| P2093 | author name string | Kim YH | |
| | Kim H | |
| | Park C | |
| | Kim NG | |
| | Lim JG | |
| P2860 | cites work | A genetic model for colorectal tumorigenesis | Q27860582 |
| | A comprehensive genetic map of the human genome based on 5,264 microsatellites | Q27860812 |
| | A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer | Q28289377 |
| | The sequential accumulation of genetic alterations characteristic of the colorectal adenoma-carcinoma sequence does not occur between gastric adenoma and adenocarcinoma | Q28297428 |
| | K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes | Q28609638 |
| | The two histological main types of gastric carcinoma: diffuse and so called intestinal-type carcinoma: an attempt at a histo-clinical classification | Q29618627 |
| | Microsatellite instability in cancer of the proximal colon | Q29620692 |
| | Allelotype of gastric adenocarcinoma. | Q30303889 |
| | Analysis of chromosome 17p13 (p53 locus) alterations in gastric carcinoma cells by dual-color fluorescence in situ hybridization | Q35782454 |
| | Fingerprinting genomes using PCR with arbitrary primers | Q35894620 |
| | Chromosome band 16q24 is frequently deleted in human gastric cancer | Q36617849 |
| | Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization | Q38500639 |
| | Deletion mapping on chromosome 1p in well-differentiated gastric cancer | Q39993827 |
| | Genetic alterations in human gastrointestinal cancers. The application to molecular diagnosis | Q40612363 |
| | Concomitant gastrin and ERBB2 gene amplifications at 17q12-q21 in the intestinal type of gastric cancer | Q40979756 |
| | Gastric cancers of the microsatellite mutator phenotype display characteristic genetic and clinical features | Q41668427 |
| | Commonly deleted region on the long arm of chromosome 7 in differentiated adenocarcinoma of the stomach | Q41812413 |
| | Allelotype analysis of adenocarcinoma of the gastric cardia | Q41931838 |
| | Microsatellite instability: the mutator that mutates the other mutator | Q44602861 |
| | Genetic alterations in primary bladder cancers and their metastases. | Q46740779 |
| | Accumulated frameshift mutations at coding nucleotide repeats during the progression of gastric carcinoma with microsatellite instability. | Q53418727 |
| | Presence of high-level DNA copy number gains in gastric carcinoma and severely dysplastic adenomas but not in moderately dysplastic adenomas. | Q53429214 |
| | Loss of FHIT expression in gastric carcinoma. | Q53429801 |
| | Identification of two distinct regions of deletion at 6q in gastric carcinoma. | Q53461477 |
| | Occurrence of microsatellite instability in gastric carcinoma is associated with enhanced expression of erbB-2 oncoprotein. | Q53464613 |
| | Allelic deletions of MCC/APC and p53 are frequent late events in human gastric carcinogenesis. | Q53471752 |
| | Frequent loss of heterozygosity on chromosomes 1q, 5q, and 17p in human gastric carcinomas. | Q53498117 |
| | Microsatellite instability in precancerous lesions and adenocarcinomas of the stomach. | Q54590327 |
| | Two distinct regions of deletion on the long arm of chromosome 5 in differentiated adenocarcinomas of the stomach. | Q54594896 |
| | Life (and death) in a malignant tumour | Q59098941 |
| | Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1 | Q59182794 |
| | Genetic alterations of the c-erbB-2 oncogene occur frequently in tubular adenocarcinoma of the stomach and are often accompanied by amplification of the v-erbA homologue | Q68131177 |
| | Loss of heterozygosity and K-ras gene mutations in gastric cancer | Q70497039 |
| | Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach | Q70840026 |
| | Differential p53 protein expression in stomach adenomas of gastric and intestinal phenotypes: possible sequences of p53 alteration in stomach carcinogenesis | Q71420571 |
| | Microsatellite instability-associated mutations associate preferentially with the intestinal type of primary gastric carcinomas in a high-risk population | Q71614110 |
| | Molecular biology of gastric cancer | Q72063761 |
| | Microsatellite alterations in adenoma and differentiated adenocarcinoma of the stomach | Q72187173 |
| | p53 gene mutations in gastric adenomas | Q72215997 |
| | Frequent loss of heterozygosity of the long arm of chromosome 7 is closely associated with progression of human gastric carcinomas | Q72804285 |
| | Allelotype of adenoma and differentiated adenocarcinoma of the stomach | Q73027868 |
| | 17q12-21 amplicon, a novel recurrent genetic change in intestinal type of gastric carcinoma: a comparative genomic hybridization study | Q73683259 |
| | Consistent genetic alterations in xenografts of proximal stomach and gastro-esophageal junction adenocarcinomas | Q74027601 |
| | Mapping of chromosomal imbalances in gastric adenocarcinoma revealed amplified protooncogenes MYCN, MET, WNT2, and ERBB2 | Q77585699 |
| | Fractional allelic loss in gastric carcinoma correlates with growth patterns | Q77640404 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 655-662 | |
| P577 | publication date | 2001-02-01 | |
| P1433 | published in | The American Journal of Pathology | Q4744259 |
| P1476 | title | Chromosomal alterations in paired gastric adenomas and carcinomas | |
| P478 | volume | 158 | |