2
Motto, D.3
Meyer, J.4
Koretzky, G.5
Campbell, K.P.6
-
10
-
-
0029149471
-
Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy
-
Brenman JE, Chao DS, Xia H, Aldape K, Bredt DS: Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy. Cell 1995, 82:743-752
-
(1995)
Cell
, vol.82
, pp. 743-752
-
-
Brenman, J.E.1
Chao, D.S.2
Xia, H.3
Aldape, K.4
Bredt, D.S.5
-
11
-
-
0026724938
-
Calmodulin specifically binds three proteins of the dystrophin-glycoprotein complex
-
Madhavan R, Massom LR, Jarrett HW: Calmodulin specifically binds three proteins of the dystrophin-glycoprotein complex. Biochem Bio- phys Res Commun 1992, 185:753-759
-
(1992)
Biochem Bio- phys Res Commun
, vol.185
, pp. 753-759
-
-
Madhavan, R.1
Massom, L.R.2
Jarrett, H.W.3
-
12
-
-
0033037910
-
Association of the dystroglycan complex isolated from bovine brain synaptosomes with proteins involved in signal transduction
-
Cavaldesi M, Macchia G, Barca S, Defilippi P, Tarone G, Petrucci TC: Association of the dystroglycan complex isolated from bovine brain synaptosomes with proteins involved in signal transduction. J Neuro- chem 1999, 72:1648-1655
-
(1999)
J Neuro- chem
, vol.72
, pp. 1648-1655
-
-
Cavaldesi, M.1
Macchia, G.2
Barca, S.3
Defilippi, P.4
Tarone, G.5
Petrucci, T.C.6
-
13
-
-
0032496393
-
Caveolin-3 is not an integral component of the dystrophin glycoprotein complex
-
Crosbie RH, Yamada H, Venzke DP, Lisanti MP, Campbell KP: Caveolin-3 is not an integral component of the dystrophin glycoprotein complex. FEBS Lett 1998, 427:279-282
-
(1998)
FEBS Lett
, vol.427
, pp. 279-282
-
-
Crosbie, R.H.1
Yamada, H.2
Venzke, D.P.3
Lisanti, M.P.4
Campbell, K.P.5
-
14
-
-
15844401780
-
Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarco- lemma and co-fractionates with dystrophin and dystrophin-associ-ated glycoproteins
-
Song KS, Scherer PE, Tang Z, Okamoto T, Li S, Chafel M, Chu C, Kohtz DS, Lisanti MP: Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarco- lemma and co-fractionates with dystrophin and dystrophin-associ-ated glycoproteins. J Biol Chem 1996, 271:15160-15165
-
(1996)
J Biol Chem
, vol.271
, pp. 15160-15165
-
-
Song, K.S.1
Scherer, P.E.2
Tang, Z.3
Okamoto, T.4
Li, S.5
Chafel, M.6
Chu, C.7
Kohtz, D.S.8
Lisanti, M.P.9
-
15
-
-
0034532164
-
Caveo- lin-3 directly interacts with the C-terminal tail of beta-dystroglycan. Identification of a central WW-like domain within caveolin family members
-
Sotgia F, Lee JK, Das K, Bedford M, Petrucci TC, Macioce P, Sargiacomo M, Bricarelli FD, Minetti C, Sudol M, Lisanti MP: Caveo- lin-3 directly interacts with the C-terminal tail of beta-dystroglycan. Identification of a central WW-like domain within caveolin family members. J Biol Chem 2000, 275:38048-38058
-
(2000)
J Biol Chem
, vol.275
, pp. 38048-38058
-
-
Sotgia, F.1
Lee, J.K.2
Das, K.3
Bedford, M.4
Petrucci, T.C.5
Macioce, P.6
Sargiacomo, M.7
Bricarelli, F.D.8
Minetti, C.9
Sudol, M.10
Lisanti, M.P.11
-
16
-
-
0345731966
-
X chromosome-linked muscular dystrophy (mdx) in the mouse
-
Bulfield G, Siller WG, Wight PAG, Moore KJ: X chromosome-linked muscular dystrophy (mdx) in the mouse. Proc Natl Acad Sci USA 1984, 81:1189-1192
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 1189-1192
-
-
Bulfield, G.1
Siller, W.G.2
Wight, P.A.G.3
Moore, K.J.4
-
17
-
-
0347915657
-
Loss of dystrophin causes aberrant mechanotransduction in skeletal muscle fibers
-
Kumar A, Khandelwal N, Malya R, Reid MB, Boriek AM: Loss of dystrophin causes aberrant mechanotransduction in skeletal muscle fibers. FASEB J 2004, 18:102-113
-
(2004)
FASEB J
, vol.18
, pp. 102-113
-
-
Kumar, A.1
Khandelwal, N.2
Malya, R.3
Reid, M.B.4
Boriek, A.M.5
-
18
-
-
2942525757
-
Altered activity of signaling pathways in diaphragm and tibialis anterior muscle of dystrophic mice
-
Lang JM, Esser KA, Dupont-Versteegden EE: Altered activity of signaling pathways in diaphragm and tibialis anterior muscle of dystrophic mice. Exp Biol Med (Maywood) 2004, 229:503-511
-
(2004)
Exp Biol Med (Maywood)
, vol.229
, pp. 503-511
-
-
Lang, J.M.1
Esser, K.A.2
Dupont-Versteegden, E.E.3
-
19
-
-
0035928793
-
Activation of JNK1 contributes to dystrophic muscle pathogenesis
-
Kolodziejczyk SM, Walsh GS, Balazsi K, Seale P, Sandoz J, Hierlihy AM, Rudnicki MA, Chamberlain JS, Miller FD, Megeney LA: Activation of JNK1 contributes to dystrophic muscle pathogenesis. Curr Biol 2001, 11:1278-1282
-
(2001)
Curr Biol
, vol.11
, pp. 1278-1282
-
-
Kolodziejczyk, S.M.1
Walsh, G.S.2
Balazsi, K.3
Seale, P.4
Sandoz, J.5
Hierlihy, A.M.6
Rudnicki, M.A.7
Chamberlain, J.S.8
Miller, F.D.9
Megeney, L.A.10
-
20
-
-
20444386565
-
Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise
-
Nakamura A, Yoshida K, Ueda H, Takeda S, Ikeda S: Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise. Biochim Biophys Acta 2005, 1740:326-331
-
(2005)
Biochim Biophys Acta
, vol.1740
, pp. 326-331
-
-
Nakamura, A.1
Yoshida, K.2
Ueda, H.3
Takeda, S.4
Ikeda, S.5
-
21
-
-
10044237735
-
Glucocorticoid treatment alleviates dystrophic myo-fiber pathology by activation of the calcineurin/NF-AT pathway
-
MegeneyLA
-
St-Pierre SJ, Chakkalakal JV, Kolodziejczyk SM, Knudson JC, Jasmin BJ, MegeneyLA: Glucocorticoid treatment alleviates dystrophic myo-fiber pathology by activation of the calcineurin/NF-AT pathway. FASEB J 2004, 18:1937-1939
-
(2004)
FASEB J
, vol.18
, pp. 1937-1939
-
-
St-Pierre, S.J.1
Chakkalakal, J.V.2
Kolodziejczyk, S.M.3
Knudson, J.C.4
Jasmin, B.J.5
-
22
-
-
33746579821
-
Regulation of phos-phatidylinositol 3-kinase (PI3K)/Akt and nuclear factor-kappa B signaling pathways in dystrophin-deficient skeletal muscle in response to mechanical stretch
-
Dogra C, Changotra H, Wergedal JE, Kumar A: Regulation of phos-phatidylinositol 3-kinase (PI3K)/Akt and nuclear factor-kappa B signaling pathways in dystrophin-deficient skeletal muscle in response to mechanical stretch. J Cell Physiol 2006, 208:575-585
-
(2006)
J Cell Physiol
, vol.208
, pp. 575-585
-
-
Dogra, C.1
Changotra, H.2
Wergedal, J.E.3
Kumar, A.4
-
23
-
-
33745856252
-
Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway
-
Peter AK, Crosbie RH: Hypertrophic response of Duchenne and limb-girdle muscular dystrophies is associated with activation of Akt pathway. Exp Cell Res 2006, 312:2580-2591
-
(2006)
Exp Cell Res
, vol.312
, pp. 2580-2591
-
-
Peter, A.K.1
Crosbie, R.H.2
-
24
-
-
0023244894
-
Muscular dystrophy in the mdx mouse: Histopathology of the soleus and extensor digitorum longus muscles
-
Carnwath JW, Shotton DM: Muscular dystrophy in the mdx mouse: histopathology of the soleus and extensor digitorum longus muscles. J Neurol Sci 1987, 80:39-54
-
(1987)
J Neurol Sci
, vol.80
, pp. 39-54
-
-
Carnwath, J.W.1
Shotton, D.M.2
-
25
-
-
0023910734
-
The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation
-
Coulton GR, Morgan JE, Partridge TA, Sloper JC: The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation. Neuropathol Appl Neurobiol 1988, 14:53-70
-
(1988)
Neuropathol Appl Neurobiol
, vol.14
, pp. 53-70
-
-
Coulton, G.R.1
Morgan, J.E.2
Partridge, T.A.3
Sloper, J.C.4
-
26
-
-
0023091942
-
The mutant mdx: Inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates
-
Torres LF, Duchen LW: The mutant mdx: inherited myopathy in the mouse. Morphological studies of nerves, muscles and end-plates. Brain 1987, 110 (Pt 2):269-299
-
(1987)
Brain
, vol.110
, Issue.PART 2
, pp. 269-299
-
-
Torres, L.F.1
Duchen, L.W.2
-
27
-
-
0023883621
-
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
-
Cooper BJ, Winand NJ, Stedman H, Valentine BA, Hoffman EP, Kunkel LM, Scott MO, Fischbeck KH, Kornegay JN, Avery RJ, Williams JR, Schmickel RD, Sylvester JE: The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs. Nature 1988, 334:154-156
-
(1988)
Nature
, vol.334
, pp. 154-156
-
-
Cooper, B.J.1
Winand, N.J.2
Stedman, H.3
Valentine, B.A.4
Hoffman, E.P.5
Kunkel, L.M.6
Scott, M.O.7
Fischbeck, K.H.8
Kornegay, J.N.9
Avery, R.J.10
Williams, J.R.11
Schmickel, R.D.12
Sylvester, J.E.13
-
28
-
-
0024263367
-
Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: Clinical studies
-
Valentine BA, Cooper BJ, de Lahunta A, O'Quinn R, Blue JT: Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies. J Neurol Sci 1988, 88:69-81
-
(1988)
J Neurol Sci
, vol.88
, pp. 69-81
-
-
Valentine, B.A.1
Cooper, B.J.2
de Lahunta, A.3
O'Quinn, R.4
Blue, J.T.5
-
29
-
-
0026538578
-
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
-
Sharp NJ, Kornegay JN, Van Camp SD, Herbstreith MH, Secore SL, Kettle S, Hung WY, Constantinou CD, Dykstra MJ, Roses AD, Bartlett RJ: An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy. Genomics 1992, 13:115-121
-
(1992)
Genomics
, vol.13
, pp. 115-121
-
-
Sharp, N.J.1
Kornegay, J.N.2
Van Camp, S.D.3
Herbstreith, M.H.4
Secore, S.L.5
Kettle, S.6
Hung, W.Y.7
Constantinou, C.D.8
Dykstra, M.J.9
Roses, A.D.10
Bartlett, R.J.11
-
30
-
-
0035736260
-
Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo
-
Bodine SC, Stitt TN, Gonzalez M, Kline WO, Stover GL, Bauerlein R, Zlotchenko E, Scrimgeour A, Lawrence JC, Glass DJ, Yancopoulos GD: Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo. Nat Cell Biol 2001, 3:1014-1019
-
(2001)
Nat Cell Biol
, vol.3
, pp. 1014-1019
-
-
Bodine, S.C.1
Stitt, T.N.2
Gonzalez, M.3
Kline, W.O.4
Stover, G.L.5
Bauerlein, R.6
Zlotchenko, E.7
Scrimgeour, A.8
Lawrence, J.C.9
Glass, D.J.10
Yancopoulos, G.D.11
-
31
-
-
23944456384
-
Skeletal muscle hypertrophy and atrophy signaling pathways
-
Glass DJ: Skeletal muscle hypertrophy and atrophy signaling pathways. Int J Biochem Cell Biol 2005, 37:1974-1984
-
(2005)
Int J Biochem Cell Biol
, vol.37
, pp. 1974-1984
-
-
Glass, D.J.1
-
32
-
-
0035735902
-
Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways
-
Rommel C, Bodine SC, Clarke BA, Rossman R, Nunez L, Stitt TN, Yancopoulos GD, Glass DJ: Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways. Nat Cell Biol 2001, 3:1009-1013
-
(2001)
Nat Cell Biol
, vol.3
, pp. 1009-1013
-
-
Rommel, C.1
Bodine, S.C.2
Clarke, B.A.3
Rossman, R.4
Nunez, L.5
Stitt, T.N.6
Yancopoulos, G.D.7
Glass, D.J.8
-
33
-
-
0036074029
-
GSK-3beta negatively regulates skeletal myotube hypertrophy
-
Vyas DR, Spangenburg EE, Abraha TW, Childs TE, Booth FW: GSK-3beta negatively regulates skeletal myotube hypertrophy. Am J Physiol Cell Physiol 2002, 283:C545-C551
-
(2002)
Am J Physiol Cell Physiol
, vol.283
-
-
Vyas, D.R.1
Spangenburg, E.E.2
Abraha, T.W.3
Childs, T.E.4
Booth, F.W.5
-
34
-
-
0029587224
-
Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B
-
Cross DA, Alessi DR, Cohen P, Andjelkovich M, Hemmings BA: Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B. Nature 1995, 378:785-789
-
(1995)
Nature
, vol.378
, pp. 785-789
-
-
Cross, D.A.1
Alessi, D.R.2
Cohen, P.3
Andjelkovich, M.4
Hemmings, B.A.5
-
35
-
-
0026659046
-
Rapamycin-FKBP specifically blocks growth-dependent activation of and signaling by the 70 kd S6 protein kinases
-
Chung J, Kuo CJ, Crabtree GR, Blenis J: Rapamycin-FKBP specifically blocks growth-dependent activation of and signaling by the 70 kd S6 protein kinases. Cell 1992, 69:1227-1236
-
(1992)
Cell
, vol.69
, pp. 1227-1236
-
-
Chung, J.1
Kuo, C.J.2
Crabtree, G.R.3
Blenis, J.4
-
36
-
-
0036713778
-
TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling
-
Inoki K, Li Y, Zhu T, Wu J, Guan KL: TSC2 is phosphorylated and inhibited by Akt and suppresses mTOR signalling. Nat Cell Biol 2002, 4:648-657
-
(2002)
Nat Cell Biol
, vol.4
, pp. 648-657
-
-
Inoki, K.1
Li, Y.2
Zhu, T.3
Wu, J.4
Guan, K.L.5
-
37
-
-
14844363721
-
Signaling by target of rapamycin proteins in cell growth control
-
Inoki K, Ouyang H, Li Y, Guan KL: Signaling by target of rapamycin proteins in cell growth control. Microbiol Mol Biol Rev 2005, 69: 79-100
-
(2005)
Microbiol Mol Biol Rev
, vol.69
, pp. 79-100
-
-
Inoki, K.1
Ouyang, H.2
Li, Y.3
Guan, K.L.4
-
38
-
-
0026759874
-
Rapamycin-in-duced inhibition of the 70-kilodalton S6 protein kinase
-
Price DJ, Grove JR, Calvo V, Avruch J, Bierer BE: Rapamycin-in-duced inhibition of the 70-kilodalton S6 protein kinase. Science 1992, 257:973-977
-
(1992)
Science
, vol.257
, pp. 973-977
-
-
Price, D.J.1
Grove, J.R.2
Calvo, V.3
Avruch, J.4
Bierer, B.E.5
-
39
-
-
0023897684
-
Type I phos-phatidylinositol kinase makes a novel inositol phospholipid, phospha-tidylinositol-3-phosphate
-
Whitman M, Downes CP, Keeler M, Keller T, Cantley L: Type I phos-phatidylinositol kinase makes a novel inositol phospholipid, phospha-tidylinositol-3-phosphate. Nature 1988, 332:644-646
-
(1988)
Nature
, vol.332
, pp. 644-646
-
-
Whitman, M.1
Downes, C.P.2
Keeler, M.3
Keller, T.4
Cantley, L.5
-
40
-
-
0031127305
-
Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha
-
Alessi DR, James SR, Downes CP, Holmes AB, Gaffney PR, Reese CB, Cohen P: Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha. Curr Biol 1997, 7:261-269
-
(1997)
Curr Biol
, vol.7
, pp. 261-269
-
-
Alessi, D.R.1
James, S.R.2
Downes, C.P.3
Holmes, A.B.4
Gaffney, P.R.5
Reese, C.B.6
Cohen, P.7
-
42
-
-
0032577699
-
The tumor suppressor. PTEN/MMAC1, de- phosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate
-
Maehama T, Dixon JE: The tumor suppressor. PTEN/MMAC1, de- phosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate. J Biol Chem 1998, 273:13375-13378
-
(1998)
J Biol Chem
, vol.273
, pp. 13375-13378
-
-
Maehama, T.1
Dixon, J.E.2
-
43
-
-
6344256238
-
Conditional activation of akt in adult skeletal muscle induces rapid hypertrophy
-
Lai KM, Gonzalez M, Poueymirou WT, Kline WO, Na E, Zlotchenko E, Stitt TN, Economides AN, Yancopoulos GD, Glass DJ: Conditional activation of akt in adult skeletal muscle induces rapid hypertrophy. Mol Cell Biol 2004, 24:9295-9304
-
(2004)
Mol Cell Biol
, vol.24
, pp. 9295-9304
-
-
Lai, K.M.1
Gonzalez, M.2
Poueymirou, W.T.3
Kline, W.O.4
Na, E.5
Zlotchenko, E.6
Stitt, T.N.7
Economides, A.N.8
Yancopoulos, G.D.9
Glass, D.J.10
-
44
-
-
33746225428
-
Regulation of PTEN function as a PIP3 gatekeeper through membrane interaction
-
Vazquez F, Devreotes P: Regulation of PTEN function as a PIP3 gatekeeper through membrane interaction. Cell Cycle 2006, 5:1523-1527
-
(2006)
Cell Cycle
, vol.5
, pp. 1523-1527
-
-
Vazquez, F.1
Devreotes, P.2
-
45
-
-
33644870152
-
Tumor suppressor PTEN acts through dynamic interaction with the plasma membrane
-
Vazquez F, Matsuoka S, Sellers WR, Yanagida T, Ueda M, Devreotes PN: Tumor suppressor PTEN acts through dynamic interaction with the plasma membrane. Proc Natl Acad Sci USA 2006, 103: 3633-3638
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 3633-3638
-
-
Vazquez, F.1
Matsuoka, S.2
Sellers, W.R.3
Yanagida, T.4
Ueda, M.5
Devreotes, P.N.6
-
46
-
-
0036382931
-
Some protein tyrosine phosphatases target in part to lipid rafts and interact with caveolin-1
-
Caselli A, Mazzinghi B, Camici G, Manao G, Ramponi G: Some protein tyrosine phosphatases target in part to lipid rafts and interact with caveolin-1. Biochem Biophys Res Commun 2002, 296:692-697
-
(2002)
Biochem Biophys Res Commun
, vol.296
, pp. 692-697
-
-
Caselli, A.1
Mazzinghi, B.2
Camici, G.3
Manao, G.4
Ramponi, G.5
-
47
-
-
0019442473
-
Freeze-fracture studies of muscle caveolae in human muscular dystrophy
-
Bonilla E, Fischbeck K, Schotland DL: Freeze-fracture studies of muscle caveolae in human muscular dystrophy. Am J Pathol 1981, 104:167-173
-
(1981)
Am J Pathol
, vol.104
, pp. 167-173
-
-
Bonilla, E.1
Fischbeck, K.2
Schotland, D.L.3
-
49
-
-
0033546753
-
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy
-
Repetto S, Bado M, Broda P, Lucania G, Masetti E, Sotgia F, Carbone I, Pavan A, Bonilla E, Cordone G, Lisanti MP, Minetti C: Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy. Biochem Biophys Res Commun 1999, 261:547-550
-
(1999)
Biochem Biophys Res Commun
, vol.261
, pp. 547-550
-
-
Repetto, S.1
Bado, M.2
Broda, P.3
Lucania, G.4
Masetti, E.5
Sotgia, F.6
Carbone, I.7
Pavan, A.8
Bonilla, E.9
Cordone, G.10
Lisanti, M.P.11
Minetti, C.12
-
50
-
-
51849086880
-
PTEN: A new guardian of the genome
-
Yin Y, Shen WH: PTEN: a new guardian of the genome. Oncogene 2008, 27:5443-5453
-
(2008)
Oncogene
, vol.27
, pp. 5443-5453
-
-
Yin, Y.1
Shen, W.H.2
-
51
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R: Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet 1997, 16:64-67
-
(1997)
Nat Genet
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
Dahia, P.L.4
Wang, S.I.5
Zheng, Z.6
Bose, S.7
Call, K.M.8
Tsou, H.C.9
Peacocke, M.10
Eng, C.11
Parsons, R.12
-
52
-
-
0242541686
-
Association of the polymorphisms in the 5'-untranslated region of PTEN gene with type 2 diabetes in a Japanese population
-
Ishihara H, Sasaoka T, Kagawa S, Murakami S, Fukui K, Kawagishi Y, Yamazaki K, Sato A, Iwata M, Urakaze M, Ishiki M, Wada T, Yaguchi S, Tsuneki H, Kimura I, Kobayashi M: Association of the polymorphisms in the 5'-untranslated region of PTEN gene with type 2 diabetes in a Japanese population. FEBS Lett 2003, 554:450-454
-
(2003)
FEBS Lett
, vol.554
, pp. 450-454
-
-
Ishihara, H.1
Sasaoka, T.2
Kagawa, S.3
Murakami, S.4
Fukui, K.5
Kawagishi, Y.6
Yamazaki, K.7
Sato, A.8
Iwata, M.9
Urakaze, M.10
Ishiki, M.11
Wada, T.12
Yaguchi, S.13
Tsuneki, H.14
Kimura, I.15
Kobayashi, M.16
-
53
-
-
0345582159
-
Caveolin-3 in muscular dystrophy
-
McNally EM, de Sa Moreira E, Duggan DJ, Bonnemann CG, Lisanti MP, Lidov HG, Vainzof M, Passos-Bueno MR, Hoffman EP, Zatz M, Kunkel LM: Caveolin-3 in muscular dystrophy. Hum Mol Genet 1998, 7:871-877
-
(1998)
Hum Mol Genet
, vol.7
, pp. 871-877
-
-
McNally, E.M.1
de Sa Moreira, E.2
Duggan, D.J.3
Bonnemann, C.G.4
Lisanti, M.P.5
Lidov, H.G.6
Vainzof, M.7
Passos-Bueno, M.R.8
Hoffman, E.P.9
Zatz, M.10
Kunkel, L.M.11
-
54
-
-
0031920515
-
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
-
Minetti C, Sotgia F, Bruno C, Scartezzini P, Broda P, Bado M, Masetti E, Mazzocco M, Egeo A, Donati MA, Volonte D, Galbiati F, Cordone G, Bricarelli FD, Lisanti MP, Zara F: Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nat Genet 1998, 18:365-368
-
(1998)
Nat Genet
, vol.18
, pp. 365-368
-
-
Minetti, C.1
Sotgia, F.2
Bruno, C.3
Scartezzini, P.4
Broda, P.5
Bado, M.6
Masetti, E.7
Mazzocco, M.8
Egeo, A.9
Donati, M.A.10
Volonte, D.11
Galbiati, F.12
Cordone, G.13
Bricarelli, F.D.14
Lisanti, M.P.15
Zara, F.16
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