Pages that link to "Q72127241"

The following pages link to Characteristics of imprinted genes (Q72127241):

Displaying 50 items.

• Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain (Q24534447) (← 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)
• Overlapping antisense transcription in the human genome (Q24646474) (← links)
• The complete nucleotide sequence of the human immunoglobulin heavy chain variable region locus (Q24647015) (← links)
• Mouse U2af1-rs1 is a neomorphic imprinted gene (Q24647321) (← links)
• Genomic imprinting and assisted reproduction (Q24793282) (← links)
• Genomic imprinting in mammals (Q26828858) (← links)
• New insights into establishment and maintenance of DNA methylation imprints in mammals (Q26852971) (← links)
• The specification of imprints in mammals (Q26861311) (← links)
• The evolution of the DLK1-DIO3 imprinted domain in mammals (Q27333130) (← links)
• Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma (Q28140252) (← links)
• The expanding snoRNA world (Q28216313) (← links)
• A downstream CpG island controls transcript initiation and elongation and the methylation state of the imprinted Airn macro ncRNA promoter (Q28481336) (← links)
• Genomic imprinting: parental influence on the genome (Q29616227) (← links)
• Cytosine methylation and the ecology of intragenomic parasites (Q29618264) (← links)
• A conserved structural element in horse and mouse IGF2 genes binds a methylation sensitive factor (Q32085871) (← links)
• Evolution and control of imprinted FWA genes in the genus Arabidopsis (Q33326979) (← links)
• A cis-acting element that directs the activity of the murine methylation modifier locus Ssm1. (Q33552210) (← links)
• Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian Ascl2/Mash2-Igf2-H19 region (Q33596180) (← links)
• Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene. (Q33781581) (← links)
• Genomic imprinting-an epigenetic gene-regulatory model (Q33814499) (← links)
• Improving the safety of embryo technologies: possible role of genomic imprinting (Q33873823) (← links)
• Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome (Q33897588) (← links)
• Genomic imprinting in plants: observations and evolutionary implications (Q33918746) (← 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)
• Genomic imprinting, uniparental disomy and foetal growth (Q33987666) (← links)
• Dynamic stage-specific changes in imprinted differentially methylated regions during early mammalian development and prevalence of non-CpG methylation in oocytes (Q34159815) (← links)
• The marks, mechanisms and memory of epigenetic states in mammals (Q34241071) (← links)
• Shared role for differentially methylated domains of imprinted genes (Q34276347) (← links)
• Imprinting and transgenerational modulation of gene expression; human growth as a model (Q34402875) (← links)
• Peg3/Pw1 is an imprinted gene involved in the TNF-NFkappaB signal transduction pathway. (Q34460141) (← links)
• The causes of synonymous rate variation in the rodent genome. Can substitution rates be used to estimate the sex bias in mutation rate? (Q34607045) (← links)
• An essential role for the DXPas34 tandem repeat and Tsix transcription in the counting process of X chromosome inactivation (Q34624543) (← links)
• Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. (Q34939534) (← links)
• Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity (Q35020593) (← links)
• Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes (Q35131567) (← links)
• Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus. (Q35170038) (← links)
• A comprehensive analysis of allelic methylation status of CpG islands on human chromosome 21q (Q35728480) (← links)
• Unique patterns of evolutionary conservation of imprinted genes (Q36001933) (← links)
• Comparative analysis of sequence characteristics of imprinted genes in human, mouse, and cattle (Q36023346) (← links)
• Genomic imprinting: cis-acting sequences and regional control (Q36083462) (← links)
• The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins (Q36283882) (← links)
• Comparative analyses of human single- and multilocus tandem repeats (Q36778181) (← links)
• Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. (Q36820044) (← links)
• Transcription is required for establishment of germline methylation marks at imprinted genes (Q37075687) (← links)
• Epigenetic profiling at mouse imprinted gene clusters reveals novel epigenetic and genetic features at differentially methylated regions (Q37287372) (← links)
• Epigenetic regulation of photoperiodic flowering (Q37744460) (← links)
• Genomic Imprinting Syndromes and Cancer (Q37797697) (← links)
• Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse (Q38291049) (← links)