Pages that link to "Q28288348"
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The following pages link to An enhancer deletion affects both H19 and Igf2 expression (Q28288348):
Displaying 50 items.
- Birth of parthenogenetic mice that can develop to adulthood (Q22122493) (← links)
- Alterations in specific gene expression and focal neoplastic growth during spontaneous hepatocarcinogenesis in albumin-SV40 T antigen transgenic rats (Q23924152) (← links)
- CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 (Q24295238) (← links)
- Regulation of alpha-fetoprotein expression by Nkx2.8 (Q24304079) (← links)
- Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome (Q24634411) (← links)
- Transcription of the sodium/myo-inositol cotransporter gene is regulated by multiple tonicity-responsive enhancers spread over 50 kilobase pairs in the 5'-flanking region (Q24647556) (← links)
- H19 overexpression in breast adenocarcinoma stromal cells is associated with tumor values and steroid receptor status but independent of p53 and Ki-67 expression (Q24682023) (← links)
- Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans (Q24810018) (← links)
- Regulatory links between imprinted genes: evolutionary predictions and consequences (Q28075832) (← links)
- gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome (Q28137721) (← links)
- Steroid hormones modulate H19 gene expression in both mammary gland and uterus (Q28141832) (← links)
- CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus (Q28145756) (← links)
- CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease (Q28214592) (← links)
- Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma (Q28215251) (← links)
- Dissociation of IGF2 and H19 imprinting in human brain (Q28288697) (← links)
- Bisphenol a exposure disrupts genomic imprinting in the mouse (Q28485979) (← links)
- FoxA proteins regulate H19 endoderm enhancer E1 and exhibit developmental changes in enhancer binding in vivo (Q28505087) (← links)
- The H19 locus acts in vivo as a tumor suppressor (Q28508794) (← links)
- Role of CTCF binding sites in the Igf2/H19 imprinting control region (Q28512182) (← links)
- The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA (Q28594499) (← links)
- Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans (Q28594559) (← links)
- Transcription regulation and animal diversity (Q29618752) (← links)
- An upstream repressor element plays a role in Igf2 imprinting (Q30684867) (← links)
- Antisense transcripts with FANTOM2 clone set and their implications for gene regulation (Q31147226) (← links)
- Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain. (Q31864191) (← links)
- Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5' region (Q33259112) (← links)
- Statistical significance of cis-regulatory modules (Q33269955) (← links)
- Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3 (Q33294657) (← links)
- Insulin gene expression is regulated by DNA methylation (Q33501742) (← links)
- Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region (Q33596180) (← links)
- H19 imprinting control region methylation requires an imprinted environment only in the male germ line. (Q33648826) (← links)
- Complete biallelic insulation at the H19/Igf2 imprinting control region position results in fetal growth retardation and perinatal lethality (Q33691538) (← links)
- Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome (Q33721384) (← links)
- An intragenic methylated region in the imprinted Igf2 gene augments transcription. (Q33757992) (← links)
- Turnover of primary transcripts is a major step in the regulation of mouse H19 gene expression (Q33758082) (← links)
- CTCF-dependent chromatin bias constitutes transient epigenetic memory of the mother at the H19-Igf2 imprinting control region in prospermatogonia. (Q33760850) (← links)
- Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster (Q33774256) (← links)
- Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways (Q33875930) (← links)
- Genomic imprinting recapitulated in the human beta-globin locus (Q33900452) (← links)
- Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene (Q33957648) (← links)
- The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells (Q33994222) (← links)
- Regulatory mechanisms at the mouse Igf2/H19 locus. (Q34012897) (← links)
- Imprinting: focusing on the center (Q34026945) (← links)
- Parent-of-origin-specific binding of nuclear hormone receptor complexes in the H19-Igf2 imprinting control region (Q34181759) (← links)
- Paternally expressed Peg3 controls maternally expressed Zim1 as a trans factor (Q34270424) (← links)
- Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting (Q34277546) (← links)
- H19 antisense RNA can up-regulate Igf2 transcription by activation of a novel promoter in mouse myoblasts (Q34291425) (← links)
- Epigenetic control of the genome-lessons from genomic imprinting (Q34347672) (← links)
- Developmental profile of H19 differentially methylated domain (DMD) deletion alleles reveals multiple roles of the DMD in regulating allelic expression and DNA methylation at the imprinted H19/Igf2 locus (Q34353718) (← links)
- DNA methylation in genomic imprinting, development, and disease (Q34378421) (← links)