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Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
by
Haaf, Thomas
, Hajj, Nady El
, Potabattula, Ramya
, Müller, Tobias
, Schorsch, Martin
, Hahn, Thomas
, Dittrich, Marcus
, Böck, Julia
, Haertle, Larissa
in
Adult
/ Age
/ Aging
/ allele-specific methylation
/ Alleles
/ Blood
/ Cell division
/ Colorectal cancer
/ Cord blood
/ Correlation analysis
/ deep bisulphite sequencing
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA polymerase
/ Epigenetics
/ epimutation rates
/ Female
/ Fetal Blood - metabolism
/ fetal cord blood samples
/ Fetuses
/ Gene expression
/ Gene sequencing
/ Genes
/ Genetic diversity
/ Genomes
/ Genomic Imprinting
/ Genotyping
/ Haplotypes
/ Humans
/ imprinted genes
/ In vitro fertilization
/ Male
/ Maternal Age
/ Middle Aged
/ Miscarriage
/ Mutation
/ parental age and BMI effects
/ Paternal Age
/ Peg3 protein
/ Polymorphism, Single Nucleotide
/ Regression analysis
/ Reproductive technologies
/ single nucleotide polymorphism haplotypes
/ Single-nucleotide polymorphism
/ Sperm
/ Spermatogenesis
/ Studies
/ unmethylated and methylated alleles
2018
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Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
by
Haaf, Thomas
, Hajj, Nady El
, Potabattula, Ramya
, Müller, Tobias
, Schorsch, Martin
, Hahn, Thomas
, Dittrich, Marcus
, Böck, Julia
, Haertle, Larissa
in
Adult
/ Age
/ Aging
/ allele-specific methylation
/ Alleles
/ Blood
/ Cell division
/ Colorectal cancer
/ Cord blood
/ Correlation analysis
/ deep bisulphite sequencing
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA polymerase
/ Epigenetics
/ epimutation rates
/ Female
/ Fetal Blood - metabolism
/ fetal cord blood samples
/ Fetuses
/ Gene expression
/ Gene sequencing
/ Genes
/ Genetic diversity
/ Genomes
/ Genomic Imprinting
/ Genotyping
/ Haplotypes
/ Humans
/ imprinted genes
/ In vitro fertilization
/ Male
/ Maternal Age
/ Middle Aged
/ Miscarriage
/ Mutation
/ parental age and BMI effects
/ Paternal Age
/ Peg3 protein
/ Polymorphism, Single Nucleotide
/ Regression analysis
/ Reproductive technologies
/ single nucleotide polymorphism haplotypes
/ Single-nucleotide polymorphism
/ Sperm
/ Spermatogenesis
/ Studies
/ unmethylated and methylated alleles
2018
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Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
by
Haaf, Thomas
, Hajj, Nady El
, Potabattula, Ramya
, Müller, Tobias
, Schorsch, Martin
, Hahn, Thomas
, Dittrich, Marcus
, Böck, Julia
, Haertle, Larissa
in
Adult
/ Age
/ Aging
/ allele-specific methylation
/ Alleles
/ Blood
/ Cell division
/ Colorectal cancer
/ Cord blood
/ Correlation analysis
/ deep bisulphite sequencing
/ Deoxyribonucleic acid
/ DNA
/ DNA Methylation
/ DNA polymerase
/ Epigenetics
/ epimutation rates
/ Female
/ Fetal Blood - metabolism
/ fetal cord blood samples
/ Fetuses
/ Gene expression
/ Gene sequencing
/ Genes
/ Genetic diversity
/ Genomes
/ Genomic Imprinting
/ Genotyping
/ Haplotypes
/ Humans
/ imprinted genes
/ In vitro fertilization
/ Male
/ Maternal Age
/ Middle Aged
/ Miscarriage
/ Mutation
/ parental age and BMI effects
/ Paternal Age
/ Peg3 protein
/ Polymorphism, Single Nucleotide
/ Regression analysis
/ Reproductive technologies
/ single nucleotide polymorphism haplotypes
/ Single-nucleotide polymorphism
/ Sperm
/ Spermatogenesis
/ Studies
/ unmethylated and methylated alleles
2018
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Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
Journal Article
Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
2018
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Overview
To examine the effects of genetic variation, parental age and BMI on parental allele-specific methylation of imprinted genes in fetal cord blood samples.
We have developed SNP genotyping and deep bisulphite sequencing assays for six imprinted genes to determine parental allele-specific methylation patterns in diploid somatic tissues.
Multivariate linear regression analyses revealed a negative correlation of paternal age with paternal
allele methylation in fetal cord blood. Methylation of the maternal
allele showed a positive correlation with maternal age. Paternal BMI was positively correlated with paternal
allele methylation. In addition to parental origin, allele-specific methylation of most imprinted genes was largely dependent on the underlying SNP haplotype.
Our study supports the idea that parental factors can have an impact, although of small effect size, on the epigenome of the next generation, providing an additional layer of complexity to phenotypic diversity.
Publisher
Future Medicine Ltd
Subject
/ Age
/ Aging
/ Alleles
/ Blood
/ DNA
/ Female
/ Fetuses
/ Genes
/ Genomes
/ Humans
/ Male
/ Mutation
/ parental age and BMI effects
/ Polymorphism, Single Nucleotide
/ single nucleotide polymorphism haplotypes
/ Single-nucleotide polymorphism
/ Sperm
/ Studies
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