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Page 1
Septins at the annulus of mammalian sperm.
Toure A, Rode B, Hunnicutt GR, Escalier D, Gacon G. Toure A, et al. Among authors: gacon g. Biol Chem. 2011 Aug;392(8-9):799-803. doi: 10.1515/BC.2011.074. Epub 2011 Jul 11. Biol Chem. 2011. PMID: 21740329 Review.
The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.
Rode B, Dirami T, Bakouh N, Rizk-Rabin M, Norez C, Lhuillier P, Lorès P, Jollivet M, Melin P, Zvetkova I, Bienvenu T, Becq F, Planelles G, Edelman A, Gacon G, Touré A. Rode B, et al. Among authors: gacon g. Hum Mol Genet. 2012 Mar 15;21(6):1287-98. doi: 10.1093/hmg/ddr558. Epub 2011 Nov 25. Hum Mol Genet. 2012. PMID: 22121115
Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia.
Dirami T, Rode B, Jollivet M, Da Silva N, Escalier D, Gaitch N, Norez C, Tuffery P, Wolf JP, Becq F, Ray PF, Dulioust E, Gacon G, Bienvenu T, Touré A. Dirami T, et al. Among authors: gacon g. Am J Hum Genet. 2013 May 2;92(5):760-6. doi: 10.1016/j.ajhg.2013.03.016. Epub 2013 Apr 11. Am J Hum Genet. 2013. PMID: 23582645 Free PMC article.
Absence of annulus in human asthenozoospermia: case report.
Lhuillier P, Rode B, Escalier D, Lorès P, Dirami T, Bienvenu T, Gacon G, Dulioust E, Touré A. Lhuillier P, et al. Among authors: gacon g. Hum Reprod. 2009 Jun;24(6):1296-303. doi: 10.1093/humrep/dep020. Epub 2009 Feb 15. Hum Reprod. 2009. PMID: 19221096
[Human asthenozoospermia and structural defects of the annulus].
Lhuillier P, Escalier D, Gacon G, Dulioust E, Touré A. Lhuillier P, et al. Among authors: gacon g. Med Sci (Paris). 2010 Aug-Sep;26(8-9):688-9. doi: 10.1051/medsci/2010268-9688. Med Sci (Paris). 2010. PMID: 20819699 Free article. French. No abstract available.
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.
El Khouri E, Thomas L, Jeanson L, Bequignon E, Vallette B, Duquesnoy P, Montantin G, Copin B, Dastot-Le Moal F, Blanchon S, Papon JF, Lorès P, Yuan L, Collot N, Tissier S, Faucon C, Gacon G, Patrat C, Wolf JP, Dulioust E, Crestani B, Escudier E, Coste A, Legendre M, Touré A, Amselem S. El Khouri E, et al. Among authors: gacon g. Am J Hum Genet. 2016 Aug 4;99(2):489-500. doi: 10.1016/j.ajhg.2016.06.022. Am J Hum Genet. 2016. PMID: 27486783 Free PMC article.
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.
Lorès P, Coutton C, El Khouri E, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, Papon JF, Gacon G, Escudier E, Arnoult C, Bonhivers M, Savinov SN, Amselem S, Ray PF, Dulioust E, Touré A. Lorès P, et al. Among authors: gacon g. Hum Mol Genet. 2018 Apr 1;27(7):1196-1211. doi: 10.1093/hmg/ddy034. Hum Mol Genet. 2018. PMID: 29365104 Clinical Trial.
118 results