Published in Hum Mol Genet on July 01, 1999
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A 330 kb CENP-A binding domain and altered replication timing at a human neocentromere. EMBO J (2001) 1.65
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Identification of two distinct subfamilies of alpha satellite DNA that are highly specific for human chromosome 15. Genomics (1990) 1.51
Mouse major (gamma) satellite DNA is highly conserved and organized into extremely long tandem arrays: implications for recombination between nonhomologous chromosomes. Genomics (1989) 1.47
Sequence analysis of an 80 kb human neocentromere. Hum Mol Genet (1999) 1.45
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Further evidence that CENP-C is a necessary component of active centromeres: studies of a dic(X; 15) with simultaneous immunofluorescence and FISH. Hum Mol Genet (1995) 1.26
Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21. Genome Res (1999) 1.22
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A homologous subfamily of satellite III DNA on human chromosomes 14 and 22. Nucleic Acids Res (1990) 1.18
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Isolation and characterization of a myeloma--spleen-cell hybrid producing antibody to phenylalanine hydroxylase. Biochem J (1980) 1.12
A chromosome 14-specific human satellite III DNA subfamily that shows variable presence on different chromosomes 14. Am J Hum Genet (1992) 1.10
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome. Ann Hum Genet (1984) 1.10
Direct cloning of human 10q25 neocentromere DNA using transformation-associated recombination (TAR) in yeast. Genomics (1998) 1.10
Evolution of alpha-satellite DNA on human acrocentric chromosomes. Genomics (1989) 1.10
Prospects for epigenetic research within cohort studies of psychological disorder: a pilot investigation of a peripheral cell marker of epigenetic risk for depression. Biol Psychol (2009) 1.10
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Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism. Clin Genet (2009) 1.08
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Long-range analyses of the centromeric regions of human chromosomes 13, 14 and 21: identification of a narrow domain containing two key centromeric DNA elements. Hum Mol Genet (1993) 1.07
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A chromosome 13-specific human satellite I DNA subfamily with minor presence on chromosome 21: further studies on Robertsonian translocations. Genomics (1993) 1.04
Four distinct alpha satellite subfamilies shared by human chromosomes 13, 14 and 21. Nucleic Acids Res (1991) 1.04
Specific tumour-associated methylation in normal human term placenta and first-trimester cytotrophoblasts. Mol Hum Reprod (2008) 1.03
Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation. Hum Mol Genet (1996) 1.03
Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints. Am J Hum Genet (1994) 1.03
Identification of DNA sequences flanking the breakpoint of human t(14q21q) Robertsonian translocations. Am J Hum Genet (1992) 1.02
Identification and characterization of satellite III subfamilies to the acrocentric chromosomes. Chromosome Res (2001) 1.02
Observations indicating the nature of the mutation in phenylketonuria. J Inherit Metab Dis (1980) 1.01
Wheel running and environmental enrichment differentially modify exon-specific BDNF expression in the hippocampus of wild-type and pre-motor symptomatic male and female Huntington's disease mice. Hippocampus (2010) 1.01
Conservation of centromere protein in vertebrates. Chromosome Res (1999) 1.01
Non-neutralizing monoclonal antibodies to a trypsin-sensitive site on the major glycoprotein of rotavirus which discriminate between virus serotypes. Arch Virol (1987) 1.01
Individual and overlapping roles of BH3-only proteins Bim and Bad in apoptosis of lymphocytes and platelets and in suppression of thymic lymphoma development. Cell Death Differ (2010) 1.00
Microbial exposure, interferon gamma gene demethylation in naïve T-cells, and the risk of allergic disease. Allergy (2009) 1.00
Methylation of the adenomatous polyposis coli (APC) gene in human placenta and hypermethylation in choriocarcinoma cells. Cancer Lett (2008) 1.00
Trisomy 20p resulting from inverted duplication and neocentromere formation. Am J Med Genet (1999) 0.98