Published in Somatic Cell Genet on September 01, 1978
Incomplete X chromosome dosage compensation in chorionic villi of human placenta. Proc Natl Acad Sci U S A (1985) 1.53
Regulation of the capacity for O6-methylguanine removal from DNA in human lymphoblastoid cells studied by cell hybridization. Mol Cell Biol (1982) 0.83
Isolation of diploid human lymphoblast mutants presumably homozygous for ouabain resistance. Proc Natl Acad Sci U S A (1980) 0.76
Artificial food colors and childhood behavior disorders. Bull N Y Acad Med (1982) 0.75
Enhancing the efficiency of DNA-mediated gene transfer in mammalian cells. Somatic Cell Genet (1981) 7.07
Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation. Proc Natl Acad Sci U S A (1984) 3.53
DNA restriction endonuclease analysis for localization of human beta- and delta-globin genes on chromosome 11. Proc Natl Acad Sci U S A (1979) 3.02
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells. Proc Natl Acad Sci U S A (1981) 2.83
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations. Science (1968) 2.69
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. Am J Hum Genet (1976) 2.51
Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation. Proc Natl Acad Sci U S A (1980) 2.48
Studies of X chromosome DNA methylation in normal human cells. Nature (1982) 2.34
Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity. Proc Natl Acad Sci U S A (1975) 2.30
D-valine as a selective agent for normal human and rodent epithelial cells in culture. Cell (1975) 2.05
Three related centromere proteins are absent from the inactive centromere of a stable isodicentric chromosome. Chromosoma (1985) 2.04
Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes. Nature (1985) 1.96
Human-mouse somatic cell hybrids with single human chromosome (group E): link with thymidine kinase activity. Science (1968) 1.96
Isolation and characterization of cloned DNA sequences that hybridize to the human X chromosome. Cell (1980) 1.96
Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation. Proc Natl Acad Sci U S A (1984) 1.86
Differential expression of steroid sulphatase locus on active and inactive human X chromosome. Nature (1982) 1.75
Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cells. Cell (1982) 1.62
Genetic inactivation of the alpha-galactosidase locus in carriers of Fabry's disease. Science (1970) 1.61
Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations. Somat Cell Mol Genet (1990) 1.58
Mechanism of origin of complete hydatidiform moles. Nature (1980) 1.55
Incomplete X chromosome dosage compensation in chorionic villi of human placenta. Proc Natl Acad Sci U S A (1985) 1.53
Complex chromosome rearrangements. Report of a new case and literature review. Clin Genet (1980) 1.51
Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA. EMBO J (1988) 1.50
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse. Proc Natl Acad Sci U S A (1981) 1.48
Human and mouse hypoxanthine-guanine phosphoribosyltransferase: dimers and tetramers. Science (1979) 1.42
Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3' CpG clusters: implications for X chromosome dosage compensation. Nucleic Acids Res (1984) 1.42
Stability of X chromosomal inactivation in human somatic cells. Nature (1972) 1.38
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cells. Science (1971) 1.37
Evidence for the inactivation of an X chromosome early in the development of the human female. Am J Hum Genet (1975) 1.32
Short arm deletions in group E and chromosomal "deletion" syndromes. J Pediatr (1966) 1.31
Haptoglobin: a locus on the D1 chromosome? Am J Hum Genet (1967) 1.30
Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation. Am J Hum Genet (1971) 1.29
DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation. Proc Natl Acad Sci U S A (1987) 1.22
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells. Nature (1974) 1.22
Isolation and analysis of somatic hybrids derived from two human diploid cells. Proc Natl Acad Sci U S A (1974) 1.18
Asynchronous replication of homologous loci on human active and inactive X chromosomes. Proc Natl Acad Sci U S A (1990) 1.17
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency? Am J Hum Genet (1977) 1.17
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: detection of heterozygotes by selective medium. Biochem Genet (1970) 1.16
Effect of intercellular communication on the selection of intraspecific human hybrids in HAT and ouabain. Somatic Cell Genet (1978) 1.15
The Barr body is a looped X chromosome formed by telomere association. Proc Natl Acad Sci U S A (1991) 1.15
Interferon production and action in mouse, hamster and somatic hybrid mouse-hamster cells. Science (1968) 1.13
Comparison of factor IX methylation on human active and inactive X chromosomes: implications for X inactivation and transcription of tissue-specific genes. EMBO J (1986) 1.13
Assignment of the haemophilia B (factor IX) locus to the q26-qter region of the X chromosome. Ann Hum Genet (1984) 1.10
Signal sequence and DNA-mediated expression of human lysosomal alpha-galactosidase A. Eur J Biochem (1987) 1.09
Stability of the "two active X" phenotype in triploid somatic cells. Cell (1979) 1.07
Quantitation of contact-feeding between somatic cells in culture. Exp Cell Res (1975) 1.07
X-linked Hunter syndrome: the heterozygous phenotype in cell culture. Am J Hum Genet (1977) 1.07
The human NTT gene: identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells. Genomics (1997) 1.06
In search of non-random X inactivation: studies of fetal membranes heterozygous for glucose-6-phosphate dehydrogenase. Am J Hum Genet (1979) 1.06
The nature of thymidine kinase in the human-mouse hybrid cell. Biochem Genet (1969) 1.05
Stability of X chromosomal inactivation in human somatic cells transformed by SV-40. Humangenetik (1975) 1.04
Complete reactivation of X chromosomes from human chorionic villi with a switch to early DNA replication. Proc Natl Acad Sci U S A (1986) 1.03
Implications for X-chromosome regulation from studies of human X-chromosome DNA. Cold Spring Harb Symp Quant Biol (1983) 1.02
Centromeric inactivation in a dicentric human Y;21 translocation chromosome. Chromosoma (1997) 1.01
Selection and cell communication as determinants of female phenotype. Basic Life Sci (1978) 0.99
Characterization of reiterated human DNA with respect to mammalian X chromosome homology. Somat Cell Mol Genet (1984) 0.99
Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genes. Cytogenet Cell Genet (1985) 0.94
Non-random loss of human markers from man-mouse somatic cell hybrids. Nature (1974) 0.93
Comparison of contact-mediated communication in normal and transformed human cells in culture. Proc Natl Acad Sci U S A (1977) 0.89
Studies of human-mouse cell hybrids with respect to X-chromosome inactivation. Basic Life Sci (1978) 0.89
DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation. Somat Cell Mol Genet (1993) 0.89
Genetic disorders of male sexual differentiation. Adv Hum Genet (1980) 0.88
Androgen receptors and metabolism in cultured human fetal fibroblasts. Pediatr Res (1980) 0.88
Relationship of finite proliferative lifespan, senescence, and quiescence in human cells. J Cell Physiol (1985) 0.88
Hybridization of mammalian somatic cells. Prog Med Genet (1970) 0.87
Competence for DNA transfer of ouabain resistance and thymidine kinase: clonal variation in mouse L-cell recipients. Somatic Cell Genet (1981) 0.87
Effect of ouabain resistance on human diploid fibroblasts carrying other genetic variants. Exp Cell Res (1975) 0.86
In search of nonrandom X inactivation: studies of the placenta from newborns heterozygous for glucose-6-phosphate dehydrogenase. Basic Life Sci (1978) 0.86
Unreliability of the microcomplement fixation method for Xga typing of cultured fibroblasts. Birth Defects Orig Artic Ser (1976) 0.86
Sex differences in activity of glucose 6-phosphate dehydrogenase from cultured human fetal lung cells despite X-inactivation. Biochem Genet (1973) 0.86
Contact-mediated communication of ouabain resistance in mammalian cells in culture. Nature (1977) 0.85
Translocation of the nucleolus organizer region to the human X chromosome. Am J Hum Genet (1986) 0.85
DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late. Am J Hum Genet (1994) 0.85
Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation. Am J Hum Genet (1974) 0.85
The postulated X-inactivation center at Xq27 is most reasonably explained by ascertainment bias: heterozygous expression of recessive mutations is a powerful means of detecting unbalanced X inactivation. Am J Hum Genet (1993) 0.84
Hybridization of somatic cells derived from mouse and syrian hamster: evolution of karyotype and enzyme studies. Biochem Genet (1968) 0.84
Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters. Mol Cell Biol (1989) 0.83
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland. Pediatr Res (1982) 0.83
Familial skewed X inactivation and X-linked mutations: unbalanced X inactivation is a powerful means to ascertain X-linked genes that affect cell proliferation. Am J Hum Genet (1998) 0.83
Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase. Am J Hum Genet (1981) 0.82
Hyperexpression of HPRT induced by 5-azacytidine in mouse-human hybrid reactivants. Am J Hum Genet (1985) 0.82
Studies of X-chromosome inactivation in trisomies. Cytogenet Cell Genet (1989) 0.81
Familial occurrence of the somatic phenotype of Turner's syndrome. Johns Hopkins Med J (1967) 0.81
Evidence for a relationship between DNA methylation and DNA replication from studies of the 5-azacytidine-reactivated allocyclic X chromosome. Exp Cell Res (1985) 0.81
Molecular characterization of tiny ring X chromosomes from females with functional X chromosome disomy and lack of cis X inactivation. Genomics (1995) 0.81
Thyroxin, satellite association and trisomy. Nature (1966) 0.80
XIST expression is repressed when X inactivation is reversed in human placental cells: a model for study of XIST regulation. Somat Cell Mol Genet (1995) 0.80
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome. Ann Genet (2001) 0.80
Evidence for two active X chromosomes in germ cells of female before meiotic entry. Nature (1977) 0.80
Enrichment of human heterokaryons by Ficoll gradient for complementation analysis of iduronate sulfatase deficiency. Somatic Cell Genet (1979) 0.79
Glucose-6-phosphate dehydrogenase as a probe for the study of X-chromosome inactivation in hunan females. Isozymes Curr Top Biol Med Res (1983) 0.78
Reactivation of X-linked genes in human fibroblasts transformed by origin-defective SV40. Somat Cell Mol Genet (1986) 0.78
The XIST locus replicates late on the active X, and earlier on the inactive X based on FISH DNA replication analysis of somatic cell hybrids. Somat Cell Mol Genet (1995) 0.78
Renal enzymes in kidney cells selected by D-valine medium. J Cell Physiol (1977) 0.78