(Q34830485)

4 August 2017

1 reference

title

Epigenetic contributors to the discordance of monozygotic twins (English)

1 reference

4 August 2017

Singh SM

1

1 reference

PubMed ID

12220446

4 August 2017

Murphy B

series ordinal

2

1 reference

PubMed ID

12220446

4 August 2017

O'Reilly R

series ordinal

3

1 reference

4 August 2017

1 August 2002

1 reference

4 August 2017

1 reference

4 August 2017

62

1 reference

4 August 2017

2

1 reference

4 August 2017

97-103

1 reference

Mechanisms for differences in monozygous twins

4 August 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Twin study: relationship between birth weight, zygosity, placentation, and pathologic placental changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Placental transport rather than maternal concentration of amino acids regulates fetal growth in monochorionic twins: implications for fetal origin hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Twinning: mechanisms and genetic implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Environmental effects on genomic imprinting in mammals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Epigenetic lesions causing genetic lesions in human cancer: promoter hypermethylation of DNA repair genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Constitutively methylated CpG dinucleotides as mutation hot spots in the retinoblastoma gene (RB1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Localization of the human SP3 gene to chromosome 7p14-p15.2. The lack of expression in multiple sclerosis does not reflect abnormal gene organization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Schizophrenia: an epigenetic puzzle?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Beyond Watson and Crick: DNA methylation and molecular enzymology of DNA methyltransferases

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Overexpression of 5-methylcytosine DNA glycosylase in human embryonic kidney cells EcR293 demethylates the promoter of a hormone-regulated reporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Cytosine methylation and the ecology of intragenomic parasites

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

DNA methylation in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Allele-specific non-CpG methylation of the Nf1 gene during early mouse development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Creation of genomic methylation patterns

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

The Sequence of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Initial sequencing and analysis of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Methyl CpG-binding proteins and transcriptional repression

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Methyl-CpG-binding proteins. Targeting specific gene repression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Methylation of promoter proximal-transcribed sequences of an embryonic globin gene inhibits transcription in primary erythroid cells and promotes formation of a cell type-specific methyl cytosine binding complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

DNA methylation and gene activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Cytosine methylation and mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Role for DNA methylation in genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Cooperativity between DNA methyltransferases in the maintenance methylation of repetitive elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Preferential methylation of unmethylated DNA by Mammalian de novo DNA methyltransferase Dnmt3a.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Differential activity of maternally and paternally derived chromosome regions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Dynamic reprogramming of DNA methylation in the early mouse embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Epigenetic reprogramming in mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Genomic imprinting: parental influence on the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Genetics. Do X chromosomes set boundaries?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Xce haplotypes show modified methylation in a region of the active X chromosome lying 3' to Xist

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

X-chromosome inactivation: counting, choice and initiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

CTCF, a candidate trans-acting factor for X-inactivation choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Genome imprinting, cellular mosaicism and carcinogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Trinucleotide repeats: mechanisms and pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Linkage and associated studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Molecular genetics of schizophrenia: past, present and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Molecular characterization of a 2.7-kb, 12q13-specific, retroviral-related sequence isolated by RDA from monozygotic twin pairs discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Retroviruses and schizophrenia revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Methylation-specific oligonucleotide microarray: a new potential for high-throughput methylation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Demethylation of the zygotic paternal genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

Fetal blood sampling demonstrating chimerism in monozygotic twins discordant for sex and tissue karyotype (46,XY and 45,X)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

A comparative study of X-inactivation in Rett syndrome probands and control subjects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

A novel mutation of the KAL1 gene in monozygotic twins with Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

CTG trinucleotide repeat variability in identical twins with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

Genomic discordance between monozygotic twins discordant for schizophrenia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

Phenotypic discordance in monozygotic twins with 22q11.2 deletion.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620201.X

7 January 2021

10.1034/J.1399-0004.2002.620201.X

Identifiers

DOI

1 reference

4 August 2017

1 reference

PubMed ID

12220446