Published in Somat Cell Mol Genet on July 01, 1987
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Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease. J Biol Chem (1986) 2.54
Localization of the X inactivation centre on the human X chromosome in Xq13. Nature (1991) 2.48
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Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome. Mol Cell Biol (1987) 2.18
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Chromosome-specific organization of human alpha satellite DNA. Am J Hum Genet (1985) 2.10
Defining the sequence specificity of the Saccharomyces cerevisiae DNA binding protein REB1p by selecting binding sites from random-sequence oligonucleotides. Yeast (1994) 2.09
Evolutionary conservation of possible functional domains of the human and murine XIST genes. Hum Mol Genet (1993) 2.05
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The amygdala central nucleus and appetitive Pavlovian conditioning: lesions impair one class of conditioned behavior. J Neurosci (1990) 1.91
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A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation. Nat Genet (1997) 1.88
Nucleotide sequence heterogeneity of alpha satellite repetitive DNA: a survey of alphoid sequences from different human chromosomes. Nucleic Acids Res (1987) 1.87
Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation. Cell (1992) 1.87
Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes. Science (1984) 1.85
The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus. Nature (1986) 1.84
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Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. Am J Hum Genet (1978) 1.80
MSP RFLP for X-linked proteolipid protein gene (PLP) identified with either rat or human PLP cDNA clone. Nucleic Acids Res (1987) 1.80
A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome. J Cell Biol (2001) 1.79
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. Proc Natl Acad Sci U S A (1989) 1.79
PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis. Genomics (1991) 1.74
Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism. Am J Hum Genet (1989) 1.74
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Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. Hum Mol Genet (2001) 1.71
Adult forms of the Ca2+ATPase of sarcoplasmic reticulum. Expression in developing skeletal muscle. J Biol Chem (1987) 1.69
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes. Cancer Res (1988) 1.67
BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes. Chromosoma (1976) 1.66
Differential effects of two ways of devaluing the unconditioned stimulus after Pavlovian appetitive conditioning. J Exp Psychol Anim Behav Process (1979) 1.65
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Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA. Hum Mol Genet (1997) 1.60
The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA. Am J Hum Genet (1998) 1.60
Removal of cholinergic input to rat posterior parietal cortex disrupts incremental processing of conditioned stimuli. J Neurosci (1998) 1.60
The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1. Hum Mol Genet (1993) 1.57
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene. J Biol Chem (1988) 1.56
Tra1p is a component of the yeast Ada.Spt transcriptional regulatory complexes. J Biol Chem (1998) 1.55
Cloning of DNA from double minutes of Y1 mouse adrenocortical tumor cells: evidence for gene amplification. Cell (1981) 1.54
Physical and genetic mapping of the human X chromosome centromere: repression of recombination. Genome Res (1998) 1.53
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Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells. Hum Genet (1976) 1.52
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Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome. Science (1988) 1.49
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Stable dicentric X chromosomes with two functional centromeres. Nat Genet (1998) 1.47
The amygdala complex: multiple roles in associative learning and attention. Proc Natl Acad Sci U S A (1994) 1.47
Direct regional assignment of the gene for vitamin D binding protein (Gc-globulin) to human chromosome 4q11-q13 and identification of an associated DNA polymorphism. Hum Genet (1986) 1.45
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. Genomics (1991) 1.43
Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation. Proc Natl Acad Sci U S A (1998) 1.43
Basal forebrain cholinergic lesions disrupt increments but not decrements in conditioned stimulus processing. J Neurosci (1995) 1.43
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Second-order conditioning with food unconditioned stimulus. J Comp Physiol Psychol (1975) 1.38
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end. Science (1988) 1.38
Structure of the rabbit fast-twitch skeletal muscle Ca2+-ATPase gene. J Biol Chem (1988) 1.38
Expression of genes from the human active and inactive X chromosomes. Am J Hum Genet (1997) 1.38