Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies (Q36251483)

13 August 2017

Gametes and embryo epigenetic reprogramming affect developmental outcome: implication for assisted reproductive technologies (English)

1 reference

13 August 2017

Saji Jacob

1

1 reference

13 August 2017

Kelle H Moley

series ordinal

2

1 reference

13 August 2017

language of work or name

English

0 references

publication date

1 September 2005

1 reference

13 August 2017

1 reference

13 August 2017

58

1 reference

13 August 2017

3

1 reference

13 August 2017

437-446

1 reference

https://scigraph.springernature.com/pub.10.1203/01.pdr.0000179401.17161.d3

13 August 2017

0 references

cites work

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Low and very low birth weight in infants conceived with use of assisted reproductive technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic reprogramming in mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic reprogramming in mouse primordial germ cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Reprogramming of primordial germ cells begins before migration into the genital ridge, making these cells inadequate donors for reproductive cloning

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Maternal primary imprinting is established at a specific time for each gene throughout oocyte growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Dynamic reprogramming of DNA methylation in the early mouse embryo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

A 5' 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Undermethylation of structural gene sequences in extraembryonic lineages of the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic inheritance at the agouti locus in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Inheritance of allelic blueprints for methylation patterns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic inheritance in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Decreased birthweights in infants after maternal in utero exposure to the Dutch famine of 1944-1945

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Dnmt3L and the establishment of maternal genomic imprints.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Completion of mouse embryogenesis requires both the maternal and paternal genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Delayed and incomplete reprogramming of chromosome methylation patterns in bovine cloned embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Differential activity of maternally and paternally derived chromosome regions in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Imprinting of genes and the Barker hypothesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Parental imprinting of the mouse insulin-like growth factor II gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Structure of human DNMT2, an enigmatic DNA methyltransferase homolog that displays denaturant-resistant binding to DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Cloning of a mammalian transcriptional activator that binds unmethylated CpG motifs and shares a CXXC domain with DNA methyltransferase, human trithorax, and methyl-CpG binding domain protein 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

CpG binding protein is crucial for early embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

DNA methylation in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genetic variation in ICF syndrome: evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

MECP2 is highly mutated in X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Molecular-clinical spectrum of the ATR-X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The transcriptional coactivators p300 and CBP are histone acetyltransferases

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

A mouse model of Rubinstein-Taybi syndrome: defective long-term memory is ameliorated by inhibitors of phosphodiesterase 4

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic risks related to assisted reproductive technologies: risk analysis and epigenetic inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Differential mRNA expression of the human DNA methyltransferases (DNMTs) 1, 3a and 3b during the G(0)/G(1) to S phase transition in normal and tumor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genomic imprinting: parental influence on the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The epigenetic basis of gender in flowering plants and mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Conservation of Dnmt1o cytosine methyltransferase in the marsupial Monodelphis domestica.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Shared role for differentially methylated domains of imprinted genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genomic imprinting and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genomic imprinting: implications for human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Genomic imprinting: mother maintains methylation marks.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Uniparental paternal disomy in Angelman's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

A global disorder of imprinting in the human female germ line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The genetics of the Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The history of cancer epigenetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Blockade of EphA receptor tyrosine kinase activation inhibits vascular endothelial cell growth factor-induced angiogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Aberrant methylation and impaired expression of the p15(INK4b) cell cycle regulatory gene in chronic myelomonocytic leukemia (CMML).

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Oocyte maturation and embryonic failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

In vitro follicular growth affects oocyte imprinting establishment in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Hypermethylation of the neurofibromatosis type 1 (NF1) gene promoter is not a common event in the inactivation of the NF1 gene in NF1-specific tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Rare congenital disorders, imprinted genes, and assisted reproductive technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Danish National In-Vitro Fertilization Registry 1994 and 1995: a controlled study of births, malformations and cytogenetic findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

The increased risk of complication observed in singleton pregnancies resulting from in-vitro fertilization (IVF) does not seem to be related to the IVF method itself

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Culture of preimplantation embryos and its long-term effects on gene expression and phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

In-utero overgrowth in ruminants following embryo culture: lessons from mice and a warning to men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Improving the safety of embryo technologies: possible role of genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Transposable elements: targets for early nutritional effects on epigenetic gene regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Birth weight and sex ratio after transfer at the blastocyst stage in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Intracytoplasmic sperm injection may increase the risk of imprinting defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Incidence of retinoblastoma in children born after in-vitro fertilisation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Congenital malformations after intracytoplasmic injection of spermatids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Status of genomic imprinting in mouse spermatids

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Developmental changes in methylation of spermatogenesis-specific genes include reprogramming in the epididymis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Neonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999).

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Maturation of human oocytes in vitro and their developmental competence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Frequent RASSF1A tumour suppressor gene promoter methylation in Wilms' tumour and colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

Demethylation of the zygotic paternal genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000179401.17161.D3

10.1203/01.PDR.0000179401.17161.D3

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

13 August 2017

0 references

1 reference