-
1
-
-
16644403759
-
Guidelines for the diagnosis and management of heart failure
-
Hobbs RE. Guidelines for the diagnosis and management of heart failure. Am J Ther. 2004;11:467-472.
-
(2004)
Am J Ther
, vol.11
, pp. 467-472
-
-
Hobbs, R.E.1
-
2
-
-
34347403248
-
Signaling pathways mediating cardiac myocyte gene expression in physiological and stress responses
-
Clerk A, Cullingford TE, Fuller SJ, Giraldo A, Markou T, Pikkarainen S, Sugden PH. Signaling pathways mediating cardiac myocyte gene expression in physiological and stress responses. J Cell Physiol. 2007;212:311-322.
-
(2007)
J Cell Physiol
, vol.212
, pp. 311-322
-
-
Clerk, A.1
Cullingford, T.E.2
Fuller, S.J.3
Giraldo, A.4
Markou, T.5
Pikkarainen, S.6
Sugden, P.H.7
-
3
-
-
0033604644
-
SHP-2 Tyrosine phosphatase: Signaling one cell or many
-
Feng G. SHP-2 Tyrosine phosphatase: signaling one cell or many. Exp Cell Res. 1999;253:47-54.
-
(1999)
Exp Cell Res
, vol.253
, pp. 47-54
-
-
Feng, G.1
-
4
-
-
0035313868
-
Combinatorial control of the specificity of protein tyrosine phosphatases
-
Tonks NK, Neel BG. Combinatorial control of the specificity of protein tyrosine phosphatases. Curr Opin Cell Biol. 2001;13:182-195.
-
(2001)
Curr Opin Cell Biol
, vol.13
, pp. 182-195
-
-
Tonks, N.K.1
Neel, B.G.2
-
5
-
-
0038771965
-
The "Shp"ing news: SH2 domain-containing tyrosine phosphatases in cell signaling
-
Neel BG, Gu H, Pao L. The "Shp"ing news: SH2 domain-containing tyrosine phosphatases in cell signaling. Trends Biochem Sci. 2003;28:284-293.
-
(2003)
Trends Biochem Sci
, vol.28
, pp. 284-293
-
-
Neel, B.G.1
Gu, H.2
Pao, L.3
-
6
-
-
0034735945
-
The protein tyrosine phosphatase Shp-2 regulates RhoA activity
-
Schoenwaelder SM, Petch LA, Williamson D, Shen R, Feng GS, Burridge K. The protein tyrosine phosphatase Shp-2 regulates RhoA activity. Curr Biol. 2000;10:1523-1526.
-
(2000)
Curr Biol
, vol.10
, pp. 1523-1526
-
-
Schoenwaelder, S.M.1
Petch, L.A.2
Williamson, D.3
Shen, R.4
Feng, G.S.5
Burridge, K.6
-
7
-
-
0037031978
-
Nitric oxide-induced motility in aortic smooth muscle cells: Role of protein tyrosine phosphatase SHP-2 and GTP-binding protein Rho
-
Chang Y, Ceacareanu B, Dixit M, Sreejayan N, Hassid A. Nitric oxide-induced motility in aortic smooth muscle cells: role of protein tyrosine phosphatase SHP-2 and GTP-binding protein Rho. Circ Res. 2002;91:390-397.
-
(2002)
Circ Res
, vol.91
, pp. 390-397
-
-
Chang, Y.1
Ceacareanu, B.2
Dixit, M.3
Sreejayan, N.4
Hassid, A.5
-
8
-
-
2942589265
-
SHP-2 positively regulates myogenesis by coupling to the Rho GTPase signaling pathway
-
Kontaridis MI, Eminaga S, Fornaro M, Zito CI, Sordella R, Settleman J, Bennett AM. SHP-2 positively regulates myogenesis by coupling to the Rho GTPase signaling pathway. Mol Cell Biol. 2004;24:5340-5352.
-
(2004)
Mol Cell Biol
, vol.24
, pp. 5340-5352
-
-
Kontaridis, M.I.1
Eminaga, S.2
Fornaro, M.3
Zito, C.I.4
Sordella, R.5
Settleman, J.6
Bennett, A.M.7
-
9
-
-
0032570586
-
The Shp-2 tyrosine phosphatase has opposite effects in mediating the activation of extracellular signal-regulated and c-Jun NH2-terminal mitogen-activated protein kinases
-
Shi ZQ, Lu W, Feng GS. The Shp-2 tyrosine phosphatase has opposite effects in mediating the activation of extracellular signal-regulated and c-Jun NH2-terminal mitogen-activated protein kinases. J Biol Chem. 1998;273:4904-4908.
-
(1998)
J Biol Chem
, vol.273
, pp. 4904-4908
-
-
Shi, Z.Q.1
Lu, W.2
Feng, G.S.3
-
10
-
-
0032980574
-
Shp-2 tyrosine phosphatase functions as a negative regulator of the interferon-stimulated Jak/STAT pathway
-
You M, Yu DH, Feng GS. Shp-2 tyrosine phosphatase functions as a negative regulator of the interferon-stimulated Jak/STAT pathway. Mol Cell Biol. 1999;19:2416-2424.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 2416-2424
-
-
You, M.1
Yu, D.H.2
Feng, G.S.3
-
11
-
-
0034614626
-
Cytosolic tyrosine dephosphorylation of STAT5: Potential role of SHP-2 in STAT5 regulation
-
Yu CL, Jin YJ, Burakoff SJ. Cytosolic tyrosine dephosphorylation of STAT5: potential role of SHP-2 in STAT5 regulation. J Biol Chem. 2000;275:599-604.
-
(2000)
J Biol Chem
, vol.275
, pp. 599-604
-
-
Yu, C.L.1
Jin, Y.J.2
Burakoff, S.J.3
-
12
-
-
33749577870
-
SHP-2 activates signaling of the nuclear factor of activated T cells to promote skeletal muscle growth
-
Fornaro M, Burch PM, Yang W, Zhang L, Hamilton CE, Kim JH, Neel BG, Bennett AM. SHP-2 activates signaling of the nuclear factor of activated T cells to promote skeletal muscle growth. J Cell Biol. 2006;175:87-97.
-
(2006)
J Cell Biol
, vol.175
, pp. 87-97
-
-
Fornaro, M.1
Burch, P.M.2
Yang, W.3
Zhang, L.4
Hamilton, C.E.5
Kim, J.H.6
Neel, B.G.7
Bennett, A.M.8
-
13
-
-
33144473897
-
Gain-of-function/Noonan syndrome SHP-2/Ptpn11 mutants enhance calcium oscillations and impair NFAT signaling
-
Uhlen P, Burch PM, Zito CI, Estrada M, Ehrlich BE, Bennett AM. Gain-of-function/Noonan syndrome SHP-2/Ptpn11 mutants enhance calcium oscillations and impair NFAT signaling. Proc Natl Acad Sci U S A. 2006;103:2160-2165.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 2160-2165
-
-
Uhlen, P.1
Burch, P.M.2
Zito, C.I.3
Estrada, M.4
Ehrlich, B.E.5
Bennett, A.M.6
-
14
-
-
18344385476
-
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
-
Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, van der Burgt I, Crosby AH, Ion A, Jeffery S, Kalidas K, Patton MA, Kucherlapati RS, Gelb BD. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet. 2001;29:465-468.
-
(2001)
Nat Genet
, vol.29
, pp. 465-468
-
-
Tartaglia, M.1
Mehler, E.L.2
Goldberg, R.3
Zampino, G.4
Brunner, H.G.5
Kremer, H.6
van der Burgt, I.7
Crosby, A.H.8
Ion, A.9
Jeffery, S.10
Kalidas, K.11
Patton, M.A.12
Kucherlapati, R.S.13
Gelb, B.D.14
-
15
-
-
18344370436
-
PTPN11 mutations in Noonan syndrome: Molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
-
Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet. 2002;70:1555-1563.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1555-1563
-
-
Tartaglia, M.1
Kalidas, K.2
Shaw, A.3
Song, X.4
Musat, D.L.5
van der Burgt, I.6
Brunner, H.G.7
Bertola, D.R.8
Crosby, A.9
Ion, A.10
Kucherlapati, R.S.11
Jeffery, S.12
Patton, M.A.13
Gelb, B.D.14
-
16
-
-
34547530823
-
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
-
Pandit B, Sarkozy A, Pennacchio LA, Carta C, Oishi K, Martinelli S, Pogna EA, Schackwitz W, Ustaszewska A, Landstrom A, Bos JM, Ommen SR, Esposito G, Lepri F, Faul C, Mundel P, López Siguero JP, Tenconi R, Selicorni A, Rossi C, Mazzanti L, Torrente I, Marino B, Digilio MC, Zampino G, Ackerman MJ, Dallapiccola B, Tartaglia M, Gelb BD. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007;39:1007-1012.
-
(2007)
Nat Genet
, vol.39
, pp. 1007-1012
-
-
Pandit, B.1
Sarkozy, A.2
Pennacchio, L.A.3
Carta, C.4
Oishi, K.5
Martinelli, S.6
Pogna, E.A.7
Schackwitz, W.8
Ustaszewska, A.9
Landstrom, A.10
Bos, J.M.11
Ommen, S.R.12
Esposito, G.13
Lepri, F.14
Faul, C.15
Mundel, P.16
López Siguero, J.P.17
Tenconi, R.18
Selicorni, A.19
Rossi, C.20
Mazzanti, L.21
Torrente, I.22
Marino, B.23
Digilio, M.C.24
Zampino, G.25
Ackerman, M.J.26
Dallapiccola, B.27
Tartaglia, M.28
Gelb, B.D.29
more..
-
17
-
-
1542619343
-
Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation
-
Fragale A, Tartaglia M, Wu J, Gelb BD. Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation. Hum Mutat. 2004;23:267-277.
-
(2004)
Hum Mutat
, vol.23
, pp. 267-277
-
-
Fragale, A.1
Tartaglia, M.2
Wu, J.3
Gelb, B.D.4
-
18
-
-
4043056497
-
Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation
-
Araki T, Mohi MG, Ismat FA, Bronson RT, Williams IR, Kutok JL, Yang W, Pao LI, Gilliland DG, Epstein JA, Neel BG. Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation. Nat Med. 2004;10:849-857.
-
(2004)
Nat Med
, vol.10
, pp. 849-857
-
-
Araki, T.1
Mohi, M.G.2
Ismat, F.A.3
Bronson, R.T.4
Williams, I.R.5
Kutok, J.L.6
Yang, W.7
Pao, L.I.8
Gilliland, D.G.9
Epstein, J.A.10
Neel, B.G.11
-
19
-
-
24744465207
-
Diverse biochemical properties of Shp2 mutants: Implications for disease phenotypes
-
Keilhack H, David FS, McGregor M, Cantley LC, Neel BG. Diverse biochemical properties of Shp2 mutants: implications for disease phenotypes. J Biol Chem. 2005;280:30984-30993.
-
(2005)
J Biol Chem
, vol.280
, pp. 30984-30993
-
-
Keilhack, H.1
David, F.S.2
McGregor, M.3
Cantley, L.C.4
Neel, B.G.5
-
20
-
-
21044458262
-
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
-
Niihori T, Aoki Y, Ohashi H, Kurosawa K, Kondoh T, Ishikiriyama S, Kawame H, Kamasaki H, Yamanaka T, Takada F, Nishio K, Sakurai M, Tamai H, Nagashima T, Suzuki Y, Kure S, Fujii K, Imaizumi M, Matsubara Y. Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia. J Hum Genet. 2005;50:192-202.
-
(2005)
J Hum Genet
, vol.50
, pp. 192-202
-
-
Niihori, T.1
Aoki, Y.2
Ohashi, H.3
Kurosawa, K.4
Kondoh, T.5
Ishikiriyama, S.6
Kawame, H.7
Kamasaki, H.8
Yamanaka, T.9
Takada, F.10
Nishio, K.11
Sakurai, M.12
Tamai, H.13
Nagashima, T.14
Suzuki, Y.15
Kure, S.16
Fujii, K.17
Imaizumi, M.18
Matsubara, Y.19
-
21
-
-
31544452561
-
Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease
-
Tartaglia M, Martinelli S, Stella L, Bocchinfuso G, Flex E, Cordeddu V, Zampino G, Burgt I, Palleschi A, Petrucci TC, Sorcini M, Schoch C, Foa R, Emanuel PD, Gelb BD. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Am J Hum Genet. 2006;78:279-290.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 279-290
-
-
Tartaglia, M.1
Martinelli, S.2
Stella, L.3
Bocchinfuso, G.4
Flex, E.5
Cordeddu, V.6
Zampino, G.7
Burgt, I.8
Palleschi, A.9
Petrucci, T.C.10
Sorcini, M.11
Schoch, C.12
Foa, R.13
Emanuel, P.D.14
Gelb, B.D.15
-
22
-
-
22044452124
-
Functional analysis of leukemia-associated PTPN11 mutations in primary hematopoietic cells
-
Schubbert S, Lieuw K, Rowe SL, Lee CM, Li X, Loh ML, Clapp DW, Shannon KM. Functional analysis of leukemia-associated PTPN11 mutations in primary hematopoietic cells. Blood. 2005;106:311-317.
-
(2005)
Blood
, vol.106
, pp. 311-317
-
-
Schubbert, S.1
Lieuw, K.2
Rowe, S.L.3
Lee, C.M.4
Li, X.5
Loh, M.L.6
Clapp, D.W.7
Shannon, K.M.8
-
24
-
-
20444371557
-
PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes
-
Ogata T, Yoshida R. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes. Pediatr Endocrinol Rev. 2005;2:669-674.
-
(2005)
Pediatr Endocrinol Rev
, vol.2
, pp. 669-674
-
-
Ogata, T.1
Yoshida, R.2
-
25
-
-
33748610364
-
Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy
-
Limongelli G, Hawkes L, Calabro R, McKenna WJ, Syrris P. Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy. Eur J Med Genet. 2006;49:426-430.
-
(2006)
Eur J Med Genet
, vol.49
, pp. 426-430
-
-
Limongelli, G.1
Hawkes, L.2
Calabro, R.3
McKenna, W.J.4
Syrris, P.5
-
26
-
-
33646901973
-
LEOPARD syndrome: Clinical diagnosis in the first year of life
-
Digilio MC, Sarkozy A, de Zorzi A, Pacileo G, Limongelli G, Mingarelli R, Calabro R, Marino B, Dallapiccola B. LEOPARD syndrome: clinical diagnosis in the first year of life. Am J Med Genet A. 2006;140A:740-746.
-
(2006)
Am J Med Genet A
, vol.140 A
, pp. 740-746
-
-
Digilio, M.C.1
Sarkozy, A.2
de Zorzi, A.3
Pacileo, G.4
Limongelli, G.5
Mingarelli, R.6
Calabro, R.7
Marino, B.8
Dallapiccola, B.9
-
27
-
-
33646096207
-
PTPN11 (Shp2) mutations in LEOPARD syndrome have dominant negative, not activating, effects
-
Kontaridis MI, Swanson KD, David FS, Barford D, Neel BG. PTPN11 (Shp2) mutations in LEOPARD syndrome have dominant negative, not activating, effects. J Biol Chem. 2006;281:6785-6792.
-
(2006)
J Biol Chem
, vol.281
, pp. 6785-6792
-
-
Kontaridis, M.I.1
Swanson, K.D.2
David, F.S.3
Barford, D.4
Neel, B.G.5
-
28
-
-
33847404953
-
Response of caspase-independent apoptotic factors to high salt diet-induced heart failure
-
Siu PM, Bae S, Bodyak N, Rigor DL, Kang PM. Response of caspase-independent apoptotic factors to high salt diet-induced heart failure. J Mol Cell Cardiol. 2007;42:678-686.
-
(2007)
J Mol Cell Cardiol
, vol.42
, pp. 678-686
-
-
Siu, P.M.1
Bae, S.2
Bodyak, N.3
Rigor, D.L.4
Kang, P.M.5
-
29
-
-
0037109094
-
Cardiac-specific overexpression of GLUT1 prevents the development of heart failure attributable to pressure overload in mice
-
Liao R, Jain M, Cui L, D'Agostino J, Aiello F, Luptak I, Ngoy S, Mortensen RM, Tian R. Cardiac-specific overexpression of GLUT1 prevents the development of heart failure attributable to pressure overload in mice. Circulation. 2002;106:2125-2131.
-
(2002)
Circulation
, vol.106
, pp. 2125-2131
-
-
Liao, R.1
Jain, M.2
Cui, L.3
D'Agostino, J.4
Aiello, F.5
Luptak, I.6
Ngoy, S.7
Mortensen, R.M.8
Tian, R.9
-
30
-
-
0036841474
-
Side population cells from diverse adult tissues are capable of in vitro hematopoietic differentiation
-
Asakura A, Rudnicki MA. Side population cells from diverse adult tissues are capable of in vitro hematopoietic differentiation. Exp Hematol. 2002;30:1339-1345.
-
(2002)
Exp Hematol
, vol.30
, pp. 1339-1345
-
-
Asakura, A.1
Rudnicki, M.A.2
-
31
-
-
0037236642
-
-
Brancaccio M, Fratta L, Notte A, Hirsch E, Poulet R, Guazzone S, De Acetis M, Vecchione C, Marino G, Altruda F, Silengo L, Tarone G, Lembo G. Melusin, a muscle-specific integrin beta1-interacting protein, is required to prevent cardiac failure in response to chronic pressure overload. Nat Med. 2003;9:68-75.
-
Brancaccio M, Fratta L, Notte A, Hirsch E, Poulet R, Guazzone S, De Acetis M, Vecchione C, Marino G, Altruda F, Silengo L, Tarone G, Lembo G. Melusin, a muscle-specific integrin beta1-interacting protein, is required to prevent cardiac failure in response to chronic pressure overload. Nat Med. 2003;9:68-75.
-
-
-
-
32
-
-
20344399430
-
Cardiac overexpression of melusin protects from dilated cardiomyopathy due to long-standing pressure overload
-
De Acetis M, Notte A, Accornero F, Selvetella G, Brancaccio M, Vecchione C, Sbroggiò M, Collino F, Pacchioni B, Lanfranchi G, Aretini A, Ferretti R, Maffei A, Altruda F, Silengo L, Tarone G, Lembo G. Cardiac overexpression of melusin protects from dilated cardiomyopathy due to long-standing pressure overload. Circ Res. 2005;96:1087-1094.
-
(2005)
Circ Res
, vol.96
, pp. 1087-1094
-
-
De Acetis, M.1
Notte, A.2
Accornero, F.3
Selvetella, G.4
Brancaccio, M.5
Vecchione, C.6
Sbroggiò, M.7
Collino, F.8
Pacchioni, B.9
Lanfranchi, G.10
Aretini, A.11
Ferretti, R.12
Maffei, A.13
Altruda, F.14
Silengo, L.15
Tarone, G.16
Lembo, G.17
-
33
-
-
10744223870
-
Shp2 regulates SRC family kinase activity and Ras/Erk activation by controlling Csk recruitment
-
Zhang SQ, Yang W, Kontaridis MI, Bivona TG, Wen G, Araki T, Luo J, Thompson JA, Schraven BL, Philips MR, Neel BG. Shp2 regulates SRC family kinase activity and Ras/Erk activation by controlling Csk recruitment. Mol Cell. 2004;13:341-355.
-
(2004)
Mol Cell
, vol.13
, pp. 341-355
-
-
Zhang, S.Q.1
Yang, W.2
Kontaridis, M.I.3
Bivona, T.G.4
Wen, G.5
Araki, T.6
Luo, J.7
Thompson, J.A.8
Schraven, B.L.9
Philips, M.R.10
Neel, B.G.11
-
34
-
-
0032214652
-
A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance
-
Bruning JC, Michael MD, Winnay JN, Hayashi T, Horsch D, Accili D, Goodyear LJ, Kahn CR. A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance. Mol Cell. 1998;2:559-569.
-
(1998)
Mol Cell
, vol.2
, pp. 559-569
-
-
Bruning, J.C.1
Michael, M.D.2
Winnay, J.N.3
Hayashi, T.4
Horsch, D.5
Accili, D.6
Goodyear, L.J.7
Kahn, C.R.8
-
35
-
-
33748323383
-
Regulation of cardiac hypertrophy by intracellular signalling pathways
-
Heineke J, Molkentin JD. Regulation of cardiac hypertrophy by intracellular signalling pathways. Nat Rev Mol Cell Biol. 2006;7:589-600.
-
(2006)
Nat Rev Mol Cell Biol
, vol.7
, pp. 589-600
-
-
Heineke, J.1
Molkentin, J.D.2
-
36
-
-
33748278519
-
Targeted ablation of ILK from the murine heart results in dilated cardiomyopathy and spontaneous heart failure
-
White DE, Coutu P, Shi YF, Tardif JC, Nattel S, St Arnaud R, Dedhar S, Muller WJ. Targeted ablation of ILK from the murine heart results in dilated cardiomyopathy and spontaneous heart failure. Genes Dev. 2006;20:2355-2360.
-
(2006)
Genes Dev
, vol.20
, pp. 2355-2360
-
-
White, D.E.1
Coutu, P.2
Shi, Y.F.3
Tardif, J.C.4
Nattel, S.5
St Arnaud, R.6
Dedhar, S.7
Muller, W.J.8
-
37
-
-
0037040839
-
Cardiac myocyte-specific excision of the beta1 integrin gene results in myocardial fibrosis and cardiac failure
-
Shai SY, Harpf AE, Babbitt CJ, Jordan MC, Fishbein MC, Chen J, Omura M, Leil TA, Becker KD, Jiang M, Smith DJ, Cherry SR, Loftus JC, Ross RS. Cardiac myocyte-specific excision of the beta1 integrin gene results in myocardial fibrosis and cardiac failure. Circ Res. 2002;90:458-464.
-
(2002)
Circ Res
, vol.90
, pp. 458-464
-
-
Shai, S.Y.1
Harpf, A.E.2
Babbitt, C.J.3
Jordan, M.C.4
Fishbein, M.C.5
Chen, J.6
Omura, M.7
Leil, T.A.8
Becker, K.D.9
Jiang, M.10
Smith, D.J.11
Cherry, S.R.12
Loftus, J.C.13
Ross, R.S.14
-
38
-
-
0032694585
-
Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure
-
Sah VP, Minamisawa S, Tam SP, Wu TH, Dorn GW 2nd, Ross J Jr, Chien KR, Brown JH. Cardiac-specific overexpression of RhoA results in sinus and atrioventricular nodal dysfunction and contractile failure. J Clin Invest. 1999;103:1627-1634.
-
(1999)
J Clin Invest
, vol.103
, pp. 1627-1634
-
-
Sah, V.P.1
Minamisawa, S.2
Tam, S.P.3
Wu, T.H.4
Dorn 2nd, G.W.5
Ross Jr, J.6
Chien, K.R.7
Brown, J.H.8
-
39
-
-
0030878260
-
Gene recombination in postmitotic cells: Targeted expression of Cre recombinase provokes cardiac-restricted, site-specific rearrangement in adult ventricular muscle in vivo
-
Agah R, Frenkel PA, French BA, Michael LH, Overbeek PA, Schneider MD. Gene recombination in postmitotic cells: targeted expression of Cre recombinase provokes cardiac-restricted, site-specific rearrangement in adult ventricular muscle in vivo. J Clin Invest. 1997;100:169-179.
-
(1997)
J Clin Invest
, vol.100
, pp. 169-179
-
-
Agah, R.1
Frenkel, P.A.2
French, B.A.3
Michael, L.H.4
Overbeek, P.A.5
Schneider, M.D.6
-
40
-
-
20444480174
-
Morphogenesis of the right ventricle requires myocardial expression of Gata4
-
Zeisberg EM, Ma Q, Juraszek AL, Moses K, Schwartz RJ, Izumo S, Pu WT. Morphogenesis of the right ventricle requires myocardial expression of Gata4. J Clin Invest. 2005;115:1522-1531.
-
(2005)
J Clin Invest
, vol.115
, pp. 1522-1531
-
-
Zeisberg, E.M.1
Ma, Q.2
Juraszek, A.L.3
Moses, K.4
Schwartz, R.J.5
Izumo, S.6
Pu, W.T.7
-
41
-
-
84990609891
-
Proliferation of cardiomyocytes and interstitial cells in the cardiac muscle of the mouse during pre- and postnatal development
-
Cluzeaut F, and Maurer-Schultze B. Proliferation of cardiomyocytes and interstitial cells in the cardiac muscle of the mouse during pre- and postnatal development. Cell Tissue Kinet. 1986;19:267-274.
-
(1986)
Cell Tissue Kinet
, vol.19
, pp. 267-274
-
-
Cluzeaut, F.1
Maurer-Schultze, B.2
-
42
-
-
27744569175
-
Temporally controlled onset of dilated cardiomyopathy through disruption of the SRF gene in adult heart
-
Parlakian A, Charvet C, Escoubet B, Mericskay M, Molkentin JD, Gary-Bobo G, De Windt LJ, Ludosky MA, Paulin D, Daegelen D, Tuil D, Li Z. Temporally controlled onset of dilated cardiomyopathy through disruption of the SRF gene in adult heart. Circulation. 2005;112:2930-2939.
-
(2005)
Circulation
, vol.112
, pp. 2930-2939
-
-
Parlakian, A.1
Charvet, C.2
Escoubet, B.3
Mericskay, M.4
Molkentin, J.D.5
Gary-Bobo, G.6
De Windt, L.J.7
Ludosky, M.A.8
Paulin, D.9
Daegelen, D.10
Tuil, D.11
Li, Z.12
-
43
-
-
0037172982
-
Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy
-
Ozcelik C, Erdmann B, Pilz B, Wettschureck N, Britsch S, Hubner N, Chien KR, Birchmeier C, Garratt AN. Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy. Proc Natl Acad Sci U S A. 2002;99:8880-8885.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 8880-8885
-
-
Ozcelik, C.1
Erdmann, B.2
Pilz, B.3
Wettschureck, N.4
Britsch, S.5
Hubner, N.6
Chien, K.R.7
Birchmeier, C.8
Garratt, A.N.9
-
44
-
-
33847216159
-
Essential role of insulin and insulin-like growth factor 1 receptor signaling in cardiac development and function
-
Laustsen PG, Russell SJ, Cui L, Entingh-Pearsall A, Holzenberger M, Liao R, Kahn CR. Essential role of insulin and insulin-like growth factor 1 receptor signaling in cardiac development and function. Mol Cell Biol. 2007;27:1649-1664.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 1649-1664
-
-
Laustsen, P.G.1
Russell, S.J.2
Cui, L.3
Entingh-Pearsall, A.4
Holzenberger, M.5
Liao, R.6
Kahn, C.R.7
-
45
-
-
9644295769
-
Cardiac-specific disruption of the c-raf-1 gene induces cardiac dysfunction and apoptosis
-
Yamaguchi O, Watanabe T, Nishida K, Kashiwase K, Higuchi Y, Takeda T, Hikoso S, Hirotani S, Asahi M, Taniike M, Nakai A, Tsujimoto I, Matsumura Y, Miyazaki J, Chien KR, Matsuzawa A, Sadamitsu C, Ichijo H, Baccarini M, Hori M, Otsu K. Cardiac-specific disruption of the c-raf-1 gene induces cardiac dysfunction and apoptosis. J Clin Invest. 2004;114:937-943.
-
(2004)
J Clin Invest
, vol.114
, pp. 937-943
-
-
Yamaguchi, O.1
Watanabe, T.2
Nishida, K.3
Kashiwase, K.4
Higuchi, Y.5
Takeda, T.6
Hikoso, S.7
Hirotani, S.8
Asahi, M.9
Taniike, M.10
Nakai, A.11
Tsujimoto, I.12
Matsumura, Y.13
Miyazaki, J.14
Chien, K.R.15
Matsuzawa, A.16
Sadamitsu, C.17
Ichijo, H.18
Baccarini, M.19
Hori, M.20
Otsu, K.21
more..
-
46
-
-
35348921181
-
Genetic inhibition of cardiac ERK1/2 promotes stress-induced apoptosis and heart failure but has no effect on hypertrophy in vivo
-
Purcell NH, Wilkins BJ, York A, Saba-El-Leil MK, Meloche S, Robbins J, Molkentin JD. Genetic inhibition of cardiac ERK1/2 promotes stress-induced apoptosis and heart failure but has no effect on hypertrophy in vivo. Proc Natl Acad Sci U S A. 2007;104:14074-14079.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 14074-14079
-
-
Purcell, N.H.1
Wilkins, B.J.2
York, A.3
Saba-El-Leil, M.K.4
Meloche, S.5
Robbins, J.6
Molkentin, J.D.7
-
47
-
-
0036099675
-
ErbB2 is essential in the prevention of dilated cardiomyopathy
-
Crone SA, Zhao YY, Fan L, Gu Y, Minamisawa S, Liu Y, Peterson KL, Chen J, Kahn R, Condorelli G, Ross J Jr, Chien KR, Lee KF. ErbB2 is essential in the prevention of dilated cardiomyopathy. Nat Med. 2002;8:459-465.
-
(2002)
Nat Med
, vol.8
, pp. 459-465
-
-
Crone, S.A.1
Zhao, Y.Y.2
Fan, L.3
Gu, Y.4
Minamisawa, S.5
Liu, Y.6
Peterson, K.L.7
Chen, J.8
Kahn, R.9
Condorelli, G.10
Ross Jr, J.11
Chien, K.R.12
Lee, K.F.13
-
48
-
-
3242739935
-
Protein-tyrosine phosphatase, non-receptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome
-
Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Protein-tyrosine phosphatase, non-receptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. J Clin Endocrinol Metab. 2004;89:3359-3364.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 3359-3364
-
-
Yoshida, R.1
Hasegawa, T.2
Hasegawa, Y.3
Nagai, T.4
Kinoshita, E.5
Tanaka, Y.6
Kanegane, H.7
Ohyama, K.8
Onishi, T.9
Hanew, K.10
Okuyama, T.11
Horikawa, R.12
Tanaka, T.13
Ogata, T.14
-
49
-
-
0029940955
-
Hypertrophic cardiomyopathy in Noonan syndrome
-
Nishikawa T, Ishiyama S, Shimojo T, Takeda K, Kasajima T, Momma K. Hypertrophic cardiomyopathy in Noonan syndrome. Acta Paediatr Jpn. 1996;38:91-98.
-
(1996)
Acta Paediatr Jpn
, vol.38
, pp. 91-98
-
-
Nishikawa, T.1
Ishiyama, S.2
Shimojo, T.3
Takeda, K.4
Kasajima, T.5
Momma, K.6
-
50
-
-
0031790484
-
Noonan syndrome and aortic coarctation
-
Digilio MC, Marino B, Picchio F, Prandstraller D, Toscano A, Giannotti A, Dallapiccola B. Noonan syndrome and aortic coarctation. Am J Med Genet. 1998;80:160-162.
-
(1998)
Am J Med Genet
, vol.80
, pp. 160-162
-
-
Digilio, M.C.1
Marino, B.2
Picchio, F.3
Prandstraller, D.4
Toscano, A.5
Giannotti, A.6
Dallapiccola, B.7
|