-
1
-
-
0029090221
-
Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)
-
Ahn, J., H.-J. Ludecke, S. Lindow, W.A. Horton, B. Lee, M.J. Wagner, B. Horsthemke, and D.E. Wells. 1995. Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1). Nature Genet. 11: 137-143.
-
(1995)
Nature Genet.
, vol.11
, pp. 137-143
-
-
Ahn, J.1
Ludecke, H.-J.2
Lindow, S.3
Horton, W.A.4
Lee, B.5
Wagner, M.J.6
Horsthemke, B.7
Wells, D.E.8
-
2
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S., W. Gish, W. Miller, E. Meyers, and D. Lipman. 1990. Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.1
Gish, W.2
Miller, W.3
Meyers, E.4
Lipman, D.5
-
3
-
-
19144373472
-
Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm of chromosome 11
-
Bartsch, O., W. Wuyts, W. Van Hul, J.T. Hecht, P. Meinecke, D. Hogue, W. Werner, B. Zabel, G.K. Hinkel, C.M. Powell, L.G. Shaffer, and P.J. Willems. 1996. Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions on the short arm of chromosome 11. Am. J. Hum. Genet. 58: 734-742.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 734-742
-
-
Bartsch, O.1
Wuyts, W.2
Van Hul, W.3
Hecht, J.T.4
Meinecke, P.5
Hogue, D.6
Werner, W.7
Zabel, B.8
Hinkel, G.K.9
Powell, C.M.10
Shaffer, L.G.11
Willems, P.J.12
-
4
-
-
0027155128
-
Two distinct regions involved in 1p deletion in human primary breast cancer
-
Bieche, I., M.-H. Champeme, F. Matifas, C.S. Cropp, R. Callahan, and R. Lidereau. 1993. Two distinct regions involved in 1p deletion in human primary breast cancer. Cancer Res. 53: 1990-1994.
-
(1993)
Cancer Res.
, vol.53
, pp. 1990-1994
-
-
Bieche, I.1
Champeme, M.-H.2
Matifas, F.3
Cropp, C.S.4
Callahan, R.5
Lidereau, R.6
-
5
-
-
0023349389
-
Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors
-
Burke, D.T., G.F. Carle, and M.V. Olson. 1987. Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. Science 236: 806-812.
-
(1987)
Science
, vol.236
, pp. 806-812
-
-
Burke, D.T.1
Carle, G.F.2
Olson, M.V.3
-
6
-
-
0027366989
-
Genetic heterogeneity in families with hereditary multiple exostoses
-
Cook, A., W. Raskind, S.H. Blanton, R.M. Pauli, R.G. Gregg, C.A. Francomano, E. Puffenberger, E.U. Conrad, G. Schmale, G. Schellenberg, E. Wijsman, J.T. Hecht, D. Wells, and M.J. Wagner. 1993. Genetic heterogeneity in families with hereditary multiple exostoses. Am. J. Hum. Genet. 53: 71-79.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 71-79
-
-
Cook, A.1
Raskind, W.2
Blanton, S.H.3
Pauli, R.M.4
Gregg, R.G.5
Francomano, C.A.6
Puffenberger, E.7
Conrad, E.U.8
Schmale, G.9
Schellenberg, G.10
Wijsman, E.11
Hecht, J.T.12
Wells, D.13
Wagner, M.J.14
-
7
-
-
0028835213
-
Human chromosome-specific cDNA Libraries: New tools for gene identification and genome annotation
-
Del Mastro, R., L. Wang, A.D. Simmons, T.D. Gallardo, G.A. Clines, J.A. Ashley, C.J. Hilliard, J.J. Wasmuth, J.D. McPherson, and M. Lovett. 1995. Human chromosome-specific cDNA Libraries: New tools for gene identification and genome annotation. Genome Res. 5: 185-194.
-
(1995)
Genome Res.
, vol.5
, pp. 185-194
-
-
Del Mastro, R.1
Wang, L.2
Simmons, A.D.3
Gallardo, T.D.4
Clines, G.A.5
Ashley, J.A.6
Hilliard, C.J.7
Wasmuth, J.J.8
McPherson, J.D.9
Lovett, M.10
-
8
-
-
9044231362
-
Deletion mapping on chromosome 1p in well-differentiated gastric cancer
-
Ezaki, T., A. Yanagisawa, K. Ohta, S. Aiso, M. Watanabe, T. Hibi, Y. Kato, T. Nakajima, T. Ariyama, J. Inazawa, Y. Nakamura, and A. Horii. 1996. Deletion mapping on chromosome 1p in well-differentiated gastric cancer. Br. J. Cancer 73: 424-428.
-
(1996)
Br. J. Cancer
, vol.73
, pp. 424-428
-
-
Ezaki, T.1
Yanagisawa, A.2
Ohta, K.3
Aiso, S.4
Watanabe, M.5
Hibi, T.6
Kato, Y.7
Nakajima, T.8
Ariyama, T.9
Inazawa, J.10
Nakamura, Y.11
Horii, A.12
-
9
-
-
15144344073
-
Large-insert cloning and analysis
-
(ed. N.C. Dracopoli, J. Haines, B.R. Korf, D.T. Moir, C.C. Morton, C.E. Seidman, J.G. Seidman, and D.R. Smith). John Wiley & Sons, New York, NY
-
Gemmill, R.M., R. Bolin, and H. Albertsen. 1996. Large-insert cloning and analysis. In Current protocols in human genetics (ed. N.C. Dracopoli, J. Haines, B.R. Korf, D.T. Moir, C.C. Morton, C.E. Seidman, J.G. Seidman, and D.R. Smith). John Wiley & Sons, New York, NY.
-
(1996)
Current Protocols in Human Genetics
-
-
Gemmill, R.M.1
Bolin, R.2
Albertsen, H.3
-
11
-
-
0028917663
-
Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8
-
Hecht, J.T., D. Hogue, L.C. Strong, M.F. Hansen, S.H. Blanton, and M. Wagner. 1995. Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8. Am. J. Hum. Genet. 56: 1125-1131.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1125-1131
-
-
Hecht, J.T.1
Hogue, D.2
Strong, L.C.3
Hansen, M.F.4
Blanton, S.H.5
Wagner, M.6
-
12
-
-
0031020756
-
Hereditary multiple exostoses: Mutational studies of familial EXT1 cases and EXT associated malignancies
-
in press
-
Hecht, J.T. , D. Hogue, Y.Wang, S.H. Blanton, M. Wagner, L.C. Strong, W. Raskind, M.F. Hansen, and D. Wells. 1996. Hereditary multiple exostoses: Mutational studies of familial EXT1 cases and EXT associated malignancies. Am. J. Hum. Genet, (in press).
-
(1996)
Am. J. Hum. Genet
-
-
Hecht, J.T.1
Hogue, D.2
Wang, Y.3
Blanton, S.H.4
Wagner, M.5
Strong, L.C.6
Raskind, W.7
Hansen, M.F.8
Wells, D.9
-
13
-
-
0025810316
-
Hereditary multiple exostoses
-
Hennekam, R.C.M. 1991. Hereditary multiple exostoses. J. Med. Genet 28: 262-266.
-
(1991)
J. Med. Genet
, vol.28
, pp. 262-266
-
-
Hennekam, R.C.M.1
-
14
-
-
0028819584
-
Allelic imbalance on chromosome 1 in human breast cancer. II. Microsatellite repeat analysis
-
Hoggard, N., B. Brintnell, A. Howell, J. Weissenbach, and J. Varley. 1995. Allelic imbalance on chromosome 1 in human breast cancer. II. Microsatellite repeat analysis. Genes Chromosomes Cancer 12: 24-31.
-
(1995)
Genes Chromosomes Cancer
, vol.12
, pp. 24-31
-
-
Hoggard, N.1
Brintnell, B.2
Howell, A.3
Weissenbach, J.4
Varley, J.5
-
15
-
-
0028304908
-
On global sequence alignment
-
Huang, X. 1994. On global sequence alignment. Comput. Appl. Biosci. 10: 227-235.
-
(1994)
Comput. Appl. Biosci.
, vol.10
, pp. 227-235
-
-
Huang, X.1
-
16
-
-
0029115296
-
Chromosome 1p terminal deletion: Report of new findings and confirmation of two characteristic phenotypes
-
Keppler-Noreuil, K.M., A.J. Carroll, W.H. Finley, and S.L. Rutledge. 1995. Chromosome 1p terminal deletion: Report of new findings and confirmation of two characteristic phenotypes. J. Med. Genet. 32: 619-622.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 619-622
-
-
Keppler-Noreuil, K.M.1
Carroll, A.J.2
Finley, W.H.3
Rutledge, S.L.4
-
17
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
Knudson, A.G. 1971. Mutation and cancer: Statistical study of retinoblastoma. Proc. Natl. Acad. Sci 68: 820-823.
-
(1971)
Proc. Natl. Acad. Sci
, vol.68
, pp. 820-823
-
-
Knudson, A.G.1
-
18
-
-
0027366690
-
PCR probes for chromosome in situ hybridization of large-insert bacterial recombinants
-
Kroisel, P.M., P.A. Ioannou, P.J. de Jong. 1993. PCR probes for chromosome in situ hybridization of large-insert bacterial recombinants. Cytogenet. Cell Genet. 65: 97-100.
-
(1993)
Cytogenet. Cell Genet.
, vol.65
, pp. 97-100
-
-
Kroisel, P.M.1
Ioannou, P.A.2
De Jong, P.J.3
-
19
-
-
0028351625
-
A gene for hereditary multiple exostoses maps to chromosome 19p
-
Le Merrer, M., L. Legeai-Mallet, P.M. Jeannin, B. Horsthemke, A. Schinzel, H. Plauchu, A. Toutain, F. Achard, A. Munnich, and P. Maroteaux. 1994. A gene for hereditary multiple exostoses maps to chromosome 19p. Hum. Mol. Genet. 3: 717-722.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 717-722
-
-
Le Merrer, M.1
Legeai-Mallet, L.2
Jeannin, P.M.3
Horsthemke, B.4
Schinzel, A.5
Plauchu, H.6
Toutain, A.7
Achard, F.8
Munnich, A.9
Maroteaux, P.10
-
20
-
-
0030005755
-
The I.M.A.G.E. consortium: An integrated molecular analysis of genomes and their expression
-
Lennon, G., C. Auffray, M. Polymeropoulos, and M.B. Soares. 1996. The I.M.A.G.E. consortium: An integrated molecular analysis of genomes and their expression. Genomics 33: 151-152.
-
(1996)
Genomics
, vol.33
, pp. 151-152
-
-
Lennon, G.1
Auffray, C.2
Polymeropoulos, M.3
Soares, M.B.4
-
21
-
-
0028786695
-
Deletion of 1p loci and microsatellite instability in colorectal polyps
-
Lothe, R.A., S.N. Andersen, B. Hofstad, G.I. Meling, P. Peltomaki, S. Heim, A. Brogger, M. Vatn, T.O. Rognum, and A.-L. Borresen. 1995. Deletion of 1p loci and microsatellite instability in colorectal polyps. Genes Chromosomes Cancer 14: 182-188.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 182-188
-
-
Lothe, R.A.1
Andersen, S.N.2
Hofstad, B.3
Meling, G.I.4
Peltomaki, P.5
Heim, S.6
Brogger, A.7
Vatn, M.8
Rognum, T.O.9
Borresen, A.-L.10
-
22
-
-
0027410857
-
Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2
-
Mulligan, L.M., E. Gardner. B.A. Smith, C.G.P. Mathew, and B.A.J. Ponder. 1993. Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2. Genes Chromosomes Cancer 6: 166-177.
-
(1993)
Genes Chromosomes Cancer
, vol.6
, pp. 166-177
-
-
Mulligan, L.M.1
Gardner, E.2
Smith, B.A.3
Mathew, C.G.P.4
Ponder, B.A.J.5
-
23
-
-
0028918250
-
Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer
-
Nagai, H., M. Negrini, S.L. Carter, D.R. Gillum, A.L. Rosenberg, G.F. Schwartz, and C.M. Croce. 1995. Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer. Cancer Res. 55: 1752-1757.
-
(1995)
Cancer Res.
, vol.55
, pp. 1752-1757
-
-
Nagai, H.1
Negrini, M.2
Carter, S.L.3
Gillum, D.R.4
Rosenberg, A.L.5
Schwartz, G.F.6
Croce, C.M.7
-
24
-
-
0028916693
-
Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11
-
Raskind, W.H., E.U. Conrad, H. Chansky, and M. Matsushita. 1995. Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11. Am. J. Hum. Genet. 56: 1132-1139.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1132-1139
-
-
Raskind, W.H.1
Conrad, E.U.2
Chansky, H.3
Matsushita, M.4
-
25
-
-
0028861983
-
Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome
-
Reish, O., S.A. Berry, and B. Hirsch. 1995. Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome. Am. J. Med. Genet. 59: 467-475.
-
(1995)
Am. J. Med. Genet.
, vol.59
, pp. 467-475
-
-
Reish, O.1
Berry, S.A.2
Hirsch, B.3
-
26
-
-
0028049832
-
Construction and characterization of a normalized cDNA library
-
Soares, M.B., M.F. Bonaldo, P. Jelene, L. Su, L. Lawton, and A. Efstratiadis. 1994. Construction and characterization of a normalized cDNA library. Proc. Natl. Acad. Sci. 91: 9228-9232.
-
(1994)
Proc. Natl. Acad. Sci.
, vol.91
, pp. 9228-9232
-
-
Soares, M.B.1
Bonaldo, M.F.2
Jelene, P.3
Su, L.4
Lawton, L.5
Efstratiadis, A.6
-
27
-
-
0001509847
-
Bone growth in diaphyseal acalasis
-
Solomon, L. 1961. Bone growth in diaphyseal acalasis. J. Bone Joint Surg. 43: 700-716.
-
(1961)
J. Bone Joint Surg.
, vol.43
, pp. 700-716
-
-
Solomon, L.1
-
28
-
-
0029764629
-
The EXT2 multiple exostoses gene defines a family of putative tumor suppressor genes
-
Stickens, D., G. Clines, D. Burbee, P. Ramos, S. Thomas, D. Hogue, J.T. Hecht, M. Lovett, and G.A. Evans. 1996. The EXT2 multiple exostoses gene defines a family of putative tumor suppressor genes. Nature Genet. 14: 25-32.
-
(1996)
Nature Genet.
, vol.14
, pp. 25-32
-
-
Stickens, D.1
Clines, G.2
Burbee, D.3
Ramos, P.4
Thomas, S.5
Hogue, D.6
Hecht, J.T.7
Lovett, M.8
Evans, G.A.9
-
29
-
-
0027171533
-
Suppression of tumourigenicity in human colon carcinoma cells by introduction of normal chromosome 1p36 region
-
Tanaka, K., R. Yanoshita, M. Konishi, M. Oshimura, Y. Maeda, T. Mori, and M. Miyaki. 1993. Suppression of tumourigenicity in human colon carcinoma cells by introduction of normal chromosome 1p36 region. Oncogens 8: 2253-2258.
-
(1993)
Oncogens
, vol.8
, pp. 2253-2258
-
-
Tanaka, K.1
Yanoshita, R.2
Konishi, M.3
Oshimura, M.4
Maeda, Y.5
Mori, T.6
Miyaki, M.7
-
30
-
-
0026736251
-
Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
-
Telenius, H., N.P. Carter, C. Bebb, M. Nordenskjold, B.A. Ponder, and A. Tunnacliffe. 1992. Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer. Genomics 13: 718-725.
-
(1992)
Genomics
, vol.13
, pp. 718-725
-
-
Telenius, H.1
Carter, N.P.2
Bebb, C.3
Nordenskjold, M.4
Ponder, B.A.5
Tunnacliffe, A.6
-
31
-
-
0001029139
-
Fluorescence in situ hybridization
-
(ed. B. Birren, E. Green, P. Hieter, and R. Myers). Cold Spring Harbor Laboratory Press (in press)
-
Trask, B.J. 1996. Fluorescence in situ hybridization. In Genome analysis: A laboratory manual (ed. B. Birren, E. Green, P. Hieter, and R. Myers). Cold Spring Harbor Laboratory Press (in press).
-
(1996)
Genome Analysis: A Laboratory Manual
-
-
Trask, B.J.1
-
32
-
-
0029049717
-
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3
-
White, P.S., J.M. Maris, C. Beltinger, E. Sulman, H.N. Marshall, M. Fujimori, B.A. Kaufman, J.A. Biegel, C. Allen, C. Hilliard, M.B. Valentine, A.T. Look, H. Enomoto, S. Sakiyama, and G.M. Brodeur. 1995. A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. Proc. Natl. Acad. Sci. 92: 5520-5524.
-
(1995)
Proc. Natl. Acad. Sci.
, vol.92
, pp. 5520-5524
-
-
White, P.S.1
Maris, J.M.2
Beltinger, C.3
Sulman, E.4
Marshall, H.N.5
Fujimori, M.6
Kaufman, B.A.7
Biegel, J.A.8
Allen, C.9
Hilliard, C.10
Valentine, M.B.11
Look, A.T.12
Enomoto, H.13
Sakiyama, S.14
Brodeur, G.M.15
-
33
-
-
0028908915
-
Natural history study of hereditary multiple exostoses
-
Wicklund, C.L., R.M. Pauli, D. Johnston, and J.T. Hecht. 1995. Natural history study of hereditary multiple exostoses. Am. J. Med. Genet. 55: 43-46.
-
(1995)
Am. J. Med. Genet.
, vol.55
, pp. 43-46
-
-
Wicklund, C.L.1
Pauli, R.M.2
Johnston, D.3
Hecht, J.T.4
-
34
-
-
0028047748
-
Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11
-
Wu, Y.-Q., P. Heutink, B.B.A. de Vries, L.A. Sandkuijl, A.M.W. van den Ouweland, M.F. Niermeijer, H. Galjaard, E. Reyneirs, P.J. Willems, and D.J.J. Halley. 1994. Assignment of a second locus for multiple exostoses to the pericentromeric region of chromosome 11. Hum. Mol. Genet. 3: 167-171.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 167-171
-
-
Wu, Y.-Q.1
Heutink, P.2
De Vries, B.B.A.3
Sandkuijl, L.A.4
Van Den Ouweland, A.M.W.5
Niermeijer, M.F.6
Galjaard, H.7
Reyneirs, E.8
Willems, P.J.9
Halley, D.J.J.10
-
35
-
-
0029047022
-
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11
-
Wuyts, W., S. Ramlakhan, W. Van Hul, J.T. Hecht, A.M W. van den Ouweland, W.H. Raskind, F.C. Hofstede, E. Reyniers, D.E. Wells, B. de Vries, E.U. Conrad, A. Hill, D. Zalatayev, J. Weissenbach, M.J. Wagner, E. Bakker, D.J.J. Halley, and P.J. Willems. 1995. Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11. Am. J. Hum. Genet. 57: 382-387.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 382-387
-
-
Wuyts, W.1
Ramlakhan, S.2
Van Hul, W.3
Hecht, J.T.4
Van Den Ouweland, A.M.W.5
Raskind, W.H.6
Hofstede, F.C.7
Reyniers, E.8
Wells, D.E.9
De Vries, B.10
Conrad, E.U.11
Hill, A.12
Zalatayev, D.13
Weissenbach, J.14
Wagner, M.J.15
Bakker, E.16
Halley, D.J.J.17
Willems, P.J.18
-
36
-
-
0029129535
-
Molecular cytogenetics of human papillomavirus-negative cervical carcinoma cell lines
-
Zimonjic, D.B., S. Simpson, N.C. Popescu, and J.A. DiPaolo. 1995. Molecular cytogenetics of human papillomavirus-negative cervical carcinoma cell lines. Cancer Genet. Cytogenet. 82: 1-8.
-
(1995)
Cancer Genet. Cytogenet.
, vol.82
, pp. 1-8
-
-
Zimonjic, D.B.1
Simpson, S.2
Popescu, N.C.3
DiPaolo, J.A.4
|