Publications

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2011
J. - L. Gao, Ding, X. - P., Liu, D. - S., and Zhu, Y. - J., Detection of Klinefelter syndrome by G-banding analysis combined with primed in situ labeling technique, vol. 10, pp. 4026-4033, 2011.
Barch MJ (1991). The ACT Cytogenetics Laboratory Manual. 2nd edn. Raven Press, New York. PMid:1747941   Bhasin S, de Kretser DM and Baker HW (1994). Clinical review 64: Pathophysiology and natural history of male infertility. J. Clin. Endocrinol. Metab. 79: 1525-1529. http://dx.doi.org/10.1210/jc.79.6.1525 PMid:7989450   Ding X-P (2002). Modern Clinical Molecular Genetic and Cytogenetic Techniques. 1st edn. Sichuan University Press, Sichuan.   Gao LJ, Song F and Zhou L (2006). Effect of trypsin of different sources on G-banding analysis. J. Baotou Med. College 22: 77-78.   Koch JE, Kolvraa S, Petersen KB, Gregersen N, et al. (1989). Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ. Chromosoma 98: 259-265. http://dx.doi.org/10.1007/BF00327311 PMid:2612286   Liu DS and Ding XP (2007). Triple-color primed in situ labeling protocol of human metaphase chromosomes. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 24: 514-517. PMid:17922416   Maduro MR and Lamb DJ (2002). Understanding new genetics of male infertility. J. Urol. 168: 2197-2205. http://dx.doi.org/10.1016/S0022-5347(05)64355-8   Medica I, Gligorievska N, Prenc M and Peterlin B (2005). Y microdeletions in the Istria county, Croatia. Asian J. Androl. 7: 213-216. http://dx.doi.org/10.1111/j.1745-7262.2005.00028.x PMid:15897979   Speel EJ, Ramaekers FC and Hopman AH (1997). Sensitive multicolor fluorescence in situ hybridization using catalyzed reporter deposition (CARD) amplification. J. Histochem. Cytochem. 45: 1439-1446. http://dx.doi.org/10.1177/002215549704501013 PMid:9313806   Tharapel AT and Wachtel SS (2006). PRINS for mapping single-copy genes. Methods Mol. Biol. 338: 59-67. PMid:16888350   Therkelsen AJ, Nielsen A, Koch J, Hindkjaer J, et al. (1995). Staining of human telomeres with primed in situ labeling (PRINS). Cytogenet. Cell Genet. 68: 115-118. http://dx.doi.org/10.1159/000133903 PMid:7525160   Van Assche E, Bonduelle M, Tournaye H, Joris H, et al. (1996). Cytogenetics of infertile men. Hum. Reprod. 11 (Suppl 4): 1-24. http://dx.doi.org/10.1093/humrep/11.suppl_4.1 PMid:9147109   Yan J, Bronsard M and Drouin R (2001). Creating a new color by omission of 3 end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique. Chromosoma 109: 565-570. http://dx.doi.org/10.1007/s004120000111 PMid:11305789
J. - L. Gao, Nie, Y., and Ding, X. - P., Primed in situ labeling for detecting single-copy genes, vol. 10, pp. 1884-1890, 2011.
Chandley AC, Gosden JR, Hargreave TB, Spowart G, et al. (1989). Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs). J. Med. Genet. 26: 145-153. http://dx.doi.org/10.1136/jmg.26.3.145 PMid:2709392    PMCid:1015574 Cinti C, Stuppia L and Maraldi NM (2002). Combined use of PRINS and FISH in the study of the dystrophin gene. Am. J. Med. Genet. 107: 115-118. http://dx.doi.org/10.1002/ajmg.10104 PMid:11807884 Habermann B, Mi HF, Edelmann A, Bohring C, et al. (1998). DAZ (Deleted in AZoospermia) genes encode proteins located in human late spermatids and in sperm tails. Hum. Reprod. 13: 363-369. http://dx.doi.org/10.1093/humrep/13.2.363 PMid:9557839 Hargreave TB (2000). Genetic basis of male fertility. Br. Med. Bull. 56: 650-671. http://dx.doi.org/10.1258/0007142001903454 PMid:11255552 Kadandale JS, Wachtel SS, Tunca Y, Wilroy RS Jr, et al. (2000). Localization of SRY by primed in situ labeling in XX and XY sex reversal. Am. J. Med. Genet. 95: 71-74. http://dx.doi.org/10.1002/1096-8628(20001106)95:1<71::AID-AJMG14>3.0.CO;2-Y Kadandale JS, Wachtel SS, Tunca Y, Martens PR, et al. (2002). Deletion of RBM and DAZ in azoospermia: evaluation by PRINS. Am. J. Med. Genet. 107: 105-108. http://dx.doi.org/10.1002/ajmg.10107 PMid:11807882 Kallioniemi A, Kallioniemi O-P, Waldman FM, Chen LC, et al. (1992). Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization. Cytogenet. Cell Genet. 60: 190-193. http://dx.doi.org/10.1159/000133333 Kent-First M, Muallem A, Shultz J, Pryor J, et al. (1999). Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. Mol. Reprod. Dev. 53: 27-41. http://dx.doi.org/10.1002/(SICI)1098-2795(199905)53:1<27::AID-MRD4>3.0.CO;2-W Koch JE, Kolvraa S, Petersen KB, Gregersen N, et al. (1989). Oligonucleotide-priming methods for the chromosome-specific labelling of alpha satellite DNA in situ. Chromosoma 98: 259-265. http://dx.doi.org/10.1007/BF00327311 PMid:2612286 Koch JE, Hindkjaer J, Kolvraa S and Bolund L (1995). Construction of a panel of chromosome-specific oligonucleotide probes (PRINS-primers) useful for the identification of individual human chromosomes in situ. Cytogenet. Cell Genet. 71: 142-147. http://dx.doi.org/10.1159/000134094 Pellestor F (2006). Development and adaptation of the PRINS technology: an overview. Methods Mol. Biol. 334: 211-220. PMid:16861766 Pellestor F, Girardet A, Lefort G, Andreo B, et al. (1995). PRINS as a method for rapid chromosomal labeling on human spermatozoa. Mol. Reprod. Dev. 40: 333-337. http://dx.doi.org/10.1002/mrd.1080400309 PMid:7772343 Pellestor F, Girardet A, Lefort G, Andreo B, et al. (1996). Rapid chromosome detection in human gametes, zygotes, and preimplantation embryos using the PRINS technique. J. Assist. Reprod. Genet. 13: 675-680. http://dx.doi.org/10.1007/BF02069648 PMid:8897129 Pellestor F, Imbert I and Andreo B (2002). Rapid chromosome detection by PRINS in human sperm. Am. J. Med. Genet. 107: 109-114. http://dx.doi.org/10.1002/ajmg.10101 PMid:11807883 Tharapel AT and Wachtel SS (2006). PRINS for mapping single-copy genes. Methods Mol. Biol. 338: 59-67. PMid:16888350 Tharapel SA and Kadandale JS (2002). Primed in situ labeling (PRINS) for evaluation of gene deletions in cancer. Am. J. Med. Genet. 107: 123-126. http://dx.doi.org/10.1002/ajmg.10105 PMid:11807886 Velagelati GV, Shulman LP, Phillips OP, Tharapel SA, et al. (1998). Primed in situ labeling for rapid prenatal diagnosis. Am. J. Obstet. Gynecol. 178: 1313-1320. http://dx.doi.org/10.1016/S0002-9378(98)70338-2 Wachtel SS (1998). X-linked sex-reversing genes. Cytogenet. Cell Genet. 80: 222-225. http://dx.doi.org/10.1159/000014984 Yan J, Bronsard M and Drouin R (2001). Creating a new color by omission of 3 end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique. Chromosoma 109: 565-570. http://dx.doi.org/10.1007/s004120000111 PMid:11305789 Zeng M, Ding X, Jiang M, Li X (2006). Rapid chromosome detection by PRINS in human sperm. Reprod. Contracept. 26: 241-244.