-
1
-
-
0013805802
-
Persisting clone of cells with an abnormal chromosome in a woman previously irradiated
-
DEKABAN, A. 1965. Persisting clone of cells with an abnormal chromosome in a woman previously irradiated. J. Nucl. Med. 6: 740-746.
-
(1965)
J. Nucl. Med.
, vol.6
, pp. 740-746
-
-
Dekaban, A.1
-
2
-
-
0017381277
-
Fragile sites on human chromosomes: Demonstration of their dependence on the type of tissue culture medium
-
SUTHERLAND, G.R. 1977. Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium. Science 197: 265-266.
-
(1977)
Science
, vol.197
, pp. 265-266
-
-
Sutherland, G.R.1
-
3
-
-
0024469656
-
Spontaneous chromosome fragility in band 3q21, 11p11, or 11q13 of cultured bone marrow cells from two patients with hematologic disorders
-
ABE, S. et al. 1989. Spontaneous chromosome fragility in band 3q21, 11p11, or 11q13 of cultured bone marrow cells from two patients with hematologic disorders. Cancer Genet. Cytogenet. 40: 47-53.
-
(1989)
Cancer Genet. Cytogenet.
, vol.40
, pp. 47-53
-
-
Abe, S.1
-
4
-
-
0028934193
-
New heritable fragile site with spontaneous expression at 1q41
-
DAR, H. et al. 1995. New heritable fragile site with spontaneous expression at 1q41. Am. J. Med. Genet. 55: 145-146.
-
(1995)
Am. J. Med. Genet.
, vol.55
, pp. 145-146
-
-
Dar, H.1
-
5
-
-
0022591794
-
Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11)
-
GOLLIN, S.M. et al. 1986. Spontaneous expression of fra(11)(q23) in a patient with Ewing's sarcoma and t(11;22)(q23;q11). Cancer Genet. Cytogenet. 20: 331-339.
-
(1986)
Cancer Genet. Cytogenet.
, vol.20
, pp. 331-339
-
-
Gollin, S.M.1
-
6
-
-
0025995253
-
"Spontaneous" FRA16B is a hot spot for sister chromatid exchanges
-
LUKUSA, T. et al. 1991. "Spontaneous" FRA16B is a hot spot for sister chromatid exchanges. Hum. Genet. 87: 583-586.
-
(1991)
Hum. Genet.
, vol.87
, pp. 583-586
-
-
Lukusa, T.1
-
7
-
-
0037469080
-
Preferential integration of a transfected marker gene into spontaneously expressed fragile sites of a breast cancer cell line
-
MATZNER, I., L. SAVELYEVA & M. SCHWAB. 2003. Preferential integration of a transfected marker gene into spontaneously expressed fragile sites of a breast cancer cell line. Cancer Lett. 189: 207-219.
-
(2003)
Cancer Lett.
, vol.189
, pp. 207-219
-
-
Matzner, I.1
Savelyeva, L.2
Schwab, M.3
-
8
-
-
0025996714
-
Spontaneous chromosome fragility in chorionic villus cells
-
MIGUEZ, L. et al. 1991. Spontaneous chromosome fragility in chorionic villus cells. Early Hum. Dev. 26: 93-99.
-
(1991)
Early Hum. Dev.
, vol.26
, pp. 93-99
-
-
Miguez, L.1
-
9
-
-
0020662470
-
Spontaneous expression of the chromosome fragile site fra(10)(q25)
-
TAYLOR, A.M. & S. BUNDEY. 1983. Spontaneous expression of the chromosome fragile site fra(10)(q25). Am. J. Hum. Genet. 35: 123-125.
-
(1983)
Am. J. Hum. Genet.
, vol.35
, pp. 123-125
-
-
Taylor, A.M.1
Bundey, S.2
-
10
-
-
0023753486
-
New common fragile sites
-
HECHT, F. et al. 1988. New common fragile sites. Cancer Genet. Cytogenet. 33: 1-9.
-
(1988)
Cancer Genet. Cytogenet.
, vol.33
, pp. 1-9
-
-
Hecht, F.1
-
11
-
-
0031005091
-
Aphidicolin-sensitive specific common fragile sites: A biomarker of exposure to pesticides
-
MUSIO, A. & I. SBRANA. 1997. Aphidicolin-sensitive specific common fragile sites: a biomarker of exposure to pesticides. Environ. Mol. Mutagen. 29: 250-255.
-
(1997)
Environ. Mol. Mutagen.
, vol.29
, pp. 250-255
-
-
Musio, A.1
Sbrana, I.2
-
13
-
-
0029878014
-
The enigma of common fragile sites
-
SIMONIC, I. & G.S. GERICKE. 1996. The enigma of common fragile sites. Hum. Genet. 97: 524-531.
-
(1996)
Hum. Genet.
, vol.97
, pp. 524-531
-
-
Simonic, I.1
Gericke, G.S.2
-
14
-
-
0035081264
-
Regional localization of 10 mariner transposon-like ESTs by means of FISH-evidence for a correlation with fragile sites
-
LIEHR, T. et al. 2001. Regional localization of 10 mariner transposon-like ESTs by means of FISH-evidence for a correlation with fragile sites. Mamm. Genome 12: 326-328.
-
(2001)
Mamm. Genome
, vol.12
, pp. 326-328
-
-
Liehr, T.1
-
15
-
-
0031899979
-
Common fragile sites on human chromosomes represent transcriptionally active regions: Evidence from camptothecin
-
SBRANA, I. et al. 1998. Common fragile sites on human chromosomes represent transcriptionally active regions: evidence from camptothecin. Hum. Genet. 102: 409-414.
-
(1998)
Hum. Genet.
, vol.102
, pp. 409-414
-
-
Sbrana, I.1
-
16
-
-
0024333576
-
Fibroblast-specific common fragile sites induced by aphidicolin
-
MURANO, I., A. KUWANO & T. KAJII. 1989. Fibroblast-specific common fragile sites induced by aphidicolin. Hum. Genet. 83: 45-48.
-
(1989)
Hum. Genet.
, vol.83
, pp. 45-48
-
-
Murano, I.1
Kuwano, A.2
Kajii, T.3
-
18
-
-
0022371326
-
Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites
-
BERGER, R., C.D. BLOOMFIELD & G.R. SUTHERLAND. 1985. Report of the Committee on Chromosome Rearrangements in Neoplasia and on Fragile Sites. Cytogenet. Cell Genet. 40: 490-535.
-
(1985)
Cytogenet. Cell Genet.
, vol.40
, pp. 490-535
-
-
Berger, R.1
Bloomfield, C.D.2
Sutherland, G.R.3
-
19
-
-
0032242325
-
Instability at chromosomal fragile sites
-
GLOVER, T.W. 1998. Instability at chromosomal fragile sites. Recent Results Cancer Res. 154: 185-199.
-
(1998)
Recent Results Cancer Res.
, vol.154
, pp. 185-199
-
-
Glover, T.W.1
-
20
-
-
0029061046
-
The molecular basis of fragile sites in human chromosomes
-
SUTHERLAND, G.R. & R.I. RICHARDS. 1995. The molecular basis of fragile sites in human chromosomes. Curr. Opin. Genet. Dev. 5: 323-327.
-
(1995)
Curr. Opin. Genet. Dev.
, vol.5
, pp. 323-327
-
-
Sutherland, G.R.1
Richards, R.I.2
-
21
-
-
0021278143
-
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
-
GLOVER, T.W. et al. 1984. DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum. Genet. 67: 136-142.
-
(1984)
Hum. Genet.
, vol.67
, pp. 136-142
-
-
Glover, T.W.1
-
22
-
-
0028907045
-
Effect of radiation and cigarette smoking on expression of FUdR- Inducible common fragile sites in human peripheral lymphocytes
-
BAN, S., J.B. COLOGNE & K. NERIISHI. 1995. Effect of radiation and cigarette smoking on expression of FUdR- inducible common fragile sites in human peripheral lymphocytes. Mutat... Res. 334: 197-203.
-
(1995)
Mutat. Res.
, vol.334
, pp. 197-203
-
-
Ban, S.1
Cologne, J.B.2
Neriishi, K.3
-
23
-
-
0032413191
-
The role of the FHIT/FRA3B locus in cancer
-
HUEBNER, K. et al. 1998. The role of the FHIT/FRA3B locus in cancer. Annu. Rev. Genet. 32: 7-31.
-
(1998)
Annu. Rev. Genet.
, vol.32
, pp. 7-31
-
-
Huebner, K.1
-
24
-
-
0035753424
-
FRA3B and other common fragile sites: The weakest links
-
HUEBNER, K. & C.M. CROCE. 2001. FRA3B and other common fragile sites: the weakest links. Nat. Rev. Cancer 1: 214-221.
-
(2001)
Nat. Rev. Cancer
, vol.1
, pp. 214-221
-
-
Huebner, K.1
Croce, C.M.2
-
25
-
-
0037473048
-
Characterization of the common fragile site FRA9E and its potential role in ovarian cancer
-
CALLAHAN, G. et al. 2003. Characterization of the common fragile site FRA9E and its potential role in ovarian cancer. Oncogene 22: 590-601.
-
(2003)
Oncogene
, vol.22
, pp. 590-601
-
-
Callahan, G.1
-
26
-
-
0141864371
-
Molecular basis for expression of common and rare fragile sites
-
ZLOTORYNSKI, E. et al. 2003. Molecular basis for expression of common and rare fragile sites. Mol. Cell Biol. 23: 7143-7151.
-
(2003)
Mol. Cell Biol.
, vol.23
, pp. 7143-7151
-
-
Zlotorynski, E.1
-
27
-
-
0023204641
-
Fragile sites are targets of diverse mutagens and carcinogens
-
YUNIS, J.J., A.L. SORENG & A.E. BOWE. 1987. Fragile sites are targets of diverse mutagens and carcinogens. Oncogene 1: 59-69.
-
(1987)
Oncogene
, vol.1
, pp. 59-69
-
-
Yunis, J.J.1
Soreng, A.L.2
Bowe, A.E.3
-
28
-
-
0036159474
-
Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution
-
RUIZ-HERRERA, A. et al. 2002. Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution. Chromosome Res. 10: 33-44.
-
(2002)
Chromosome Res.
, vol.10
, pp. 33-44
-
-
Ruiz-Herrera, A.1
-
29
-
-
0023269925
-
A comparative mapping study of fragile sites in the human and murine genomes
-
DJALALI, M. et al. 1987. A comparative mapping study of fragile sites in the human and murine genomes. Hum. Genet. 77: 157-162.
-
(1987)
Hum. Genet.
, vol.77
, pp. 157-162
-
-
Djalali, M.1
-
30
-
-
0036266065
-
The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at Fra8E1
-
KRUMMEL, K.A. et al. 2002. The common fragile site FRA16D and its associated gene WWOX are highly conserved in the mouse at Fra8E1. Genes Chromosomes Cancer 34: 154-167.
-
(2002)
Genes Chromosomes Cancer
, vol.34
, pp. 154-167
-
-
Krummel, K.A.1
-
31
-
-
0023090923
-
Fragile sites, chromosome evolution, and human neoplasia
-
MIRO, R. et al. 1987. Fragile sites, chromosome evolution, and human neoplasia. Hum. Genet. 75: 345-349.
-
(1987)
Hum. Genet.
, vol.75
, pp. 345-349
-
-
Miro, R.1
-
32
-
-
0021690129
-
Constitutive fragile sites and cancer
-
YUNIS, J.J. & A.L. SORENG. 1984. Constitutive fragile sites and cancer. Science 226: 1199-1204.
-
(1984)
Science
, vol.226
, pp. 1199-1204
-
-
Yunis, J.J.1
Soreng, A.L.2
-
33
-
-
0022373122
-
Evolutionary conservation of fragile sites induced by 5-azacytidine and 5-azadeoxycytidine in man, gorilla, and chimpanzee
-
SCHMID, M. et al. 1985. Evolutionary conservation of fragile sites induced by 5-azacytidine and 5-azadeoxycytidine in man, gorilla, and chimpanzee. Hum Genet. 71: 342-350.
-
(1985)
Hum Genet.
, vol.71
, pp. 342-350
-
-
Schmid, M.1
-
34
-
-
0035826908
-
Sequence conservation at human and mouse orthologous common fragile regions, FRA3B/FHIT and Fra14A2/Fhit
-
SHIRAISHI, T. et al. 2001. Sequence conservation at human and mouse orthologous common fragile regions, FRA3B/FHIT and Fra14A2/Fhit. Proc. Natl. Acad. Sci. USA 98: 5722-5727.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 5722-5727
-
-
Shiraishi, T.1
-
35
-
-
0022580241
-
Fragile sites: Overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression
-
GLOVER, T.W., J. COYLE-MORRIS & R. MORGAN. 1986. Fragile sites: overview, occurrence in acute nonlymphocytic leukemia and effects of caffeine on expression. Cancer Genet. Cytogenet. 19: 141-150.
-
(1986)
Cancer Genet. Cytogenet.
, vol.19
, pp. 141-150
-
-
Glover, T.W.1
Coyle-Morris, J.2
Morgan, R.3
-
36
-
-
0031924605
-
Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: Implications for the mechanism of fragile site induction
-
LE BEAU, M.M. et al. 1998. Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction. Hum Mol Genet. 7: 755-761.
-
(1998)
Hum Mol Genet.
, vol.7
, pp. 755-761
-
-
Le Beau, M.M.1
-
37
-
-
0033051760
-
Allele-specific late replication and fragility of the most active common fragile site, FRA3B
-
WANG, L. et al. 1999. Allele-specific late replication and fragility of the most active common fragile site, FRA3B. Hum. Mol. Genet. 8: 431-437.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 431-437
-
-
Wang, L.1
-
38
-
-
0034117095
-
Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability
-
HELLMAN, A. et al. 2000. Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Mol. Cell Biol. 20: 4420-4427.
-
(2000)
Mol. Cell Biol.
, vol.20
, pp. 4420-4427
-
-
Hellman, A.1
-
39
-
-
13144283613
-
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site
-
MISHMAR, D. et al. 1998. Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site. Proc. Natl. Acad. Sci. USA 95: 8141-8146.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 8141-8146
-
-
Mishmar, D.1
-
40
-
-
0033595004
-
Cancer-specific chromosome alterations in the constitutive fragile region FRA3B
-
MIMORI, K. et al. 1999. Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. Proc. Natl. Acad. Sci. USA 96: 7456-7461.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 7456-7461
-
-
Mimori, K.1
-
41
-
-
0037126393
-
Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors
-
MORELLI, C. et al. 2002. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors. Oncogene 21: 7266-7276.
-
(2002)
Oncogene
, vol.21
, pp. 7266-7276
-
-
Morelli, C.1
-
42
-
-
17444440946
-
Common chromosomal fragile site FRA16D sequence: Identification of the for gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
-
RIED, K. et al. 2000. Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells. Hum. Mol. Genet. 9: 1651-1663.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1651-1663
-
-
Ried, K.1
-
43
-
-
0037074013
-
ATR regulates fragile site stability
-
CASPER, A.M. et al. 2002. ATR regulates fragile site stability. Cell 111: 779-789.
-
(2002)
Cell
, vol.111
, pp. 779-789
-
-
Casper, A.M.1
-
44
-
-
0034312277
-
Requirement for Atr in phosphorylation of Chk1 and cell cycle regulation in response to DNA replication blocks and UV-damaged DNA in Xenopus egg extracts
-
Guo, Z. et al. 2000. Requirement for Atr in phosphorylation of Chk1 and cell cycle regulation in response to DNA replication blocks and UV-damaged DNA in Xenopus egg extracts. Genes Dev. 14: 2745-2756.
-
(2000)
Genes Dev.
, vol.14
, pp. 2745-2756
-
-
Guo, Z.1
-
45
-
-
0032472330
-
Overexpression of a kinase-inactive ATR protein causes sensitivity to DNA-damaging agents and defects in cell cycle checkpoints
-
CLIBY, W.A. et al. 1998. Overexpression of a kinase-inactive ATR protein causes sensitivity to DNA-damaging agents and defects in cell cycle checkpoints. EMBO J. 17: 159-169.
-
(1998)
EMBO J.
, vol.17
, pp. 159-169
-
-
Cliby, W.A.1
-
46
-
-
0034649590
-
Xenopus ATR is a replication-dependent chromatin-binding protein required for the DNA replication checkpoint
-
HEKMAT-NEJAD, M. et al. 2000. Xenopus ATR is a replication-dependent chromatin-binding protein required for the DNA replication checkpoint. Curr. Biol. 10: 1565-1573.
-
(2000)
Curr. Biol.
, vol.10
, pp. 1565-1573
-
-
Hekmat-Nejad, M.1
-
47
-
-
0037452872
-
Fragile sites: Breaking up over a slowdown
-
CIMPRICH, K. A. 2003. Fragile sites: breaking up over a slowdown. Curr. Biol. 13: R231-233.
-
(2003)
Curr. Biol.
, vol.13
-
-
Cimprich, K.A.1
-
48
-
-
0023789150
-
Chromosome breakage and recombination at fragile sites
-
GLOVER, T.W. & C.K. STEIN. 1988. Chromosome breakage and recombination at fragile sites. Am. J. Hum. Genet. 43: 265-273.
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 265-273
-
-
Glover, T.W.1
Stein, C.K.2
-
49
-
-
0343035597
-
Comparative study of chromosome aberrations induced with aphidicolin in women affected by breast cancer and cervix uterine cancer
-
PAZ-Y-MINO, C. et al. 1997. Comparative study of chromosome aberrations induced with aphidicolin in women affected by breast cancer and cervix uterine cancer. Cancer Genet. Cytogenet. 94: 120-124.
-
(1997)
Cancer Genet. Cytogenet.
, vol.94
, pp. 120-124
-
-
Paz-Y-Mino, C.1
-
50
-
-
0037288332
-
Expression of aphidicolin-induced fragile sites and their relationship between genetic susceptibility in breast cancer, ovarian cancer, and non-small-cell lung cancer patients
-
DHILLON, V.S., S.A. HUSAIN & G.N. RAY. 2003. Expression of aphidicolin-induced fragile sites and their relationship between genetic susceptibility in breast cancer, ovarian cancer, and non-small-cell lung cancer patients. Terat. Carcin. Mutagen. Suppl 1: 35-45.
-
(2003)
Terat. Carcin. Mutagen.
, Issue.SUPPL. 1
, pp. 35-45
-
-
Dhillon, V.S.1
Husain, S.A.2
Ray, G.N.3
-
51
-
-
0033836494
-
The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites
-
EGELI, U. et al. 2000. The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites. Head Neck 22: 591-598.
-
(2000)
Head Neck
, vol.22
, pp. 591-598
-
-
Egeli, U.1
-
52
-
-
0028871656
-
Expression of common fragile sites in lymphocytes of Wilms tumor in patients, their parents, and siblings
-
SUNDARESHAN, T.S. & M. AUGUSTUS. 1995. Expression of common fragile sites in lymphocytes of Wilms tumor in patients, their parents, and siblings. Cancer Genet. Cytogenet. 84: 51-55.
-
(1995)
Cancer Genet. Cytogenet.
, vol.84
, pp. 51-55
-
-
Sundareshan, T.S.1
Augustus, M.2
-
53
-
-
0024268761
-
Common fragile sites and human cancer: A study on lymphocytes from neuroblastoma patients
-
VERNOLE, P. et al. 1988. Common fragile sites and human cancer: a study on lymphocytes from neuroblastoma patients. Cancer Genet. Cytogenet. 36: 13-23.
-
(1988)
Cancer Genet. Cytogenet.
, vol.36
, pp. 13-23
-
-
Vernole, P.1
-
55
-
-
0035954234
-
Amplification of oncogenes revisited: From expression profiling to clinical application
-
SAVELYEVA, L. & M. SCHWAB. 2001. Amplification of oncogenes revisited: from expression profiling to clinical application. Cancer Lett. 167: 115-123.
-
(2001)
Cancer Lett.
, vol.167
, pp. 115-123
-
-
Savelyeva, L.1
Schwab, M.2
-
56
-
-
0026645532
-
Co-amplified markers alternate in megabase long chromosomal inverted repeats and cluster independently in interphase nuclei at early steps of mammalian gene amplification
-
TOLEDO, F. et al. 1992. Co-amplified markers alternate in megabase long chromosomal inverted repeats and cluster independently in interphase nuclei at early steps of mammalian gene amplification. EMBO J. 11: 2665-2673.
-
(1992)
EMBO J.
, vol.11
, pp. 2665-2673
-
-
Toledo, F.1
-
57
-
-
0030904279
-
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
-
COQUELLE, A. et al. 1997. Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons. Cell 89: 215-225.
-
(1997)
Cell
, vol.89
, pp. 215-225
-
-
Coquelle, A.1
-
58
-
-
0027982007
-
Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug-resistant CHO cells
-
KUO, M.T. et al. 1994. Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug-resistant CHO cells. Mol Cell Biol. 14: 5202-11.
-
(1994)
Mol Cell Biol.
, vol.14
, pp. 5202-5211
-
-
Kuo, M.T.1
-
59
-
-
12944329959
-
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
-
GISSELSSON, D. et al. 2000. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. Proc. Natl. Acad. Sci. USA 97: 5357-5362.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5357-5362
-
-
Gisselsson, D.1
-
60
-
-
0036463767
-
A role for common fragile site induction in amplification of human oncogenes
-
HELLMAN, A. et al. 2002. A role for common fragile site induction in amplification of human oncogenes. Cancer Cell. 1: 89-97.
-
(2002)
Cancer Cell
, vol.1
, pp. 89-97
-
-
Hellman, A.1
-
61
-
-
0036849512
-
Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: The model of PIP gene duplication from a break at FRA7I
-
CIULLO, M. et al. 2002. Initiation of the breakage-fusion-bridge mechanism through common fragile site activation in human breast cancer cells: the model of PIP gene duplication from a break at FRA7I. Hum. Mol. Genet. 11: 2887-2894.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2887-2894
-
-
Ciullo, M.1
-
62
-
-
0023805880
-
Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpoints
-
CANNIZZARO, L.A. et al. 1988. Regional chromosome localization of human papillomavirus integration sites near fragile sites, oncogenes, and cancer chromosome breakpoints. Cancer Genet. Cytogenet. 33: 93-98.
-
(1988)
Cancer Genet. Cytogenet.
, vol.33
, pp. 93-98
-
-
Cannizzaro, L.A.1
-
63
-
-
0024453311
-
Preferential sites for viral integration on mammalian genome
-
POPESCU, N.C. & J.A. DIPAOLO. 1989. Preferential sites for viral integration on mammalian genome. Cancer Genet. Cytogenet. 42: 157-171.
-
(1989)
Cancer Genet. Cytogenet.
, vol.42
, pp. 157-171
-
-
Popescu, N.C.1
Dipaolo, J.A.2
-
64
-
-
0025265727
-
Viral integration, fragile sites, and proto-oncogenes in human neoplasia
-
POPESCU, N.C., D. ZIMONJIC & J.A. DIPAOLO. 1990. Viral integration, fragile sites, and proto-oncogenes in human neoplasia. Hum. Genet. 84: 383-386.
-
(1990)
Hum. Genet.
, vol.84
, pp. 383-386
-
-
Popescu, N.C.1
Zimonjic, D.2
Dipaolo, J.A.3
-
65
-
-
0037468256
-
Common fragile sites are preferential targets for HPV16 integrations in cervical tumors
-
THORLAND, E.C. et al. 2003. Common fragile sites are preferential targets for HPV16 integrations in cervical tumors. Oncogene 22: 1225-1237.
-
(2003)
Oncogene
, vol.22
, pp. 1225-1237
-
-
Thorland, E.C.1
-
66
-
-
0034326237
-
Human papillomavirus type 16 integrations in cervical tumors frequently occur in common fragile sites
-
THORLAND, E.C. et al. 2000. Human papillomavirus type 16 integrations in cervical tumors frequently occur in common fragile sites. Cancer Res. 60: 5916-5921.
-
(2000)
Cancer Res.
, vol.60
, pp. 5916-5921
-
-
Thorland, E.C.1
-
67
-
-
0242720711
-
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinoma
-
FERBER, M.J. et al. 2003. Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinoma. Oncogene 22: 7233-42.
-
(2003)
Oncogene
, vol.22
, pp. 7233-7242
-
-
Ferber, M.J.1
-
68
-
-
0031916693
-
Sites of recombinant adeno-associated virus integration
-
RIVADENEIRA, E. D. et al. 1998. Sites of recombinant adeno-associated virus integration. Int. J. Oncol. 12: 805-810.
-
(1998)
Int. J. Oncol.
, vol.12
, pp. 805-810
-
-
Rivadeneira, E.D.1
-
69
-
-
0037294118
-
Characterization of the human common fragile site FRA2G
-
LIMONGI, M.Z., F. PELLICCIA & A. ROCCHI. 2003. Characterization of the human common fragile site FRA2G. Genomics 81: 93-97.
-
(2003)
Genomics
, vol.81
, pp. 93-97
-
-
Limongi, M.Z.1
Pelliccia, F.2
Rocchi, A.3
-
70
-
-
0030201095
-
Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2
-
RASSOOL, F.V. et al. 1996. Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2. Genomics 35: 109-117.
-
(1996)
Genomics
, vol.35
, pp. 109-117
-
-
Rassool, F.V.1
-
71
-
-
0026017993
-
Preferential integration of marker DNA into the chromosomal fragile site at 3p14: An approach to cloning fragile sites
-
RASSOOL, F.V. et al. 1991. Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites. Proc. Natl. Acad. Sci. USA 88: 6657-6661.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 6657-6661
-
-
Rassool, F.V.1
-
72
-
-
0028169985
-
Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma
-
WILKE, C.M. et al. 1994. Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the t(3;8) associated with hereditary renal cell carcinoma. Genomics 22: 319-326.
-
(1994)
Genomics
, vol.22
, pp. 319-326
-
-
Wilke, C.M.1
-
73
-
-
0030890750
-
Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene
-
ZIMONJIC, D. B. et al. 1997. Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene. Cancer Res. 57: 1166-1170.
-
(1997)
Cancer Res.
, vol.57
, pp. 1166-1170
-
-
Zimonjic, D.B.1
-
74
-
-
0031447174
-
Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion
-
INOUE, H. et al. 1997. Sequence of the FRA3B common fragile region: implications for the mechanism of FHIT deletion. Proc. Natl. Acad. Sci. USA 94: 14584-14589.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 14584-14589
-
-
Inoue, H.1
-
75
-
-
0032493124
-
FRA7G extends over a broad region: Coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites
-
HUANG, H. et al. 1998. FRA7G extends over a broad region: coincidence of human endogenous retroviral sequences (HERV-H) and small polydispersed circular DNAs (spcDNA) and fragile sites. Oncogene 16: 2311-2319.
-
(1998)
Oncogene
, vol.16
, pp. 2311-2319
-
-
Huang, H.1
-
76
-
-
0034704856
-
Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site
-
ZENKLUSEN, J.C. et al. 2000. Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site. Oncogene 19: 1729-1733.
-
(2000)
Oncogene
, vol.19
, pp. 1729-1733
-
-
Zenklusen, J.C.1
-
77
-
-
0034306548
-
The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations
-
KRUMMEL, K.A. et al. 2000. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations. Genomics 69: 37-46.
-
(2000)
Genomics
, vol.69
, pp. 37-46
-
-
Krummel, K.A.1
-
78
-
-
0034654641
-
Chromosomal fragile site FRA16D and DNA instability in cancer
-
MANGELSDORF, M. et al. 2000. Chromosomal fragile site FRA16D and DNA instability in cancer. Cancer Res. 60: 1683-1689.
-
(2000)
Cancer Res.
, vol.60
, pp. 1683-1689
-
-
Mangelsdorf, M.1
-
79
-
-
0036131979
-
Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells
-
ARLT, M.F. et al. 2002. Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells. Genes Chromosomes Cancer 33: 82-92.
-
(2002)
Genes Chromosomes Cancer
, vol.33
, pp. 82-92
-
-
Arlt, M.F.1
-
80
-
-
0037293054
-
Candidate tumor suppressor genes at FRA7G are coamplified with MET and do not suppress malignancy in a gastric cancer
-
HAN, S.Y., T. DRUCK & K. HUEBNER. 2003. Candidate tumor suppressor genes at FRA7G are coamplified with MET and do not suppress malignancy in a gastric cancer. Genomics 81: 105-107.
-
(2003)
Genomics
, vol.81
, pp. 105-107
-
-
Han, S.Y.1
Druck, T.2
Huebner, K.3
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