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TypeTitleAuthor(s)YearViews
Characterization of a complex chromosome rearrangement involving 6q in a melanoma cell line by chromosome microdissectionGuan, XY; Zhang, HE; Zhou, H; Sham, JST; Fung, JMW; Trent, JM200269
 
Chromosome microdissection for detection of subchromosomal alterations by FISHGuan, XY; Trent, JM2001181
 
Recurrent chromosome changes in 62 primary gastric carcinomas detected by comparative genomic hybridizationGuan, XY; Fu, SB; Xia, JC; Fang, Y; Sham, JST; Du, BD; Zhou, H; Lu, S; Wang, BQ; Lin, YZ; Liang, Q; Li, XM; Du, B; Ning, XM; Du, JR; Li, P; Trent, JM2000143
 
Analysis of genetic alterations in primary nasopharyngeal carcinoma by comparative genomic hybridization (CGH)Sun, L; Fang, Y; Sham, JST; Guo, Y; Deng, M; Liang, Q; Zhang, H; Zhou, H; Tideman, H; Trent, JM; Guan, XY2000144
 
Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative hybridizationGuan, XY; Fang, Y; Sham, JST; Kwong, DLW; Zhang, Y; Liang, Q; Li, H; Zhou, H; Trent, JM2000111
 
Analysis of genetic alterations in primary nasopharyngeal carcinoma by comparative genomic hybridization (CGH)Sun, L; Fong, Y; Sham, JST; Guo, Y; Deng, M; Liang, Q; Zhang, H; Zhou, H; Tideman, H; Trent, JM; Guan, XY2000220
 
Characterization of a complex chromosome rearrangement involving 6q in a melanoma cell line: isolation of a candidate tumor suppressor gene interrupted by the breakpoint at 6q16Guan, XY; Zhou, H; Sham, JST; Zhang, H; Trent, JM2000196
 
A nuclear factor, ASC-2, as a cancer-amplified transcriptional coactivator essential for ligand-dependent transactivation by nuclear receptors in vivoLee, SK; Anzick, SL; Choi, JE; Bubendorf, L; Guan, XY; Jung, YK; Kallioniemi, OP; Kononen, J; Trent, JM; Azorsa, D; Jhun, BH; Cheong, JH; Lee, YC; Meltzer, PS; Lee, JW1999121
 
The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinomaQin, LX; Tang, ZY; Sham, JST; Ma, ZC; Ye, SL; Zhou, XD; Wu, ZQ; Trent, JM; Guan, XY199980
 
The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinomaGuan, XY; Qin, LX; Tang, ZY; Sham, JST; Ma, ZC; Ye, SL; Zhou, XD; Wu, ZQ; Trent, JM1999170
 
Identification of a ring chromosome in a myxoid malignant fibrous histiocytoma with chromosome microdissection and fluorescence in situ hybridizationMeloniEhrig, AM; Chen, Z; Guan, XY; Notohamiprodjo, M; Shepard, RR; Spanier, SS; Trent, JM; Sandberg, AA199971
 
Gain of 9p in the pathogenesis of polycythemia veraChen, Z; Notohamiprodjo, M; Guan, XY; Paietta, E; Blackwell, S; Stout, K; Turner, A; Richkind, K; Trent, JM; Lamb, A; Sandberg, AA1998104
 
Detection of chromosome 6 abnormalities in melanoma cell lines by chromosome arm painting probesGuan, XY; Zhang, H; Yang, JM; Wang, J; Taetle, R; Meltzer, PS; Trent, JM1998101
 
Chromosome 22q11.2 Interstitial deletions among childhood-onset schizophrenics and 'multidimensionally impaired'Yan, W; Jacobsen, LK; Krasnewich, DM; Guan, XY; Lenane, MC; Paul, SP; Dalwadi, HN; Zhang, H; Long, RT; Kumra, S; Martin, BM; Scambler, PJ; Trent, JM; Sidransky, E; Ginns, EI; Rapoport, JL199893
 
AIB1, a steroid receptor coactivator amplified in breast and ovarian cancerAnzick, SL; Kononen, J; Walker, RL; Azorsa, DO; Tanner, MM; Guan, XY; Sauter, G; Kallioniemi, OP; Trent, JM; Meltzer, PS1997158
 
Increased chromosome 20 copy number detected by fluorescence in situ hybridization (FISH) in malignant melanomaBarks, JH; Thompson, FH; Taetle, R; Yang, JM; Stone, JF; Wymer, JA; Khavari, R; Guan, XY; Trent, JM; Pinkel, D; Nelson, MA1997109
 
Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: Cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissectionChen, Z; Grebe, TA; Guan, XY; Notohamiprodjo, M; Nutting, PJ; Stone, JF; Trent, JM; Sandberg, AA1997120
 
Identification of region specific genes by chromosome microdissectionMeltzer, PS; Guan, XY; Su, YA; Gracia, E; Trent, JM199774
 
Localization by chromosome microdissection of a recurrent breakpoint region on chromosome 6 in human B-cell lymphomaGuan, XY; Horsman, D; Zhang, HE; Parsa, NZ; Meltzer, PS; Trent, JM199698
 
Isolation of a cosmid sublibrary for a region of chromosome 12 frequently amplified in human cancers using a complex chromosome microdissection probeElkahloun, AG; Meltzer, PS; Guan, XY; Mcninch, JS; Trent, JM; De Jong, PJ1996100
 
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