-
2
-
-
0033990725
-
Comparison of cancers of the oral cavity and pharynx worldwide: Etiological clues
-
Franceschi S, Bidoli E, Herrero R, Munoz N. Comparison of cancers of the oral cavity and pharynx worldwide: Etiological clues. Oral Oncol 2000;36:106-115.
-
(2000)
Oral Oncol
, vol.36
, pp. 106-115
-
-
Franceschi, S.1
Bidoli, E.2
Herrero, R.3
Munoz, N.4
-
3
-
-
0037001672
-
The epidemiology of oral and pharynx cancer in Brazil
-
Wunsch-Filho V. The epidemiology of oral and pharynx cancer in Brazil. Oral Oncol 2002;38:737-746.
-
(2002)
Oral Oncol
, vol.38
, pp. 737-746
-
-
Wunsch-Filho, V.1
-
4
-
-
0024318873
-
Risk factors for oral cancer in Brazil: A case-control study
-
Franco EL, Kowalski LP, Oliveira BV, et al. Risk factors for oral cancer in Brazil: A case-control study. Int J Cancer 1989; 43:992-1000.
-
(1989)
Int J Cancer
, vol.43
, pp. 992-1000
-
-
Franco, E.L.1
Kowalski, L.P.2
Oliveira, B.V.3
-
5
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer-Analyses of cohorts of twins from Sweden, Denmark, and Finland
-
Lichtenstein P, Holm NV, Verkasalo PK, et al. Environmental and heritable factors in the causation of cancer-Analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000;343:78-85.
-
(2000)
N Engl J Med
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
-
6
-
-
0033647141
-
Distinct chromosomal deleted regions defining different subsets of head and neck tumors
-
Miracca EC, Yamamoto L, Contado D, Takimoto MSS, Kowalski LP, Nagai MA. Distinct chromosomal deleted regions defining different subsets of head and neck tumors. Diagn Mol Pathol 2000;9:229-233.
-
(2000)
Diagn Mol Pathol
, vol.9
, pp. 229-233
-
-
Miracca, E.C.1
Yamamoto, L.2
Contado, D.3
Takimoto, M.S.S.4
Kowalski, L.P.5
Nagai, M.A.6
-
7
-
-
0038006218
-
Allelic imbalance at chromosome 11 in head and neck squamous cell carcinoma in an Indian patient population
-
Mondal G, Tripathi A, Bhattacharya N, et al. Allelic imbalance at chromosome 11 in head and neck squamous cell carcinoma in an Indian patient population. J Clin Pathol 2003;56: 512-518.
-
(2003)
J Clin Pathol
, vol.56
, pp. 512-518
-
-
Mondal, G.1
Tripathi, A.2
Bhattacharya, N.3
-
8
-
-
0029953162
-
Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: Association with aggressive biological features
-
El-Naggar AK, Hurr K, Huff V, Luna MA, Goepfert H, Batsakis JG. Allelic loss and replication errors at microsatellite loci on chromosome 11p in head and neck squamous carcinoma: Association with aggressive biological features. Clin Cancer Res 1996;2:903-907.
-
(1996)
Clin Cancer Res
, vol.2
, pp. 903-907
-
-
El-Naggar, A.K.1
Hurr, K.2
Huff, V.3
Luna, M.A.4
Goepfert, H.5
Batsakis, J.G.6
-
9
-
-
0027104205
-
Chromosomal localization of two putative 11p oncosuppressor genes involved in human ovarian tumours
-
Viel A, Giannini F, Tumiotto L, Sopracordevole F, Visentin C, Boiocchi M. Chromosomal localization of two putative 11p oncosuppressor genes involved in human ovarian tumours. Br J Cancer 1992;66:1030-1036.
-
(1992)
Br J Cancer
, vol.66
, pp. 1030-1036
-
-
Viel, A.1
Giannini, F.2
Tumiotto, L.3
Sopracordevole, F.4
Visentin, C.5
Boiocchi, M.6
-
10
-
-
0029936996
-
High-density marker analysis of 11p15.5 in non-small cell lung carcinomas reveals allelic deletion of one shared and one distinct region when compared to breast carcinomas
-
Tran YK, Newsham IF. High-density marker analysis of 11p15.5 in non-small cell lung carcinomas reveals allelic deletion of one shared and one distinct region when compared to breast carcinomas. Cancer Res 1996;56:2916-2921.
-
(1996)
Cancer Res
, vol.56
, pp. 2916-2921
-
-
Tran, Y.K.1
Newsham, I.F.2
-
11
-
-
0030027206
-
Population variation at the polymorphic ApaI restriction enzyme site in intron 5 of the WT1 gene
-
Bernard-Guérin C, Newsham I, Winqwist R, Cavenee WK. Population variation at the polymorphic ApaI restriction enzyme site in intron 5 of the WT1 gene. Hum Genet 1996; 97:163-170.
-
(1996)
Hum Genet
, vol.97
, pp. 163-170
-
-
Bernard-Guérin, C.1
Newsham, I.2
Winqwist, R.3
Cavenee, W.K.4
-
12
-
-
0027231784
-
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11
-
Koi M, Johnson LA, Kalikin LM, Little PFR, Nakamura Y, Feinberg AP. Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11. Science 1993;260:361-364.
-
(1993)
Science
, vol.260
, pp. 361-364
-
-
Koi, M.1
Johnson, L.A.2
Kalikin, L.M.3
Little, P.F.R.4
Nakamura, Y.5
Feinberg, A.P.6
-
13
-
-
0031820625
-
Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast
-
Lichy JH, Zavar M, Tsai MM, O'Leary TJ, Taubenberger JK. Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast. Am J Pathol 1998;153:271-278.
-
(1998)
Am J Pathol
, vol.153
, pp. 271-278
-
-
Lichy, J.H.1
Zavar, M.2
Tsai, M.M.3
O'Leary, T.J.4
Taubenberger, J.K.5
-
14
-
-
0033118754
-
Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction
-
Feinberg AP. Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: An introduction. Cancer Res 1999;59:1743s-1746s.
-
(1999)
Cancer Res
, vol.59
-
-
Feinberg, A.P.1
-
15
-
-
0036144048
-
DNA methylation patterns and epigenetic memory
-
Bird A. DNA methylation patterns and epigenetic memory. Genes Dev 2002;16:6-21.
-
(2002)
Genes Dev
, vol.16
, pp. 6-21
-
-
Bird, A.1
-
16
-
-
0035839136
-
Translating the histone code
-
Jenuwein T, Allis CD. Translating the histone code. Science 2001;293:1074-1080.
-
(2001)
Science
, vol.293
, pp. 1074-1080
-
-
Jenuwein, T.1
Allis, C.D.2
-
17
-
-
0036733675
-
Chromatin modification and epigenetic reprogramming in mammalian development
-
Li E. Chromatin modification and epigenetic reprogramming in mammalian development. Nat Rev Genet 2002;3:662-673.
-
(2002)
Nat Rev Genet
, vol.3
, pp. 662-673
-
-
Li, E.1
-
18
-
-
0034713080
-
Genomic imprinting: Silence across the border
-
Reik W, Murrel A. Genomic imprinting: Silence across the border. Nature 2000;405:408-409.
-
(2000)
Nature
, vol.405
, pp. 408-409
-
-
Reik, W.1
Murrel, A.2
-
19
-
-
0027322519
-
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
-
Ohlsson R, Nystrom A, Pfeifer-Ohlsson S, et al. IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nat Genet 1993;4: 94-97.
-
(1993)
Nat Genet
, vol.4
, pp. 94-97
-
-
Ohlsson, R.1
Nystrom, A.2
Pfeifer-Ohlsson, S.3
-
20
-
-
0026732759
-
Parental imprinting of the human H19 gene
-
Rachmilewitz J, Goshen R, Ariel I, Schneider T, de Groot N, Hochberg A. Parental imprinting of the human H19 gene. FEBS Lett 1992;309:25-28.
-
(1992)
FEBS Lett
, vol.309
, pp. 25-28
-
-
Rachmilewitz, J.1
Goshen, R.2
Ariel, I.3
Schneider, T.4
De Groot, N.5
Hochberg, A.6
-
21
-
-
0027442239
-
Tumour-suppressor activity of H19 RNA
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B. Tumour-suppressor activity of H19 RNA. Nature 1993;365: 764-767.
-
(1993)
Nature
, vol.365
, pp. 764-767
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
22
-
-
0028370014
-
H19, a tumour suppressing RNA?
-
Wrana JL. H19, a tumour suppressing RNA? Bioassays 1994; 16:89-90.
-
(1994)
Bioassays
, vol.16
, pp. 89-90
-
-
Wrana, J.L.1
-
23
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and IGF2
-
Thorvaldsen JL, Duran KL, Bartolomei MS. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and IGF2. Genes Dev 1998;12: 3693-3702.
-
(1998)
Genes Dev
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
-
24
-
-
0034713375
-
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
-
Bell AC, Felsenfeld G. Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene. Nature 2000;405:482-485.
-
(2000)
Nature
, vol.405
, pp. 482-485
-
-
Bell, A.C.1
Felsenfeld, G.2
-
25
-
-
0034713275
-
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus
-
Hark AT, Schoenherr CJ, Katz DJ, Ingram RS, Levorse JM, Tilghman SM. CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus. Nature 2000;405: 486-489.
-
(2000)
Nature
, vol.405
, pp. 486-489
-
-
Hark, A.T.1
Schoenherr, C.J.2
Katz, D.J.3
Ingram, R.S.4
Levorse, J.M.5
Tilghman, S.M.6
-
26
-
-
0035451090
-
CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease
-
Ohlsson R, Renkawitz R, Lobanenkov V. CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease. Trends Genet 2001;17:520-527.
-
(2001)
Trends Genet
, vol.17
, pp. 520-527
-
-
Ohlsson, R.1
Renkawitz, R.2
Lobanenkov, V.3
-
27
-
-
0032545688
-
Promoter-specific methylation and expression alterations of igf2 and h19 are involved in human hepatoblastoma
-
Li X, Kogner P, Sandstedt B, Haas AO, Ekström TJ. Promoter-specific methylation and expression alterations of igf2 and h19 are involved in human hepatoblastoma. Int J Cancer 1998;75:176-180.
-
(1998)
Int J Cancer
, vol.75
, pp. 176-180
-
-
Li, X.1
Kogner, P.2
Sandstedt, B.3
Haas, A.O.4
Ekström, T.J.5
-
28
-
-
0033604466
-
Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma
-
El-Naggar AK, Lai S, Tucker Sa, et al. Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma. Oncogene 1999;18:7063-7069.
-
(1999)
Oncogene
, vol.18
, pp. 7063-7069
-
-
El-Naggar, A.K.1
Lai, S.2
Tucker, Sa.3
-
29
-
-
0034835563
-
Loss of imprinting and loss of heterozygosity on 11p15.5 in head and neck squamous cell carcinomas
-
Rainho CA, Kowalski LP, Rogatto SR. Loss of imprinting and loss of heterozygosity on 11p15.5 in head and neck squamous cell carcinomas. Head Neck 2001;23:851-859.
-
(2001)
Head Neck
, vol.23
, pp. 851-859
-
-
Rainho, C.A.1
Kowalski, L.P.2
Rogatto, S.R.3
-
30
-
-
0033902038
-
Loss of imprinting and genetic alterations of the cyclin-dependent kinase inhibitor p57KIP2 gene in head and neck squamous cell carcinoma
-
Lai S, Goepfert H, Gillenwater AM, Luna MA, El-Naggar AK. Loss of imprinting and genetic alterations of the cyclin-dependent kinase inhibitor p57KIP2 gene in head and neck squamous cell carcinoma. Clin Cancer Res 2000;6:3172-3176.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 3172-3176
-
-
Lai, S.1
Goepfert, H.2
Gillenwater, A.M.3
Luna, M.A.4
El-Naggar, A.K.5
-
33
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang Y, Tycko B. Monoallelic expression of the human H19 gene. Nat Genet 1992;1:40-44.
-
(1992)
Nat Genet
, vol.1
, pp. 40-44
-
-
Zhang, Y.1
Tycko, B.2
-
34
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer M, McDonald LE, Millar DS, et al. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci USA 1992;89:1827-1831.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
-
35
-
-
0031978181
-
Base-calling of automated sequencer traces using phred. II. Error probabilities
-
Ewing B, Green P. Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res 1998; 8:186-194.
-
(1998)
Genome Res
, vol.8
, pp. 186-194
-
-
Ewing, B.1
Green, P.2
-
36
-
-
0031955518
-
Base-calling of automated sequencer traces using phred. I. Accuracy assessment
-
Ewing B, Hillier I, Wendl MC, Green P. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res 1998;8:175-185.
-
(1998)
Genome Res
, vol.8
, pp. 175-185
-
-
Ewing, B.1
Hillier, I.2
Wendl, M.C.3
Green, P.4
-
38
-
-
0036311202
-
Identification and resolution of artifacts in bisulfite sequencing
-
Warnecke PM, Stizaker C, Song J, Grunau C, Melki JR, Clarck S. Identification and resolution of artifacts in bisulfite sequencing. Methods 2002;27:101-107.
-
(2002)
Methods
, vol.27
, pp. 101-107
-
-
Warnecke, P.M.1
Stizaker, C.2
Song, J.3
Grunau, C.4
Melki, J.R.5
Clarck, S.6
-
39
-
-
2642673070
-
Genomic alterations associated with malignancy in head and neck cancer
-
Bockmuhl U, Wolf G, Schmidt S, et al. Genomic alterations associated with malignancy in head and neck cancer. Head Neck 1998;20:145-151.
-
(1998)
Head Neck
, vol.20
, pp. 145-151
-
-
Bockmuhl, U.1
Wolf, G.2
Schmidt, S.3
-
40
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche NA, Kress C, Poirrer F, Dandolo L. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev 1997;11:1596-1604.
-
(1997)
Genes Dev
, vol.11
, pp. 1596-1604
-
-
Ripoche, N.A.1
Kress, C.2
Poirrer, F.3
Dandolo, L.4
-
41
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms' tumour patients
-
Moulton T, Crenshaw T, Hao Y, et al. Epigenetic lesions at the H19 locus in Wilms' tumour patients. Nat Genet 1994;7: 440-447.
-
(1994)
Nat Genet
, vol.7
, pp. 440-447
-
-
Moulton, T.1
Crenshaw, T.2
Hao, Y.3
-
42
-
-
0032865667
-
High frequency of inactivation of the imprinted H19 gene in "sporadic" hepatoblastoma
-
Fukuzawa R, Umezawa A, Ochi K, Urano F, Ikeda H, Hata J. High frequency of inactivation of the imprinted H19 gene in "sporadic" hepatoblastoma. Int J Cancer 1999;82:490-497.
-
(1999)
Int J Cancer
, vol.82
, pp. 490-497
-
-
Fukuzawa, R.1
Umezawa, A.2
Ochi, K.3
Urano, F.4
Ikeda, H.5
Hata, J.6
-
43
-
-
0037339969
-
Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site
-
Ulaner GA, Vu Th, Li T, et al. Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site. Hum Mol Genet 2003; 12:535-549.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 535-549
-
-
Ulaner, G.A.1
Vu, Th.2
Li, T.3
-
44
-
-
0035393429
-
Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site
-
Cui H, Niemitz EL, Ravenel JD, et al. Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site. Cancer Res 2001;61:4947-4950.
-
(2001)
Cancer Res
, vol.61
, pp. 4947-4950
-
-
Cui, H.1
Niemitz, E.L.2
Ravenel, J.D.3
-
45
-
-
0347622294
-
Targeting DNA methylation in cancer
-
Szyf M. Targeting DNA methylation in cancer. Ageing Res Rev 2003;2:299-328.
-
(2003)
Ageing Res Rev
, vol.2
, pp. 299-328
-
-
Szyf, M.1
-
46
-
-
0035510088
-
Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer
-
Takay D, Gonzales FA, Tsai YC, Thayer MJ, Jones P. Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer. Hum Mol Genet 2001;10:2619-2626.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2619-2626
-
-
Takay, D.1
Gonzales, F.A.2
Tsai, Y.C.3
Thayer, M.J.4
Jones, P.5
-
47
-
-
0035895208
-
Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer
-
Nakagawa H, Chadwick RB, Peltomäki P, Plass C, Nakamura Y, de la Chapelle A. Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer. Proc Natl Acad Sci USA 2001;98:591-596.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 591-596
-
-
Nakagawa, H.1
Chadwick, R.B.2
Peltomäki, P.3
Plass, C.4
Nakamura, Y.5
De La Chapelle, A.6
-
48
-
-
0037112364
-
Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2
-
Cui H, Onyango P, Brandenburg S, Wu Y, Hsieh CL, Feinberg AP. Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2. Cancer Res 2002;62:6442-6446.
-
(2002)
Cancer Res
, vol.62
, pp. 6442-6446
-
-
Cui, H.1
Onyango, P.2
Brandenburg, S.3
Wu, Y.4
Hsieh, C.L.5
Feinberg, A.P.6
-
49
-
-
0028905376
-
Frequent loss of imprinting of the H19 gene is often associated with its over-expression in human lung cancers
-
Kondo M, Suzuki H, Ueda R, et al. Frequent loss of imprinting of the H19 gene is often associated with its over-expression in human lung cancers. Oncogene 1995;19: 1193-1198.
-
(1995)
Oncogene
, vol.19
, pp. 1193-1198
-
-
Kondo, M.1
Suzuki, H.2
Ueda, R.3
-
50
-
-
0030031360
-
Loss of H19 imprinting in esophageal cancer
-
Hibi K, Nakamura H, Hirai A, et al. Loss of H19 imprinting in esophageal cancer. Cancer Res 1996;56:480-482.
-
(1996)
Cancer Res
, vol.56
, pp. 480-482
-
-
Hibi, K.1
Nakamura, H.2
Hirai, A.3
-
51
-
-
0029240550
-
The imprinted H19 gene as a tumor marker in bladder carcinoma
-
Ariel I, Lustig O, Schneider T, et al. The imprinted H19 gene as a tumor marker in bladder carcinoma. Urology 1995;45: 335-338.
-
(1995)
Urology
, vol.45
, pp. 335-338
-
-
Ariel, I.1
Lustig, O.2
Schneider, T.3
-
52
-
-
0033673204
-
The imprinted H19 gene is a marker of early recurrence in human bladder carcinoma
-
Ariel I, Sughayer M, Felling Y, et al. The imprinted H19 gene is a marker of early recurrence in human bladder carcinoma. Mol Pathol 2000;54:320-323.
-
(2000)
Mol Pathol
, vol.54
, pp. 320-323
-
-
Ariel, I.1
Sughayer, M.2
Felling, Y.3
-
53
-
-
18544405060
-
H19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and ki-67 expression
-
Adrienssens E, Dumont L, Lottin S, et al. H19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and ki-67 expression. Am J Pathol 1998;153:1597-1607.
-
(1998)
Am J Pathol
, vol.153
, pp. 1597-1607
-
-
Adrienssens, E.1
Dumont, L.2
Lottin, S.3
-
54
-
-
0036789524
-
Possible physiological role of H19 RNA
-
Ayesh S, Matouk I, Schneider T, et al. Possible physiological role of H19 RNA. Mol Carcinog 2002;35:63-74.
-
(2002)
Mol Carcinog
, vol.35
, pp. 63-74
-
-
Ayesh, S.1
Matouk, I.2
Schneider, T.3
|