-
1
-
-
0032541318
-
FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates
-
PMID: 9714712
-
Grewal PK, Todd LC, van der Maarel S, Frants RR, Hewitt JE (1998) FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates. Gene 216: 13-19. PMID: 9714712
-
(1998)
Gene
, vol.216
, pp. 13-19
-
-
Grewal, P.K.1
Todd, L.C.2
Van Der Maarel, S.3
Frants, R.R.4
Hewitt, J.E.5
-
2
-
-
33644522383
-
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1
-
PMID: 16341202
-
Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, et al. (2006) Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature 439: 973-977. PMID: 16341202
-
(2006)
Nature
, vol.439
, pp. 973-977
-
-
Gabellini, D.1
D'Antona, G.2
Moggio, M.3
Prelle, A.4
Zecca, C.5
-
3
-
-
33846589302
-
FRG1P-mediated aggregation of proteins involved in pre-mRNA processing
-
PMID: 17103222
-
van Koningsbruggen S, Straasheijm KR, Sterrenburg E, de Graaf N, Dauwerse HG, et al. (2007) FRG1P-mediated aggregation of proteins involved in pre-mRNA processing. Chromosoma 116: 53-64. PMID: 17103222
-
(2007)
Chromosoma
, vol.116
, pp. 53-64
-
-
Van Koningsbruggen, S.1
Straasheijm, K.R.2
Sterrenburg, E.3
De Graaf, N.4
Dauwerse, H.G.5
-
4
-
-
84873515320
-
Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD)
-
PMID: 23300487
-
Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, et al. (2013) Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD). Plos Genetics 9: e1003186. doi: 10.1371/journal.pgen.1003186 PMID: 23300487
-
(2013)
Plos Genetics
, vol.9
, pp. e1003186
-
-
Pistoni, M.1
Shiue, L.2
Cline, M.S.3
Bortolanza, S.4
Neguembor, M.V.5
-
5
-
-
79960737300
-
Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein
-
PMID: 21699900
-
Sun CY, van Koningsbruggen S, Long SW, Straasheijm K, Klooster R, et al. (2011) Facioscapulohumeral muscular dystrophy region gene 1 is a dynamic RNA-associated and actin-bundling protein. Journal of Molecular Biology 411: 397-416. doi: 10.1016/j.jmb.2011.06.014 PMID: 21699900
-
(2011)
Journal of Molecular Biology
, vol.411
, pp. 397-416
-
-
Sun, C.Y.1
Van Koningsbruggen, S.2
Long, S.W.3
Straasheijm, K.4
Klooster, R.5
-
6
-
-
77951145598
-
Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites
-
PMID: 20215405
-
Liu Q, Jones TI, Tang VW, Brieher WM, Jones PL (2010) Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites. Journal of Cell Science 123: 1116-1123. doi: 10.1242/jcs.058958 PMID: 20215405
-
(2010)
Journal of Cell Science
, vol.123
, pp. 1116-1123
-
-
Liu, Q.1
Jones, T.I.2
Tang, V.W.3
Brieher, W.M.4
Jones, P.L.5
-
7
-
-
66349093652
-
Muscular dystrophy candidate gene FRG1 is critical for muscle development
-
PMID: 19097195
-
Hanel ML, Wuebbles RD, Jones PL (2009) Muscular dystrophy candidate gene FRG1 is critical for muscle development. Dev Dyn 238: 1502-1512. doi: 10.1002/dvdy.21830 PMID: 19097195
-
(2009)
Dev Dyn
, vol.238
, pp. 1502-1512
-
-
Hanel, M.L.1
Wuebbles, R.D.2
Jones, P.L.3
-
8
-
-
84902517476
-
Facioscapulohumeral dystrophy: The path to consensus on pathophysiology
-
PMID: 24940479
-
Tawil R, van der Maarel SM, Tapscott SJ (2014) Facioscapulohumeral dystrophy: the path to consensus on pathophysiology. Skelet Muscle 4: 12. doi: 10.1186/2044-5040-4-12 PMID: 24940479
-
(2014)
Skelet Muscle
, vol.4
, pp. 12
-
-
Tawil, R.1
Van Der Maarel, S.M.2
Tapscott, S.J.3
-
9
-
-
0028918407
-
Facioscapulohumeral muscular dystrophy in the Dutch population
-
PMID: 23573591
-
Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, et al. (1995) Facioscapulohumeral muscular dystrophy in the Dutch population. Muscle Nerve Suppl 2: S81-84. PMID: 23573591
-
(1995)
Muscle Nerve Suppl
, vol.2
, pp. S81-S84
-
-
Padberg, G.W.1
Frants, R.R.2
Brouwer, O.F.3
Wijmenga, C.4
Bakker, E.5
-
10
-
-
0034882438
-
Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy
-
PMID: 11525880
-
Flanigan KM, Coffeen CM, Sexton L, Stauffer D, Brunner S, et al. (2001) Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy. Neuromuscul Disord 11: 525-529. PMID: 11525880
-
(2001)
Neuromuscul Disord
, vol.11
, pp. 525-529
-
-
Flanigan, K.M.1
Coffeen, C.M.2
Sexton, L.3
Stauffer, D.4
Brunner, S.5
-
11
-
-
66549122709
-
Facioscapulohumeral muscular dystrophy: Epidemiological and molecular study in a north-east Italian population sample
-
PMID: 19320656
-
Mostacciuolo ML, Pastorello E, Vazza G, Miorin M, Angelini C, et al. (2009) Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample. Clin Genet 75: 550-555. doi: 10.1111/j.1399-0004.2009.01158.x PMID: 19320656
-
(2009)
Clin Genet
, vol.75
, pp. 550-555
-
-
Mostacciuolo, M.L.1
Pastorello, E.2
Vazza, G.3
Miorin, M.4
Angelini, C.5
-
12
-
-
84915829052
-
Population-based incidence and prevalence of facioscapulohumeral dystrophy
-
PMID: 25122204
-
Deenen JC, Arnts H, van der Maarel SM, Padberg GW, Verschuuren JJ, et al. (2014) Population-based incidence and prevalence of facioscapulohumeral dystrophy. Neurology 83: 1056-1059. doi: 10.1212/WNL.0000000000000797 PMID: 25122204
-
(2014)
Neurology
, vol.83
, pp. 1056-1059
-
-
Deenen, J.C.1
Arnts, H.2
Van Der Maarel, S.M.3
Padberg, G.W.4
Verschuuren, J.J.5
-
13
-
-
0026080958
-
Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization
-
PMID: 2037288
-
Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, et al. (1991) Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics 9: 570-575. PMID: 2037288
-
(1991)
Genomics
, vol.9
, pp. 570-575
-
-
Wijmenga, C.1
Padberg, G.W.2
Moerer, P.3
Wiegant, J.4
Liem, L.5
-
14
-
-
0344436078
-
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
-
PMID: 10433963
-
Gabriels J, Beckers MC, Ding H, De Vriese A, Plaisance S, et al. (1999) Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element. Gene 236: 25-32. PMID: 10433963
-
(1999)
Gene
, vol.236
, pp. 25-32
-
-
Gabriels, J.1
Beckers, M.C.2
Ding, H.3
De Vriese, A.4
Plaisance, S.5
-
15
-
-
77957327192
-
A unifying genetic model for facioscapulohumeral muscular dystrophy
-
PMID: 20724583
-
Lemmers RJ, van der Vliet PJ, Klooster R, Sacconi S, Camano P, et al. (2010) A unifying genetic model for facioscapulohumeral muscular dystrophy. Science 329: 1650-1653. doi: 10.1126/science.1189044 PMID: 20724583
-
(2010)
Science
, vol.329
, pp. 1650-1653
-
-
Lemmers, R.J.1
Van Der Vliet, P.J.2
Klooster, R.3
Sacconi, S.4
Camano, P.5
-
16
-
-
36749026295
-
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
-
PMID: 17984056
-
Dixit M, Ansseau E, Tassin A, Winokur S, Shi R, et al. (2007) DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1. Proceedings of the National Academy of Sciences of the United States of America 104: 18157-18162. PMID: 17984056
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, pp. 18157-18162
-
-
Dixit, M.1
Ansseau, E.2
Tassin, A.3
Winokur, S.4
Shi, R.5
-
17
-
-
84855956147
-
DUX4 Activates Germ line Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy
-
PMID: 22209328
-
Geng LN, Yao ZZ, Snider L, Fong AP, Cech JN, et al. (2012) DUX4 Activates Germ line Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy. Developmental Cell 22: 38-51. doi: 10.1016/j.devcel.2011.11.013 PMID: 22209328
-
(2012)
Developmental Cell
, vol.22
, pp. 38-51
-
-
Geng, L.N.1
Yao, Z.Z.2
Snider, L.3
Fong, A.P.4
Cech, J.N.5
-
18
-
-
84888236297
-
DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis
-
PMID: 24278031
-
Young JM, Whiddon JL, Yao Z, Kasinathan B, Snider L, et al. (2013) DUX4 binding to retroelements creates promoters that are active in FSHD muscle and testis. Plos Genetics 9: e1003947. doi: 10.1371/journal.pgen.1003947 PMID: 24278031
-
(2013)
Plos Genetics
, vol.9
, pp. e1003947
-
-
Young, J.M.1
Whiddon, J.L.2
Yao, Z.3
Kasinathan, B.4
Snider, L.5
-
19
-
-
84964817861
-
Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice
-
PMID: 23125914
-
Pandey SN, Cabotage J, Shi R, Dixit M, Sutherland M, et al. (2012) Conditional over-expression of PITX1 causes skeletal muscle dystrophy in mice. Biol Open 1: 629-639. PMID: 23125914
-
(2012)
Biol Open
, vol.1
, pp. 629-639
-
-
Pandey, S.N.1
Cabotage, J.2
Shi, R.3
Dixit, M.4
Sutherland, M.5
-
20
-
-
84872415036
-
Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy
-
PMID: 23108159
-
Mitsuhashi H, Mitsuhashi S, Lynn-Jones T, Kawahara G, Kunkel LM (2013) Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy. Human Molecular Genetics 22: 568-577. doi: 10.1093/hmg/dds467 PMID: 23108159
-
(2013)
Human Molecular Genetics
, vol.22
, pp. 568-577
-
-
Mitsuhashi, H.1
Mitsuhashi, S.2
Lynn-Jones, T.3
Kawahara, G.4
Kunkel, L.M.5
-
21
-
-
84876821220
-
Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD
-
PMID: 23593020
-
Krom YD, Thijssen PE, Young JM, den Hamer B, Balog J, et al. (2013) Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD. Plos Genetics 9: e1003415. doi: 10.1371/journal.pgen.1003415 PMID: 23593020
-
(2013)
Plos Genetics
, vol.9
, pp. e1003415
-
-
Krom, Y.D.1
Thijssen, P.E.2
Young, J.M.3
Den Hamer, B.4
Balog, J.5
-
22
-
-
84922547186
-
Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene
-
PMID: 25176645
-
Dandapat A, Bosnakovski D, Hartweck LM, Arpke RW, Baltgalvis KA, et al. (2014) Dominant Lethal Pathologies in Male Mice Engineered to Contain an X-Linked DUX4 Transgene. Cell Reports 8: 1484-1496. doi: 10.1016/j.celrep.2014.07.056 PMID: 25176645
-
(2014)
Cell Reports
, vol.8
, pp. 1484-1496
-
-
Dandapat, A.1
Bosnakovski, D.2
Hartweck, L.M.3
Arpke, R.W.4
Baltgalvis, K.A.5
-
23
-
-
9244232833
-
Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35
-
PMID: 8733123
-
van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, et al. (1996) Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. Human Molecular Genetics 5: 581-590. PMID: 8733123
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 581-590
-
-
Van Deutekom, J.C.1
Lemmers, R.J.2
Grewal, P.K.3
Van Geel, M.4
Romberg, S.5
-
24
-
-
0030009384
-
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
-
PMID: 8733044
-
Tupler R, Berardinelli A, Barbierato L, Frants R, Hewitt JE, et al. (1996) Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. J Med Genet 33: 366-370. PMID: 8733044
-
(1996)
J Med Genet
, vol.33
, pp. 366-370
-
-
Tupler, R.1
Berardinelli, A.2
Barbierato, L.3
Frants, R.4
Hewitt, J.E.5
-
26
-
-
84860885909
-
A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy
-
PMID: 22541069
-
Cabianca DS, Casa V, Bodega B, Xynos A, Ginelli E, et al. (2012) A long ncRNA links copy number variation to a polycomb/trithorax epigenetic switch in FSHD muscular dystrophy. Cell 149: 819-831. doi: 10.1016/j.cell.2012.03.035 PMID: 22541069
-
(2012)
Cell
, vol.149
, pp. 819-831
-
-
Cabianca, D.S.1
Casa, V.2
Bodega, B.3
Xynos, A.4
Ginelli, E.5
-
27
-
-
0037047439
-
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
PMID: 12176321
-
Gabellini D, Green MR, Tupler R (2002) Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110: 339-348. PMID: 12176321
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
28
-
-
33847234593
-
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
-
PMID: 17151338
-
Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R (2007) Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 68: 569-577. PMID: 17151338
-
(2007)
Neurology
, vol.68
, pp. 569-577
-
-
Osborne, R.J.1
Welle, S.2
Venance, S.L.3
Thornton, C.A.4
Tawil, R.5
-
29
-
-
70450275779
-
Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
-
PMID: 19809486
-
Klooster R, Straasheijm K, Shah B, Sowden J, Frants R, et al. (2009) Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level. European Journal of Human Genetics 17: 1615-1624. doi: 10.1038/ejhg.2009.62 PMID: 19809486
-
(2009)
European Journal of Human Genetics
, vol.17
, pp. 1615-1624
-
-
Klooster, R.1
Straasheijm, K.2
Shah, B.3
Sowden, J.4
Frants, R.5
-
30
-
-
0344875044
-
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
-
PMID: 14519683
-
Winokur ST, Chen YW, Masny PS, Martin JH, Ehmsen JT, et al. (2003) Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Human Molecular Genetics 12: 2895-2907. PMID: 14519683
-
(2003)
Human Molecular Genetics
, vol.12
, pp. 2895-2907
-
-
Winokur, S.T.1
Chen, Y.W.2
Masny, P.S.3
Martin, J.H.4
Ehmsen, J.T.5
-
31
-
-
0345227304
-
Testing the position-effectvariegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
-
PMID: 14506132
-
Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, et al. (2003) Testing the position-effectvariegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Human Molecular Genetics 12: 2909-2921. PMID: 14506132
-
(2003)
Human Molecular Genetics
, vol.12
, pp. 2909-2921
-
-
Jiang, G.1
Yang, F.2
Van Overveld, P.G.3
Vedanarayanan, V.4
Van Der Maarel, S.5
-
32
-
-
77949656794
-
Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei
-
PMID: 19888305
-
Masny PS, Chan OYA, de Greef JC, Bengtsson U, Ehrlich M, et al. (2010) Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei. European Journal of Human Genetics 18: 448-456. doi: 10.1038/ejhg.2009.183 PMID: 19888305
-
(2010)
European Journal of Human Genetics
, vol.18
, pp. 448-456
-
-
Masny, P.S.1
Chan, O.Y.A.2
De Greef, J.C.3
Bengtsson, U.4
Ehrlich, M.5
-
33
-
-
84879856340
-
Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells
-
PMID: 23525014
-
Xynos A, Neguembor MV, Caccia R, Licastro D, Nonis A, et al. (2013) Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells. Journal of Cell Science 126: 2236-2245. doi: 10.1242/jcs.121533 PMID: 23525014
-
(2013)
Journal of Cell Science
, vol.126
, pp. 2236-2245
-
-
Xynos, A.1
Neguembor, M.V.2
Caccia, R.3
Licastro, D.4
Nonis, A.5
-
34
-
-
67650314502
-
FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy
-
PMID: 25608223
-
Wuebbles RD, Hanel ML, Jones PL (2009) FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy. Disease Models &Mechanisms 2: 267-274. doi: 10.1111/jvh.12392 PMID: 25608223
-
(2009)
Disease Models &Mechanisms
, vol.2
, pp. 267-274
-
-
Wuebbles, R.D.1
Hanel, M.L.2
Jones, P.L.3
-
35
-
-
84885342118
-
FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis
-
PMID: 23720823
-
Neguembor MV, Xynos A, Onorati MC, Caccia R, Bortolanza S, et al. (2013) FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis. Journal of Molecular Cell Biology 5: 294-307. doi: 10.1093/jmcb/mjt018 PMID: 23720823
-
(2013)
Journal of Molecular Cell Biology
, vol.5
, pp. 294-307
-
-
Neguembor, M.V.1
Xynos, A.2
Onorati, M.C.3
Caccia, R.4
Bortolanza, S.5
-
36
-
-
33749605124
-
Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes
-
PMID: 17013991
-
Celegato B, Capitanio D, Pescatori M, Romualdi C, Pacchioni B, et al. (2006) Parallel protein and transcript profiles of FSHD patient muscles correlate to the D4Z4 arrangement and reveal a common impairment of slow to fast fibre differentiation and a general deregulation of MyoD-dependent genes. Proteomics 6: 5303-5321. PMID: 17013991
-
(2006)
Proteomics
, vol.6
, pp. 5303-5321
-
-
Celegato, B.1
Capitanio, D.2
Pescatori, M.3
Romualdi, C.4
Pacchioni, B.5
-
37
-
-
79958759071
-
Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
-
PMID: 21695143
-
Cheli S, Francois S, Bodega B, Ferrari F, Tenedini E, et al. (2011) Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns. Plos One 6: e20966. doi: 10.1371/journal.pone.0020966 PMID: 21695143
-
(2011)
Plos One
, vol.6
, pp. e20966
-
-
Cheli, S.1
Francois, S.2
Bodega, B.3
Ferrari, F.4
Tenedini, E.5
-
38
-
-
84871296824
-
FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes
-
PMID: 23272181
-
Tassin A, Leroy B, Laoudj-Chenivesse D, Wauters A, Vanderplanck C, et al. (2012) FSHD Myotubes with Different Phenotypes Exhibit Distinct Proteomes. Plos One 7: e51865. doi: 10.1371/journal.pone.0051865 PMID: 23272181
-
(2012)
Plos One
, vol.7
, pp. e51865
-
-
Tassin, A.1
Leroy, B.2
Laoudj-Chenivesse, D.3
Wauters, A.4
Vanderplanck, C.5
-
39
-
-
80053349950
-
Gene expression during normal and FSHD myogenesis
-
PMID: 21951698
-
Tsumagari K, Chang SC, Lacey M, Baribault C, Chittur SV, et al. (2011) Gene expression during normal and FSHD myogenesis. Bmc Medical Genomics 4: 67-84. doi: 10.1186/1755-8794-4-67 PMID: 21951698
-
(2011)
Bmc Medical Genomics
, vol.4
, pp. 67-84
-
-
Tsumagari, K.1
Chang, S.C.2
Lacey, M.3
Baribault, C.4
Chittur, S.V.5
-
40
-
-
0034815139
-
Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts
-
PMID: 11595515
-
Furling D, Lemieux D, Taneja K, Puymirat J (2001) Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts. Neuromuscular Disorders 11: 728-735. PMID: 11595515
-
(2001)
Neuromuscular Disorders
, vol.11
, pp. 728-735
-
-
Furling, D.1
Lemieux, D.2
Taneja, K.3
Puymirat, J.4
-
41
-
-
0034806973
-
Molecular basis for impaired muscle differentiation in myotonic dystrophy
-
PMID: 11564876
-
Timchenko NA, Iakova P, Cai ZJ, Smith JR, Timchenko LT (2001) Molecular basis for impaired muscle differentiation in myotonic dystrophy. Molecular and Cellular Biology 21: 6927-6938. PMID: 11564876
-
(2001)
Molecular and Cellular Biology
, vol.21
, pp. 6927-6938
-
-
Timchenko, N.A.1
Iakova, P.2
Cai, Z.J.3
Smith, J.R.4
Timchenko, L.T.5
-
42
-
-
12144288743
-
Inhibition of myogenesis in transgenic mice expressing the human DMPK 3 '-UTR
-
PMID: 14734627
-
Storbeck CJ, Drmanic S, Daniel K, Waring JD, Jirik FR, et al. (2004) Inhibition of myogenesis in transgenic mice expressing the human DMPK 3 '-UTR. Human Molecular Genetics 13: 589-600. PMID: 14734627
-
(2004)
Human Molecular Genetics
, vol.13
, pp. 589-600
-
-
Storbeck, C.J.1
Drmanic, S.2
Daniel, K.3
Waring, J.D.4
Jirik, F.R.5
-
43
-
-
0033578613
-
Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication
-
PMID: 10480922
-
Brown S, McGrath MJ, Ooms LM, Gurung R, Maimone MM, et al. (1999) Characterization of two isoforms of the skeletal muscle LIM protein 1, SLIM1. Localization of SLIM1 at focal adhesions and the isoform slimmer in the nucleus of myoblasts and cytoplasm of myotubes suggests distinct roles in the cytoskeleton and in nuclear-cytoplasmic communication. Journal of Biological Chemistry 274: 27083-27091. PMID: 10480922
-
(1999)
Journal of Biological Chemistry
, vol.274
, pp. 27083-27091
-
-
Brown, S.1
McGrath, M.J.2
Ooms, L.M.3
Gurung, R.4
Maimone, M.M.5
-
44
-
-
40549108276
-
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy
-
PMID: 18274675
-
Schessl J, Zou Y, McGrath MJ, Cowling BS, Maiti B, et al. (2008) Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. Journal of Clinical Investigation 118: 904-912. doi: 10.1172/JCI34450 PMID: 18274675
-
(2008)
Journal of Clinical Investigation
, vol.118
, pp. 904-912
-
-
Schessl, J.1
Zou, Y.2
McGrath, M.J.3
Cowling, B.S.4
Maiti, B.5
-
45
-
-
38749136299
-
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1
-
PMID: 18179901
-
Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, et al. (2008) X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American Journal of Human Genetics 82: 208-213. doi: 10.1016/j.ajhg.2007.09.013 PMID: 18179901
-
(2008)
American Journal of Human Genetics
, vol.82
, pp. 208-213
-
-
Quinzii, C.M.1
Vu, T.H.2
Min, K.C.3
Tanji, K.4
Barral, S.5
-
46
-
-
38749121773
-
An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1
-
PMID: 18179888
-
Windpassinger C, Schoser B, Straub V, Hochmeister S, Noor A, et al. (2008) An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1. American Journal of Human Genetics 82: 88-99. doi: 10.1016/j.ajhg.2007.09.004 PMID: 18179888
-
(2008)
American Journal of Human Genetics
, vol.82
, pp. 88-99
-
-
Windpassinger, C.1
Schoser, B.2
Straub, V.3
Hochmeister, S.4
Noor, A.5
-
47
-
-
69749088309
-
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy
-
PMID: 19716112
-
Gueneau L, Bertrand AT, Jais JP, Salih MA, Stojkovic T, et al. (2009) Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy. American Journal of Human Genetics 85: 338-353. doi: 10.1016/j.ajhg.2009.07.015 PMID: 19716112
-
(2009)
American Journal of Human Genetics
, vol.85
, pp. 338-353
-
-
Gueneau, L.1
Bertrand, A.T.2
Jais, J.P.3
Salih, M.A.4
Stojkovic, T.5
-
48
-
-
58249091742
-
Identification of FHL1 as a regulator of skeletal muscle mass: Implications for human myopathy
-
PMID: 19075112
-
Cowling BS, McGrath MJ, Nguyen MA, Cottle DL, Kee AJ, et al. (2008) Identification of FHL1 as a regulator of skeletal muscle mass: implications for human myopathy. Journal of Cell Biology 183: 1033-1048. doi: 10.1083/jcb.200804077 PMID: 19075112
-
(2008)
Journal of Cell Biology
, vol.183
, pp. 1033-1048
-
-
Cowling, B.S.1
McGrath, M.J.2
Nguyen, M.A.3
Cottle, D.L.4
Kee, A.J.5
-
49
-
-
0017759258
-
Serial Passing and Differentiation of Myogenic Cells Isolated from Dystrophic Mouse Muscle
-
PMID: 563524
-
Yaffe D, Saxel O (1977) Serial Passing and Differentiation of Myogenic Cells Isolated from Dystrophic Mouse Muscle. Nature 270: 725-727. PMID: 563524
-
(1977)
Nature
, vol.270
, pp. 725-727
-
-
Yaffe, D.1
Saxel, O.2
-
50
-
-
36348958434
-
Transgenic overexpression of ADAM12 suppresses muscle regeneration and aggravates dystrophy in aged mdx mice
-
PMID: 17982130
-
Jorgensen LH, Jensen CH, Wewer UM, Schroder HD (2007) Transgenic overexpression of ADAM12 suppresses muscle regeneration and aggravates dystrophy in aged mdx mice. American Journal of Pathology 171: 1599-1607. PMID: 17982130
-
(2007)
American Journal of Pathology
, vol.171
, pp. 1599-1607
-
-
Jorgensen, L.H.1
Jensen, C.H.2
Wewer, U.M.3
Schroder, H.D.4
-
51
-
-
44949231424
-
Analyzing real-time PCR data by the comparative C(T) method
-
PMID: 18546601
-
Schmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3: 1101-1108. PMID: 18546601
-
(2008)
Nat Protoc
, vol.3
, pp. 1101-1108
-
-
Schmittgen, T.D.1
Livak, K.J.2
-
52
-
-
34249044300
-
FHL3 binds MyoD and negatively regulates myotube formation
-
PMID: 17389685
-
Cottle DL, McGrath MJ, Cowling BS, Coghill ID, Brown S, et al. (2007) FHL3 binds MyoD and negatively regulates myotube formation. Journal of Cell Science 120: 1423-1435. PMID: 17389685
-
(2007)
Journal of Cell Science
, vol.120
, pp. 1423-1435
-
-
Cottle, D.L.1
McGrath, M.J.2
Cowling, B.S.3
Coghill, I.D.4
Brown, S.5
-
53
-
-
84880617578
-
Elucidation of target muscle and detailed development of dorsal motor neurons in chick embryo spinal cord
-
PMID: 23504940
-
Kobayashi N, Homma S, Okada T, Masuda T, Sato N, et al. (2013) Elucidation of target muscle and detailed development of dorsal motor neurons in chick embryo spinal cord. J Comp Neurol 521: 2987-3002. doi: 10.1002/cne.23326 PMID: 23504940
-
(2013)
J Comp Neurol
, vol.521
, pp. 2987-3002
-
-
Kobayashi, N.1
Homma, S.2
Okada, T.3
Masuda, T.4
Sato, N.5
-
54
-
-
0037764082
-
Class III beta-tubulin in human development and cancer
-
PMID: 12740870
-
Katsetos CD, Herman MM, Mork SJ (2003) Class III beta-tubulin in human development and cancer. Cell Motil Cytoskeleton 55: 77-96. PMID: 12740870
-
(2003)
Cell Motil Cytoskeleton
, vol.55
, pp. 77-96
-
-
Katsetos, C.D.1
Herman, M.M.2
Mork, S.J.3
-
56
-
-
84892454097
-
Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy
-
PMID: 24087791
-
D'Arcy CE, Feeney SJ, McLean CA, Gehrig SM, Lynch GS, et al. (2014) Identification of FHL1 as a therapeutic target for Duchenne muscular dystrophy. Human Molecular Genetics 23: 618-636. doi: 10. 1093/hmg/ddt449 PMID: 24087791
-
(2014)
Human Molecular Genetics
, vol.23
, pp. 618-636
-
-
D'Arcy, C.E.1
Feeney, S.J.2
McLean, C.A.3
Gehrig, S.M.4
Lynch, G.S.5
-
57
-
-
21844436541
-
EID3 is a novel EID family member and an inhibitor of CBP-dependent co-activation
-
PMID: 15987788
-
Bavner A, Matthews J, Sanyal S, Gustafsson JA, Treuter E (2005) EID3 is a novel EID family member and an inhibitor of CBP-dependent co-activation. Nucleic Acids Research 33: 3561-3569. PMID: 15987788
-
(2005)
Nucleic Acids Research
, vol.33
, pp. 3561-3569
-
-
Bavner, A.1
Matthews, J.2
Sanyal, S.3
Gustafsson, J.A.4
Treuter, E.5
-
58
-
-
4444305799
-
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse
-
PMID: 15351425
-
Briguet A, Courdier-Fruh I, Foster M, Meier T, Magyar JP (2004) Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse. Neuromuscul Disord 14: 675-682. PMID: 15351425
-
(2004)
Neuromuscul Disord
, vol.14
, pp. 675-682
-
-
Briguet, A.1
Courdier-Fruh, I.2
Foster, M.3
Meier, T.4
Magyar, J.P.5
-
59
-
-
84885346693
-
Spatiotemporal patterns of Pax3, Pax6, and Pax7 expression in the developing brain of a urodele amphibian, Pleurodeles waltl
-
PMID: 23784810
-
Joven A, Morona R, Gonzalez A, Moreno N (2013) Spatiotemporal patterns of Pax3, Pax6, and Pax7 expression in the developing brain of a urodele amphibian, Pleurodeles waltl. J Comp Neurol 521: 3913-3953. doi: 10.1002/cne.23385 PMID: 23784810
-
(2013)
J Comp Neurol
, vol.521
, pp. 3913-3953
-
-
Joven, A.1
Morona, R.2
Gonzalez, A.3
Moreno, N.4
-
60
-
-
41849143809
-
In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy
-
PMID: 18317591
-
Bruusgaard JC, Gundersen K (2008) In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy. Journal of Clinical Investigation 118: 1450-1457. doi: 10.1172/JCI34022 PMID: 18317591
-
(2008)
Journal of Clinical Investigation
, vol.118
, pp. 1450-1457
-
-
Bruusgaard, J.C.1
Gundersen, K.2
-
61
-
-
77957921360
-
Astroglial loss and edema formation in the rat piriform cortex and hippocampus following pilocarpine-induced status epilepticus
-
PMID: 20886625
-
Kim JE, Yeo SI, Ryu HJ, Kim MJ, Kim DS, et al. (2010) Astroglial loss and edema formation in the rat piriform cortex and hippocampus following pilocarpine-induced status epilepticus. J Comp Neurol 518: 4612-4628. doi: 10.1002/cne.22482 PMID: 20886625
-
(2010)
J Comp Neurol
, vol.518
, pp. 4612-4628
-
-
Kim, J.E.1
Yeo, S.I.2
Ryu, H.J.3
Kim, M.J.4
Kim, D.S.5
-
62
-
-
77649309210
-
Dynamics of muscle fibre growth during postnatal mouse development
-
PMID: 20175910
-
White RB, Bierinx AS, Gnocchi VF, Zammit PS (2010) Dynamics of muscle fibre growth during postnatal mouse development. Bmc Developmental Biology 10: 21. doi: 10.1186/1471-213X-10-21 PMID: 20175910
-
(2010)
Bmc Developmental Biology
, vol.10
, pp. 21
-
-
White, R.B.1
Bierinx, A.S.2
Gnocchi, V.F.3
Zammit, P.S.4
-
63
-
-
84859910158
-
Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
-
PMID: 22495301
-
Gehrig SM, van der Poel C, Sayer TA, Schertzer JD, Henstridge DC, et al. (2012) Hsp72 preserves muscle function and slows progression of severe muscular dystrophy. Nature 484: 394-398. doi: 10.1038/nature10980 PMID: 22495301
-
(2012)
Nature
, vol.484
, pp. 394-398
-
-
Gehrig, S.M.1
Van Der Poel, C.2
Sayer, T.A.3
Schertzer, J.D.4
Henstridge, D.C.5
-
64
-
-
84858800356
-
Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy
-
PMID: 22153988
-
Wang CH, Leung M, Liang WC, Hsieh TJ, Chen TH, et al. (2012) Correlation between muscle involvement, phenotype and D4Z4 fragment size in facioscapulohumeral muscular dystrophy. Neuromuscul Disord 22: 331-338. doi: 10.1016/j.nmd.2011.10.018 PMID: 22153988
-
(2012)
Neuromuscul Disord
, vol.22
, pp. 331-338
-
-
Wang, C.H.1
Leung, M.2
Liang, W.C.3
Hsieh, T.J.4
Chen, T.H.5
-
65
-
-
67149122523
-
Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies
-
PMID: 18808326
-
Wallace GQ, McNally EM (2009) Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies. Annu Rev Physiol 71: 37-57. doi: 10.1146/annurev.physiol.010908.163216 PMID: 18808326
-
(2009)
Annu Rev Physiol
, vol.71
, pp. 37-57
-
-
Wallace, G.Q.1
McNally, E.M.2
-
66
-
-
79956137778
-
Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1
-
PMID: 21603621
-
Chen SC, Frett E, Marx J, Bosnakovski D, Reed X, et al. (2011) Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1. Plos One 6: e19780. doi: 10.1371/journal.pone.0019780 PMID: 21603621
-
(2011)
Plos One
, vol.6
, pp. e19780
-
-
Chen, S.C.1
Frett, E.2
Marx, J.3
Bosnakovski, D.4
Reed, X.5
-
67
-
-
0027476102
-
Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice
-
PMID: 7678010
-
Brennan KJ, Hardeman EC (1993) Quantitative analysis of the human alpha-skeletal actin gene in transgenic mice. Journal of Biological Chemistry 268: 719-725. PMID: 7678010
-
(1993)
Journal of Biological Chemistry
, vol.268
, pp. 719-725
-
-
Brennan, K.J.1
Hardeman, E.C.2
-
68
-
-
0033210772
-
Gene targeting restricted to mouse striated muscle lineage
-
PMID: 10481039
-
Miniou P, Tiziano D, Frugier T, Roblot N, Le Meur M, et al. (1999) Gene targeting restricted to mouse striated muscle lineage. Nucleic Acids Research 27: e27. PMID: 10481039
-
(1999)
Nucleic Acids Research
, vol.27
, pp. e27
-
-
Miniou, P.1
Tiziano, D.2
Frugier, T.3
Roblot, N.4
Le Meur, M.5
-
69
-
-
84876274371
-
Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration
-
PMID: 23582327
-
Heredia JE, Mukundan L, Chen FM, Mueller AA, Deo RC, et al. (2013) Type 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration. Cell 153: 376-388. doi: 10.1016/j.cell.2013.02.053 PMID: 23582327
-
(2013)
Cell
, vol.153
, pp. 376-388
-
-
Heredia, J.E.1
Mukundan, L.2
Chen, F.M.3
Mueller, A.A.4
Deo, R.C.5
-
70
-
-
0037726553
-
IL-4 acts as a myoblast recruitment factor during mammalian muscle growth
-
PMID: 12757709
-
Horsley V, Jansen KM, Mills ST, Pavlath GK (2003) IL-4 acts as a myoblast recruitment factor during mammalian muscle growth. Cell 113: 483-494. PMID: 12757709
-
(2003)
Cell
, vol.113
, pp. 483-494
-
-
Horsley, V.1
Jansen, K.M.2
Mills, S.T.3
Pavlath, G.K.4
-
71
-
-
77951700255
-
Regulatory interactions between muscle and the immune system during muscle regeneration
-
PMID: 20219869
-
Tidball JG, Villalta SA (2010) Regulatory interactions between muscle and the immune system during muscle regeneration. Am J Physiol Regul Integr Comp Physiol 298: R1173-1187. doi: 10.1152/ajpregu.00735.2009 PMID: 20219869
-
(2010)
Am J Physiol Regul Integr Comp Physiol
, vol.298
, pp. R1173-R1187
-
-
Tidball, J.G.1
Villalta, S.A.2
-
72
-
-
84861014560
-
Sphingosine-1-phosphate enhances satellite cell activation in dystrophic muscles through a S1PR2/STAT3 signaling pathway
-
PMID: 22606352
-
Loh KC, Leong WI, Carlson ME, Oskouian B, Kumar A, et al. (2012) Sphingosine-1-phosphate enhances satellite cell activation in dystrophic muscles through a S1PR2/STAT3 signaling pathway. Plos One 7: e37218. doi: 10.1371/journal.pone.0037218 PMID: 22606352
-
(2012)
Plos One
, vol.7
, pp. e37218
-
-
Loh, K.C.1
Leong, W.I.2
Carlson, M.E.3
Oskouian, B.4
Kumar, A.5
-
74
-
-
84880397926
-
Myomaker is a membrane activator of myoblast fusion and muscle formation
-
PMID: 23868259
-
Millay DP, O'Rourke JR, Sutherland LB, Bezprozvannaya S, Shelton JM, et al. (2013) Myomaker is a membrane activator of myoblast fusion and muscle formation. Nature 499: 301-305. doi: 10.1038/nature12343 PMID: 23868259
-
(2013)
Nature
, vol.499
, pp. 301-305
-
-
Millay, D.P.1
O'Rourke, J.R.2
Sutherland, L.B.3
Bezprozvannaya, S.4
Shelton, J.M.5
-
75
-
-
84893019463
-
Galphai2 signaling is required for skeletal muscle growth, regeneration, and satellite cell proliferation and differentiation
-
PMID: 24298018
-
Minetti GC, Feige JN, Bombard F, Heier A, Morvan F, et al. (2014) Galphai2 signaling is required for skeletal muscle growth, regeneration, and satellite cell proliferation and differentiation. Molecular and Cellular Biology 34: 619-630. doi: 10.1128/MCB.00957-13 PMID: 24298018
-
(2014)
Molecular and Cellular Biology
, vol.34
, pp. 619-630
-
-
Minetti, G.C.1
Feige, J.N.2
Bombard, F.3
Heier, A.4
Morvan, F.5
-
76
-
-
84903469617
-
Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma
-
PMID: 24927541
-
Fu W, Asp P, Canter B, Dynlacht BD (2014) Primary cilia control hedgehog signaling during muscle differentiation and are deregulated in rhabdomyosarcoma. Proc Natl Acad Sci U S A 111: 9151-9156. doi: 10.1073/pnas.1323265111 PMID: 24927541
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, pp. 9151-9156
-
-
Fu, W.1
Asp, P.2
Canter, B.3
Dynlacht, B.D.4
-
77
-
-
84879864816
-
Brain and muscle Arnt-like 1 is a key regulator of myogenesis
-
PMID: 23525013
-
Chatterjee S, Nam D, Guo B, Kim JM, Winnier GE, et al. (2013) Brain and muscle Arnt-like 1 is a key regulator of myogenesis. Journal of Cell Science 126: 2213-2224. doi: 10.1242/jcs.120519 PMID: 23525013
-
(2013)
Journal of Cell Science
, vol.126
, pp. 2213-2224
-
-
Chatterjee, S.1
Nam, D.2
Guo, B.3
Kim, J.M.4
Winnier, G.E.5
-
78
-
-
85027917443
-
Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts
-
PMID: 21502976
-
Ge X, McFarlane C, Vajjala A, Lokireddy S, Ng ZH, et al. (2011) Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts. Cell Res 21: 1591-1604. doi: 10.1038/cr.2011.72 PMID: 21502976
-
(2011)
Cell Res
, vol.21
, pp. 1591-1604
-
-
Ge, X.1
McFarlane, C.2
Vajjala, A.3
Lokireddy, S.4
Ng, Z.H.5
-
79
-
-
0038273864
-
Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle
-
PMID: 12743106
-
Nicole S, Desforges B, Millet G, Lesbordes J, Cifuentes-Diaz C, et al. (2003) Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle. Journal of Cell Biology 161: 571-582. PMID: 12743106
-
(2003)
Journal of Cell Biology
, vol.161
, pp. 571-582
-
-
Nicole, S.1
Desforges, B.2
Millet, G.3
Lesbordes, J.4
Cifuentes-Diaz, C.5
-
80
-
-
37149022054
-
Muscle-specific overexpression of the type 1 IGF receptor results in myoblast-independent muscle hypertrophy via PI3K, and not calcineurin, signaling
-
PMID: 17940216
-
Quinn LS, Anderson BG, Plymate SR (2007) Muscle-specific overexpression of the type 1 IGF receptor results in myoblast-independent muscle hypertrophy via PI3K, and not calcineurin, signaling. Am J Physiol Endocrinol Metab 293: E1538-1551. PMID: 17940216
-
(2007)
Am J Physiol Endocrinol Metab
, vol.293
, pp. E1538-E1551
-
-
Quinn, L.S.1
Anderson, B.G.2
Plymate, S.R.3
-
81
-
-
84855306505
-
Down-Regulation of Myogenin Can Reverse Terminal Muscle Cell Differentiation
-
PMID: 23349657
-
Mastroyiannopoulos NP, Nicolaou P, Anayasa M, Uney JB, Phylactou LA (2012) Down-Regulation of Myogenin Can Reverse Terminal Muscle Cell Differentiation. Plos One 7. doi: 10.1371/journal.pone.0051204 PMID: 23349657
-
(2012)
Plos One
, vol.7
-
-
Mastroyiannopoulos, N.P.1
Nicolaou, P.2
Anayasa, M.3
Uney, J.B.4
Phylactou, L.A.5
-
82
-
-
0038236734
-
Calcineurin is a potent regulator for skeletal muscle regeneration by association with NFATc1 and GATA-2
-
PMID: 12557015
-
Sakuma K, Nishikawa J, Nakao R, Watanabe K, Totsuka T, et al. (2003) Calcineurin is a potent regulator for skeletal muscle regeneration by association with NFATc1 and GATA-2. Acta Neuropathologica 105: 271-280. PMID: 12557015
-
(2003)
Acta Neuropathologica
, vol.105
, pp. 271-280
-
-
Sakuma, K.1
Nishikawa, J.2
Nakao, R.3
Watanabe, K.4
Totsuka, T.5
-
83
-
-
78650972892
-
Calcineurin-NFAT signaling critically regulates early lineage specification in mouse embryonic stem cells and embryos
-
PMID: 21211781
-
Li X, Zhu L, Yang A, Lin J, Tang F, et al. (2011) Calcineurin-NFAT signaling critically regulates early lineage specification in mouse embryonic stem cells and embryos. Cell Stem Cell 8: 46-58. doi: 10.1016/j.stem.2010.11.027 PMID: 21211781
-
(2011)
Cell Stem Cell
, vol.8
, pp. 46-58
-
-
Li, X.1
Zhu, L.2
Yang, A.3
Lin, J.4
Tang, F.5
-
84
-
-
0037073786
-
Requirement of nuclear factor of activated T-cells in calcineurin-mediated cardiomyocyte hypertrophy
-
PMID: 12226086
-
van Rooij E, Doevendans PA, de Theije CC, Babiker FA, Molkentin JD, et al. (2002) Requirement of nuclear factor of activated T-cells in calcineurin-mediated cardiomyocyte hypertrophy. Journal of Biological Chemistry 277: 48617-48626. PMID: 12226086
-
(2002)
Journal of Biological Chemistry
, vol.277
, pp. 48617-48626
-
-
Van Rooij, E.1
Doevendans, P.A.2
De Theije, C.C.3
Babiker, F.A.4
Molkentin, J.D.5
-
85
-
-
0035897418
-
Regulation of the growth of multinucleated muscle cells by an NFATC2-dependent pathway
-
PMID: 11309414
-
Horsley V, Friday BB, Matteson S, Kegley KM, Gephart J, et al. (2001) Regulation of the growth of multinucleated muscle cells by an NFATC2-dependent pathway. Journal of Cell Biology 153: 329-338. PMID: 11309414
-
(2001)
Journal of Cell Biology
, vol.153
, pp. 329-338
-
-
Horsley, V.1
Friday, B.B.2
Matteson, S.3
Kegley, K.M.4
Gephart, J.5
-
86
-
-
2342640319
-
Cell fusion in skeletal muscle - Central role of NFATC2 in regulating muscle cell size
-
PMID: 12963831
-
Pavlath GK, Horsley V (2003) Cell fusion in skeletal muscle - central role of NFATC2 in regulating muscle cell size. Cell Cycle 2: 420-423. PMID: 12963831
-
(2003)
Cell Cycle
, vol.2
, pp. 420-423
-
-
Pavlath, G.K.1
Horsley, V.2
-
87
-
-
84877775057
-
Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion
-
PMID: 23615608
-
Hochreiter-Hufford AE, Lee CS, Kinchen JM, Sokolowski JD, Arandjelovic S, et al. (2013) Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion. Nature 497: 263-267. doi: 10.1038/nature12135 PMID: 23615608
-
(2013)
Nature
, vol.497
, pp. 263-267
-
-
Hochreiter-Hufford, A.E.1
Lee, C.S.2
Kinchen, J.M.3
Sokolowski, J.D.4
Arandjelovic, S.5
-
88
-
-
79551686645
-
Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein
-
PMID: 20970242
-
Hanel ML, Sun CYJ, Jones TI, Long SW, Zanotti S, et al. (2011) Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein. Differentiation 81: 107-118. doi: 10.1016/j.diff.2010.09.185 PMID: 20970242
-
(2011)
Differentiation
, vol.81
, pp. 107-118
-
-
Hanel, M.L.1
Sun, C.Y.J.2
Jones, T.I.3
Long, S.W.4
Zanotti, S.5
-
89
-
-
84892576144
-
Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)
-
PMID: 24305066
-
Sancisi V, Germinario E, Esposito A, Morini E, Peron S, et al. (2014) Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1). Am J Physiol Regul Integr Comp Physiol 306: R124-137. doi: 10.1152/ajpregu.00379.2013 PMID: 24305066
-
(2014)
Am J Physiol Regul Integr Comp Physiol
, vol.306
, pp. R124-R137
-
-
Sancisi, V.1
Germinario, E.2
Esposito, A.3
Morini, E.4
Peron, S.5
-
90
-
-
84862212313
-
Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response
-
PMID: 22560623
-
Cohen TV, Cohen JE, Partridge TA (2012) Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response. Neuromuscular Disorders 22: 648-658. doi: 10.1016/j.nmd.2012.03.002 PMID: 22560623
-
(2012)
Neuromuscular Disorders
, vol.22
, pp. 648-658
-
-
Cohen, T.V.1
Cohen, J.E.2
Partridge, T.A.3
-
91
-
-
84900796161
-
FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation
-
PMID: 24634512
-
Wilding BR, McGrath MJ, Bonne G, Mitchell CA (2014) FHL1 mutants that cause clinically distinct human myopathies form protein aggregates and impair myoblast differentiation. Journal of Cell Science 127: 2269-2281. doi: 10.1242/jcs.140905 PMID: 24634512
-
(2014)
Journal of Cell Science
, vol.127
, pp. 2269-2281
-
-
Wilding, B.R.1
McGrath, M.J.2
Bonne, G.3
Mitchell, C.A.4
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