scholarly article | Q13442814 |
P2093 | author name string | A L Webber | |
S M Tilghman | |||
P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway | Q24308083 | ||
Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose | Q24611198 | ||
Detection of specific sequences among DNA fragments separated by gel electrophoresis | Q25939003 | ||
A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae | Q27860636 | ||
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I | Q27860885 | ||
Ectopic expression of the H19 gene in mice causes prenatal lethality | Q28281671 | ||
Disruption of imprinting caused by deletion of the H19 gene region in mice | Q28287765 | ||
An enhancer deletion affects both H19 and Igf2 expression | Q28288348 | ||
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element | Q28588115 | ||
Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
Role for DNA methylation in genomic imprinting | Q29618669 | ||
Position-independent, high-level expression of the human beta-globin gene in transgenic mice | Q29620032 | ||
The human HPRT gene on a yeast artificial chromosome is functional when transferred to mouse cells by cell fusion | Q30980451 | ||
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. | Q34059933 | ||
Parental-origin-specific epigenetic modification of the mouse H19 gene | Q34363043 | ||
A method for high efficiency YAC lipofection into murine embryonic stem cells | Q34620762 | ||
Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction | Q34993293 | ||
The structural H19 gene is required for transgene imprinting | Q35934507 | ||
A 5' differentially methylated sequence and the 3'-flanking region are necessary for H19 transgene imprinting | Q36564819 | ||
Use of yeast artificial chromosomes (YACs) for studying control of gene expression: correct regulation of the genes of a human beta-globin locus YAC following transfer to mouse erythroleukemia cell lines | Q36695335 | ||
Yeast kar1 mutants provide an effective method for YAC transfer to new hosts | Q36726786 | ||
Germ line transmission of a yeast artificial chromosome spanning the murine alpha 1(I) collagen locus | Q36741219 | ||
Construction of a large-insert yeast artificial chromosome library of the mouse genome | Q36767726 | ||
Two regulatory domains flank the mouse H19 gene | Q36848651 | ||
Multiple regulatory elements in the intergenic region between the alpha-fetoprotein and albumin genes | Q36909561 | ||
An electrophoretic karyotype for yeast | Q37690127 | ||
Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse | Q38291049 | ||
Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
Location of enhancers is essential for the imprinting of H19 and Igf2 genes | Q39450419 | ||
A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development | Q40022869 | ||
Transcriptional regulation of multigene loci: multilevel control | Q40919870 | ||
Conservation of a maternal-specific methylation signal at the human IGF2R locus | Q41285894 | ||
Genomic imprinting: nature and clinical relevance | Q41360424 | ||
Germ-line transmission and expression of a human-derived yeast artificial chromosome | Q41565454 | ||
Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome | Q41566242 | ||
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene. | Q41979401 | ||
Separation of large DNA molecules by contour-clamped homogeneous electric fields | Q44137486 | ||
Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus | Q48061527 | ||
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 | ||
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
A yeast artificial chromosome covering the tyrosinase gene confers copy number-dependent expression in transgenic mice | Q49150314 | ||
Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes. | Q52201995 | ||
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain. | Q52204453 | ||
H19 is imprinted in the choroid plexus and leptomeninges of the mouse foetus | Q52208588 | ||
Comparative analysis of Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region. | Q52213159 | ||
Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes | Q52214150 | ||
Importance of globin gene order for correct developmental expression. | Q52236177 | ||
Developmental regulation of human fetal-to-adult globin gene switching in transgenic mice. | Q52241950 | ||
Human gamma- to beta-globin gene switching in transgenic mice. | Q52242246 | ||
Relaxation of imprinted genes in human cancer. | Q52545355 | ||
Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene | Q72094721 | ||
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1903-1910 | |
P577 | publication date | 1998-04-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | The absence of enhancer competition between Igf2 and H19 following transfer into differentiated cells | |
P478 | volume | 18 |
Q90279933 | Disruption of the Igf2 gene alters hepatic lipid homeostasis and gene expression in the newborn mouse |
Q42489595 | H19 sense and antisense transgenes modify insulin-like growth factor-II mRNA levels |
Q36091303 | Insulators are fundamental components of the eukaryotic genomes |
Q51545297 | Ontogeny of the H19 gene in sheep and effect of maternal fasting on its expression in the fetus. |
Q33957648 | Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene |
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