Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility
about
A preliminary study of copy number variation in TibetansTudor, MBT and chromo domains gauge the degree of lysine methylationThe AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertilityEpigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime healthHigh mutation rates have driven extensive structural polymorphism among human Y chromosomesCharacterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markersLack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts.Screening for Y-chromosome microdeletions in a population of infertile males in the Gaza Strip.The Y deletion gr/gr and susceptibility to testicular germ cell tumorAssociation of spermatogenic failure with the b2/b3 partial AZFc deletionClinical data for 185 infertile Iranian men with Y-chromosome microdeletionImpaired spermatogenesis and gr/gr deletions related to Y chromosome haplogroups in Korean men.Developmental model for the pathogenesis of testicular carcinoma in situ: genetic and environmental aspects.Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.Screening for AZFc partial deletions in Dravidian men with nonobstructive azoospermia and oligozoospermia.Structural variation of the human genome: mechanisms, assays, and role in male infertilityCommon AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination.Copy number variation in the human Y chromosome in the UK population.Organizational and functional status of the Y-linked genes and loci in the infertile patients having normal spermiogramSusceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions.Discrimination of Deletion and Duplication Subtypes of the Deleted in Azoospermia Gene Family in the Context of Frequent Interloci Gene Conversion.Multiplex PCR based screening for micro/partial deletions in the AZF region of Y-chromosome in severe oligozoospermic and azoospermic infertile men in IranQuantitative PCR technique for the identification of microrearrangements of the AZFc region.Y chromosome variants and male reproductive function.Gr/gr deletions on Y-chromosome correlate with male infertility: an original study, meta-analyses, and trial sequential analysesGenetic risk factors in male infertility.Susceptibility alleles for testicular germ cell tumour: a review.Partial deletions are associated with an increased risk of complete deletion in AZFc: a new insight into the role of partial AZFc deletions in male infertility.Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.Partial AZFc duplications not deletions are associated with male infertility in the Yi population of Yunnan Province, China.Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background.Human Y-chromosome variation and male dysfunctionGenetic testing in couples undergoing assisted reproduction technique protocols.Partial Deletions of Y-Chromosome in Infertile Men with Non-obstructive Azoospermia and Oligoasthenoteratozoospermia in a Turkish Population.Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia.Associations of Y-chromosome subdeletion gr/gr with the prevalence of Y-chromosome haplogroups in infertile patients.Y Chromosome Microdeletions in Infertile Men with Non-obstructive Azoospermia and Severe Oligozoospermia.A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.Genetics of the human Y chromosome and its association with male infertility.An infertile patient with Y chromosome b1/b3 deletion presenting with congenital bilateral absence of the vas deferens with normal spermatogenesis.
P2860
Q21134117-2C4D10C6-7FFC-46AF-B2E3-1EDAD902BCBCQ24301294-E46F44BB-2A9E-4020-8835-C0803BF9CB18Q24634263-064E4EDE-E0A7-4BD7-8EA6-702EA2519745Q26777239-DB9C8EE8-778C-4323-B00E-EE6107B186CDQ28299248-6DA98C98-3089-492D-9DBF-9D4EA8B17F59Q33300786-BDA59072-976D-4C25-9AAF-74596EAB8C8AQ33490988-82A18256-A7EC-4BE0-8A13-CAE9B0BA53D8Q33844530-A7D8B932-98CA-4037-937B-3BDDB8CAC43CQ34137428-82BE5447-8673-4E6F-92FA-E6E6DC2E4427Q34238802-33DA2D43-5776-4F93-B50F-EF4D973E2577Q34286910-9645AB61-8BFF-4BEE-BB3C-D99F13DC707EQ34395812-2BCF6B54-3B53-4A73-9C03-850B8CB51580Q34502475-EAA26D57-BC8A-49D3-B55C-D45B79709700Q34649789-52245EEF-F6BE-4158-A89A-070013E924EBQ35180500-499D9C45-9AC8-478B-831F-AFD2D170EBB4Q35230286-DB3D167B-A7B4-4C3F-B392-C009BDB1B843Q35635789-8CD8AED2-E0F5-4218-A546-74A51D4AC02DQ35698091-4FBBAB40-BBD4-4F66-90DC-3DB2EFB400D4Q36109559-E24B726E-266A-4A79-95B8-21941A495372Q36127728-846443C0-977F-4C95-9FA7-E594DFCD0079Q36159296-600C8803-433F-4BA4-A090-9107B22F4118Q36260018-244FE179-203A-4FFC-81F0-0D753D145EEAQ36268496-3330BF33-ADE5-44B7-9668-10FCBE3E30B7Q36391095-462E3846-EB8D-462C-BC65-68314F7616EBQ36579477-39493FD4-F849-4BD9-9758-C46506BD2144Q36870998-43E590D9-7C9D-4251-A62E-FA83ED911149Q36913143-C6C24D7F-833E-4E97-8094-8AC9CC6937C1Q37004678-968C0A4A-59B4-4DE5-A54E-EE5F5867BFEDQ37004683-9D613E11-FB66-4936-9EB1-91AE4AF223DAQ37172321-FD273D1B-189E-460F-959B-E0D3F69B1C21Q37232357-9FF8AAC8-CB86-489D-81D9-DF6B70A12F60Q37241871-381EAE3D-62A8-4259-8647-AE523B590F07Q38089822-5AD9BE03-ABC0-4B8B-A0C5-19595723B772Q38822079-68A09B6A-5E24-4E0C-B681-0BE04701554FQ41259226-C5B50E1A-66E1-4AE9-8E59-BEC5BDDB57D3Q41821478-7082B279-BC8E-4DA4-8DB5-7EE16136DBF7Q42957013-2684EEF5-A79D-48D1-BB80-6868D9324113Q44372433-1E13371E-05F8-4638-B496-4950B86D95D5Q49900644-11D8112D-ADFA-4546-AA5E-885BFDAEF5A9Q52584237-E70A0707-3372-4ACD-9BEA-2658E20C5443
P2860
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility
description
2004 nî lūn-bûn
@nan
2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Sequence family variant loss f ...... sociated with male infertility
@ast
Sequence family variant loss f ...... sociated with male infertility
@en
type
label
Sequence family variant loss f ...... sociated with male infertility
@ast
Sequence family variant loss f ...... sociated with male infertility
@en
prefLabel
Sequence family variant loss f ...... sociated with male infertility
@ast
Sequence family variant loss f ...... sociated with male infertility
@en
P2093
P2860
P50
P356
P1476
Sequence family variant loss f ...... sociated with male infertility
@en
P2093
Belougne J
Chiaroni J
Clemente E
Collignon P
Ducourneau A
Frances AM
Guichaoua M
Longepied G
P2860
P304
P356
10.1136/JMG.2004.022111
P407
P577
2004-11-01T00:00:00Z