Pages that link to "Q33887777"

The following pages link to Competition--a common motif for the imprinting mechanism? (Q33887777):

Displaying 50 items.

• Functional characterization of ORCTL2--an organic cation transporter expressed in the renal proximal tubules (Q24315129) (← links)
• Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control (Q24539092) (← links)
• Silencing by imprinted noncoding RNAs: is transcription the answer? (Q24610022) (← links)
• A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome (Q24644175) (← links)
• An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus (Q24678820) (← links)
• Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma (Q28140252) (← links)
• Prader-Willi and Angelman syndromes: sister imprinted disorders (Q28200133) (← links)
• Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma (Q28215251) (← links)
• Epigenetic reprogramming in early embryonic development: effects of in-vitro production and somatic nuclear transfer (Q28241243) (← links)
• Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4 (Q28941781) (← links)
• Genomic imprinting: implications for human disease (Q33541538) (← links)
• Mechanisms of genomic imprinting (Q33632372) (← links)
• Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster (Q33774256) (← links)
• Complex patterns of inheritance of an imprinted murine transgene suggest incomplete germline erasure (Q33786662) (← links)
• Beckwith-Wiedemann syndrome: imprinting in clusters revisited (Q33838090) (← links)
• Improving the safety of embryo technologies: possible role of genomic imprinting (Q33873823) (← links)
• The uniqueness of the imprinting mechanism (Q33885040) (← links)
• Identification of a methylation imprint mark within the mouse Gnas locus (Q33964982) (← links)
• Investigation of elements sufficient to imprint the mouse Air promoter (Q33969040) (← links)
• RNA-directed DNA methylation. (Q34041209) (← links)
• A novel antisense long noncoding RNA within the IGF1R gene locus is imprinted in hematopoietic malignancies (Q34115325) (← links)
• Molecular and biochemical regulation of early mammalian development (Q34250637) (← links)
• Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting (Q34277546) (← links)
• Minireview: Parthenogenesis in mammals (Q34316722) (← links)
• Beckwith-Wiedemann syndrome and isolated hemihyperplasia (Q35200576) (← links)
• The Dlk1 and Gtl2 genes are linked and reciprocally imprinted (Q35201020) (← links)
• Igf2 imprinting does not require its own DNA methylation or H19 RNA. (Q35205921) (← links)
• Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. (Q35211749) (← links)
• A Bayesian model for the analysis of transgenerational epigenetic variation. (Q35330100) (← links)
• p57(KIP2) is not mutated in hepatoblastoma but shows increased transcriptional activity in a comparative analysis of the three imprinted genes p57(KIP2), IGF2, and H19 (Q35745855) (← links)
• Consequences of paternally inherited effects on the genetic evaluation of maternal effects. (Q35945663) (← links)
• A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2 (Q36452285) (← links)
• The Effects of ISM1 Medium on Embryo Quality and Outcomes of IVF/ICSI Cycles (Q37362939) (← links)
• Monoallelic gene expression in mammals. (Q37401175) (← links)
• The spatial and temporal expression pattern of Nesp and its antisense Nespas, in mid-gestation mouse embryos (Q38305736) (← links)
• An intragenic long noncoding RNA interacts epigenetically with the RUNX1 promoter and enhancer chromatin DNA in hematopoietic malignancies (Q39002254) (← links)
• Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center. (Q39458709) (← links)
• The imprinted Air ncRNA is an atypical RNAPII transcript that evades splicing and escapes nuclear export (Q41829208) (← links)
• Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7. (Q47973503) (← links)
• Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. (Q48000452) (← links)
• The sins of the fathers and mothers: genomic imprinting in mammalian development (Q50532990) (← links)
• Imprinting mechanisms in mammals. (Q52187194) (← links)
• Imprinting and the initiation of gene silencing in the germ line. (Q52187741) (← links)
• H19 gene expression is up-regulated exclusively by stabilization of the RNA during muscle cell differentiation. (Q53900112) (← links)
• The imprinting box of the mouse Igf2r gene (Q59073140) (← links)
• An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript (Q60035843) (← links)
• Competitive edge at the imprinted Prader-Willi/Angelman region? (Q62075692) (← links)
• Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitus (Q73738916) (← links)
• The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1 (Q73765902) (← links)
• Regulation of the Wilms' tumour suppressor (WT1) gene by an antisense RNA: a link with genomic imprinting? (Q77600644) (← links)