-
1
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
Hewitt, J. E., Lyle, R., Clark, L. N., Valleley, E. M., Wright, T. J., Wijmenga, C. et al. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum. Mol. Genet. 3, 1287-1295 (1994).
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
Wijmenga, C.6
-
2
-
-
2642534599
-
Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients
-
Matsumura, T., Goto, K., Yamanaka, G., Lee, J., Zhang, C., Hayashi, Y. K. et al. Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients. BMC Neurol. 2, 7 (2002).
-
(2002)
BMC Neurol.
, vol.2
, pp. 7
-
-
Matsumura, T.1
Goto, K.2
Yamanaka, G.3
Lee, J.4
Zhang, C.5
Hayashi, Y.K.6
-
3
-
-
77649231841
-
Worldwide population analysis of the 4q and 10q subtelomeres Identifies only four discrete interchromosomal sequence transfers in human evolution
-
Lemmers, R. J., van der Vliet, P. J., van der Gaag, K. J., Zuniga, S., Frants, R. R., de Knijff, P. et al. Worldwide population analysis of the 4q and 10q subtelomeres Identifies only four discrete interchromosomal sequence transfers in human evolution. Am. J. Hum. Genet. 86, 364-377 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 364-377
-
-
Lemmers, R.J.1
Der Vliet, P.J.2
Der Gaag, K.J.3
Zuniga, S.4
Frants, R.R.5
De Knijff, P.6
-
4
-
-
34447104322
-
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein
-
Kowaljow, V., Marcowycz, A., Ansseau, E., Conde, C. B., Sauvage, S., Matteotti, C. et al. The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein. Neuromuscul. Disord. 17, 611-623 (2007).
-
(2007)
Neuromuscul. Disord.
, vol.17
, pp. 611-623
-
-
Kowaljow, V.1
Marcowycz, A.2
Ansseau, E.3
Conde, C.B.4
Sauvage, S.5
Matteotti, C.6
-
5
-
-
77957327192
-
A unifying genetic model for facioscapulohumeral muscular dystrophy
-
Lemmers, R. J., van der Vliet, P. J., Klooster, R., Sacconi, S., Camano, P., Dauwerse, J. G. et al. A unifying genetic model for facioscapulohumeral muscular dystrophy. Science 329, 1650-1653 (2010).
-
(2010)
Science
, vol.329
, pp. 1650-1653
-
-
Lemmers, R.J.1
Der Vliet, P.J.2
Klooster, R.3
Sacconi, S.4
Camano, P.5
Dauwerse, J.G.6
-
6
-
-
78449250235
-
Facioscapulohumeral dystrophy: Incomplete suppression of a retrotransposed gene
-
Snider, L., Geng, L. N., Lemmers, R. J., Kyba, M., Ware, C. B., Nelson, A. M. et al. Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene. PLoS Genet. 6, e1001181 (2010).
-
(2010)
PLoS Genet.
, vol.6
-
-
Snider, L.1
Geng, L.N.2
Lemmers, R.J.3
Kyba, M.4
Ware, C.B.5
Nelson, A.M.6
-
7
-
-
53049110907
-
Facioscapulohumeral muscular dystrophy
-
Tawil, R. Facioscapulohumeral muscular dystrophy. Neurotherapeutics 5, 601-606 (2008).
-
(2008)
Neurotherapeutics
, vol.5
, pp. 601-606
-
-
Tawil, R.1
-
8
-
-
84859505154
-
Facioscapulohumeral muscular dystrophy: New insights from compound heterozygotes and implication for prenatal genetic counselling
-
Scionti, I., Fabbri, G., Fiorillo, C., Ricci, G., Greco, F., D'Amico, R. et al. Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling. J. Med. Genet. (2011).
-
(2011)
J. Med. Genet.
-
-
Scionti, I.1
Fabbri, G.2
Fiorillo, C.3
Ricci, G.4
Greco, F.5
D'Amico, R.6
-
9
-
-
13844278432
-
Molecular diagnosis of FSHD
-
Upadhyaya, M. & Cooper, D. N. eds, BIOS Scientific Publishers, New York, NY
-
Lemmers, R. J. L. F., van der Wielen, M., Bakker, E. & van der Maarel, S. Molecular diagnosis of FSHD. in FSHD Facioscapulohumeral Muscular Dystrophy: Clinical Medicine and Molecular Cell Biology. Upadhyaya, M. & Cooper, D. N. (eds) 211-234 (BIOS Scientific Publishers, New York, NY, 2004).
-
(2004)
FSHD Facioscapulohumeral Muscular Dystrophy: Clinical Medicine and Molecular Cell Biology.
, pp. 211-234
-
-
Lemmers, R.J.L.F.1
Der Wielen, M.2
Bakker, E.3
Der Maarel, S.4
-
10
-
-
33645971656
-
Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy
-
Goto, K., Nishino, I. & Hayashi, Y. K. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy. Neuromuscul. Disord. 16, 256-261 (2006).
-
(2006)
Neuromuscul. Disord.
, vol.16
, pp. 256-261
-
-
Goto, K.1
Nishino, I.2
Hayashi, Y.K.3
-
11
-
-
84855370315
-
Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy
-
Nguyen, K., Walrafen, P., Bernard, R., Attarian, S., Chaix, C., Vovan, C. et al. Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy. Ann. Neurol. 70, 627-633 (2011).
-
(2011)
Ann. Neurol.
, vol.70
, pp. 627-633
-
-
Nguyen, K.1
Walrafen, P.2
Bernard, R.3
Attarian, S.4
Chaix, C.5
Vovan, C.6
-
12
-
-
79952736706
-
Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt?
-
Fitzsimons, R. B. Retinal vascular disease and the pathogenesis of facioscapulohumeral muscular dystrophy. A signalling message from Wnt? Neuromuscul. Disord. 21, 263-271 (2011).
-
(2011)
Neuromuscul. Disord.
, vol.21
, pp. 263-271
-
-
Fitzsimons, R.B.1
-
13
-
-
0029017568
-
DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: Clinical correlations
-
Goto, K., Lee, J. H., Matsuda, C., Hirabayashi, K., Kojo, T., Nakamura, A. et al. DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations. Neuromuscul. Disord. 5, 201-208 (1995).
-
(1995)
Neuromuscul. Disord.
, vol.5
, pp. 201-208
-
-
Goto, K.1
Lee, J.H.2
Matsuda, C.3
Hirabayashi, K.4
Kojo, T.5
Nakamura, A.6
-
14
-
-
8644275568
-
A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment
-
Dorobek, M. & Kabzinska, D. A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment. Eur. J. Paediatr. Neurol. 8, 313-316 (2004).
-
(2004)
Eur. J. Paediatr. Neurol.
, vol.8
, pp. 313-316
-
-
Dorobek, M.1
Kabzinska, D.2
-
15
-
-
59149092904
-
Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: A case study
-
Tsuji, M., Kinoshita, M., Imai, Y., Kawamoto, M. & Kohara, N. Facioscapulohumeral muscular dystrophy presenting with hypertrophic cardiomyopathy: a case study. Neuromuscul. Disord. 19, 140-142 (2009).
-
(2009)
Neuromuscul. Disord.
, vol.19
, pp. 140-142
-
-
Tsuji, M.1
Kinoshita, M.2
Imai, Y.3
Kawamoto, M.4
Kohara, N.5
-
16
-
-
3242666915
-
Ventilatory support in facioscapulohumeral muscular dystrophy
-
Wohlgemuth, M., van der Kooi, E. L., van Kesteren, R. G., van der Maarel, S. M. & Padberg, G. W. Ventilatory support in facioscapulohumeral muscular dystrophy. Neurology 63, 176-178 (2004).
-
(2004)
Neurology
, vol.63
, pp. 176-178
-
-
Wohlgemuth, M.1
Der Kooi, E.L.2
Kesteren, R.G.3
Der Maarel, S.M.4
Padberg, G.W.5
-
17
-
-
12544250255
-
Ventilatory support in facioscapulohumeral muscular dystrophy
-
Carter, G. T. & Bird, T. D. Ventilatory support in facioscapulohumeral muscular dystrophy. Neurology 64, 401 (2005).
-
(2005)
Neurology
, vol.64
, pp. 401
-
-
Carter, G.T.1
Bird, T.D.2
-
18
-
-
0034069726
-
An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy
-
Saito, A., Higuchi, I., Nakagawa, M., Saito, M., Uchida, Y., Inose, M. et al. An overexpression of fibroblast growth factor (FGF) and FGF receptor 4 in a severe clinical phenotype of facioscapulohumeral muscular dystrophy. Muscle Nerve 23, 490-497 (2000).
-
(2000)
Muscle Nerve
, vol.23
, pp. 490-497
-
-
Saito, A.1
Higuchi, I.2
Nakagawa, M.3
Saito, M.4
Uchida, Y.5
Inose, M.6
-
19
-
-
33846004205
-
Cochlear function in facioscapulohumeral muscular dystrophy
-
Balatsouras, D. G., Korres, S., Manta, P., Panousopoulou, A. & Vassilopoulos, D. Cochlear function in facioscapulohumeral muscular dystrophy. Otol. Neurotol. 28, 7-10 (2007).
-
(2007)
Otol. Neurotol.
, vol.28
, pp. 7-10
-
-
Balatsouras, D.G.1
Korres, S.2
Manta, P.3
Panousopoulou, A.4
Vassilopoulos, D.5
-
20
-
-
0022996407
-
Facioscapulohumeral dystrophy associated with mental retardation, hearing loss, and tortuosity of retinal arterioles
-
Matsuzaka, T., Sakuragawa, N., Terasawa, K. & Kuwabara, H. Facioscapulohumeral dystrophy associated with mental retardation, hearing loss, and tortuosity of retinal arterioles. J. Child Neurol. 1, 218-223 (1986).
-
(1986)
J. Child Neurol.
, vol.1
, pp. 218-223
-
-
Matsuzaka, T.1
Sakuragawa, N.2
Terasawa, K.3
Kuwabara, H.4
-
21
-
-
3042576275
-
Exploring hypotheses about the molecular etiology of FSHD: Loss of heterochromatin spreading and other long-range interaction models
-
Cooper, D. N. & Upadhyaya, M. eds, BIOS Scientific Pub, New York, NY
-
Ehrlich, M. Exploring hypotheses about the molecular etiology of FSHD: loss of heterochromatin spreading and other long-range interaction models. in FSHD Facioscapulohumeral Muscular Dystrophy: Molecular Cell Biology & Clinical Medicine. Cooper, D. N. & Upadhyaya, M. (eds) 253-276 (BIOS Scientific Pub, New York, NY, 2004).
-
(2004)
FSHD Facioscapulohumeral Muscular Dystrophy: Molecular Cell Biology & Clinical Medicine
, pp. 253-276
-
-
Ehrlich, M.1
-
22
-
-
33846315519
-
Facioscapulohumeral muscular dystrophy
-
van der Maarel, S. M., Frants, R. R. & Padberg, G. W. Facioscapulohumeral muscular dystrophy. Biochim. Biophys. Acta 1772, 186-194 (2007).
-
(2007)
Biochim. Biophys. Acta
, vol.1772
, pp. 186-194
-
-
Van Der Maarel, S.M.1
Frants, R.R.2
Padberg, G.W.3
-
23
-
-
33846433695
-
RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA
-
Alexiadis, V., Ballestas, M. E., Sanchez, C., Winokur, S., Vedanarayanan, V., Warren, M. et al. RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA. Biochem. Biophys. Acta (1769) 29-40, 2007.
-
(1769)
Biochem. Biophys. Acta
, vol.29-40
, pp. 2007
-
-
Alexiadis, V.1
Ballestas, M.E.2
Sanchez, C.3
Winokur, S.4
Vedanarayanan, V.5
Warren, M.6
-
24
-
-
0037047439
-
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
Gabellini, D., Green, M. R. & Tupler, R. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110, 339-348 (2002).
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
25
-
-
0345227304
-
Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q
-
Jiang, G., Yang, F., van Overveld, P. G., Vedanarayanan, V., van der Maarel, S. & Ehrlich, M. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Hum. Mol. Genet. 12, 2909-2921 (2003).
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2909-2921
-
-
Jiang, G.1
Yang, F.2
Overveld, P.G.3
Vedanarayanan, V.4
Der Maarel, S.5
Ehrlich, M.6
-
26
-
-
0344436078
-
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3kb element
-
Gabriels, J., Beckers, M. C., Ding, H., De Vriese, A., Plaisance, S., van der Maarel, S. M. et al. Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3kb element. Gene 236, 25-32 (1999).
-
(1999)
Gene
, vol.236
, pp. 25-32
-
-
Gabriels, J.1
Beckers, M.C.2
Ding, H.3
De Vriese, A.4
Plaisance, S.5
Der Maarel, S.M.6
-
27
-
-
36749026295
-
DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1
-
Dixit, M., Ansseau, E., Tassin, A., Winokur, S., Shi, R., Qian, H. et al. DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1. Proc. Natl Acad. Sci. USA 104, 18157-18162 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 18157-18162
-
-
Dixit, M.1
Ansseau, E.2
Tassin, A.3
Winokur, S.4
Shi, R.5
Qian, H.6
-
28
-
-
53949112045
-
DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation
-
Bosnakovski, D., Lamb, S., Simsek, T., Xu, Z., Belayew, A., Perlingeiro, R. et al. DUX4c, an FSHD candidate gene, interferes with myogenic regulators and abolishes myoblast differentiation. Exp. Neurol. 214, 87-96 (2008).
-
(2008)
Exp. Neurol.
, vol.214
, pp. 87-96
-
-
Bosnakovski, D.1
Lamb, S.2
Simsek, T.3
Xu, Z.4
Belayew, A.5
Perlingeiro, R.6
-
29
-
-
67650314502
-
Region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy
-
Wuebbles, R. D., Hanel, M. L. & Jones, P. L. F. S. H. D. region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy. Dis. Model Mech. 2, 267-274 (2009).
-
(2009)
Dis. Model Mech.
, vol.2
, pp. 267-274
-
-
Wuebbles, R.D.1
Hanel, M.L.2
Jones, P.L.F.S.H.D.3
-
30
-
-
70450275779
-
Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level
-
Klooster, R., Straasheijm, K., Shah, B., Sowden, J., Frants, R., Thornton, C. et al. Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level. Eur. J Hum. Genet. 17, 1615-1624 (2009).
-
(2009)
Eur. J Hum. Genet.
, vol.17
, pp. 1615-1624
-
-
Klooster, R.1
Straasheijm, K.2
Shah, B.3
Sowden, J.4
Frants, R.5
Thornton, C.6
-
31
-
-
0344875044
-
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation
-
Winokur, S. T., Chen, Y. W., Masny, P. S., Martin, J. H., Ehmsen, J. T., Tapscott, S. J. et al. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum. Mol. Genet. 12, 2895-2907 (2003).
-
(2003)
Hum. Mol. Genet.
, 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
Tapscott, S.J.6
-
32
-
-
33847234593
-
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
-
Osborne, R. J., Welle, S., Venance, S. L., Thornton, C. A. & Tawil, R. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 68, 569-577 (2007).
-
(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
-
33
-
-
35348907287
-
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy
-
Lemmers, R. J., Wohlgemuth, M., van der Gaag, K. J., van der Vliet, P. J., van Teijlingen, C. M., de Knijff, P. et al. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy. Am. J. Hum. Genet. 81, 884-894 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 884-894
-
-
Lemmers, R.J.1
Wohlgemuth, M.2
Der Gaag, K.J.3
Der Vliet, P.J.4
Teijlingen, C.M.5
De Knijff, P.6
-
34
-
-
78149342810
-
FSH dystrophy and a subtelomeric 4q haplotype: A new assay and associations with disease
-
Tsumagari, K., Chen, D., Hackman, J. R., Bossler, A. D. & Ehrlich, M. FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease. J Med. Genet. 47, 745-751 (2010).
-
(2010)
J Med. Genet.
, vol.47
, pp. 745-751
-
-
Tsumagari, K.1
Chen, D.2
Hackman, J.R.3
Bossler, A.D.4
Ehrlich, M.5
-
35
-
-
78149354416
-
Confirmation that the specific SSLP microsatellite allele 4qA161 segregates with fascioscapulohumeral muscular dystrophy (FSHD) in a cohort of multiplex and simplex FSHD families
-
Spurlock, G., Jim, H. P. & Upadhyaya, M. Confirmation that the specific SSLP microsatellite allele 4qA161 segregates with fascioscapulohumeral muscular dystrophy (FSHD) in a cohort of multiplex and simplex FSHD families. Muscle Nerve 42, 820-821 (2010).
-
(2010)
Muscle Nerve
, vol.42
, pp. 820-821
-
-
Spurlock, G.1
Jim, H.P.2
Upadhyaya, M.3
-
36
-
-
78649330207
-
A family history of DUX4: Phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene
-
Leidenroth, A. & Hewitt, J. E. A family history of DUX4: phylogenetic analysis of DUXA, B, C and Duxbl reveals the ancestral DUX gene. BMC Evol. Biol. 10, 364 (2010).
-
(2010)
BMC Evol. Biol.
, vol.10
, pp. 364
-
-
Leidenroth, A.1
Hewitt, J.E.2
-
37
-
-
0030009384
-
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
-
Tupler, R., Berardinelli, A., Barbierato, L., Frants, R., Hewitt, J. E., Lanzi, G. et al. Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy. J. Med. Genet. 33, 366-370 (1996).
-
(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
Lanzi, G.6
-
38
-
-
75649084888
-
DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2
-
Xu, X., Tsumagari, K., Sowden, J., Tawil, R., Boyle, A. P., Song, L. et al. DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2. Nucleic Acids Res. 37, 7381-7393 (2009).
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. 7381-7393
-
-
Xu, X.1
Tsumagari, K.2
Sowden, J.3
Tawil, R.4
Boyle, A.P.5
Song, L.6
-
39
-
-
70450222400
-
Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD
-
de Greef, J. C., Lemmers, R. J., van Engelen, B. G., Sacconi, S., Venance, S. L., Frants, R. R. et al. Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD. Hum. Mutat. 30, 1-11 (2009).
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1-11
-
-
De Greef, J.C.1
Lemmers, R.J.2
Engelen, B.G.3
Sacconi, S.4
Venance, S.L.5
Frants, R.R.6
-
40
-
-
1642487857
-
FSHDlike patients without 4q35 deletion
-
Yamanaka, G., Goto, K., Ishihara, T., Oya, Y., Miyajima, T., Hoshika, A. et al. FSHDlike patients without 4q35 deletion. J Neurol. Sci. 219, 89-93 (2004).
-
(2004)
J Neurol. Sci.
, vol.219
, pp. 89-93
-
-
Yamanaka, G.1
Goto, K.2
Ishihara, T.3
Oya, Y.4
Miyajima, T.5
Hoshika, A.6
-
41
-
-
84865255518
-
Diagnosis by sequencing: Correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis
-
Leidenroth, A., Sorte, H. S., Gilfillan, G., Ehrlich, M., Lyle, R. & Hewitt, J. E. Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis. Eur. J Hum. Genet. 20, 999-1003 (2012).
-
(2012)
Eur. J Hum. Genet.
, vol.20
, pp. 999-1003
-
-
Leidenroth, A.1
Sorte, H.S.2
Gilfillan, G.3
Ehrlich, M.4
Lyle, R.5
Hewitt, J.E.6
-
42
-
-
67249104052
-
RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: New candidates for the pathophysiology of facioscapulohumeral dystrophy
-
Snider, L., Asawachaicharn, A., Tyler, A. E., Geng, L. N., Petek, L. M., Maves, L. et al. RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy. Hum. Mol. Genet. 18, 2414-2430 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2414-2430
-
-
Snider, L.1
Asawachaicharn, A.2
Tyler, A.E.3
Geng, L.N.4
Petek, L.M.5
Maves, L.6
-
44
-
-
79251580715
-
HP1 recruits activity-dependent neuroprotective protein to H3K9me3 marked pericentromeric heterochromatin for silencing of major satellite repeats
-
Mosch, K., Franz, H., Soeroes, S., Singh, P. B. & Fischle, W. HP1 recruits activity-dependent neuroprotective protein to H3K9me3 marked pericentromeric heterochromatin for silencing of major satellite repeats. PLoS One 6, e15894 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Mosch, K.1
Franz, H.2
Soeroes, S.3
Singh, P.B.4
Fischle, W.5
-
45
-
-
70350215746
-
Loss of epigenetic silencing in tumors preferentially affects primate-specific retroelements
-
Szpakowski, S., Sun, X., Lage, J. M., Dyer, A., Rubinstein, J., Kowalski, D. et al. Loss of epigenetic silencing in tumors preferentially affects primate-specific retroelements. Gene 448, 151-167 (2009).
-
(2009)
Gene
, vol.448
, pp. 151-167
-
-
Szpakowski, S.1
Sun, X.2
Lage, J.M.3
Dyer, A.4
Rubinstein, J.5
Kowalski, D.6
-
46
-
-
68249088114
-
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD)
-
Zeng, W., de Greef, J. C., Chen, Y. Y., Chien, R., Kong, X., Gregson, H. C. et al. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD). PLoS Genet. 5, e1000559 (2009).
-
(2009)
PLoS Genet.
, vol.5
-
-
Zeng, W.1
De Greef, J.C.2
Chen, Y.Y.3
Chien, R.4
Kong, X.5
Gregson, H.C.6
-
47
-
-
0035201141
-
Hypermethylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cells but not in ICF syndrome cells
-
Tsien, F., Sun, B., Hopkins, N. E., Vedanarayanan, V., Figlewicz, D., Winokur, S. et al. Hypermethylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cells but not in ICF syndrome cells. Molec. Gen. Metab. 74, 322-331 (2001).
-
(2001)
Molec. Gen. Metab.
, vol.74
, pp. 322-331
-
-
Tsien, F.1
Sun, B.2
Hopkins, N.E.3
Vedanarayanan, V.4
Figlewicz, D.5
Winokur, S.6
-
48
-
-
34548392207
-
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD
-
de Greef, J. C., Wohlgemuth, M., Chan, O. A., Hansson, K. B., Smeets, D., Frants, R. R. et al. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD. Neurology 69, 1018-1026 (2007).
-
(2007)
Neurology
, vol.69
, pp. 1018-1026
-
-
De Greef, J.C.1
Wohlgemuth, M.2
Chan, O.A.3
Hansson, K.B.4
Smeets, D.5
Frants, R.R.6
-
49
-
-
0029113034
-
The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes
-
Lyle, R., Wright, T. J., Clark, L. N. & Hewitt, J. E. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes. Genomics 28, 389-397 (1995).
-
(1995)
Genomics
, vol.28
, pp. 389-397
-
-
Lyle, R.1
Wright, T.J.2
Clark, L.N.3
Hewitt, J.E.4
-
50
-
-
0029798271
-
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region
-
Winokur, S. T., Bengtsson, U., Vargas, J. C., Wasmuth, J. J., Altherr, M. R., Weiffenbach, B. et al. The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region. Hum. Mol. Genet. 5, 1567-1575 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1567-1575
-
-
Winokur, S.T.1
Bengtsson, U.2
Vargas, J.C.3
Wasmuth, J.J.4
Altherr, M.R.5
Weiffenbach, B.6
-
51
-
-
73949125304
-
Function and specificity of Hox genes
-
Foronda, D., de Navas, L. F., Garaulet, D. L. & Sanchez-Herrero, E. Function and specificity of Hox genes. Int. J. Dev. Biol. 53, 1404-1419 (2009).
-
(2009)
Int. J. Dev. Biol.
, vol.53
, pp. 1404-1419
-
-
Foronda, D.1
De Navas, L.F.2
Garaulet, D.L.3
Sanchez-Herrero, E.4
-
52
-
-
84859514536
-
Facioscapulohumeral muscular dystrophy (FSHD): An enigma unravelled?
-
Richards, M., Coppee, F., Thomas, N., Belayew, A. & Upadhyaya, M. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled? Hum. Genet. 131, 325-340 (2011).
-
(2011)
Hum. Genet.
, vol.131
, pp. 325-340
-
-
Richards, M.1
Coppee, F.2
Thomas, N.3
Belayew, A.4
Upadhyaya, M.5
-
53
-
-
80053349950
-
Gene expression during normal and FSHD myogenesis
-
Tsumagari, K., Chang, S.-C., Lacey, M., Baribault, C., Chittur, S. V., Sowden, J. et al. Gene expression during normal and FSHD myogenesis. BMC Med. Genomics 4, 67 (2011).
-
(2011)
BMC Med. Genomics
, vol.4
, pp. 67
-
-
Tsumagari, K.1
Chang, S.-C.2
Lacey, M.3
Baribault, C.4
Chittur, S.V.5
Sowden, J.6
-
54
-
-
1942534070
-
Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD)
-
Wood-Allum, C., Brennan, P., Hewitt, M., Lowe, J., Tyfield, L. & Wills, A. Clinical and histopathological heterogeneity in patients with 4q35 facioscapulohumeral muscular dystrophy (FSHD). Neuropathol. Appl. Neurobiol. 30, 188-191 (2004).
-
(2004)
Neuropathol. Appl. Neurobiol.
, vol.30
, pp. 188-191
-
-
Wood-Allum, C.1
Brennan, P.2
Hewitt, M.3
Lowe, J.4
Tyfield, L.5
Wills, A.6
-
55
-
-
32044454237
-
Sarcolemmal reorganization in facioscapulohumeral muscular dystrophy
-
Reed, P., Porter, N. C., Strong, J., Pumplin, D. W., Corse, A. M., Luther, P. W. et al. Sarcolemmal reorganization in facioscapulohumeral muscular dystrophy. Ann. Neurol. 59, 289-297 (2006).
-
(2006)
Ann. Neurol.
, vol.59
, pp. 289-297
-
-
Reed, P.1
Porter, N.C.2
Strong, J.3
Pumplin, D.W.4
Corse, A.M.5
Luther, P.W.6
-
56
-
-
78650239733
-
Impact of ageing on muscle cell regeneration
-
Carosio, S., Berardinelli, M. G., Aucello, M. & Musaro, A. Impact of ageing on muscle cell regeneration. Ageing Res. Rev. 10, 35-42 (2011).
-
(2011)
Ageing Res. Rev
, vol.10
, pp. 35-42
-
-
Carosio, S.1
Berardinelli, M.G.2
Aucello, M.3
Musaro, A.4
-
57
-
-
0347989458
-
Cellular and molecular regulation of muscle regeneration
-
Charge, S. B. & Rudnicki, M. A. Cellular and molecular regulation of muscle regeneration. Physiol. Rev. 84, 209-238 (2004).
-
(2004)
Physiol. Rev.
, vol.84
, pp. 209-238
-
-
Charge, S.B.1
Rudnicki, M.A.2
-
58
-
-
84857488690
-
The muscle satellite cell at 50: The formative years
-
Scharner, J. & Zammit, P. S. The muscle satellite cell at 50: the formative years. Skelet. Muscle 1, 28 (2011).
-
(2011)
Skelet. Muscle
, vol.1
, pp. 28
-
-
Scharner, J.1
Zammit, P.S.2
-
59
-
-
54349088194
-
An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies
-
Bosnakovski, D., Xu, Z., Gang, E. J., Galindo, C. L., Liu, M., Simsek, T. et al. An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies. EMBO J. 27, 2766-2779 (2008).
-
(2008)
EMBO J
, vol.27
, pp. 2766-2779
-
-
Bosnakovski, D.1
Xu, Z.2
Gang, E.J.3
Galindo, C.L.4
Liu, M.5
Simsek, T.6
-
60
-
-
84858334928
-
A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: Family, disease and cell function
-
Homma, S., Chen, J. C., Rahimov, F., Beermann, M. L., Hanger, K., Bibat, G. M. et al. A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function. Eur. J. Hum. Genet. 20, 204-210 (2011).
-
(2011)
Eur. J. Hum. Genet.
, vol.20
, pp. 204-210
-
-
Homma, S.1
Chen, J.C.2
Rahimov, F.3
Beermann, M.L.4
Hanger, K.5
Bibat, G.M.6
-
61
-
-
84855956147
-
DUX4 activates germline genes, retroelements, and immune mediators: Implications for facioscapulohumeral dystrophy
-
Geng, L. N., Yao, Z., Snider, L., Fong, A. P., Cech, J. N., Young, J. M. et al. DUX4 activates germline genes, retroelements, and immune mediators: Implications for facioscapulohumeral dystrophy. Dev. Cell 22, 38-51 (2012).
-
(2012)
Dev. Cell
, vol.22
, pp. 38-51
-
-
Geng, L.N.1
Yao, Z.2
Snider, L.3
Fong, A.P.4
Cech, J.N.5
Young, J.M.6
-
62
-
-
79953292473
-
DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo
-
Wallace, L. M., Garwick, S. E., Mei, W., Belayew, A., Coppee, F., Ladner, K. J. et al. DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo. Ann. Neurol. 69, 540-552 (2011).
-
(2011)
Ann. Neurol.
, vol.69
, pp. 540-552
-
-
Wallace, L.M.1
Garwick, S.E.2
Mei, W.3
Belayew, A.4
Coppee, F.5
Ladner, K.J.6
-
63
-
-
80055040201
-
The FSHD atrophic myotube phenotype is caused by DUX4 expression
-
Vanderplanck, C., Ansseau, E., Charron, S., Stricwant, N., Tassin, A., Laoudj-Chenivesse, D. et al. The FSHD atrophic myotube phenotype is caused by DUX4 expression. PLoS One 6, e26820 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Vanderplanck, C.1
Ansseau, E.2
Charron, S.3
Stricwant, N.4
Tassin, A.5
Laoudj-Chenivesse, D.6
-
64
-
-
38049041930
-
An in situ hybridization-based screen for heterogeneously expressed genes in mouse ES cells
-
Carter, M. G., Stagg, C. A., Falco, G., Yoshikawa, T., Bassey, U. C., Aiba, K. et al. An in situ hybridization-based screen for heterogeneously expressed genes in mouse ES cells. Gene. Expr. Patterns 8, 181-198 (2008).
-
(2008)
Gene. Expr. Patterns
, vol.8
, pp. 181-198
-
-
Carter, M.G.1
Stagg, C.A.2
Falco, G.3
Yoshikawa, T.4
Bassey, U.C.5
Aiba, K.6
-
65
-
-
77954150150
-
Hes1 regulates embryonic stem cell differentiation by suppressing Notch signaling
-
Kobayashi, T. & Kageyama, R. Hes1 regulates embryonic stem cell differentiation by suppressing Notch signaling. Genes Cells 15, 689-698 (2010).
-
(2010)
Genes Cells
, vol.15
, pp. 689-698
-
-
Kobayashi, T.1
Kageyama, R.2
-
66
-
-
80455131192
-
Oscillatory protein expression dynamics endows stem cells with robust differentiation potential
-
Suzuki, N., Furusawa, C. & Kaneko, K. Oscillatory protein expression dynamics endows stem cells with robust differentiation potential. PLoS One 6, e27232 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Suzuki, N.1
Furusawa, C.2
Kaneko, K.3
-
67
-
-
34347263069
-
Zscan4: A novel gene expressed exclusively in late 2-cell embryos and embryonic stem cells
-
Falco, G., Lee, S. L., Stanghellini, I., Bassey, U. C., Hamatani, T. & Ko, M. S. Zscan4: a novel gene expressed exclusively in late 2-cell embryos and embryonic stem cells. Dev. Biol. 307, 539-550 (2007).
-
(2007)
Dev. Biol.
, vol.307
, pp. 539-550
-
-
Falco, G.1
Lee, S.L.2
Stanghellini, I.3
Bassey, U.C.4
Hamatani, T.5
Ko, M.S.6
-
68
-
-
57449111124
-
Transcriptional heterogeneity in mouse embryonic stem cells
-
Tanaka, T. S. Transcriptional heterogeneity in mouse embryonic stem cells. Reprod. Fertil. Dev. 21, 67-75 (2009).
-
(2009)
Reprod. Fertil. Dev.
, vol.21
, pp. 67-75
-
-
Tanaka, T.S.1
-
69
-
-
0033607231
-
Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy
-
Tupler, R., Perini, G., Pellegrino, M. A. & Green, M. R. Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy. Proc. Natl Acad. Sci. USA 96, 12650-12654 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 12650-12654
-
-
Tupler, R.1
Perini, G.2
Pellegrino, M.A.3
Green, M.R.4
-
70
-
-
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
-
Celegato, B., Capitanio, D., Pescatori, M., Romualdi, C., Pacchioni, B., Cagnin, S. et al. 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 (2006).
-
(2006)
Proteomics
, vol.6
, pp. 5303-5321
-
-
Celegato, B.1
Capitanio, D.2
Pescatori, M.3
Romualdi, C.4
Pacchioni, B.5
Cagnin, S.6
-
71
-
-
65549085668
-
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers
-
Arashiro, P., Eisenberg, I., Kho, A. T., Cerqueira, A. M., Canovas, M., Silva, H. C. et al. Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers. Proc. Natl Acad. Sci. USA 106, 6220-6225 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 6220-6225
-
-
Arashiro, P.1
Eisenberg, I.2
Kho, A.T.3
Cerqueira, A.M.4
Canovas, M.5
Silva, H.C.6
-
72
-
-
79958759071
-
Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns
-
Cheli, S., Francois, S., Bodega, B., Ferrari, F., Tenedini, E., Roncaglia, E. et al. Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns. PLoS One 6, e20966 (2011).
-
(2011)
PLoS One
, vol.6
-
-
Cheli, S.1
Francois, S.2
Bodega, B.3
Ferrari, F.4
Tenedini, E.5
Roncaglia, E.6
-
73
-
-
0028094533
-
Facioscapulohumeral dystrophy: The role of inflammation
-
Fitzsimons, R. B. Facioscapulohumeral dystrophy: the role of inflammation. Lancet 344, 902-903 (1994).
-
(1994)
Lancet
, vol.344
, pp. 902-903
-
-
Fitzsimons, R.B.1
-
74
-
-
0028961960
-
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): Immunocytochemical and genetic analyses
-
Arahata, K., Ishihara, T., Fukunaga, H., Orimo, S., Lee, J. H., Goto, K. et al. Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses. Muscle Nerve 2, S56-S66 (1995).
-
(1995)
Muscle Nerve
, vol.2
-
-
Arahata, K.1
Ishihara, T.2
Fukunaga, H.3
Orimo, S.4
Lee, J.H.5
Goto, K.6
-
75
-
-
67349284686
-
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy
-
Kan, H. E., Scheenen, T. W., Wohlgemuth, M., Klomp, D. W., van Loosbroek-Wagenmans, I., Padberg, G. W. et al. Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy. Neuromuscul. Disord. 19, 357-362 (2009).
-
(2009)
Neuromuscul. Disord.
, vol.19
, pp. 357-362
-
-
Kan, H.E.1
Scheenen, T.W.2
Wohlgemuth, M.3
Klomp, D.W.4
Van Loosbroek-Wagenmans, I.5
Padberg, G.W.6
-
76
-
-
79959688961
-
CD8 (+) T Cells infacioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRI
-
Frisullo, G., Frusciante, R., Nociti, V., Tasca, G., Renna, R., Iorio, R. et al. CD8 (+) T Cells infacioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRI. J. Clin. Immunol. 31, 155-166 (2011).
-
(2011)
J. Clin. Immunol.
, vol.31
, pp. 155-166
-
-
Frisullo, G.1
Frusciante, R.2
Nociti, V.3
Tasca, G.4
Renna, R.5
Iorio, R.6
-
77
-
-
39049164607
-
Connective tissue growth factor is overexpressed in muscles of human muscular dystrophy
-
Sun, G., Haginoya, K., Wu, Y., Chiba, Y., Nakanishi, T., Onuma, A. et al. Connective tissue growth factor is overexpressed in muscles of human muscular dystrophy. J. Neurol. Sci. 267, 48-56 (2008).
-
(2008)
J. Neurol. Sci.
, vol.267
, pp. 48-56
-
-
Sun, G.1
Haginoya, K.2
Wu, Y.3
Chiba, Y.4
Nakanishi, T.5
Onuma, A.6
-
78
-
-
16844364725
-
Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle
-
Laoudj-Chenivesse, D., Carnac, G., Bisbal, C., Hugon, G., Bouillot, S., Desnuelle, C. et al. Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle. J. Mol. Med. 83, 216-224 (2005).
-
(2005)
J. Mol. Med
, vol.83
, pp. 216-224
-
-
Laoudj-Chenivesse, D.1
Carnac, G.2
Bisbal, C.3
Hugon, G.4
Bouillot, S.5
Desnuelle, C.6
-
79
-
-
84859771580
-
Zscan4 transiently reactivates early embryonic genes during the generation of induced pluripotent stem cells
-
Hirata, T., Amano, T., Nakatake, Y., Amano, M., Piao, Y., Hoang, H. G. et al. Zscan4 transiently reactivates early embryonic genes during the generation of induced pluripotent stem cells. Sci. Rep. 2, 208 (2012).
-
(2012)
Sci. Rep.
, vol.2
, pp. 208
-
-
Hirata, T.1
Amano, T.2
Nakatake, Y.3
Amano, M.4
Piao, Y.5
Hoang, H.G.6
-
80
-
-
84857120620
-
Cdx function is required for maintenance of intestinal identity in the adult
-
Hryniuk, A., Grainger, S., Savory, J. G. & Lohnes, D. Cdx function is required for maintenance of intestinal identity in the adult. Dev. Biol. 363, 426-437 (2012).
-
(2012)
Dev. Biol.
, vol.363
, pp. 426-437
-
-
Hryniuk, A.1
Grainger, S.2
Savory, J.G.3
Lohnes, D.4
-
81
-
-
79960421165
-
Excitation-transcription coupling in skeletal muscle: The molecular pathways of exercise
-
Gundersen, K. Excitation-transcription coupling in skeletal muscle: the molecular pathways of exercise. Biol. Rev. Camb. Philos. Soc. 86, 564-600 (2011).
-
(2011)
Biol. Rev. Camb. Philos. Soc.
, vol.86
, pp. 564-600
-
-
Gundersen, K.1
-
82
-
-
77956616754
-
Epigenetic control of Hox genes during neurogenesis, development, and disease
-
Barber, B. A. & Rastegar, M. Epigenetic control of Hox genes during neurogenesis, development, and disease. Ann. Anat. 192, 261-274 (2010).
-
(2010)
Ann. Anat.
, vol.192
, pp. 261-274
-
-
Barber, B.A.1
Rastegar, M.2
-
83
-
-
74549147547
-
Epigenetic regulation of vertebrate Hox genes: A dynamic equilibrium
-
Soshnikova, N. & Duboule, D. Epigenetic regulation of vertebrate Hox genes: a dynamic equilibrium. Epigenetics 4, 537-540 (2009).
-
(2009)
Epigenetics
, vol.4
, pp. 537-540
-
-
Soshnikova, N.1
Duboule, D.2
-
85
-
-
74249098205
-
The role of transcription factor Pitx3 in dopamine neuron development and Parkinson's disease
-
Li, J., Dani, J. A. & Le, W. The role of transcription factor Pitx3 in dopamine neuron development and Parkinson's disease. Curr. Top Med. Chem. 9, 855-859 (2009).
-
(2009)
Curr. Top Med. Chem.
, vol.9
, pp. 855-859
-
-
Li, J.1
Dani, J.A.2
Le, W.3
-
86
-
-
67949085111
-
Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements
-
Lepper, C., Conway, S. J. & Fan, C. M. Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements. Nature 460, 627-631 (2009).
-
(2009)
Nature
, vol.460
, pp. 627-631
-
-
Lepper, C.1
Conway, S.J.2
Fan, C.M.3
-
87
-
-
80755169506
-
A genetic approach to the transcriptional regulation of Hox gene clusters
-
Tschopp, P. & Duboule, D. A genetic approach to the transcriptional regulation of Hox gene clusters. Annu. Rev. Genet. 45, 145-166 (2011).
-
(2011)
Annu. Rev. Genet.
, vol.45
, pp. 145-166
-
-
Tschopp, P.1
Duboule, D.2
-
88
-
-
78649974534
-
Taf1 regulates Pax3 protein by monoubiquitination in skeletal muscle progenitors
-
Boutet, S. C., Biressi, S., Iori, K., Natu, V. & Rando, T. A. Taf1 regulates Pax3 protein by monoubiquitination in skeletal muscle progenitors. Mol. Cell 40, 749-761 (2010).
-
(2010)
Mol. Cell
, vol.40
, pp. 749-761
-
-
Boutet, S.C.1
Biressi, S.2
Iori, K.3
Natu, V.4
Rando, T.A.5
-
89
-
-
77956370863
-
MicroRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7
-
Chen, J. F., Tao, Y., Li, J., Deng, Z., Yan, Z., Xiao, X. et al. microRNA-1 and microRNA-206 regulate skeletal muscle satellite cell proliferation and differentiation by repressing Pax7. J. Cell. Biol. 190, 867-879 (2010).
-
(2010)
J. Cell. Biol.
, vol.190
, pp. 867-879
-
-
Chen, J.F.1
Tao, Y.2
Li, J.3
Deng, Z.4
Yan, Z.5
Xiao, X.6
-
90
-
-
35548949865
-
Transcriptional activation of p53 by Pitx1
-
Liu, D. X. & Lobie, P. E. Transcriptional activation of p53 by Pitx1. Cell Death Differ. 14, 1893-1907 (2007).
-
(2007)
Cell Death Differ
, vol.14
, pp. 1893-1907
-
-
Liu, D.X.1
Lobie, P.E.2
-
91
-
-
33744947569
-
Endocrine regulation of HOX genes
-
Daftary, G. S. & Taylor, H. S. Endocrine regulation of HOX genes. Endocr. Rev. 27, 331-355 (2006).
-
(2006)
Endocr. Rev.
, vol.27
, pp. 331-355
-
-
Daftary, G.S.1
Taylor, H.S.2
-
92
-
-
67749095703
-
Hox specificity unique roles for cofactors and collaborators
-
Mann, R. S., Lelli, K. M. & Joshi, R. Hox specificity unique roles for cofactors and collaborators. Curr. Top Dev. Biol. 88, 63-101 (2009).
-
(2009)
Curr. Top Dev. Biol.
, vol.88
, pp. 63-101
-
-
Mann, R.S.1
Lelli, K.M.2
Joshi, R.3
-
93
-
-
77955053847
-
Hox genes and regional patterning of the vertebrate body plan
-
Mallo, M., Wellik, D. M. & Deschamps, J. Hox genes and regional patterning of the vertebrate body plan. Dev. Biol. 344, 7-15 (2010).
-
(2010)
Dev. Biol.
, vol.344
, pp. 7-15
-
-
Mallo, M.1
Wellik, D.M.2
Deschamps, J.3
-
94
-
-
34547754037
-
Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy
-
Clapp, J., Mitchell, L. M., Bolland, D. J., Fantes, J., Corcoran, A. E., Scotting, P. J. et al. Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy. Am. J. Hum. Genet. 81, 264-279 (2007).
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 264-279
-
-
Clapp, J.1
Mitchell, L.M.2
Bolland, D.J.3
Fantes, J.4
Corcoran, A.E.5
Scotting, P.J.6
-
95
-
-
77149125886
-
Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl
-
Wu, S. L., Tsai, M. S., Wong, S. H., Hsieh-Li, H. M., Tsai, T. S., Chang, W. T. et al. Characterization of genomic structures and expression profiles of three tandem repeats of a mouse double homeobox gene: Duxbl. Dev. Dyn. 239, 927-940 (2010).
-
(2010)
Dev. Dyn.
, vol.239
, pp. 927-940
-
-
Wu, S.L.1
Tsai, M.S.2
Wong, S.H.3
Hsieh-Li, H.M.4
Tsai, T.S.5
Chang, W.T.6
-
96
-
-
38449121233
-
Expression profiling of immature thymocytes revealed a novel homeobox gene that regulates double-negative thymocyte development
-
Kawazu, M., Yamamoto, G., Yoshimi, M., Yamamoto, K., Asai, T., Ichikawa, M. et al. Expression profiling of immature thymocytes revealed a novel homeobox gene that regulates double-negative thymocyte development. J. Immunol. 179, 5335-5345 (2007).
-
(2007)
J. Immunol.
, vol.179
, pp. 5335-5345
-
-
Kawazu, M.1
Yamamoto, G.2
Yoshimi, M.3
Yamamoto, K.4
Asai, T.5
Ichikawa, M.6
-
97
-
-
77951954873
-
Myoblasts from affected and non affected FSHD muscles exhibit morphological differentiation defects
-
Barro, M., Carnac, G., Flavier, S., Mercier, J., Vassetzky, Y. & Laoudj-Chenivesse, D. Myoblasts from affected and non affected FSHD muscles exhibit morphological differentiation defects. J. Cell Mol. Med. 275-289 (2010).
-
(2010)
J. Cell Mol. Med.
, pp. 275-289
-
-
Barro, M.1
Carnac, G.2
Flavier, S.3
Mercier, J.4
Vassetzky, Y.5
Laoudj-Chenivesse, D.6
-
98
-
-
36049044111
-
Analysis of the genetic interactions between Cyclin A1, Atm and p53 during spermatogenesis
-
Baumer, N., Sandstede, M. L., Diederichs, S., Kohler, G., Readhead, C., Ji, P. et al. Analysis of the genetic interactions between Cyclin A1, Atm and p53 during spermatogenesis. Asian J. Androl. 9, 739-750 (2007).
-
(2007)
Asian J. Androl.
, vol.9
, pp. 739-750
-
-
Baumer, N.1
Sandstede, M.L.2
Diederichs, S.3
Kohler, G.4
Readhead, C.5
Ji, P.6
-
99
-
-
80052396196
-
Extrinsic regulation of satellite cell specification
-
Bentzinger, C. F., von Maltzahn, J. & Rudnicki, M. A. Extrinsic regulation of satellite cell specification. Stem Cell Res. Ther. 1, 27 (2011).
-
(2011)
Stem Cell Res. Ther.
, vol.1
, pp. 27
-
-
Bentzinger, C.F.1
Von Maltzahn, J.2
Rudnicki, M.A.3
-
100
-
-
77949789594
-
Retention of Pax3 expression in satellite cells of muscle spindles
-
Kirkpatrick, L. J., Yablonka-Reuveni, Z. & Rosser, B. W. Retention of Pax3 expression in satellite cells of muscle spindles. J. Histochem. Cytochem. 58, 317-327 (2010).
-
(2010)
J. Histochem. Cytochem.
, vol.58
, pp. 317-327
-
-
Kirkpatrick, L.J.1
Yablonka-Reuveni, Z.2
Rosser, B.W.3
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