Published in Am J Pathol on January 01, 1974
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A definitive cloning technique for human fibroblast cultures. Proc Soc Exp Biol Med (1966) 1.08
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Clonal variation of derepressed phosphatase in chromosomally mosaic cell cultures from a child with Down's syndrome. Exp Cell Res (1967) 0.80
Isolation, purification, and chemical characterization of the serum mitogen for diploid human fibroblasts. J Cell Physiol (1973) 0.79
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Increased activity-regulating and neuroprotective efficacy of alpha-secretase-derived secreted amyloid precursor protein conferred by a C-terminal heparin-binding domain. J Neurochem (1996) 1.66
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group. Am J Hum Genet (1997) 1.52
Increased susceptibility of Down's syndrome fibroblasts to transformation by SV40. Proc Soc Exp Biol Med (1967) 1.49
Alzheimer's PS-1 mutation perturbs calcium homeostasis and sensitizes PC12 cells to death induced by amyloid beta-peptide. Neuroreport (1996) 1.48
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Variegated translocation mosaicism in human skin fibroblast cultures. Cytogenet Cell Genet (1975) 1.45
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A genetically inactivated herpes simplex virus type 2 (HSV-2) vaccine provides effective protection against primary and recurrent HSV-2 disease. J Infect Dis (1997) 1.44
Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells. Hum Genet (1996) 1.43
Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome. Hum Genet (1976) 1.41
Growth characteristics of Werner syndrome cells in vitro. Adv Exp Med Biol (1985) 1.39
Enhanced cell proliferation and biosynthesis mediate improved wound repair in refed, caloric-restricted mice. Mech Ageing Dev (1996) 1.38
Werner helicase is localized to transcriptionally active nucleoli of cycling cells. Exp Cell Res (1998) 1.37
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers. Am J Hum Genet (1996) 1.31
The Werner syndrome protein is involved in RNA polymerase II transcription. Mol Biol Cell (1999) 1.29
Cultivated cells from diagnostic amniocentesis in second trimester pregnancies. I. Clonal morphology and growth potential. Pediatr Res (1974) 1.29
Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts. Hum Genet (1981) 1.24
Increased vulnerability of hippocampal neurons from presenilin-1 mutant knock-in mice to amyloid beta-peptide toxicity: central roles of superoxide production and caspase activation. J Neurochem (1999) 1.22
Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation. Nature (1979) 1.21
Homozygous and compound heterozygous mutations at the Werner syndrome locus. Hum Mol Genet (1996) 1.19
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Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population. Am J Med Genet (1997) 1.17
cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein. Hum Mol Genet (1996) 1.17
Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients. Hum Genet (1990) 1.16
Comparative heterokaryon study of cellular senescence and the serum-deprived state. Exp Cell Res (1980) 1.16
Mammalian mutator mutant with an aphidicolin-resistant DNA polymerase alpha. Proc Natl Acad Sci U S A (1983) 1.16
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Preparation of cell-size unilamellar liposomes with high captured volume and defined size distribution. Biochim Biophys Acta (1981) 1.11
Increased chromosomal aberrations in first metaphases of cells isolated from the kidneys of aged mice. Isr J Med Sci (1985) 1.10
A novel human gene encoding HECT domain and RCC1-like repeats interacts with cyclins and is potentially regulated by the tumor suppressor proteins. Biochem Biophys Res Commun (1999) 1.10
Trisomy of the long arm of human chromosome 1. Humangenetik (1974) 1.09
Evidence of clonal attenuation, clonal succession, and clonal expansion in mass cultures of aging Werner's syndrome skin fibroblasts. Cytogenet Cell Genet (1981) 1.08
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Exceptional cellular resistance to oxidative damage in long-lived birds requires active gene expression. J Gerontol A Biol Sci Med Sci (2001) 1.07
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Abnormal skin fibroblast cytogenetics in four dysmorphic patients with normal lymphocyte chromosomes. Am J Hum Genet (1979) 1.05
Hypermutable ligation of plasmid DNA ends in cells from patients with Werner syndrome. J Invest Dermatol (1994) 1.05
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Preparation of multivesicular liposomes. Biochim Biophys Acta (1983) 0.99
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Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines. Hum Genet (1999) 0.98
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Effects of cytochalasin B on cultivated human diploid fibroblasts and its use for the isolation of tetraploid clones. Exp Cell Res (1973) 0.96
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Proliferative potential of human fibroblasts: an inverse dependence on cell size. J Cell Physiol (1987) 0.95
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