Published in Hum Genet on October 14, 1977
Elevated spontaneous mutation rate in Bloom syndrome fibroblasts. Proc Natl Acad Sci U S A (1981) 1.62
The human Bloom syndrome gene suppresses the DNA replication and repair defects of yeast dna2 mutants. Proc Natl Acad Sci U S A (2003) 1.42
Roles of the Werner syndrome RecQ helicase in DNA replication. DNA Repair (Amst) (2008) 1.20
Sister chromatid exchange analysis. Am J Hum Genet (1980) 1.02
Different mutations are responsible for the elevated sister-chromatid exchange frequencies characteristic of Bloom's syndrome and hamster EM9 cells. Proc Natl Acad Sci U S A (1987) 0.96
Clastogenic activity from Bloom syndrome fibroblast cultures. Proc Natl Acad Sci U S A (1981) 0.91
DNA polymerases alpha beta and gamma in inherited diseases affecting DNA repair. Nucleic Acids Res (1978) 0.80
The Bloom's syndrome gene product is homologous to RecQ helicases. Cell (1995) 9.91
A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes. Proc Natl Acad Sci U S A (1974) 6.51
Eucaryotic DNA: organization of the genome for replication. Cell (1978) 4.53
Evidence that xeroderma pigmentosum cells do not perform the first step in the repair of ultraviolet damage to their DNA. Proc Natl Acad Sci U S A (1969) 3.97
Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients. Am J Hum Genet (1969) 2.87
Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. Proc Natl Acad Sci U S A (1989) 2.22
A retarded rate of DNA chain growth in Bloom's syndrome. Proc Natl Acad Sci U S A (1975) 2.06
Action of dichlorobenzimidazole riboside on RNA synthesis in L-929 and HeLa cells. J Cell Biol (1976) 1.96
Bloom's syndrome. III. Analysis of the chromosome aberration characteristic of this disorder. Chromosoma (1974) 1.82
Genetically determined sex-reversal in 46,XY humans. Science (1978) 1.76
Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes. Am J Hum Genet (1977) 1.67
Initiation of DNA replication in mammalian cells and its inhibition by reovirus infection. J Mol Biol (1974) 1.67
Molecular evidence that homologous recombination occurs in proliferating human somatic cells. Proc Natl Acad Sci U S A (1990) 1.65
Evidence for chromosome instability in vivo in Bloom syndrome: increased numbers of micronuclei in exfoliated cells. Hum Genet (1985) 1.61
Regulation of DNA replication on subchromosomal units of mammalian cells. J Cell Biol (1975) 1.58
An abnormal profile of DNA replication intermediates in Bloom's syndrome. Cancer Res (1990) 1.54
Altered DNA ligase I activity in Bloom's syndrome cells. Nature (1987) 1.54
DNA replication: direction and rate of chain growth in mammalian cells. J Cell Biol (1973) 1.51
The Roberts syndrome. Clin Genet (1974) 1.45
Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells. Am J Hum Genet (1995) 1.35
Bloom's syndrome: evidence for an increased mutation frequency in vivo. Science (1983) 1.34
Rate of DNA chain growth in mammalian cells infected with cytocidal RNA viruses. Virology (1972) 1.33
Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth. Ann Intern Med (1966) 1.33
Molecular genetics of Bloom's syndrome. Hum Mol Genet (1996) 1.33
Sensitivity of Bloom's syndrome lymphocytes to ethyl methanesulfonate. Hum Genet (1979) 1.29
Mapping human autosomes: assignment of the MN locus to a specific segment in the long arm of chromosome no. 2. Science (1973) 1.27
Protein kinase activity associated with the D2 hybrid protein related to simian virus 40 T antigen: some characteristics of the reaction products. Proc Natl Acad Sci U S A (1979) 1.24
A previously unrecognized X-linked syndrome of dysmorphia. Birth Defects Orig Artic Ser (1975) 1.22
Functions of T antigens of SV40 and polyomavirus. Biochim Biophys Acta (1981) 1.20
Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population. Mol Genet Metab (1998) 1.19
Cellular DNA replication in infections with cytocidal RNA viruses. Virology (1971) 1.19
Unilateral agenesis of the diaphragm. Humangenetik (1968) 1.18
Bloom's syndrome protein, BLM, colocalizes with replication protein A in meiotic prophase nuclei of mammalian spermatocytes. Proc Natl Acad Sci U S A (1999) 1.16
Roberts' syndrome. I. Cytological evidence for a disturbance in chromatid pairing. Clin Genet (1979) 1.14
Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome. Am J Hum Genet (1994) 1.12
Chromosomal effects of mitomycin, a potential recombinogen in mammalian cell genetics. Tex Rep Biol Med (1969) 1.12
Bloom's syndrome and Fanconi's anemia: demonstration of two distinctive patterns of chromosome disruption and rearrangement. Humangenetik (1974) 1.12
Mongolism, delayed fertilization and human sexual behaviour. Nature (1968) 1.09
Hospital-acquired bacterial meningitis in neurosurgical patients. J Neurosurg (1977) 1.08
The Ashkenazic Jewish Bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry. Am J Hum Genet (1998) 1.06
Genes which increase chromosomal instability in somatic cells and predispose to cancer. Prog Med Genet (1972) 1.06
Abnormal immune responses of Bloom's syndrome lymphocytes in vitro. J Clin Invest (1975) 1.06
BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins. Cytogenet Cell Genet (2000) 1.05
A test for Fanconi's anemia. Blood (1987) 1.04
Trimethadione and human teratogenesis. Teratology (1970) 1.04
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. Am J Hum Genet (1977) 1.03
Phosphorylation and dephosphorylation alter the structure of D2 hybrid T antigen. J Virol (1982) 1.02
Bloom's syndrome. V. Surveillance for cancer in affected families. Clin Genet (1977) 1.02
Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients. Mutat Res (1989) 1.01
In vitro labelling of human meiotic chromosomes with H3-thymidine. Hereditas (1968) 0.99
Reovirus: effect of noninfective viral components on cellular deoxyribonucleic acid synthesis. J Virol (1973) 0.99
Testicular feminisation and inguinal hernia. Lancet (1973) 0.98
Familial congenital heart disease. II. Chromosomal studies. Circulation (1966) 0.98
Bloom's syndrome. VII. Progress report for 1978. Clin Genet (1979) 0.98
DNA replication in mammalian cells. Altered patterns of initiation during inhibition of protein synthesis. J Cell Biol (1975) 0.98
Bloom's syndrome and EM9 cells in BrdU-containing medium exhibit similarly elevated frequencies of sister chromatid exchange but dissimilar amounts of cellular proliferation and chromosome disruption. Chromosoma (1984) 0.97
Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum. Cytogenet Cell Genet (1978) 0.97
Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations. Am J Hum Genet (1984) 0.96
Different mutations are responsible for the elevated sister-chromatid exchange frequencies characteristic of Bloom's syndrome and hamster EM9 cells. Proc Natl Acad Sci U S A (1987) 0.96
Bloom's syndrome XI. Progress report for 1983. Clin Genet (1984) 0.96
Embryonic stress hypothesis of teratogenesis. Am J Med (1984) 0.96
Pseudovaginal perineoscrotal hypospadias. Clin Genet (1972) 0.96
[Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)]. Ann Genet (1970) 0.95
Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locus. Hum Genet (1992) 0.94
Mapping human autosomes: evidence supporting assignment of rhesus to the short arm of chromosome No. 1. Science (1974) 0.94
Characterization of a ts mutant of BALB/3T3 cells and correction of the defect by in vitro addition of extracts from wild-type cells. Mol Cell Biol (1984) 0.94
Long-term study of the immunodeficiency of Bloom's syndrome. Acta Paediatr (1992) 0.93
Back mutation can produce phenotype reversion in Bloom syndrome somatic cells. Hum Genet (2001) 0.93
Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal. Am J Hum Genet (1999) 0.92
MN blood-group locus: data concerning the possible chromosomal location. Science (1968) 0.92
Decreased initiation of DNA synthesis in a temperature-sensitive mutant of hamster cells. J Cell Physiol (1980) 0.91
Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp. Nat Genet (1994) 0.90
Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam. Ann Genet (1973) 0.89
Possible teratogenicity of trimethadione and paramethadione. Lancet (1970) 0.88
Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation. Birth Defects Orig Artic Ser (1975) 0.88
Alternative therapies used by patients with AIDS. N Engl J Med (1989) 0.87
Physical mapping of the bloom syndrome region by the identification of YAC and P1 clones from human chromosome 15 band q26.1. Genomics (1996) 0.87
Plasma membrane orientation of simian virus 40 T antigen in three transformed cell lines mapped with monoclonal antibodies. J Virol (1985) 0.87
Approaches to meeting health needs of large poverty populations. Am J Public Health Nations Health (1967) 0.86
[Duplication of an X chromosome in a case of Turner's syndrome (45,X-46,XXp+)]. Ann Genet (1970) 0.86
Testicular feminization in monozygotic twins with 47 chromosomes (XXY). Ann Genet (1966) 0.86
Replication of mammalian DNA in vitro. Evidence for initiation from fiber autoradiography. J Cell Biol (1979) 0.86
Familial predisposition to cancer and age at onset of disease in randomly selected cancer patients. Am J Hum Genet (1983) 0.86
The human Y chromosome homologue of XG: transcription of a naturally truncated gene. Hum Mol Genet (1995) 0.85
The cis AB phenotype in three generations of one family: serological, enzymatic and cytogenetic studies. J Immunogenet (1978) 0.85
Immunological cross-reactivity between simian virus 40 large T antigen and D2 hybrid T antigen. J Virol (1981) 0.85
Roberts's syndrome. II. Aberrant Y-chromosome behavior. Clin Genet (1981) 0.85
A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene. Hum Mutat (1998) 0.84
Alterations in nuclear structure and function in reovirus-infected cells. Clin Invest Med (1979) 0.84
Reovirus: analysis of proteins from released and cell-associated virus. J Gen Virol (1971) 0.84
Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization. Cytogenet Cell Genet (1993) 0.83
Autoradiographic studies of human chromosomes. 4. Comparison of the end-of-S patterns in lymphocytes and amniotic epithelial cells. Chromosoma (1971) 0.83
The Aarskog-Scott syndrome in four brothers. Birth Defects Orig Artic Ser (1975) 0.83
Males with a uterus and fallopian tubes, a rare disorder of sexual development. Birth Defects Orig Artic Ser (1971) 0.82
Infective endocarditis due to Actinobacillus actinomycetemcomitans in a patient with a porcine prosthetic mitral valve. Can Med Assoc J (1980) 0.82
Chromosome abnormalities of leukaemic B lymphocytes in chronic lymphocytic leukaemia. Nature (1980) 0.82
Secondary diagnoses as predictive factors for survival or mortality in Medicare patients with acute pneumonia. Am J Med Qual (1996) 0.82
Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest. Am J Hum Genet (1979) 0.82
Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits. Humangenetik (1974) 0.81