Citations for
1NBL, TSG11I, TSG1A
Chromosome 1p and 11q deletions and outcome in neuroblastoma.
Attiyeh EF, London WB, Mosse YP, Wang Q, Winter C, Khazi D, McGrady PW, Seeger RC, Look AT, Shimada H, Brodeur GM, Cohn SL, Matthay KK, Maris JM; Children's Oncology Group.
N Engl J Med 353(21):2243-53. 2005
2TSG1A, TSG1C, TSG1G, TSG19A
Clinical, histological, and immunohistochemical features predicting 1p/19q loss of heterozygosity in oligodendroglial tumors.
Kim SH, Kim H, Kim TS.
Acta Neuropathol (Berl) 110(1):27-38. Epub 2005 May 26. 2005
3TSG1A
Genomic annotation of the meningioma tumor suppressor locus on chromosome 1p34.
Sulman EP, White PS, Brodeur GM.
Oncogene 23(4):1014-20. 2004
4TSG1A
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis.
Riva P, Crosti F, Orzan F, Dalpra L, Mortini P, Parafioriti A, Pollo B, Fuhrman Conti AM, Miozzo M, Larizza L.
Int J Cancer 107(3):493-7. 2003
5TSG1A
Frequent allelic losses on the short arm of chromosome 1 and decreased expression of the p73 gene at 1p36.3 in squamous cell carcinoma of the oral cavity.
Araki D, Uzawa K, Watanabe T, Shiiba M, Miyakawa A, Yokoe H, Tanzawa H.
Int J Oncol 20(2):355-60. 2002
6TSG1A
Distinction in gene expression profiles of oligodendrogliomas with and without allelic loss of 1p.
Mukasa A, Ueki K, Matsumoto S, Tsutsumi S, Nishikawa R, Fujimaki T, Asai A, Kirino T, Aburatani H.
Oncogene 21(25):3961-8. 2002
7TSG10B, TSG12C, TSG13D, TSG14C, CRAC1, TSG16H, TSG19A, TSG1A
Detection of three novel translocations and specific common chromosomal break sites in malignant melanoma by spectral karyotyping.
Sargent LM, Nelson MA, Lowry DT, Senft JR, Jefferson AM, Ariza ME, Reynolds SH.
Genes Chromosomes Cancer 32(1):18-25. 2001
8TSG1A
Homozygous deletion in a neuroblastoma cell line defined by a high-density STS map spanning human chromosome band 1p36.
Chen YZ, Soeda E, Yang HW, Takita J, Chai L, Horii A, Inazawa J, Ohki M, Hayashi Y.
Genes Chromosomes Cancer 31(4):326-32. 2001
9TSG1A, TSG1C, TSG1G
Chromosome bands 1p35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted.
Caron H, Spieker N, Godfried M, Veenstra M, van Sluis P, de Kraker J, Voute P, Versteeg R.
Genes Chromosomes Cancer 30(2):168-74. 2001
10ST3, TSG14B, TSG1A, DLEC1
Analysis of genetic alterations in primary nasopharyngeal carcinoma by comparative genomic hybridization.
Fang Y, Guan X, Guo Y, Sham J, Deng M, Liang Q, Li H, Zhang H, Zhou H, Trent J.
Genes Chromosomes Cancer 30(3):254-60. 2001
11RAD54L, TSG1A
hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas.
Bello MJ, de Campos JM, Vaquero J, Ruiz-Barnes P, Kusak ME, Sarasa JL, Rey JA.
Cancer Genet Cytogenet 116(2):142-7. 2000
12TSG1A
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36.
Miozzo M, Dalpra L, Riva P, Volonta M, Macciardi F, Pericotti S, Tibiletti MG, Cerati M, Rohde K, Larizza L, Fuhrman Conti AM.
Int J Cancer 87(1):68-72. 2000
13TSG1A, TSG19A, TSG22D
Chromosomal aberrations detected by comparative genomic hybridization (CGH) in human astrocytic tumors.
Maruno M, et al.
Cancer Lett 135(1):61-6. 1999
14TSG19A,TSG1A
Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype.
Smith JS, et al.
Oncogene 18(28):4144-52 1999
15TSG1A, TSG1F, TSG1J
Allelic loss on chromosome 1 is associated with tumor progression of cervical carcinoma.
Cheung TH, Chung TK, Poon CS, Hampton GM, Wang VW, Wong YF.
Cancer 86(7):1294-8 1999
16TP73, TSG1A
Search for mutations and examination of allelic expression imbalance of the p73 gene at 1p36.33 in human lung cancers.
Nomoto S, et al.
Cancer Res 58 : 1380-1383. 1998
17TSG1A
Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
Van Gele M, et al.
Genes Chromosomes Cancer 23 : 67-71. 1998
18TSG1A, TSG1J
Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome.
Iolascon A, et al.
Cancer Lett 130 : 83-92. 1998
19TSG1A, TSG1B
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma.
Caron H, et al.
N Engl J Med 334 : 225-230. 1996
20TNFRSF1B, TSG1A
Physical mapping and genomic structure of the human TNFR2 gene.
Beltinger CP, et al.
Genomics 35 : 94-100. 1996
21TSG1A, TSG1C, TSG1K
Molecular and genetic studies on the region of translocation and duplication in the neuroblastoma cell line NGP at the 1p36.13-p36.32 chromosomal site.
Casciano I, et al.
Oncogene 12 : 2101-2108. 1996
22TSG1A, TSG1C
Familial predisposition to neuroblastoma does not map to chromosome band 1p36.
Maris JM, et al.
Cancer Res 56 : 3421-3425. 1996
23CDK11A, CDK11B, NBL, TSG1A, TSG1C
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.
White PS, et al.
Proc Natl Acad Sci U S A 92 : 5520-5524. 1995
24TSG1A
Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double-target fluorescence in situ hybridization and microsatellite analysis.
Hashimoto N, et al.
Genes Chromosomes Cancer 14 : 295-300. 1995
25TSG1A, TSG1C
The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma.
Gehring M, et al.
Cancer Res 55 : 5366-5369. 1995
26TSG1A
Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms.
Martinsson T, et al.
Cancer Res 55 : 5681-5686. 1995
27TSG1A, TSG1C
Significance of chromosome 1p loss of heterozygosity in neuroblastoma.
Maris JM, et al.
Cancer Res 55 : 4664-4669. 1995
28TSG1A, TSG10A, TSG14B
Allelic losses on chromosome 14, 10 and 1 in atypical and malignant meningiomas : a genetic model of meningioma progression.
Simon M, et al.
Cancer Res 55 : 4696-4701. 1995
29TSG1A, TSG19A
Shared allelic losses on chromosomes 1p and 19q suggest a common origin of oligodendroglioma and oligoastrocytoma.
Kraus JA, et al.
J Neuropathol Exp Neurol 54 : 91-95. 1995
30TSG1A, TSG1C, NBL
Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma : one probably imprinted, another associated with N-myc amplification.
Caron H, et al.
Hum Mol Genet 4 : 535-539. 1995
31TSG1A, TSG1B, TSG1H, TSG1J
Detection and cloning of a common region of loss of heterozygosity at chromosome 1p in breast cancer.
Nagai H, et al.
Cancer Res 55 : 1752-1757. 1995
32TSG1A, NBL, TSG1C
Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.
Cheng NC, et al.
Oncogene 10 : 291-297. 1995
33TSG1A
Deletion of chromosome arm Ip in a Merkel cell carcinoma (MCC).
Gibas Z, et al.
Genes Chromosomes Cancer 9 : 216-220. 1994
34TSG1A, TSG22A
Allelic loss at Ip is associated with tumor progression of meningiomas.
Bello MJ, et al.
Genes Chromosomes Cancer 9 : 296-298. 1994
35TSG1A, TSG1C
There may be two tumor suppressor genes on chromosome arm Ip closely associated with biologically distinct subtypes of neuroblastoma.
Takeda O, et al.
Genes Chromosomes Cancer 10 : 30-39. 1994
36MGCR, TSG1A
Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression.
Lindblom A, et al.
Int J Cancer 56 : 354-357. 1994
37TSG1A, NBL
Two distinct deleted regions on the short arm of chromosome I in neuroblastoma.
Schleiermacher G, et al.
Genes Chromosomes Cancer 10 : 275-281. 1994
38TSG1A
Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells.
Savelyeva L, et al.
Am J Hum Genet 55 : 334-340. 1994
39TSG1A
Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.
Caron H, et al.
Am J Hum Genet 55 : 341-347. 1994
40TSG1A
Molecular analysis of chromosome 1 abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors.
Bello MJ, et al.
Int J Cancer 57 : 172-175. 1994
41NBL, TSG1A
Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells.
Barker PE, et al.
Oncogene 8 : 3353-3358. 1993
42NBL, TSG1A
Constitutional 1p36 deletion in a child with neuroblastoma.
Biegel JA, et al.
Am J Hum Genet 52 : 176-182. 1993
43TSG1A
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.
Caron H, et al.
Nat Genet 4 : 187-190. 1993
44TSG1A, TSG14B
Deletion mapping of chromosomes 14q and 1p in human neuroblastoma.
Takayama H, et al.
Oncogene 7 : 1185-1189. 1992
45TSG1A
Analysis of chromosome band 1p36 alterations by chromosomal in situ suppression hybridization with a microclone DNA bank.
Zink D, et al.
Genes Chromosomes Cancer 3 : 407-410. 1991
46TSG1A, TSG1C
Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood.
Devilee P, et al.
Int J Cancer 47 : 817-821. 1991
47TSG1A
Loss of allelic heterozygosity on distal chromosome 1p in merkel cell carcinoma.
Harnett PR, et al.
Cancer Genet Cytogenet 54 : 109-113. 1991
48TSG1A, D1S7, D1S47, D1S94, D1S95, D1S96, D1S97, D1S98
Neuroblastoma consensus deletion maps to 1p36.1-2.
Weith A, et al.
Genes Chromosomes Cancer 1 : 159-166. 1989
49TSG1A
Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas : correlation with N-myc amplification.
Fong C, et al.
Proc Natl Acad Sci U S A 86 : 3753-3757. 1989