Publications
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“Detection of Klinefelter syndrome by G-banding analysis combined with primed in situ labeling technique”, vol. 10, pp. 4026-4033, 2011.
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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
“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.