Published in EMBO J on November 01, 1995
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Telomeres shorten during ageing of human fibroblasts. Nature (1990) 23.97
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Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res (1989) 15.35
A telomeric sequence in the RNA of Tetrahymena telomerase required for telomere repeat synthesis. Nature (1989) 13.18
Telomere reduction in human colorectal carcinoma and with ageing. Nature (1990) 11.24
An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide. Nucleic Acids Res (1989) 10.50
The human telomere terminal transferase enzyme is a ribonucleoprotein that synthesizes TTAGGG repeats. Cell (1989) 8.68
Complex gene conversion events in germline mutation at human minisatellites. Nat Genet (1994) 5.70
Minisatellite repeat coding as a digital approach to DNA typing. Nature (1991) 5.25
Hypervariable ultra-long telomeres in mice. Nature (1990) 4.76
Human telomeres contain at least three types of G-rich repeat distributed non-randomly. Nucleic Acids Res (1989) 4.72
Telomerase activity in human ovarian carcinoma. Proc Natl Acad Sci U S A (1994) 3.86
Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal. Nature (1985) 3.63
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Molecular cloning of human telomeres in yeast. Nature (1989) 2.67
Extensive telomere repeat arrays in mouse are hypervariable. Nucleic Acids Res (1990) 2.56
Clustering of hypervariable minisatellites in the proterminal regions of human autosomes. Genomics (1988) 2.34
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes. Nature (1985) 2.14
Genetics and molecular biology of telomeres. Adv Genet (1992) 1.88
Complex recombination events at the hypermutable minisatellite CEB1 (D2S90). EMBO J (1994) 1.79
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
The pseudoautosomal regions of the human sex chromosomes. Hum Genet (1993) 1.77
Identification of clusters of biallelic polymorphic sequence-tagged sites (pSTSs) that generate highly informative and automatable markers for genetic linkage mapping. Genomics (1992) 1.55
Mammalian telomere dynamics: healing, fragmentation shortening and stabilization. Curr Opin Genet Dev (1994) 1.54
Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping. Hum Mol Genet (1993) 1.38
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A subterminal satellite located adjacent to telomeres in chimpanzees is absent from the human genome. Nat Genet (1994) 1.15
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary. Am J Hum Genet (1990) 1.13
Allele-specific MVR-PCR analysis at minisatellite D1S8. Hum Mol Genet (1993) 1.04
Identification of new human repetitive sequences: characterization of the corresponding cDNAs and their expression in embryonal carcinoma cells. Nucleic Acids Res (1989) 0.93
Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes. Am J Hum Genet (1994) 0.81
Hypervariable 'minisatellite' regions in human DNA. Nature (1985) 31.03
DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man. Cell (1979) 15.74
A physical map of the DNA regions flanking the rabbit beta-globin gene. Cell (1977) 12.96
Individual-specific 'fingerprints' of human DNA. Nature (1985) 10.38
Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. Nature (1988) 9.47
Characterization of a panel of highly variable minisatellites cloned from human DNA. Ann Hum Genet (1987) 7.58
The rabbit beta-globin gene contains a large large insert in the coding sequence. Cell (1977) 6.45
Forensic application of DNA 'fingerprints'. Nature (1986) 5.19
Chromosome 5 allele loss in human colorectal carcinomas. Nature (1987) 4.46
Linkage of adult alpha- and beta-globin genes in X. laevis and gene duplication by tetraploidization. Cell (1980) 4.09
Identification of the skeletal remains of a murder victim by DNA analysis. Nature (1991) 3.73
Human minisatellite mutation rate after the Chernobyl accident. Nature (1996) 3.46
Systematic cloning of human minisatellites from ordered array charomid libraries. Genomics (1990) 3.21
DNA fingerprints of dogs and cats. Anim Genet (1987) 3.12
Positive identification of an immigration test-case using human DNA fingerprints. Nature (1985) 3.07
Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite. Nucleic Acids Res (1986) 2.70
DNA fingerprints applied to gene introgression in breeding programs. Genetics (1990) 2.70
DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees. Am J Hum Genet (1986) 2.55
Mouse DNA 'fingerprints': analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains. Nucleic Acids Res (1987) 2.47
Clustering of hypervariable minisatellites in the proterminal regions of human autosomes. Genomics (1988) 2.34
Evolution of the beta-globin gene cluster in man and the primates. J Mol Biol (1981) 2.31
Deletion of genes on chromosome 1 in endocrine neoplasia. Nature (1987) 2.27
Uniparental paternal disomy in Angelman's syndrome. Lancet (1991) 2.26
Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively. Somat Cell Mol Genet (1987) 2.21
The retinoblastoma gene is frequently altered leading to loss of expression in primary breast tumours. Oncogene (1989) 2.02
Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci. Genomics (1989) 1.93
Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident. Mutat Res (1997) 1.92
A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16. Genomics (1990) 1.84
Minisatellite diversity supports a recent African origin for modern humans. Nat Genet (1996) 1.84
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. N Engl J Med (1992) 1.78
Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. Br J Cancer (1987) 1.74
Highly variable minisatellites and DNA fingerprints. Biochem Soc Trans (1987) 1.71
DNA fingerprinting Dolly. Nature (1998) 1.69
Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events. Proc Biol Sci (1991) 1.56
Induction of minisatellite mutations in the mouse germline by low-dose chronic exposure to gamma-radiation and fission neutrons. Mutat Res (2000) 1.54
Characterization of a highly unstable mouse minisatellite locus: evidence for somatic mutation during early development. Genomics (1989) 1.51
Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism. Nat Genet (1994) 1.50
Organization of the human myoglobin gene. EMBO J (1984) 1.49
The seal myoglobin gene: an unusually long globin gene. Nature (1983) 1.44
Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. Nucleic Acids Res (1989) 1.41
Isolation of human simple repeat loci by hybridization selection. Hum Mol Genet (1994) 1.39
Use of vectorette and subvectorette PCR to isolate transgene flanking DNA. PCR Methods Appl (1994) 1.38
Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping. Hum Mol Genet (1993) 1.38
Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309). Hum Mol Genet (1996) 1.33
Processes of gene duplication. Nature (1982) 1.33
Minisatellite instability and germline mutation. Cell Mol Life Sci (1999) 1.28
Analysis of somatic mutations at human minisatellite loci in tumors and cell lines. Genomics (1989) 1.28
Isolation and sequence analysis of a hybrid delta-globin pseudogene from the brown lemur. J Mol Biol (1982) 1.27
Influences of array size and homogeneity on minisatellite mutation. EMBO J (1998) 1.26
High-resolution sperm typing of meiotic recombination in the mouse MHC Ebeta gene. EMBO J (2003) 1.26
Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7. Hum Mol Genet (1999) 1.23
A comparison of vertebrate interferon gene families detected by hybridization with human interferon DNA. J Mol Biol (1983) 1.23
Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination. Hum Mol Genet (2000) 1.22
Biology and applications of human minisatellite loci. Curr Opin Genet Dev (1992) 1.20
Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. Nature (1979) 1.19
Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. Hum Mol Genet (1993) 1.19
Mouse minisatellite mutations induced by ionizing radiation. Nat Genet (1993) 1.18
Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition. Am J Hum Genet (2000) 1.17
A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development. Genomics (1993) 1.16
A subterminal satellite located adjacent to telomeres in chimpanzees is absent from the human genome. Nat Genet (1994) 1.15
Stage specificity, dose response, and doubling dose for mouse minisatellite germ-line mutation induced by acute radiation. Proc Natl Acad Sci U S A (1998) 1.14
Molecular cloning of seal myoglobin mRNA. Nucleic Acids Res (1982) 1.14
A novel unstable mouse VNTR family expanded from SINE B1 elements. Genomics (1998) 1.11
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A DNA marker for human chromosome 8 that detects alleles of differing sizes. Cytogenet Cell Genet (1986) 1.08
Detection of a novel minisatellite-specific DNA-binding protein. Nucleic Acids Res (1990) 1.08
High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution. Am J Hum Genet (2000) 1.08
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Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90). Am J Hum Genet (2000) 1.07
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Allele-specific MVR-PCR analysis at minisatellite D1S8. Hum Mol Genet (1993) 1.04
Use of minisatellite DNA probes for determination of twin zygosity at birth. Lancet (1986) 1.03
Comparative sequence analysis of human minisatellites showing meiotic repeat instability. Genome Res (1999) 1.03
Transgenerational mutation by radiation. Nature (2000) 1.03
Identification of post-transplant cell population by DNA fingerprint analysis. Lancet (1986) 1.03
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"Major minisatellite loci" detected by minisatellite clones 33.6 and 33.15 correspond to the cognate loci D1S111 and D7S437. Genomics (1990) 0.99
Minisatellite "isoallele" discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping. Genomics (1991) 0.99
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The plasticity of human telomeres demonstrated by a hypervariable telomere repeat array that is located on some copies of 16p and 16q. Hum Mol Genet (1999) 0.98
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes. Hum Mol Genet (2000) 0.98
STS for minisatellite MS607 (D22S163). Nucleic Acids Res (1991) 0.96
Minisatellite binding protein Msbp-1 is a sequence-specific single-stranded DNA-binding protein. Nucleic Acids Res (1991) 0.94
Gestational and nongestational trophoblastic tumors distinguished by DNA analysis. Cancer (1992) 0.93
Isolation of telomere junction fragments by anchored polymerase chain reaction. Proc Biol Sci (1992) 0.93
The CEPH consortium linkage map of human chromosome 16. Genomics (1995) 0.92
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Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration. Nucleic Acids Res (1994) 0.90
Isolation and characterization of mouse minisatellites. Genomics (1998) 0.89
Isolation and detailed characterization of human cell lines resistant to D-threo-chloramphenicol. Exp Cell Res (1976) 0.89
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Minisatellite mutation frequency in human sperm following radiotherapy. Mutat Res (2000) 0.88
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