Published in Nucleic Acids Res on April 24, 1981
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes. Nucleic Acids Res (1982) 4.67
Isolation and characterization of a major tandem repeat family from the human X chromosome. Nucleic Acids Res (1983) 2.94
KpnI families of long, interspersed repetitive DNAs in human and other primate genomes. Nucleic Acids Res (1982) 2.26
Genomic representation of the Hind II 1.9 kb repeated DNA. Nucleic Acids Res (1982) 2.02
Members of the KpnI family of long interspersed repeated sequences join and interrupt alpha-satellite in the monkey genome. Nucleic Acids Res (1983) 1.93
Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex. Proc Natl Acad Sci U S A (1983) 1.60
Interruption of an alpha-satellite array by a short member of the KpnI family of interspersed, highly repeated monkey DNA sequences. Mol Cell Biol (1983) 1.59
Nucleotide sequence definition of a major human repeated DNA, the Hind III 1.9 kb family. Nucleic Acids Res (1982) 1.55
Rearranged sequences of a human Kpn I element. Proc Natl Acad Sci U S A (1984) 1.52
Some KpnI family members are associated with the Alu family in the human genome. Nucleic Acids Res (1983) 1.26
Characterization and evolution of a single-copy sequence from the human Y chromosome. Mol Cell Biol (1985) 1.25
Chromosomal localization of several families of repetitive sequences by in situ hybridization. Am J Hum Genet (1985) 1.14
Unusual domains of human alphoid satellite DNA with contiguous non-satellite sequences: sequence analysis of a junction region. Nucleic Acids Res (1983) 1.09
Translocation and amplification of an X-chromosome DNA repeat in inbred strains of mice. Nucleic Acids Res (1987) 0.96
An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72]. Nucleic Acids Res (1985) 0.88
Analysis of LINE-1 family sequences on a single monkey chromosome. Nucleic Acids Res (1986) 0.80
Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol (1975) 503.08
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J Mol Biol (1977) 205.11
Screening lambdagt recombinant clones by hybridization to single plaques in situ. Science (1977) 83.82
A membrane-filter technique for the detection of complementary DNA. Biochem Biophys Res Commun (1966) 71.25
The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA. Cell (1978) 22.88
A physical map of the DNA regions flanking the rabbit beta-globin gene. Cell (1977) 12.96
Ubiquitous, interspersed repeated sequences in mammalian genomes. Proc Natl Acad Sci U S A (1980) 9.48
Translocatable elements in procaryotes. Cell (1977) 9.12
Molecular cloning and characterization of the human beta-like globin gene cluster. Cell (1980) 7.77
DNA rearrangements associated with a transposable element in yeast. Cell (1980) 7.03
X-chromosome inactivation and developmental patterns in mammals. Biol Rev Camb Philos Soc (1972) 4.80
Localization of the human alpha-globin structural gene to chromosome 16 in somatic cell hybrids by molecular hybridization assay. Cell (1977) 4.34
A family of long reiterated DNA sequences, one copy of which is next to the human beta globin gene. Nucleic Acids Res (1980) 3.91
Insertion of the Drosophila transposable element copia generates a 5 base pair duplication. Cell (1980) 3.63
Effect of chemical modification on the rate of renaturation of deoxyribonucleic acid. Deaminated and glyoxalated deoxyribonucleic acid. Biochemistry (1973) 3.12
Cloning of human satellite III DNA: different components are on different chromosomes. Nucleic Acids Res (1979) 3.01
Construction and characterization of the hybrid bacteriophage lambda Charon vectors for DNA cloning. J Virol (1979) 2.99
Chromosomal localization of human beta globin gene on human chromosome 11 in somatic cell hybrids. Proc Natl Acad Sci U S A (1978) 2.65
Chromosomal localization of complex and simple repeated human DNAs. Chromosoma (1978) 2.65
Insertion of DNA carrying ribosomal protein genes of Escherichia coli into Charon vector phages. J Biol Chem (1977) 2.13
Human Y-chromosome-specific reiterated DNA. Science (1976) 2.02
Isolation and characterization of cloned DNA sequences that hybridize to the human X chromosome. Cell (1980) 1.96
Gene transfer by means of cell fusion I. Statistical mapping of the human X-chromosome by analysis of radiation-induced gene segregation. J Cell Sci (1977) 1.77
Specific arrangements of human satellite III DNA sequences in human chromosomes. Chromosoma (1979) 1.57
Use of formamide in nucleic acid reassociation. Biochemistry (1972) 1.56
The isolation and partial characterization of recombinant DNA containing genomic globin sequences from the goat. J Biol Chem (1979) 1.44
Evolution of a human Y chromosome-specific repeated sequence. Cell (1978) 1.23
The gene numbers game. Cell (1974) 1.21
The specific organisation of satellite DNA sequences on the X-chromosome of Mus musculus: partial independence of chromosome evolution. Nucleic Acids Res (1980) 1.13
Regional mapping of human genes for hexosaminidase B and diphtheria toxin sensitivity on chromosome 5 using mouse X human hybrid cells. Somatic Cell Genet (1977) 1.10
Localisation of 5S ribosomal RNA genes on human chromosome 1. Nature (1974) 1.08
Partial purification and characterization of DNA from the human X chromosome. Proc Natl Acad Sci U S A (1979) 1.01
Organization and heterogeneity of sequences within a repeating unit of human Y chromosome deoxyribonucleic acid. Biochemistry (1979) 1.01
Assignments of the human genes for lactate dehydrogenase-A and thymidine kinase to specific chromosomal regions. Cytogenet Cell Genet (1975) 0.85
The innate immune response to bacterial flagellin is mediated by Toll-like receptor 5. Nature (2001) 14.24
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci U S A (1977) 13.87
The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between toll-like receptors. Proc Natl Acad Sci U S A (2000) 9.67
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature (1991) 8.22
The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell (1992) 8.05
A first-generation X-inactivation profile of the human X chromosome. Proc Natl Acad Sci U S A (1999) 6.59
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure. J Cell Biol (1996) 5.51
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet (1989) 5.48
Five polymorphic microsatellite VNTRs on the human X chromosome. Am J Hum Genet (1990) 5.38
Toll-like receptor-2 mediates mycobacteria-induced proinflammatory signaling in macrophages. Proc Natl Acad Sci U S A (1999) 4.49
Genomic and genetic definition of a functional human centromere. Science (2001) 4.28
Formation of de novo centromeres and construction of first-generation human artificial microchromosomes. Nat Genet (1997) 4.27
Clonal analysis using recombinant DNA probes from the X-chromosome. Cancer Res (1987) 4.25
Uniparental disomy as a mechanism for human genetic disease. Am J Hum Genet (1988) 4.21
Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. J Biol Chem (1990) 3.87
The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts. Blood (1998) 3.69
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature (1991) 3.59
Isolation of cDNA clones coding for the beta subunit of human beta-hexosaminidase. Proc Natl Acad Sci U S A (1985) 3.50
Assignment of the gene for myelin proteolipid protein to the X chromosome: implications for X-linked myelin disorders. Science (1985) 3.43
Cloning of human androgen receptor complementary DNA and localization to the X chromosome. Science (1988) 3.40
Report of the committee on the genetic constitution of the X chromosome. Cytogenet Cell Genet (1989) 3.37
Characterization of a murine gene expressed from the inactive X chromosome. Nature (1991) 3.21
Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes. Proc Natl Acad Sci U S A (1986) 3.21
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence. Genomics (1987) 3.21
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet (1985) 3.08
Isolation and characterization of a major tandem repeat family from the human X chromosome. Nucleic Acids Res (1983) 2.94
The UTX gene escapes X inactivation in mice and humans. Hum Mol Genet (1998) 2.91
Structure, organization, and sequence of alpha satellite DNA from human chromosome 17: evidence for evolution by unequal crossing-over and an ancestral pentamer repeat shared with the human X chromosome. Mol Cell Biol (1986) 2.81
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques. Cytogenet Cell Genet (1984) 2.70
Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques. Cytogenet Cell Genet (1985) 2.70
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome. Cell (1990) 2.70
X inactivation in females with X-linked disease. N Engl J Med (1998) 2.67
Isolation of human fibroblast catalase cDNA clones. Sequence of clones derived from spliced and unspliced mRNA. J Biol Chem (1984) 2.57
Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. Proc Natl Acad Sci U S A (1986) 2.54
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
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosome. J Mol Biol (1985) 2.39
SV40 recombinants carrying rabbit beta-globin gene coding sequences. Cell (1979) 2.35
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation. Nature (1994) 2.32
Chromosome-specific alpha satellite DNA: nucleotide sequence analysis of the 2.0 kilobasepair repeat from the human X chromosome. Nucleic Acids Res (1985) 2.28
Report of the committee on human gene mapping by recombinant DNA techniques. Cytogenet Cell Genet (1987) 2.24
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
Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant. Chromosome Res (2013) 2.12
Translation of immunoglobulin mRNAs in a wheat germ cell-free system. Mol Biol Rep (1974) 2.11
Chromosome-specific organization of human alpha satellite DNA. Am J Hum Genet (1985) 2.10
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy. Nat Med (1998) 2.08
Evolutionary conservation of possible functional domains of the human and murine XIST genes. Hum Mol Genet (1993) 2.05
Human Y-chromosome-specific reiterated DNA. Science (1976) 2.02
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. Am J Hum Genet (1976) 1.90
Replication timing of DNA sequences associated with human centromeres and telomeres. Mol Cell Biol (1990) 1.89
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 introduction of radioisotopes into RNA by methylation in vitro. Biochim Biophys Acta (1967) 1.84
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
Statistical analysis of MPSS measurements: application to the study of LPS-activated macrophage gene expression. Proc Natl Acad Sci U S A (2005) 1.84
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
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotyping. Ann Hum Genet (1999) 1.78
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
Prenatal diagnosis of sickle cell anemia by restriction and endonuclease analysis: HindIII polymorphisms in gamma-globin genes extend test applicability. Proc Natl Acad Sci U S A (1980) 1.71
Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening. Ann Neurol (2001) 1.71
Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. Hum Mol Genet (2001) 1.71
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
Low HLA-C expression at cell surfaces correlates with increased turnover of heavy chain mRNA. J Exp Med (1995) 1.63
Heritability of X chromosome--inactivation phenotype in a large family. Am J Hum Genet (1996) 1.62
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood (1992) 1.62
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
Pharmacological induction of peroxisomes in peroxisome biogenesis disorders. Ann Neurol (2000) 1.59
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
Use of formamide in nucleic acid reassociation. Biochemistry (1972) 1.56
Physical and genetic mapping of the human X chromosome centromere: repression of recombination. Genome Res (1998) 1.53
Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. Proc Natl Acad Sci U S A (1999) 1.52
Adrenoleukodystrophy: phenotypic variability and implications for therapy. J Inherit Metab Dis (1992) 1.52
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
Report of the committee on the genetic constitution of the X chromosome. Cytogenet Cell Genet (1990) 1.51
Gene encoding the beta subunit of S100 protein is on chromosome 21: implications for Down syndrome. Science (1988) 1.49
Stable dicentric X chromosomes with two functional centromeres. Nat Genet (1998) 1.47
Human beta satellite DNA: genomic organization and sequence definition of a class of highly repetitive tandem DNA. Proc Natl Acad Sci U S A (1989) 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
Fecal Isolation of Corynebacterium equi from a Foal with Chronic Diarrhea. Can Vet J (1984) 1.43
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). Cytogenet Cell Genet (1987) 1.40
Recognition and destruction of Bacillus Calmette-Guerin-infected human monocytes. J Exp Med (1993) 1.39
Clinical use of a concomitant boost technique using a gypsum compensator. Int J Radiat Oncol Biol Phys (1994) 1.39
Human ribosomal RNA genes: orientation of the tandem array and conservation of the 5' end. Science (1988) 1.38
A familial centric chromosome fragment. Cytogenetics (1965) 1.38
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