Pages that link to "Q33841575"
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The following pages link to Genome-wide prediction of imprinted murine genes (Q33841575):
Displaying 50 items.
- Genome-wide interrogation of Mammalian stem cell fate determinants by nested chromosome deletions (Q21144967) (← links)
- Genomic imprinting in mammals: emerging themes and established theories (Q21145256) (← links)
- RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer (Q24298388) (← links)
- Epigenetics in mood disorders (Q24644659) (← links)
- Genomic imprinting disorders in humans: a mini-review (Q24646016) (← links)
- Computational and experimental identification of novel human imprinted genes (Q24684684) (← links)
- Genome-wide in silico identification and analysis of cis natural antisense transcripts (cis-NATs) in ten species (Q24685558) (← links)
- The opossum genome: insights and opportunities from an alternative mammal (Q28657449) (← links)
- Sex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat diet (Q28744059) (← links)
- Environmental epigenomics and disease susceptibility (Q29547452) (← links)
- SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data. (Q30425530) (← links)
- Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse (Q30433075) (← links)
- High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta. (Q30981538) (← links)
- A genomic imprinting test for ordinal traits in pedigree data (Q31132501) (← links)
- Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes (Q33157676) (← links)
- Evidence of influence of genomic DNA sequence on human X chromosome inactivation (Q33256101) (← links)
- Genomic environment predicts expression patterns on the human inactive X chromosome (Q33258823) (← links)
- Circular chromosome conformation capture (4C) uncovers extensive networks of epigenetically regulated intra- and interchromosomal interactions. (Q33260024) (← links)
- A maternal-offspring coadaptation theory for the evolution of genomic imprinting (Q33263582) (← links)
- A novel approach to detect parent-of-origin effects from pedigree data with application to Beckwith-Wiedemann syndrome (Q33288182) (← links)
- Joint linkage and imprinting analyses of GAW15 rheumatoid arthritis and gene expression data (Q33332985) (← links)
- Genome-wide analysis reveals a complex pattern of genomic imprinting in mice (Q33340977) (← links)
- Sex dependent imprinting effects on complex traits in mice (Q33381858) (← links)
- Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain (Q33389173) (← links)
- EpiGRAPH: user-friendly software for statistical analysis and prediction of (epi)genomic data (Q33408033) (← links)
- Modeling genetic imprinting effects of DNA sequences with multilocus polymorphism data (Q33492605) (← links)
- The human retinoblastoma gene is imprinted (Q33521315) (← links)
- Postnatal survival of mice with maternal duplication of distal chromosome 7 induced by a Igf2/H19 imprinting control region lacking insulator function (Q33523010) (← links)
- Imprinted genes show unique patterns of sequence conservation (Q33751959) (← links)
- Metabolic syndrome components in murine models (Q33790395) (← links)
- Conservation of Repeats at the Mammalian KCNQ1OT1-CDKN1C Region Suggests a Role in Genomic Imprinting (Q33812168) (← links)
- Early transcription from the maternal genome controlling blastomere integrity in mouse two-cell-stage embryos (Q33840433) (← links)
- Imbalanced class learning in epigenetics (Q33847534) (← links)
- Using next-generation RNA sequencing to identify imprinted genes. (Q33927875) (← links)
- Successful computational prediction of novel imprinted genes from epigenomic features. (Q33963896) (← links)
- Molecular targets of chromatin repressive mark H3K9me3 in primate progenitor cells within adult neurogenic niches. (Q33972484) (← links)
- The impact of assisted reproductive technologies on genomic imprinting and imprinting disorders (Q34011361) (← links)
- Genome-wide association studies for bivariate sparse longitudinal data (Q34047770) (← links)
- Genetic, epigenetic, and gene-by-diet interaction effects underlie variation in serum lipids in a LG/JxSM/J murine model (Q34116418) (← links)
- The imprinted gene DIO3 is a candidate gene for litter size in pigs. (Q34185730) (← links)
- A framework for detecting and characterizing genetic background-dependent imprinting effects (Q34287133) (← links)
- Differential decay of parent-of-origin-specific genomic sharing in cystic fibrosis-affected sib pairs maps a paternally imprinted locus to 7q34. (Q34329053) (← links)
- Quantification of leukocyte genomic 5-methylcytosine levels reveals epigenetic plasticity in healthy adult cloned cattle (Q34356807) (← links)
- Genomic imprinting and parent-of-origin effects on complex traits. (Q34362002) (← links)
- Genomic imprinting and genetic effects on muscle traits in mice (Q34385720) (← links)
- Induced Pluripotent Stem Cells Can Be Used to Model the Genomic Imprinting Disorder Prader-Willi Syndrome (Q34401155) (← links)
- An imprinted locus epistatically influences Nstr1 and Nstr2 to control resistance to nerve sheath tumors in a neurofibromatosis type 1 mouse model (Q34448414) (← links)
- dsPIG: a tool to predict imprinted genes from the deep sequencing of whole transcriptomes (Q34452763) (← links)
- Intronic parent-of-origin dependent differential methylation at the Actn1 gene is conserved in rodents but is not associated with imprinted expression (Q34473768) (← links)
- Brain function and chromatin plasticity (Q34620395) (← links)