- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1868-7083
- Extent
-
Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Is ZFP57 binding to H19/IGF2:IG-DMR affected in Silver-Russell syndrome? ; volume:10 ; number:1 ; day:21 ; month:2 ; year:2018 ; pages:1-5 ; date:12.2018
Clinical epigenetics ; 10, Heft 1 (21.2.2018), 1-5, 12.2018
- Creator
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Sparago, Angela
- Contributor
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Cerrato, Flavia
Riccio, Andrea
SpringerLink (Online service)
- DOI
-
10.1186/s13148-018-0454-7
- URN
-
urn:nbn:de:101:1-2018080213470810054702
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:39 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sparago, Angela
- Cerrato, Flavia
- Riccio, Andrea
- SpringerLink (Online service)
Other Objects (12)
Untersuchungen zur Expression der Gene IGF2 und H19 in kultivierten Hautfibroblasten von Kindern mit Silver-Russell-Syndrom und Epimutation des IGF2/H19-Locus
IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome
The IGF2 mRNA binding protein p62 as a regulator of IGF2 and H19 expression : potential implications in tumorigenesis
Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2
Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2
DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Molekulare Ursachen des idiopathischen Silver-Russell-Syndroms: Untersuchungen zur Beteiligung der Chromosomen 6, 14 und 20 sowie des IGF2-Gens
DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice
Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine
Adrenarche bei Kindern mit Silver-Russell-Syndrom
Untersuchungen zur Expression der Gene IGF2 und H19 in kultivierten Hautfibroblasten von Kindern mit Silver-Russell-Syndrom und Epimutation des IGF2/H19-Locus
IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome
The IGF2 mRNA binding protein p62 as a regulator of IGF2 and H19 expression : potential implications in tumorigenesis
Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2
Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2
DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Molekulare Ursachen des idiopathischen Silver-Russell-Syndroms: Untersuchungen zur Beteiligung der Chromosomen 6, 14 und 20 sowie des IGF2-Gens
DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice
Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine
Adrenarche bei Kindern mit Silver-Russell-Syndrom
Untersuchungen zur Expression der Gene IGF2 und H19 in kultivierten Hautfibroblasten von Kindern mit Silver-Russell-Syndrom und Epimutation des IGF2/H19-Locus
IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome
The IGF2 mRNA binding protein p62 as a regulator of IGF2 and H19 expression : potential implications in tumorigenesis
Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2
Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2
DNA methylation of the IGF2/H19 imprinting control region and adiposity distribution in young adults
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Molekulare Ursachen des idiopathischen Silver-Russell-Syndroms: Untersuchungen zur Beteiligung der Chromosomen 6, 14 und 20 sowie des IGF2-Gens
DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice
Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine