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Isoform-specific imprinting of the human PEG1/MEST gene
scientific article
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instance of
scholarly article
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title
Isoform-specific imprinting of the human PEG1/MEST gene
(English)
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author name string
K Kosaki
series ordinal
1
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R Kosaki
series ordinal
2
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W J Craigen
series ordinal
3
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N Matsuo
series ordinal
4
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language of work or name
English
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publication date
January 2000
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published in
American Journal of Human Genetics
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volume
66
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issue
1
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page(s)
309-12
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cites work
IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
24 March 2017
Human PEG1/MEST, an imprinted gene on chromosome 7
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
24 March 2017
Uniparental disomy as a mechanism for human genetic disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
24 March 2017
PEG1 expression in maternal uniparental disomy 7
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
24 March 2017
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
24 March 2017
A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
27 September 2017
Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
27 September 2017
Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
27 September 2017
Genomic structure and parent-of-origin-specific methylation of Peg1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
27 September 2017
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
30 May 2018
Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
30 May 2018
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
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30 May 2018
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
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30 May 2018
Embryological and molecular investigations of parental imprinting on mouse chromosome 7.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
19 June 2018
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
29 November 2018
Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
29 November 2018
Promoter-specific imprinting of the human insulin-like growth factor-II gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
29 November 2018
Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288335
retrieved
29 November 2018
Promoter-specific IGF2 imprinting status and its plasticity during human liver development
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10631159
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1086/302712
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PMC publication ID
1288335
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PubMed publication ID
10631159
0 references
ResearchGate publication ID
12683509
0 references
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