Published in Chromosoma on March 14, 1974
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Initiation of DNA synthesis in the prematurely condensed chromosomes of G1 cells. J Cell Biol (1980) 0.77
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Mitotic factors from mammalian cells induce germinal vesicle breakdown and chromosome condensation in amphibian oocytes. Proc Natl Acad Sci U S A (1979) 2.43
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Movement and segregation of kinetochores experimentally detached from mammalian chromosomes. Nature (1988) 2.10
A case revisited: recent presentation of incontinentia pigmenti in association with a previously reported X;autosome translocation. Am J Med Genet (1997) 2.05
Mitotic synchrony in mammalian cells treated with nitrous oxide at high pressure. Science (1968) 1.95
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Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. Am J Hum Genet (2001) 1.68
Characterization of ATM gene mutations in 66 ataxia telangiectasia families. Hum Mol Genet (1999) 1.66
DNA topoisomerase II alpha is the major chromosome protein recognized by the mitotic phosphoprotein antibody MPM-2. Proc Natl Acad Sci U S A (1993) 1.66
Activity of rifabutin alone or in combination with clofazimine or ethambutol or both against acute and chronic experimental Mycobacterium intracellulare infections. Am Rev Respir Dis (1987) 1.62
Nucleo-cytoplasmic interactions in the acheivement of nuclear synchrony in DNA synthesis and mitosis in multinucleate cells. Biol Rev Camb Philos Soc (1971) 1.61
Rabl's model of the interphase chromosome arrangement tested in Chinese hamster cells by premature chromosome condensation and laser-UV-microbeam experiments. Hum Genet (1982) 1.53
Blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) associated with interstitial deletion of band 3q22: review and gene assignment to the interface of band 3q22.3 and 3q23. Am J Med Genet (1993) 1.47
A new chromosomal instability disorder confirmed by complementation studies. Clin Genet (1988) 1.45
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. Am J Hum Genet (1997) 1.41
Death from metastatic donor-derived ovarian cancer in a male kidney transplant recipient. Am J Transplant (2009) 1.41
Study of clonality in myelodysplastic syndromes: detection of trisomy 8 in bone marrow cell smears by fluorescence in situ hybridization. Leuk Res (1996) 1.37
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK). Nat Genet (1994) 1.36
Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p. J Med Genet (2005) 1.36
Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature. Prenat Diagn (2001) 1.35
G2 phase-specific proteins of HeLa cells. Proc Natl Acad Sci U S A (1978) 1.35
Mammalian cell fusion. 3. A HeLa cell inducer of premature chromosome condensation active in cells from a variety of animal species. J Cell Physiol (1970) 1.34
A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene. J Med Genet (2001) 1.31
Distribution of cytoskeletal proteins sharing a conserved phosphorylated epitope. Eur J Cell Biol (1986) 1.30
Localization of mitotic factors on metaphase chromosomes. J Cell Sci (1982) 1.27
Hydrogeochemical characterization of fluoride rich groundwater of Wailpalli watershed, Nalgonda District, Andhra Pradesh, India. Environ Monit Assess (2010) 1.24
Mitosis-specific monoclonal antibody MPM-2 inhibits Xenopus oocyte maturation and depletes maturation-promoting activity. Proc Natl Acad Sci U S A (1989) 1.23
Radioimmunoassay of 3 alpha-hydroxy-5 alpha-pregnan-20-one in rat and human plasma. Steroids (1990) 1.23
Premature chromosome condensation and cell cycle analysis. J Cell Physiol (1977) 1.19
The cause of G2-arrest in Chinese hamster ovary cells treated with anticancer drugs. J Natl Cancer Inst (1976) 1.19
DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes. Hum Mol Genet (2001) 1.19
Premature chromosome condensation. I. Visualization of x-ray-induced chromosome damage in interphase cells. Mutat Res (1974) 1.17
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse. Hum Mol Genet (1994) 1.16
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations. Eur J Hum Genet (2000) 1.15
Premature chromosome condensation: a mechanism for the elimination of chromosomes in virus-fused cells. J Cell Sci (1972) 1.15
Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation. Mol Cell Biol (1997) 1.15
Neuroendocrine-gonadal axis in men: frequent sampling of LH, FSH, and testosterone. Am J Physiol (1988) 1.15
Activity of amikacin against Mycobacterium avium complex under simulated in vivo conditions. Antimicrob Agents Chemother (1988) 1.13
Environmental trichlorfon and cluster of congenital abnormalities. Lancet (1993) 1.10
A nidus, crystalluria and aggregation: key ingredients for stone enlargement. Urol Res (2007) 1.08
Evolutionary trends in 18S ribosomal RNA nucleotide sequences of rat, mouse, hamster and man. Nucleic Acids Res (1976) 1.08
Inhalation challenge effects of perfume scent strips in patients with asthma. Ann Allergy Asthma Immunol (1995) 1.07
Extrahepatic portal hypertension: a review of 70 cases. J Pediatr Surg (1978) 1.07
The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1. Am J Hum Genet (1995) 1.06
Nijmegen breakage syndrome: consequences of defective DNA double strand break repair. Bioessays (1999) 1.05
Regulation of DNA synthesis: age-dependent cooperation among G1 cells upon fusion. Proc Natl Acad Sci U S A (1977) 1.04
Mitotic non-disjunction of sister chromatids and anomalous mitosis induced by low temperatures in HeLa cells. Exp Cell Res (1966) 1.04
Antibodies specific for mitotic human chromosomes. Exp Cell Res (1982) 1.04
Molecular characterization of human and mouse photoreceptor guanylate cyclase-activating protein (GCAP) and chromosomal localization of the human gene. J Biol Chem (1994) 1.04
Nuclear magnetic resonance patterns of intracellular water as a function of HeLa cell cycle. Science (1976) 1.04
Mitotic factors from mammalian cells: a preliminary characterization. J Supramol Struct (1979) 1.02
Giemsa banding in prematurely condensed chromosomes obtained by cell fusion. Nat New Biol (1973) 1.01
Putrescine biosynthesis in mammalial cells: essential for DNA synthesis but not for mitosis. Biochem Biophys Res Commun (1977) 1.01
Cytogenetic investigations in a new case of Bloom's syndrome. Hum Genet (1976) 1.01
Her-2/neu gene amplification in low to moderately expressing breast cancers: possible role of chromosome 17/Her-2/neu polysomy. Breast J (2002) 1.01
Differential effects of inhibition of polyamine biosynthesis on cell cycle traverse and structure of the prematurely condensed chromosomes of normal and transformed cells. J Cell Physiol (1979) 1.00
Fluid absorption during transurethral resection. Br Med J (1980) 1.00
Characterization of human and mouse rod cGMP phosphodiesterase delta subunit (PDE6D) and chromosomal localization of the human gene. Genomics (1998) 1.00
Restoration of pliability to the mitral leaflets during reconstruction. J Heart Valve Dis (1995) 0.99
Severe sepsis following percutaneous or endoscopic procedures for urinary tract stones. Br J Urol (1993) 0.99
The spectrum of abnormal patterns of gonadotropin-releasing hormone secretion in men with idiopathic hypogonadotropic hypogonadism: clinical and laboratory correlations. J Clin Endocrinol Metab (1987) 0.98
Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome. Am J Hum Genet (1997) 0.97
Effect of gossypol on DNA synthesis and cell cycle progression of mammalian cells in vitro. Cancer Res (1984) 0.97
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations. J Med Genet (2007) 0.96
The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysis. Genomics (1995) 0.96
Arrangement of prematurely condensed chromosomes in cultured cells and lymphocytes of the Indian muntjac. Chromosoma (1981) 0.95
A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22. Am J Hum Genet (2000) 0.95
A comparative analysis of nephrostomy, JJ stent and urgent in situ extracorporeal shock wave lithotripsy for obstructing ureteric stones. BJU Int (1999) 0.95
Multiple forms of maturation-promoting factor in unfertilized Xenopus eggs. Proc Natl Acad Sci U S A (1991) 0.94
Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation. Blood (1999) 0.94
V(D)J rearrangement in Nijmegen breakage syndrome. Mol Immunol (2000) 0.93
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability. J Med Genet (2005) 0.93
Chromosome condensation and decondensation factors in the life cycle of eukaryotic cells. Symp Fundam Cancer Res (1984) 0.93
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. Eur J Hum Genet (2000) 0.93
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival. Hum Genet (1997) 0.93
Partial purification and characterization of mitotic factors from HeLa cells. Exp Cell Res (1985) 0.93
A novel M phase-specific H1 kinase recognized by the mitosis-specific monoclonal antibody MPM-2. Dev Biol (1991) 0.92
Bleomycin-induced damage in prematurely condensed chromosomes and its relationship to cell cycle progression in CHO cells. Cancer Res (1974) 0.92
Localization of the ileal sodium-bile acid cotransporter gene (SLC10A2) to human chromosome 13q33. Genomics (1996) 0.92
Study of the normal conjunctival flora (bacterial and fungal) and its relations to external ocular infections. Indian J Ophthalmol (1972) 0.92
Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21. Hum Genet (1992) 0.91
Prostatodynia--physiological characteristics and rational management with muscle relaxants. Br J Urol (1981) 0.91
Early observations of the effect of extracorporeal shockwave lithotripsy on blood pressure: a prospective randomized control clinical trial. BJU Int (2000) 0.91
Deficiency of DNA ligase activity in Fanconi's anemia. Hum Genet (1978) 0.91
Analysis of protein patterns in two-dimensional gels of cultured human cells with trisomy 21. Clin Chem (1982) 0.91
Distribution of phosphorylated spindle-associated proteins in the diatom Stephanopyxis turris. Cell Motil Cytoskeleton (1989) 0.91
Conditional absence of mitosis-specific antigens in a temperature-sensitive embryonic-arrest mutant of Caenorhabditis elegans. J Cell Sci (1987) 0.90
Corrosive acid ingestion in man - a clinical and endoscopic study. Gut (1984) 0.90
Protein phosphorylation and dynamics of cytoskeletal structures associated with basal bodies in Paramecium. Cell Motil Cytoskeleton (1987) 0.90