A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme

A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme

Item
http://www.wikidata.org/entity/Q24337425
Group III secreted phospholipase A2 regulates epididymal sperm maturation and fertility in mice.Mammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypesSperm-associated antigen-17 gene is essential for motile cilia function and neonatal survivalFunctional deficiencies and a reduced response to calcium in the flagellum of mouse sperm lacking SPAG16LSpag16, an axonemal central apparatus gene, encodes a male germ cell nuclear speckle protein that regulates SPAG16 mRNA expression.Genetic variation in SPAG16 regions encoding the WD40 repeats is not associated with reduced sperm motility and axonemal defects in a population of infertile malesClinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.Identification of male gametogenesis expressed genes from the scallop Nodipecten subnodosus by suppressive subtraction hybridization and pyrosequencing.Association between a Tetranucleotide Repeat Polymorphism of SPAG16 Gene and Cataract in Male Children.Computer-assisted image analysis of human cilia and Chlamydomonas flagella reveals both similarities and differences in axoneme structure.Mendelian genetics of male infertilityGenetic causes of spermatogenic failure.The Central Apparatus of Cilia and Eukaryotic Flagella.Fused (Stk36) is a ciliary protein required for central pair assembly and motile cilia orientation in the mammalian oviduct.Identification of a genetic variant for joint damage progression in autoantibody-positive rheumatoid arthritis.Formation and function of sperm tail structures in association with sperm motility defects.A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole-exome sequencing.
P2860

A heterozygous mutation disrupting the SPAG16 gene results in biochemical instability of central apparatus components of the human sperm axoneme

Item
http://www.wikidata.org/entity/Q24337425
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@ast
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en-gb
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@nl
type
label
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@ast
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en-gb
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@nl
prefLabel
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@ast
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en-gb
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P5875
P698
P921
P356
P1433
P1476
A heterozygous mutation disrup ...... nts of the human sperm axoneme
@en
P2093
P304
P31
P356
10.1095/BIOLREPROD.107.063206
P407
P433
P478
P50
P577
P5875
P698
P921