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R. - L. Dai, Wang, R. - X., Jin, J. - L., Niu, G. - N., Lee, J. - Y., Li, S. - B., and Liu, R. - Z., Correlation of Y-chromosome multiple segmental deletions and chromosomal anomalies in non-obstructive azoospermic males from northeastern China, vol. 11, pp. 2422-2431, 2012.
Balaresque P, Bowden GR, Parkin EJ, Omran GA, et al. (2008). Dynamic nature of the proximal AZFc region of the human Y chromosome: multiple independent deletion and duplication events revealed by microsatellite analysis. Hum. Mutat. 29: 1171-1180. PMid:18470947 PMCid:2689608   Balkan M, Tekes S and Gedik A (2008). Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey. J. Assist. Reprod. Genet. 25: 559-565. PMid:18953646 PMCid:2593766   Briton-Jones C and Haines CJ (2000). Microdeletions on the long arm of the Y chromosome and their association with male-factor infertility. Hong Kong Med. J. 6: 184-189. PMid:10895142   Chiang HS, Yeh SD, Wu CC, Huang BC, et al. (2004). Clinical and pathological correlation of the microdeletion of Y chromosome for the 30 patients with azoospermia and severe oligoasthenospermia. Asian J. Androl. 6: 369-375. PMid:15546032   Devroey P, Fauser BC and Diedrich K (2009). Approaches to improve the diagnosis and management of infertility. Hum. Reprod. Update 15: 391-408. PMid:19380415 PMCid:2691653   Ferlin A, Arredi B, Speltra E, Cazzadore C, et al. (2007). Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy. J. Clin. Endocrinol. Metab. 92: 762-770. PMid:17213277   Foresta C, Ferlin A and Moro E (2000). Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility. Hum. Mol. Genet. 9: 1161-1169. PMid:10767340   Foresta C, Moro E and Ferlin A (2001). Y chromosome microdeletions and alterations of spermatogenesis. Endocr. Rev. 22: 226-239. PMid:11294825   Gatta V, Stuppia L, Calabrese G, Morizio E, et al. (2002). A new case of Yq microdeletion transmitted from a normal father to two infertile sons. J. Med. Genet. 39: E27. PMid:12070259 PMCid:1735151   Imken L, El HB, Chafik A, Nahili H, et al. (2007). AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men. Asian J. Androl. 9: 674-678. PMid:17712485   Kato H, Komori S, Nakata Y, Sakata K, et al. (2001). Screening for deletions in interval D16-22 of the Y chromosome in azoospermic and oligozoospermic Japanese men. J. Hum. Genet. 46: 110-114. PMid:11310577   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.<27::AID-MRD4>3.0.CO;2-W   Kihaile PE, Yasui A and Shuto Y (2005). Prospective assessment of Y-chromosome microdeletions and reproductive outcomes among infertile couples of Japanese and African origin. J. Exp. Clin. Assist. Reprod. 2: 9. PMid:15987528 PMCid:1198247   Krausz C, Rajpert-De ME, Frydelund-Larsen L, Quintana-Murci L, et al. (2001). Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: microdeletions are specific for spermatogenic failure. J. Clin. Endocrinol. Metab. 86: 2638-2642. PMid:11397865   Krausz C, Forti G and McElreavey K (2003). The Y chromosome and male fertility and infertility. Int. J. Androl. 26: 70-75. PMid:12641824   Le Bourhis C, Siffroi JP, McElreavey K and Dadoune JP (2000). Y chromosome microdeletions and germinal mosaicism in infertile males. Mol. Hum. Reprod. 6: 688-693. PMid:10908277   Lin YM, Chen CW, Sun HS, Hsu CC, et al. (2000). Y-chromosome microdeletion and its effect on reproductive decisions in taiwanese patients presenting with nonobstructive azoospermia. Urology 56: 1041-1046.   Lin YM, Lin YH, Teng YN, Hsu CC, et al. (2002). Gene-based screening for Y chromosome deletions in Taiwanese men presenting with spermatogenic failure. Fertil. Steril. 77: 897-903.   Mafra FA, Christofolini DM, Bianco B, Gava MM, et al. (2011). Chromosomal and molecular abnormalities in a group of Brazilian infertile men with severe oligozoospermia or non-obstructive azoospermia attending an infertility service. Int. Braz. J. Urol. 37: 244-250. PMid:21557841   Martinez MC, Bernabe MJ, Gomez E, Ballesteros A, et al. (2000). Screening for AZF deletion in a large series of severely impaired spermatogenesis patients. J. Androl. 21: 651-655. PMid:10975411   Medica I, Gligorievska N, Prenc M and Peterlin B (2005). Y microdeletions in the Istria county, Croatia. Asian J. Androl. 7: 213-216. PMid:15897979   Mirfakhraie R, Mirzajani F, Kalantar SM, Montazeri M, et al. (2010). High prevalence of AZFb microdeletion in Iranian Y-chromosome microdeletions and chromosomal anomalies patients with idiopathic non-obstructive azoospermia. Ind. J. Med. Res. 132: 265-270. PMid:20847372   Mitra A, Dada R, Kumar R, Gupta NP, et al. (2008). Screening for Y-chromosome microdeletions in infertile Indian males: utility of simplified multiplex PCR. Ind. J. Med. Res. 127: 124-132. PMid:18403789   Organization WH (1999). Laboratory Manual for the Examination of Human Semen and Semen-Cervical Mucus Interaction. Cambridge University Press, Cambridge.   Osterlund C, Segersteen E, Arver S and Pousette A (2000). Low number of Y-chromosome deletions in infertile azoospermic men at a Swedish andrology centre. Int. J. Androl. 23: 225-229. PMid:10886425   Peterlin B, Kunej T and Hristovski D (2004). Diagnostic test for Y chromosome microdeletion screening in male infertility. Genet. Test. 8: 45-49. PMid:15140373   Shaffer LG, Slovak ML and Campbell LJ (2009). ISCN 2009: An International System for Human Cytogenetic Nomenclature, Karger.   Simoni M, Bakker E and Krausz C (2004). EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int. J. Androl. 27: 240-249. PMid:15271204   Tiepolo L and Zuffardi O (1976). Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Genet. 34: 119-124. PMid:1002136   Tsujimura A, Matsumiya K, Takao T, Miyagawa Y, et al. (2004). Clinical analysis of patients with azoospermia factor deletions by microdissection testicular sperm extraction. Int. J. Androl. 27: 76-81. PMid:15149464   Vicdan A, Vicdan K, Gunalp S, Kence A, et al. (2004). Genetic aspects of human male infertility: the frequency of chromosomal abnormalities and Y chromosome microdeletions in severe male factor infertility. Eur. J. Obstet. Gynecol. Reprod. Biol. 117: 49-54. PMid:15474244   Vutyavanich T, Piromlertamorn W, Sirirungsi W and Sirisukkasem S (2007). Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Thai men with oligozoospermia and azoospermia. Asian J. Androl. 9: 68-75. PMid:17187159   Yang Y, Ma MY, Xiao CY, Li L, et al. (2008). Massive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/ or maturation arrest. Int. J. Androl. 31: 573-578. PMid:17877719