Establishment and maintenance of H19 imprinting in the germline and preimplantation embryo.

scientific article published in January 2006

Establishment and maintenance of H19 imprinting in the germline and preimplantation embryo. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1159/000090827
P698PubMed publication ID16575175

P50authorMarisa S. BartolomeiQ85577670
P2093author name stringReese KJ
P2860cites workParental imprinting of the mouse H19 geneQ22122365
Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19Q24615581
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 geneQ28145754
CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locusQ28145756
CTCF is a uniquely versatile transcription regulator linked to epigenetics and diseaseQ28214592
Role of CTCF binding sites in the Igf2/H19 imprinting control regionQ28512182
Transgenic RNAi reveals essential function for CTCF in H19 gene imprintingQ28590627
CTCF maintains differential methylation at the Igf2/H19 locusQ28593901
Role for DNA methylation in genomic imprintingQ29618669
Dynamic reprogramming of DNA methylation in the early mouse embryo.Q34108785
Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprintingQ34277546
The nucleotides responsible for the direct physical contact between the chromatin insulator protein CTCF and the H19 imprinting control region manifest parent of origin-specific long-distance insulation and methylation-free domainsQ35964289
A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprintingQ36564819
Two regulatory domains flank the mouse H19 geneQ36848651
Intracytoplasmic sperm injection may increase the risk of imprinting defectsQ37361933
A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout developmentQ40022869
Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injectionQ43202295
Maternal primary imprinting is established at a specific time for each gene throughout oocyte growthQ43802401
The ubiquitin ligase Hyperplastic discs negatively regulates hedgehog and decapentaplegic expression by independent mechanismsQ47071133
Selective loss of imprinting in the placenta following preimplantation development in cultureQ47232748
Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.Q47590866
The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell developmentQ47811571
Gene-specific timing and epigenetic memory in oocyte imprintingQ48004990
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndromeQ48177276
Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb.Q48563905
Epigenetic instability in ES cells and cloned miceQ48882976
The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during foetal testis developmentQ48886136
A paternal-specific methylation imprint marks the alleles of the mouse H19 geneQ49057890
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.Q52177094
Parental imprinting of the mouse insulin-like growth factor II gene.Q55052428
Epigenetic reprogramming in mouse primordial germ cellsQ57086629
P433issue1-4
P304page(s)153-158
P577publication date2006-01-01
P1433published inCytogenetics and Genome ResearchQ1524623
P1476titleEstablishment and maintenance of H19 imprinting in the germline and preimplantation embryo.
P478volume113

Reverse relations

cites work (P2860)
Q33303250Assisted Reproductive Technology affects developmental kinetics, H19 Imprinting Control Region methylation and H19 gene expression in individual mouse embryos
Q33294657Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3
Q38310406Reduced MiR-675 in exosome in H19 RNA-related melanogenesis via MITF as a direct target
Q24309357Thymine DNA glycosylase is essential for active DNA demethylation by linked deamination-base excision repair

Search more.