Published in Chromosoma on January 01, 1974
The Bloom's syndrome gene product promotes branch migration of holliday junctions. Proc Natl Acad Sci U S A (2000) 4.67
Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance. Mol Cell Biol (1997) 2.76
Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. Proc Natl Acad Sci U S A (1989) 2.22
Phosphorylation of the Bloom's syndrome helicase and its role in recovery from S-phase arrest. Mol Cell Biol (2004) 2.20
A retarded rate of DNA chain growth in Bloom's syndrome. Proc Natl Acad Sci U S A (1975) 2.06
The molecular pathogenesis of osteosarcoma: a review. Sarcoma (2011) 1.91
Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes. Am J Hum Genet (1977) 1.67
Molecular evidence that homologous recombination occurs in proliferating human somatic cells. Proc Natl Acad Sci U S A (1990) 1.65
Elevated spontaneous mutation rate in Bloom syndrome fibroblasts. Proc Natl Acad Sci U S A (1981) 1.62
Substrate-specific inhibition of RecQ helicase. Nucleic Acids Res (2001) 1.46
Genetic control of chromosome breakage and rejoining in Drosophila melanogaster: spontaneous chromosome aberrations in X-linked mutants defective in DNA metabolism. Proc Natl Acad Sci U S A (1979) 1.42
Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1. Nucleic Acids Res (2001) 1.41
Relationships among chromatid interchanges, sister chromatid exchanges, and meiotic recombination in Drosophila melanogaster. Proc Natl Acad Sci U S A (1980) 1.32
Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF). Orphanet J Rare Dis (2006) 1.17
Region-specific effects on chromosome integrity of mutations at essential loci in Drosophila melanogaster. Proc Natl Acad Sci U S A (1982) 1.15
Abnormal immune responses of Bloom's syndrome lymphocytes in vitro. J Clin Invest (1975) 1.06
Structural and functional characterizations reveal the importance of a zinc binding domain in Bloom's syndrome helicase. Nucleic Acids Res (2005) 1.02
The relative efficiency of homology-directed repair has distinct effects on proper anaphase chromosome separation. Nucleic Acids Res (2011) 0.97
Sister chromatid exchange frequencies in Progeria and Werner syndrome patients. Am J Hum Genet (1981) 0.96
The role of post-translational modifications in fine-tuning BLM helicase function during DNA repair. DNA Repair (Amst) (2014) 0.91
Most Uv-Induced Reciprocal Translocations in SORDARIA MACROSPORA Occur in or near Centromere Regions. Genetics (1986) 0.91
Specific aneusomies in Chinese hamster cells at different stages of neoplastic transformation, initiated by nitrosomethylurea. Proc Natl Acad Sci U S A (2002) 0.86
Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases. Ageing Res Rev (2016) 0.84
Disruption of SUMO-targeted ubiquitin ligases Slx5-Slx8/RNF4 alters RecQ-like helicase Sgs1/BLM localization in yeast and human cells. DNA Repair (Amst) (2014) 0.82
Bloom's Syndrome: Clinical Spectrum, Molecular Pathogenesis, and Cancer Predisposition. Mol Syndromol (2016) 0.81
Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM. Cytogenet Genome Res (2015) 0.77
Mutator Phenotype and DNA Double-Strand Break Repair in BLM Helicase-Deficient Human Cells. Mol Cell Biol (2016) 0.75
Loss of RMI2 Increases Genome Instability and Causes a Bloom-Like Syndrome. PLoS Genet (2016) 0.75
Endocrine abnormalities and myopathy in Bloom's syndrome. J Med Genet (1977) 0.75
Smc5/6 complex regulates Sgs1 recombination functions. Curr Genet (2016) 0.75
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
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
A Canadian multicenter placebo-controlled study of fixed doses of risperidone and haloperidol in the treatment of chronic schizophrenic patients. J Clin Psychopharmacol (1993) 2.92
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
Clinical assessment of urethral sphincter function. J Urol (1993) 2.17
A retarded rate of DNA chain growth in Bloom's syndrome. Proc Natl Acad Sci U S A (1975) 2.06
Replacement of chlorpromazine with other neuroleptics: effect on abnormal skin pigmentation and ocular changes. J Psychiatry Neurosci (1993) 2.02
Polyglutamine-containing proteins in schizophrenia. Mol Psychiatry (1999) 1.77
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
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
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
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
The syndrome of congenital telangiectatic erythema and stunted growth. J Pediatr (1966) 1.34
Bloom's syndrome: evidence for an increased mutation frequency in vivo. Science (1983) 1.34
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
Adventitious knots in urethral catheters: report of 5 cases. J Urol (1992) 1.27
Mapping human autosomes: assignment of the MN locus to a specific segment in the long arm of chromosome no. 2. Science (1973) 1.27
A previously unrecognized X-linked syndrome of dysmorphia. Birth Defects Orig Artic Ser (1975) 1.22
Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population. Mol Genet Metab (1998) 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
T102C polymorphism in the 5HT2A gene and schizophrenia: relation to phenotype and drug response variability. J Psychiatry Neurosci (1999) 1.10
Atypical presentation of Clostridium difficile colitis in patients with cystic fibrosis. AJR Am J Roentgenol (1999) 1.09
Mongolism, delayed fertilization and human sexual behaviour. Nature (1968) 1.09
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
Trimethadione and human teratogenesis. Teratology (1970) 1.04
A test for Fanconi's anemia. Blood (1987) 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
Bloom's syndrome. V. Surveillance for cancer in affected families. Clin Genet (1977) 1.02
Analysis of 14 CAG repeat-containing genes in schizophrenia. Am J Med Genet (1999) 1.02
Reduction of hospital days in chronic schizophrenic patients treated with risperidone: a retrospective study. Clin Ther (1994) 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
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
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
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
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
Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations. Am J Hum 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
Long-term study of the immunodeficiency of Bloom's syndrome. Acta Paediatr (1992) 0.93
Association between the methylenetetrahydrofolate reductase 677C-->T missense mutation and schizophrenia. Mol Psychiatry (2000) 0.93
Back mutation can produce phenotype reversion in Bloom syndrome somatic cells. Hum Genet (2001) 0.93
Calcineurin inhibitor withdrawal after renal transplantation with alemtuzumab: clinical outcomes and effect on T-regulatory cells. Am J Transplant (2008) 0.92
Clinical evaluation of indoramin as the sole agent for the treatment of hypertension. S Afr Med J (1974) 0.92
MN blood-group locus: data concerning the possible chromosomal location. Science (1968) 0.92
Bloom's syndrome: DNA replication in cultured fibroblasts and lymphocytes. Hum Genet (1977) 0.92
Transfection of BLM into cultured bloom syndrome cells reduces the sister-chromatid exchange rate toward normal. Am J Hum Genet (1999) 0.92
Proceedings: The effects of jaundiced plasma on vascular sensitivity to noradrenaline. J Physiol (1974) 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
The effects of hypercholesterolaemic plasma on vascular sensitivity to noradrenaline. Br J Pharmacol (1975) 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
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
[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
Approaches to meeting health needs of large poverty populations. Am J Public Health Nations Health (1967) 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
Memory impairment in schizophrenia: a study using event-related potentials in implicit and explicit tasks. Psychiatry Res (2001) 0.85
Roberts's syndrome. II. Aberrant Y-chromosome behavior. Clin Genet (1981) 0.85
The cis AB phenotype in three generations of one family: serological, enzymatic and cytogenetic studies. J Immunogenet (1978) 0.85
Denouement and discussion. Bloom's syndrome. (Congenital telangiectasis erythema and stunted growth). Am J Dis Child (1966) 0.84
Event-related brain potentials during an extended visual recognition memory task depict delayed development of cerebral inhibitory processes among 6-month-old infants with Down syndrome. Int J Psychophysiol (1998) 0.84
A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene. Hum Mutat (1998) 0.84
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
Confirmation of 15q26.1 as the site of the FES protooncogene by fluorescence in situ hybridization. Cytogenet Cell Genet (1993) 0.83
Effects of jaundiced plasma on vascular sensitivity to noradrenalin. Kidney Int (1975) 0.83
Males with a uterus and fallopian tubes, a rare disorder of sexual development. Birth Defects Orig Artic Ser (1971) 0.82
Human male infertility, probably genetically determined, due to defective meiosis and spermatogenic arrest. Am J Hum Genet (1979) 0.82
Sibling reflux: a dual center retrospective study. J Urol (1996) 0.82