-
1
-
-
0037366067
-
Neuroblastoma: biological insights into a clinical enigma
-
Brodeur G.M. Neuroblastoma: biological insights into a clinical enigma. Nat Rev Cancer 3 (2003) 203-216
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 203-216
-
-
Brodeur, G.M.1
-
2
-
-
4544236943
-
Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q
-
McArdle L., McDermott M., Purcell R., Grehan D., O'Meara A., Breatnach F., Catchpoole D., Culhane A.C., Jeffery I., Gallagher W.M., and Stallings R.L. Oligonucleotide microarray analysis of gene expression in neuroblastoma displaying loss of chromosome 11q. Carcinogenesis 25 (2004) 1599-1609
-
(2004)
Carcinogenesis
, vol.25
, pp. 1599-1609
-
-
McArdle, L.1
McDermott, M.2
Purcell, R.3
Grehan, D.4
O'Meara, A.5
Breatnach, F.6
Catchpoole, D.7
Culhane, A.C.8
Jeffery, I.9
Gallagher, W.M.10
Stallings, R.L.11
-
3
-
-
0031665929
-
Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization
-
Vandesompele J., Van Roy N., Van Gele M., Laureys G., Ambros P., Heimann P., Devalck C., Schuuring E., Brock P., Otten J., Gyselinck J., De Paepe A., and Speleman F. Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization. Genes Chromosomes Cancer 23 (1998) 141-152
-
(1998)
Genes Chromosomes Cancer
, vol.23
, pp. 141-152
-
-
Vandesompele, J.1
Van Roy, N.2
Van Gele, M.3
Laureys, G.4
Ambros, P.5
Heimann, P.6
Devalck, C.7
Schuuring, E.8
Brock, P.9
Otten, J.10
Gyselinck, J.11
De Paepe, A.12
Speleman, F.13
-
4
-
-
0034237508
-
Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization
-
Breen C.J., O'Meara A., McDermott M., Mullarkey M., and Stallings R.L. Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization. Cancer Genet Cytogenet 120 (2000) 44-49
-
(2000)
Cancer Genet Cytogenet
, vol.120
, pp. 44-49
-
-
Breen, C.J.1
O'Meara, A.2
McDermott, M.3
Mullarkey, M.4
Stallings, R.L.5
-
5
-
-
0037239718
-
Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma
-
Spitz R., Hero B., Ernestus K., and Berthold F. Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma. Clin Cancer Res 9 (2003) 52-58
-
(2003)
Clin Cancer Res
, vol.9
, pp. 52-58
-
-
Spitz, R.1
Hero, B.2
Ernestus, K.3
Berthold, F.4
-
6
-
-
0037438886
-
Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?
-
Stallings R.L., Howard J., Dunlop A., Mullarkey M., McDermott M., Breatnach F., and O'Meara A. Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?. Cancer Genet Cytogenetics 140 (2003) 133-137
-
(2003)
Cancer Genet Cytogenetics
, vol.140
, pp. 133-137
-
-
Stallings, R.L.1
Howard, J.2
Dunlop, A.3
Mullarkey, M.4
McDermott, M.5
Breatnach, F.6
O'Meara, A.7
-
7
-
-
20244370742
-
Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma
-
Vandesompele J., Baudis M., De Preter K., Van Roy N., Ambros P., Bown N., Combaret V., De Preter K., Brinkschmidt C., Christiansen H., Combaret V., Lastowska M., Nicholson J., O'Meara A., Plantaz D., Stallings R., Brichard B., Van den Broecke De Bie S., De Paepe A., Laureys G., and Speleman F. Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma. J Clin Oncol 23 (2005) 2280-2299
-
(2005)
J Clin Oncol
, vol.23
, pp. 2280-2299
-
-
Vandesompele, J.1
Baudis, M.2
De Preter, K.3
Van Roy, N.4
Ambros, P.5
Bown, N.6
Combaret, V.7
De Preter, K.8
Brinkschmidt, C.9
Christiansen, H.10
Combaret, V.11
Lastowska, M.12
Nicholson, J.13
O'Meara, A.14
Plantaz, D.15
Stallings, R.16
Brichard, B.17
Van den Broecke De Bie, S.18
De Paepe, A.19
Laureys, G.20
Speleman, F.21
more..
-
8
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
-
Bronner C.E., Baker S.M., Morrison P.T., Warren G., Smith L.G., Lescoe M.K., Kane M., Earabino C., Lipford J., and Lindblom A. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature 368 (1994) 258-261
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
Warren, G.4
Smith, L.G.5
Lescoe, M.K.6
Kane, M.7
Earabino, C.8
Lipford, J.9
Lindblom, A.10
-
9
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F., Tory K., Gnarra J., Yao M., Duh F.M., Orcutt M.L., Stackhouse T., Kuzmin I., Modi W., and Geil L. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 260 (1993) 1317-1320
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.M.5
Orcutt, M.L.6
Stackhouse, T.7
Kuzmin, I.8
Modi, W.9
Geil, L.10
-
10
-
-
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. 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 4 (1996) 587-597
-
(1996)
Cell
, vol.4
, 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
-
11
-
-
0037081278
-
Human semaphorin 3B (SEMA3B) located at chromosome 3p21.3 suppresses tumor formation in an adenocarcinoma cell line
-
Tse C., Xiang R.H., Bracht T., and Naylor S.L. Human semaphorin 3B (SEMA3B) located at chromosome 3p21.3 suppresses tumor formation in an adenocarcinoma cell line. Cancer Res 62 (2002) 542-546
-
(2002)
Cancer Res
, vol.62
, pp. 542-546
-
-
Tse, C.1
Xiang, R.H.2
Bracht, T.3
Naylor, S.L.4
-
12
-
-
0029871193
-
Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancer
-
Xiang R.H., Hensel C.H., Garcia D.K., Carlson H.C., Kok K., Daly M.C., Kerbacher K., van den Berg A., Veldhuis P., Buys C.H., and Naylor S.L. Isolation of the human semaphorin III/F gene (SEMA3F) at chromosome 3p21, a region deleted in lung cancer. Genomics 32 (1996) 39-48
-
(1996)
Genomics
, vol.32
, pp. 39-48
-
-
Xiang, R.H.1
Hensel, C.H.2
Garcia, D.K.3
Carlson, H.C.4
Kok, K.5
Daly, M.C.6
Kerbacher, K.7
van den Berg, A.8
Veldhuis, P.9
Buys, C.H.10
Naylor, S.L.11
-
13
-
-
0032408496
-
Semaphorin-neuropilin interactions underlying sympathetic axon responses to class 3 semaphorins
-
Chen H., He Z., Bagri A., and Tessier-Lavigne M. Semaphorin-neuropilin interactions underlying sympathetic axon responses to class 3 semaphorins. Neuron 21 (1998) 1283-1290
-
(1998)
Neuron
, vol.21
, pp. 1283-1290
-
-
Chen, H.1
He, Z.2
Bagri, A.3
Tessier-Lavigne, M.4
-
14
-
-
0032817550
-
Semaphorins as mediators of neuronal apoptosis
-
Shirvan A., Ziv I., Fleminger G., Shina R., He Z., Brudo I., Melamed E., and Barzilai A. Semaphorins as mediators of neuronal apoptosis. J Neurochem 73 (1999) 961-971
-
(1999)
J Neurochem
, vol.73
, pp. 961-971
-
-
Shirvan, A.1
Ziv, I.2
Fleminger, G.3
Shina, R.4
He, Z.5
Brudo, I.6
Melamed, E.7
Barzilai, A.8
-
15
-
-
0035923529
-
Inhibition of lung cancer cell growth and induction of apoptosis after reexpression of 3p21.3 candidate tumor suppressor gene SEMA3B
-
Tomizawa Y., Sekido Y., Kondo M., Gao B., Yokota J., Roche J., Drabkin H., Lerman M.I., Gazdar A.F., and Minna J.D. Inhibition of lung cancer cell growth and induction of apoptosis after reexpression of 3p21.3 candidate tumor suppressor gene SEMA3B. Proc Natl Acad Sci U S A 98 (2001) 13954-13959
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 13954-13959
-
-
Tomizawa, Y.1
Sekido, Y.2
Kondo, M.3
Gao, B.4
Yokota, J.5
Roche, J.6
Drabkin, H.7
Lerman, M.I.8
Gazdar, A.F.9
Minna, J.D.10
-
16
-
-
4644290536
-
Molecular cytogenetic analysis of recurrent unbalanced t(11;17)'s in neuroblastoma
-
Stallings R.L., Carty P., McArdle L., Mullarkey M., McDermott M., Breatnach F., and O'Meara A. Molecular cytogenetic analysis of recurrent unbalanced t(11;17)'s in neuroblastoma. Cancer Genet Cytogenetics 154 (2004) 44-51
-
(2004)
Cancer Genet Cytogenetics
, vol.154
, pp. 44-51
-
-
Stallings, R.L.1
Carty, P.2
McArdle, L.3
Mullarkey, M.4
McDermott, M.5
Breatnach, F.6
O'Meara, A.7
-
17
-
-
25844494223
-
Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH
-
Selzer R.R., Richmond T.A., Pofahl N.J., Green R.D., Eis P., Nair P., Brothman A.R., and Stallings R.L. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH. Genes Chromosomes Cancer 44 (2005) 305-319
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 305-319
-
-
Selzer, R.R.1
Richmond, T.A.2
Pofahl, N.J.3
Green, R.D.4
Eis, P.5
Nair, P.6
Brothman, A.R.7
Stallings, R.L.8
-
18
-
-
33645749497
-
High-resolution analysis of chromosomal breakpoints and genomic instability identifies PTPRD as a candidate tumor suppressor gene in neuroblastoma
-
Stallings R.L., Nair P., Maris J.M., Catchpoole D., McDermott M., O'Meara A., and Breatnach F. High-resolution analysis of chromosomal breakpoints and genomic instability identifies PTPRD as a candidate tumor suppressor gene in neuroblastoma. Cancer Res 66 (2006) 3673-3680
-
(2006)
Cancer Res
, vol.66
, pp. 3673-3680
-
-
Stallings, R.L.1
Nair, P.2
Maris, J.M.3
Catchpoole, D.4
McDermott, M.5
O'Meara, A.6
Breatnach, F.7
-
19
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer M., McDonald L.E., Millar D.S., Collis C.M., Watt F., Grigg G.W., Molloy P.L., and Paul C.L. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci U S A 89 (1992) 1827-1831
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
Collis, C.M.4
Watt, F.5
Grigg, G.W.6
Molloy, P.L.7
Paul, C.L.8
-
20
-
-
0038068926
-
Allelic loss on chromosome 3p21.3 and promoter hypermethylation of semaphorin 3B in non-small cell lung cancer
-
Kuroki T., Trapasso F., Yendamuri S., Matsuyama A., Alder H., Williams N.N., Kaiser L.R., and Croce C.M. Allelic loss on chromosome 3p21.3 and promoter hypermethylation of semaphorin 3B in non-small cell lung cancer. Cancer Res 63 (2003) 3352-3355
-
(2003)
Cancer Res
, vol.63
, pp. 3352-3355
-
-
Kuroki, T.1
Trapasso, F.2
Yendamuri, S.3
Matsuyama, A.4
Alder, H.5
Williams, N.N.6
Kaiser, L.R.7
Croce, C.M.8
-
21
-
-
0033563255
-
HMGI(Y) and HMGI-C genes are expressed in neuroblastoma cell lines and tumors and affect retinoic acid responsiveness
-
Giannini G., Di Marcotullio L., Ristori E., Zani M., Crescenzi M., Scarpa S., Piaggio G., Vacca A., Peverali F.A., Diana F., Screpanti I., Frati L., and Gulino A. HMGI(Y) and HMGI-C genes are expressed in neuroblastoma cell lines and tumors and affect retinoic acid responsiveness. Cancer Res 59 (1999) 2484-2492
-
(1999)
Cancer Res
, vol.59
, pp. 2484-2492
-
-
Giannini, G.1
Di Marcotullio, L.2
Ristori, E.3
Zani, M.4
Crescenzi, M.5
Scarpa, S.6
Piaggio, G.7
Vacca, A.8
Peverali, F.A.9
Diana, F.10
Screpanti, I.11
Frati, L.12
Gulino, A.13
-
22
-
-
4344688973
-
Clustering of gene hypermethylation associated with clinical risk groups in neuroblastoma
-
Alaminos M., Davalos V., Cheung N.K.V., Gerald W.L., and Esteller M. Clustering of gene hypermethylation associated with clinical risk groups in neuroblastoma. J Natl Cancer Inst 96 (2004) 1208-1219
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 1208-1219
-
-
Alaminos, M.1
Davalos, V.2
Cheung, N.K.V.3
Gerald, W.L.4
Esteller, M.5
-
23
-
-
21744443423
-
High-resolution detection and mapping of genomic DNA alterations in neuroblastoma
-
Mosse Y.P., Greshock J., Margolin A., Naylor T., Cole K., Khazi D., Hii G., Winter C., Shahzad S., Asziz M., Biegel J.A., Weber B.L., and Maris J.M. High-resolution detection and mapping of genomic DNA alterations in neuroblastoma. Genes Chromosomes Cancer 43 (2005) 390-403
-
(2005)
Genes Chromosomes Cancer
, vol.43
, pp. 390-403
-
-
Mosse, Y.P.1
Greshock, J.2
Margolin, A.3
Naylor, T.4
Cole, K.5
Khazi, D.6
Hii, G.7
Winter, C.8
Shahzad, S.9
Asziz, M.10
Biegel, J.A.11
Weber, B.L.12
Maris, J.M.13
-
24
-
-
11144229611
-
Association of epigenetic inactivation of RASSF1A with poor outcome in human neuroblastoma
-
Yang Q., Zage P., Kagan D., Tian Y., Seshadri R., Salwen H.R., Liu S., Chlenski A., and Cohn S.L. Association of epigenetic inactivation of RASSF1A with poor outcome in human neuroblastoma. Clin Cancer Res 10 (2004) 8493-8500
-
(2004)
Clin Cancer Res
, vol.10
, pp. 8493-8500
-
-
Yang, Q.1
Zage, P.2
Kagan, D.3
Tian, Y.4
Seshadri, R.5
Salwen, H.R.6
Liu, S.7
Chlenski, A.8
Cohn, S.L.9
-
25
-
-
13444270332
-
CpG island methylator phenotype is a strong determinant of poor prognosis in neuroblastomas
-
Abe M., Ohira M., Kaneda A., Yagi Y., Yamamoto S., Kitano Y., Takato T., Nakagawara A., and Ushijima T. CpG island methylator phenotype is a strong determinant of poor prognosis in neuroblastomas. Cancer Res 65 (2005) 828-834
-
(2005)
Cancer Res
, vol.65
, pp. 828-834
-
-
Abe, M.1
Ohira, M.2
Kaneda, A.3
Yagi, Y.4
Yamamoto, S.5
Kitano, Y.6
Takato, T.7
Nakagawara, A.8
Ushijima, T.9
-
26
-
-
33745494694
-
Von Hippel-Lindau tumor suppressor gene expression level has prognostic value in neuroblastoma
-
Hoebeeck J., Vandesompele J., Nilsson H., De Preter K., Van Roy N., De Smet E., Yigit N., De Paepe A., Laureys G., Pahlman S., and Speleman F. Von Hippel-Lindau tumor suppressor gene expression level has prognostic value in neuroblastoma. Int J Cancer 19 (2006) 624-629
-
(2006)
Int J Cancer
, vol.19
, pp. 624-629
-
-
Hoebeeck, J.1
Vandesompele, J.2
Nilsson, H.3
De Preter, K.4
Van Roy, N.5
De Smet, E.6
Yigit, N.7
De Paepe, A.8
Laureys, G.9
Pahlman, S.10
Speleman, F.11
-
27
-
-
33745700217
-
Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number
-
Wang Q., Diskin S., Rappaport E., Attiyeh E., Mosse Y., Shue D., Seiser E., Jagannathan J., Shusterman S., Bansal M., Khazi D., Winter C., Okawa E., Grant G., Cnaan A., Zhao H., Cheung N.K., Gerald W., London W., Matthay K.K., Brodeur G.M., and Maris J.M. Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number. Cancer Res 66 (2006) 6050-6062
-
(2006)
Cancer Res
, vol.66
, pp. 6050-6062
-
-
Wang, Q.1
Diskin, S.2
Rappaport, E.3
Attiyeh, E.4
Mosse, Y.5
Shue, D.6
Seiser, E.7
Jagannathan, J.8
Shusterman, S.9
Bansal, M.10
Khazi, D.11
Winter, C.12
Okawa, E.13
Grant, G.14
Cnaan, A.15
Zhao, H.16
Cheung, N.K.17
Gerald, W.18
London, W.19
Matthay, K.K.20
Brodeur, G.M.21
Maris, J.M.22
more..
|