-
1
-
-
0034103927
-
Transcriptional augmentation: Modulation of gene expression by scaffold/matrix-attached regions (S/MAR elements)
-
Bode, J., Benham, C., Knopp, A., and Mielke, C. 2000. Transcriptional augmentation: Modulation of gene expression by scaffold/matrix-attached regions (S/MAR elements). Crit. Rev. Eukaryot. Gene Expr. 10: 73-90.
-
(2000)
Crit. Rev. Eukaryot. Gene Expr
, vol.10
, pp. 73-90
-
-
Bode, J.1
Benham, C.2
Knopp, A.3
Mielke, C.4
-
2
-
-
0022553738
-
Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites
-
Cockerill, P.N. and Garrard, W.T. 1986. Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites. Cell 44: 273-282.
-
(1986)
Cell
, vol.44
, pp. 273-282
-
-
Cockerill, P.N.1
Garrard, W.T.2
-
3
-
-
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., Weemaes, C.M., Padberg, G.W., and van der Maarel, S.M. 2007. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD. Neurology 69: 1018-1026.
-
(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
Weemaes, C.M.7
Padberg, G.W.8
van der Maarel, S.M.9
-
4
-
-
0037047439
-
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle
-
Gabellini, D., Green, M.R., and Tupler, R. 2002. Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110: 339-348.
-
(2002)
Cell
, vol.110
, pp. 339-348
-
-
Gabellini, D.1
Green, M.R.2
Tupler, R.3
-
5
-
-
33644522383
-
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1
-
Gabellini, D., D'Antona, G., Moggio, M., Prelle, A., Zecca, C., Adami, R., Angeletti, B., Ciscato, P., Pellegrino, M.A., Bottinelli, R., et al. 2005. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature 439: 973-977
-
(2005)
Nature
, vol.439
, pp. 973-977
-
-
Gabellini, D.1
D'Antona, G.2
Moggio, M.3
Prelle, A.4
Zecca, C.5
Adami, R.6
Angeletti, B.7
Ciscato, P.8
Pellegrino, M.A.9
Bottinelli, R.10
-
6
-
-
0344436078
-
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
-
Gabriels, J., Beckers, M.C., Ding, H., De Vriese, A., Plaisance, S., van der Maarel, S.M., Padberg, G.W., Frants, R.R., Hewitt, J.E., Collen, D., 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.
-
(1999)
Gene
, vol.236
, pp. 25-32
-
-
Gabriels, J.1
Beckers, M.C.2
Ding, H.3
De Vriese, A.4
Plaisance, S.5
van der Maarel, S.M.6
Padberg, G.W.7
Frants, R.R.8
Hewitt, J.E.9
Collen, D.10
-
7
-
-
0005061982
-
Analysis of nuclear scaffold attachment regions
-
ed. H. Gould, pp, Oxford University Press, Oxford, UK
-
Gasser, S.M. and Vassetzky, Y.S. 1998. Analysis of nuclear scaffold attachment regions. In Chromatin: A Practical Approach (ed. H. Gould), pp. 111-124. Oxford University Press, Oxford, UK.
-
(1998)
Chromatin: A Practical Approach
, pp. 111-124
-
-
Gasser, S.M.1
Vassetzky, Y.S.2
-
8
-
-
33747453473
-
Insulators: Exploiting transcriptional and epigenetic mechanisms
-
doi: 10.1038/nrg1925
-
Gaszner, M. and Felsenfeld, G. 2006. Insulators: Exploiting transcriptional and epigenetic mechanisms. Nat. Rev. Genet. 7: 703-713. doi: 10.1038/nrg1925.
-
(2006)
Nat. Rev. Genet
, vol.7
, pp. 703-713
-
-
Gaszner, M.1
Felsenfeld, G.2
-
9
-
-
2442606618
-
DNA replication initiates at domains overlapping with nuclear matrix attachment regions in the xenopus and mouse c-myc promoter
-
Girard-Reydet, C., Gregoire, D., Vassetzky, Y., and Mechali, M. 2004. DNA replication initiates at domains overlapping with nuclear matrix attachment regions in the xenopus and mouse c-myc promoter. Gene 332: 129-138.
-
(2004)
Gene
, vol.332
, pp. 129-138
-
-
Girard-Reydet, C.1
Gregoire, D.2
Vassetzky, Y.3
Mechali, M.4
-
10
-
-
0028966045
-
Different topoisomerase II antitumor drugs direct similar specific long-range fragmentation of an amplified c-MYC gene locus in living cells and in high-salt-extracted nuclei
-
Gromova, I.I., Thomsen, B., and Razin, S.V. 1995. Different topoisomerase II antitumor drugs direct similar specific long-range fragmentation of an amplified c-MYC gene locus in living cells and in high-salt-extracted nuclei. Proc. Natl. Acad. Sci. 92: 102-106.
-
(1995)
Proc. Natl. Acad. Sci
, vol.92
, pp. 102-106
-
-
Gromova, I.I.1
Thomsen, B.2
Razin, S.V.3
-
11
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
doi: 10.1038/ng1491
-
Horike, S., Cai, S., Miyano, M., Cheng, J.F., and Kohwi-Shigematsu, T. 2005. Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat. Genet. 37: 31-40. doi: 10.1038/ng1491.
-
(2005)
Nat. Genet
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
Cheng, J.F.4
Kohwi-Shigematsu, T.5
-
12
-
-
10644297060
-
Mapping long-range chromatin organization within the chicken α-globin gene domain using oligonucleotide DNA arrays
-
Ioudinkova, E., Petrov, A., Razin, S.V., and Vassetzky, Y.S. 2005. Mapping long-range chromatin organization within the chicken α-globin gene domain using oligonucleotide DNA arrays. Genomics 85: 143-151.
-
(2005)
Genomics
, vol.85
, pp. 143-151
-
-
Ioudinkova, E.1
Petrov, A.2
Razin, S.V.3
Vassetzky, Y.S.4
-
13
-
-
0028988485
-
Position-independent transgene expression mediated by boundary elements from the apolipoprotein B chromatin domain
-
Kalos, M. and Fournier, R.E. 1995. Position-independent transgene expression mediated by boundary elements from the apolipoprotein B chromatin domain. Mol. Cell. Biol. 15: 198-207.
-
(1995)
Mol. Cell. Biol
, vol.15
, pp. 198-207
-
-
Kalos, M.1
Fournier, R.E.2
-
14
-
-
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., Vassetzky, Y., and Fernandez, A. 2005. 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)
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
Vassetzky, Y.7
Fernandez, A.8
-
15
-
-
0025836092
-
Genetic counselling in facioscapulohumeral muscular dystrophy
-
Lunt, P.W. and Harper, P.S. 1991. Genetic counselling in facioscapulohumeral muscular dystrophy. J. Med. Genet. 28: 655-664.
-
(1991)
J. Med. Genet
, vol.28
, pp. 655-664
-
-
Lunt, P.W.1
Harper, P.S.2
-
16
-
-
0021675784
-
Organization of the higher-order chromatin loop: Specific DNA attachment sites on nuclear scaffold
-
Mirkovitch, J., Mirault, M.E., and Laemmli, U.K. 1984. Organization of the higher-order chromatin loop: Specific DNA attachment sites on nuclear scaffold. Cell 39: 223-232.
-
(1984)
Cell
, vol.39
, pp. 223-232
-
-
Mirkovitch, J.1
Mirault, M.E.2
Laemmli, U.K.3
-
17
-
-
9444294990
-
Genetics and epigenetics of progressive facioscapulohumeral (Landouzy-Dejerine) muscular dystrophy
-
Petrov, A.P., Laoudj, D., and Vassetzky, Y.S. 2003. Genetics and epigenetics of progressive facioscapulohumeral (Landouzy-Dejerine) muscular dystrophy. Genetika 39: 147-151.
-
(2003)
Genetika
, vol.39
, pp. 147-151
-
-
Petrov, A.P.1
Laoudj, D.2
Vassetzky, Y.S.3
-
18
-
-
33646485687
-
Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts
-
Petrov, A., Pirozhkova, I., Laoudj, D., Carnac, G., Lipinski, M., and Vassetzky, Y.S. 2006. Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts. Proc. Natl. Acad. Sci. 103: 6982-6987.
-
(2006)
Proc. Natl. Acad. Sci
, vol.103
, pp. 6982-6987
-
-
Petrov, A.1
Pirozhkova, I.2
Laoudj, D.3
Carnac, G.4
Lipinski, M.5
Vassetzky, Y.S.6
-
19
-
-
8744240156
-
FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients
-
Rijkers, T., Deidda, G., van Koningsbruggen, S., van Geel, M., Lemmers, R.J., van Deutekom, J.C., Figlewicz, D., Hewitt, J.E., Padberg, G.W., Frants, R.R., et al. 2004. FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. J. Med. Genet. 41: 826-836.
-
(2004)
J. Med. Genet
, vol.41
, pp. 826-836
-
-
Rijkers, T.1
Deidda, G.2
van Koningsbruggen, S.3
van Geel, M.4
Lemmers, R.J.5
van Deutekom, J.C.6
Figlewicz, D.7
Hewitt, J.E.8
Padberg, G.W.9
Frants, R.R.10
-
20
-
-
0040411236
-
Excision of an integrated provirus by the action of FLP recombinase
-
Schubeler, D., Mielke, C., and Bode, J. 1997. Excision of an integrated provirus by the action of FLP recombinase. In Vitro Cell. Dev. Biol. 33: 825-830.
-
(1997)
In Vitro Cell. Dev. Biol
, vol.33
, pp. 825-830
-
-
Schubeler, D.1
Mielke, C.2
Bode, J.3
-
21
-
-
0342316480
-
Origin and roles of nuclear matrix proteins. Specific functions of the MAR-binding protein MeCP2/ARBP
-
Stratling, W.H. and Yu, F. 1999. Origin and roles of nuclear matrix proteins. Specific functions of the MAR-binding protein MeCP2/ARBP. Crit. Rev. Eukaryot. Gene Expr. 9: 311-318.
-
(1999)
Crit. Rev. Eukaryot. Gene Expr
, vol.9
, pp. 311-318
-
-
Stratling, W.H.1
Yu, F.2
-
22
-
-
0033607231
-
Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy
-
Tupler, R., Perini, G., Pellegrino, M.A., and Green, M.R. 1999. Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy. Proc. Natl. Acad. Sci. 96: 12650-12654.
-
(1999)
Proc. Natl. Acad. Sci
, vol.96
, pp. 12650-12654
-
-
Tupler, R.1
Perini, G.2
Pellegrino, M.A.3
Green, M.R.4
-
23
-
-
33846315519
-
Facioscapulohumeral muscular dystrophy
-
van der Maarel, S.M., Frants, R.R., and Padberg, G.W. 2006. Facioscapulohumeral muscular dystrophy. Biochim Biophys Acta 1772: 186-194.
-
(2006)
Biochim Biophys Acta
, vol.1772
, pp. 186-194
-
-
van der Maarel, S.M.1
Frants, R.R.2
Padberg, G.W.3
-
24
-
-
0027744223
-
FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
-
van Deutekom, J.C., Wijmenga, C., van Tienhoven, E.A., Gruter, A.M., Hewitt, J.E., Padberg, G.W., van Ommen, G.J., Hofker, M.H., and Frants, R.R. 1993. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. Hum. Mol. Genet. 2: 2037-2042.
-
(1993)
Hum. Mol. Genet
, vol.2
, pp. 2037-2042
-
-
van Deutekom, J.C.1
Wijmenga, C.2
van Tienhoven, E.A.3
Gruter, A.M.4
Hewitt, J.E.5
Padberg, G.W.6
van Ommen, G.J.7
Hofker, M.H.8
Frants, R.R.9
-
25
-
-
0032862871
-
The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements
-
van Geel, M., Heather, L.J., Lyle, R., Hewitt, J.E., Frants, R.R., and de Jong, P.J. 1999. The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements. Genomics 61: 55-65.
-
(1999)
Genomics
, vol.61
, pp. 55-65
-
-
van Geel, M.1
Heather, L.J.2
Lyle, R.3
Hewitt, J.E.4
Frants, R.R.5
de Jong, P.J.6
-
26
-
-
33846589302
-
FRG1P-mediated aggregation of proteins involved in pre-mRNA processing
-
van Koningsbruggen, S., Straasheijm, K.R., Sterrenburg, E., de Graaf, N., Dauwerse, H.G., Frants, R.R., and van der Maarel, S.M. 2006. FRG1P-mediated aggregation of proteins involved in pre-mRNA processing. Chromosoma 116: 53-64.
-
(2006)
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
Frants, R.R.6
van der Maarel, S.M.7
-
27
-
-
0345257778
-
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy
-
doi: 10.1038/ng1262
-
van Overveld, P.G., Lemmers, R.J., Sandkuijl, L.A., Enthoven, L., Winokur, S.T., Bakels, F., Padberg, G.W., van Ommen, G.J., Frants, R.R., and van der Maarel, S.M. 2003. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy. Nat. Genet. 35: 315-317. doi: 10.1038/ng1262.
-
(2003)
Nat. Genet
, vol.35
, pp. 315-317
-
-
van Overveld, P.G.1
Lemmers, R.J.2
Sandkuijl, L.A.3
Enthoven, L.4
Winokur, S.T.5
Bakels, F.6
Padberg, G.W.7
van Ommen, G.J.8
Frants, R.R.9
van der Maarel, S.M.10
-
28
-
-
0034075901
-
Specification of chromatin domains and regulation of replication and transcription during development
-
Vassetzky, Y., Lemaitre, J.M., and Mechali, M. 2000. Specification of chromatin domains and regulation of replication and transcription during development. Crit. Rev. Eukaryot. Gene Expr. 10: 31-38.
-
(2000)
Crit. Rev. Eukaryot. Gene Expr
, vol.10
, pp. 31-38
-
-
Vassetzky, Y.1
Lemaitre, J.M.2
Mechali, M.3
-
29
-
-
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., Van Der Maarel, S.M., Hayashi, Y., and Flanigan, K.M. 2003. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum. Mol. Genet. 12: 2895-2907.
-
(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
Van Der Maarel, S.M.7
Hayashi, Y.8
Flanigan, K.M.9
-
30
-
-
10744222546
-
Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles
-
Wohlgemuth, M., Lemmers, R.J., Van Der Kooi, E.L., Van Der Wielen, M.J., Van Overveld, P.G., Dauwerse, H., Bakker, E., Frants, R.R., Padberg, G.W., and Van Der Maarel, S.M. 2003. Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles. Neurology 61: 909-913.
-
(2003)
Neurology
, vol.61
, pp. 909-913
-
-
Wohlgemuth, M.1
Lemmers, R.J.2
Van Der Kooi, E.L.3
Van Der Wielen, M.J.4
Van Overveld, P.G.5
Dauwerse, H.6
Bakker, E.7
Frants, R.R.8
Padberg, G.W.9
Van Der Maarel, S.M.10
|