Published in Genet Res on August 01, 1981
Use of a HpaII-polymerase chain reaction assay to study DNA methylation in the Pgk-1 CpG island of mouse embryos at the time of X-chromosome inactivation. Mol Cell Biol (1990) 3.78
Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation. Nucleic Acids Res (1997) 1.20
Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation. Proc Natl Acad Sci U S A (1992) 1.19
Genetic control of X chromosome inactivation in mice: definition of the Xce candidate interval. Genetics (2006) 1.14
An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse. Genetics (2003) 0.87
Genetic architecture of skewed X inactivation in the laboratory mouse. PLoS Genet (2013) 0.84
X-inactivation analysis of embryonic lethality in Ocrl wt/-; Inpp5b-/- mice. Mamm Genome (2010) 0.83
Nonrandom X chromosome inactivation is influenced by multiple regions on the murine X chromosome. Genetics (2012) 0.80
Differential activity of maternally and paternally derived chromosome regions in mice. Nature (1985) 4.02
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nat Genet (1997) 3.32
Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature (1993) 3.11
Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature (1991) 2.31
Risks of radiation at low dose rates. Lancet (1981) 1.78
Parental origin effects in mice. J Embryol Exp Morphol (1986) 1.77
Sex-reversed mice: XX and XO males. Cytogenetics (1971) 1.76
Gonadotrophin-releasing hormone deficiency in a mutant mouse with hypogonadism. Nature (1977) 1.71
Mouse homologues of the human AZF candidate gene RBM are expressed in spermatogonia and spermatids, and map to a Y chromosome deletion interval associated with a high incidence of sperm abnormalities. Hum Mol Genet (1998) 1.69
Position effect variegation in the mouse. Genet Res (1974) 1.63
Tumour induction by methyl-nitroso-urea following preconceptional paternal contamination with plutonium-239. Br J Cancer (1998) 1.50
Nodisjunction and reduced fertility caused by the tobacco mouse metacentric chromosomes. Cytogenet Cell Genet (1973) 1.45
Mapping the murine Xce locus with (CA)n repeats. Mamm Genome (1993) 1.41
Evidence of non-random X chromosome activity in the mouse. Genet Res (1972) 1.39
Chromosomal instability in the descendants of unirradiated surviving cells after alpha-particle irradiation. Proc Natl Acad Sci U S A (1998) 1.35
Meitoic crossing-over between the X and Y chromosomes of male mice carrying the sex-reversing (Sxr) factor. Nature (1982) 1.35
Controlling elements in the mouse X chromosome. Genetics (1967) 1.29
Molecular genetic characterization of six recessive viable alleles of the mouse agouti locus. Genetics (1995) 1.28
Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2. Dev Biol (1997) 1.27
The location of Cattanach's translocation in the X-chromosome linkage map of the mouse. Genet Res (1966) 1.21
Controlling elements in the mouse. IV. Evidence of non-random X-inactivation. Genet Res (1981) 1.21
Controlling elements in the mouse X-chromosome. I. Interaction with the X-linked genes. Genet Res (1969) 1.20
Control of chromosome inactivation. Annu Rev Genet (1975) 1.18
Male, female and intersex development in mice of identical chromosome constitution. Nature (1982) 1.13
The response of spontaneous and transplantable murine tumors to vasoactive agents measured by 31P magnetic resonance spectroscopy. Int J Radiat Oncol Biol Phys (1992) 1.10
In vivo chromosomal instability and transmissible aberrations in the progeny of haemopoietic stem cells induced by high- and low-LET radiations. Int J Radiat Biol (2001) 1.08
Ethyl methanesulfonate-induced chromosome breakage in the mouse. Mutat Res (1969) 1.06
Serological evidence for H-Y antigen in Sxr, XX sex-reversal phenotypic males. Nature (1977) 1.05
Controlling elements in the mouse X-chromosome. II. Location in the linkage map. Genet Res (1970) 1.04
Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal. Nat Genet (1993) 0.99
A test of distributive pairing between two specific non-homologous chromosomes in the mouse. Cytogenetics (1967) 0.98
Genetic control over the inactivation of autosomal genes attached to the X-chromosome. Z Vererbungsl (1965) 0.98
Imprinting of distal mouse chromosome 2 is associated with phenotypic anomalies in utero. Genet Res (1998) 0.98
Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7. Genomics (2000) 0.97
Controlling elements in the mouse X-chromosome. 3. Influence upon both parts of an X divided by rearrangement. Genet Res (1970) 0.93
Activation of an imprinted Igf 2 gene in mouse somatic cell cultures. Mol Cell Biol (1993) 0.91
Chemically induced mutations in mice. Mutat Res (1966) 0.91
Chromosome 2 hypersensitivity and clonal development in murine radiation acute myeloid leukaemia. Int J Radiat Biol (1997) 0.91
Susceptibility to radiation-induced leukaemia/lymphoma is genetically separable from sensitivity to radiation-induced genomic instability. Int J Radiat Biol (2001) 0.90
Time of initiation and site of action of the mouse chromosome 11 imprinting effects. Genet Res (1996) 0.90
Ubiquitous expression and imprinting of Snrpn in the mouse. Mamm Genome (1995) 0.90
Dose- and time-response relationships for lethal mutations and chromosomal instability induced by ionizing radiation in an immortalized human keratinocyte cell line. Int J Radiat Biol (2000) 0.89
Induction of paternal sex-chromosome losses and deletions and of autosomal gene mutations by the treatment of mouse post-meiotic germ cells with triethylenemelamine. Mutat Res (1967) 0.89
Identification of the linkage groups carried by the metacentric chromosomes of the tobacco mouse (Mus poschiavinus). Cytogenetics (1972) 0.88
Dependence of the yield of DNA double-strand breaks in Chinese hamster V79-4 cells on the photon energy of ultrasoft X rays. Radiat Res (2001) 0.86
Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2. Cytogenet Cell Genet (1998) 0.86
Investigation of lung tumour induction in BALB/cJ mice following paternal X-irradiation. Int J Radiat Biol (1995) 0.86
Abnormally high variability in the uncrossed retinofugal pathway of mice with albino mosaicism. Development (1987) 0.86
A comparative study of the coats of chimaeric mice and those of heterozygotes for X-linked genes. Genet Res (1972) 0.86
Genetic mechanisms determining the central visual pathways of mice. Science (1973) 0.86
Molecular genetic analysis of the Ta25H deletion: evidence for additional deleted loci. Mamm Genome (1991) 0.86
Rumpshaker mouse: a new X-linked mutation affecting myelination: evidence for a defect in PLP expression. J Neurocytol (1990) 0.86
Y chromosome short arm-Sxr recombination in XSxr/Y males causes deletion of Rbm and XY female sex reversal. Proc Natl Acad Sci U S A (1995) 0.85
Murine radiation myeloid leukaemogenesis: a possible role for radiation-sensitive sites on chromosome 2. Genes Chromosomes Cancer (1991) 0.85
A search for chromosome aberrations induced in mouse spermatogonia by chemical mutagens. Mutat Res (1971) 0.85
Sex chromosome pairing patterns in male mice of novel Sxr genotypes. Chromosoma (1989) 0.84
Interaction between the Xce locus and imprinting of the paternal X chromosome in mouse yolk-sac endoderm. Nature (1983) 0.84
X-inactivation of the Sts locus in the mouse: an anomaly of the dosage compensation mechanism. Genet Res (1989) 0.82
Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes disease. J Med Genet (1997) 0.81
Crossover suppression in mice heterozygous for tobacco mouse metacentrics. Cytogenet Cell Genet (1978) 0.81
The mouse mutation ulnaless on chromosome 2. J Hered (1990) 0.81
Haematopoietic role for Patch (Ph) revealed by new W mutant (Wct) in mice. Genet Res (1983) 0.81
Murine radiation myeloid leukaemogenesis: relationship between interstitial telomere-like sequences and chromosome 2 fragile sites. Genes Chromosomes Cancer (1993) 0.81
Rumpshaker: an X-linked mutation affecting CNS myelination. A study of the female heterozygote. Neuropathol Appl Neurobiol (1991) 0.81
The naevoid basal-cell carcinoma syndrome (Gorlin syndrome) is a chromosomal instability syndrome. Mutat Res (1998) 0.80
A genetically determined variant of the A-subunit of lactic dehydrogenase in the deer mouse. Biochem Genet (1969) 0.80
Investigation of lung tumour induction in C3H/HeH mice, with and without tumour promotion with urethane, following paternal X-irradiation. Mutat Res (1998) 0.79
Conscious sedation for interventional neuroradiology: a comparison of midazolam and propofol infusion. Can J Anaesth (1997) 0.78
Irradiation of DNA with 193 nm light yields formamidopyrimidine-DNA glycosylase(Fpg) protein-sensitive lesions. Photochem Photobiol (1997) 0.78
Carcinogenicity of radon/radon decay product inhalation in rats--effect of dose, dose rate and unattached fraction. Int J Radiat Biol (2005) 0.78
An XYY sex-chromosome constitution in the mouse. Cytogenetics (1969) 0.78
Parental influence on X-autosome translocation-induced variegation in the mouse. Genet Res (1970) 0.78
Testicular steroidogenesis in X/X sex-reversed mice. Int J Androl (1991) 0.77
Translocation yield from the immature mouse testis and the nature of spermatogonial stem cell heterogeneity. Mutat Res (1977) 0.77
Regulation of the apoptotic response to radiation damage in B cell development. Cell Death Differ (1998) 0.77
An attempt to distinguish a modified genetic response of the mouse testis to X-ray exposure by the action of a spermatogonial chalone. Mutat Res (1979) 0.77
Induction of specific-locus mutations in female mice by triethylenemelamine (TEM). Mutat Res (1982) 0.77
Evidence of chromosomal instability in the lymphocytes of Gorlin basal-cell carcinoma patients. Mutat Res (1995) 0.77
Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa. Mech Dev (2000) 0.76
The genetics of Sleek: a possible regulatory mutation of the tabby-crinkled-downless syndrome. Genet Res (1979) 0.76
The radiosensitivity of spermatogonial stem cells in C3H/101 F1 hybrid mice. Mutat Res (1993) 0.75
Comments on the estimated distance over which electrons can migrate in solid DNA before being trapped by misonidazole. Radiat Res (1991) 0.75
Spermatogonial stem cell killing in the mouse following single and fractionated x-ray doses, as assessed by length of sterile period. Mutat Res (1974) 0.75
The molars of tabby chimaeras in the mouse. Proc R Soc Lond B Biol Sci (1972) 0.75
Genetic effects of combined chemical-X-ray treatments in male mouse germ cells. Int J Radiat Biol Relat Stud Phys Chem Med (1987) 0.75
Hindshaker, a novel myelin mutant showing hypomyelination preferentially affecting the spinal cord. J Neurocytol (1997) 0.75
The mutagenicity of cyclamates and their metabolites. Mutat Res (1976) 0.75
Control scheme for familial nephropathy in cocker spaniels. Vet Rec (1987) 0.75
Translocation and specific locus mutation response of mouse spermatogonial stem cells to fractionated and combined X-ray chemical mutagen treatments. Prog Clin Biol Res (1986) 0.75
Evidence for the re-establishment of a heterogeneity in radiosensitivity among spermatogonial stem cells repopulating the mouse testis following depletion by X-rays. Mutat Res (1984) 0.75
Modified genetic response to X-irradiation of mouse spermatogonial stem cells surviving treatment with TEM. Mutat Res (1980) 0.75
Translocation yield from mouse spermatogonial stem cells following unequal-sized x-ray fractionations: evidence of radiation-induced loss of heterogeneity. Mutat Res (1979) 0.75
X-ray induction of translocations in mice carrying metacentrics (Robertsonian fusions); detection of whole arm chromosome exchanges. Mutat Res (1981) 0.75
Enhanced spermatogonial stem cell killing and reduced translocation yield from X-irradiated 101/H mice. Mutat Res (1987) 0.75
Enzyme levels in testis and other tissues of genetically sex-reversed mice. J Reprod Fertil (1979) 0.75
Mutagenicity tests with cyclohexylamine in the mouse. Mutat Res (1971) 0.75
Snaker: a dominant abnormality caused by chromosomal imbalance. Z Vererbungsl (1965) 0.75
Sterile period, translocation and specific locus mutation in the mouse following fractionated x-ray treatments with different fractionation intervals. Mutat Res (1974) 0.75
Genetic tests for autosomal non-disjunction and chromosome loss in mice. Mutat Res (1984) 0.75