참고문헌
- Bhasin, S., K. Ma and D. M. de Kretser, 1997. Y-chromosome microdeletions and male infertility. Ann. Med. 29, 261-263 https://doi.org/10.3109/07853899708999344
- Brown, G. M., R. A. Furlong, C. A Sargent, R. P. Erickson, G. Longepied, M. Mitchell, M. H. Jones, T. B. Hargreave, H. J. Cooke and N. A. Affara. 1998. Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene. Hum. Mol. Genet. 7, 97-107 https://doi.org/10.1093/hmg/7.1.97
- Chai, N. N., E. C. Salido and P. H. Yen. 1997. Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome. Genomics 45, 355-361 https://doi.org/10.1006/geno.1997.4944
- Chandley, A .C. and H. J. Cooke. 1994. Human male infertility Y-linked genes and spermatogenesis. Hum. Mol. Genet. 3, 1449-1452 https://doi.org/10.1093/hmg/3.suppl_1.1449
- Cooke, H. J. and P. T. Saunders. 2002. Mouse models of male infertility. Nat. Rev. Genet. 3, 790-801 https://doi.org/10.1038/nrg911
- Dorus, S., S. L. Gilbert, M. L. Forster, R. J. Barndt and B. T. Lahn. 2003. The CDY-related gene family: coordinated evolution in copy number, expression profile and protein sequence. Hum. Mol. Genet. 12, 1643-1650 https://doi.org/10.1093/hmg/ddg185
- Elliott, D. J. 2004. The role of potential splicing factors including RBMY, RBMX, hnRNPG-T and STAR proteins in spermatogenesis. Int. J. Androl. 27, 328-334 https://doi.org/10.1111/j.1365-2605.2004.00496.x
- Elliott, D. J., M. R. Millar, K. Oghene, A. Ross, F. Kiesewetter, J. Pryor, M. McIntyre, T. B. Hargreave, P. T. Saunders, P. H. Vogt, A. C. Chandley and H. Cooke. 1997. Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm. Proc. Natl. Acad. Sci. USA. 94, 3848-3853 https://doi.org/10.1073/pnas.94.8.3848
- Foresta, C., A. Ferlin, A. Garolla, M. Rossato, S. Barbaux and A. de Bertoli. 1997. Y-chromosome deletions in idiopathic severe testiculopathies. J. Clin. Endocrinol. Metab. 82, 1075-1080 https://doi.org/10.1210/jc.82.4.1075
- Friel, A., J. A. Houghton, M. Maher, T. Smith, S. Noel, A Nolan, D. Egan and M. Glennon. 2001. Molecular detection of Y chromosome microdeletions: an Irish study. Int. J. Androl. 24, 31-36 https://doi.org/10.1046/j.1365-2605.2001.00264.x
- Hargreave, T. B. 2000. Genetic basis of male fertility. Br. Med. Bull. 56, 650-671 https://doi.org/10.1258/0007142001903454
- Kleiman, S. E., A. Lagziel, L. Yogev, A. Botchan, C. Paz and H. Yavetz. 2001. Expression of CDY1 may identify complete spermatogenesis. Fertil. Steril. 75, 166-173 https://doi.org/10.1016/S0015-0282(00)01639-3
- Kleiman, S. E.., L. Yogev, R. Hauser, A. Botchan, B. Bar-Shira Maymon, L. Schreiber, G. Paz and H. Yavetz. 2003. Members of the CDY family have different expression patterns: CDY1 transcripts have the best correlation with complete spermatogenesis. Hum. Genet. 113. 486-492 https://doi.org/10.1007/s00439-003-0990-9
- Kuroda-Kawaguchi, T., H. Skaletsky, L. G. Brown, P. J. Minx, H. S. Cordum, R. H. Waterston, R. K. Wilson, S. Silber, R. Oates, S. Rozen and D. C. Page. 2001. The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nat. Genet. 29, 279-286 https://doi.org/10.1038/ng757
- Lahn, B. T. and D. C. Page. 1999. Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome. Nat. Genet. 21, 429-433 https://doi.org/10.1038/7771
- Mazeyrat, S., N. Saut, M. G. Mattei and M. J. Mitchell. 1999. RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene. Nat. Genet. 22, 224-226 https://doi.org/10.1038/10282
- Namiki, M. 2000. Genetic aspects of male infertility. World J. Surg. 24, 1176-1179 https://doi.org/10.1007/s002680010198
- Peterlin. B., T. Kunej, J. Sinkovec, N. Gligorievska and B. Zorn. 2002. Screening for Y chromosome micro deletions in 226 Slovenian subfertile men. Hum. Reprod. 17, 17-24
- Reijo, R., T. Y. Lee, P. Salo, R Alagappan, L. G. Brown, M. Rosenberg, S. Rozen, T. Jaffe, D. Straus and O. Hovatta. 1995. Diverse spermatogenic defect in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat. Genet. 10, 383-393 https://doi.org/10.1038/ng0895-383
- Skaletsky, H., T. Kuroda-Kawaguchi, P. J. Minx, H. S. Cordum, L. Hillier, L. C. Brown, S. Repping, T. Pyntikova, J. Ali, T. Bieri, A. Chinwalla, A. Delehaunty, K. Delehaunty, H. Du, G. Fewell, L. Fulton, R. Fulton, T. Graves, S. F. Hou, P. Latrielle, S. Leonard, E. Mardis, R. Maupin, J. McPherson, T. Miner, W. Nash, C. Nguyen, P. Ozersky, K. Pepin, S. Rock, T. Rohlfing, K. Scott, B. Schultz, C. Strong, A. Tin-Wollam, S. P. Yang, R. H. Waterston, R. K. Wilson, S. Rozen and D. C. Page. 2003. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423, 825-837 https://doi.org/10.1038/nature01722
- Thonneau, P., S. Marchand, A. Tallec, M. L. Ferial, B. Ducor, J. Lansac, P. Lopes, J. M. Tabaste and A. Spira. 1991. Incidence and main causes of infertility in a resident population (1,850,000) of three French regions (1988-1989). Hum. Reprod. 6, 811-816 https://doi.org/10.1093/oxfordjournals.humrep.a137433
- Tiepolo, L. and O. Zuffardi. 1976. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Gent. 28, 119-124
- Tse, J. Y., E. Y. Wong, A. N. Cheung, W. S. O, P. C. Tam and W. S. Yeung. 2003. Specific expression of VCY2 in human male germ cells and its involvement in the pathogenesis of male infertility. Biol. Reprod. 69, 746-751 https://doi.org/10.1095/biolreprod.103.015792
- Venables, J. P., D. J. Elliott, O. V. Makarova, E. M. Makarov, H. J. Cooke and I. C. Eperon. 2000. RBMY, a probable human spermatogenesis factor, and other hnRNP G proteins interact with Tra2beta and affect splicing. Hum. Mol. Genet. 9, 685-694 https://doi.org/10.1093/hmg/9.5.685
- Vogt, P. H., A. Edelmann, S. Kirsch, O. Henegariu, P. Hirschmann, F. Kiesewetter, F. M. Kohn, W. B. Schill, S. Farah, C. Ramos, M. Hartmann, W. Hartschuh, D. Meschede, H. M. Behre, A. Castel, E. Nieschlag, W. Weidner, H. J. Grone, A. Jung, W. Engel and G. Haidl. 1996. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum. Mol. Genet. 5, 933-943 https://doi.org/10.1093/hmg/5.7.933
- Wong, E. Y., J. Y. Tse, K. M. Yao, V. C. Lui, P. C. Tam and W. S. Yeung. 2004. Identification and characterization of human VCY2-interacting protein: VCY2IP-1, a microtubule-associated protein-like protein. Biol. Reprod. 70, 775-784 https://doi.org/10.1095/biolreprod.103.018531
- Yen, P. H. 1998. A long-range restriction map of deletion interval 6 of the human Y chromosome: a region frequently deleted in azoospermic males. Genomics 54, 5-12 https://doi.org/10.1006/geno.1998.5526