(Q36312101)

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Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

0 references

author name string

Cristina Camprubí

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Marta Pladevall

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Mark Grossmann

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Nicolás Garrido

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Maria Carme Pons

5

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Joan Blanco

6

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

publication date

13 August 2012

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1115-1124

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Genome-wide reprogramming in the mouse germ line entails the base excision repair pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Fetal programming: link between early nutrition, DNA methylation, and complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Genomic imprinting effects in a compromised in utero environment: implications for a healthy pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Potential role of estrogen in regulation of the insulin-like growth factor2-H19 locus in the rat testis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Distinctive chromatin in human sperm packages genes for embryo development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

DNA methylation errors at imprinted loci after assisted conception originate in the parental sperm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Low frequency of imprinting defects in ICSI children born small for gestational age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Effect of tamoxifen treatment on global and insulin-like growth factor 2-H19 locus-specific DNA methylation in rat spermatozoa and its association with embryo loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

A review of known imprinting syndromes and their association with assisted reproduction technologies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Chromatin dynamics during epigenetic reprogramming in the mouse germ line

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Epigenetic programming of the germ line: effects of endocrine disruptors on the development of transgenerational disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Mammalian meiotic recombination hot spots

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Human imprinted chromosomal regions are historical hot-spots of recombination.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Consequences of paternal cocaine exposure in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Epigenetic transgenerational actions of endocrine disruptors and male fertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

The structural organization of sperm chromatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Intracytoplasmic sperm injection may increase the risk of imprinting defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Shared role for differentially methylated domains of imprinted genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

30 September 2017

Aberrant DNA methylation at imprinted genes in testicular sperm retrieved from men with obstructive azoospermia and undergoing vasectomy reversal.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Methylation defects of imprinted genes in human testicular spermatozoa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Role of the Dnmt3 family in de novo methylation of imprinted and repetitive sequences during male germ cell development in the mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Adverse effects of 5-aza-2'-deoxycytidine on spermatogenesis include reduced sperm function and selective inhibition of de novo DNA methylation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Aberrant DNA methylation of imprinted loci in superovulated oocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

MTHFR C677T polymorphism associates with unexplained infertile male factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Influence of global sperm DNA methylation on IVF results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Genomic imprinting in disruptive spermatogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Dnmt3L and the establishment of maternal genomic imprints

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469453

22 September 2018

Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

1 reference

https://api.crossref.org/works/10.4161%2FEPI.21743

21 January 2018

Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation analysis by pyrosequencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal methylation of imprinted genes in human sperm is associated with oligozoospermia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal DNA methyltransferase expression in mouse germline stem cells results in spermatogenic defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations in sperm DNA methylation patterns at imprinted loci in two classes of infertility

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal methylation patterns at the IGF2/H19 imprinting control region in phenotypically normal babies conceived by assisted reproductive technologies

1 reference

https://pubmed.ncbi.nlm.nih.gov/22885410

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.4161/EPI.21743

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

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