-
1
-
-
0027169927
-
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
-
Glenn CC, Nicholls RD, Robinson WP, et al. Modification of 15q11-13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum Mol Genet 1993;2:1377-1382 (Pubitemid 23271180)
-
(1993)
Human Molecular Genetics
, vol.2
, Issue.9
, pp. 1377-1382
-
-
Glenn, C.C.1
Nicholls, R.D.2
Robinson, W.P.3
Saitoh, S.4
Niikawa, N.5
Schinzel, A.6
Horsthemke, B.7
Driscoll, D.J.8
-
2
-
-
0029806141
-
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
-
Brown KW, Villar AJ, Bickmore W, et al. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19- independent pathway. Hum Mol Genet 1996;5: 2027-2032 (Pubitemid 26413650)
-
(1996)
Human Molecular Genetics
, vol.5
, Issue.12
, pp. 2027-2032
-
-
Brown, K.W.1
Villar, A.J.2
Bickmore, W.3
Clayton-Smith, J.4
Catchpoole, D.5
Maher, E.R.6
Reik, W.7
-
3
-
-
34347218214
-
Chromatin structure of repeating CTG/ CAG and CGG/CCG sequences in human disease
-
Wang YH. Chromatin structure of repeating CTG/ CAG and CGG/CCG sequences in human disease. Front Biosci 2007;12:4731-4741
-
(2007)
Front Biosci
, vol.12
, pp. 4731-4741
-
-
Wang, Y.H.1
-
4
-
-
0038581890
-
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
-
DOI 10.1038/ng1157
-
Tufarelli C, Stanley JA, Garrick D, et al. Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease. Nat Genet 2003;34:157-165 (Pubitemid 36666926)
-
(2003)
Nature Genetics
, vol.34
, Issue.2
, pp. 157-165
-
-
Tufarelli, C.1
Sloane Stanley, J.A.2
Garrick, D.3
Sharpe, J.A.4
Ayyub, H.5
Wood, W.G.6
Higgs, D.R.7
-
5
-
-
58149144567
-
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
-
Ligtenberg MJ, Kuiper RP, Chan TL, et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1. Nat Genet 2009;41: 112-117
-
(2009)
Nat Genet
, vol.41
, pp. 112-117
-
-
Ligtenberg, M.J.1
Kuiper, R.P.2
Chan, T.L.3
-
6
-
-
34249314024
-
Downregulation of Death-Associated Protein Kinase 1 (DAPK1) in Chronic Lymphocytic Leukemia
-
DOI 10.1016/j.cell.2007.03.043, PII S0092867407005120
-
Raval A, Tanner SM, Byrd JC, et al. Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia. Cell 2007;129: 879-890 (Pubitemid 46813150)
-
(2007)
Cell
, vol.129
, Issue.5
, pp. 879-890
-
-
Raval, A.1
Tanner, S.M.2
Byrd, J.C.3
Angerman, E.B.4
Perko, J.D.5
Chen, S.-S.6
Hackanson, B.7
Grever, M.R.8
Lucas, D.M.9
Matkovic, J.J.10
Lin, T.S.11
Kipps, T.J.12
Murray, F.13
Weisenburger, D.14
Sanger, W.15
Lynch, J.16
Watson, P.17
Jansen, M.18
Yoshinaga, Y.19
Rosenquist, R.20
De Jong, P.J.21
Coggill, P.22
Beck, S.23
Lynch, H.24
De La Chapelle, A.25
Plass, C.26
more..
-
7
-
-
0030723262
-
A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation
-
DOI 10.1038/ng1197-353
-
Plenge RM, Hendrich BD, Schwartz C, et al. A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. Nat Genet 1997;17:353-356 (Pubitemid 27476005)
-
(1997)
Nature Genetics
, vol.17
, Issue.3
, pp. 353-356
-
-
Plenge, R.M.1
Hendrich, B.D.2
Schwartz, C.3
Arena, J.F.4
Naumova, A.5
Sapienza, C.6
Winter, R.M.7
Willard, H.F.8
-
8
-
-
85047695538
-
Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay
-
Tomkins DJ, McDonald HL, Farrell SA, Brown CJ. Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay. Eur J Hum Genet 2002; 10:44-51.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 44-51
-
-
Tomkins, D.J.1
McDonald, H.L.2
Farrell, S.A.3
Brown, C.J.4
-
9
-
-
17344363494
-
Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation
-
DOI 10.1093/hmg/ddi089
-
Pugacheva EM, Tiwari VK, Abdullaev Z, et al. Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation. Hum Mol Genet 2005;14:953-965 (Pubitemid 40533106)
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.7
, pp. 953-965
-
-
Pugacheva, E.M.1
Tiwari, V.K.2
Abdullaev, Z.3
Vostrov, A.A.4
Flanagan, P.T.5
Quitschke, W.W.6
Loukinov, D.I.7
Ohlsson, R.8
Lobanenkov, V.V.9
-
10
-
-
70449366014
-
Detection of MGMT promoter methylation in normal individuals is strongly associated with the T allele of the rs16906252 MGMT promoter single nucleotide polymorphism
-
Candiloro ILM, Dobrovic A. Detection of MGMT promoter methylation in normal individuals is strongly associated with the T allele of the rs16906252 MGMT promoter single nucleotide polymorphism. Cancer Prev Res 2009;2:862-867
-
(2009)
Cancer Prev Res
, vol.2
, pp. 862-867
-
-
Candiloro, I.L.M.1
Dobrovic, A.2
-
11
-
-
19244370208
-
6-Methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to a mutations in K-ras in colorectal tumorigenesis
-
Esteller M, Toyota M, Sanchez-Cespedes M, et al. Inactivation of the DNA repair gene O6- methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis. Cancer Res 2000;60:2368-2371 (Pubitemid 30262424)
-
(2000)
Cancer Research
, vol.60
, Issue.9
, pp. 2368-2371
-
-
Esteller, M.1
Toyota, M.2
Sanchez-Cespedes, M.3
Capella, G.4
Peinado, M.A.5
Watkins, D.N.6
Issa, J.-P.J.7
Sidransky, D.8
Baylin, S.B.9
Herman, J.G.10
-
12
-
-
44449147948
-
Role of mismatch repair and MGMT in response to anticancer therapies
-
DOI 10.2174/187152008784220276
-
Casorelli I, Russo MT, Bignami M. Role of mismatch repair and MGMT in response to anticancer therapies. Anticanc Agents Med Chem 2008;8: 368-380 (Pubitemid 351761422)
-
(2008)
Anti-Cancer Agents in Medicinal Chemistry
, vol.8
, Issue.4
, pp. 368-380
-
-
Casorelli, I.1
Russo, M.T.2
Bignami, M.3
-
13
-
-
34948886186
-
MGMT germline polymorphism is associated with somatic MGMT promoter methylation and gene silencing in colorectal cancer
-
DOI 10.1093/carcin/bgm160
-
Ogino S, Hazra A, Tranah GJ, et al. MGMT germline polymorphism is associated with somatic MGMT promoter methylation and gene silencing in colorectal cancer. Carcinogenesis 2007;28:1985-1990 (Pubitemid 47514483)
-
(2007)
Carcinogenesis
, vol.28
, Issue.9
, pp. 1985-1990
-
-
Ogino, S.1
Hazra, A.2
Tranah, G.J.3
Kirkner, G.J.4
Kawasaki, T.5
Nosho, K.6
Ohnishi, M.7
Suemoto, Y.8
Meyerhardt, J.A.9
Hunter, D.J.10
Fuchs, C.S.11
-
14
-
-
71149121511
-
MGMT methylation is associated primarily with the germline C>T SNP (rs16906252) in colorectal cancer and normal colonic mucosa
-
In press
-
Hawkins N, Lee J, Wong J, Ward R, Hitchins M. MGMT methylation is associated primarily with the germline C>T SNP (rs16906252) in colorectal cancer and normal colonic mucosa. Mod Pathol, In press 2009.
-
(2009)
Mod Pathol
-
-
Hawkins, N.1
Lee, J.2
Wong, J.3
Ward, R.4
Hitchins, M.5
-
15
-
-
25144518262
-
MGMT promoter methylation and field defect in sporadic colorectal cancer
-
DOI 10.1093/jnci/dji275
-
Shen L, Kondo Y, Rosner GL, et al. MGMT promoter methylation and field defect in sporadic colorectal cancer. J Natl Cancer Inst 2005;97: 1330-1338 (Pubitemid 41487800)
-
(2005)
Journal of the National Cancer Institute
, vol.97
, Issue.18
, pp. 1330-1338
-
-
Shen, L.1
Kondo, Y.2
Rosner, G.L.3
Xiao, L.4
Hernandez, N.S.5
Vilaythong, J.6
Houlihan, P.S.7
Krouse, R.S.8
Prasad, A.R.9
Einspahr, J.G.10
Buckmeier, J.11
Alberts, D.S.12
Hamilton, S.R.13
Issa, J.-P.J.14
-
16
-
-
34548008398
-
O6- Methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis
-
Menigatti M, Pedroni M, Verrone AM, et al. O6- methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis. Oncol Rep 2007;17:1421-1427
-
(2007)
Oncol Rep
, vol.17
, pp. 1421-1427
-
-
Menigatti, M.1
Pedroni, M.2
Verrone, A.M.3
-
17
-
-
33748528622
-
Promoter methylation status of the MGMT, hMLH1, and CDKN2A/ p16 genes in non-neoplastic mucosa of patients with and without colorectal adenomas
-
Ye C, Shrubsole MJ, Cai Q, et al. Promoter methylation status of the MGMT, hMLH1, and CDKN2A/ p16 genes in non-neoplastic mucosa of patients with and without colorectal adenomas. Oncol Rep 2006;16:429-435
-
(2006)
Oncol Rep
, vol.16
, pp. 429-435
-
-
Ye, C.1
Shrubsole, M.J.2
Cai, Q.3
-
18
-
-
78651056338
-
Field cancerization in oral stratified squamous epithelium;cllnical implications of multicentric origin
-
Slaughter DP, Southwick HW, Smejkal W. Field cancerization in oral stratified squamous epithelium;cllnical implications of multicentric origin. Cancer 1953;6:963-968
-
(1953)
Cancer
, vol.6
, pp. 963-968
-
-
Slaughter, D.P.1
Southwick, H.W.2
Smejkal, W.3
-
19
-
-
0028138905
-
Identification of a 59 bp enhancer located at the first exon/intron boundary of the human O6-methylguanine DNA methyltransferase gene
-
Harris LC, Remack JS, Brent TP. Identification of a 59 bp enhancer located at the first exon/intron boundary of the human O6-methylguanine DNA methyltransferase gene. Nucleic Acids Res 1994;22:4614-4619
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 4614-4619
-
-
Harris, L.C.1
Remack, J.S.2
Brent, T.P.3
-
20
-
-
0030611199
-
Cytoplasmic sequestration of an O6-methylguanine- DNA methyltransferase enhancer binding protein in DNA repair-deficient human cells
-
Chen FY, Hams LC, Remack JS, Brent TP. Cytoplasmic sequestration of an O6-methylguanine- DNA methyltransferase enhancer binding protein in DNA repair-deficient human cells. Proc Natl Acad Sci U S A 1997;94:4348-4353
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 4348-4353
-
-
Chen, F.Y.1
Hams, L.C.2
Remack, J.S.3
Brent, T.P.4
-
21
-
-
62849100430
-
Aberrant epigenetic silencing is triggered by a transient reduction in gene expression
-
Oyer JA, Chu A, Brar S, Turker MS. Aberrant epigenetic silencing is triggered by a transient reduction in gene expression. PLoS One 2009;4:e4832.
-
(2009)
PLoS One
, vol.4
-
-
Oyer, J.A.1
Chu, A.2
Brar, S.3
Turker, M.S.4
-
22
-
-
67349237892
-
Histone deacetylase inhibitor induced modulation of anti-estrogen therapy
-
Thomas S, Munster PN. Histone deacetylase inhibitor induced modulation of anti-estrogen therapy. Cancer Lett 2009;280:184-191
-
(2009)
Cancer Lett
, vol.280
, pp. 184-191
-
-
Thomas, S.1
Munster, P.N.2
|