Published in Nature on March 19, 1966
Satellite association and trisomy in thyrotoxicosis. J Med Genet (1968) 0.75
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
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
Human and mouse hypoxanthine-guanine phosphoribosyltransferase: dimers and tetramers. Science (1979) 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
The Barr body is a looped X chromosome formed by telomere association. Proc Natl Acad Sci U S A (1991) 1.15
Effect of intercellular communication on the selection of intraspecific human hybrids in HAT and ouabain. Somatic Cell Genet (1978) 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
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
Stability of the "two active X" phenotype in triploid somatic cells. Cell (1979) 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
The influence of patients' age and tumor grade on the prognosis of carcinoma of the cervix. Cancer (1983) 1.01
Management of adenoid cystic carcinoma of the uterine cervix (cylindroma): report of six cases and reappraisal of all cases reported in the medical literature. Cancer (1980) 1.00
A comparison of unscheduled DNA synthesis, D 0 , cell recovery, and chromosome number in x-irradiated mammalian cell lines. Radiat Res (1971) 0.99
Characterization of reiterated human DNA with respect to mammalian X chromosome homology. Somat Cell Mol Genet (1984) 0.99
Selection and cell communication as determinants of female phenotype. Basic Life Sci (1978) 0.99
Angiosarcomas of the uterus and ovary: clinicopathologic report. Cancer (1982) 0.98
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
Unusual metastases from carcinoma of the lung. J Can Assoc Radiol (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
Gene expression in euploid human hybrid cells: ouabain resistance is codominant. Somatic Cell Genet (1978) 0.88
Pathophysiology of chronic communicating hydrocephalus in dogs (Canis familiaris). Experimental studies. J Neurol Sci (1975) 0.88
Androgen receptors and metabolism in cultured human fetal fibroblasts. Pediatr Res (1980) 0.88
Hybridization of mammalian somatic cells. Prog Med Genet (1970) 0.87
Effect of ouabain resistance on human diploid fibroblasts carrying other genetic variants. Exp Cell Res (1975) 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
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
Translocation of the nucleolus organizer region to the human X chromosome. Am J Hum Genet (1986) 0.85
Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation. Am J Hum Genet (1974) 0.85
Contact-mediated communication of ouabain resistance in mammalian cells in culture. Nature (1977) 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
Hybridization of somatic cells derived from mouse and syrian hamster: evolution of karyotype and enzyme studies. Biochem Genet (1968) 0.84
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
The mechanism of 67 Ga association with lymphocytes. Cancer Res (1974) 0.83
Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters. Mol Cell Biol (1989) 0.83
Compensatory renal hyperplasia. J Urol (1967) 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
Radiosensitivity and repair time: the repair time of chromosome breaks produced during the different stages of the cell cycle. Mutat Res (1969) 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
Angiosarcoma of the vagina: a clinicopathologic report. A reappraisal of the radiation treatment of angiosarcomas of the female genital tract. Cancer (1983) 0.82
Hyperexpression of HPRT induced by 5-azacytidine in mouse-human hybrid reactivants. Am J Hum Genet (1985) 0.82
Retreatment of very late recurrent invasive squamous cell carcinoma of the cervix with irradiation. II. Criteria for patients' selection to achieve the success. Cancer (1984) 0.82
The repair time of chromosome breaks induced by pulsed x-rays on ultra-high dose-rate. Int J Radiat Biol Relat Stud Phys Chem Med (1969) 0.82
Technetium-99m-labeled lymphocytes: a radiotoxicity study. J Nucl Med (1986) 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
Familial occurrence of the somatic phenotype of Turner's syndrome. Johns Hopkins Med J (1967) 0.81
Studies of X-chromosome inactivation in trisomies. Cytogenet Cell Genet (1989) 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
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome. Ann Genet (2001) 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