Citations for
1TSG8D
Identification of a region of homozygous deletion on 8p22-23.1 in medulloblastoma.
Yin XL, Pang JC, Ng HK.
Oncogene 21(9):1461-8. 2002
2TSG8D
Frequent germline deletion polymorphism of chromosomal region 8p12-p21 identified as a recurrent homozygous deletion in human tumors.
Ryu B, Song J, Sohn T, Hruban RH, Kern SE.
Genomics 72(1):108-12. 2001
3TSG8D
Two putative tumor suppressor genes on chromosome arm 8p may play different roles in prostate cancer.
Oba K, Matsuyama H, Yoshihiro S, Kishi F, Takahashi M, Tsukamoto M, Kinjo M, Sagiyama K, Naito K.
Cancer Genet Cytogenet 124(1):20-6. 2001
4TUSC3, TSG8D
High-resolution physical map and transcript identification of a prostate cancer deletion interval on 8p22.
Arbieva ZH, Banerjee K, Kim SY, Edassery SL, Maniatis VS, Horrigan SK, Westbrook CA.
Genome Res 10(2):244-57. 2000
5TSG8D
Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer.
Sigbjornsdottir BI, Ragnarsson G, Agnarsson BA, Huiping C, Barkardottir RB, Egilsson V, Ingvarsson S.
J Med Genet 37(5):342-7. 2000
6TSG8D
Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma.
Ahmed MN, Kim K, Haddad B, Berchuck A, Qumsiyeh MB.
Cancer Genet Cytogenet 116(1):10-5. 2000
7TSG8D
Allelic loss at the 8p22 region as a prognostic factor in large and estrogen receptor negative breast carcinomas.
Utada Y, Haga S, Kajiwara T, Kasumi F, Sakamoto G, Nakamura Y, Emi M.
Cancer 88(6):1410-6. 2000
8TSG8D
Loss of heterozygosity at chromosome segments 8p22 and 8p11.2-21.1 in transitional-cell carcinoma of the urinary bladder.
Choi C, Kim MH, Juhng SW, Oh BR.
Int J Cancer 86(4):501-5. 2000
9TSG8A, TSG8B, TSG8D
Identification of a homozygous deletion at 8p12-21 in a human prostate cancer xenograft.
Van Alewijk DC, et al.
Genes Chromosomes Cancer 24 : 119-126. 1999
10TSG8A, TSG8D
Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cM interval of 8p22-p23.1.
Yokota T, et al.
Cancer 85(2):447-52. 1999
11TSG8D
Deletion mapping of the tumor suppressor locus involved in colorectal cancer on chromosome band 8p21.
Lerebours F, et al.
Genes Chromosomes Cancer 25(2):147-53. 1999
12TSG3D, TSG3G, TSG4A, TSG4E, TSG5A, ST8, TSG8D, TSG9A, ST3, TSG13A, TSG13D, TSG14C, TSG15B, TSG18C, TSG21C
Novel recurrent genetic imbalances in human hepatocellular carcinoma cell lines identified by comparative genomic hybridization.
Zimonjic DB, et al.
Hepatology 29(4):1208-14. 1999
13TSG8A, TSG8D
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma.
Pineau P, et al.
Oncogene 18(20):3127-34. 1999
14TSG8A, TSG8D
Deletion mapping on the short arm of chromosome 8 in hepatocellular carcinoma.
Piao Z, et al.
Cancer Lett 138(1-2):227-32. 1999
15TSG8D
The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinoma.
Qin LX, Tang ZY, Sham JS, Ma ZC, Ye SL, Zhou XD, Wu ZQ, Trent JM, Guan XY.
Cancer Res 59(22):5662-5. 1999
16EXTL3, TSG8D
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.
Van Hul W, Wuyts W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Bossuyt P, Willems PJ.
Genomics 47(2):230-7. 1998
17TSG8D
Chromosome region 8p11-p21 : refined mapping and molecular alterations in breast cancer.
AdŽla•de J, et al.
Genes Chromosomes Cancer 22 : 186-199. 1998
18DLC1, TSG8D
Cloning, characterization, and chromosomal localization of a gene frequently deleted in human liver cancer (DLC-1) homologous to Rat RhoGAP.
Yuan BZ, et al.
Cancer Res 58 : 2196-2199. 1998
19TSG8D, TSG17A, VHL
Intratumoral heterogeneity of von Hippel-Lindau gene deletions in renal cell carcinoma detected by fluorescence in situ hybridization.
Moch H, Schraml P, Bubendorf L, Richter J, Gasser TC, Mihatsch MJ, Sauter G.
Cancer Res 58 : 2304-2309. 1998
20TSG8A, TSG8D
Frequent loss of heterozygosity and three critical regions on the short arm of chromosome 8 in ovarian adenocarcinomas.
Wright K, et al.
Oncogene 17 : 1185-1188. 1998
21TNFRSF10B, TSG8D
Genomic organization and mutation analyses of the DR5/TRAIL receptor 2 gene in colorectal carcinomas.
Arai T, et al.
Cancer Lett 133(2):197-204. 1998
22TSG8A, TSG8D
Deletion mapping defines three discrete areas of allelic imbalance on chromosome arm 8p in oral and oropharyngeal squamous cell carcinomas.
Wu CL, Roz L, Sloan P, Read AP, Holland S, Porter S, Scully C, Speight PM, Thakker N.
Genes Chromosomes Cancer 20(4):347-53. 1997
23TSG8D
Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis.
Seitz S, Rohde K, Bender E, Nothnagel A, Pidde H, Ullrich OM, El-Zehairy A, Haensch W, Jandrig B, Kolble K, Schlag PM, Scherneck S.
Br J Cancer 76(8):983-91. 1997