-
1
-
-
0029977194
-
Role of ploidy, chromosome 1p, and Schwann cells in the maturation of neuroblastoma
-
Ambros IM, Zellner A, Roald B, et al (1996). Role of ploidy, chromosome 1p, and Schwann cells in the maturation of neuroblastoma. The New England J Med, 334, 1505-11.
-
(1996)
The New England J Med
, vol.334
, pp. 1505-1511
-
-
Ambros, I.M.1
Zellner, A.2
Roald, B.3
-
2
-
-
19044380776
-
Loss of a Fyn-regulated differentiation and growth arrest pathway in advanced stage neuroblastoma
-
Berwanger B, Hartmann O, Bergmann E, et al (2002). Loss of a Fyn-regulated differentiation and growth arrest pathway in advanced stage neuroblastoma. Cancer Cell, 2, 377-86.
-
(2002)
Cancer Cell
, vol.2
, pp. 377-386
-
-
Berwanger, B.1
Hartmann, O.2
Bergmann, E.3
-
3
-
-
0017698493
-
Chromosomal aberrations in human neuroblastomas
-
Brodeur GM, Sekhon GS, Goldstein MN, (1977). Chromosomal aberrations in human neuroblastomas. Cancer, 40, 2256-63.
-
(1977)
Cancer
, vol.40
, pp. 2256-2263
-
-
Brodeur, G.M.1
Sekhon, G.S.2
Goldstein, M.N.3
-
4
-
-
0019777535
-
Cytogenetic features of human neuroblastomas and cell lines
-
Brodeur GM, Green AA, Hayes FA, et al (1981). Cytogenetic features of human neuroblastomas and cell lines. Cancer Res, 41, 4678-86.
-
(1981)
Cancer Res
, vol.41
, pp. 4678-4686
-
-
Brodeur, G.M.1
Green, A.A.2
Hayes, F.A.3
-
5
-
-
0037366067
-
Neuroblastoma: biological insights into a clinical enigma
-
Brodeur G (2003). Neuroblastoma: biological insights into a clinical enigma. Nat Rev Cancer, 3, 203-16.
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 203-216
-
-
Brodeur, G.1
-
6
-
-
77956632267
-
Genetics and genomics of neuroblastoma
-
Capasso M, Diskin SJ, (2010). Genetics and genomics of neuroblastoma. Cancer Treat Res, 155, 65-84.
-
(2010)
Cancer Treat Res
, vol.155
, pp. 65-84
-
-
Capasso, M.1
Diskin, S.J.2
-
7
-
-
15844421386
-
Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus
-
Caron H, van Sluis P, Buschman R, et al (1996). Allelic loss of the short arm of chromosome 4 in neuroblastoma suggests a novel tumour suppressor gene locus. Hum Genet, 97, 834-37.
-
(1996)
Hum Genet
, vol.97
, pp. 834-837
-
-
Caron, H.1
van Sluis, P.2
Buschman, R.3
-
8
-
-
33845743957
-
Aurora kinases: new targets for cancer therapy
-
Carvajal RD, Tse A, Schwartz GK, (2006). Aurora kinases: new targets for cancer therapy. Clin Cancer Res, 12, 6869-75.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 6869-6875
-
-
Carvajal, R.D.1
Tse, A.2
Schwartz, G.K.3
-
9
-
-
0029962469
-
The human chromosome 22-located genes and malignancies of the central nervous system
-
Dumanski JP (1996). The human chromosome 22-located genes and malignancies of the central nervous system. Neuropathol Appl Neurobiol, 22, 412-7.
-
(1996)
Neuropathol Appl Neurobiol
, vol.22
, pp. 412-417
-
-
Dumanski, J.P.1
-
10
-
-
0031749533
-
Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumoursuppressor locus distal to the FHIT gene
-
Ejeskar K, Aburatani H, Abrahamsson J, et al (1998). Loss of heterozygosity of 3p markers in neuroblastoma tumours implicate a tumoursuppressor locus distal to the FHIT gene. Br J Cancer, 77, 1787-91.
-
(1998)
Br J Cancer
, vol.77
, pp. 1787-1791
-
-
Ejeskar, K.1
Aburatani, H.2
Abrahamsson, J.3
-
11
-
-
0025056930
-
Identification of a chromosome 18q gene that is altered in colorectal cancers
-
Fearon ER, Cho KR, Nigro JM, et al (1990). Identification of a chromosome 18q gene that is altered in colorectal cancers. Sci, 247, 49-56.
-
(1990)
Sci
, vol.247
, pp. 49-56
-
-
Fearon, E.R.1
Cho, K.R.2
Nigro, J.M.3
-
12
-
-
0026769255
-
Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas
-
Fong CT, White PS, Peterson K, et al (1992). Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas. Cancer Res, 52, 1780-5.
-
(1992)
Cancer Res
, vol.52
, pp. 1780-1785
-
-
Fong, C.T.1
White, P.S.2
Peterson, K.3
-
13
-
-
0024448398
-
Coincidence in Fragile Site Expression with Fluorodeoxyuridine and Bromodeoxyuridine
-
Fundia AF, Larripa IB, (1989). Coincidence in Fragile Site Expression with Fluorodeoxyuridine and Bromodeoxyuridine. Cancer Genet Cytogenet, 41, 41-8.
-
(1989)
Cancer Genet Cytogenet
, vol.41
, pp. 41-48
-
-
Fundia, A.F.1
Larripa, I.B.2
-
14
-
-
0020314732
-
Abnormalities of chromosome 1p in neuroblastoma tumours and cell lines
-
Gilbert F, Balaban G, Moorhead P, et al (1982). Abnormalities of chromosome 1p in neuroblastoma tumours and cell lines. Cancer Genet Cytogenet, 7, 33-42.
-
(1982)
Cancer Genet Cytogenet
, vol.7
, pp. 33-42
-
-
Gilbert, F.1
Balaban, G.2
Moorhead, P.3
-
15
-
-
44349185433
-
Array comparative genomic hybridization analysis of olfactory neuroblastoma
-
Guled M, Myllykangas S, Frierson HF Jr, et al (2008). Array comparative genomic hybridization analysis of olfactory neuroblastoma. Mod Pathol, 21, 770-8.
-
(2008)
Mod Pathol
, vol.21
, pp. 770-778
-
-
Guled, M.1
Myllykangas, S.2
Frierson Jr., H.F.3
-
16
-
-
0033517349
-
Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas
-
Guo C, White PS, Weiss MJ, et al (1999). Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas. Oncogene, 18, 4948-57.
-
(1999)
Oncogene
, vol.18
, pp. 4948-4957
-
-
Guo, C.1
White, P.S.2
Weiss, M.J.3
-
17
-
-
0030593038
-
-
Wash. DC
-
Hahn SA, Schutte M, Hoque AT, et al (1996). DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1. Science (Wash. DC), 271, 350-3.
-
(1996)
DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1. Science
, vol.271
, pp. 350-353
-
-
Hahn, S.A.1
Schutte, M.2
Hoque, A.T.3
-
18
-
-
0344936702
-
Cytogenetic findings in thirty lung carcinoma patients
-
Karaüzüm SB, Lüleci G, özbilim G, et al (1998). Cytogenetic findings in thirty lung carcinoma patients. Cancer Genet Cytogenet, 100, 114-23.
-
(1998)
Cancer Genet Cytogenet
, vol.100
, pp. 114-123
-
-
Karaüzüm, S.B.1
Lüleci, G.2
Özbilim, G.3
-
19
-
-
0021047844
-
Transposition and amplification of oncogene-related sequences in human neuroblastomas
-
Kohl NE, Kanda N, Schreck RR, et al (1983). Transposition and amplification of oncogene-related sequences in human neuroblastomas. Cell, 35, 359-67.
-
(1983)
Cell
, vol.35
, pp. 359-367
-
-
Kohl, N.E.1
Kanda, N.2
Schreck, R.R.3
-
20
-
-
40249110396
-
Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis
-
Krona C, Caren H, Sjöberg RM, et al (2008). Analysis of neuroblastoma tumour progression; loss of PHOX2B on 4p13 and 17q gain are early events in neuroblastoma tumourigenesis. Int J of Oncol, 32, 575-83.
-
(2008)
Int J of Oncol
, vol.32
, pp. 575-583
-
-
Krona, C.1
Caren, H.2
Sjöberg, R.M.3
-
21
-
-
0033034390
-
Molecular biology of neuroblastoma
-
Maris JM, Matthay KK, (1999). Molecular biology of neuroblastoma. J Clin Oncol, 17, 2264-79.
-
(1999)
J Clin Oncol
, vol.17
, pp. 2264-2279
-
-
Maris, J.M.1
Matthay, K.K.2
-
22
-
-
0030839811
-
Loss of heterozygosity at chromosome 9p21 in primary neuroblastomas: evidence for two deleted regions
-
Marshall B, Isidro G, Martins AG, Boavida MG (1997). Loss of heterozygosity at chromosome 9p21 in primary neuroblastomas: evidence for two deleted regions. Cancer Genet Cytogenet, 96, 134-9.
-
(1997)
Cancer Genet Cytogenet
, vol.96
, pp. 134-139
-
-
Marshall, B.1
Isidro, G.2
Martins, A.G.3
Boavida, M.G.4
-
23
-
-
0026352160
-
The 1991 catalog of mapped genes and report of the nomenclature committee, human gene mapping 11
-
McAlpine PJ, Shows TB, Boucheli C, Huebner M, Anderson WA (1991). The 1991 catalog of mapped genes and report of the nomenclature committee, human gene mapping 11. Cytogenet Cell Genet, 58, 5-102.
-
(1991)
Cytogenet Cell Genet
, vol.58
, pp. 5-102
-
-
McAlpine, P.J.1
Shows, T.B.2
Boucheli, C.3
Huebner, M.4
Anderson, W.A.5
-
24
-
-
38149108611
-
ISCN: An international system for humn cytogenetics nomenclature
-
Mitelman F (ed.), Skarger, (1995). ISCN: An international system for humn cytogenetics nomenclature. Basel.
-
(1995)
Basel.
-
-
Mitelman, F.S.1
-
25
-
-
0034907626
-
Loss of heterozygosity at 19q13.3 is associated with locally aggressive neuroblastoma.
-
Mora J, Cheung NK, Chen L, et al (2001). Loss of heterozygosity at 19q13.3 is associated with locally aggressive neuroblastoma. Clin Cancer Res, 7, 1358-61.
-
(2001)
Clin Cancer Res
, vol.7
, pp. 1358-1361
-
-
Mora, J.1
Cheung, N.K.2
Chen, L.3
-
26
-
-
0030754254
-
Aneusomy of chromosome 18 is associated with the development of colorectal carcinoma
-
Nanashima A, Tagawa Y, Yasutake T, et al (1997). Aneusomy of chromosome 18 is associated with the development of colorectal carcinoma. J Gastroenterology, 32, 487-91.
-
(1997)
J Gastroenterology
, vol.32
, pp. 487-491
-
-
Nanashima, A.1
Tagawa, Y.2
Yasutake, T.3
-
27
-
-
57849107571
-
Stabilization of N-Myc is a critical function of aurora a in human neuroblastoma
-
Otto T, Horn S, Brockmann M, et al (2009). Stabilization of N-Myc is a critical function of aurora a in human neuroblastoma. Cancer Cell, 15, 67-78.
-
(2009)
Cancer Cell
, vol.15
, pp. 67-78
-
-
Otto, T.1
Horn, S.2
Brockmann, M.3
-
28
-
-
0028948713
-
Chromosome analysis of 97 primary carcinomas of the breast: Identification of eight karyotypic subgroups
-
Pandis N, Jin Y, Gorunova L, et al (1995). Chromosome analysis of 97 primary carcinomas of the breast: Identification of eight karyotypic subgroups. Genes Chrom Cancer, 12, 173-85.
-
(1995)
Genes Chrom Cancer
, vol.12
, pp. 173-185
-
-
Pandis, N.1
Jin, Y.2
Gorunova, L.3
-
29
-
-
0025833886
-
Cytogenetic analysis of primary neuroblastoma with del(1), del(14), hsr, and dmin chromosomes
-
Petkovic I, Cepulic M (1991). Cytogenetic analysis of primary neuroblastoma with del(1), del(14), hsr, and dmin chromosomes. Cancer Genet Cytogenet, 55, 231-4.
-
(1991)
Cancer Genet Cytogenet
, vol.55
, pp. 231-234
-
-
Petkovic, I.1
Cepulic, M.2
-
30
-
-
0031049728
-
N-myc gene amplification is a major prognostic factor in localized neuroblastoma: results of the French NBL90 study
-
Rubie H, Hartmann O, Michon J, et al (1997). N-myc gene amplification is a major prognostic factor in localized neuroblastoma: results of the French NBL90 study. J Clin Oncol, 15, 1171-82.
-
(1997)
J Clin Oncol
, vol.15
, pp. 1171-1182
-
-
Rubie, H.1
Hartmann, O.2
Michon, J.3
-
31
-
-
0037239718
-
Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4 s neuroblastoma
-
Spitz R, Hero B, Ernestus K, Berthold F, (2003). Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4 s neuroblastoma. Clin Cancer Res, 9, 52-8.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 52-58
-
-
Spitz, R.1
Hero, B.2
Ernestus, K.3
Berthold, F.4
-
32
-
-
9644252853
-
MYCN status in neuroblastoma: characteristics of tumours showing amplification, gain, and non-amplification
-
Spitz R, Hero B, Skowron M, Ernestus K, Berthold F, (2004). MYCN status in neuroblastoma: characteristics of tumours showing amplification, gain, and non-amplification. Eur J Cancer, 40, 2753-9.
-
(2004)
Eur J Cancer
, vol.40
, pp. 2753-2759
-
-
Spitz, R.1
Hero, B.2
Skowron, M.3
Ernestus, K.4
Berthold, F.5
-
33
-
-
0023810844
-
Chromosome 1 abnormalities in cervical carcinoma
-
Sreekantaiah C, Bhargava MK, Shetty NJ, (1988). Chromosome 1 abnormalities in cervical carcinoma. Cancer, 62, 1317-24.
-
(1988)
Cancer
, vol.62
, pp. 1317-1324
-
-
Sreekantaiah, C.1
Bhargava, M.K.2
Shetty, N.J.3
-
34
-
-
79952189457
-
A novel t(4;22) (q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor
-
Sumegi J, Nishio J, Nelson M, et al (2011). A novel t(4;22) (q31;q12) produces an EWSR1-SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor. Mod Pathol, 24, 333-42.
-
(2011)
Mod Pathol
, vol.24
, pp. 333-342
-
-
Sumegi, J.1
Nishio, J.2
Nelson, M.3
-
35
-
-
0024581779
-
Frequent loss of heterozygosity on chromosome 14q in neuroblastoma
-
Suzuki T, Yokota J, Mugishima H, et al (1989). Frequent loss of heterozygosity on chromosome 14q in neuroblastoma. Cancer Res, 49, 1095-8.
-
(1989)
Cancer Res
, vol.49
, pp. 1095-1098
-
-
Suzuki, T.1
Yokota, J.2
Mugishima, H.3
-
36
-
-
0035169984
-
Loss of heterozygosity for chromosome 14q in neuroblastoma
-
Thompson PM, Seifried BA, Kyemba SK, et al (2001). Loss of heterozygosity for chromosome 14q in neuroblastoma. Med Pediatr Oncol, 36, 28-31.
-
(2001)
Med Pediatr Oncol
, vol.36
, pp. 28-31
-
-
Thompson, P.M.1
Seifried, B.A.2
Kyemba, S.K.3
-
37
-
-
0033646871
-
Localization of a hereditary neuroblastoma predisposition gene to 16p12- p13
-
Weiss MJ, Guo C, Shusterman S, et al (2000). Localization of a hereditary neuroblastoma predisposition gene to 16p12- p13. Med Pediatr Oncol, 35, 526-30.
-
(2000)
Med Pediatr Oncol
, vol.35
, pp. 526-530
-
-
Weiss, M.J.1
Guo, C.2
Shusterman, S.3
-
38
-
-
78649740699
-
Chromosome 4q31 locus in COPD is also associated with lung cancer
-
Young RP, Whittington CF, Hopkins RJ, et al (2010). Chromosome 4q31 locus in COPD is also associated with lung cancer. Eur Respir J, 36, 1375-82.
-
(2010)
Eur Respir J
, vol.36
, pp. 1375-1382
-
-
Young, R.P.1
Whittington, C.F.2
Hopkins, R.J.3
-
39
-
-
0031714080
-
Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation
-
Zhou H, Kuang J, Zhong L, et al (1998). Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation. Nat Genet, 20, 89-193.
-
(1998)
Nat Genet
, vol.20
, pp. 89-193
-
-
Zhou, H.1
Kuang, J.2
Zhong, L.3
|