(Q53472940)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

author name string

Wei Zhang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Dan Su

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Yongxin Ma

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

Sizhong Zhang

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

publication date

1 March 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

Systems Biology in Reproductive Medicine

8 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

volume

54

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

page(s)

93-95

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

Genomic instability in mice lacking histone H2AX

8 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Sperm chromatin proteomics identifies evolutionarily conserved fertility factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

gammaH2AX signalling during sperm chromatin remodelling in the mouse zygote.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

H2AX: the histone guardian of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Mutant meiotic chromosome core components in mice can cause apparent sexual dimorphic endpoints at prophase or X-Y defective male-specific sterility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Genetic risk factors in male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

H2AX: tailoring histone H2A for chromatin-dependent genomic integrity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Platelet-activating factor receptor and ADAM10 mediate responses to Staphylococcus aureus in epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Azoospermia in patients heterozygous for a mutation in SYCP3

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Absence of constitutional H2AX gene mutations in 101 hereditary breast cancer families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Mouse models for genes involved in impaired spermatogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

SYCP3 mutations are uncommon in patients with azoospermia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Mutations in the chromosome pairing gene FKBP6 are not a common cause of non-obstructive azoospermia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F19396360701883266

10.1080/19396360701883266

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18536151%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference