(Q42135922)

English

Genome-wide analysis identifies changes in histone retention and epigenetic modifications at developmental and imprinted gene loci in the sperm of infertile men.

scientific article published on 17 June 2011

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Genome-wide analysis identifies changes in histone retention and epigenetic modifications at developmental and imprinted gene loci in the sperm of infertile men. (English)

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

author name string

Saher Sue Hammoud

1

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

David A Nix

2

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Ahmad O Hammoud

3

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Mark Gibson

4

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Bradley R Cairns

5

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Douglas T Carrell

6

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

language of work or name

0 references

publication date

17 June 2011

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

Human Reproduction

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

26

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

9

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

2558-2569

1 reference

Europe PubMed Central

PMC publication ID

17 October 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=3157626

29 May 2018

Endonuclease-sensitive regions of human spermatozoal chromatin are highly enriched in promoter and CTCF binding sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

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=3157626

29 May 2018

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=3157626

29 May 2018

Imprinting disorders and assisted reproductive technology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Assisted reproductive technology and major structural birth defects in the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Sperm DNA damage is associated with an increased risk of pregnancy loss after IVF and ICSI: systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Contributions of spermatozoa to embryogenesis: assays to evaluate their genetic and epigenetic fitness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

A bivalent chromatin structure marks key developmental genes in embryonic stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

DNA integrity is compromised in protamine-deficient human sperm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Paternal effects on cell division in the human preimplantation embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Imprinting and assisted reproductive technology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

Epigenetic silencing of the imprinted gene ZAC by DNA methylation is an early event in the progression of human ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

29 May 2018

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=3157626

29 May 2018

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=3157626

29 May 2018

Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

17 August 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=3157626

17 August 2018

Selective loss of imprinting in the placenta following preimplantation development in culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

17 August 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=3157626

17 August 2018

A prospective longitudinal study of the physical, psychomotor, and intellectual development of singleton children up to 5 years who were conceived by intracytoplasmic sperm injection compared with children conceived spontaneously and by in vitro fer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

17 August 2018

The risk of major birth defects after intracytoplasmic sperm injection and in vitro fertilization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

17 August 2018

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3157626

17 August 2018

Aberrant DNA methylation of imprinted loci in sperm from oligospermic patients

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDER192

21 January 2018

Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia

1 reference

https://api.crossref.org/works/10.1093%2FHUMREP%2FDER192

21 January 2018

Culture of preimplantation mouse embryos affects fetal development and the expression of imprinted genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21685136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered protamine 2 expression is uncommon in donors of known fertility, but common among men with poor fertilizing capacity, and may reflect other abnormalities of spermiogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21685136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assisted reproductive technology in the United States

1 reference

https://pubmed.ncbi.nlm.nih.gov/21685136

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/21685136

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/21685136

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/21685136

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HUMREP/DER192

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 October 2017

ResearchGate publication ID

0 references

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