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Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
title
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
main subject
patient
0 references
Dynein axonemal heavy chain 11
1 reference
stated in
GOA release 2020-03-11
Dynein axonemal heavy chain 5
1 reference
stated in
GOA release 2020-03-11
Dynein axonemal intermediate chain 1
1 reference
stated in
GOA release 2020-03-11
flagellated sperm motility
1 reference
stated in
GOA release 2020-03-11
asthenozoospermia
1 reference
based on heuristic
inferred from title
author
Alberto Ferlin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
Sandro Francavilla
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author name string
D Zuccarello
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
C Cazzadore
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
A Pepe
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
A Garolla
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
A Moretti
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
G Cordeschi
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
C Foresta
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
language of work or name
English
0 references
publication date
20 May 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Human Reproduction
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
1957-1962
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
cites work
Genetic aspects of immotile cilia syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Motor apparatus in human spermatozoa that lack central pair microtubules
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quantitative analysis of ciliary ultrastructure in patients with primary ciliary dyskinesia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Utrastructural analysis of asthenozoospermic ejaculates in the era of assisted procreation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Semen quality and oxidative stress scores in fertile and infertile patients with varicocele
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical characteristics and light and transmission electron microscopic sperm defects of infertile men with persistent unexplained asthenozoospermia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Combination of hypoosmotic swelling/eosin Y test for sperm membrane integrity evaluation: correlations with other sperm parameters to predict ICSI cycles.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic and biochemical dissection of the eucaryotic flagellum
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ultrastructural pathology of the sperm flagellum: association between flagellar pathology and fertility prognosis in severely asthenozoospermic men
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene deletions in an infertile man with sperm fibrous sheath dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: Case Report
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Quantitative ultrastructural analysis of sperm tails reveals flagellar defects associated with persistent asthenozoospermia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic defects in ciliary structure and function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Movement: the emerging genetics of primary ciliary dyskinesia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ureaplasma urealyticum, Ureaplasma parvum, Mycoplasma hominis and Mycoplasma genitalium infections and semen quality of infertile men.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathophysiology of sperm motility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1093%2FHUMREP%2FDEN193
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1093/HUMREP/DEN193
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
PubMed publication ID
18492703
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18492703
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18492703%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
ResearchGate publication ID
5357088
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