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“Genetic association of UBE2B variants with susceptibility to male infertility in a Northeast Chinese population”, vol. 11, pp. 4226-4234, 2012.
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Baarends WM, Wassenaar E, Hoogerbrugge JW, van Cappellen G, et al. (2003). Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase. Mol. Cell. Biol. 23: 1151-1162.
http://dx.doi.org/10.1128/MCB.23.4.1151-1162.2003
PMid:12556476 PMCid:141135
Ciechanover A (1996). Ubiquitin-mediated proteolysis and male sterility. Nat. Med. 2: 1188-1190.
http://dx.doi.org/10.1038/nm1196-1188
PMid:8898739
Escalier D and Serres C (1985). Aberrant distribution of the peri-axonemal structures in the human spermatozoon: possible role of the axoneme in the spatial organization of the flagellar components. Biol. Cell 53: 239-250.
http://dx.doi.org/10.1111/j.1768-322X.1985.tb00372.x
PMid:3160418
Escalier D, Bai XY, Silvius D, Xu PX, et al. (2003). Spermatid nuclear and sperm periaxonemal anomalies in the mouse Ube2b null mutant. Mol. Reprod. Dev. 65: 298-308.
http://dx.doi.org/10.1002/mrd.10290
PMid:12784252
Grootegoed JA, Siep M and Baarends WM (2000). Molecular and cellular mechanisms in spermatogenesis. Baillieres Best Pract. Res. Clin. Endocrinol. Metab. 14: 331-343.
http://dx.doi.org/10.1053/beem.2000.0083
PMid:11097779
Huang I, Emery BR, Christensen GL, Griffin J, et al. (2008). Novel UBE2B-associated polymorphisms in an azoospermic/ oligozoospermic population. Asian J. Androl. 10: 461-466.
http://dx.doi.org/10.1111/j.1745-7262.2008.00386.x
PMid:18385908
Li Z, Zhang Z, He Z, Tang W, et al. (2009). A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn). Cell Res. 19: 519-523.
http://dx.doi.org/10.1038/cr.2009.33
PMid:19290020
Nishimune Y and Tanaka H (2006). Infertility caused by polymorphisms or mutations in spermatogenesis-specific genes. J. Androl. 27: 326-334.
http://dx.doi.org/10.2164/jandrol.05162
PMid:16474012
Pengo M, Ferlin A, Arredi B, Ganz F, et al. (2006). FSH receptor gene polymorphisms in fertile and infertile Italian men. Reprod. Biomed. Online 13: 795-800.
http://dx.doi.org/10.1016/S1472-6483(10)61026-7
Rajapurohitam V, Morales CR, El-Alfy M, Lefrancois S, et al. (1999). Activation of a UBC4-dependent pathway of ubiquitin conjugation during postnatal development of the rat testis. Dev. Biol. 212: 217-228.
http://dx.doi.org/10.1006/dbio.1999.9342
PMid:10419697
Rajapurohitam V, Bedard N and Wing SS (2002). Control of ubiquitination of proteins in rat tissues by ubiquitin conjugating enzymes and isopeptidases. Am. J. Physiol. Endocrinol. Metab. 282: E739-E745.
PMid:11882492
Roest HP, van Klaveren J, de Wit J, van Gurp CG, et al. (1996). Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification. Cell 86: 799-810.
http://dx.doi.org/10.1016/S0092-8674(00)80154-3
Serres C, Feneux D and Jouannet P (1986). Abnormal distribution of the periaxonemal structures in a human sperm flagellar dyskinesia. Cell Motil. Cytoskeleton 6: 68-76.
http://dx.doi.org/10.1002/cm.970060109
PMid:3698108
Shi YY and He L (2005). SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 15: 97-98.
http://dx.doi.org/10.1038/sj.cr.7290272
PMid:15740637
Suryavathi V, Khattri A, Gopal K, Rani DS, et al. (2008). Novel variants in UBE2B gene and idiopathic male infertility. J. Androl. 29: 564-571.
http://dx.doi.org/10.2164/jandrol.107.004580
PMid:18497339
World Health Organization (1999). WHO Laboratory Manual for the Examination of Human Semen and Sperm-Cervical Mucus Interaction. 4th edn. Cambridge University Press, Cambridge.