-
1
-
-
0028832281
-
Circular structures in retroviral and cellular genomes
-
Albert, F. G., Bronson, E. C., Fitzgerald, D. J. and Anderson, J. N. (1995). Circular structures in retroviral and cellular genomes. J. Biol. Chem. 270, 23570-23581.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 23570-23581
-
-
Albert, F.G.1
Bronson, E.C.2
Fitzgerald, D.J.3
Anderson, J.N.4
-
2
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S. F., Madden, T. L., Schaffer, A. A., Zhang, J., Zhnag, Z., Miller, W. and Lipman, D. J. (1997). Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucl. Acids Res. 25, 3389-3402.
-
(1997)
Nucl. Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
Zhang, J.4
Zhnag, Z.5
Miller, W.6
Lipman, D.J.7
-
3
-
-
0026547285
-
Aphidicolin-inducible common fragile site expression: Results from a population survey of twins
-
Austin, M. J., Collins, J. M., Corty, L. A., Nance, W. E., Neale, M. C., Schicken, R. M. and Brown, J. A. (1992). Aphidicolin-inducible common fragile site expression: Results from a population survey of twins. Am. J. Hum. Genet. 50, 76-83.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 76-83
-
-
Austin, M.J.1
Collins, J.M.2
Corty, L.A.3
Nance, W.E.4
Neale, M.C.5
Schicken, R.M.6
Brown, J.A.7
-
4
-
-
0028786921
-
Adenovirus type 12-induced fragility of the human RNU2 locus requires U2 small nuclear RNA transcriptional regulatory elements
-
Bailey, A. D., Li, Z., Pavelitz, T. and Weiner, A. M. (1995). Adenovirus type 12-induced fragility of the human RNU2 locus requires U2 small nuclear RNA transcriptional regulatory elements. Mul. Cell. Biol. 15, 6246-6255.
-
(1995)
Mul. Cell. Biol.
, vol.15
, pp. 6246-6255
-
-
Bailey, A.D.1
Li, Z.2
Pavelitz, T.3
Weiner, A.M.4
-
5
-
-
0028109387
-
Integrated YAC contig containing the 3p14 hereditary renal cell carcinoma 3:8 translocation breakpoint and the fragile site FRA3B
-
Boldog, F. L., Waggoner, B., Glover, T. W., Chumakov, I., Le Paslsier, D., Cohen, D., Gemmill, R. M. and Drabkin, H. A. (1994). Integrated YAC contig containing the 3p14 hereditary renal cell carcinoma 3:8 translocation breakpoint and the fragile site FRA3B. Genes, Chromosomes and Cancer 11, 216-221.
-
(1994)
Genes, Chromosomes and Cancer
, vol.11
, pp. 216-221
-
-
Boldog, F.L.1
Waggoner, B.2
Glover, T.W.3
Chumakov, I.4
Le Paslsier, D.5
Cohen, D.6
Gemmill, R.M.7
Drabkin, H.A.8
-
6
-
-
2042468966
-
Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B
-
Boldog, F., Gemmill, R. M., West, J., Robinson, M., Robinson, L., Li, E., Roche, J., Todd, S., Waggoner, B., Lundstrom, R., Jacobson, J., Mullokandov, M. R., Klinger, H. and Drabkin, H. A. (1997). Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B. Hum. Mol. Genet. 6, 193-203.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 193-203
-
-
Boldog, F.1
Gemmill, R.M.2
West, J.3
Robinson, M.4
Robinson, L.5
Li, E.6
Roche, J.7
Todd, S.8
Waggoner, B.9
Lundstrom, R.10
Jacobson, J.11
Mullokandov, M.R.12
Klinger, H.13
Drabkin, H.A.14
-
7
-
-
0029987173
-
Common structural features of replication origins in all life forms
-
Boulikas, T. (1996). Common structural features of replication origins in all life forms. J. Cell. Biochem. 60, 297-316.
-
(1996)
J. Cell. Biochem.
, vol.60
, pp. 297-316
-
-
Boulikas, T.1
-
8
-
-
0029082085
-
Characteristic chromosomal fragility of human embryonic cells exposed in vitro to aphidicolin
-
Caporossi, D., Vernole, P., Nicoletti, B. and Tedeschi, B. (1995). Characteristic chromosomal fragility of human embryonic cells exposed in vitro to aphidicolin. Hum. Genet. 96, 269-274.
-
(1995)
Hum. Genet.
, vol.96
, pp. 269-274
-
-
Caporossi, D.1
Vernole, P.2
Nicoletti, B.3
Tedeschi, B.4
-
9
-
-
0030904279
-
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
-
Coquelle, A., Piparas, E., Toledo, F., Buttin, G. and Debatisse, M. (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
Piparas, E.2
Toledo, F.3
Buttin, G.4
Debatisse, M.5
-
10
-
-
0023269925
-
A comparative mapping study of fragile sites in the human and murine genomes
-
Djalali, M., Adolph, S., Steinbach, P., Winking, H. and Hameister, H. (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
Adolph, S.2
Steinbach, P.3
Winking, H.4
Hameister, H.5
-
11
-
-
0028272137
-
Modular sequence elements associated with origin regions in eukaryotic chromosomal DNA
-
Dobbs, D. L., Shaiu, W.-L. and Bennow, R. M. (1994). Modular sequence elements associated with origin regions in eukaryotic chromosomal DNA. Nucl. Acids Res. 22, 2479-2489.
-
(1994)
Nucl. Acids Res.
, vol.22
, pp. 2479-2489
-
-
Dobbs, D.L.1
Shaiu, W.-L.2
Bennow, R.M.3
-
12
-
-
0023874808
-
A fragile site in the human U2 small nuclear RNA gene cluster is revealed by Adenovirus type 12 infection
-
Durnam, D. M., Menninger, J. C., Chandler, S. H., Smith, P. P. and McDougall, J. K. (1998). A fragile site in the human U2 small nuclear RNA gene cluster is revealed by Adenovirus type 12 infection. Mol. Cell. Biol. 8, 1863-1867.
-
(1998)
Mol. Cell. Biol.
, vol.8
, pp. 1863-1867
-
-
Durnam, D.M.1
Menninger, J.C.2
Chandler, S.H.3
Smith, P.P.4
McDougall, J.K.5
-
13
-
-
0023665948
-
Computer modelling of DNA structures involved in chromosome maintenance
-
Eckdahl, T. T. and Anderson, J. N. (1987) Computer modelling of DNA structures involved in chromosome maintenance. Nucl. Acids Res. 15, 8531-8545.
-
(1987)
Nucl. Acids Res.
, vol.15
, pp. 8531-8545
-
-
Eckdahl, T.T.1
Anderson, J.N.2
-
14
-
-
0025308614
-
Conserved DNA structures in origins of replication
-
Eckdahl, T. T. and Anderson, J. N. (1990) Conserved DNA structures in origins of replication. Nucl. Acids Res. 18, 1609-1612.
-
(1990)
Nucl. Acids Res.
, vol.18
, pp. 1609-1612
-
-
Eckdahl, T.T.1
Anderson, J.N.2
-
15
-
-
0028785210
-
Generation of a human X-derived minichromosome using telomere-associated chromosome fragmentation
-
Farr, C. J., Bayne, R. A. L., Kipling, D., Mills, W., Critcher, R. and Cooke, H. J. (1995). Generation of a human X-derived minichromosome using telomere-associated chromosome fragmentation. EMBO J. 14, 5444-5454.
-
(1995)
EMBO J.
, vol.14
, pp. 5444-5454
-
-
Farr, C.J.1
Bayne, R.A.L.2
Kipling, D.3
Mills, W.4
Critcher, R.5
Cooke, H.J.6
-
16
-
-
0028129558
-
Conserved patterns of bending in satellite and nucleosome positioning DNA
-
Fitzgerald, D. J., Dryden, G. L., Bronson, E. C., Williams, J. S. and Anderson, J. N. (1994) Conserved patterns of bending in satellite and nucleosome positioning DNA. J. Biol. Chem. 269, 21303-21314.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 21303-21314
-
-
Fitzgerald, D.J.1
Dryden, G.L.2
Bronson, E.C.3
Williams, J.S.4
Anderson, J.N.5
-
17
-
-
0029057763
-
Study of the relationship between common fragile sites, chromosome breakages and sister chromatid exchanges
-
Gaddini, L., Belliccia, F., Limongi, M. Z. and Rocchi, A. (1995). Study of the relationship between common fragile sites, chromosome breakages and sister chromatid exchanges. Mutagenesis 10, 257-260.
-
(1995)
Mutagenesis
, vol.10
, pp. 257-260
-
-
Gaddini, L.1
Belliccia, F.2
Limongi, M.Z.3
Rocchi, A.4
-
18
-
-
0028784797
-
The transcriptionally competent U2 gene is necessary and sufficient for Adenovirus type 12 induction ot the fragile site at 17q2l-22
-
Gargano, S., Wang, P., Rusanganwa, E. and Bacchelti, S. (1995) The transcriptionally competent U2 gene is necessary and sufficient for Adenovirus type 12 induction ot the fragile site at 17q2l-22. Mol. Cell. Biol. 15, 6256-6261.
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 6256-6261
-
-
Gargano, S.1
Wang, P.2
Rusanganwa, E.3
Bacchelti, S.4
-
19
-
-
0021278143
-
DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
-
Glover, T. M., Berger, C., Coyle, J. and Echo, B. (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.M.1
Berger, C.2
Coyle, J.3
Echo, B.4
-
20
-
-
0023614553
-
Induction of sister chromatid exchanges at common fragile sites
-
Glover, T. W. and Stein, C. K. (1987). Induction of sister chromatid exchanges at common fragile sites. Am. J. Hum. Genet. 41, 882-890.
-
(1987)
Am. J. Hum. Genet.
, vol.41
, pp. 882-890
-
-
Glover, T.W.1
Stein, C.K.2
-
21
-
-
0023789150
-
Chromosome breakage and recombination at fragile sites
-
Glover, T. W. and Stein, C. K. (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
-
22
-
-
0020480669
-
The construction of cosmid libraries which can be used to transform eukaryotic cells
-
Grosveld, K G., Lund, T., Murray, E. J., Mellor, A. L., Dahl, H. H. M. and Flavell, R. A. (1982). The construction of cosmid libraries which can be used to transform eukaryotic cells. Nucl. Acids Res. 10, 6715-6732.
-
(1982)
Nucl. Acids Res.
, vol.10
, pp. 6715-6732
-
-
Grosveld, K.G.1
Lund, T.2
Murray, E.J.3
Mellor, A.L.4
Dahl, H.H.M.5
Flavell, R.A.6
-
23
-
-
0027449978
-
The identification of a third fragile site. HRAXF in Xq27-q28 distal to both FRAXA and FRAXE
-
Hirst, M. C., Barnicoat, A., Flynn, G., Wang, Q., Daker, M., Buckle, V. J., Davies, K. E. and Bobrow, M. (1993). The identification of a third fragile site. HRAXF in Xq27-q28 distal to both FRAXA and FRAXE. Hum. Mol. Genet. 2, 197-200.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 197-200
-
-
Hirst, M.C.1
Barnicoat, A.2
Flynn, G.3
Wang, Q.4
Daker, M.5
Buckle, V.J.6
Davies, K.E.7
Bobrow, M.8
-
24
-
-
0000467231
-
Mammalian chromosomes in vitro XVII: Ideogram of the Chinese hamster
-
Hsu, T. C. and Zenzes, M. T. (1964). Mammalian chromosomes in vitro XVII: Ideogram of the Chinese hamster. J. Nat. Cancer Inst. (Bethesda) 32, 857-869.
-
(1964)
J. Nat. Cancer Inst. (Bethesda)
, vol.32
, pp. 857-869
-
-
Hsu, T.C.1
Zenzes, M.T.2
-
25
-
-
0023490455
-
A tissue specific fragile site associated with the sex reversed (SXR) mutation in the mouse
-
Hunt, P. A. and Burgoyne, P. S. (1987). A tissue specific fragile site associated with the sex reversed (SXR) mutation in the mouse. Chromosoma 96, 67-71.
-
(1987)
Chromosoma
, vol.96
, pp. 67-71
-
-
Hunt, P.A.1
Burgoyne, P.S.2
-
26
-
-
0031447174
-
Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion
-
Inoue, H., Ishii, H., Alder, H., Snyder, E., Druck, T., Huebner, K. and Croce, C. M. (1997). Sequence of the FRA3B common fragile region: Implications for the mechanism of FHIT deletion. Proc. Nat. Acad. Sci. USA 94, 14584-14589.
-
(1997)
Proc. Nat. Acad. Sci. USA
, vol.94
, pp. 14584-14589
-
-
Inoue, H.1
Ishii, H.2
Alder, H.3
Snyder, E.4
Druck, T.5
Huebner, K.6
Croce, C.M.7
-
27
-
-
0028557941
-
Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3
-
Jones, C., Slijepcevic, P., Marsh, S., Baker, E., Langdon, W. Y., Richards, R. I. and Tunnacliffe, A. (1994). Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. Hum. Mol. Genet. 3, 2123-2130.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2123-2130
-
-
Jones, C.1
Slijepcevic, P.2
Marsh, S.3
Baker, E.4
Langdon, W.Y.5
Richards, R.I.6
Tunnacliffe, A.7
-
28
-
-
0028896099
-
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2
-
Jones, C., Penny, L., Mattina, T., Yu, S., Baker, E., Voullaire, L., Langdon, W. Y., Sutherland, G. R., Richards, R. I. and Tunnacliffe, A. (1995). Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2. Nature 376, 145-149.
-
(1995)
Nature
, vol.376
, pp. 145-149
-
-
Jones, C.1
Penny, L.2
Mattina, T.3
Yu, S.4
Baker, E.5
Voullaire, L.6
Langdon, W.Y.7
Sutherland, G.R.8
Richards, R.I.9
Tunnacliffe, A.10
-
29
-
-
0025800165
-
Mapping of DNA instability at the Fragile X to a trinucleolide repeat sequence p(CCG)n
-
Kremer, E. J., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S. T., Schlessinger, D., Sutherland, G. R. and Richards, R. I. (1991). Mapping of DNA instability at the Fragile X to a trinucleolide repeat sequence p(CCG)n. Science 252, 1711-1714.
-
(1991)
Science
, vol.252
, pp. 1711-1714
-
-
Kremer, E.J.1
Pritchard, M.2
Lynch, M.3
Yu, S.4
Holman, K.5
Baker, E.6
Warren, S.T.7
Schlessinger, D.8
Sutherland, G.R.9
Richards, R.I.10
-
30
-
-
0027982007
-
Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug resistant CHO cells
-
Kuo, M. T., Vyas, R. C., Jiang, L.-X. and Hittelman, W. N. (1994). Chromosome breakage at a major fragile site associated with P-glycoprotein gene amplification in multidrug resistant CHO cells. Mol. Cell. Biol. 14, 5202-5211.
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 5202-5211
-
-
Kuo, M.T.1
Vyas, R.C.2
Jiang, L.-X.3
Hittelman, W.N.4
-
31
-
-
0026842288
-
Scaffold associated regions: Cis-acting determinants of chromatin structural loops and functional domains
-
Laemmli, U. K., Kas, E., Poljak, L. and Adachi, Y. (1992). Scaffold associated regions: Cis-acting determinants of chromatin structural loops and functional domains. Curr. Opin. Genet. Dev. 2, 275-285.
-
(1992)
Curr. Opin. Genet. Dev.
, vol.2
, pp. 275-285
-
-
Laemmli, U.K.1
Kas, E.2
Poljak, L.3
Adachi, Y.4
-
32
-
-
0021183587
-
Heritable fragile sites in cancer
-
LeBeau, M. M. and Rowley, J. D. (1984). Heritable fragile sites in cancer. Nature 308, 607-608.
-
(1984)
Nature
, vol.308
, pp. 607-608
-
-
LeBeau, M.M.1
Rowley, J.D.2
-
33
-
-
0021163617
-
An in vitro and in vivo study of a BrdU sensitive fragile site in the Chinese hamster
-
Lin, M. S., Takabayashi, T., Wilson, M. G. and Marchese, C. A. (1984) An in vitro and in vivo study of a BrdU sensitive fragile site in the Chinese hamster. Cytogenet. Cell Genet. 38, 211-215.
-
(1984)
Cytogenet. Cell Genet.
, vol.38
, pp. 211-215
-
-
Lin, M.S.1
Takabayashi, T.2
Wilson, M.G.3
Marchese, C.A.4
-
34
-
-
2642620883
-
The interactions of Adenovirus with host cell gene loci
-
McDougall, J. K. (1979). The interactions of Adenovirus with host cell gene loci. Cytogenet. Cell Genet. 25, 183.
-
(1979)
Cytogenet. Cell Genet.
, vol.25
, pp. 183
-
-
McDougall, J.K.1
-
35
-
-
0023090923
-
Fragile sites. chromosome evolution and human neoplasia
-
Miro, R., Clemente, I. C., Fuster, C. and Egozcue, J. (1987). Fragile sites. chromosome evolution and human neoplasia. Hum .Genet. 75, 345-349.
-
(1987)
Hum .Genet.
, vol.75
, pp. 345-349
-
-
Miro, R.1
Clemente, I.C.2
Fuster, C.3
Egozcue, J.4
-
36
-
-
0024333576
-
Fibroblast specific common fragile sites induced by aphidicolin
-
Murano, I., Kuwano, A. and Kajii, T. (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
-
37
-
-
0027981933
-
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
-
Nancarrow, J. K., Kremer, E., Holman, K., Eyre, H., Doggett, N. A., Le Paslier, D., Callen, D. F., Sutherland, G. R. and Richards, R. I. (1994). Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science 264, 1938-1941
-
(1994)
Science
, vol.264
, pp. 1938-1941
-
-
Nancarrow, J.K.1
Kremer, E.2
Holman, K.3
Eyre, H.4
Doggett, N.A.5
Le Paslier, D.6
Callen, D.F.7
Sutherland, G.R.8
Richards, R.I.9
-
38
-
-
0026548222
-
DNA helical stability accounts for mutational defects in a yeast replication origin
-
Natale, D. A., Schubert, A. E. and Kowalski, D. (1992). DNA helical stability accounts for mutational defects in a yeast replication origin. Proc. Nat. Acad. Sci. USA 89, 2654-2658.
-
(1992)
Proc. Nat. Acad. Sci. USA
, vol.89
, pp. 2654-2658
-
-
Natale, D.A.1
Schubert, A.E.2
Kowalski, D.3
-
39
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in Fragile X syndrome
-
Oberle, I., Rousseau, F., Heitz, D., Kretz, C., Devys, D., Hanauer, A., Boue, J., Bertheas, M. F. and Mandel, J. L. (1991). Instability of a 550-base pair DNA segment and abnormal methylation in Fragile X syndrome. Science 252, 1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberle, I.1
Rousseau, F.2
Heitz, D.3
Kretz, C.4
Devys, D.5
Hanauer, A.6
Boue, J.7
Bertheas, M.F.8
Mandel, J.L.9
-
40
-
-
13344279424
-
The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3:8) breakpoint is abnormal in digestive tract cancers
-
Ohta, M., Inoue, H., Cotticelli, M. G., Kastury, K., Baffa, R., Palazzo, J., Siprashvili, Z., Mori, M., McCue, P., Druck, T., Croce, C. M. and Huebner, K. (1996). The FHIT gene. spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3:8) breakpoint is abnormal in digestive tract cancers. Cell 84, 587-597.
-
(1996)
Cell
, vol.84
, pp. 587-597
-
-
Ohta, M.1
Inoue, H.2
Cotticelli, M.G.3
Kastury, K.4
Baffa, R.5
Palazzo, J.6
Siprashvili, Z.7
Mori, M.8
McCue, P.9
Druck, T.10
Croce, C.M.11
Huebner, K.12
-
41
-
-
0030930174
-
Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines
-
Ong, S. T., Fong, K. M., Bader, S. A., Minna, J. D., Le Beau, M. M., McKeithan, T. W. and Rassool, F. V. (1997). Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines. Genes Chromosomes Cancer 20, 16-23.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 16-23
-
-
Ong, S.T.1
Fong, K.M.2
Bader, S.A.3
Minna, J.D.4
Le Beau, M.M.5
McKeithan, T.W.6
Rassool, F.V.7
-
42
-
-
0029045840
-
Precise localization of aphidicolin induced breakpoints on the short arm of human chromosome 3
-
Paradee, W., Mullins, C., He, Z., Glover, T., Wilke, C., Opalka, B., Schutte, J. and Smith, D. I. (1995). Precise localization of aphidicolin induced breakpoints on the short arm of human chromosome 3. Genomics 27, 358-361.
-
(1995)
Genomics
, vol.27
, pp. 358-361
-
-
Paradee, W.1
Mullins, C.2
He, Z.3
Glover, T.4
Wilke, C.5
Opalka, B.6
Schutte, J.7
Smith, D.I.8
-
43
-
-
0030201105
-
A 350 kb cosmid contig in 3p14.2 that crosses the t(3:8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin induced FRA3B breakpoints
-
Paradee, W., Wilke, C. M., Wang, L., Shridhar, R., Mullins, C. M., Hoge, A., Glover, T. W. and Smith, D. I. (1996). A 350 kb cosmid contig in 3p14.2 that crosses the t(3:8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin induced FRA3B breakpoints. Genomics 35, 87-93.
-
(1996)
Genomics
, vol.35
, pp. 87-93
-
-
Paradee, W.1
Wilke, C.M.2
Wang, L.3
Shridhar, R.4
Mullins, C.M.5
Hoge, A.6
Glover, T.W.7
Smith, D.I.8
-
44
-
-
0023989064
-
Improved tools for biological sequence comparison
-
Pearson, W. R. and Lipman, D. J. (1988). Improved tools for biological sequence comparison. Proc. Nat. Acad. Sci. USA 85, 2444-2448.
-
(1988)
Proc. Nat. Acad. Sci. USA
, vol.85
, pp. 2444-2448
-
-
Pearson, W.R.1
Lipman, D.J.2
-
45
-
-
0032472367
-
Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome
-
Pipiras, E., Coquelle, A., Bieth, A. and Debatisse, M. (1998). Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome. EMBO J. 17, 325-333.
-
(1998)
EMBO J.
, vol.17
, pp. 325-333
-
-
Pipiras, E.1
Coquelle, A.2
Bieth, A.3
Debatisse, M.4
-
46
-
-
0028987794
-
Ultra-sensitive FISH using peroxidase-mediated deposition of biotin- or fluorochrome tyramides
-
Raap, A. K., van de Corput, M. P. C., Vervenne, R. A. W., van Gijlswiijk, R. P. M., Tanke, H. J. and Wiegant, J. (1995) Ultra-sensitive FISH using peroxidase-mediated deposition of biotin- or fluorochrome tyramides. Hum. Mol. Genet. 4, 529-534.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 529-534
-
-
Raap, A.K.1
Van de Corput, M.P.C.2
Vervenne, R.A.W.3
Van Gijlswiijk, R.P.M.4
Tanke, H.J.5
Wiegant, J.6
-
47
-
-
0021151878
-
Inhibitors of DNA synthesis induce sister chromatid exchanges at the early S phase of the cell cycle
-
Rainaldi, G., Sessa, M. R. and Mariani, T. (1984). Inhibitors of DNA synthesis induce sister chromatid exchanges at the early S phase of the cell cycle. Chromosoma 90, 46-49.
-
(1984)
Chromosoma
, vol.90
, pp. 46-49
-
-
Rainaldi, G.1
Sessa, M.R.2
Mariani, T.3
-
48
-
-
0026017993
-
Preferential integration of marker DNA into the chromosomal fragile site at 3p14: An approach to cloning fragile sites
-
Rassool, F. V., McKeithen, T. W., Neilly, M. E., van Melle, E., Espinosa, R. and LeBeau, M. M. (1991). Preferential integration of marker DNA into the chromosomal fragile site at 3p14: An approach to cloning fragile sites. Proc. Nat. Acad. Sci. USA 88, 6657-6661.
-
(1991)
Proc. Nat. Acad. Sci. USA
, vol.88
, pp. 6657-6661
-
-
Rassool, F.V.1
McKeithen, T.W.2
Neilly, M.E.3
Van Melle, E.4
Espinosa, R.5
LeBeau, M.M.6
-
49
-
-
0030201095
-
Direct cloning of DNA sequences from the common fragile site region at chromosome hand 3p14.2
-
Rassool, F. V., LeBeau, M. M., Shen, M.-L., Neilly, M. E., Espinosa III, R., Ong, S. T., Boldog, F., Drabkin, H., MacCarroll, R. and McKeithan, T. W. (1996). Direct cloning of DNA sequences from the common fragile site region at chromosome hand 3p14.2. Genomics 35, 109-117.
-
(1996)
Genomics
, vol.35
, pp. 109-117
-
-
Rassool, F.V.1
LeBeau, M.M.2
Shen, M.-L.3
Neilly, M.E.4
Espinosa III, R.5
Ong, S.T.6
Boldog, F.7
Drabkin, H.8
MacCarroll, R.9
McKeithan, T.W.10
-
50
-
-
0025309404
-
Regulatory elements in the introns of the human HPRT gene are necessary for its expression in embryonic stem cells
-
Reid, L. H. (1990). Regulatory elements in the introns of the human HPRT gene are necessary for its expression in embryonic stem cells. Proc. Nat. Acad. Sci. USA 87, 4299-4303.
-
(1990)
Proc. Nat. Acad. Sci. USA
, vol.87
, pp. 4299-4303
-
-
Reid, L.H.1
-
51
-
-
0023502921
-
Multiple common fragile sites are expressed in the genome of the laboratory rat
-
Robinson, T. J. and Elder, F. F. B. (1987). Multiple common fragile sites are expressed in the genome of the laboratory rat. Chromosoma 96, 45-49.
-
(1987)
Chromosoma
, vol.96
, pp. 45-49
-
-
Robinson, T.J.1
Elder, F.F.B.2
-
52
-
-
0028289026
-
Metaphase chromosome structure: Bands arise from a differential folding path of the highly AT-rich scaffold
-
Saitoh, Y. and Laemmli, U. K. (1994). Metaphase chromosome structure: Bands arise from a differential folding path of the highly AT-rich scaffold. Cell 76, 609-622.
-
(1994)
Cell
, vol.76
, pp. 609-622
-
-
Saitoh, Y.1
Laemmli, U.K.2
-
54
-
-
0025041513
-
Genetic determination of fragile site expression
-
Smeets, D. and Arets, A. (1990). Genetic determination of fragile site expression. Am. J. Hum. Genet. 47, 196-201.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 196-201
-
-
Smeets, D.1
Arets, A.2
-
55
-
-
0025268820
-
Common fragile sites in man and three closely related primate species
-
Smeets, D. F. C. M. and van de Klundert, F. A. J. M. (1990). Common fragile sites in man and three closely related primate species. Cytogenet. Cell Genet. 53, 8-14.
-
(1990)
Cytogenet. Cell Genet.
, vol.53
, pp. 8-14
-
-
Smeets, D.F.C.M.1
Van de Klundert, F.A.J.M.2
-
56
-
-
0025914298
-
Chromosomal fragile site expression in dogs: 1. Breed specific differences
-
Stone, D. M., Jacky, P. B., Hancock, D. D. and Prieur, D. J. (1991). Chromosomal fragile site expression in dogs: 1. Breed specific differences. Am. J. Med. Genet. 40, 214-222.
-
(1991)
Am. J. Med. Genet.
, vol.40
, pp. 214-222
-
-
Stone, D.M.1
Jacky, P.B.2
Hancock, D.D.3
Prieur, D.J.4
-
57
-
-
44949275580
-
Chromosomal fragile sites
-
Sutherland, G. R. (1991). Chromosomal fragile sites. GATA 8, 161-166.
-
(1991)
GATA
, vol.8
, pp. 161-166
-
-
Sutherland, G.R.1
-
58
-
-
0026865445
-
Characterisation of a new rare fragile site easily confused with the Fragile X
-
Sutherland, G. R. and Baker, E. (1992). Characterisation of a new rare fragile site easily confused with the Fragile X. Hum. Mol. Genet. 1, 111-113.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 111-113
-
-
Sutherland, G.R.1
Baker, E.2
-
59
-
-
0000524403
-
Map of distamycin, netropsin and actinomycin binding sites on heterogeneous DNA: DNA cleavage-inhibition patterns with methidiumpropyl-EDTA-Fe(II)
-
Van Dyke, M. W., Hertzberg, R. P. and Dervan, P. B. (1982). Map of distamycin, netropsin and actinomycin binding sites on heterogeneous DNA: DNA cleavage-inhibition patterns with methidiumpropyl-EDTA-Fe(II). Proc. Nat. Acad. Sci. USA 79, 5470-5474.
-
(1982)
Proc. Nat. Acad. Sci. USA
, vol.79
, pp. 5470-5474
-
-
Van Dyke, M.W.1
Hertzberg, R.P.2
Dervan, P.B.3
-
60
-
-
0025905795
-
Identification of a gene (FMRI) containing a CCG repeat coincident with a breakpoint cluster region exhibiting length variation in Fragile X syndrome
-
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F. et al (1991). Identification of a gene (FMRI) containing a CCG repeat coincident with a breakpoint cluster region exhibiting length variation in Fragile X syndrome. Cell 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
-
61
-
-
0031148646
-
Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions
-
Wang, L., Paradee, W., Mullins, C., Shridhar, R., Rosati, R., Wilke, C. M., Glover, T. W. and Smith, D. I. (1997). Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions. Genomics 41, 485-458.
-
(1997)
Genomics
, vol.41
, pp. 485-1458
-
-
Wang, L.1
Paradee, W.2
Mullins, C.3
Shridhar, R.4
Rosati, R.5
Wilke, C.M.6
Glover, T.W.7
Smith, D.I.8
-
62
-
-
0032485047
-
Frequent homozygous deletions in the FRA3B region in tumor cell lines still leave the FHIT exons intact
-
Wang, L., Darling, J., Zhang, J.-S., Qian, C.-P., Hartmann, L., Conover, C., Jenkins, R. and Smith, D. I. (1998). Frequent homozygous deletions in the FRA3B region in tumor cell lines still leave the FHIT exons intact. Oncogene 16, 635-642.
-
(1998)
Oncogene
, vol.16
, pp. 635-642
-
-
Wang, L.1
Darling, J.2
Zhang, J.-S.3
Qian, C.-P.4
Hartmann, L.5
Conover, C.6
Jenkins, R.7
Smith, D.I.8
-
63
-
-
0028598544
-
Sequence determinants of DNA bending in the ilvIH promoter and regulator region of E.coli.
-
Wang, Q., Albert, F. G., Fitzgerald, D. J., Calvo, J. M. and Anderson, J. N. (1994). Sequence determinants of DNA bending in the ilvIH promoter and regulator region of E.coli. Nucl. Acids Res. 22, 5753-5760.
-
(1994)
Nucl. Acids Res.
, vol.22
, pp. 5753-5760
-
-
Wang, Q.1
Albert, F.G.2
Fitzgerald, D.J.3
Calvo, J.M.4
Anderson, J.N.5
-
64
-
-
0028169985
-
Multicolour 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., Guo, S.-W., Hall, B. K., Boldog, F., Gemmill, R. M., Chandrasekharappa, S. C., Barcroft, C. L., Drabkin, H. A. and Glover, T. W. (1994). Multicolour 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
Guo, S.-W.2
Hall, B.K.3
Boldog, F.4
Gemmill, R.M.5
Chandrasekharappa, S.C.6
Barcroft, C.L.7
Drabkin, H.A.8
Glover, T.W.9
-
65
-
-
0030060945
-
FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: Direct evidence for the coincidence of viral integration sites and fragile sites
-
Wilke, C. M., Hall, B. K., Hoge, A., Paradee, W., Smith, D. I. and Glover, T. W. (1996). FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: Direct evidence for the coincidence of viral integration sites and fragile sites. Hum. Mol. Genet. 5, 187-195.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 187-195
-
-
Wilke, C.M.1
Hall, B.K.2
Hoge, A.3
Paradee, W.4
Smith, D.I.5
Glover, T.W.6
-
66
-
-
0021867410
-
Different sister chromatid exchange rates in XX and XY cells of a pair of human chimeric twins
-
Wulf, H. C. and Niebuhr, E. (1985). Different sister chromatid exchange rates in XX and XY cells of a pair of human chimeric twins. Cytogenet. Cell Genet. 39, 105-108.
-
(1985)
Cytogenet. Cell Genet.
, vol.39
, pp. 105-108
-
-
Wulf, H.C.1
Niebuhr, E.2
-
67
-
-
0026347628
-
Fragile X genotype characterised by an unstable region of DNA
-
Yu, S., Pritchard, M., Kremer, E., Lynch, M., Nancarrow, J., Baker, E., Holman, K., Muley, J. C., Warren, S. T., Schlessinger, D., Sutherland, G. R. and Richards, R. I. (1991). Fragile X genotype characterised by an unstable region of DNA. Science 252, 1179-1181.
-
(1991)
Science
, vol.252
, pp. 1179-1181
-
-
Yu, S.1
Pritchard, M.2
Kremer, E.3
Lynch, M.4
Nancarrow, J.5
Baker, E.6
Holman, K.7
Muley, J.C.8
Warren, S.T.9
Schlessinger, D.10
Sutherland, G.R.11
Richards, R.I.12
-
68
-
-
0030974861
-
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
-
Yu, S., Mangelsdorf, M., Hewett, D., Hobson, L., Baker, E., Eyre, H. J., Lapsys, N., le Paslier, D., Doggett, N. A., Sutherland, G. R. and Richards, R. I. (1997). Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat. Cell 88, 367-374.
-
(1997)
Cell
, vol.88
, pp. 367-374
-
-
Yu, S.1
Mangelsdorf, M.2
Hewett, D.3
Hobson, L.4
Baker, E.5
Eyre, H.J.6
Lapsys, N.7
Le Paslier, D.8
Doggett, N.A.9
Sutherland, G.R.10
Richards, R.I.11
-
69
-
-
0021690129
-
Constitutive fragile sites and cancer
-
Yunis, J. J. and Soreng, A. L. (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
-
70
-
-
0030890750
-
Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FHIT gene
-
Zimonjic, D. B., Druck, T., Kastury, K., Croce, C. M., Popescu, N. C. and Huebner, K. (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
Druck, T.2
Kastury, K.3
Croce, C.M.4
Popescu, N.C.5
Huebner, K.6
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