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Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.
Proc Natl Acad Sci U S A. 1989 Nov;86(22):8852-6
PMID: 2573067
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Hepatitis C virus infection is associated with the development of hepatocellular carcinoma.
Proc Natl Acad Sci U S A. 1990 Sep;87(17):6547-9
PMID: 2168552
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Mutations in the p53 gene occur in diverse human tumour types.
Nature. 1989 Dec 7;342(6250):705-8
PMID: 2531845
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Identification of a chromosome 18q gene that is altered in colorectal cancers.
Science. 1990 Jan 5;247(4938):49-56
PMID: 2294591
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Detection of antibody against antigen expressed by molecularly cloned hepatitis C virus cDNA: application to diagnosis and blood screening for posttransfusion hepatitis.
Proc Natl Acad Sci U S A. 1990 Feb;87(3):983-7
PMID: 2105505
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Partial deletion of the long arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: a new association.
Blood. 1983 May;61(5):994-8
PMID: 6831056
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Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association.
N Engl J Med. 1983 Sep 15;309(11):630-6
PMID: 6577285
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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma.
Nature. 1983 Oct 27-Nov 2;305(5937):779-84
PMID: 6633649
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Duplication within the haptoglobin Hp2 gene.
Nature. 1984 May 10-16;309(5964):131-5
PMID: 6325933
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Isolation and sequence of a rat chymotrypsin B gene.
J Biol Chem. 1984 Nov 25;259(22):14265-70
PMID: 6209274
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Complete nucleotide sequence of hepatitis B virus DNA of subtype adr and its conserved gene organization.
Gene. 1984 Oct;30(1-3):227-32
PMID: 6510717
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Cloning the complete human adenine phosphoribosyl transferase gene.
Gene. 1984 Nov;31(1-3):233-40
PMID: 6241170
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Detection of a restriction site polymorphism within the human alpha-globin gene complex.
Hum Genet. 1985;69(2):144-6
PMID: 2982725
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Hereditary cancer, oncogenes, and antioncogenes.
Cancer Res. 1985 Apr;45(4):1437-43
PMID: 2983882
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The hepatitis B virus.
Nature. 1985 Oct 10-16;317(6037):489-95
PMID: 2995835
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Deletion in chromosome 11p associated with a hepatitis B integration site in hepatocellular carcinoma.
Science. 1985 Oct 18;230(4723):319-22
PMID: 2996131
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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma.
Nature. 1986 Oct 16-22;323(6089):643-6
PMID: 2877398
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A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library.
Hum Genet. 1986 Dec;74(4):425-31
PMID: 2878870
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A 5' flanking region of the metallothionein, MT2A, gene identifies two moderately frequent RFLPs.
Nucleic Acids Res. 1987 Feb 11;15(3):1350
PMID: 2881275
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Relationship of histologic grade of hepatocellular carcinoma (HCC) to tumor size, and demonstration of tumor cells of multiple different grades in single small HCC.
Liver. 1987 Feb;7(1):18-26
PMID: 3033422
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Multiple RFLPs at the human cholesteryl ester transfer protein (CETP) locus.
Nucleic Acids Res. 1987 Jun 11;15(11):4698
PMID: 2884631
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Pathology of small hepatocellular carcinoma. A proposal for a new gross classification.
Cancer. 1987 Aug 15;60(4):810-9
PMID: 2439190
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Localization of the gene for familial adenomatous polyposis on chromosome 5.
Nature. 1987 Aug 13-19;328(6131):614-6
PMID: 3039373
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Chromosome 5 allele loss in human colorectal carcinomas.
Nature. 1987 Aug 13-19;328(6131):616-9
PMID: 2886919
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Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.
Hum Genet. 1987 Oct;77(2):95-103
PMID: 2888723
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Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer.
Nature. 1987 Oct 1-7;329(6138):451-4
PMID: 2821400
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Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping.
Nature. 1987 Oct 15-21;329(6140):645-7
PMID: 3657988
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Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia.
Science. 1987 Oct 9;238(4824):185-8
PMID: 3659909
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The gene for familial polyposis coli maps to the long arm of chromosome 5.
Science. 1987 Dec 4;238(4832):1411-3
PMID: 3479843
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Rearrangement of a common cellular DNA domain on chromosome 4 in human primary liver tumors.
J Virol. 1988 Feb;62(2):629-32
PMID: 2826820
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Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung.
Proc Natl Acad Sci U S A. 1987 Dec;84(24):9252-6
PMID: 2892196
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Tyrosine aminotransferase and chymotrypsinogen B are linked to haptoglobin on human chromosome 16q: comparison of genetic and physical distances.
Genomics. 1987 Dec;1(4):313-9
PMID: 2896626
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Inactivation of the retinoblastoma susceptibility gene in human breast cancers.
Science. 1988 Jul 8;241(4862):218-21
PMID: 3388033
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Abnormalities in structure and expression of the human retinoblastoma gene in SCLC.
Science. 1988 Jul 15;241(4863):353-7
PMID: 2838909
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The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.
Hum Genet. 1988 Jul;79(3):260-4
PMID: 2456982
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Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16.
Hum Genet. 1988 Jul;79(3):277-9
PMID: 2900214
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Genetic alterations during colorectal-tumor development.
N Engl J Med. 1988 Sep 1;319(9):525-32
PMID: 2841597
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Clonal origin of atypical adenomatous hyperplasia of the liver and clonal identity with hepatocellular carcinoma.
Gastroenterology. 1988 Dec;95(6):1664-6
PMID: 2846405
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Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas.
Cytogenet Cell Genet. 1988;48(2):72-8
PMID: 2904349
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Suppression of the neoplastic phenotype by replacement of the RB gene in human cancer cells.
Science. 1988 Dec 16;242(4885):1563-6
PMID: 3201247
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Report of the committee on human gene mapping by recombinant DNA techniques.
Cytogenet Cell Genet. 1987;46(1-4):390-566
PMID: 3507285
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Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.
Science. 1989 Apr 14;244(4901):217-21
PMID: 2649981
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An assay for circulating antibodies to a major etiologic virus of human non-A, non-B hepatitis.
Science. 1989 Apr 21;244(4902):362-4
PMID: 2496467
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A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q.
Nucleic Acids Res. 1989 Apr 25;17(8):3331
PMID: 2566972
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Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.
Proc Natl Acad Sci U S A. 1989 May;86(10):3753-7
PMID: 2566996
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Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix.
Cancer Res. 1989 Jul 1;49(13):3598-601
PMID: 2567206
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Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.
Proc Natl Acad Sci U S A. 1989 Jun;86(12):4614-8
PMID: 2734311
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A TaqI RFLP detected by the probe VK45C6 [D16S131] at 16p13.11.
Nucleic Acids Res. 1989 Aug 11;17(15):6430
PMID: 2570409
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Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16.
Cytogenet Cell Genet. 1989;50(2-3):145-8
PMID: 2789125
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Report of the committee on the genetic constitution of chromosome 16.
Cytogenet Cell Genet. 1989;51(1-4):299-318
PMID: 2676374
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Frequent loss of heterozygosity on chromosomes 16 and 4 in human hepatocellular carcinoma.
Jpn J Cancer Res. 1990 Feb;81(2):108-11
PMID: 1970554
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p53: a frequent target for genetic abnormalities in lung cancer.
Science. 1989 Oct 27;246(4929):491-4
PMID: 2554494