Published in J Exp Zool on March 01, 1983
Intercellular interactions, position, and polarity in establishing blastocyst cell lineages and embryonic axes. Cold Spring Harb Perspect Biol (2012) 1.00
Myosin rings and spreading in mouse blastomeres. J Cell Biol (1984) 0.80
The polycomb-group gene Ezh2 is required for early mouse development. Mol Cell Biol (2001) 7.20
Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature (1984) 4.22
Eomesodermin is required for mouse trophoblast development and mesoderm formation. Nature (2000) 3.53
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat Genet (1998) 3.38
Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature (1993) 3.11
Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science (1999) 3.07
Genomic imprinting determines methylation of parental alleles in transgenic mice. Nature (1987) 2.71
Imprinting and the epigenetic asymmetry between parental genomes. Science (2001) 2.56
Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells. EMBO J (1997) 2.34
Skin hyperkeratosis and papilloma formation in transgenic mice expressing a ras oncogene from a suprabasal keratin promoter. Cell (1990) 2.34
Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature (1991) 2.31
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. Genes Dev (1992) 2.19
Transgenes as probes for active chromosomal domains in mouse development. Nature (1988) 2.16
Role of paternal and maternal genomes in mouse development. Nature (1984) 2.12
Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. Nat Genet (1996) 2.06
Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis. Prenat Diagn (1998) 2.04
Sex determination of preimplantation embryos. Lancet (1994) 2.00
Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisation. Nucleic Acids Res (1999) 1.94
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q. Genes Cells (2000) 1.90
Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development. Cell (1994) 1.86
Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. Hum Genet (1997) 1.77
The human blastocyst: cell number, death and allocation during late preimplantation development in vitro. Development (1989) 1.77
Epigenetic control of transgene expression and imprinting by genotype-specific modifiers. Cell (1990) 1.70
The fragilis interferon-inducible gene family of transmembrane proteins is associated with germ cell specification in mice. BMC Dev Biol (2003) 1.70
Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. Development (2000) 1.68
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nat Genet (1995) 1.67
The importance of the 3'-enhancer region in immunoglobulin kappa gene expression. Nucleic Acids Res (1990) 1.56
Genomic imprinting and the differential roles of parental genomes in brain development. Brain Res Dev Brain Res (1996) 1.54
Changes in the organization of the mouse egg plasma membrane upon fertilization and first cleavage: indications from the lateral diffusion rates of fluorescent lipid analogs. Dev Biol (1981) 1.46
Epigenotype switching of imprintable loci in embryonic germ cells. Dev Genes Evol (1998) 1.44
Imprinting of Igf2 and H19 from a 130 kb YAC transgene. Development (1997) 1.43
A functional analysis of imprinting in parthenogenetic embryonic stem cells. Development (1994) 1.41
Nuclear transplantation in the mouse: heritable differences between parental genomes after activation of the embryonic genome. Cell (1986) 1.40
Preimplantation genetic diagnosis of beta-thalassaemia major. Lancet (1996) 1.39
Segmental and developmental regulation of a presumptive T-cell oncogene in the central nervous system. Nature (1990) 1.38
Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene. Proc Natl Acad Sci U S A (1998) 1.37
Establishment of pluripotential cell lines from haploid mouse embryos. J Embryol Exp Morphol (1983) 1.36
Increased number of cells and metabolic activity in male human preimplantation embryos following in vitro fertilization. J Reprod Fertil (1995) 1.35
Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome. Hum Mol Genet (2001) 1.34
Dual fluorescent in situ hybridisation for simultaneous detection of X and Y chromosome-specific probes for the sexing of human preimplantation embryonic nuclei. Hum Genet (1992) 1.34
The Splotch mutation interferes with muscle development in the limbs. Anat Embryol (Berl) (1993) 1.34
An imprinting element from the mouse H19 locus functions as a silencer in Drosophila. Nat Genet (1997) 1.34
Human preimplantation development in vitro is not adversely affected by biopsy at the 8-cell stage. Hum Reprod (1990) 1.31
Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. Development (1995) 1.31
Transgenes as molecular probes for genomic imprinting. Trends Genet (1988) 1.31
Increased body fat in mice with a targeted mutation of the paternally expressed imprinted gene Peg3. FASEB J (2005) 1.31
Imprinted genes and regulation of gene expression by epigenetic inheritance. Curr Opin Cell Biol (1996) 1.28
Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH). Hum Mol Genet (1993) 1.28
Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2. Dev Biol (1997) 1.27
Identification of the sex of human preimplantation embryos in two hours using an improved spreading method and fluorescent in-situ hybridization (FISH) using directly labelled probes. Hum Reprod (1994) 1.24
Reduced allele dropout in single-cell analysis for preimplantation genetic diagnosis of cystic fibrosis. J Assist Reprod Genet (1996) 1.22
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn (1995) 1.22
Development of gynogenetic eggs in the mouse: implications for parthenogenetic embryos. Science (1983) 1.20
Effects of pyruvate and glucose on the development of human preimplantation embryos in vitro. J Reprod Fertil (1993) 1.20
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus. Hum Mol Genet (2001) 1.20
Effect of microvilli on lateral diffusion measurements made by the fluorescence photobleaching recovery technique. Biophys J (1982) 1.19
Adult phenotype in the mouse can be affected by epigenetic events in the early embryo. Development (1993) 1.19
Loss of Xist imprinting in diploid parthenogenetic preimplantation embryos. Dev Biol (2001) 1.18
Imprinted expression of neuronatin from modified BAC transgenes reveals regulation by distinct and distant enhancers. Dev Biol (2001) 1.16
Binucleate blastomeres in preimplantation human embryos in vitro: failure of cytokinesis during early cleavage. J Reprod Fertil (1993) 1.16
Provision of the immunoglobulin heavy chain enhancer downstream of a test gene is sufficient to confer lymphoid-specific expression in transgenic mice. Eur J Immunol (1987) 1.15
Diagnosis of sex in preimplantation embryos by fluorescent in situ hybridisation. BMJ (1993) 1.13
Genomic structure and parent-of-origin-specific methylation of Peg1. Hum Mol Genet (1997) 1.12
A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice. Proc Natl Acad Sci U S A (1999) 1.12
Increasing the denaturation temperature during the first cycles of amplification reduces allele dropout from single cells for preimplantation genetic diagnosis. Mol Hum Reprod (1996) 1.11
Non-invasive measurement of glucose and pyruvate uptake by individual human oocytes and preimplantation embryos. Hum Reprod (1989) 1.10
A repertoire of monoclonal antibodies with human heavy chains from transgenic mice. Proc Natl Acad Sci U S A (1989) 1.08
Unusual cell specific expression of a major human cytomegalovirus immediate early gene promoter-lacZ hybrid gene in transgenic mouse embryos. Mech Dev (1991) 1.08
Lack of somatic mutation in a kappa light chain transgene. Eur J Immunol (1990) 1.08
Selection criteria for human embryo transfer: a comparison of pyruvate uptake and morphology. J Assist Reprod Genet (1993) 1.08
Co-expression of the HGF/SF and c-met genes during early mouse embryogenesis precedes reciprocal expression in adjacent tissues during organogenesis. Dev Genet (1996) 1.07
Cancer genetics. Genomic imprinting and embryonal tumours. Nature (1989) 1.07
A rapid procedure for visualising the inner cell mass and trophectoderm nuclei of mouse blastocysts in situ using polynucleotide-specific fluorochromes. J Exp Zool (1984) 1.06
Distribution of antibody- and lectin-binding sites on dissociated blastomeres from mouse morulae: evidence for polarization at compaction. J Embryol Exp Morphol (1980) 1.06
Comparative analysis of Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region. Genomics (1994) 1.06
Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors. J Biochem (2000) 1.05
A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC. Genomics (2000) 1.05
Clinical experience with preimplantation diagnosis of sex by dual fluorescent in situ hybridization. J Assist Reprod Genet (1994) 1.04
Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch. Development (2000) 1.04
A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis. Prenat Diagn (2001) 1.04
Developmental potential of mouse primordial germ cells. Development (1999) 1.03
Isotype exclusion and transgene down-regulation in immunoglobulin-lambda transgenic mice. Nature (1989) 1.02
Developmentally regulated and tissue specific expression of mRNAs encoding the two alternative forms of the LIM domain oncogene rhombotin: evidence for thymus expression. Oncogene (1991) 1.02
A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene. Development (2000) 1.01
Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb. Mech Dev (2000) 1.01
The origin of genetic defects in the human and their detection in the preimplantation embryo. Hum Reprod Update (1995) 1.00
Time of commitment of inside cells isolated from preimplantation mouse embryos. J Embryol Exp Morphol (1978) 1.00
XIST expression from the maternal X chromosome in human male preimplantation embryos at the blastocyst stage. Hum Mol Genet (1997) 1.00
Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes. Hum Reprod (1991) 0.99
Nuclear cytoplasmic interactions following nuclear transplantation in mouse embryos. Development (1987) 0.99
Preimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli. J Assist Reprod Genet (1998) 0.98
Genome-wide methylation patterns in normal and uniparental early mouse embryos. Hum Mol Genet (2001) 0.98
Preimplantation prevention of X-linked disease: reliable and rapid sex determination of single human cells by restriction analysis of simultaneously amplified ZFX and ZFY sequences. Hum Mol Genet (1993) 0.98
Influence of paternally imprinted genes on development. Development (1991) 0.97
Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7. Genomics (2000) 0.97
Normal postimplantation development of mouse parthenogenetic embryos to the forelimb bud stage. Nature (1977) 0.97
Use of triple tissue blastocyst reconstitution to study the development of diploid parthenogenetic primitive ectoderm in combination with fertilization-derived trophectoderm and primitive endoderm. Genet Res (1991) 0.96
Human antibody production in transgenic mice: expression from 100 kb of the human IgH locus. Eur J Immunol (1991) 0.96
Temporal and spatial patterns of the synthesis of tissue-specific polypeptides in the preimplantation mouse embryo. J Embryol Exp Morphol (1978) 0.96
Lack of cell cycle checkpoints in human cleavage stage embryos revealed by a clonal pattern of chromosomal mosaicism analysed by sequential multicolour FISH. Zygote (2000) 0.96