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The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

Data up to Jan 2025

Published1993
Citations345
References24

Total Citations Per Year

Abstract

References (24)

Parental imprinting of the mouse insulin-like growth factor II gene

1991 • 1,773 citations

Parental imprinting of the mouse H19 gene

1991 • 1,192 citations

Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryo development

1987 • 1,088 citations

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1991 • 904 citations

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line.

1992 • 729 citations

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal

1993 • 602 citations

Parental-origin-specific epigenetic modification of the mouse H19 gene

1993 • 419 citations

Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation

1987 • 363 citations

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1992 • 279 citations

Physical linkage of two mammalian imprinted genes, H19 and insulin–like growth factor 2

1992 • 261 citations

Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis

1991 • 246 citations

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region

1992 • 243 citations

A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes

1992 • 212 citations

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

1992 • 203 citations

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

1990 • 161 citations

Additional microsatellite markers for mouse genome mapping

1991 • 158 citations

Demethylation of CpG islands in embryonic cells

1991 • 151 citations

PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluation.

1992 • 123 citations

Transgenes as molecular probes for genomic imprinting

1988 • 108 citations

Methylation of CpG sites of two X–linked genes coincides with X–inactivation in the female mouse embryo but not in the germ line

1992 • 90 citations

Methylation patterns of testis-specific genes.

1991 • 85 citations

Methylation changes in the apolipoprotein AI gene during embryonic development of the mouse.

1991 • 58 citations

Parental methylation patterns of a transgenic locus in adult somatic tissues are imprinted during gametogenesis

1992 • 57 citations

Isolation of viable mouse primordial germ cells by antibody‐directed flow sorting

1987 • 36 citations

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The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. (1993) – The EMBO Journal | Metascience Observatory Explorer