Published in J Cell Sci on April 01, 1977
Mitochondria-to-nucleus stress signaling induces phenotypic changes, tumor progression and cell invasion. EMBO J (2001) 2.30
Lymphoma development in mice and humans: diversity of initiation is followed by convergent cytogenetic evolution. Proc Natl Acad Sci U S A (1979) 1.90
U1 small nuclear RNA genes are located on human chromosome 1 and are expressed in mouse-human hybrid cells. Mol Cell Biol (1983) 1.76
Homozygous deletions within human chromosome band 9p21 in melanoma. Proc Natl Acad Sci U S A (1992) 1.58
Tumor promoter induces sister chromatid exchanges: relevance to mechanisms of carcinogenesis. Proc Natl Acad Sci U S A (1978) 1.49
Introduction of a human X-6 translocation chromosome into a mouse teratocarcinoma: investigation of control of HLA-A, B, C expression. Proc Natl Acad Sci U S A (1982) 1.33
Melanoma x macrophage hybrids with enhanced metastatic potential. Clin Exp Metastasis (1998) 1.23
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) 1.21
Nonrandom cytogenetic alterations in hepatocellular carcinoma from transgenic mice overexpressing c-Myc and transforming growth factor-alpha in the liver. Am J Pathol (1999) 1.09
Genetic mapping of tumor susceptibility genes involved in mouse plasmacytomagenesis. Proc Natl Acad Sci U S A (1993) 1.07
Tumorigenicity and its suppression in cybrids of mouse and Chinese hamster cell lines. Proc Natl Acad Sci U S A (1978) 1.06
Complete suppression of tumor formation by high levels of basement membrane collagen. Mol Cancer Res (2007) 0.94
Molecular aspects of melanocytic dysplastic nevi. J Mol Diagn (2002) 0.92
Horizontal transmission of malignancy: in-vivo fusion of human lymphomas with hamster stroma produces tumors retaining human genes and lymphoid pathology. PLoS One (2013) 0.87
Cell fusion segregates progressive growth from metastasis. Br J Cancer (1983) 0.83
Tumor suppression by collagen XV is independent of the restin domain. Matrix Biol (2012) 0.82
Surface antigens of immunoprotective leukaemia x fibroblast hybrid cells which have lost malignant properties in histocompatible mice differ from the malignant parental cells. Immunology (1984) 0.81
Low-frequency loss of heterozygosity in Moloney murine leukemia virus-induced tumors in BRAKF1/J mice. J Virol (1997) 0.79
Suppression of malignancy in human cancer cells: issues and challenges. Proc Natl Acad Sci U S A (1981) 0.78
Chromosome 1 in relation to human disease. J Med Genet (1986) 0.77
Recurrent and nonrandom DNA copy number and chromosome alterations in Myc transgenic mouse model for hepatocellular carcinogenesis: implications for human disease. Cancer Genet Cytogenet (2009) 0.77
Differentiation in vitro of human-mouse teratocarcinoma hybrids. Mol Cell Biol (1983) 0.76
Suppression of properties associated with malignancy in murine melanoma-melanocyte hybrid cells. Br J Cancer (1992) 0.75
Growth control variant cell line having increased serum requirement and decreased response to platelet-derived growth factor: reversion by 5-azacytidine. J Cell Biol (1984) 0.75
Expression of microtubule networks in normal cells, transformed cells, and their hybrids. J Cell Biol (1979) 0.75
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2. Cytogenet Cell Genet (1985) 7.70
Characterization of a panel of highly variable minisatellites cloned from human DNA. Ann Hum Genet (1987) 7.58
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee. Genomics (1997) 6.44
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34. Science (1997) 6.10
Enzyme polymorphisms in man. Proc R Soc Lond B Biol Sci (1966) 5.86
A new marker for human cancer cells. 1 The Ca antigen and the Ca1 antibody. Lancet (1982) 5.63
Dynamic molecular combing: stretching the whole human genome for high-resolution studies. Science (1997) 4.86
Estimation of genetic variation at the DNA level from restriction endonuclease data. Proc Natl Acad Sci U S A (1981) 4.71
Human red cell peptidases. Nature (1967) 4.46
Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms. Ann Hum Genet (1972) 4.29
Esterase D: a new human polymorphism. Ann Hum Genet (1973) 3.85
Isolation and characterization of a cDNA encoding a human liver/bone/kidney-type alkaline phosphatase. Proc Natl Acad Sci U S A (1986) 3.62
Further data on the adenosine deaminase (ADA) polymprphism and a report of a new phenotype. Ann Hum Genet (1969) 3.60
Further studies on the genetics of placental alkaline phosphatase. Ann Hum Genet (1967) 3.49
Artificial heterokaryons of animal cells from different species. J Cell Sci (1966) 3.44
Suppression of malignancy by cell fusion. Nature (1969) 3.41
Genetically determined variation of adenylate kinase in man. Nature (1966) 3.26
Systematic cloning of human minisatellites from ordered array charomid libraries. Genomics (1990) 3.21
Rare phosphoglucomutase phenotypes. Ann Hum Genet (1966) 2.96
Evidence that the gene for tuberous sclerosis is on chromosome 9. Lancet (1987) 2.95
Data on the incidence, segregation and linkage relations of the adenylate kinase (AK) polymorphism. Ann Hum Genet (1968) 2.91
Structure of the human liver/bone/kidney alkaline phosphatase gene. J Biol Chem (1988) 2.80
New method for mapping genes in human chromosomes. Nature (1975) 2.69
A third phosphoglucomutase locus in man. Ann Hum Genet (1968) 2.37
Differential inhibition of the products of the human alkaline phosphatase loci. Ann Hum Genet (1978) 2.26
A new marker for human cancer cells, 2 immunohistochemical detection of the Ca antigen in human tissues with the Ca1 antibody. Lancet (1982) 2.17
Inherited variations in human phosphohexose isomerase. Ann Hum Genet (1968) 2.16
National Confidential Enquiry into counselling for genetic disorders by non-geneticists: general recommendations and specific standards for improving care. Br J Obstet Gynaecol (1999) 2.06
Characteristics of four new human cell lines derived from squamous cell carcinomas of the head and neck. J Natl Cancer Inst (1985) 2.03
Expression of a human placental alkaline phosphatase gene in transfected cells: use as a reporter for studies of gene expression. Proc Natl Acad Sci U S A (1988) 2.02
Assignment of the structural gene for the third component of human complement to chromosome 19. Proc Natl Acad Sci U S A (1982) 2.00
Structure and function of the Ca antigen. Br J Cancer (1983) 1.96
Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome. Nature (1983) 1.94
Tissue culture model of transitional cell carcinoma: characterization of twenty-two human urothelial cell lines. Cancer Res (1986) 1.94
Nucleotide and amino acid sequences of human intestinal alkaline phosphatase: close homology to placental alkaline phosphatase. Proc Natl Acad Sci U S A (1987) 1.93
Immunoglobulin heavy chain genes in humans are located on chromosome. Ann Hum Genet (1981) 1.85
The incidence of rare alleles determining electrophoretic variants: data on 43 enzyme loci in man. Ann Hum Genet (1974) 1.85
Genetics of the alkaline phosphatase polymorphism of the human placenta. Nature (1965) 1.83
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene. J Clin Invest (1997) 1.81
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia. Proc Natl Acad Sci U S A (1988) 1.80
The reactivation of the red cell nucleus. J Cell Sci (1967) 1.80
Developmental changes and polymorphism in human alcohol dehydrogenase. Ann Hum Genet (1971) 1.79
Gene transfer by means of cell fusion I. Statistical mapping of the human X-chromosome by analysis of radiation-induced gene segregation. J Cell Sci (1977) 1.77
An abnormal membrane glycoprotein associated with malignancy in a wide range of different tumours. Proc R Soc Lond B Biol Sci (1978) 1.76
Haemophilus influenzae resides and multiplies intracellularly in human adenoid tissue as demonstrated by in situ hybridization and bacterial viability assay. Infect Immun (1994) 1.70
Regional asssignments of the loci AK3, ACONS, and ASS on human chromosome 9. Cytogenet Cell Genet (1979) 1.68
Developmental change in human intestinal alkaline phosphatase. Proc Natl Acad Sci U S A (1978) 1.67
Profiling of bacterial flora in gastric biopsies from patients with Helicobacter pylori-associated gastritis and histologically normal control individuals by temperature gradient gel electrophoresis and 16S rDNA sequence analysis. J Med Microbiol (2000) 1.66
Immunopathology of B-cell lymphomas induced in C57BL/6 mice by dualtropic murine leukemia virus (MuLV). Am J Pathol (1982) 1.66
Enzyme and protein polymorphism in human populations. Br Med Bull (1969) 1.66
Unrelatedness of temperate Bacillus subtilis bacteriophages SP02 and phi105. J Virol (1972) 1.65
Identity of some human bladder cancer cell lines. Nature (1983) 1.65
A human X-linked antigen defined by a monoclonal antibody. Somatic Cell Genet (1980) 1.64
Products of two common alleles at the locus for human placental alkaline phosphatase differ by seven amino acids. Proc Natl Acad Sci U S A (1986) 1.63
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Am J Hum Genet (2000) 1.60
The genetic basis of tuberous sclerosis. Mol Med Today (1998) 1.60
Rapid cloning and characterization of new chromosome 10 DNA markers by Alu element-mediated PCR. Genomics (1990) 1.59
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma. Am J Hum Genet (2000) 1.58
The expression of genetic information: a study with hybrid animal cells. J Cell Sci (1969) 1.57
Inherited variants of human nucleoside phosphorylase. Ann Hum Genet (1971) 1.55
Confidential inquiry into families with two siblings with cystic fibrosis. Arch Dis Child (1997) 1.54
Hybridization of a myeloid leukemia-derived human cell line (K562) with a human Burkitt's lymphoma line (P3HR-1). J Natl Cancer Inst (1980) 1.53
Characterisation of human cell lines and differentiation from HeLa by enzyme typing. Nature (1976) 1.53
Polymorphism and the subunit structure of enzymes: a contribution to the neutralist-selectionist controversy. Proc Natl Acad Sci U S A (1977) 1.53
Adenosine deaminase isozymes in human tissues. Ann Hum Genet (1971) 1.50
Molecular cloning of the human Goodpasture antigen demonstrates it to be the alpha 3 chain of type IV collagen. J Clin Invest (1992) 1.50
Recommendations for locus-specific databases and their curation. Hum Mutat (2008) 1.49
Generation of a panel of somatic cell hybrids containing unselected fragments of human chromosome 10 by X-ray irradiation and cell fusion: application to isolating the MEN2A region in hybrid cells. Somat Cell Mol Genet (1990) 1.49
Gene transfer by means of cell fusion. II. The mapping of 8 loci on human chromosome 1 by statistical analysis of gene assortment in somatic cell hybrids. J Cell Sci (1977) 1.49
Pulmonary emphysema and alpha 1-antitrypsin deficiency. Br Med J (1971) 1.49
An ultrastructural study of inter-specific cell fusion induced by inactivated Sendai virus. J Cell Sci (1966) 1.48
Expression of alkaline phosphatase loci in mammalian tissues. Proc Natl Acad Sci U S A (1980) 1.47
Mutations of the microsomal triglyceride-transfer-protein gene in abetalipoproteinemia. Am J Hum Genet (1995) 1.47
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13. Ann Hum Genet (1975) 1.45
The analysis of malignancy by cell fusion. I. Hybrids between tumour cells and L cell derivatives. J Cell Sci (1971) 1.45
Polymerase chain reaction for the detection of Pseudomonas aeruginosa, Stenotrophomonas maltophilia and Burkholderia cepacia in sputum of patients with cystic fibrosis. Mol Cell Probes (1996) 1.45
Influence of diet on the "intestinal" component of serum alkaline phosphatase in people of different ABO blood groups and secretor status. Nature (1966) 1.44
Synthesis of an enzyme determined by an erythrocyte nucleus in a hybrid cell. J Cell Sci (1969) 1.44
Human gene mapping using an X/autosome translocation. Somatic Cell Genet (1976) 1.44
Correction of a genetic defect in a mammalian cell. Nat New Biol (1971) 1.44
A new marker for human cancer cells. 3. Immunocytochemical detection of malignant cells in serous fluids with the Ca1 antibody. Lancet (1982) 1.42
Production by EBV infection of an EBNA-positive subline from an EBNA-negative human lymphoma cell line without detectable EBV DNA. Int J Cancer (1975) 1.41
Subjective effects of 3,4-methylenedioxymethamphetamine in recreational users. Neuropsychopharmacology (1988) 1.41
Species- and tissue-specific expression of human alpha 1-antitrypsin in transgenic mice. Genes Dev (1987) 1.40
Evidence for linkage between the transferrin locus (Tf) and the serum cholinesterase locus (E1) in man. Ann Hum Genet (1966) 1.40
Genetic studies on hydatidiform moles. I. The origin of partial moles. Cancer Genet Cytogenet (1982) 1.39
Changes in the cytochemical properties of erythrocyte nuclei reactivated by cell fusion. J Cell Sci (1969) 1.39
Magic Lite Chlamydia immunoassay in urogenital samples and urine versus chlamydial culture. Int J STD AIDS (1994) 1.39
Polymorphism and protein evolution. The neutral mutation-random drift hypothesis. J Med Genet (1971) 1.39
Association of beta-glucosidase with intact cells of Thermoactinomyces. Biotechnol Bioeng (1979) 1.38
Pericentric inversion of a group C autosome: a study of three families. Ann Hum Genet (1968) 1.37
Behaviour of differentiated nuclei in heterokaryons of animal cells from different species. Nature (1965) 1.36
Fusion of tumour cells with host cells. Nat New Biol (1972) 1.34
Alcohol dehydrogenase isozymes in adult human stomach and liver: evidence for activity of the ADH 3 locus. Ann Hum Genet (1972) 1.31
Types of cutaneous reactions to drugs. Importance in recognition of adverse reactions. JAMA (1967) 1.29
Evidence for the assignment of the loci AK1, AK3 and ACONs to chromosome 9 in man. Ann Hum Genet (1976) 1.29
Peptidase D (prolidase) variants in man. Ann Hum Genet (1969) 1.28
Eccrine angiomatous hamartoma. N Y State J Med (1968) 1.28