scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1041664110 |
P356 | DOI | 10.1038/SJ.BJC.6690638 |
P932 | PMC publication ID | 2363156 |
P698 | PubMed publication ID | 10471057 |
P5875 | ResearchGate publication ID | 12829089 |
P2093 | author name string | Yamaguchi T | |
Nakamura Y | |||
Abe T | |||
Takahashi T | |||
Koyama K | |||
Yamagishi H | |||
Taniguchi H | |||
Inazawa J | |||
Hagiwara A | |||
Sakakura C | |||
P2860 | cites work | Hepatitis C and hepatocellular carcinoma | Q73717368 |
Amplification on double-minute chromosomes and partial-tandem duplication of theMILL gene in leukemic cells of a patient with acute myelogenous leukemia | Q77470736 | ||
The complete coding sequence of arg defines the Abelson subfamily of cytoplasmic tyrosine kinases | Q24292892 | ||
Detection and mapping of amplified DNA sequences in breast cancer by comparative genomic hybridization | Q24564349 | ||
The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localization | Q28114998 | ||
Monoallelically Expressed Gene Related to p53 at 1p36, a Region Frequently Deleted in Neuroblastoma and Other Human Cancers | Q29616471 | ||
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors | Q29618818 | ||
Hepatitis B virus integration in a cyclin A gene in a hepatocellular carcinoma | Q33493133 | ||
Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma | Q33772796 | ||
Detection of replicative intermediates of hepatitis C viral RNA in liver and serum of patients with chronic hepatitis C | Q34200730 | ||
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma | Q34319319 | ||
Cellular and molecular mechanisms of hepatocarcinogenesis | Q35532421 | ||
DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies | Q35765428 | ||
Hepatocellular carcinoma and dietary aflatoxin in Mozambique and Transkei | Q35992152 | ||
Gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization | Q38500639 | ||
Chromosomal translocation and inverted duplication associated with integrated hepatitis B virus in hepatocellular carcinomas | Q40141359 | ||
Tumor suppressor genes, growth factor genes, and oncogenes in hepatitis B virus-associated hepatocellular carcinoma | Q40681068 | ||
Report of a complex karyotype in recurrent metastatic fibrolamellar hepatocellular carcinoma and a review of hepatocellular carcinoma cytogenetics | Q40993259 | ||
Pathogenesis of hepatocellular carcinoma: a review from the viewpoint of molecular analysis | Q41051463 | ||
Integration of hepatitis B virus and alteration of the 1p36 region found in cancerous tissue of primary hepatocellular carcinoma with viral replication evidenced only in noncancerous, cirrhotic tissue | Q41277761 | ||
Alteration of cell cycle-related genes in hepatocarcinogenesis | Q41596787 | ||
Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas | Q41686912 | ||
Expression of ERBB2 in human gastric carcinomas: relationship between p185ERBB2 expression and the gene amplification | Q41710662 | ||
Hepatitis C and hepatitis B in the etiology of hepatocellular carcinoma in the Japanese population | Q42986643 | ||
Incidence of hepatocellular carcinoma in chronic hepatitis B and C: a prospective study of 251 patients | Q43040870 | ||
Rearrangement and enhanced expression of c-myc in hepatocellular carcinoma of hepatitis virus infected woodchucks | Q43470081 | ||
Allelotype study of primary hepatocellular carcinoma | Q43578355 | ||
Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma. | Q44654607 | ||
Chromosome 1 alterations in breast cancer: allelic loss on 1p and 1q is related to lymphogenic metastases and poor prognosis | Q46404137 | ||
Alterations of tumor suppressor genes and allelic losses in human hepatocellular carcinomas in China | Q46681132 | ||
Accumulation of genetic changes during development and progression of hepatocellular carcinoma: Loss of heterozygosity on chromosome arm Ip occurs at an early stage of hepatocarcinogenesis | Q53462750 | ||
Phenotype variants, malignancy, and additional copies of 6p in retinoblastoma | Q53470260 | ||
Allelic loss on chromosomes 4q and 16q in hepatocellular carcinoma: Association with elevated alpha-fetoprotein production | Q57205641 | ||
Comprehensive allelotyping of human hepatocellular carcinoma | Q57981015 | ||
Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization | Q57981016 | ||
Association between HCV and HBV infection in hepatocellular carcinoma and alcoholic liver disease | Q62658393 | ||
p53 gene mutation spectrum in hepatocellular carcinoma | Q67864181 | ||
Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas | Q70801336 | ||
A 3-Mb physical map of the chromosome region 8p21.3-p22, including a 600-kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non-small cell lung cancer | Q71639487 | ||
Recurrent chromosomal abnormalities in hepatocellular carcinoma detected by comparative genomic hybridization | Q71970809 | ||
Molecular biology of gastric cancer | Q72063761 | ||
Allelic loss at chromosome band 8p21.3-p22 is associated with progression of hepatocellular carcinoma | Q72088881 | ||
Frequent genetic alterations at the distal region of chromosome 1p in human hepatocellular carcinomas | Q72685147 | ||
Predictive factors for long term prognosis after partial hepatectomy for patients with hepatocellular carcinoma in Japan. The Liver Cancer Study Group of Japan | Q72789397 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | hepatitis C | Q154869 |
Hepatitis C virus | Q708693 | ||
P304 | page(s) | 2034-2039 | |
P577 | publication date | 1999-08-01 | |
P1433 | published in | British Journal of Cancer | Q326309 |
P1476 | title | Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization | |
P478 | volume | 80 |
Q33941031 | A novel human striated muscle RING zinc finger protein, SMRZ, interacts with SMT3b via its RING domain |
Q45585418 | Allelic loss of chromosome 4q21 approximately 23 associates with hepatitis B virus-related hepatocarcinogenesis and elevated alpha-fetoprotein |
Q57205409 | Allelic loss of chromosome 4q21?23 associates with hepatitis B virus-related hepatocarcinogenesis and elevated alpha-fetoprotein |
Q35870437 | Amplification and overexpression of the EMS 1 oncogene, a possible prognostic marker, in human hepatocellular carcinoma |
Q42984930 | Analysis of DNA copy number aberrations in hepatitis C virus-associated hepatocellular carcinomas by conventional CGH and array CGH. |
Q33336700 | Analysis of chromosomal aberrations in large hepatocellular carcinomas by comparative genomic hybridization |
Q74238775 | Assessment of chromosomal losses and gains in hepatocellular carcinoma |
Q41550872 | CHD1L Is a Marker for Poor Prognosis of Hepatocellular Carcinoma after Surgical Resection. |
Q55066691 | Characterization of human gastric adenocarcinoma cell lines established from peritoneal ascites. |
Q37777019 | Chromosome 1q21 amplification and oncogenes in hepatocellular carcinoma. |
Q36622040 | Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas |
Q34693285 | Compilation of published comparative genomic hybridization studies |
Q78368622 | Comprehensive allelotyping of well-differentiated human hepatocellular carcinoma with semiquantitative determination of chromosomal gain or loss |
Q35491733 | Copy number gain of granulin-epithelin precursor (GEP) at chromosome 17q21 associates with overexpression in human liver cancer. |
Q34606310 | Detection of chromosomal imbalances in hepatocellular carcinoma |
Q38610074 | Difference of polymorphism VEGF-gene rs699947 in Indonesian chronic liver disease population. |
Q54696630 | Discrete breakpoint mapping and shortest region of overlap of chromosome arm 1q gain and 1p loss in human hepatocellular carcinoma detected by semiquantitative microsatellite analysis. |
Q53406747 | Distinct chromosomal abnormality pattern in primary liver cancer of non-B, non-C patients. |
Q54312067 | Expression and prognostic value of ING3 in human primary hepatocellular carcinoma. |
Q74840940 | Genetic alterations in hepatocellular carcinoma and intrahepatic cholangiocarcinoma |
Q40771342 | HBV integrants of hepatocellular carcinoma cell lines contain an active enhancer |
Q39556322 | Hepatitis B and C virus infections as possible risk factor for pancreatic adenocarcinoma |
Q39639979 | Hepatitis C Virus Inhibits DNA Damage Repair through Reactive Oxygen and Nitrogen Species and by Interfering with the ATM-NBS1/Mre11/Rad50 DNA Repair Pathway in Monocytes and Hepatocytes |
Q29615767 | Hepatocellular carcinoma pathogenesis: from genes to environment |
Q34136464 | Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1-24.1. |
Q48343925 | Identification of target genes within an amplicon at 14q12-q13 in esophageal squamous cell carcinoma |
Q24645549 | Loss of HOP tumour suppressor expression in head and neck squamous cell carcinoma |
Q54630974 | MYH Y165C and G382D mutations in hepatocellular carcinoma and cholangiocarcinoma patients. |
Q35800003 | Malignant and benign ganglioglioma: a pathological and molecular study |
Q37295572 | Methylation-regulated miR-124-1 suppresses tumorigenesis in hepatocellular carcinoma by targeting CASC3. |
Q78357688 | Molecular pathogenesis of human hepatocellular carcinoma |
Q30054218 | NECC1, a candidate choriocarcinoma suppressor gene that encodes a homeodomain consensus motif☆☆Sequence data from this article have been deposited with the DDBJ/EMBL/GenBank Data Libraries under Accession No. AB059410 |
Q28212534 | PTK2 and EIF3S3 genes may be amplification targets at 8q23-q24 and are associated with large hepatocellular carcinomas |
Q34162207 | Pathogenesis of hepatocellular carcinoma |
Q43569197 | Pattern of chromosomal imbalances in non-B virus related hepatocellular carcinoma detected by comparative genomic hybridization |
Q37175500 | Predominant modifier of extreme liver cancer susceptibility in C57BR/cdJ female mice localized to 6 Mb on chromosome 17. |
Q34083417 | Presence of CHD1L over-expression is associated with aggressive tumor biology and is a novel prognostic biomarker for patient survival in human breast cancer |
Q41621586 | Recurrent genetic alterations in hepatitis C-associated hepatocellular carcinoma detected by genomic microarray: a genetic, clinical and pathological correlation study |
Q35543614 | Rising incidence of hepatocellular carcinoma: the role of hepatitis B and C; the impact on transplantation and outcomes |
Q38998210 | Rsf-1 overexpression serves as a prognostic marker in human hepatocellular carcinoma |
Q92478385 | SH3BGRL2 inhibits growth and metastasis in clear cell renal cell carcinoma via activating hippo/TEAD1-Twist1 pathway |
Q27004699 | The homeobox only protein homeobox (HOPX) and colorectal cancer |
Q30165324 | The identification of a novel human homologue of the SH3 binding glutamic acid-rich (SH3BGR) gene establishes a new family of highly conserved small proteins related to Thioredoxin Superfamily |
Q33433774 | Thrombopoietic cytokines in patients with hepatitis C virus-associated immune thrombocytopenia. |
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