- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1868-7083
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
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
- Urheber
-
Sparago, Angela
- Beteiligte Personen und Organisationen
-
Cerrato, Flavia
Riccio, Andrea
SpringerLink (Online service)
- DOI
-
10.1186/s13148-018-0454-7
- URN
-
urn:nbn:de:101:1-2018080213470810054702
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:39 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sparago, Angela
- Cerrato, Flavia
- Riccio, Andrea
- SpringerLink (Online service)
Ähnliche Objekte (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
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
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
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
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
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Epigenetic dysregulation of H19/IGF2 in hepatic cells exposed to toxic metal mixtures in vitro
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