-
1
-
-
0025992756
-
A map of 22 loci on human chromosome 22
-
Dumanski, J.P., Carlbom, E., Collins, V.P., Nordenskjöld, M., Emanuel, B.S., Budarf, M.L., McDermid, H., Wolff, R., O'Connell, P., White, R. et al. (1991) A map of 22 loci on human chromosome 22. Genomics, 11, 709-719.
-
(1991)
Genomics
, vol.11
, pp. 709-719
-
-
Dumanski, J.P.1
Carlbom, E.2
Collins, V.P.3
Nordenskjöld, M.4
Emanuel, B.S.5
Budarf, M.L.6
McDermid, H.7
Wolff, R.8
O'Connell, P.9
White, R.10
-
2
-
-
0029653651
-
A high resolution integrated yeast artificial chromosome clone map of human chromosome 22
-
Collins, J.E., Cole, C.G., Smink, L.J., Garrett, C.L., Leversha, M.A., Soderlund, C.A., Maslen, G.L., Everett, L.A., Rice, K.M., Coffey, A.J. et al. (1995) A high resolution integrated yeast artificial chromosome clone map of human chromosome 22. Nature, 377, 367-379.
-
(1995)
Nature
, vol.377
, pp. 367-379
-
-
Collins, J.E.1
Cole, C.G.2
Smink, L.J.3
Garrett, C.L.4
Leversha, M.A.5
Soderlund, C.A.6
Maslen, G.L.7
Everett, L.A.8
Rice, K.M.9
Coffey, A.J.10
-
3
-
-
79960655760
-
The DNA sequence of human chromosome 22
-
Dunham, I., Shimizu, N., Roe, B.A., Chissoc, S., Hunt, A.R., Collins, J.E., Bruskiewich, R., Beare, D.M., Clamp, M., Smink, L.J. et al. (1999) The DNA sequence of human chromosome 22. Nature, 402, 489-495.
-
(1999)
Nature
, vol.402
, pp. 489-495
-
-
Dunham, I.1
Shimizu, N.2
Roe, B.A.3
Chissoc, S.4
Hunt, A.R.5
Collins, J.E.6
Bruskiewich, R.7
Beare, D.M.8
Clamp, M.9
Smink, L.J.10
-
4
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo, S., Lampel, S., Stilgenbauer, S., Nickolenko, J., Benner, A., Dohner, H., Cremer, T. and Lichter, P. (1997) Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer, 20, 399-407.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
5
-
-
17344371740
-
High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
-
Pinkel, D., Segraves, R., Sudar, D., Clark, S., Poole, I., Kowbel, D., Collins, C., Kuo, W.L., Chen, C., Zhai, Y. et al. (1998) High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat. Genet., 20, 207-211.
-
(1998)
Nat. Genet.
, vol.20
, pp. 207-211
-
-
Pinkel, D.1
Segraves, R.2
Sudar, D.3
Clark, S.4
Poole, I.5
Kowbel, D.6
Collins, C.7
Kuo, W.L.8
Chen, C.9
Zhai, Y.10
-
6
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders, A.M., Nowak, N., Segraves, R., Blackwood, S., Brown, N., Conroy, J., Hamilton, G., Hindle, A.K., Huey, B., Kimura, K. et al. (2001) Assembly of microarrays for genome-wide measurement of DNA copy number. Nat. Genet., 29, 263-264.
-
(2001)
Nat. Genet.
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
-
7
-
-
0036138187
-
Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22
-
Bailey, J.A., Yavor, A.M., Viggiano, L., Misceo, D., Horvath, J.E., Archidiacono, N., Schwartz, S., Rocchi, M. and Eichler, E.E. (2002) Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22. Am. J. Hum. Genet., 70, 83-100.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 83-100
-
-
Bailey, J.A.1
Yavor, A.M.2
Viggiano, L.3
Misceo, D.4
Horvath, J.E.5
Archidiacono, N.6
Schwartz, S.7
Rocchi, M.8
Eichler, E.E.9
-
8
-
-
0028074376
-
Characterization of a new member of the human b-adaptin gene family from chromosome 22q12, a candidate meningioma gene
-
Peyrard, M., Fransson, I., Xie, Y.-G., Han, F.-Y., Ruttledge, M.H., Swahn, S., Collins, J.E., Dunham, I., Collins, V.P. and Dumanski, J.P. (1994) Characterization of a new member of the human b-adaptin gene family from chromosome 22q12, a candidate meningioma gene. Hum. Mol. Genet., 3, 1393-1399.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1393-1399
-
-
Peyrard, M.1
Fransson, I.2
Xie, Y.-G.3
Han, F.-Y.4
Ruttledge, M.H.5
Swahn, S.6
Collins, J.E.7
Dunham, I.8
Collins, V.P.9
Dumanski, J.P.10
-
9
-
-
0035252636
-
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
-
Bruder, C.E., Hirvela, C., Tapia-Paez, I., Fransson, I., Segraves, R., Hamilton, G., Zhang, XX, Evans, D.G., Wallace, A.J., Baser, M.E. et al. (2001) High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Hum. Mol. Genet., 10, 271-282.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 271-282
-
-
Bruder, C.E.1
Hirvela, C.2
Tapia-Paez, I.3
Fransson, I.4
Segraves, R.5
Hamilton, G.6
Zhang, X.X.7
Evans, D.G.8
Wallace, A.J.9
Baser, M.E.10
-
10
-
-
0032956279
-
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4 MB constitutional deletion on chromosome 22: Possible localization of a neurofibromatosis type 2 modifier gene?
-
Bruder, C.E., Ichimura, K., Blennow, E., Ikeuchi, T., Yamaguchi, T., Yuasa, Y., Collins, V.P. and Dumanski, J.P. (1999) Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4 MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene? Genes Chromosomes Cancer, 25, 184-190.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 184-190
-
-
Bruder, C.E.1
Ichimura, K.2
Blennow, E.3
Ikeuchi, T.4
Yamaguchi, T.5
Yuasa, Y.6
Collins, V.P.7
Dumanski, J.P.8
-
11
-
-
0032809735
-
Common regions of deletion on chromosome 22q12.3-q13.1 and 22q13.2 in human astrocytomas appear related to malignancy grade
-
Ino, Y., Silver, J. S., Blazejewski, L., Nishikawa, R., Matsutani, M., von Deimling, A. and Louis, D.N. (1999) Common regions of deletion on chromosome 22q12.3-q13.1 and 22q13.2 in human astrocytomas appear related to malignancy grade. J. Neuropathol. Exp. Neurol., 58, 881-885.
-
(1999)
J. Neuropathol. Exp. Neurol.
, vol.58
, pp. 881-885
-
-
Ino, Y.1
Silver, J.S.2
Blazejewski, L.3
Nishikawa, R.4
Matsutani, M.5
von Deimling, A.6
Louis, D.N.7
-
12
-
-
0033987633
-
A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression
-
Oskam, N.T., Bijleveld, E.H. and Hulsebos, T.J. (2000) A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression. Int. J. Cancer, 85, 336-339.
-
(2000)
Int. J. Cancer
, vol.85
, pp. 336-339
-
-
Oskam, N.T.1
Bijleveld, E.H.2
Hulsebos, T.J.3
-
13
-
-
0034117078
-
14-3-3 proteins: Structure, function, and regulation
-
Fu, H., Subramanian, R.R. and Masters, S.C. (2000) 14-3-3 proteins: structure, function, and regulation. Annu. Rev. Pharmacol. Toxicol., 40, 617-647.
-
(2000)
Annu. Rev. Pharmacol. Toxicol.
, vol.40
, pp. 617-647
-
-
Fu, H.1
Subramanian, R.R.2
Masters, S.C.3
-
14
-
-
0037138389
-
How do 14-3-3 proteins work? Gatekeeper phosphorylation and the molecular anvil hypothesis
-
Yaffe, M.B. (2002) How do 14-3-3 proteins work? Gatekeeper phosphorylation and the molecular anvil hypothesis. FEBS Lett., 513, 53-57.
-
(2002)
FEBS Lett.
, vol.513
, pp. 53-57
-
-
Yaffe, M.B.1
-
15
-
-
0035132141
-
Proteomic analysis reveals that 14-3-3sigma is down-regulated in human breast cancer cells
-
Vercoutter-Edouart, A.S., Lemoine, J., Le Bourhis, X., Louis, H., Boilly, B., Nurcombe, V., Revillion, F., Peyrat,,J.P. and Hondermarck, H. (2001) Proteomic analysis reveals that 14-3-3sigma is down-regulated in human breast cancer cells. Cancer Res., 61, 76-80.
-
(2001)
Cancer Res.
, vol.61
, pp. 76-80
-
-
Vercoutter-Edouart, A.S.1
Lemoine, J.2
Le Bourhis, X.3
Louis, H.4
Boilly, B.5
Nurcombe, V.6
Revillion, F.7
Peyrat, J.P.8
Hondermarck, H.9
-
16
-
-
0035821727
-
Hypermethylation of 14-3-3 sigma (stratifin) is an early event in breast cancer
-
Umbricht, C.B., Evron, E., Gabrielson, E., Ferguson, A., Marks, J. and Sukumar, S. (2001) Hypermethylation of 14-3-3 sigma (stratifin) is an early event in breast cancer. Oncogene, 20, 3348-3353.
-
(2001)
Oncogene
, vol.20
, pp. 3348-3353
-
-
Umbricht, C.B.1
Evron, E.2
Gabrielson, E.3
Ferguson, A.4
Marks, J.5
Sukumar, S.6
-
17
-
-
0034072726
-
Gene amplifications characterize acral melanoma and permit the detection of occult tumor cells in the surrounding skin
-
Bastian, B.C., Kashani-Sabet, M., Hamm, H., Godfrey, T., Moore, D.H., 2nd, Brocker, E.B., LeBoit, P.E. and Pinkel, D. (2000) Gene amplifications characterize acral melanoma and permit the detection of occult tumor cells in the surrounding skin. Cancer Res., 60, 1968-1973.
-
(2000)
Cancer Res.
, vol.60
, pp. 1968-1973
-
-
Bastian, B.C.1
Kashani-Sabet, M.2
Hamm, H.3
Godfrey, T.4
Moore D.H. II5
Brocker, E.B.6
LeBoit, P.E.7
Pinkel, D.8
-
18
-
-
0034161932
-
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: Genomic organization and deletion endpoint analysis
-
Shaikh, T.H., Kurahashi, H., Saitta, S.C., O'Hare, A.M., Hu, P., Roe, B.A., Driscoll, D.A., McDonald-McGinn, D.M., Zackai, E.H., Budarf, M.L. et al. (2000) Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Hum. Mol. Genet., 9, 489-501.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 489-501
-
-
Shaikh, T.H.1
Kurahashi, H.2
Saitta, S.C.3
O'Hare, A.M.4
Hu, P.5
Roe, B.A.6
Driscoll, D.A.7
McDonald-McGinn, D.M.8
Zackai, E.H.9
Budarf, M.L.10
-
19
-
-
0029875843
-
Translocation t(17;22) (q22;q13) in dermatofibrosarcoma protuberans. A new tumor-associated chromosome rearrangement
-
Pedeutour, F., Simon, M.P., Minoletti, F., Barcelo, G., Terrier-Lacombe, M.J., Combemale, P., Sozzi, G., Ayraud, N. and Turc-Carel, C. (1996) Translocation t(17;22) (q22;q13) in dermatofibrosarcoma protuberans. A new tumor-associated chromosome rearrangement. Cytogenet. Cell Genet., 72, 171-174.
-
(1996)
Cytogenet. Cell Genet.
, vol.72
, pp. 171-174
-
-
Pedeutour, F.1
Simon, M.P.2
Minoletti, F.3
Barcelo, G.4
Terrier-Lacombe, M.J.5
Combemale, P.6
Sozzi, G.7
Ayraud, N.8
Turc-Carel, C.9
-
20
-
-
0035146991
-
Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: A fluorescence in situ hybridization and comparative genomic hybridization analysis
-
Nishio, J., Iwasaki, H., Ishiguro, M., Ohjimi, Y., Yo, S., Isayama, T., Naito, M. and Kikuchi, M. (2001) Supernumerary ring chromosome in a Bednar tumor (pigmented dermatofibrosarcoma protuberans) is composed of interspersed sequences from chromosomes 17 and 22: a fluorescence in situ hybridization and comparative genomic hybridization analysis. Genes Chromosomes Cancer, 30, 305-309.
-
(2001)
Genes Chromosomes Cancer
, vol.30
, pp. 305-309
-
-
Nishio, J.1
Iwasaki, H.2
Ishiguro, M.3
Ohjimi, Y.4
Yo, S.5
Isayama, T.6
Naito, M.7
Kikuchi, M.8
-
21
-
-
0031012850
-
Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma
-
Simon, M.P., Pedeutour, F., Sirvent, N., Grosgeorge, J., Minoletti, F., Coindre, J.M., Terrier-Lacombe, M.J., Mandahl, N., Craver, R.D., Blin, N. et al. (1997) Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma. Nat. Genet., 15, 95-98.
-
(1997)
Nat. Genet.
, vol.15
, pp. 95-98
-
-
Simon, M.P.1
Pedeutour, F.2
Sirvent, N.3
Grosgeorge, J.4
Minoletti, F.5
Coindre, J.M.6
Terrier-Lacombe, M.J.7
Mandahl, N.8
Craver, R.D.9
Blin, N.10
-
22
-
-
0031661840
-
Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas
-
O'Brien, K.P., Seroussi, E., Dal Cin, P., Sciot, R., Mandahl, N., Fletcher, J.A., Turc-Carel, C. and Dumanski, J.P. (1998) Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas. Genes Chromosomes Cancer, 23, 187-193.
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 187-193
-
-
O'Brien, K.P.1
Seroussi, E.2
Dal Cin, P.3
Sciot, R.4
Mandahl, N.5
Fletcher, J.A.6
Turc-Carel, C.7
Dumanski, J.P.8
-
23
-
-
0029006919
-
Ring chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences
-
Pedeutour, F., Simon, M.-P., Minoletti, F., Sozzi, G., Pierotti, M.A., Hecht, F. and Turc-Carel, C. (1995) Ring chromosomes in dermatofibrosarcoma protuberans are low-level amplifiers of chromosome 17 and 22 sequences. Cancer Res., 55, 2400-2403.
-
(1995)
Cancer Res.
, vol.55
, pp. 2400-2403
-
-
Pedeutour, F.1
Simon, M.-P.2
Minoletti, F.3
Sozzi, G.4
Pierotti, M.A.5
Hecht, F.6
Turc-Carel, C.7
-
24
-
-
0345711466
-
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
-
Gisselsson, D., Hoglund, M., Mertens, F., Johansson, B., Dal Cin, P., Van den Berghe, H., Earnshaw, W.C., Mitelman, F. and Mandahl, N. (1999) The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum. Genet., 104, 315-325.
-
(1999)
Hum. Genet.
, vol.104
, pp. 315-325
-
-
Gisselsson, D.1
Hoglund, M.2
Mertens, F.3
Johansson, B.4
Dal Cin, P.5
Van den Berghe, H.6
Earnshaw, W.C.7
Mitelman, F.8
Mandahl, N.9
-
25
-
-
4243264396
-
Gene dosage arrays, their production and use thereof
-
Swedish patent application, no. SE0200865-4. Sweden
-
Dumanski, J.P. (2002) Gene dosage arrays, their production and use thereof, Swedish patent application, no. SE0200865-4. Sweden.
-
(2002)
-
-
Dumanski, J.P.1
-
26
-
-
0034830935
-
Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification
-
Dean, F.B., Nelson, J.R., Giesler, T.L. and Lasken, R.S. (2001) Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification. Genome Res., 11, 1095-1099.
-
(2001)
Genome Res.
, vol.11
, pp. 1095-1099
-
-
Dean, F.B.1
Nelson, J.R.2
Giesler, T.L.3
Lasken, R.S.4
-
27
-
-
18344396798
-
Comprehensive human genome amplification using multiple displacement amplification
-
Dean, F.B., Hosono, S., Fang, L., Wu, X., Faruqi, A.F., Bray-Ward, P., Sun, Z., Zong, Q., Du, Y., Du, J. et al. (2002) Comprehensive human genome amplification using multiple displacement amplification. Proc. Natl Acad. Sci. USA, 99, 5261-5266.
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 5261-5266
-
-
Dean, F.B.1
Hosono, S.2
Fang, L.3
Wu, X.4
Faruqi, A.F.5
Bray-Ward, P.6
Sun, Z.7
Zong, Q.8
Du, Y.9
Du, J.10
-
28
-
-
0026704681
-
Dermatofibrosarcoma protuberans: Treatment and prognosis
-
Rutgers, E.J., Kroon, B.B., Albus-Lutter, C.E. and Gortzak, E. (1992) Dermatofibrosarcoma protuberans: treatment and prognosis. Eur. J. Surg. Oncol., 18, 241-248.
-
(1992)
Eur. J. Surg. Oncol.
, vol.18
, pp. 241-248
-
-
Rutgers, E.J.1
Kroon, B.B.2
Albus-Lutter, C.E.3
Gortzak, E.4
-
29
-
-
0029871934
-
Soft tissue sarcomas in dermatology
-
Fish, F.S. (1996) Soft tissue sarcomas in dermatology. Dermatologic Surgery, 22, 268-273.
-
(1996)
Dermatologic Surgery
, vol.22
, pp. 268-273
-
-
Fish, F.S.1
-
30
-
-
0000264522
-
The nature of lymphoid cell lines and their relationship to the virus
-
Epstein, M. and Achong, B. (eds.), Springer-Verlag, New York
-
Nilsson, K. (1979) The nature of lymphoid cell lines and their relationship to the virus. In Epstein, M. and Achong, B. (eds.), The Epstein-Barr Virus. Springer-Verlag, New York, pp. 227-266.
-
(1979)
The Epstein-Barr Virus
, pp. 227-266
-
-
Nilsson, K.1
-
31
-
-
0029962469
-
The human chromosome 22-located genes and malignancies of the central nervous system
-
Dumanski, J.P. (1996) The human chromosome 22-located genes and malignancies of the central nervous system. Neuropathol. Appl. Neurobiol., 22, 412-417.
-
(1996)
Neuropathol. Appl. Neurobiol.
, vol.22
, pp. 412-417
-
-
Dumanski, J.P.1
-
32
-
-
0021381028
-
A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity
-
Feinberg, A.P. and Vogelstein, B. (1984) A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Addendum. Anal. Biochem., 137, 266-267.
-
(1984)
Addendum. Anal. Biochem.
, vol.137
, pp. 266-267
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
33
-
-
0033753819
-
The 22q11 deletion syndromes
-
Scambler, P.J. (2000) The 22q11 deletion syndromes. Hum. Mol. Genet., 9, 2421-2426.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2421-2426
-
-
Scambler, P.J.1
-
34
-
-
0033064584
-
A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene
-
Bruder, C.E., Ichimura, K., Tingby, O., Hirakawa, K., Komatsuzaki, A., Tamura, A., Yuasa, Y., Collins, V.P. and Dumanski, J.P. (1999) A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene. Hum. Genet., 104, 418-424.
-
(1999)
Hum. Genet.
, vol.104
, pp. 418-424
-
-
Bruder, C.E.1
Ichimura, K.2
Tingby, O.3
Hirakawa, K.4
Komatsuzaki, A.5
Tamura, A.6
Yuasa, Y.7
Collins, V.P.8
Dumanski, J.P.9
|