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Science. 1968 Apr 26;160(3826):425-7
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Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells.
Proc Natl Acad Sci U S A. 1968 Jun;60(2):545-52
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Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes.
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Non-inactivation of an x-chromosome locus in man.
Science. 1979 Jun 15;204(4398):1224-6
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Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier.
Lancet. 1980 Jan 12;1(8159):63-5
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Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
Proc Natl Acad Sci U S A. 1981 Aug;78(8):5066-70
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Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cells.
Cell. 1982 Jun;29(2):595-600
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Genetic homology and crossing over in the X and Y chromosomes of Mammals.
Hum Genet. 1982;61(2):85-90
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Differential expression of steroid sulphatase locus on active and inactive human X chromosome.
Nature. 1982 Oct 28;299(5886):838-40
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Isolation and characterization of a major tandem repeat family from the human X chromosome.
Nucleic Acids Res. 1983 Apr 11;11(7):2017-33
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Cytologic evidence for three human X-chromosomal segments escaping inactivation.
Hum Genet. 1983;63(2):171-4
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Cytologic and molecular analysis of 46,XXq- cells to identify a DNA segment that might serve as a probe for a putative human X chromosome inactivation center.
Hum Genet. 1983;64(1):33-8
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Mammalian X-chromosome inactivation.
Annu Rev Genet. 1983;17:155-90
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A sensitive and dependable assay for distinguishing hamster and human X-linked steroid sulfatase activity in somatic cell hybrids.
Hum Genet. 1984;66(2-3):272-5
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The cell surface antigen locus, MIC2X, escapes X-inactivation.
Am J Hum Genet. 1984 Jul;36(4):777-82
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Mammalian X chromosome inactivation: testing the hypothesis of transcriptional control.
Somat Cell Mol Genet. 1986 May;12(3):275-80
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Fine mapping of the distal short arm of the human X chromosome using X/Y translocations.
Am J Hum Genet. 1986 Jun;38(6):884-90
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Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.
Mol Cell Biol. 1986 Nov;6(11):4122-5
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Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
N Engl J Med. 1987 Feb 19;316(8):427-31
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The sex-determining region of the human Y chromosome encodes a finger protein.
Cell. 1987 Dec 24;51(6):1091-104
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Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome.
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5605-9
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A-11: cell type-specific and single-active-X transcription controls of newly found gene in cultured human cells.
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Cytogenet Cell Genet. 1988;49(1-3):254-6
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The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome.
Nature. 1989 Jan 5;337(6202):81-4
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Gene on short arm of human X chromosome complements murine tsA1S9 DNA synthesis mutation.
Somat Cell Mol Genet. 1989 Mar;15(2):173-8
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DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS.
Proc Natl Acad Sci U S A. 1963 Sep;50:481-5
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Enzyme electrophoresis on cellulose acetate gel: zymogram patterns in mgh-mouse and man--Chinese hamster somatic cell hybrids.
Arch Biochem Biophys. 1971 Aug;145(2):470-83
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X-chromosome inactivation and developmental patterns in mammals.
Biol Rev Camb Philos Soc. 1972 Jan;47(1):1-35
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X chromosome inactivation in cells from an individual heterozygous for two X-linked genes.
Nat New Biol. 1972 Apr 5;236(66):149-50
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X chromosome inactivation in X-linked hypohidrotic ectodermal dysplasia.
Nat New Biol. 1973 Sep 12;245(141):58-9
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Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity.
Proc Natl Acad Sci U S A. 1975 Apr;72(4):1469-72
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Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy.
Am J Hum Genet. 1976 May;28(3):213-27
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Preliminary characterization of the temperature-sensitive defect in DNA replication in a mutant mouse L cell.
Cell. 1976 Jan;7(1):49-57
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