-
1
-
-
0021675966
-
Nonrandom distribution of methotrexate-induced aberrations on human chromosomes: Detection of further folie acid sensitive fragile sites
-
Barbi G, Steinbach P, Vogel W (1984) Nonrandom distribution of methotrexate-induced aberrations on human chromosomes: Detection of further folie acid sensitive fragile sites. Hum Genet 68:290-294.
-
(1984)
Hum Genet
, vol.68
, pp. 290-294
-
-
Barbi, G.1
Steinbach, P.2
Vogel, W.3
-
2
-
-
0026808763
-
Mapping the whole human genome by fingerprinting yeast artificial chromosomes
-
Bellanne-Chantelot C, Lacroix B, Qugen R Billault A, Beautils S, Bertraut S, Georges I, Gilbert F, Lucotte G, Susm I, Jean-Jacques C, Gesnouin P, Pook S, Vaysseix G, Lu-Kuo J, Ried T, Ward D, Chumakov I, Le Paslier D, Barillot E, Cohen D (1992) Mapping the whole human genome by fingerprinting yeast artificial chromosomes. Cell 70:1059-1068.
-
(1992)
Cell
, vol.70
, pp. 1059-1068
-
-
Bellanne-Chantelot, C.1
Lacroix, B.2
Qugen, R.3
Billault, A.4
Beautils, S.5
Bertraut, S.6
Georges, I.7
Gilbert, F.8
Lucotte, G.9
Susm, I.10
Jean-Jacques, C.11
Gesnouin, P.12
Pook, S.13
Vaysseix, G.14
Lu-Kuo, J.15
Ried, T.16
Ward, D.17
Chumakov, I.18
Le Paslier, D.19
Barillot, E.20
Cohen, D.21
more..
-
3
-
-
0022371326
-
Report of the committee on chromosome rearrangements on neoplasia and on fragile sites (HGM8)
-
Berger R, Bloomfield CD, Sutherland GR (1985) Report of the committee on chromosome rearrangements on neoplasia and on fragile sites (HGM8). 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
-
4
-
-
0028109387
-
Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B
-
Boldog FC, Wagoner B, Glover TW, Chumakov I, le Paslier D, Cohen D, Gemmill RM, Drabkin HA (1994) Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B. Genes Chromosomes Cancer 11:216-221.
-
(1994)
Genes Chromosomes Cancer
, vol.11
, pp. 216-221
-
-
Boldog, F.C.1
Wagoner, B.2
Glover, T.W.3
Chumakov, I.4
Le Paslier, D.5
Cohen, D.6
Gemmill, R.M.7
Drabkin, H.A.8
-
5
-
-
2042468966
-
Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B
-
Boldog FC, Gemmill RM, West J, Robinson M, Robinson L, Li E, Roche J, Todd S, Waggoner B, Lundstrom R, Jacobson J, Mullokandov MR, Klinger H, Drabkin HA (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.C.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
-
6
-
-
0026683521
-
YAC mapping by FISH using Alu-PCR-generated probes
-
Breen M, Arveiler B, Murray I, Gosden JR, Porteous DJ (1990) YAC mapping by FISH using Alu-PCR-generated probes. Genomics 13:726-730:
-
(1990)
Genomics
, vol.13
, pp. 726-730
-
-
Breen, M.1
Arveiler, B.2
Murray, I.3
Gosden, J.R.4
Porteous, D.J.5
-
8
-
-
0018736628
-
Hereditary renal cell carcinoma associated with a chromosomal translocation
-
Cohen AJ, Li FP, Berg S, Marchetto DJ, Tasai S, Jacobs SC, Brown RS (1979) Hereditary renal cell carcinoma associated with a chromosomal translocation. N Engl J Med 301:592-595.
-
(1979)
N Engl J Med
, vol.301
, pp. 592-595
-
-
Cohen, A.J.1
Li, F.P.2
Berg, S.3
Marchetto, D.J.4
Tasai, S.5
Jacobs, S.C.6
Brown, R.S.7
-
9
-
-
0030904279
-
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early amplicons
-
Coquelle A, Pipiras E, Toledo F, Buttin G, 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
Pipiras, E.2
Toledo, F.3
Buttin, G.4
Debatisse, M.5
-
10
-
-
0030891546
-
Loss of heterozygosity at 7q31 in breast cancer: Results from an international collaborative study group
-
Devilee P, Hermans J, Eyfjord J, Borresen A-L, Lidereau R, Sobol H, Borg A, Cleton-Jansen A-M, Olah E, Cohen BB, Scherneck S, Hamann U, Peterlin B, Caligo M, Bignon Y-J, Maugard CH, the Breast Cancer Somatic Genetics Consortium (1997) Loss of heterozygosity at 7q31 in breast cancer: Results from an international collaborative study group. Genes Chromosomes Cancer 18:193-199.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 193-199
-
-
Devilee, P.1
Hermans, J.2
Eyfjord, J.3
Borresen, A.-L.4
Lidereau, R.5
Sobol, H.6
Borg, A.7
Cleton-Jansen, A.-M.8
Olah, E.9
Cohen, B.B.10
Scherneck, S.11
Hamann, U.12
Peterlin, B.13
Caligo, M.14
Bignon, Y.-J.15
Ch, M.16
-
11
-
-
0026345716
-
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Fu Y-H, Kuhl DPA, Pizzuti A, Pieretti M, Sutcliffe JS, Richards R, Verkerk AJMH, Holden JJA, Fenwick RG Jr, Warren ST, Oostra BA, Nelson DL, Caskey CT (1991) Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell 67:1047-1058.
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.-H.1
Kuhl, D.P.A.2
Pizzuti, A.3
Pieretti, M.4
Sutcliffe, J.S.5
Richards, R.6
Verkerk, A.J.M.H.7
Holden, J.J.A.8
Fenwick R.G., Jr.9
Warren, S.T.10
Oostra, B.A.11
Nelson, D.L.12
Caskey, C.T.13
-
12
-
-
0021278143
-
DNA polymerase inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes
-
Glover TW, Berger C, Coyle-Morris J, Echo B (1984) DNA polymerase inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:882-890.
-
(1984)
Hum Genet
, vol.67
, pp. 882-890
-
-
Glover, T.W.1
Berger, C.2
Coyle-Morris, J.3
Echo, B.4
-
13
-
-
0023789150
-
Chromosome breakage and recombination at fragile sites
-
Glover TW, Stein CK (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
-
14
-
-
0026007187
-
Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artitical chromosomes
-
Green ED, Mohr RM, Idol JR, Jones M, Buckingham JM, Deaven L, Moyzis RK, Olson MV (1991) Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artitical chromosomes. Genomics 11:548-564.
-
(1991)
Genomics
, vol.11
, pp. 548-564
-
-
Green, E.D.1
Mohr, R.M.2
Idol, J.R.3
Jones, M.4
Buckingham, J.M.5
Deaven, L.6
Moyzis, R.K.7
Olson, M.V.8
-
15
-
-
0025914050
-
Sister chromid exchanges are preferentially induced at expressed and nonexpressed common fragile sites
-
Hirsch B (1991) Sister chromid exchanges are preferentially induced at expressed and nonexpressed common fragile sites. Hum Genet 87:302-306.
-
(1991)
Hum Genet
, vol.87
, pp. 302-306
-
-
Hirsch, B.1
-
16
-
-
0025319997
-
Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells
-
Jones NJ, Stewart SA, Thompson LH (1990) Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cells. Mutagenesis 5:15-23.
-
(1990)
Mutagenesis
, vol.5
, pp. 15-23
-
-
Jones, N.J.1
Stewart, S.A.2
Thompson, L.H.3
-
17
-
-
0028557941
-
Physical linkage of the fragile site FRA11B and Jacobsen syndrome chromosome deletion breakpoint in 11q23.3
-
Jones C, Slijepcevic P, March S, Baker E, Langdon WY, Richards RI, Tunnacliffe A (1994) Physical linkage of the fragile site FRA11B and 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
March, S.3
Baker, E.4
Langdon, W.Y.5
Richards, R.I.6
Tunnacliffe, A.7
-
18
-
-
0342591692
-
Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines
-
Kastury K, Baffa R, Druck T, Ohta M, Cotticelli MG, Inoue H, Negrini M, Rugge M, Huang D, Croce CM, Palazzo J, Huebner K (1997) Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines. Cancer Res 56:978-983.
-
(1997)
Cancer Res
, vol.56
, pp. 978-983
-
-
Kastury, K.1
Baffa, R.2
Druck, T.3
Ohta, M.4
Cotticelli, M.G.5
Inoue, H.6
Negrini, M.7
Rugge, M.8
Huang, D.9
Croce, C.M.10
Palazzo, J.11
Huebner, K.12
-
19
-
-
0027203684
-
Tri-nucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
-
Knight SJL, Flannery AV, Hirst MC, Campbell L, Christodoulou Z, Phelps SR, Pointon J, Middleton-Price HR, Barnicoat A, Pembrey ME (1993) Tri-nucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell 74:127-134.
-
(1993)
Cell
, vol.74
, pp. 127-134
-
-
Knight, S.J.L.1
Flannery, A.V.2
Hirst, M.C.3
Campbell, L.4
Christodoulou, Z.5
Phelps, S.R.6
Pointon, J.7
Middleton-Price, H.R.8
Barnicoat, A.9
Pembrey, M.E.10
-
20
-
-
0030939065
-
Frequent loss of heterozygosity in the region of the D7S523 locus in advanced ovarian cancer
-
Koike M, Takeuchi S, Yokota J, Park S, Hatta Y, Miller CW, Tsuruoka N, Koeffler HP (1997) Frequent loss of heterozygosity in the region of the D7S523 locus in advanced ovarian cancer. Genes Chromosomes Cancer 19:1-5.
-
(1997)
Genes Chromosomes Cancer
, vol.19
, pp. 1-5
-
-
Koike, M.1
Takeuchi, S.2
Yokota, J.3
Park, S.4
Hatta, Y.5
Miller, C.W.6
Tsuruoka, N.7
Koeffler, H.P.8
-
21
-
-
0028037032
-
Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas
-
Kuniyasu H, Yasui W, Yokozaki H, Akagi M, Kitahara K, Fujii K, Tahara E (1994) Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas. Int J Cancer 59:597-600.
-
(1994)
Int J Cancer
, vol.59
, pp. 597-600
-
-
Kuniyasu, H.1
Yasui, W.2
Yokozaki, H.3
Akagi, M.4
Kitahara, K.5
Fujii, K.6
Tahara, E.7
-
22
-
-
0025262465
-
Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts
-
Kuwano A, Murano I, Kajii T (1990) Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts. Hum Genet 84:527-531.
-
(1990)
Hum Genet
, vol.84
, pp. 527-531
-
-
Kuwano, A.1
Murano, I.2
Kajii, T.3
-
23
-
-
0029014972
-
Genetic alterations in localized cancers of the prostate: Identification of a common region of deletion on the chromosome 18q
-
Latil A, Baron JC, Cussenot O, Fournier G, Soussi T, Boccon-Gibod L, Le Duc A, Rouesse J, Lidereau R (1995) Genetic alterations in localized cancers of the prostate: Identification of a common region of deletion on the chromosome 18q. Bull Cancer 82:589-597.
-
(1995)
Bull Cancer
, vol.82
, pp. 589-597
-
-
Latil, A.1
Baron, J.C.2
Cussenot, O.3
Fournier, G.4
Soussi, T.5
Boccon-Gibod, L.6
Le Duc, A.7
Rouesse, J.8
Lidereau, R.9
-
24
-
-
0025609090
-
"PCR-karyotype" of human chromosomes in somatic cell hybrids
-
Ledbetter SA, Garcia-Heras J, Ledbetter DH (1990) "PCR-karyotype" of human chromosomes in somatic cell hybrids. Genomics 8:614-622.
-
(1990)
Genomics
, vol.8
, pp. 614-622
-
-
Ledbetter, S.A.1
Garcia-Heras, J.2
Ledbetter, D.H.3
-
25
-
-
0029963491
-
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET
-
Lin JC, Scherer SW, Tongas L, Traverso G, Tsui L-C, Andrulis I, Jothy S, Park M (1996) Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET. Oncogene 13:2001-2008.
-
(1996)
Oncogene
, vol.13
, pp. 2001-2008
-
-
Lin, J.C.1
Scherer, S.W.2
Tongas, L.3
Traverso, G.4
Tsui, L.-C.5
Andrulis, I.6
Jothy, S.7
Park, M.8
-
26
-
-
0027936274
-
Oncogene amplification in human gliomas: A molecular cytogenetic analysis
-
Muleris M, Almeida A, Dutrillaux AM, Prochon E, Vega F, Delattre JY, Poisson M, Malfoy B, Dutrillaux (1994) Oncogene amplification in human gliomas: A molecular cytogenetic analysis. Oncogene 9:2717-2722.
-
(1994)
Oncogene
, vol.9
, pp. 2717-2722
-
-
Muleris, M.1
Almeida, A.2
Dutrillaux, A.M.3
Prochon, E.4
Vega, F.5
Delattre, J.Y.6
Poisson, M.7
Malfoy, B.8
Dutrillaux9
-
27
-
-
0027981933
-
Implication of FRA16A structure for the mechanism of chromosomal fragile site genesis
-
Nancrarrow JK, Kremer E, Holman K, Eyre H, Doggett NA, le Paslier D, Callen DF, Sutherland GR, Richards RI (1994) Implication of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science 264:1938-1941.
-
(1994)
Science
, vol.264
, pp. 1938-1941
-
-
Nancrarrow, 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
-
28
-
-
1542471167
-
Alu polymerase chain reaction: A method for rapid isolation of human-specific sequences from complex DNa sources
-
Nelson DL, Ledbetter SA, Corbo L, Victoria MF, Ramirez-Solis R, Webster TD, Ledbetter DH, Caskey CT (1989) Alu polymerase chain reaction: A method for rapid isolation of human-specific sequences from complex DNA sources. Proc Natl Acad Sci USA 86:6686-6690.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 6686-6690
-
-
Nelson, D.L.1
Ledbetter, S.A.2
Corbo, L.3
Victoria, M.F.4
Ramirez-Solis, R.5
Webster, T.D.6
Ledbetter, D.H.7
Caskey, C.T.8
-
29
-
-
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 MG, Kastury K, Baffa R, Palazzo J, Siprashvili Z, Mori M, McCue P, Druck T, Croce CM, 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
-
31
-
-
0030201105
-
A 350-kb cosmid contig in 3p14.2 that cross the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints
-
Paradee W, Wilke CM, Wang L, Shridhar R, Mullins CM, Hoge A, Glover TW, Smith DI (1996) A 350-kb cosmid contig in 3p14.2 that cross 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
-
32
-
-
0025833298
-
Absence of expression of the FMR-1 gene in fragile X syndrome
-
Pieretti M, Zhang F, Fu Y-H, Warren ST, Oostra BA, Caskey CT, Nelson DL (1991) Absence of expression of the FMR-1 gene in fragile X syndrome. Cell 66:817-822.
-
(1991)
Cell
, vol.66
, pp. 817-822
-
-
Pieretti, M.1
Zhang, F.2
Fu, Y.-H.3
Warren, S.T.4
Oostra, B.A.5
Caskey, C.T.6
Nelson, D.L.7
-
33
-
-
0026623368
-
Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA
-
Rassool FV, Le Beau MM, Neilly ME, van Melle E, Espinosa R 3d, McKeithan TW (1992) Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA. Am J Hum Genet 50:1243-1251.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1243-1251
-
-
Rassool, F.V.1
Le Beau, M.M.2
Neilly, M.E.3
Van Melle, E.4
Espinosa R. III5
McKeithan, T.W.6
-
34
-
-
0028567730
-
The cloning of FRAXF: Trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter
-
Ritchie RJ, Knight SJL, Hirst MC, Crewal PK, Bobrow M, Cross GS, Davies KE (1994) The cloning of FRAXF: Trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter. Hum Mol Genet 3:2115-2121.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2115-2121
-
-
Ritchie, R.J.1
Knight, S.J.L.2
Hirst, M.C.3
Crewal, P.K.4
Bobrow, M.5
Cross, G.S.6
Davies, K.E.7
-
35
-
-
0029122417
-
Increased levels of MYC and MET co-amplification during tumor progression of a case of gastric cancer
-
Seruca R, Suijkerbuik RF, Gartner F, Criado B, Veiga I, Olde-Weghuis D, David L, Castedo S, Sobrinho-Simoes M (1995) Increased levels of MYC and MET co-amplification during tumor progression of a case of gastric cancer. Cancer Genet Cytogenet 82:104-145.
-
(1995)
Cancer Genet Cytogenet
, vol.82
, pp. 104-145
-
-
Seruca, R.1
Suijkerbuik, R.F.2
Gartner, F.3
Criado, B.4
Veiga, I.5
Olde-Weghuis, D.6
David, L.7
Castedo, S.8
Sobrinho-Simoes, M.9
-
36
-
-
10144234126
-
Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors
-
Shridhar R, Shridhar V, Wang X, Paradee W, Dugan M, Sarkar F, Wilke C, Glover TW, Vaitkevicius VK, Smith DI (1997a) Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors. Cancer Res 56:4347-1350.
-
(1997)
Cancer Res
, vol.56
, pp. 4347-11350
-
-
Shridhar, R.1
Shridhar, V.2
Wang, X.3
Paradee, W.4
Dugan, M.5
Sarkar, F.6
Wilke, C.7
Glover, T.W.8
Vaitkevicius, V.K.9
Smith, D.I.10
-
37
-
-
0030700907
-
Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas
-
In Press
-
Shridhar V, Sun QC, Miller OJ, Kalemkerian GP, Petros J, Smith DI (1997b) Loss of heterozygosity on the long arm of human chromosome 7 in sporadic renal cell carcinomas. Oncogene, In Press.
-
(1997)
Oncogene
-
-
Shridhar, V.1
Sun, Q.C.2
Miller, O.J.3
Kalemkerian, G.P.4
Petros, J.5
Smith, D.I.6
-
40
-
-
0029116273
-
Frequent loss of heterozygosity at 7q31.1 in primary prostate cancer is associated with tumor aggressiveness and progression
-
Takahashi S, Shan AL, Ritland SR, Delacey KA, Bostwick DG, Lieber MM, Thibodeau SN, Jenkins RB (1995) Frequent loss of heterozygosity at 7q31.1 in primary prostate cancer is associated with tumor aggressiveness and progression. Cancer Res 55:4114-4119.
-
(1995)
Cancer Res
, vol.55
, pp. 4114-4119
-
-
Takahashi, S.1
Shan, A.L.2
Ritland, S.R.3
Delacey, K.A.4
Bostwick, D.G.5
Lieber, M.M.6
Thibodeau, S.N.7
Jenkins, R.B.8
-
41
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJMH, Pieretti, Sutcliffe JS, Fu Y-H, Kuhl DPA, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang F, Eussen BE, van Ommen G-JB, Blonden LAJ, Riggins GJ, Chastain JL, Kunst GH, Caskey CT, Nelson DL, Oostra BA, Warren ST (1991) Identification of a gene (FMR-1) containing a CGG 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
Pieretti2
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
Eussen, B.E.11
Van Ommen, G.-J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, G.H.16
Caskey, C.T.17
Nelson, D.L.18
Oostra, B.A.19
Warren, S.T.20
more..
-
42
-
-
0030575839
-
Long CCG triplet repeat blocks exclude nucleosomes: A possible mechanism for the nature of fragile sites in chromosomes
-
Wang YH, Gellibolian R, Shimizu M, Wells RD, Griffith J (1996) Long CCG triplet repeat blocks exclude nucleosomes: A possible mechanism for the nature of fragile sites in chromosomes. J Mol Biol 263:511-516.
-
(1996)
J Mol Biol
, vol.263
, pp. 511-516
-
-
Wang, Y.H.1
Gellibolian, R.2
Shimizu, M.3
Wells, R.D.4
Griffith, J.5
-
43
-
-
0028169985
-
Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the 7(3;8) associated with renal cell carcinoma
-
Wilke CM, Guo S-W, Hall BK, Boldog F, Gemmill RM, Chandrasekharappa SC, Barcroft CL, Drabkin HA, Grover TW (1994) Multicolor FISH mapping of YAC clones in 3p14 and identification of a YAC spanning both FRA3B and the 7(3;8) associated with 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
Grover, T.W.9
-
44
-
-
0028004727
-
Two independent amplification events on chromosome 7 in glioma: Amplification of rhe epidermal growth factor receptor gene and amplification of the oncogene MET
-
Wullich B, Sattler HP, Fisher U, Meese E (1994) Two independent amplification events on chromosome 7 in glioma: Amplification of rhe epidermal growth factor receptor gene and amplification of the oncogene MET. Anticancer Res 14:577-579.
-
(1994)
Anticancer Res
, vol.14
, pp. 577-579
-
-
Wullich, B.1
Sattler, H.P.2
Fisher, U.3
Meese, E.4
-
45
-
-
0026347628
-
Fragile X genotype characterized by an unstable region of DNA
-
Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, Sutherland GR, Richard RI (1991) Fragile X genotype characterized 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
Mulley, J.C.8
Warren, S.T.9
Schlessinger, D.10
Sutherland, G.R.11
Richard, R.I.12
-
46
-
-
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, Lapsys N, le Paslier D, Doggett NA, Sutherland GR, Richards RI (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.6
Lapsys, N.7
Le Paslier, D.8
Doggett, N.A.9
Sutherland, G.R.10
Richards, R.I.11
-
47
-
-
0021690129
-
Constitutive fragile sites and cancer
-
Yunis JJ, Soreng AL (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
-
48
-
-
0028091664
-
n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer
-
n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer. Proc Natl Acad Sci USA 91:12155-12158.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 12155-12158
-
-
Zenklusen, J.1
Bieche, I.2
Lidereau, R.3
Conti, C.4
-
49
-
-
0028641304
-
Loss of heterozygosity in human prostate carcinomas: A possible tumor suppressor gene at 7q31.1
-
Zenklusen JC, Thompson JC, Troncoso P, Kagan J, Conti CJ (1994b) Loss of heterozygosity in human prostate carcinomas: A possible tumor suppressor gene at 7q31.1. Cancer Res 54:6370-6373.
-
(1994)
Cancer Res
, vol.54
, pp. 6370-6373
-
-
Zenklusen, J.C.1
Thompson, J.C.2
Troncoso, P.3
Kagan, J.4
Conti, C.J.5
-
50
-
-
0028929987
-
Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 1q31.1: Evidence for a broad range tumor suppressor gene
-
Zenklusen JC, Thompson JC, Klein-Szanto AJP, Conti CJ (1995a) Frequent loss of heterozygosity in human primary squamous cell and colon carcinomas at 1q31.1: Evidence for a broad range tumor suppressor gene. Cancer Res 55:1347-1350.
-
(1995)
Cancer Res
, vol.55
, pp. 1347-1350
-
-
Zenklusen, J.C.1
Thompson, J.C.2
Klein-Szanto, A.J.P.3
Conti, C.J.4
-
51
-
-
0029121078
-
Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene
-
Zenklusen J, Weitzel J, Ball H, Conti C (1995b) Allelic loss at 7q31.1 in human primary ovarian carcinomas suggests the existence of a tumor suppressor gene. Oneogcne 11:359-363.
-
(1995)
Oneogcne
, vol.11
, pp. 359-363
-
-
Zenklusen, J.1
Weitzel, J.2
Ball, H.3
Conti, C.4
-
52
-
-
0030890750
-
Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FIHT gene
-
Zimonjic DB, Druck T, Ohta M, Kastury K, Carlo MC, Popescu NC (1997) Positions of chromosome 3p14.2 fragile sites (FRA3B) within the FIHT gene. Cancer Res 57:1166-1170.
-
(1997)
Cancer Res
, vol.57
, pp. 1166-1170
-
-
Zimonjic, D.B.1
Druck, T.2
Ohta, M.3
Kastury, K.4
Carlo, M.C.5
Popescu, N.C.6
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