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Disruption of imprinting caused by deletion of the H19 gene region in mice
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title
Disruption of imprinting caused by deletion of the H19 gene region in mice
(English)
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author name string
P A Leighton
series ordinal
1
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R S Ingram
series ordinal
2
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J Eggenschwiler
series ordinal
3
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A Efstratiadis
series ordinal
4
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S M Tilghman
series ordinal
5
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language of work or name
English
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publication date
4 May 1995
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published in
Nature
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volume
375
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page(s)
34-9
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issue
6526
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cites work
Differential imprinting and expression of maternal and paternal genomes
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7 January 2021
based on heuristic
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Parental imprinting of autosomal mammalian genes
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Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors
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Genomic imprinting of Mash2, a mouse gene required for trophoblast development
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Essential role of Mash-2 in extraembryonic development
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Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting.
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Parental imprinting of the mouse insulin-like growth factor II gene.
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
The product of the H19 gene may function as an RNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F375034A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the mouse H19 gene
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F375034A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
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7 January 2021
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inferred from DOI database lookup
Parental-origin-specific epigenetic modification of the mouse H19 gene
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Crossref
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Role for DNA methylation in genomic imprinting
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The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.
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A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.
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The mouse Pgk-1 gene promoter contains an upstream activator sequence
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Cloning and expression of the mouse pgk-1 gene and the nucleotide sequence of its promoter.
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Ectopic expression of the H19 gene in mice causes prenatal lethality
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A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.
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Tumour-suppressor activity of H19 RNA
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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
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7 January 2021
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Two regulatory domains flank the mouse H19 gene
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7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
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7 January 2021
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Epigenetic lesions at the H19 locus in Wilms' tumour patients
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Crossref
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7 January 2021
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inferred from DOI database lookup
Cell-specific expression of the rat insulin gene: evidence for role of two distinct 5' flanking elements
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7 January 2021
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Novel insulin promoter- and enhancer-binding proteins that discriminate between pancreatic alpha- and beta-cells
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Crossref
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inferred from DOI database lookup
Developmental regulation of beta-globin gene switching.
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Crossref
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7 January 2021
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inferred from DOI database lookup
Individual stage selector element mutations lead to reciprocal changes in beta- vs. epsilon-globin gene transcription: genetic confirmation of promoter competition during globin gene switching
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7 January 2021
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inferred from DOI database lookup
A position-effect assay for boundaries of higher order chromosomal domains
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7 January 2021
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The su(Hw) protein insulates expression of the Drosophila melanogaster white gene from chromosomal position-effects.
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7 January 2021
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inferred from DOI database lookup
The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
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inferred from DOI database lookup
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
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Crossref
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inferred from DOI database lookup
Evolutionary conservation of possible functional domains of the human and murine XIST genes
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based on heuristic
inferred from DOI database lookup
Expression of Xist during mouse development suggests a role in the initiation of X chromosome inactivation
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inferred from DOI database lookup
Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
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Allele-specific gene expression in mammals: the curious case of the imprinted RNAs
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7 January 2021
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inferred from DOI database lookup
Absolute quantification of target DNA: a simple competitive PCR for efficient analysis of multiple samples
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https://api.crossref.org/works/10.1038%2F375034A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F375034A0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
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Germ-line transmission of genes introduced into cultured pluripotential cells by retroviral vector
1 reference
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Detection of specific sequences among DNA fragments separated by gel electrophoresis
1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
1 reference
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reference URL
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7 January 2021
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inferred from DOI database lookup
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose
1 reference
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reference URL
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7 January 2021
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inferred from DOI database lookup
The gene family encoding the mouse ribosomal protein L32 contains a uniquely expressed intron-containing gene and an unmutated processed gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F375034A0
retrieved
7 January 2021
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inferred from DOI database lookup
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1 reference
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Crossref
reference URL
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7 January 2021
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inferred from DOI database lookup
Identifiers
DOI
10.1038/375034A0
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3658797
Dimensions Publication ID
1052910955
0 references
OpenCitations bibliographic resource ID
3658797
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3658797
PubMed ID
7536897
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3658797
Springer Nature article ID
10.1038/375034a0
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