-
1
-
-
33646869229
-
Chromatin remodelling in mammalian differentiation: Lessons from ATP-dependent remodellers
-
DOI 10.1038/nrg1882, PII N1882
-
de la Serna, I. L., Y. Ohkawa & A. N. Imbalzano: Chromatin remodelling in mammalian differentiation: lessons from ATP-dependent remodellers. Nat Rev Genet, 7, 461-73 (2006) (Pubitemid 43780489)
-
(2006)
Nature Reviews Genetics
, vol.7
, Issue.6
, pp. 461-473
-
-
De La Serna, I.L.1
Ohkawa, Y.2
Imbalzano, A.N.3
-
2
-
-
0037010187
-
The complexity of chromatin remodeling and its links to cancer
-
DOI 10.1016/S0304-419X(02)00067-7, PII S0304419X02000677
-
Neely, K. E. & J. L. Workman: The complexity of chromatin remodeling and its links to cancer. Biochim Biophys Acta, 1603, 19-29. (2002) (Pubitemid 35264614)
-
(2002)
Biochimica et Biophysica Acta - Reviews on Cancer
, vol.1603
, Issue.1
, pp. 19-29
-
-
Neely, K.E.1
Workman, J.L.2
-
3
-
-
1542358189
-
Multiple roles for ISWI in transcription, chromosome organization and DNA replication
-
DOI 10.1016/j.bbaexp.2003.09.018, PII S0167478103002835
-
Corona, D. F. V. & J. W. Tamkun: Multiple roles for ISWI in transcription, chromosome organization and DNA replication. Biochim Biophys Acta (BBA) - Gene Structure and Expression Chromatin structure and function, 1677, 113-119 (2004) (Pubitemid 38327095)
-
(2004)
Biochimica et Biophysica Acta - Gene Structure and Expression
, vol.1677
, Issue.1-3
, pp. 113-119
-
-
Corona, D.F.V.1
Tamkun, J.W.2
-
4
-
-
17444368701
-
Histone modifying and chromatin remodelling enzymes in cancer and dysplastic syndromes
-
DOI 10.1093/hmg/ddi106
-
Gibbons, R. J.: Histone modifying and chromatin remodelling enzymes in cancer and dysplastic syndromes. Hum Mol Genet, 14 Spec No 1, R85-92 (2005) (Pubitemid 40542624)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.SPEC. ISS. 1
-
-
Gibbons, R.J.1
-
5
-
-
33645279534
-
Epigenetics and cancer: Altered chromatin remodeling via Snf5 loss leads to aberrant cell cycle regulation
-
Sansam, C. G. & C. W. Roberts: Epigenetics and cancer: altered chromatin remodeling via Snf5 loss leads to aberrant cell cycle regulation. Cell Cycle, 5, 621-4 (2006)
-
(2006)
Cell Cycle
, vol.5
, pp. 621-624
-
-
Sansam, C.G.1
Roberts, C.W.2
-
6
-
-
35848958821
-
Chromatin remodeling: Insights and intrigue from single-molecule studies
-
DOI 10.1038/nsmb1333, PII NSMB1333
-
Cairns, B. R.: Chromatin remodeling: insights and intrigue from single-molecule studies. Nat Struct Mol Biol, 14, 989-996 (2007) (Pubitemid 350060341)
-
(2007)
Nature Structural and Molecular Biology
, vol.14
, Issue.11
, pp. 989-996
-
-
Cairns, B.R.1
-
7
-
-
0035839136
-
Translating the histone code
-
DOI 10.1126/science.1063127
-
Jenuwein, T. & C. D. Allis: Translating the histone code. Science, 293, 1074-80 (2001) (Pubitemid 32758077)
-
(2001)
Science
, vol.293
, Issue.5532
, pp. 1074-1080
-
-
Jenuwein, T.1
Allis, C.D.2
-
8
-
-
33745698871
-
Neural mechanisms in Williams syndrome: A unique window to genetic influences on cognition and behaviour
-
Meyer-Lindenberg, A., C. B. Mervis & K. F. Berman: Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour. Nat Rev Neurosci, 7, 380-93 (2006)
-
(2006)
Nat Rev Neurosci
, vol.7
, pp. 380-393
-
-
Meyer-Lindenberg, A.1
Mervis, C.B.2
Berman, K.F.3
-
9
-
-
25444442079
-
Chromatin remodeling by WSTF-ISWI at the replication site: Opening a window of opportunity for epigenetic inheritance?
-
Poot, R. A., L. Bozhenok, D. L. van den Berg, N. Hawkes & P. D. Varga-Weisz: Chromatin remodeling by WSTF-ISWI at the replication site: opening a window of opportunity for epigenetic inheritance? Cell Cycle, 4, 543-6 (2005) (Pubitemid 41359776)
-
(2005)
Cell Cycle
, vol.4
, Issue.4
, pp. 543-546
-
-
Poot, R.A.1
Bozhenok, L.2
Van Den Berg, D.L.C.3
Hawkes, N.4
Varga-Weisz, P.D.5
-
10
-
-
34547774654
-
Different epigenetic layers engage in complex crosstalk to define the epigenetic state of mammalian rRNA genes
-
DOI 10.1093/hmg/ddm020, Cancer Genetics
-
Grummt, I.: Different epigenetic layers engage in complex crosstalk to define the epigenetic state of mammalian rRNA genes. Hum Mol Genet, 16 Spec No 1, R21-7 (2007) (Pubitemid 47241840)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.R1
-
-
Grummt, I.1
-
11
-
-
0031706111
-
Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of drosophila ISWI
-
Aihara, T., Y. Miyoshi, K. Koyama, M. Suzuki, E. Takahashi, M. Monden & Y. Nakamura: Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI. Cytogenet Cell Genet, 81, 191-3 (1998) (Pubitemid 28431939)
-
(1998)
Cytogenetics and Cell Genetics
, vol.81
, Issue.3-4
, pp. 191-193
-
-
Aihara, T.1
Miyoshi, Y.2
Koyama, K.3
Suzuki, M.4
Takahashi, E.5
Monden, M.6
Nakamura, Y.7
-
12
-
-
0035007781
-
Cloning and characterization of the murine Imitation S witch (ISWI) genes: Differential expression patterns suggest distinct developmental roles for Snf2h and Snf2l
-
DOI 10.1046/j.1471-4159.2001.00324.x
-
Lazzaro, M. A. & D. J. Picketts: Cloning and characterization of the murine Imitation Switch (ISWI) genes: differential expression patterns suggest distinctdevelopmental roles for Snf2h and Snf2l. J Neurochem, 77, 1145-56. (2001) (Pubitemid 32467069)
-
(2001)
Journal of Neurochemistry
, vol.77
, Issue.4
, pp. 1145-1156
-
-
Lazzaro, M.A.1
Picketts, D.J.2
-
13
-
-
0036565656
-
WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci
-
DOI 10.1093/emboj/21.9.2231
-
Bozhenok, L., P. A. Wade & P. Varga-Weisz: WSTFISWI chromatin remodeling complex targets heterochromatic replication foci. EMBO J, 21, 2231-41. (2002) (Pubitemid 34516782)
-
(2002)
EMBO Journal
, vol.21
, Issue.9
, pp. 2231-2241
-
-
Bozhenok, L.1
Wade, P.A.2
Varga-Weisz, P.3
-
14
-
-
0037158744
-
Dynamics of ATP-dependent chromatin assembly by ACF
-
Fyodorov, D. V. & J. T. Kadonaga: Dynamics of ATPdependent chromatin assembly by ACF. Nature, 418, 897-900. (2002) (Pubitemid 34966311)
-
(2002)
Nature
, vol.418
, Issue.6900
, pp. 897-900
-
-
Fyodorov, D.V.1
Kadonaga, J.T.2
-
16
-
-
34247641746
-
Modifiers of epigenetic reprogramming show paternal effects in the mouse
-
DOI 10.1038/ng2031, PII NG2031
-
Chong, S., N. Vickaryous, A. Ashe, N. Zamudio, N. Youngson, S. Hemley, T. Stopka, A. Skoultchi, J. Matthews, H. S. Scott, D. de Kretser, M. O'Bryan, M. Blewitt & E. Whitelaw: Modifiers of epigenetic reprogramming show paternal effects in the mouse. Nat Genet, 39, 614-622 (2007) (Pubitemid 46676114)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 614-622
-
-
Chong, S.1
Vickaryous, N.2
Ashe, A.3
Zamudio, N.4
Youngson, N.5
Hemley, S.6
Stopka, T.7
Skoultchi, A.8
Matthews, J.9
Scott, H.S.10
De Kretser, D.11
O'Bryan, M.12
Blewitt, M.13
Whitelaw, E.14
-
17
-
-
4444239112
-
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
-
DOI 10.1038/ng1407
-
Vissers, L. E., C. M. van Ravenswaaij, R. Admiraal, J. A. Hurst, B. B. de Vries, I. M. Janssen, W. A. van der Vliet, E. H. Huys, P. J. de Jong, B. C. Hamel, E. F. Schoenmakers, H. G. Brunner, J. A. Veltman & A. G. van Kessel: Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet, 36, 955-7 (2004) (Pubitemid 39167490)
-
(2004)
Nature Genetics
, vol.36
, Issue.9
, pp. 955-957
-
-
Vissers, L.E.L.M.1
Van Ravenswaaij, C.M.A.2
Admiraal, R.3
Hurst, J.A.4
De Vries, B.B.A.5
Janssen, I.M.6
Van Der Vliet, W.A.7
Huys, E.H.L.P.G.8
De Jong, P.J.9
Hamel, B.C.J.10
Schoenmakers, E.F.P.M.11
Brunner, H.G.12
Veltman, J.A.13
Van Kessel, A.G.14
-
18
-
-
37349090075
-
Molecular analysis of the CHD7 gene in CHARGE syndrome: Identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions
-
DOI 10.1097/GIM.0b013e318156e68e, PII 0012581720071000000004
-
Vuorela, P., S. Ala-Mello, C. Saloranta, M. Penttinen, M. Poyhonen, K. Huoponen, W. Borozdin, B. Bausch, E. M. Botzenhart, C. Wilhelm, H. Kaariainen & J. Kohlhase: Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. Genet Med, 9, 690-4 (2007) (Pubitemid 350287154)
-
(2007)
Genetics in Medicine
, vol.9
, Issue.10
, pp. 690-694
-
-
Vuorela, P.1
Ala-Mello, S.2
Saloranta, C.3
Penttinen, M.4
Poyhonen, M.5
Huoponen, K.6
Borozdin, W.7
Bausch, B.8
Botzenhart, E.M.9
Wilhelm, C.10
Kaariainen, H.11
Kohlhase, J.12
-
19
-
-
37549039003
-
Familial CHARGE syndrome and the CHD7 gene: A recurrent missense mutation intrafamilial recurrence and variability
-
Jongmans, M. C., L. H. Hoefsloot, K. P. van der Donk, R. J. Admiraal, A. Magee, I. van de Laar, Y. Hendriks, J. B. Verheij, I. Walpole, H. G. Brunner & C. M. van Ravenswaaij: Familial CHARGE syndrome and the CHD7 gene: a recurrent missense mutation, intrafamilial recurrence and variability. Am J Med Genet. Part A, 146, 43-50 (2008)
-
(2008)
Am J Med Genet
, vol.146 PART. A
, pp. 43-50
-
-
Jongmans, M.C.1
Hoefsloot, L.H.2
Van Der, D.K.P.3
Admiraal, R.J.4
Magee, A.5
Van De Laa, I.6
Hendriks, Y.7
Verheij, J.B.8
Walpole, I.9
Brunner, H.G.10
Van Ravenswaaij, C.M.11
-
20
-
-
27944478666
-
Multiple mutations in mouse Chd7 provide models for CHARGE syndrome
-
DOI 10.1093/hmg/ddi375
-
Bosman, E. A., A. C. Penn, J. C. Ambrose, R. Kettleborough, D. L. Stemple & K. P. Steel: Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Hum Mol Genet, 14, 3463-76 (2005) (Pubitemid 41672129)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.22
, pp. 3463-3476
-
-
Bosman, E.A.1
Penn, A.C.2
Ambrose, J.C.3
Kettleborough, R.4
Stemple, D.L.5
Steel, K.P.6
-
21
-
-
33947266958
-
Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues
-
DOI 10.1007/s00335-006-0107-6
-
Hurd, E. A., P. L. Capers, M. N. Blauwkamp, M. E. Adams, Y. Raphael, H. K. Poucher & D. M. Martin: Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues. Mamm Genome, 18, 94-104 (2007) (Pubitemid 46425379)
-
(2007)
Mammalian Genome
, vol.18
, Issue.2
, pp. 94-104
-
-
Hurd, E.A.1
Capers, P.L.2
Blauwkamp, M.N.3
Adams, M.E.4
Raphael, Y.5
Poucher, H.K.6
Martin, D.M.7
-
22
-
-
20944437124
-
Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma
-
DOI 10.1038/sj.onc.1208306
-
White, P. S., P. M. Thompson, T. Gotoh, E. R. Okawa, J. Igarashi, M. Kok, C. Winter, S. G. Gregory, M. D. Hogarty, J. M. Maris & G. M. Brodeur: Definition and characterization of a region of 1p36.3 consistently deleted in neuroblastoma. Oncogene, 24, 2684-94 (2005) (Pubitemid 40593096)
-
(2005)
Oncogene
, vol.24
, Issue.16
, pp. 2684-2694
-
-
White, P.S.1
Thompson, P.M.2
Gotoh, T.3
Okawa, E.R.4
Igarashi, J.5
Kok, M.6
Winter, C.7
Gregory, S.G.8
Hogarty, M.D.9
Maris, J.M.10
Brodeur, G.M.11
-
23
-
-
18544381908
-
Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno- osseous dysplasia
-
Boerkoel, C. F., H. Takashima, J. John, J. Yan, P. Stankiewicz, L. Rosenbarker, J. L. Andre, R. Bogdanovic, A. Burguet, S. Cockfield, I. Cordeiro, S. Frund, F. Illies, M. Joseph, I. Kaitila, G. Lama, C. Loirat, D. R. McLeod, D. V. Milford, E. M. Petty, F. Rodrigo, J. M. Saraiva, B. Schmidt, G. C. Smith, J. Spranger, A. Stein, H. Thiele, J. Tizard, R. Weksberg, J. R. Lupski & D. W. Stockton: Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno- osseous dysplasia. Nat Genet, 30, 215-20. (2002)
-
(2002)
Nat Genet
, vol.30
, pp. 215-220
-
-
Boerkoel, C.F.1
Takashima, H.2
John, J.3
Yan, J.4
Stankiewicz, P.5
Rosenbarker, L.6
Andre, J.L.7
Bogdanovic, R.8
Burguet, A.9
Cockfield, S.10
Cordeiro, I.11
Frund, S.12
Illies, F.13
Joseph, M.14
Kaitila, I.15
Lama, G.16
Loirat, C.17
McLeod, D.R.18
Milford, D.V.19
Petty, E.M.20
Rodrigo, F.21
Saraiva, J.M.22
Schmidt, B.23
Smith, G.C.24
Spranger, J.25
Stein, A.26
Thiele, H.27
Tizard, J.28
Weksberg, R.29
Lupski, J.R.30
Stockton, D.W.31
more..
-
24
-
-
33847186637
-
Schimke immunoosseous dysplasia: Suggestions of genetic diversity
-
Clewing, J. M., H. Fryssira, D. Goodman, S. F. Smithson, E. A. Sloan, S. Lou, Y. Huang, K. Choi, T. Lucke, H. Alpay, J. L. Andre, Y. Asakura, N. Biebuyck- Gouge, R. Bogdanovic, D. Bonneau, C. Cancrini, P. Cochat, S. Cockfield, L. Collard, I. Cordeiro, V. Cormier- Daire, K. Cransberg, K. Cutka, G. Deschenes, J. H. Ehrich, S. Frund, H. Georgaki, E. Guillen-Navarro, B. Hinkelmann, M. Kanariou, B. Kasap, S. S. Kilic, G. Lama, P. Lamfers, C. Loirat, S. Majore, D. Milford, D. Morin, N. Ozdemir, B. F. Pontz, W. Proesmans, S. Psoni, H. Reichenbach, S. Reif, C. Rusu, J. M. Saraiva, O. Sakallioglu, B. Schmidt, L. Shoemaker, S. Sigaudy, G. Smith, F. Sotsiou, N. Stajic, A. Stein, A. Stray-Pedersen, D. Taha, S. Taque, J. Tizard, M. Tsimaratos, N. A. Wong & C. F. Boerkoel: Schimke immunoosseous dysplasia: suggestions of genetic diversity. Hum Mutat, 28, 273-83 (2007)
-
(2007)
Hum Mutat
, vol.28
, pp. 273-283
-
-
Clewing, J.M.1
Fryssira, H.2
Goodman, D.3
Smithson, S.F.4
Sloan, E.A.5
Lou, S.6
Huang, Y.7
Choi, K.8
Lucke, T.9
Alpay, H.10
Andre, J.L.11
Asakura, Y.12
Biebuyck- Gouge, N.13
Bogdanovic, R.14
Bonneau, D.15
Cancrini, C.16
Cochat, P.17
Cockfield, S.18
Collard, L.19
Cordeiro, I.20
Cormier- Daire, V.21
Cransberg, K.22
Cutka, K.23
Deschenes, G.24
Ehrich, J.H.25
Frund, S.26
Georgaki, H.27
Guillen-Navarro, E.28
Hinkelmann, B.29
Kanariou, M.30
Kasap, B.31
Kilic, S.S.32
Lama, G.33
Lamfers, P.34
Loirat, C.35
Majore, S.36
Milford, D.37
Morin, D.38
Ozdemir, N.39
Pontz, B.F.40
Proesmans, W.41
Psoni, S.42
Reichenbach, H.43
Reif, S.44
Rusu, C.45
Saraiva, J.M.46
Sakallioglu, O.47
Schmidt, B.48
Shoemaker, L.49
Sigaudy, S.50
Smith, G.51
Sotsiou, F.52
Stajic, N.53
Stein, A.54
Stray-Pedersen, A.55
Taha, D.56
Taque, S.57
Tizard, J.58
Tsimaratos, M.59
Wong, N.A.60
Boerkoel, C.F.61
more..
-
25
-
-
0032403109
-
Altered control of cellular proliferation in the absence of mammalian brahma (SNF2α)
-
Reyes, J. C., J. Barra, C. Muchardt, A. Camus, C. Babinet & M. Yaniv: Altered control of cellular proliferation in the absence of mammalian brahma (SNF2alpha). Embo J, 17, 6979-91. (1998) (Pubitemid 28550292)
-
(1998)
EMBO Journal
, vol.17
, Issue.23
, pp. 6979-6991
-
-
Reyes, J.C.1
Barra, J.2
Muchardt, C.3
Camus, A.4
Babinet, C.5
Yaniv, M.6
-
26
-
-
0034502484
-
A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes
-
DOI 10.1016/S1097-2765(00)00127-1
-
Bultman, S., T. Gebuhr, D. Yee, C. La Mantia, J. Nicholson, A. Gilliam, F. Randazzo, D. Metzger, P. Chambon, G. Crabtree & T. Magnuson: A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes. Mol Cell, 6, 1287-95. (2000) (Pubitemid 32045922)
-
(2000)
Molecular Cell
, vol.6
, Issue.6
, pp. 1287-1295
-
-
Bultman, S.1
Gebuhr, T.2
Yee, D.3
La Mantia, C.4
Nicholson, J.5
Gilliam, A.6
Randazzo, F.7
Metzger, D.8
Chambon, P.9
Crabtree, G.10
Magnuson, T.11
-
27
-
-
0035037801
-
Disruption of INI1 leads to peri-implantation lethality and tumorigenesis in mice
-
DOI 10.1128/MCB.21.10.3598-3603.2001
-
Guidi, C. J., A. T. Sands, B. P. Zambrowicz, T. K. Turner, D. A. Demers, W. Webster, T. W. Smith, A. N. Imbalzano & S. N. Jones: Disruption of Ini1 leads to peri implantation lethality and tumorigenesis in mice. Mol Cell Biol, 21, 3598-603. (2001) (Pubitemid 32381795)
-
(2001)
Molecular and Cellular Biology
, vol.21
, Issue.10
, pp. 3598-3603
-
-
Guidi, C.J.1
Sands, A.T.2
Zambrowicz, B.P.3
Turner, T.K.4
Demers, D.A.5
Webster, W.6
Smith, T.W.7
Imbalzano, A.N.8
Jones, S.N.9
-
28
-
-
33748067731
-
Functional interaction of the retinoblastoma and Ini1/Snf5 tumor suppressors in cell growth and pituitary tumorigenesis
-
DOI 10.1158/0008-5472.CAN-06-1451
-
Guidi, C. J., R. Mudhasani, K. Hoover, A. Koff, I. Leav, A. N. Imbalzano & S. N. Jones: Functional interaction of the retinoblastoma and Ini1/Snf5 tumor suppressors in cell growth and pituitary tumorigenesis. Cancer Res, 66, 8076-82 (2006) (Pubitemid 44299173)
-
(2006)
Cancer Research
, vol.66
, Issue.16
, pp. 8076-8082
-
-
Guidi, C.J.1
Mudhasani, R.2
Hoover, K.3
Koff, A.4
Leav, I.5
Imbalzano, A.N.6
Jones, S.N.7
-
29
-
-
29144453238
-
Inactivation of the Snf5 tumor suppressor stimulates cell cycle progression and cooperates with p53 loss in oncogenic transformation
-
DOI 10.1073/pnas.0509014102
-
Isakoff, M. S., C. G. Sansam, P. Tamayo, A. Subramanian, J. A. Evans, C. M. Fillmore, X. Wang, J. A. Biegel, S. L. Pomeroy, J. P. Mesirov & C. W. Roberts: Inactivation of the Snf5 tumor suppressor stimulates cell cycle progression and cooperates with p53 loss in oncogenic transformation. P Natl Acad Sci USA, 102, 17745-50 (2005) (Pubitemid 41803568)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.49
, pp. 17745-17750
-
-
Isakoff, M.S.1
Sansam, C.G.2
Tamayo, P.3
Subramanian, A.4
Evans, J.A.5
Fillmore, C.M.6
Wang, X.7
Biegel, J.A.8
Pomeroy, S.L.9
Mesirov, J.P.10
Roberts, C.W.M.11
-
30
-
-
0034326257
-
BRG1, a component of the SWI-SNF complex, is mutated in multiple human tumor cell lines
-
Wong, A. K., F. Shanahan, Y. Chen, L. Lian, P. Ha, K. Hendricks, S. Ghaffari, D. Iliev, B. Penn, A. M. Woodland, R. Smith, G. Salada, A. Carillo, K. Laity, J. Gupte, B. Swedlund, S. V. Tavtigian, D. H. Teng & E. Lees: BRG1, a component of the SWI-SNF complex, is mutated in multiple human tumor cell lines. Cancer Res, 60, 6171-7. (2000)
-
(2000)
Cancer Res
, vol.60
, pp. 6171-6177
-
-
Wong, A.K.1
Shanahan, F.2
Chen, Y.3
Lian, L.4
Ha, P.5
Hendricks, K.6
Ghaffari, S.7
Iliev, D.8
Penn, B.9
Woodland, A.M.10
Smith, R.11
Salada, G.12
Carillo, A.13
Laity, K.14
Gupte, J.15
Swedlund, B.16
Tavtigian, S.V.17
Teng, D.H.18
Lees, E.19
-
31
-
-
0035874880
-
Mutation analyses of 268 candidate genes in human tumor cell lines
-
Teng, D. H., Y. Chen, L. Lian, P. C. Ha, S. V. Tavtigian & A. K. Wong: Mutation analyses of 268 candidate genes in human tumor cell lines. Genomics, 74, 352-64. (2001)
-
(2001)
Genomics
, vol.74
, pp. 352-364
-
-
Teng, D.H.1
Chen, Y.2
Lian, L.3
Ha, P.C.4
Tavtigian, S.V.5
Wong, A.K.6
-
32
-
-
0034697973
-
BRCA1 is associated with a human SWI/SNF-related complex: Linking chromatin remodeling to breast cancer
-
Bochar, D. A., L. Wang, H. Beniya, A. Kinev, Y. Xue, W. S. Lane, W. Wang, F. Kashanchi & R. Shiekhattar: BRCA1 is associated with a human SWI/SNF-related complex: linking chromatin remodeling to breast cancer. Cell, 102, 257-65. (2000)
-
(2000)
Cell
, vol.102
, pp. 257-265
-
-
Bochar, D.A.1
Wang, L.2
Beniya, H.3
Kinev, A.4
Xue, Y.5
Lane, W.S.6
Wang, W.7
Kashanchi, F.8
Shiekhattar, R.9
-
33
-
-
17344371525
-
Transcriptional targets of the chromatin-remodelling factor SMARCA4/BRG1 in lung cancer cells
-
DOI 10.1093/hmg/ddi091
-
Medina, P. P., J. Carretero, E. Ballestar, B. Angulo, F. Lopez-Rios, M. Esteller & M. Sanchez-Cespedes: Transcriptional targets of the chromatin-remodelling factor SMARCA4/BRG1 in lung cancer cells. Hum Mol Genet, 14, 973-82 (2005) (Pubitemid 40533108)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.7
, pp. 973-982
-
-
Medina, P.P.1
Carretero, J.2
Ballestar, E.3
Angulo, B.4
Lopez-Rios, F.5
Esteller, M.6
Sanchez-Cespedes, M.7
-
34
-
-
30944436854
-
SWI/SNF complex is essential for NRSF-mediated suppression of neuronal genes in human nonsmall cell lung carcinoma cell lines
-
DOI 10.1038/sj.onc.1209068, PII 1209068
-
Watanabe, H., T. Mizutani, T. Haraguchi, N. Yamamichi, S. Minoguchi, M. Yamamichi-Nishina, N. Mori, T. Kameda, T. Sugiyama & H. Iba: SWI/SNF complex is essential for NRSF-mediated suppression of neuronal genes in human nonsmall cell lung carcinoma cell lines. Oncogene, 25, 470-9 (2006) (Pubitemid 43117632)
-
(2006)
Oncogene
, vol.25
, Issue.3
, pp. 470-479
-
-
Watanabe, H.1
Mizutani, T.2
Haraguchi, T.3
Yamamichi, N.4
Minoguchi, S.5
Yamamichi-Nishina, M.6
Mori, N.7
Kameda, T.8
Sugiyama, T.9
Iba, H.10
-
35
-
-
3042851775
-
Chromatin remodeling factors and BRM/BRG1 expression as prognostic indicators in non-small cell lung cancer
-
DOI 10.1158/1078-0432.CCR-03-0489
-
Fukuoka, J., T. Fujii, J. H. Shih, T. Dracheva, D. Meerzaman, A. Player, K. Hong, S. Settnek, A. Gupta, K. Buetow, S. Hewitt, W. D. Travis & J. Jen: Chromatin remodeling factors and BRM/BRG1 expression as prognostic indicators in non-small cell lung cancer. Clin Cancer Res, 10, 4314-24 (2004) (Pubitemid 38878869)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.13
, pp. 4314-4324
-
-
Fukuoka, J.1
Fujii, T.2
Shih, J.H.3
Dracheva, T.4
Meerzaman, D.5
Player, A.6
Hong, K.7
Settnek, S.8
Gupta, A.9
Buetow, K.10
Hewitt, S.11
Travis, W.D.12
Jen, J.13
-
36
-
-
33846616766
-
Aberrant expression of SWI/SNF catalytic subunits BRG1/BRM is associated with tumor development and increased invasiveness in prostate cancers
-
DOI 10.1002/pros.20521
-
Sun, A., O. Tawfik, B. Gayed, J. B. Thrasher, S. Hoestje, C. Li & B. Li: Aberrant expression of SWI/SNF catalytic subunits BRG1/BRM is associated with tumor development and increased invasiveness in prostate cancers. Prostate, 67, 203-13 (2007) (Pubitemid 46185323)
-
(2007)
Prostate
, vol.67
, Issue.2
, pp. 203-213
-
-
Sun, A.1
Tawfik, O.2
Gayed, B.3
Thrasher, J.B.4
Hoestje, S.5
Li, C.6
Li, B.7
-
37
-
-
36349006592
-
Frequent loss of Brm expression in gastric cancer correlates with histologic features and differentiation state
-
DOI 10.1158/0008-5472.CAN-07-2601
-
Yamamichi, N., K. Inada, M. Ichinose, M. Yamamichi- Nishina, T. Mizutani, H. Watanabe, K. Shiogama, M. Fujishiro, T. Okazaki, N. Yahagi, T. Haraguchi, S. Fujita, Y. Tsutsumi, M. Omata & H. Iba: Frequent loss of Brm expression in gastric cancer correlates with histologic features and differentiation state. Cancer Res, 67, 10727-35 (2007) (Pubitemid 350145899)
-
(2007)
Cancer Research
, vol.67
, Issue.22
, pp. 10727-10735
-
-
Yamamichi, N.1
Inada, K.-I.2
Ichinose, M.3
Yamamichi-Nishina, M.4
Mizutani, T.5
Watanabe, H.6
Shiogama, K.7
Fujishiro, M.8
Okazaki, T.9
Yahagi, N.10
Haraguchi, T.11
Fujita, S.12
Tsutsumi, Y.13
Omata, M.14
Iba, H.15
-
38
-
-
0030966842
-
CD44: Structure, function, and association with the malignant process
-
Naor, D., R. V. Sionov & D. Ish-Shalom: CD44: structure, function, and association with the malignant process. Adv Cancer Res, 71, 241-319 (1997) (Pubitemid 27197761)
-
(1997)
Advances in Cancer Research
, vol.71
, pp. 241-319
-
-
Naor, D.1
Sionov, R.V.2
Ish-Shalom, D.3
-
39
-
-
33751235842
-
Downregulation of BRG-1 repressed expression of CD44s in cervical neuroendocrine carcinoma and adenocarcinoma
-
Kuo, K. T., C. W. Liang, C. H. Hsiao, C. H. Lin, C. A. Chen, B. C. Sheu & M. C. Lin: Downregulation of BRG-1 repressed expression of CD44s in cervical neuroendocrine carcinoma and adenocarcinoma. Modern Pathol, 19, 1570-7 (2006)
-
(2006)
Modern Pathol
, vol.19
, pp. 1570-1577
-
-
Kuo, K.T.1
Liang, C.W.2
Hsiao, C.H.3
Lin, C.H.4
Chen, C.A.5
Sheu, B.C.6
Lin, M.C.7
-
40
-
-
0035937776
-
The BRG-1 Subunit of the SWI/SNF Complex Regulates CD44 Expression 10.1074/jbc.M009747200
-
Strobeck, M. W., M. F. DeCristofaro, F. Banine, B. E. Weissman, L. S. Sherman & E. S. Knudsen: The BRG-1 Subunit of the SWI/SNF Complex Regulates CD44 Expression 10.1074/jbc.M009747200. J Biol Chem, 276, 9273-9278 (2001)
-
(2001)
J Biol Chem
, vol.276
, pp. 9273-9278
-
-
Strobeck, M.W.1
Decristofaro, M.F.2
Banine, F.3
Weissman, B.E.4
Sherman, L.S.5
Knudsen, E.S.6
-
41
-
-
0036009569
-
Aberrations of the hSNF5/INII gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors
-
DOI 10.1002/gcc.10052
-
Uno, K., J. Takita, K. Yokomori, Y. Tanaka, S. Ohta, H. Shimada, F. H. Gilles, K. Sugita, S. Abe, M. Sako, K. Hashizume & Y. Hayashi: Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors. Gene Chromosome Canc, 34, 33-41 (2002) (Pubitemid 34260594)
-
(2002)
Genes Chromosomes and Cancer
, vol.34
, Issue.1
, pp. 33-41
-
-
Uno, K.1
Takita, J.2
Yokomori, K.3
Tanaka, Y.4
Ohta, S.5
Shimada, H.6
Gilles, F.H.7
Sugita, K.8
Abe, S.9
Sako, M.10
Hashizume, K.11
Hayashi, Y.12
-
42
-
-
20144386270
-
SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas
-
DOI 10.1158/0008-5472.CAN-04-3050
-
Modena, P., E. Lualdi, F. Facchinetti, L. Galli, M. R. Teixeira, S. Pilotti & G. Sozzi: SMARCB1/INI1 tumor suppressor gene is frequently inactivated in epithelioid sarcomas. Cancer Res, 65, 4012-9 (2005) (Pubitemid 40775637)
-
(2005)
Cancer Research
, vol.65
, Issue.10
, pp. 4012-4019
-
-
Modena, P.1
Lualdi, E.2
Facchinetti, F.3
Galli, L.4
Teixeira, M.R.5
Pilotti, S.6
Sozzi, G.7
-
43
-
-
34147192050
-
Germline mutation of INI1/SMARCB1 in familial schwannomatosis
-
Hulsebos, T. J., A. S. Plomp, R. A. Wolterman, E. C. Robanus-Maandag, F. Baas & P. Wesseling: Germline mutation of INI1/SMARCB1 in familial schwannomatosis. Am J Hum Genet, 80, 805-10 (2007)
-
(2007)
Am J Hum Genet
, vol.80
, pp. 805-8010
-
-
Hulsebos, T.J.1
Plomp, A.S.2
Wolterman, R.A.3
Robanus-Maandag, E.C.4
Baas, F.5
Wesseling, P.6
-
44
-
-
0033949274
-
Chromatin remodeling gene SMARCA5 is dysregulated in primitive hematopoietic cells of acute leukemia
-
Stopka, T., D. Zakova, O. Fuchs, O. Kubrova, J. Blafkova, J. Jelinek, E. Necas & J. Zivny: Chromatin remodeling gene SMARCA5 is dysregulated in primitive hematopoietic cells of acute leukemia. Leukemia, 14, 1247-52. (2000)
-
(2000)
Leukemia
, vol.14
, pp. 1247-1452
-
-
Stopka, T.1
Zakova, D.2
Fuchs, O.3
Kubrova, O.4
Blafkova, J.5
Jelinek, J.6
Necas, E.7
Zivny, J.8
-
45
-
-
36549015191
-
Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2
-
DOI 10.1016/j.cancergencyto.2007.09.010, PII S0165460807005882
-
Helias, C., S. Struski, C. Gervais, V. Leymarie, L. Mauvieux, R. Herbrecht & M. Lessard: Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2. Cancer Genet Cytogen, 180, 51-5 (2008) (Pubitemid 350192681)
-
(2008)
Cancer Genetics and Cytogenetics
, vol.180
, Issue.1
, pp. 51-55
-
-
Helias, C.1
Struski, S.2
Gervais, C.3
Leymarie, V.4
Mauvieux, L.5
Herbrecht, R.6
Lessard, M.7
-
46
-
-
0019981972
-
Production of a monoclonal antibody specific for Hodgkin and Sternberg-Reed cells of Hodgkin's disease and a subset of normal lymphoid cells
-
DOI 10.1038/299065a0
-
Schwab, U., H. Stein, J. Gerdes, H. Lemke, H. Kirchner, M. Schaadt & V. Diehl: Production of a monoclonal antibody specific for Hodgkin and Sternberg- Reed cells of Hodgkin's disease and a subset of normal lymphoid cells. Nature, 299, 65-7 (1982) (Pubitemid 12049770)
-
(1982)
Nature
, vol.299
, Issue.5878
, pp. 65-67
-
-
Schwab, U.1
Stein, H.2
Gerdes, J.3
-
47
-
-
34147158728
-
The Chd family of chromatin remodelers
-
DOI 10.1016/j.mrfmmm.2006.07.012, PII S0027510707000309, Chromatin: Repair, Remodeling and Regulation
-
Marfella, C. G. & A. N. Imbalzano: The Chd family of chromatin remodelers. Mutat Res, 618, 30-40 (2007) (Pubitemid 46574742)
-
(2007)
Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
, vol.618
, Issue.1-2
, pp. 30-40
-
-
Marfella, C.G.A.1
Imbalzano, A.N.2
-
48
-
-
33847076849
-
Chromatin modifications and their function
-
DOI 10.1016/j.cell.2007.02.005, PII S0092867407001845
-
Kouzarides, T.: Chromatin modifications and their function. Cell, 128, 693-705 (2007) (Pubitemid 46273577)
-
(2007)
Cell
, vol.128
, Issue.4
, pp. 693-705
-
-
Kouzarides, T.1
-
49
-
-
33847065486
-
The epigenomics of cancer
-
DOI 10.1016/j.cell.2007.01.029, PII S0092867407001274
-
Jones, P. A. & S. B. Baylin: The epigenomics of cancer. Cell, 128, 683-92 (2007) (Pubitemid 46273572)
-
(2007)
Cell
, vol.128
, Issue.4
, pp. 683-692
-
-
Jones, P.A.1
Baylin, S.B.2
|