-
1
-
-
0033681250
-
Ordered recruitment of chromatin modifying and general transcription factors to the IFN-beta promoter
-
Agalioti, T., Lomvardas, S., Parekh, B., Yie, J., Maniatis, T., and Thanos, D. (2000). Ordered recruitment of chromatin modifying and general transcription factors to the IFN-beta promoter. Cell 103, 667-678. doi: 10.1016/S0092-8674(00)00169-0
-
(2000)
Cell
, vol.103
, pp. 667-678
-
-
Agalioti, T.1
Lomvardas, S.2
Parekh, B.3
Yie, J.4
Maniatis, T.5
Thanos, D.6
-
2
-
-
0034254857
-
NuRD and SIN3: Histone deacetylase complexes in development
-
Ahringer, J. (2000). NuRD and SIN3: histone deacetylase complexes in development. Trends Genet. 16, 351-356. doi:10.1016/S0168-9525(00)02066-7
-
(2000)
Trends Genet
, vol.16
, pp. 351-356
-
-
Ahringer, J.1
-
3
-
-
0346969980
-
Dendrite development regulated by CREST, a calcium-regulated transcriptional activator
-
Aizawa, H. (2004). Dendrite development regulated by CREST, a calcium-regulated transcriptional activator. Science 303, 197-202. doi: 10.1126/sci-ence.1089845
-
(2004)
Science
, vol.303
, pp. 197-202
-
-
Aizawa, H.1
-
4
-
-
2942705826
-
Chromatin acetylation, memory, and LTP are impaired in CBP+/-mice: A model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration
-
Alarcon, J. M., Malleret, G., Touzani, K., Vronskaya, S., Ishii, S., Kandel, E. R., et al. (2004). Chromatin acetylation, memory, and LTP are impaired in CBP+/-mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration. Neuron 42, 947-959. doi: 10.1016/j.neuron.2004.05.021
-
(2004)
Neuron
, vol.42
, pp. 947-959
-
-
Alarcon, J.M.1
Malleret, G.2
Touzani, K.3
Vronskaya, S.4
Ishii, S.5
Kandel, E.R.6
-
5
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 Nat
-
Amir, R. E., Van den Veyver, I. B., Wan, M., Tran, C. Q., Francke, U., and Zoghbi, H. Y. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 Nat. Genet. 23, 185-188
-
(1999)
Genet
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van Den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
6
-
-
0043234687
-
Nucleosome sliding induced by the xMi-2 complex does not occur exclusively via a simple twist-diffusion mechanism
-
Aoyagi, S., Wade, P. A., and Hayes, J. J. (2003). Nucleosome sliding induced by the xMi-2 complex does not occur exclusively via a simple twist-diffusion mechanism. J. Biol. Chem. 278, 30562-30568. doi: 10.1074/jbc.M304148200
-
(2003)
J. Biol. Chem
, vol.278
, pp. 30562-30568
-
-
Aoyagi, S.1
Wade, P.A.2
Hayes, J.J.3
-
7
-
-
78651098091
-
A balanced translocation t(6;14)(q25.3;q 13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum
-
Backx, L., Seuntjens, E., Devriendt, K., Vermeesch, J., and Van Esch, H. (2011). A balanced translocation t(6;14)(q25.3;q 13.2) leading to reciprocal fusion transcripts in a patient with intellectual disability and agenesis of corpus callosum. Cytogenet. GenomeRes. 132, 135-143. doi: 10.1159/000321577
-
(2011)
Cytogenet. Genomeres
, vol.132
, pp. 135-143
-
-
Backx, L.1
Seuntjens, E.2
Devriendt, K.3
Vermeesch, J.4
Van Esch, H.5
-
8
-
-
84929172199
-
ACTL6a enforced the epidermal progenitor state by suppressing SWI/SNF-dependent induction of KLF4
-
Bao, X., Tang, J., Lopez-Pajared, V., Tao, S., Qu, K., Crabtree, G. R., et al. (2012). ACTL6a enforced the epidermal progenitor state by suppressing SWI/SNF-dependent induction of KLF4. Cell Stem Cell 29, 997-1003. doi:10.1016/j.biotechadv.2011.08.02
-
(2012)
Cell Stem Cell
, vol.29
, pp. 997-1003
-
-
Bao, X.1
Tang, J.2
Lopez-Pajared, V.3
Tao, S.4
Qu, K.5
Crabtree, G.R.6
-
9
-
-
34247465955
-
Snapshot: Chromatin remodeling complexes
-
Secreted Bao, Y., and Shen, X. (2007). Snapshot: chromatin remodeling complexes. Cell 129, 18-19. doi: 10.1016/j.cell.2007.04.018
-
(2007)
Cell
, vol.129
, pp. 18-19
-
-
Secreted Bao, Y.1
Shen, X.2
-
10
-
-
85027948621
-
Hippocampal focal knockout of CBP affects specific histone modifications, long-term potentiation, and longterm memory
-
Barrett, R. M., Malvaez, M., Kramar, E., Matheos, D. P., Arrizon, A., Cabrera, S. M., et al. (2011). Hippocampal focal knockout of CBP affects specific histone modifications, long-term potentiation, and longterm memory. Neuropsychopharmacology 36, 1545-1556. doi: 10.1038/npp.2011.61
-
(2011)
Neuropsychopharmacology
, vol.36
, pp. 1545-1556
-
-
Barrett, R.M.1
Malvaez, M.2
Kramar, E.3
Matheos, D.P.4
Arrizon, A.5
Cabrera, S.M.6
-
11
-
-
47549109984
-
Beyond transcription factors: The role of chromatin modifying enzymes in regulating transcription required for memory
-
Barrett, R. M., and Wood, M. A. (2008). Beyond transcription factors: the role of chromatin modifying enzymes in regulating transcription required for memory. Learn. Mem. 15, 460-467. doi: 10.1101/lm.917508
-
(2008)
Learn. Mem
, vol.15
, pp. 460-467
-
-
Barrett, R.M.1
Wood, M.A.2
-
12
-
-
84902168468
-
Regulating the chromatin landscape: Structural and mechanistic perspectives
-
Bartholomew, B. (2014). Regulating the chromatin landscape: structural and mechanistic perspectives. Annu. Rev. Biochem. 83, 671-696. doi: 10.1146/annurev-biochem-051810-093157
-
(2014)
Annu. Rev. Biochem
, vol.83
, pp. 671-696
-
-
Bartholomew, B.1
-
13
-
-
0029786398
-
The Caenorhabditis elegans gene sere-4 controls neuronal and mesodermal cell development and encodes a zmc finger protein
-
Basson, M., and Horvitz, H. R. (1996). The Caenorhabditis elegans gene sere-4 controls neuronal and mesodermal cell development and encodes a zmc finger protein. Genes Dev. 4, 1953-1965
-
(1996)
Genes Dev
, vol.4
, pp. 1953-1965
-
-
Basson, M.1
Horvitz, H.R.2
-
14
-
-
0035997356
-
ATP-dependent nucleosome remodeling
-
Becker, P. B., and Hörz, W. (2002). ATP-dependent nucleosome remodeling. Annu. Rev. Biochem. 71, 247-273. doi: 10.1146/annurev.biochem.71.110601.135400
-
(2002)
Annu. Rev. Biochem
, vol.71
, pp. 247-273
-
-
Becker, P.B.1
Hörz, W.2
-
15
-
-
84884669130
-
Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism
-
Ben-David, E., and Shifman, S. (2012). Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism. Mol Psychiatry 18, 1054-1056. doi: 10.1038/mp.2012.148
-
(2012)
Mol Psychiatry
, vol.18
, pp. 1054-1056
-
-
Ben-David, E.1
Shifman, S.2
-
16
-
-
0038094501
-
Nucleo-somes unfold completely at a transcriptionally active promoter
-
Boeger, H., Griesenbeck, J., Strattan, J. S., and Kornberg, R. D. (2003). Nucleo-somes unfold completely at a transcriptionally active promoter. Mol. Cell 11, 1587-1598. doi: 10.1016/S1097-2765(03)00231-4
-
(2003)
Mol. Cell
, vol.11
, pp. 1587-1598
-
-
Boeger, H.1
Griesenbeck, J.2
Strattan, J.S.3
Kornberg, R.D.4
-
17
-
-
1542268361
-
Mi-2/NuRD: Multiple complexes for many purposes
-
Bowen, N. J., Fujita, N., Kajita, M., and Wade, P. A. (2004). Mi-2/NuRD: multiple complexes for many purposes. Biochim. Biophys. Acta 1677, 52-57. doi: 10.1016/j.bbaexp.2003.10.010
-
(2004)
Biochim. Biophys. Acta
, vol.1677
, pp. 52-57
-
-
Bowen, N.J.1
Fujita, N.2
Kajita, M.3
Wade, P.A.4
-
18
-
-
0023652328
-
Cell cycle control of the yeast HO gene: Cis- and trans-acting regulators
-
Breeden, L., and Nasmyth, K. (1987). Cell cycle control of the yeast HO gene: cis- and trans-acting regulators. Cell 48, 389-397. doi: 10.1016/0092-8674(87)90190-5
-
(1987)
Cell
, vol.48
, pp. 389-397
-
-
Breeden, L.1
Nasmyth, K.2
-
19
-
-
18344410319
-
Dmi-2 and ISWI chromatin remodelling factors have distinct nucle-osome binding and mobilization properties
-
Brehm, A., Langst, G., Kehle, J., Clapier, C. R., Imhof, A., Eberharter, A., et al. (2000). Dmi-2 and ISWI chromatin remodelling factors have distinct nucle-osome binding and mobilization properties. EMBO J. 19, 4332-4341. doi: 10.1093/emboj/19.16.4332
-
(2000)
EMBO J
, vol.19
, pp. 4332-4341
-
-
Brehm, A.1
Langst, G.2
Kehle, J.3
Clapier, C.R.4
Imhof, A.5
Eberharter, A.6
-
20
-
-
0032216667
-
Rubinstein-taybi syndrome. Review of 732 cases and analysis of the typical traits
-
Cantani, A., and Gagliesi, D. (1998). Rubinstein-taybi syndrome. review of 732 cases and analysis of the typical traits. Eur. Rev. Med. Pharmacol. Sci. 2, 81-87
-
(1998)
Eur. Rev. Med. Pharmacol. Sci
, vol.2
, pp. 81-87
-
-
Cantani, A.1
Gagliesi, D.2
-
21
-
-
84856252670
-
MeCP2: Only 100% will do
-
Chao, H.-T., and Zoghbi, H. Y. (2012). MeCP2: only 100% will do. Nat. Neurosci. 15, 176-177. doi: 10.1038/nn.3027
-
(2012)
Nat. Neurosci
, vol.15
, pp. 176-177
-
-
Chao, H.-T.1
Zoghbi, H.Y.2
-
22
-
-
84887404098
-
Exome sequencing to identify de novo mutations in sporadic ALS trios
-
Chesi, A., Staahl, B. T., Jovicic„ A., Couthouis, J., Fasolino, M., Raphael, A. R., et al. (2013). Exome sequencing to identify de novo mutations in sporadic ALS trios. Nat. Neurosci. 16, 851-855. doi: 10.1038/nn.3412
-
(2013)
Nat. Neurosci
, vol.16
, pp. 851-855
-
-
Chesi, A.1
Staahl, B.T.2
Jovicic„, A.3
Couthouis, J.4
Fasolino, M.5
Raphael, A.R.6
-
23
-
-
0014783843
-
Mental retardation with absent fifth fingernail and terminal phalanx
-
Coffin, G. S., and Siris, E. (1970). Mental retardation with absent fifth fingernail and terminal phalanx. Am. J. Dis. Child. 119, 433-439. doi: 10.1001/arch-pedi.1970.02100050435009
-
(1970)
Am. J. Dis. Child
, vol.119
, pp. 433-439
-
-
Coffin, G.S.1
Siris, E.2
-
24
-
-
0033400343
-
Nuclear receptors: Coactivators, corepressors and chromatin remodeling in the control of transcription
-
Collingwood, T. N., Urnov, F. D., and Wolffe, A. P. (1999). Nuclear receptors: Coactivators, corepressors and chromatin remodeling in the control of transcription. J. Mol. Endocrinol. 23, 255-275. doi: 10.1677/jme.0.0230255
-
(1999)
J. Mol. Endocrinol
, vol.23
, pp. 255-275
-
-
Collingwood, T.N.1
Urnov, F.D.2
Wolffe, A.P.3
-
25
-
-
0033617334
-
Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle— and developmentally regulated promoter
-
Cosma, M. P., Tanaka, T., Nasmyth, K., Ii, F., and Pasini, V. S. (1999). Ordered recruitment of transcription and chromatin remodeling factors to a cell cycle— and developmentally regulated promoter. Cell 97, 299-311
-
(1999)
Cell
, vol.97
, pp. 299-311
-
-
Cosma, M.P.1
Tanaka, T.2
Nasmyth, K.3
Ii, F.4
Pasini, V.S.5
-
26
-
-
33646054905
-
Repressed by a NuRD
-
Crook, J. M., Dunn, N. R., and Colman, A. (2006). Repressed by a NuRD. Nat. Cell Biol. 8,212-214. doi: 10.1038/ncb0306-212
-
(2006)
Nat. Cell Biol
, vol.8
, pp. 212-214
-
-
Crook, J.M.1
Dunn, N.R.2
Colman, A.3
-
27
-
-
34547856653
-
The human Mi-2/NuRD complex and gene regulation
-
Denslow, S. A., and Wade, P. A. (2007). The human Mi-2/NuRD complex and gene regulation. Oncogene 26, 5433-5438. doi: 10.1038/sj.onc.1210611
-
(2007)
Oncogene
, vol.26
, pp. 5433-5438
-
-
Denslow, S.A.1
Wade, P.A.2
-
28
-
-
84887408417
-
HAM-2 and HAM-3 are central for the assembly of the NeurosporaSTRIPAK complex at the nuclear envelope and regulate nuclear accumulation of the MAP kinase MAK-1 in a MAK-2-dependent manner
-
Dettmann, A., Heilig, Y., Ludwig, S., Schmitt, K., Illgen, J., Fleitëner, A., et al. (2013). HAM-2 and HAM-3 are central for the assembly of the NeurosporaSTRIPAK complex at the nuclear envelope and regulate nuclear accumulation of the MAP kinase MAK-1 in a MAK-2-dependent manner. Mol. Microbiol. 90, 796-812. doi: 10.1111/mmi.12399
-
(2013)
Mol. Microbiol
, vol.90
, pp. 796-812
-
-
Dettmann, A.1
Heilig, Y.2
Ludwig, S.3
Schmitt, K.4
Illgen, J.5
Fleitëner, A.6
-
29
-
-
0034081137
-
Mechanism for specificity by HMG-1 in enhanceosome assembly
-
Ellwood, K. B., Yen, Y. M., Johnson, R. C., and Carey, M. (2000). Mechanism for specificity by HMG-1 in enhanceosome assembly. Mol. Cell. Biol. 20, 4359-4370. doi: 10.1128/MCB.20.12.4359-4370.2000
-
(2000)
Mol. Cell. Biol
, vol.20
, pp. 4359-4370
-
-
Ellwood, K.B.1
Yen, Y.M.2
Johnson, R.C.3
Carey, M.4
-
30
-
-
33847266846
-
Reversal of neurological defects in a mouse model of Rett syndrome
-
Guy, J., Gan, J., Selfridge, J., Cobb, S., and Bird, A. (2007). Reversal of neurological defects in a mouse model of Rett syndrome. Science 315, 1143-1147. doi: 10.1126/science.1138389
-
(2007)
Science
, vol.315
, pp. 1143-1147
-
-
Guy, J.1
Gan, J.2
Selfridge, J.3
Cobb, S.4
Bird, A.5
-
31
-
-
0017738954
-
A new gene affecting the efficiency of mating-type interconversions in homothallic strains of Saccharomyces cerevisiae
-
Haber, J. E., and Garvik, B. (1977). A new gene affecting the efficiency of mating-type interconversions in homothallic strains of Saccharomyces cerevisiae. Genetics 87, 33-50
-
(1977)
Genetics
, vol.87
, pp. 33-50
-
-
Haber, J.E.1
Garvik, B.2
-
32
-
-
79251506941
-
HDAC inhibition modulates hippocampus-dependent long-term memory for object location in a CBP-dependent manner
-
Haettig, J., Stefanko, D. P., Multani, M. L., Figueroa, D. X., McQuown, S. C., and Wood, M. A. (2011). HDAC inhibition modulates hippocampus-dependent long-term memory for object location in a CBP-dependent manner. Learn. Mem. 18, 71-79. doi: 10.1101/lm.1986911
-
(2011)
Learn. Mem
, vol.18
, pp. 71-79
-
-
Haettig, J.1
Stefanko, D.P.2
Multani, M.L.3
Figueroa, D.X.4
McQuown, S.C.5
Wood, M.A.6
-
33
-
-
84865071031
-
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
-
Halgren, C., Kjaergaard, S., Bak, M., Hansen, C., El-Schich, Z., Anderson, C. M., et al. (2012). Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B. Clin. Genet. 82, 248-255. doi: 10.1111/j.1399-0004.2011.01755.x
-
(2012)
Clin. Genet
, vol.82
, pp. 248-255
-
-
Halgren, C.1
Kjaergaard, S.2
Bak, M.3
Hansen, C.4
El-Schich, Z.5
Erson, C.M.6
-
34
-
-
79952539053
-
ATP-dependent chromatin remodeling: Genetics, genomics and mechanisms
-
Hargreaves, D. C., and Crabtree, G. R. (2011). ATP-dependent chromatin remodeling: genetics, genomics and mechanisms. Cell Res. 21, 396-420. doi: 10.1038/cr.2011.32
-
(2011)
Cell Res
, vol.21
, pp. 396-420
-
-
Hargreaves, D.C.1
Crabtree, G.R.2
-
35
-
-
0000247720
-
Promoter targeting of chromatin-modifying complexes
-
Hassan, A., Neely, K., and Vignali, M. (2001). Promoter targeting of chromatin-modifying complexes. Front. Biosci. 6, 1054-1064. doi: 10.2741/Hassan
-
(2001)
Front. Biosci
, vol.6
, pp. 1054-1064
-
-
Hassan, A.1
Neely, K.2
Vignali, M.3
-
36
-
-
0034704235
-
Generation of superhelical torsion by ATP-dependent chromatin remodeling activities
-
Havas, K., Flaus, A., Phelan, M., Kingston, R., Wade, P. A., Lilley, D. M. J., et al. (2000). Generation of superhelical torsion by ATP-dependent chromatin remodeling activities. Cell 103, 1133-1142. doi: 10.1016/S0092-8674(00)00215-4
-
(2000)
Cell
, vol.103
, pp. 1133-1142
-
-
Havas, K.1
Flaus, A.2
Phelan, M.3
Kingston, R.4
Wade, P.A.5
Lilley, D.6
-
37
-
-
84904976180
-
Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice
-
Heckman, L. D., Chahrour, M. H., and Zoghbi, H. Y. (2014). Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice. Elife 3:e02676. doi: 10.7554/eLife.02676
-
(2014)
Elife
, vol.3
-
-
Heckman, L.D.1
Chahrour, M.H.2
Zoghbi, H.Y.3
-
38
-
-
84898058158
-
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
-
Helsmoortel, C., Vulto-van Silfhout, A. T., Coe, B. P., Vandeweyer, G., Rooms, L., van den Ende, J., et al. (2014). A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. Nat. Genet. 46, 380-384. doi: 10.1038/ng.2899
-
(2014)
Nat. Genet
, vol.46
, pp. 380-384
-
-
Helsmoortel, C.1
Vulto-Van Silfhout, A.T.2
Coe, B.P.3
Vandeweyer, G.4
Rooms, L.5
Van Den Ende, J.6
-
39
-
-
0031792779
-
Identification and characterization of a family of mammalian methyl-CpG binding proteins
-
Hendrich, B., and Bird,A. (1998). Identification and characterization of a family of mammalian methyl-CpG binding proteins. Mol. Cell. Biol. 18, 6538-6547. doi: 10.1017/S0016672398533307
-
(1998)
Mol. Cell. Biol
, vol.18
, pp. 6538-6547
-
-
Hendrich, B.1
-
40
-
-
0035868824
-
Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development
-
Hendrich, B., Guy, J., Ramsahoye, B., Wilson, V. A., and Bird, A. (2001). Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development. Genes Dev. 15, 710-723. doi: 10.1101/gad.194101
-
(2001)
Genes Dev
, vol.15
, pp. 710-723
-
-
Hendrich, B.1
Guy, J.2
Ramsahoye, B.3
Wilson, V.A.4
Bird, A.5
-
41
-
-
0026631456
-
Psychological and speech studies in Rubinstein-Taybi syndrome
-
Hennekam, R., Baselier, A., Beyaert, E., Bos, A., Blok, J., Jansma, H., et al. (1992). Psychological and speech studies in Rubinstein-Taybi syndrome. Am. J. Ment. Retard. 96, 645-660
-
(1992)
Am. J. Ment. Retard
, vol.96
, pp. 645-660
-
-
Hennekam, R.1
Baselier, A.2
Beyaert, E.3
Bos, A.4
Blok, J.5
Jansma, H.6
-
42
-
-
84858021960
-
Haploinsufficiency of ARID1B, a member of the SWI/SNF-A chromatin-remodeling complex, is a frequent cause of intellectual disability
-
Hoyer, J., Ekici, A. B., Endele, S., Popp, B., Zweier, C., Wiesener, A., et al. (2012). Haploinsufficiency of ARID1B, a member of the SWI/SNF-A chromatin-remodeling complex, is a frequent cause of intellectual disability. Am. J. Hum. Genet. 90, 565-572. doi: 10.1016/j.ajhg.2012.02.007
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 565-572
-
-
Hoyer, J.1
Ekici, A.B.2
Endele, S.3
Popp, B.4
Zweier, C.5
Wiesener, A.6
-
43
-
-
84891868802
-
STRIPAK complexes: Structure, biological function, and involvement in human diseases
-
Hwang, J., and Pallas, D. C. (2014). STRIPAK complexes: structure, biological function, and involvement in human diseases. Int. J. Biochem. Cell Biol. 47, 118-148. doi: 10.1016/j.biocel.2013.11.021
-
(2014)
Int. J. Biochem. Cell Biol
, vol.47
, pp. 118-148
-
-
Hwang, J.1
Pallas, D.C.2
-
44
-
-
0028889159
-
Regulation of cell-type-specific interleukin-2 receptor alpha-chain gene expression: Potential role of physical interactions between Elf-1, HMG-I(Y), and NF-kappa B familyproteins
-
John, S., Reeves, R. B., Lin, J. X., Child, R., Leiden, J. M., Thompson, C. B., et al. (1995). Regulation of cell-type-specific interleukin-2 receptor alpha-chain gene expression: potential role of physical interactions between Elf-1, HMG-I(Y), and NF-kappa B familyproteins. Mol Cell. Biol. 15, 1786-1796
-
(1995)
Mol Cell. Biol
, vol.15
, pp. 1786-1796
-
-
John, S.1
Reeves, R.B.2
Lin, J.X.3
Child, R.4
Leiden, J.M.5
Thompson, C.B.6
-
45
-
-
33644764030
-
The NuRD component Mbd3 is required for pluripotencyofembryonic stem cells
-
Kaji, K., Caballero, I. M., MacLeod, R., Nichols, J., Wilson, V. A., and Hendrich, B. (2006). The NuRD component Mbd3 is required for pluripotencyofembryonic stem cells. Nat. Cell Biol. 8, 285-292. doi: 10.1038/ncb1372
-
(2006)
Nat. Cell Biol
, vol.8
, pp. 285-292
-
-
Kaji, K.1
Caballero, I.M.2
Macleod, R.3
Nichols, J.4
Wilson, V.A.5
Hendrich, B.6
-
46
-
-
84870018625
-
Preclinical research in Rett syndrome: Setting the foundation for translational success
-
Katz, D. M., Berger-Sweeney, J. E., Eubanks, J. H., Justice, M. J., Neul, J. L., Pozzo-Miller, L., et al. (2012). Preclinical research in Rett syndrome: setting the foundation for translational success. Dis. Model Mech. 5, 733-745. doi: 10.1242/dmm.011007
-
(2012)
Dis. Model Mech
, vol.5
, pp. 733-745
-
-
Katz, D.M.1
Berger-Sweeney, J.E.2
Eubanks, J.H.3
Justice, M.J.4
Neul, J.L.5
Pozzo-Miller, L.6
-
47
-
-
0032484081
-
Dmi-2, a hunchback-interacting protein that functions in polycomb repression
-
New York, N.Y
-
Kehle, J., Beuchle, D., Treuheit, S., Christen, B., Kennison, J. A., Bienz, M., et al. (1998). Dmi-2, a hunchback-interacting protein that functions in polycomb repression. Science (New York, N.Y.), 282, 1897-1900. doi: 10.1126/sci-ence.282.5395.1897
-
(1998)
Science
, vol.282
, pp. 1897-1900
-
-
Kehle, J.1
Beuchle, D.2
Treuheit, S.3
Christen, B.4
Kennison, J.A.5
Bienz, M.6
-
48
-
-
0031310825
-
The mechanism of transcriptional synergy of an in vitro assembled interferon-beta enhanceosome
-
Kim, T. K., and Maniatis, T. (1997). The mechanism of transcriptional synergy of an in vitro assembled interferon-beta enhanceosome. Mol. Cell 1, 119-129. doi: 10.1016/S1097-2765(00)80013-1
-
(1997)
Mol. Cell
, vol.1
, pp. 119-129
-
-
Kim, T.K.1
Maniatis, T.2
-
49
-
-
67249131065
-
Involvement ofSMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia
-
Koga, M., Ishiguro, H., Yazaki, S., Horiuchi, Y., Arai, M., Niizato, K., et al. (2009). Involvement ofSMARCA2/BRM in the SWI/SNF chromatin-remodeling complex in schizophrenia. Hum. Mol. Genet. 18, 2483-2494. doi: 10.1093/hmg/ddp166
-
(2009)
Hum. Mol. Genet
, vol.18
, pp. 2483-2494
-
-
Koga, M.1
Ishiguro, H.2
Yazaki, S.3
Horiuchi, Y.4
Arai, M.5
Niizato, K.6
-
50
-
-
2942731425
-
CBP histone acetyltrans-ferase activity is a critical component of memory consolidation
-
Korzus, E., Rosenfeld, M. G., and Mayford, M. (2004). CBP histone acetyltrans-ferase activity is a critical component of memory consolidation. Neuron 42, 961-972. doi: 10.1016/j.neuron.2004.06.002
-
(2004)
Neuron
, vol.42
, pp. 961-972
-
-
Korzus, E.1
Rosenfeld, M.G.2
Mayford, M.3
-
51
-
-
38549119844
-
Bypassing the requirements for epigenetic modifications in gene transcription by increasing enhancer strength
-
Koutroubas, G., Merika, M., and Thanos, D. (2008). Bypassing the requirements for epigenetic modifications in gene transcription by increasing enhancer strength. Mol. Cell. Biol. 28, 926-938. doi: 10.1128/MCB.01344-07
-
(2008)
Mol. Cell. Biol
, vol.28
, pp. 926-938
-
-
Koutroubas, G.1
Merika, M.2
Thanos, D.3
-
52
-
-
0034269239
-
Global role for chromatin remodeling enzymes in mitotic gene expression
-
Krebs, J. E., Fry, C. J., Samuels, M. L., and Peterson, C. L. (2000). Global role for chromatin remodeling enzymes in mitotic gene expression. Cell 102, 587-598. doi: 10.1016/S0092-8674(00)00081-7
-
(2000)
Cell
, vol.102
, pp. 587-598
-
-
Krebs, J.E.1
Fry, C.J.2
Samuels, M.L.3
Peterson, C.L.4
-
53
-
-
0033152279
-
Cell-cycle regulated histone acetylation required for expression of the yeast HO gene
-
Krebs, J. E., Kuo, M. H., Allis, C. D., and Peterson, C. L. (1999). Cell-cycle regulated histone acetylation required for expression of the yeast HO gene. Genes Dev. 13, 1412-1421. doi: 10.1101/gad.13.11.1412
-
(1999)
Genes Dev
, vol.13
, pp. 1412-1421
-
-
Krebs, J.E.1
Kuo, M.H.2
Allis, C.D.3
Peterson, C.L.4
-
54
-
-
84964871806
-
NuRD-dependentDNAmethylationprevents ES cells from accessing a trophectoderm fate
-
Latos, P. A., Helliwell, C., Mosaku, O., Dudzinska, D. A., Stubbs, B., Berdasco, M., et al. (2012). NuRD-dependentDNAmethylationprevents ES cells from accessing a trophectoderm fate. Biol. Open 1, 341-352. doi: 10.1242/bio.2012513
-
(2012)
Biol. Open
, vol.1
, pp. 341-352
-
-
Latos, P.A.1
Helliwell, C.2
Mosaku, O.3
Dudzinska, D.A.4
Stubbs, B.5
Berdasco, M.6
-
55
-
-
34447249019
-
An essential switch in subunit composition of a chromatin remodeling complex during neural development
-
Lessard, J., Wu, J. I., Ranish, J. A., Wan, M., Winslow, M. M., Staahl, B. T., et al. (2007). An essential switch in subunit composition of a chromatin remodeling complex during neural development. Neuron 55, 201-215. doi: 10.1016/j.neuron.2007.06.019
-
(2007)
Neuron
, vol.55
, pp. 201-215
-
-
Lessard, J.1
Wu, J.I.2
Ranish, J.A.3
Wan, M.4
Winslow, M.M.5
Staahl, B.T.6
-
56
-
-
33847070442
-
The role of chromatin during transcription
-
Li, B., Carey, M., and Workman, J. L. (2007). The role of chromatin during transcription. Cell 128, 707-719. doi: 10.1016/j.cell.2007.01.015
-
(2007)
Cell
, vol.128
, pp. 707-719
-
-
Li, B.1
Carey, M.2
Workman, J.L.3
-
57
-
-
80155131102
-
Binding of the JmjC demethylase JARID1B to LSD1/NuRD suppresses angio-genesis and metastasis in breast cancer cells by repressing chemokine CCL14
-
Li, Q., Shi, L., Gui, B., Yu, W., Wang, J., Zhang, D., et al. (2011). Binding of the JmjC demethylase JARID1B to LSD1/NuRD suppresses angio-genesis and metastasis in breast cancer cells by repressing chemokine CCL14. Cancer Res. 71, 6899-6908. doi: 10.1158/0008-5472.CAN-11-1523
-
(2011)
Cancer Res
, vol.71
, pp. 6899-6908
-
-
Li, Q.1
Shi, L.2
Gui, B.3
Yu, W.4
Wang, J.5
Zhang, D.6
-
58
-
-
33644753839
-
Chromatin remodeling by nucleosome disassembly in vitro
-
Lorch, Y., Maier-Davis, B., and Kornberg, R. D. (2006). Chromatin remodeling by nucleosome disassembly in vitro. Proc. Natl. Acad. Sci. U.S.A. 103, 3090-3093. doi: 10.1073/pnas.0511050103
-
(2006)
Proc. Natl. Acad. Sci. U.S.A
, vol.103
, pp. 3090-3093
-
-
Lorch, Y.1
Maier-Davis, B.2
Kornberg, R.D.3
-
59
-
-
15544369061
-
Distinct activities of CHD1 and ACF in ATP-dependent chromatin assembly
-
Lusser, A., Urwin, D. L., and Kadonaga, J. T. (2005). Distinct activities of CHD1 and ACF in ATP-dependent chromatin assembly. Nat. Struct. Mol. Biol. 12, 160-166. doi: 10.1038/nsmb884
-
(2005)
Nat. Struct. Mol. Biol
, vol.12
, pp. 160-166
-
-
Lusser, A.1
Urwin, D.L.2
Kadonaga, J.T.3
-
60
-
-
36348968997
-
Activity-dependent neuroprotective protein constitutes a novel element in the SWI/SNF chromatin remodeling complex
-
Mandel, S., and Gozes, I. (2007). Activity-dependent neuroprotective protein constitutes a novel element in the SWI/SNF chromatin remodeling complex. J. Biol. Chem. 282, 34448-34456. doi: 10.1074/jbc.M704756200
-
(2007)
J. Biol. Chem
, vol.282
, pp. 34448-34456
-
-
Mandel, S.1
Gozes, I.2
-
61
-
-
55949085986
-
Keeping things quiet: Roles of NuRD and Sin3 co-repressor complexes during mammalian development
-
McDonel, P., Costello, I., and Hendrich, B. (2009). Keeping things quiet: roles of NuRD and Sin3 co-repressor complexes during mammalian development. Int. J. Biochem. Cell Biol. 41, 108-116. doi: 10.1016/j.biocel.2008.07.022
-
(2009)
Int. J. Biochem. Cell Biol
, vol.41
, pp. 108-116
-
-
McDonel, P.1
Costello, I.2
Hendrich, B.3
-
62
-
-
79960075356
-
Adult neural function requires MeCP2
-
McGraw, C. M., Samaco, R. C., and Zoghbi, H. Y. (2011). Adult neural function requires MeCP2. Science 333, 186. doi: 10.1126/science.1206593
-
(2011)
Science
, vol.333
, pp. 186
-
-
McGraw, C.M.1
Samaco, R.C.2
Zoghbi, H.Y.3
-
63
-
-
78651479525
-
HDAC3 is a critical negative regulator of long-term memory formation
-
McQuown, S. C., Barrett, R. M., Matheos, D. P., Post, R. J., Rogge, G. A., Aleng-hat, T., et al. (2011). HDAC3 is a critical negative regulator of long-term memory formation. J. Neurosci. 31, 764-774. doi: 10.1523/JNEUROSCI.5052-10.2011
-
(2011)
J. Neurosci
, vol.31
, pp. 764-774
-
-
McQuown, S.C.1
Barrett, R.M.2
Matheos, D.P.3
Post, R.J.4
Rogge, G.A.5
Aleng-Hat, T.6
-
64
-
-
79958008166
-
HDAC3 and the molecular brake pad hypothesis
-
McQuown, S. C., and Wood, M. A. (2011). HDAC3 and the molecular brake pad hypothesis. Neurobiol. Learn. Mem. 96, 27-34. doi: 10.1016/j.nlm.2011.04.005
-
(2011)
Neurobiol. Learn. Mem
, vol.96
, pp. 27-34
-
-
McQuown, S.C.1
Wood, M.A.2
-
65
-
-
0035313726
-
Enhanceosomes
-
Merika, M., and Thanos, D. (2001). Enhanceosomes. Curr. Opin. Genet. Dev 11, 205-208. doi: 10.1016/S0959-437X(00)00180-5
-
(2001)
Curr. Opin. Genet. Dev
, vol.11
, pp. 205-208
-
-
Merika, M.1
Thanos, D.2
-
66
-
-
0031604766
-
Recruitment of CBP/p300 by the IFN beta enhanceosome is required for synergistic activation oftranscription
-
Merika, M., Williams, A. J., Chen, G., Collins, T., and Thanos, D. (1998). Recruitment of CBP/p300 by the IFN beta enhanceosome is required for synergistic activation oftranscription. Mol. Cell 1,277-287. doi: 10.1016/S1097-2765(00)80028-3
-
(1998)
Mol. Cell
, vol.1
, pp. 277-287
-
-
Merika, M.1
Williams, A.J.2
Chen, G.3
Collins, T.4
Thanos, D.5
-
67
-
-
33646856673
-
SWI/SNF binding to the HO promoter requires histone acetylation and stimulates TATA-binding protein recruitment
-
Mitra, D., Parnell, E. J., Landon, J. W., Yu, Y., and Stillman, D. J. (2006). SWI/SNF binding to the HO promoter requires histone acetylation and stimulates TATA-binding protein recruitment. Mol. Cell. Biol. 26, 4095-4110. doi: 10.1128/MCB.01849-05
-
(2006)
Mol. Cell. Biol
, vol.26
, pp. 4095-4110
-
-
Mitra, D.1
Parnell, E.J.2
Landon, J.W.3
Yu, Y.4
Stillman, D.J.5
-
68
-
-
84908686761
-
Numerous BAF complex genes are mutated in Coffin-Siris syndrome
-
Miyake, N., Tsurusaki, Y., and Matsumoto, N. (2014). Numerous BAF complex genes are mutated in Coffin-Siris syndrome. Am. J. Med. Genet. C Semin. Med. Genet. 166C, 257-261. doi: 10.1002/ajmg.c.31406
-
(2014)
Am. J. Med. Genet. C Semin. Med. Genet
, vol.166C
, pp. 257-261
-
-
Miyake, N.1
Tsurusaki, Y.2
Matsumoto, N.3
-
69
-
-
0023182563
-
Transcriptional regulation
-
Nasmyth, K., and Shore, D. (2011). Transcriptional regulation. Science 237, 1162-1170. doi: 10.1126/science.3306917
-
(2011)
Science
, vol.237
, pp. 1162-1170
-
-
Nasmyth, K.1
Shore, D.2
-
70
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
Neale, B. M., Kou, Y., Liu, L., Ma'ayan, A., Samocha, K. E., Sabo, A., et al. (2012). Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485,242-245. doi: 10.1038/nature11011
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'ayan, A.4
Samocha, K.E.5
Sabo, A.6
-
71
-
-
0027275531
-
An unusual syndrome with mental retardation and sparse hair
-
Nicolaides, P., and Baraitser, M. (1993). An unusual syndrome with mental retardation and sparse hair. Clin. Dysmorphol. 2, 232-236
-
(1993)
Clin. Dysmorphol
, vol.2
, pp. 232-236
-
-
Nicolaides, P.1
Baraitser, M.2
-
72
-
-
79956294419
-
Reduced transcript expression of genes affected by inherited and de novo CNVs in autism
-
Nord, A. S., Roeb, W., Dickel, D. E., Walsh, T., Kusenda, M., O'Connor, K. L., et al. (2011). Reduced transcript expression of genes affected by inherited and de novo CNVs in autism. Eur. J. Hum. Genet. 19, 727-731. doi: 10.1038/ejhg.2011.24
-
(2011)
Eur. J. Hum. Genet
, vol.19
, pp. 727-731
-
-
Nord, A.S.1
Roeb, W.2
Dickel, D.E.3
Walsh, T.4
Kusenda, M.5
O'connor, K.L.6
-
73
-
-
0033018277
-
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: Implications for a dominant-negative mechanism
-
Oike, Y., Hata, A., Mamiya, T., Kaname, T., Noda, Y., Suzuki, M., et al. (1999). Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism. Hum. Mol. Genet. 8, 387-396. doi: 10.1093/hmg/8.3.387
-
(1999)
Hum. Mol. Genet
, vol.8
, pp. 387-396
-
-
Oike, Y.1
Hata, A.2
Mamiya, T.3
Kaname, T.4
Noda, Y.5
Suzuki, M.6
-
74
-
-
0036791792
-
Identification of a polymorphic, neuron-specific chromatin remodeling complex
-
Olave, I., Wang, W., Xue, Y., Kuo, A., and Crabtree, G. R. (2002). Identification of a polymorphic, neuron-specific chromatin remodeling complex. Genes Dev. 16, 2509-2517. doi: 10.1101/gad.992102
-
(2002)
Genes Dev
, vol.16
, pp. 2509-2517
-
-
Olave, I.1
Wang, W.2
Xue, Y.3
Kuo, A.4
Crabtree, G.R.5
-
75
-
-
0014248150
-
The rubinstein-taybi syndrome
-
Padfield, C. J., Partington, M. W., and Simpson, N. E. (1968). The rubinstein-taybi syndrome, Arch. Dis. Child. 43, 94-101
-
(1968)
Arch. Dis. Child
, vol.43
, pp. 94-101
-
-
Padfield, C.J.1
Partington, M.W.2
Simpson, N.E.3
-
76
-
-
41949113742
-
The enhanceosome
-
Panne, D. (2008). The enhanceosome. Curr. Opin. Struct. Biol. 18, 236-242. doi: 10.1016/j.sbi.2007.12.002
-
(2008)
Curr. Opin. Struct. Biol
, vol.18
, pp. 236-242
-
-
Panne, D.1
-
77
-
-
84889561601
-
Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism
-
Parikshak, N. N., Luo, R., Zhang, A., Won, H., Lowe, J. K., Chandran, V., et al. (2013). Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell 155, 1008-1021. doi: 10.1016/j.cell.2013.10.031
-
(2013)
Cell
, vol.155
, pp. 1008-1021
-
-
Parikshak, N.N.1
Luo, R.2
Zhang, A.3
Won, H.4
Lowe, J.K.5
Chandran, V.6
-
78
-
-
84894260092
-
Epigenetic mechanisms of Rubinstein-Taybi syndrome
-
Park, E., Kim, Y., Ryu, H., Kowall, N. W., Lee, J., and Ryu, H. (2014). Epigenetic mechanisms of Rubinstein-Taybi syndrome. Neuromolecular Med. 16, 16-24. doi: 10.1007/s12017-013-8285-3
-
(2014)
Neuromolecular Med
, vol.16
, pp. 16-24
-
-
Park, E.1
Kim, Y.2
Ryu, H.3
Kowall, N.W.4
Lee, J.5
Ryu, H.6
-
79
-
-
0036173140
-
BAF53 forms distinct nuclear complexes and functions as a critical c-Myc-interacting nuclear cofactor for oncogenic transformation
-
Park, J., Wood, M. A., and Cole, M. D. (2002). BAF53 forms distinct nuclear complexes and functions as a critical c-Myc-interacting nuclear cofactor for oncogenic transformation. Mol. Cell. Biol. 22, 1307-1316. doi: 10.1128/MCB.22.5.1307-1316.2002
-
(2002)
Mol. Cell. Biol
, vol.22
, pp. 1307-1316
-
-
Park, J.1
Wood, M.A.2
Cole, M.D.3
-
80
-
-
70349645266
-
Ageing-related chromatin defects through loss of the NURD complex
-
Pegoraro, G., Kubben, N., Wickert, U., Göhler, H., Hoffmann, K., and Misteli, T. (2009). Ageing-related chromatin defects through loss of the NURD complex. Nat. CellBiol. 11, 1261-1267. doi: 10.1038/ncb1971
-
(2009)
Nat. Cellbiol
, vol.11
, pp. 1261-1267
-
-
Pegoraro, G.1
Kubben, N.2
Wickert, U.3
Göhler, H.4
Hoffmann, K.5
Misteli, T.6
-
81
-
-
0029022770
-
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
-
Petrif, F., Giles, R., and Dauwerse, H. (1995). Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Lett. Nat. 376, 348-351. doi: 10.1038/376348a0
-
(1995)
Lett. Nat
, vol.376
, pp. 348-351
-
-
Petrif, F.1
Giles, R.2
Dauwerse, H.3
-
82
-
-
0030881740
-
Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression
-
Pollard, K. J., and Peterson, C. L. (1997). Role for ADA/GCN5 products in antagonizing chromatin-mediated transcriptional repression. Mol. Cell. Biol. 17, 6212-6222
-
(1997)
Mol. Cell. Biol
, vol.17
, pp. 6212-6222
-
-
Pollard, K.J.1
Peterson, C.L.2
-
83
-
-
84857427738
-
Chromatin and transcription in yeast
-
Rando, O. J., and Winston, F. (2012). Chromatin and transcription in yeast. Genetics 190, 351-387. doi: 10.1534/genetics.111.132266
-
(2012)
Genetics
, vol.190
, pp. 351-387
-
-
Rando, O.J.1
Winston, F.2
-
84
-
-
77957853227
-
Drosophila transcription factor Tramtrack69 binds MEP1 to recruit the chromatin remodeler NuRD
-
Reddy, B. A., Bajpe, P. K., Bassett, A., Moshkin, Y. M., Kozhevnikova, E., Bezstarosti, K., et al. (2010). Drosophila transcription factor Tramtrack69 binds MEP1 to recruit the chromatin remodeler NuRD. Mol. Cell. Biol. 30, 5234-5244. doi: 10.1128/MCB.00266-10
-
(2010)
Mol. Cell. Biol
, vol.30
, pp. 5234-5244
-
-
Reddy, B.A.1
Bajpe, P.K.2
Bassett, A.3
Moshkin, Y.M.4
Kozhevnikova, E.5
Bezstarosti, K.6
-
85
-
-
0014011176
-
On a unusual brain atrophy syndrome in hyperammonemia in childhood
-
Rett, A. (1966). On a unusual brain atrophy syndrome in hyperammonemia in childhood. Wien. Med. Wochenschr. 116, 723-726
-
(1966)
Wien. Med. Wochenschr
, vol.116
, pp. 723-726
-
-
Rett, A.1
-
86
-
-
84856431427
-
NuRD-mediated deacetylation of H3K27 facilitates recruitment of Polycomb Repressive Complex 2 to direct gene repression
-
Reynolds, N., Salmon-Divon, M., Dvinge, H., Hynes-Allen, A., Balasooriya, G., Leaford, D., et al. (2011). NuRD-mediated deacetylation of H3K27 facilitates recruitment of Polycomb Repressive Complex 2 to direct gene repression. EMBO J. 31, 593-605. doi: 10.1038/emboj.2011.431
-
(2011)
EMBO J
, vol.31
, pp. 593-605
-
-
Reynolds, N.1
Salmon-Divon, M.2
Dvinge, H.3
Hynes-Allen, A.4
Balasooriya, G.5
Leaford, D.6
-
87
-
-
73649208151
-
Broad thumbs and toes and facial abnormalities
-
Rubinstein, J. H., and Taybi, H. (1963). Broad thumbs and toes and facial abnormalities. JAMA 105, 588-608. doi: 10.1001/archpedi.1963.02080040590010
-
(1963)
JAMA
, vol.105
, pp. 588-608
-
-
Rubinstein, J.H.1
Taybi, H.2
-
88
-
-
84862830331
-
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome
-
Santen, G. W. E., Aten, E., Sun, Y., Almomani, R., Gilissen, C., Nielsen, M., et al. (2012a). Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. Nat. Genet. 44, 379-380. doi: 10.1038/ng.2217
-
(2012)
Nat. Genet
, vol.44
, pp. 379-380
-
-
Santen, G.1
Aten, E.2
Sun, Y.3
Almomani, R.4
Gilissen, C.5
Nielsen, M.6
-
89
-
-
84885422201
-
Coffin-Siris syndrome and the BAF complex: Genotype-phenotype study in 63 patients
-
Santen, G. W. E., Aten, E., Vulto-van Silfhout, A. T., Pottinger, C., van Bon, B. W. M., van Minderhout, I. J. H. M., et al. (2013). Coffin-Siris syndrome and the BAF complex: genotype-phenotype study in 63 patients. Hum. Mutat. 34, 1519-1528. doi: 10.1002/humu.22394
-
(2013)
Hum. Mutat
, vol.34
, pp. 1519-1528
-
-
Santen, G.1
Aten, E.2
Vulto-Van Silfhout, A.T.3
Pottinger, C.4
Van Bon, B.5
Van Minderhout, I.6
-
90
-
-
84868344895
-
SWI/SNF complex in disorder switching from malignancies to intellectual disability
-
Santen, G. W. E., Kriek, M., and van Attikum, H. (2012b). SWI/SNF complex in disorder switching from malignancies to intellectual disability. Epigenetics 7, 1219-1224. doi: 10.4161/epi.22299
-
(2012)
Epigenetics
, vol.7
, pp. 1219-1224
-
-
Santen, G.1
Kriek, M.2
Van Attikum, H.3
-
91
-
-
74549220013
-
Ephexin1 is required for structural maturation and neurotransmission at the neuromus-cularjunction
-
Shi, L., Butt, B., Ip, F. C. F., Dai, Y., Jiang, L., Yung, W. H., et al. (2010a). Ephexin1 is required for structural maturation and neurotransmission at the neuromus-cularjunction. Neuron 65, 204-216. doi: 10.1016/j.neuron.2010.01.012
-
(2010)
Neuron
, vol.65
, pp. 204-216
-
-
Shi, L.1
Butt, B.2
Ip, F.3
Dai, Y.4
Jiang, L.5
Yung, W.H.6
-
92
-
-
84862758818
-
Multiple roles of the Rho GEF ephexin1 in synapse remodeling
-
Shi, L., Fu, A. K., and Ip, N. Y. (2010b). Multiple roles of the Rho GEF ephexin1 in synapse remodeling. Commun. Integr. Biol. 3, 622-624. doi: 10.4161/cib.3.6.13481
-
(2010)
Commun. Integr. Biol
, vol.3
, pp. 622-624
-
-
Shi, L.1
Fu, A.K.2
Ip, N.Y.3
-
93
-
-
24944535335
-
Regulation of LSD1 histone demethylase activity by its associated factors
-
Shi, Y. J., Matson, C., Lan, F., Iwase, S., Baba, T., and Shi, Y. (2005). Regulation of LSD1 histone demethylase activity by its associated factors. Mol. Cell 19, 857-864. doi: 10.1016/j.molcel.2005.08.027
-
(2005)
Mol. Cell
, vol.19
, pp. 857-864
-
-
Shi, Y.J.1
Matson, C.2
Lan, F.3
Iwase, S.4
Baba, T.5
Shi, Y.6
-
94
-
-
84887404456
-
Creating a neural specific chromatin landscape by npBAF and nBAF complexes
-
Staahl, B. T., and Crabtree, G. R. (2013). Creating a neural specific chromatin landscape by npBAF and nBAF complexes. Curr. Opin. Neurobiol. 23, 903-913. doi: 10.1016/j.conb.2013.09.003
-
(2013)
Curr. Opin. Neurobiol
, vol.23
, pp. 903-913
-
-
Staahl, B.T.1
Crabtree, G.R.2
-
95
-
-
67249137941
-
Modulation of long-term memory for object recognition via HDAC inhibition
-
Stefanko, D. P., Barrett, R. M., Ly, A. R., Reolon, G. K., and Wood, M. A. (2009). Modulation of long-term memory for object recognition via HDAC inhibition. Proc. Natl. Acad. Sci. U.S.A. 106, 9447-9452. doi: 10.1073/pnas.0903964106
-
(2009)
Proc. Natl. Acad. Sci. U.S.A
, vol.106
, pp. 9447-9452
-
-
Stefanko, D.P.1
Barrett, R.M.2
Ly, A.R.3
Reolon, G.K.4
Wood, M.A.5
-
96
-
-
0021659727
-
Five SWI genes are required for expression of the HO gene in yeast
-
Stern, M., Jensen, R., and Herskowitz, I. (1984). Five SWI genes are required for expression of the HO gene in yeast. J. Mol. Biol. 178, 853-868. doi: 10.1016/0022-2836(84)90315-2
-
(1984)
J. Mol. Biol
, vol.178
, pp. 853-868
-
-
Stern, M.1
Jensen, R.2
Herskowitz, I.3
-
97
-
-
84874020298
-
New CBP mutations in Brazilian patients with Rubinstein-Taybi syndrome
-
Suzuki, K. T., Torres, L. C., Sugayama, S. M. M., Aguiar Alves, B. D. C., Moreira-Filho, C. A., and Carneiro-Sampaio, M. (2013). New CBP mutations in Brazilian patients with Rubinstein-Taybi syndrome. Clin. Genet. 83, 291-292. doi: 10.1111/j.1399-0004.2012.01894.x
-
(2013)
Clin. Genet
, vol.83
, pp. 291-292
-
-
Suzuki, K.T.1
Torres, L.C.2
Sugayama, S.3
Aguiar Alves, B.4
Moreira-Filho, C.A.5
Carneiro-Sampaio, M.6
-
98
-
-
0030923585
-
Abnormal skeletal patterning in embryos lacking a single Cbp allele: A partial similarity with Rubinstein-Taybi syndrome
-
Tanaka, Y., Naruse, I., Maekawa, T., Masuya, H., Shiroishi, T., and Ishii, S. (1997). Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein-Taybi syndrome. Proc. Natl. Acad. Sci. U.S.A. 94, 10215-10220. doi: 10.1073/pnas.94.19.10215
-
(1997)
Proc. Natl. Acad. Sci. U.S.A
, vol.94
, pp. 10215-10220
-
-
Tanaka, Y.1
Naruse, I.2
Maekawa, T.3
Masuya, H.4
Shiroishi, T.5
Ishii, S.6
-
99
-
-
77954218952
-
Structure and function of SWI/SNF chromatin remodeling complexes and mechanistic implications for transcription
-
Tang, L., Nogales, E., and Ciferri, C. (2010). Structure and function of SWI/SNF chromatin remodeling complexes and mechanistic implications for transcription. Prog. Biophys. Mol. Biol. 102, 122-128. doi: 10.1016/j.pbiomolbio.2010.05.001
-
(2010)
Prog. Biophys. Mol. Biol
, vol.102
, pp. 122-128
-
-
Tang, L.1
Nogales, E.2
Ciferri, C.3
-
100
-
-
73049098277
-
Predicting nucleosome positions on the DNA: Combining intrinsic sequence preferences and remodeler activities
-
Teif, V. B., and Rippe, K. (2009). Predicting nucleosome positions on the DNA: combining intrinsic sequence preferences and remodeler activities. Nucleic Acids Res. 37, 5641-5655. doi: 10.1093/nar/gkp610
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 5641-5655
-
-
Teif, V.B.1
Rippe, K.2
-
101
-
-
0029617947
-
Virus induction ofhuman IFN^ gene expression requires the assembly of an enhanceosome
-
Thanos, D., and Maniatis, T. (1995). Virus induction ofhuman IFN^ gene expression requires the assembly of an enhanceosome. Cell 83, 1091-1100. doi: 10.1016/0092-8674(95)90136-1
-
(1995)
Cell
, vol.83
, pp. 1091-1100
-
-
Thanos, D.1
Maniatis, T.2
-
102
-
-
0035013739
-
MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin
-
Trappe, R., Laccone, F., Cobilanschi, J., Meins, M., Huppke, P., Hanefeld, F., et al. (2001). MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin. Am. J. Hum. Genet. 68, 1093-1101. doi: 10.1086/320109
-
(2001)
Am. J. Hum. Genet
, vol.68
, pp. 1093-1101
-
-
Trappe, R.1
Laccone, F.2
Cobilanschi, J.3
Meins, M.4
Huppke, P.5
Hanefeld, F.6
-
103
-
-
84859427243
-
Mutations affectingcomponents ofthe SWI/SNF complexcause Coffin-Siris syndrome
-
Tsurusaki, Y., Okamoto, N., Ohashi, H., Kosho, T., Imai, Y., Hibi-Ko, Y., et al. (2012). Mutations affectingcomponents ofthe SWI/SNF complexcause Coffin-Siris syndrome. Nat. Genet. 44, 376-378. doi: 10.1038/ng.2219
-
(2012)
Nat. Genet
, vol.44
, pp. 376-378
-
-
Tsurusaki, Y.1
Okamoto, N.2
Ohashi, H.3
Kosho, T.4
Imai, Y.5
Hibi-Ko, Y.6
-
104
-
-
84899480136
-
Coffin-Siris syndromeis a SWI/SNF complexdisorder
-
Tsurusaki, Y., Okamoto, N., Ohashi, H., Mizuno, S., Matsumoto, N., Makita, Y., et al. (2014). Coffin-Siris syndromeis a SWI/SNF complexdisorder. Clin. Genet. 85, 548-554. doi: 10.1111/cge.12225
-
(2014)
Clin. Genet
, vol.85
, pp. 548-554
-
-
Tsurusaki, Y.1
Okamoto, N.2
Ohashi, H.3
Mizuno, S.4
Matsumoto, N.5
Makita, Y.6
-
105
-
-
0033527448
-
The nuclear factor-kappaB engages CBP/p300 and histone acetyltransferase activity for transcriptional activation of the interleukin-6 gene promoter
-
Vanden Berghe, W., De Bosscher, K., Boone, E., Plaisance, S., and Haege-man, G. (1999). The nuclear factor-kappaB engages CBP/p300 and histone acetyltransferase activity for transcriptional activation of the interleukin-6 gene promoter. J. Biol. Chem. 274, 32091-32098. doi: 10.1074/jbc.274.45.32091
-
(1999)
J. Biol. Chem
, vol.274
, pp. 32091-32098
-
-
Vanden Berghe, W.1
De Bosscher, K.2
Boone, E.3
Plaisance, S.4
Haege-Man, G.5
-
106
-
-
84908641727
-
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism
-
Vandeweyer, G., Helsmoortel, C., Van Dijck, A., Vulto-van Silfhout, A. T., Coe, B. P., Bernier, R., et al. (2014). The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. Am. J. Med. Genet. C Semin. Med. Genet. 166C, 315-326. doi: 10.1002/ajmg.c.31413
-
(2014)
Am. J. Med. Genet. C Semin. Med. Genet
, vol.166C
, pp. 315-326
-
-
Vandeweyer, G.1
Helsmoortel, C.2
Van Dijck, A.3
Vulto-Van Silfhout, A.T.4
Coe, B.P.5
Bernier, R.6
-
107
-
-
0041385955
-
Models for chromatin remodeling: A critical comparison
-
Van Holde, K., and Yager, T. (2003). Models for chromatin remodeling: a critical comparison. Biochem. Cell Biol. 81, 169-172. doi: 10.1139/o03-038
-
(2003)
Biochem. Cell Biol
, vol.81
, pp. 169-172
-
-
Van Holde, K.1
Yager, T.2
-
108
-
-
84859423484
-
Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome
-
Van Houdt, J. K. J., Nowakowska, B. A., Sousa, S. B., van Schaik, B. D. C., Seuntjens, E., Avonce, N., et al. (2012). Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome. Nat. Genet. 44, 445-449. doi: 10.1038/ng.1105
-
(2012)
Nat. Genet
, vol.44
, pp. 445-449
-
-
Van Houdt, J.1
Nowakowska, B.A.2
Sousa, S.B.3
Van Schaik, B.4
Seuntjens, E.5
Avonce, N.6
-
109
-
-
0035962662
-
ATP-dependent chromatin remodeling factors: Nucle-osome shuttlers with many missions
-
Varga-weisz, P. (2001). ATP-dependent chromatin remodeling factors: nucle-osome shuttlers with many missions. Oncogene 20, 3076-3085. doi: 10.1038/sj.onc.1204332
-
(2001)
Oncogene
, vol.20
, pp. 3076-3085
-
-
Varga-Weisz, P.1
-
110
-
-
34250026412
-
Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation
-
Vecsey, C. G., Hawk, J. D., Lattal, K. M., Stein, J. M., Fabian, S. A., Attner, M., et al. (2007). Histone deacetylase inhibitors enhance memory and synaptic plasticity via CREB:CBP-dependent transcriptional activation. J. Neurosci. 27, 6128-6140. doi: 10.1523/JNEUROSCI.0296-07.2007
-
(2007)
J. Neurosci
, vol.27
, pp. 6128-6140
-
-
Vecsey, C.G.1
Hawk, J.D.2
Lattal, K.M.3
Stein, J.M.4
Fabian, S.A.5
Attner, M.6
-
111
-
-
70450159836
-
Psychiatric profile in rubinstein-taybi syndrome
-
Verhoeven, W. M. A., Tuinier, S., Kuijpers, H. J. H., Egger, J. I. M., and Brunner, H. G. (2009). Psychiatric profile in rubinstein-taybi syndrome. Psychopathology 43, 63-68. doi: 10.1159/000260045
-
(2009)
Psychopathology
, vol.43
, pp. 63-68
-
-
Verhoeven, W.1
Tuinier, S.2
Kuijpers, H.3
Egger, J.4
Brunner, H.G.5
-
112
-
-
84876903184
-
The neuron-specific chromatin regulatory subunit BAF53b is necessary for synaptic plasticity and memory
-
Vogel-Ciernia, A., Matheos, D. P., Barrett, R.M., Kramâr, E. A., Azzawi, S., Chen, Y., et al. (2013). The neuron-specific chromatin regulatory subunit BAF53b is necessary for synaptic plasticity and memory. Nat. Neurosci. 16, 552-561. doi: 10.1038/nn.3359
-
(2013)
Nat. Neurosci
, vol.16
, pp. 552-561
-
-
Vogel-Ciernia, A.1
Matheos, D.P.2
Barrett, R.M.3
Kramâr, E.A.4
Azzawi, S.5
Chen, Y.6
-
113
-
-
84898853930
-
Neuron-specific chromatin remodeling: A missing link in epigenetic mechanisms underlying synaptic plasticity, memory, and intellectual disability disorders
-
Vogel-Ciernia, A., and Wood, M. A. (2014). Neuron-specific chromatin remodeling: a missing link in epigenetic mechanisms underlying synaptic plasticity, memory, and intellectual disability disorders. Neuropharmacology 80, 18-27. doi: 10.1016/j.neuropharm.2013.10.002
-
(2014)
Neuropharmacology
, vol.80
, pp. 18-27
-
-
Vogel-Ciernia, A.1
Wood, M.A.2
-
114
-
-
0032845039
-
Mi-2 complexcouples DNAmethylation to chromatin remodelling and histone deacetylation
-
Wade, P. A., Gegonne, A., Jones, P. L., Ballestar, E., Aubry, F., and Wolffe, A. P. (1999). Mi-2 complexcouples DNAmethylation to chromatin remodelling and histone deacetylation. Nat. Genet. 23, 62-66
-
(1999)
Nat. Genet
, vol.23
, pp. 62-66
-
-
Wade, P.A.1
Gegonne, A.2
Jones, P.L.3
Ballestar, E.4
Aubry, F.5
Wolffe, A.P.6
-
115
-
-
0032474826
-
A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase
-
Wade, P. A., Jones, P. L., Vermaak, D., and Wolffe, A. P. (1998). A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase. Curr. Biol. 8, 843-846. doi: 10.1016/S0960-9822(98)70328-8
-
(1998)
Curr. Biol
, vol.8
, pp. 843-846
-
-
Wade, P.A.1
Jones, P.L.2
Vermaak, D.3
Wolffe, A.P.4
-
116
-
-
0035875298
-
Mi2, an auto-antigen for dermatomyositis, is an ATP-dependent nucleosome remodeling factor
-
Wang, H. B., and Zhang, Y. (2001). Mi2, an auto-antigen for dermatomyositis, is an ATP-dependent nucleosome remodeling factor. Nucleic Acids Res. 29, 2517-2521. doi: 10.1093/nar/29.12.2517
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 2517-2521
-
-
Wang, H.B.1
Zhang, Y.2
-
117
-
-
74049144071
-
CBP histone acetyltransferase activity regulates embryonic neural differentiation in the normal and rubinstein-taybi syndrome brain
-
Wang, J., Weaver, I. C. G., Gauthier-Fisher, A., Wang, H., He, L., Yeomans, J., et al. (2010). CBP histone acetyltransferase activity regulates embryonic neural differentiation in the normal and rubinstein-taybi syndrome brain. Dev. Cell 18, 114-125. doi: 10.1016/j.devcel.2009.10.023
-
(2010)
Dev. Cell
, vol.18
, pp. 114-125
-
-
Wang, J.1
Weaver, I.2
Gauthier-Fisher, A.3
Wang, H.4
He, L.5
Yeomans, J.6
-
118
-
-
68749108259
-
LSD1 is a subunit of the NuRD complex and targets the metastasis programs in breast cancer
-
Wang, Y., Zhang, H., Chen, Y., Sun, Y., Yang, F., Yu, W., et al. (2009). LSD1 is a subunit of the NuRD complex and targets the metastasis programs in breast cancer. Cell 138, 660-672. doi: 10.1016/j.cell.2009.05.050
-
(2009)
Cell
, vol.138
, pp. 660-672
-
-
Wang, Y.1
Zhang, H.2
Chen, Y.3
Sun, Y.4
Yang, F.5
Yu, W.6
-
119
-
-
84877095979
-
The SWI/SNF chromatin remodeling complex selectively affects multiple aspects of serotonergic neuron differentiation
-
Weinberg, P., Flames, N., Sawa, H., Garriga, G., and Hobert, O. (2013). The SWI/SNF chromatin remodeling complex selectively affects multiple aspects of serotonergic neuron differentiation. Genetics 194, 189-198. doi: 10.1534/genet-ics.112.148742
-
(2013)
Genetics
, vol.194
, pp. 189-198
-
-
Weinberg, P.1
Flames, N.2
Sawa, H.3
Garriga, G.4
Hobert, O.5
-
120
-
-
0033584369
-
Nucleosome mobilization catalysed by the yeast SWI/SNF complex
-
Whitehouse, I., Flaus, A., Cairns, B. R., White, M. F., Workman, J. L., and Owen-Hughes, T. (1999). Nucleosome mobilization catalysed by the yeast SWI/SNF complex. Nature 400, 784-787. doi: 10.1038/23506
-
(1999)
Nature
, vol.400
, pp. 784-787
-
-
Whitehouse, I.1
Flaus, A.2
Cairns, B.R.3
White, M.F.4
Workman, J.L.5
Owen-Hughes, T.6
-
121
-
-
0028060550
-
A striking similarity in the organization ofthe E-selectin and beta interferon gene promoters
-
Whitley, M. Z., Thanos, D., Read, M. A., Maniatis, T., and Collins, T. (1994). A striking similarity in the organization ofthe E-selectin and beta interferon gene promoters. Mol. Cell. Biol. 14, 6464-6475
-
(1994)
Mol. Cell. Biol
, vol.14
, pp. 6464-6475
-
-
Whitley, M.Z.1
Thanos, D.2
Read, M.A.3
Maniatis, T.4
Collins, T.5
-
122
-
-
79959653996
-
SWI/SNF nucleosome remodellers and cancer
-
Wilson, B. G., and Roberts, C. W. M. (2011). SWI/SNF nucleosome remodellers and cancer. Nat. Rev. Cancer 11, 481-492. doi: 10.1038/nrc3068
-
(2011)
Nat. Rev. Cancer
, vol.11
, pp. 481-492
-
-
Wilson, B.G.1
Roberts, C.2
-
123
-
-
84860338936
-
In-frame deletion and missense mutations of the c-terminal helicase domain of SMARCA2 in three patients with nicolaides-baraitser syndrome
-
Wolff, D., Endele, S., Azzarello-Burri, S., Hoyer, J., Zweier, M., Schanze, I., et al. (2012). In-frame deletion and missense mutations of the c-terminal helicase domain of SMARCA2 in three patients with nicolaides-baraitser syndrome. Mol. Syndromol. 2, 237-244. doi: 10.1159/000337323
-
(2012)
Mol. Syndromol
, vol.2
, pp. 237-244
-
-
Wolff, D.1
Endele, S.2
Azzarello-Burri, S.3
Hoyer, J.4
Zweier, M.5
Schanze, I.6
-
124
-
-
17144374869
-
Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity andmemorystorage
-
Wood, M. A., Kaplan, M. P., Park, A., Blanchard, E. J., Oliveira, A. M. M., Lombardi, T. L., et al. (2005). Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity andmemorystorage. Learn.Mem. 12, 111-119. doi: 10.1101/lm.86605
-
(2005)
Learn.Mem
, vol.12
, pp. 111-119
-
-
Wood, M.A.1
Kaplan, M.P.2
Park, A.3
Blanchard, E.J.4
Oliveira, A.5
Lombardi, T.L.6
-
125
-
-
0031707751
-
Alteration of nucleosome structure as a mechanism of transcriptional regulation
-
Workman, J. L., and Kingston, R. E. (1998). Alteration of nucleosome structure as a mechanism of transcriptional regulation. Annu. Rev. Biochem. 67, 545-579. doi: 10.1146/annurev.biochem.67.1.545
-
(1998)
Annu. Rev. Biochem
, vol.67
, pp. 545-579
-
-
Workman, J.L.1
Kingston, R.E.2
-
126
-
-
34748887795
-
Regulation of dendritic development by neuron-specific chromatin remodeling complexes
-
Wu, J. I., Lessard, J., Olave, I. A., Qiu, Z., Ghosh, A., Graef, I. A., et al. (2007). Regulation of dendritic development by neuron-specific chromatin remodeling complexes. Neuron 56, 94-108. doi: 10.1016/j.neuron.2007.08.021
-
(2007)
Neuron
, vol.56
, pp. 94-108
-
-
Wu, J.I.1
Lessard, J.2
Olave, I.A.3
Qiu, Z.4
Ghosh, A.5
Graef, I.A.6
-
127
-
-
0032252209
-
NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities
-
Xue, Y., Wong, J., Moreno, G. T., Young, M. K., Côté, J., and Wang, W. (1998). NURD, a novel complex with both ATP-dependent chromatin-remodeling and histone deacetylase activities. Moï. Cell 2, 851-861. doi: 10.1016/S1097-2765(00)80299-3
-
(1998)
Moï. Cell
, vol.2
, pp. 851-861
-
-
Xue, Y.1
Wong, J.2
Moreno, G.T.3
Young, M.K.4
Côté, J.5
Wang, W.6
-
128
-
-
0033539575
-
Mechanism by which the IFN-beta enhanceosome activates transcription
-
Yie, J., Senger, K., and Thanos, D. (1999). Mechanism by which the IFN-beta enhanceosome activates transcription. Proc. Natl. Acad. Sci. U.S.A. 96, 13108-13113. doi: 10.1073/pnas.96.23.13108
-
(1999)
Proc. Natl. Acad. Sci. U.S.A
, vol.96
, pp. 13108-13113
-
-
Yie, J.1
Senger, K.2
Thanos, D.3
-
129
-
-
79958847065
-
The expanding Mi-2/NuRD complexes: A schematic glance
-
Zhang, Y., and Li, Y. (2010). The expanding Mi-2/NuRD complexes: a schematic glance. Proteomics Insights 3, 79-109. doi:10.4137/PRI.S6329
-
(2010)
Proteomics Insights
, vol.3
, pp. 79-109
-
-
Zhang, Y.1
Li, Y.2
-
130
-
-
0033180082
-
Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation
-
Zhang, Y., Ng, H. H., Erdjument-Bromage, H., Tempst, P., Bird, A., and Reinberg, D. (1999). Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation. Genes Dev. 13, 1924-1935. doi: 10.1101/gad.13.15.1924
-
(1999)
Genes Dev
, vol.13
, pp. 1924-1935
-
-
Zhang, Y.1
Ng, H.H.2
Erdjument-Bromage, H.3
Tempst, P.4
Bird, A.5
Reinberg, D.6
-
131
-
-
33947638345
-
DNA translocation and loop formation mechanism of chromatin remodeling by SWI/SNF and RSC
-
Zhang, Y., Smith, C. L., Saha, A., Grill, S. W., Mihardja, S., Smith, S. B., et al. (2006). DNA translocation and loop formation mechanism of chromatin remodeling by SWI/SNF and RSC. Mol. Cell 24, 559-568. doi: 10.1016/j.molcel.2006.10.025
-
(2006)
Mol. Cell
, vol.24
, pp. 559-568
-
-
Zhang, Y.1
Smith, C.L.2
Saha, A.3
Grill, S.W.4
Mihardja, S.5
Smith, S.B.6
-
132
-
-
0032567080
-
Rapid and phosphoinositol-dependent binding of the SWI/SNF-like BAF complex to chromatin after T lymphocyte receptor signaling
-
Zhao, K., Wang, W., Rando, O. J., Xue, Y., Swiderek, K., Kuo, A., et al. (1998). Rapid and phosphoinositol-dependent binding of the SWI/SNF-like BAF complex to chromatin after T lymphocyte receptor signaling. Cell 95, 625-636. doi: 10.1016/S0092-8674(00)81633-5
-
(1998)
Cell
, vol.95
, pp. 625-636
-
-
Zhao, K.1
Wang, W.2
Rando, O.J.3
Xue, Y.4
Swiderek, K.5
Kuo, A.6
-
133
-
-
33744916194
-
Chromatin remodeling by ISW2 and SWI/SNF requires DNA translocation inside the nucleosome
-
Zofall, M., Persinger, J., Kassabov, S. R., and Bartholomew, B. (2006). Chromatin remodeling by ISW2 and SWI/SNF requires DNA translocation inside the nucleosome. Nat. Struct. Mol. Biol. 13, 339-346. doi: 10.1038/nsmb1071
-
(2006)
Nat. Struct. Mol. Biol
, vol.13
, pp. 339-346
-
-
Zofall, M.1
Persinger, J.2
Kassabov, S.R.3
Bartholomew, B.4
|