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Items: 1 to 20 of 98

1.

The association of stromal antigen 3 (STAG3) sequence variations with spermatogenic impairment in the male Korean population.

Nam Y, Kang KM, Sung SR, Park JE, Shin YJ, Song SH, Seo JT, Yoon TK, Shim SH.

Asian J Androl. 2019 May 17. doi: 10.4103/aja.aja_28_19. [Epub ahead of print]

2.

Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C.

Hum Reprod. 2019 Jun 4;34(6):978-988. doi: 10.1093/humrep/dez042.

PMID:
31125047
3.

Pathogenic variants screening in five non-obstructive azoospermia-associated genes.

Lu C, Xu M, Wang R, Qin Y, Wang Y, Wu W, Song L, Wang S, Shen H, Sha J, Miao D, Hu Z, Xia Y, Wang X.

Mol Hum Reprod. 2014 Feb;20(2):178-83. doi: 10.1093/molehr/gat071. Epub 2013 Oct 24.

PMID:
24162948
4.

Meiosis-specific cohesin component, Stag3 is essential for maintaining centromere chromatid cohesion, and required for DNA repair and synapsis between homologous chromosomes.

Hopkins J, Hwang G, Jacob J, Sapp N, Bedigian R, Oka K, Overbeek P, Murray S, Jordan PW.

PLoS Genet. 2014 Jul 3;10(7):e1004413. doi: 10.1371/journal.pgen.1004413. eCollection 2014 Jul.

5.

STAG3 is a strong candidate gene for male infertility.

Llano E, Gomez-H L, García-Tuñón I, Sánchez-Martín M, Caburet S, Barbero JL, Schimenti JC, Veitia RA, Pendas AM.

Hum Mol Genet. 2014 Jul 1;23(13):3421-31. doi: 10.1093/hmg/ddu051. Epub 2014 Mar 7.

6.

Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L.

Ward A, Hopkins J, Mckay M, Murray S, Jordan PW.

G3 (Bethesda). 2016 Jun 1;6(6):1713-24. doi: 10.1534/g3.116.029462.

7.

A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest.

Gershoni M, Hauser R, Barda S, Lehavi O, Arama E, Pietrokovski S, Kleiman SE.

Hum Reprod. 2019 Apr 1;34(4):666-671. doi: 10.1093/humrep/dez016.

PMID:
30838384
8.

Sequence variations of the EGR4 gene in Korean men with spermatogenesis impairment.

Sung SR, Song SH, Kang KM, Park JE, Nam YJ, Shin YJ, Cha DH, Seo JT, Yoon TK, Shim SH.

BMC Med Genet. 2017 May 2;18(1):47. doi: 10.1186/s12881-017-0408-5.

9.

Genetic variants in Ser-Arg protein-coding genes are associated with the risk of nonobstructive azoospermia in Chinese men.

Ni B, Ma H, Lin Y, Dai J, Guo X, Xia Y, Sha J, Hu Z.

Fertil Steril. 2014 Jun;101(6):1711-7.e1-2. doi: 10.1016/j.fertnstert.2014.02.033. Epub 2014 Mar 21.

PMID:
24661730
10.

A novel stopgain mutation c.G992A (p.W331X) in TACR3 gene was identified in nonobstructive azoospermia by targeted next-generation sequencing.

Geng D, Yang X, Wang R, Deng S, Li L, Hu X, Jiang Y, Liu R.

J Clin Lab Anal. 2019 Mar;33(3):e22700. doi: 10.1002/jcla.22700. Epub 2018 Nov 2.

PMID:
30390321
11.

Association of the common SNPs in RNF212, STAG3 and RFX2 gene with male infertility with azoospermia in Chinese population.

Yu CH, Xie T, Zhang RP, A ZC.

Eur J Obstet Gynecol Reprod Biol. 2018 Feb;221:109-112. doi: 10.1016/j.ejogrb.2017.12.030. Epub 2017 Dec 15.

PMID:
29277047
12.

Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion.

Winters T, McNicoll F, Jessberger R.

EMBO J. 2014 Jun 2;33(11):1256-70. doi: 10.1002/embj.201387330. Epub 2014 May 5.

13.
14.

Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.

Deng Y, Zhang W, Su D, Yang Y, Ma Y, Zhang H, Zhang S.

Urology. 2008 May;71(5):878-82. doi: 10.1016/j.urology.2007.12.055. Epub 2008 Apr 18.

PMID:
18372033
15.

STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion.

Pezzi N, Prieto I, Kremer L, Pérez Jurado LA, Valero C, Del Mazo J, Martínez-A C, Barbero JL.

FASEB J. 2000 Mar;14(3):581-92.

PMID:
10698974
16.

Comprehensive pathway-based analysis identifies associations of BCL2, GNAO1 and CHD2 with non-obstructive azoospermia risk.

Qin Y, Ji J, Du G, Wu W, Dai J, Hu Z, Sha J, Hang B, Lu C, Xia Y, Wang X.

Hum Reprod. 2014 Apr;29(4):860-6. doi: 10.1093/humrep/deu013. Epub 2014 Feb 18.

PMID:
24549219
17.

STAG3-mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosis.

Fukuda T, Fukuda N, Agostinho A, Hernández-Hernández A, Kouznetsova A, Höög C.

EMBO J. 2014 Jun 2;33(11):1243-55. doi: 10.1002/embj.201387329. Epub 2014 May 5.

18.

Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure.

Akinloye O, Gromoll J, Callies C, Nieschlag E, Simoni M.

Andrologia. 2007 Oct;39(5):190-5.

PMID:
17714218
19.

Linkage disequilibrium and haplotype analysis of COX-2 and risk of colorectal adenoma development.

Kwagyan J, Apprey V, Ashktorab H.

Clin Transl Sci. 2012 Feb;5(1):60-4. doi: 10.1111/j.1752-8062.2011.00373.x. Epub 2012 Jan 10.

20.

Evaluation of the Stag3 gene and the synaptonemal complex in a rat model (as/as) for male infertility.

Bayés M, Prieto I, Noguchi J, Barbero JL, Pérez Jurado LA.

Mol Reprod Dev. 2001 Nov;60(3):414-7.

PMID:
11599053

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