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Computational and experimental identification of novel human imprinted genes

Computational and experimental identification of novel human imprinted genes

http://www.wikidata.org/entity/Q24684684

about

Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations Genomic imprinting disorders in humans: a mini-review A searchable database of genetic evidence for psychiatric disorders Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's role The pseudoautosomal region and sex chromosome aneuploidies in domestic species Environmental Influences on Genomic Imprinting Genetic aspects of autism spectrum disorders: insights from animal models Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome Maternal cadmium, iron and zinc levels, DNA methylation and birth weight Novel retrotransposed imprinted locus identified at human 6p25 Sex- and diet-specific changes of imprinted gene expression and DNA methylation in mouse placenta under a high-fat diet An analysis of gene expression in PTSD implicates genes involved in the glucocorticoid receptor pathway and neural responses to stress SNP-guided identification of monoallelic DNA-methylation events from enrichment-based sequencing data.Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.A novel mutation in the maternally imprinted PEG3 domain results in a loss of MIMT1 expression and causes abortions and stillbirths in cattle (Bos taurus).A Prevalence of Imprinted Genes within the Total Transcriptomes of Human Tissues and Cells.Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.Variants of ST8SIA1 are associated with risk of developing multiple sclerosis.Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain EpiGRAPH: user-friendly software for statistical analysis and prediction of (epi)genomic data Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete.Allelic skewing of DNA methylation is widespread across the genome.Evaluation of allelic expression of imprinted genes in adult human blood.Differentially methylated regions in maternal and paternal uniparental disomy for chromosome 7.Imprinted genes show unique patterns of sequence conservation.Epigenetic disorders and altered gene expression after use of Assisted Reproductive Technologies in domestic cattle.Metabolic syndrome components in murine models.Conservation of Repeats at the Mammalian KCNQ1OT1-CDKN1C Region Suggests a Role in Genomic Imprinting Developmental origins of health and disease: brief history of the approach and current focus on epigenetic mechanisms.Gene expression allelic imbalance in ovine brown adipose tissue impacts energy homeostasis.Parent of origin effects on age at colorectal cancer diagnosis Imprinted genes and the environment: links to the toxic metals arsenic, cadmium, lead and mercury.Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins Using next-generation RNA sequencing to identify imprinted genes.Integrative DNA methylation and gene expression analyses identify DNA packaging and epigenetic regulatory genes associated with low motility sperm.Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome Successful computational prediction of novel imprinted genes from epigenomic features.Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation.Discovery of a novel imprinted gene by transcriptional analysis of parthenogenetic embryonic stem cells.

P2860

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P2860

Computational and experimental identification of novel human imprinted genes

http://www.wikidata.org/entity/Q24684684

description

2007 nî lūn-bûn

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2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Computational and experimental identification of novel human imprinted genes

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Computational and experimental identification of novel human imprinted genes

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Computational and experimental identification of novel human imprinted genes

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type

label

Computational and experimental identification of novel human imprinted genes

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Computational and experimental identification of novel human imprinted genes

@en

Computational and experimental identification of novel human imprinted genes

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prefLabel

Computational and experimental identification of novel human imprinted genes

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Computational and experimental identification of novel human imprinted genes

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Computational and experimental identification of novel human imprinted genes

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Genome Research

P1476

Computational and experimental identification of novel human imprinted genes

@en

P2093

Alexander J Hartemink

http://www.w3.org/2001/XMLSchema#string

Fred S Dietrich

http://www.w3.org/2001/XMLSchema#string

Jason M Bosko

http://www.w3.org/2001/XMLSchema#string

Jennifer R Weidman

http://www.w3.org/2001/XMLSchema#string

Philippe P Luedi

http://www.w3.org/2001/XMLSchema#string

Randy L Jirtle

http://www.w3.org/2001/XMLSchema#string

P2860

Parental imprinting of the mouse H19 gene

Cloning, expression and chromosomal location of NKX6B TO 10Q26, a region frequently deleted in brain tumors

Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genes

Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8

Improved tools for biological sequence comparison.

The UCSC Genome Browser Database

Monoallelic expression of the human H19 gene

A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids

An imprinted PEG1/MEST antisense expressed predominantly in human testis and in mature spermatozoa

The role of HOX genes in human implantation

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1723-30

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scholarly article

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3023668

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10.1101/GR.6584707

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12

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17

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2007-12-01T00:00:00Z

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5792030

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18055845

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2099581

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