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Volumn 85, Issue 4, 2006, Pages 1061-1063

Preliminary study of the relationship between DAZ gene copy deletions and spermatogenic impairment in Chinese men

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AZOOSPERMIA; CONTROLLED STUDY; DAZ GENE; GENE; GENE DELETION; HUMAN; MAJOR CLINICAL STUDY; MALE; OLIGOSPERMIA; PREVALENCE; PRIORITY JOURNAL; SPERMATOGENESIS;

EID: 33645385369     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2005.09.025     Document Type: Article
Times cited : (11)

References (19)
  • 1
    • 0017119580 scopus 로고
    • Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
    • L. Tiepolo, O. Zuffardi Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm Hum Genet 34 1976 119 124
    • (1976) Hum Genet , vol.34 , pp. 119-124
    • Tiepolo, L.1    Zuffardi, O.2
  • 4
    • 0242298320 scopus 로고    scopus 로고
    • Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
    • S. Repping, H. Skaletsky, L. Brown, S.K. van Daalen, C.M. Korver, T. Pyntikova Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection Nat Genet 35 2003 247 251
    • (2003) Nat Genet , vol.35 , pp. 247-251
    • Repping, S.1    Skaletsky, H.2    Brown, L.3    Van Daalen, S.K.4    Korver, C.M.5    Pyntikova, T.6
  • 5
    • 0035184973 scopus 로고    scopus 로고
    • The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men
    • T. Kuroda-Kawaguchi, H. Skaletsky, L.G. Brown, P.J. Minx, H.S. Cordum, R.H. Waterston The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men Nat Genet 29 2001 279 286
    • (2001) Nat Genet , vol.29 , pp. 279-286
    • Kuroda-Kawaguchi, T.1    Skaletsky, H.2    Brown, L.G.3    Minx, P.J.4    Cordum, H.S.5    Waterston, R.H.6
  • 6
    • 0029088061 scopus 로고
    • Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
    • R. Reijo, T.Y. Lee, P. Salo, R. Alagappan, L.G. Brown, M. Rosenberg Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 1995 383 393
    • (1995) Nat Genet , vol.10 , pp. 383-393
    • Reijo, R.1    Lee, T.Y.2    Salo, P.3    Alagappan, R.4    Brown, L.G.5    Rosenberg, M.6
  • 8
    • 0031569890 scopus 로고    scopus 로고
    • Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene
    • E. Seboun, S. Barbaux, T. Bourgeron, S. Nishi, A. Agulnik, M. Egashira Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene Genomics 41 1997 227 235
    • (1997) Genomics , vol.41 , pp. 227-235
    • Seboun, E.1    Barbaux, S.2    Bourgeron, T.3    Nishi, S.4    Agulnik, A.5    Egashira, M.6
  • 12
    • 0035012270 scopus 로고    scopus 로고
    • Y chromosome microdeletions and alterations of spermatogenesis
    • C. Foresta, E. Moro, A. Ferlin Y chromosome microdeletions and alterations of spermatogenesis Endocrinol Rev 22 2001 226 239
    • (2001) Endocrinol Rev , vol.22 , pp. 226-239
    • Foresta, C.1    Moro, E.2    Ferlin, A.3
  • 13
    • 0036782130 scopus 로고    scopus 로고
    • Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure
    • S. Repping, H. Skaletsky, J. Lange, S. Silber, F. Van Der Veen, R.D. Oates Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure Am J Hum Genet 71 2002 906 922
    • (2002) Am J Hum Genet , vol.71 , pp. 906-922
    • Repping, S.1    Skaletsky, H.2    Lange, J.3    Silber, S.4    Van Der Veen, F.5    Oates, R.D.6
  • 14
    • 15044347800 scopus 로고    scopus 로고
    • Association of partial AZFc region deletions with spermatogenic impairment and male infertility
    • A. Ferlin, A. Tessari, F. Ganz, E. Marchina, S. Barlati, A. Garolla Association of partial AZFc region deletions with spermatogenic impairment and male infertility J Med Genet 42 2005 209 213
    • (2005) J Med Genet , vol.42 , pp. 209-213
    • Ferlin, A.1    Tessari, A.2    Ganz, F.3    Marchina, E.4    Barlati, S.5    Garolla, A.6
  • 15
    • 12444309408 scopus 로고    scopus 로고
    • High frequency of gr/gr chromosome Y deletions in consecutive oligozoospermic ICSI candidates
    • M. de Llanos, J.L. Ballesca, C. Gazquez, E. Margarit, R. Oliva High frequency of gr/gr chromosome Y deletions in consecutive oligozoospermic ICSI candidates Hum Reprod 20 2005 216 220
    • (2005) Hum Reprod , vol.20 , pp. 216-220
    • De Llanos, M.1    Ballesca, J.L.2    Gazquez, C.3    Margarit, E.4    Oliva, R.5
  • 16
    • 12444336969 scopus 로고    scopus 로고
    • Partial deletions in the AZFc region of the Y chromosome occur in men with impaired as well as normal spermatogenesis
    • K. Hucklenbroich, J. Gromoll, M. Heinrich, C. Hohoff, E. Nieschlag, M. Simoni Partial deletions in the AZFc region of the Y chromosome occur in men with impaired as well as normal spermatogenesis Hum Reprod 20 2005 191 197
    • (2005) Hum Reprod , vol.20 , pp. 191-197
    • Hucklenbroich, K.1    Gromoll, J.2    Heinrich, M.3    Hohoff, C.4    Nieschlag, E.5    Simoni, M.6
  • 18
    • 4043092052 scopus 로고    scopus 로고
    • EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004
    • M. Simoni, E. Bakker, C. Krausz EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004 Int J Androl 27 2004 240 249
    • (2004) Int J Androl , vol.27 , pp. 240-249
    • Simoni, M.1    Bakker, E.2    Krausz, C.3
  • 19
    • 8744291701 scopus 로고    scopus 로고
    • Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility
    • N. Machev, N. Saut, G. Longepied, P. Terriou, A. Navarro, N. Levy Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility J Med Genet 41 2004 814 825
    • (2004) J Med Genet , vol.41 , pp. 814-825
    • MacHev, N.1    Saut, N.2    Longepied, G.3    Terriou, P.4    Navarro, A.5    Levy, N.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.