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Volumn 94, Issue 7, 2010, Pages 2770.e11-2770.e16

Transmissible microdeletion of the Y-chromosome encompassing two DAZ copies, four RBMY1 copies, and both PRY copies

Author keywords

transmissible microdeletion; Y chromosome microdeletion; Y chromosome rearrangement

Indexed keywords

FOLLITROPIN; GENOMIC DNA;

EID: 78650211597     PISSN: 00150282     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2010.04.038     Document Type: Article
Times cited : (21)

References (29)
  • 1
    • 0017119580 scopus 로고
    • Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm
    • L. Tiepolo, and 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
  • 2
    • 0026726412 scopus 로고
    • The human y chromosome: Overlapping DNA clones spanning the euchromatic region
    • S. Foote, D. Vollrath, A. Hilton, and D.C. Page The human Y chromosome: overlapping DNA clones spanning the euchromatic region Science 258 1992 60 66
    • (1992) Science , vol.258 , pp. 60-66
    • Foote, S.1    Vollrath, D.2    Hilton, A.3    Page, D.C.4
  • 3
    • 0026756965 scopus 로고
    • The human y chromosome: A 43-interval map based on naturally occurring deletions
    • D. Vollrath, S. Foote, A. Hilton, L.G. Brown, P. Beer-Romero, and J.S. Bogan The human Y chromosome: a 43-interval map based on naturally occurring deletions Science 258 1992 52 59
    • (1992) Science , vol.258 , pp. 52-59
    • Vollrath, D.1    Foote, S.2    Hilton, A.3    Brown, L.G.4    Beer-Romero, P.5    Bogan, J.S.6
  • 4
    • 0027715823 scopus 로고
    • A y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis
    • K. Ma, J.D. Inglis, A. Sharkey, W.A. Bickmore, R.E. Hill, and E.J. Prosser A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis Cell 75 1993 1287 1295
    • (1993) Cell , vol.75 , pp. 1287-1295
    • Ma, K.1    Inglis, J.D.2    Sharkey, A.3    Bickmore, W.A.4    Hill, R.E.5    Prosser, E.J.6
  • 5
    • 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, and 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
  • 6
    • 0026726199 scopus 로고
    • Microdeletions in interval 6 of the y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene
    • P. Vogt, A.C. Chandley, T.B. Hargreave, R. Keil, K. Ma, and A. Sharkey Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene Hum Genet 89 1992 491 496
    • (1992) Hum Genet , vol.89 , pp. 491-496
    • Vogt, P.1    Chandley, A.C.2    Hargreave, T.B.3    Keil, R.4    Ma, K.5    Sharkey, A.6
  • 8
    • 0035014112 scopus 로고    scopus 로고
    • Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47, XXY, mosaic 46, XY/47, XXY and 47, XYY) assessed by fluorescence in-situ hybridization
    • J. Blanco, J. Egozcue, and F. Vidal Meiotic behaviour of the sex chromosomes in three patients with sex chromosome anomalies (47, XXY, mosaic 46, XY/47, XXY and 47, XYY) assessed by fluorescence in-situ hybridization Hum Reprod 16 2001 887 892
    • (2001) Hum Reprod , vol.16 , pp. 887-892
    • Blanco, J.1    Egozcue, J.2    Vidal, F.3
  • 9
    • 0034641881 scopus 로고    scopus 로고
    • Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events
    • C. Kamp, P. Hirschmann, H. Voss, K. Huellen, and P.H. Vogt Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events Hum Mol Genet 9 2000 2563 2572
    • (2000) Hum Mol Genet , vol.9 , pp. 2563-2572
    • Kamp, C.1    Hirschmann, P.2    Voss, H.3    Huellen, K.4    Vogt, P.H.5
  • 10
    • 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, and 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
  • 11
    • 0036782130 scopus 로고    scopus 로고
    • Recombination between palindromes P5 and P1 on the human y chromosome causes massive deletions and spermatogenic failure
    • C. Sun, H. Skaletsky, J. Lange, S. Silber, F. Van Der Veen, and 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
    • Sun, C.1    Skaletsky, H.2    Lange, J.3    Silber, S.4    Van Der Veen, F.5    Oates, R.D.6
  • 12
    • 0034703178 scopus 로고    scopus 로고
    • Deletion of azoospermia factor a (AZFa) region of human y chromosome caused by recombination between HERV15 proviruses
    • C. Sun, H. Skaletsky, S. Rozen, J. Gromoll, E. Nieschlag, and R. Oates Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses Hum Mol Genet 9 2000 2291 2296
    • (2000) Hum Mol Genet , vol.9 , pp. 2291-2296
    • Sun, C.1    Skaletsky, H.2    Rozen, S.3    Gromoll, J.4    Nieschlag, E.5    Oates, R.6
  • 13
    • 0141813754 scopus 로고    scopus 로고
    • Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion
    • R. Ambasudhan, K. Singh, J.K. Agarwal, S.K. Singh, A. Khanna, and R.K. Sah Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion J Biosci 28 2003 605 612
    • (2003) J Biosci , vol.28 , pp. 605-612
    • Ambasudhan, R.1    Singh, K.2    Agarwal, J.K.3    Singh, S.K.4    Khanna, A.5    Sah, R.K.6
  • 14
    • 33947546526 scopus 로고    scopus 로고
    • Molecular and clinical characterization of y chromosome microdeletions in infertile men: A 10-year experience in Italy
    • A. Ferlin, B. Arredi, E. Speltra, C. Cazzadore, R. Selice, and A. Garolla Molecular and clinical characterization of Y chromosome microdeletions in infertile men: a 10-year experience in Italy J Clin Endocrinol Metab 92 2007 762 770
    • (2007) J Clin Endocrinol Metab , vol.92 , pp. 762-770
    • Ferlin, A.1    Arredi, B.2    Speltra, E.3    Cazzadore, C.4    Selice, R.5    Garolla, A.6
  • 15
    • 0036712133 scopus 로고    scopus 로고
    • Natural transmission of a partial AZFb deletion of the y chromosome over three generations: Case report
    • C. Rolf, J. Gromoll, M. Simoni, and E. Nieschlag Natural transmission of a partial AZFb deletion of the Y chromosome over three generations: case report Hum Reprod 17 2002 2267 2271
    • (2002) Hum Reprod , vol.17 , pp. 2267-2271
    • Rolf, C.1    Gromoll, J.2    Simoni, M.3    Nieschlag, E.4
  • 16
    • 33749507234 scopus 로고    scopus 로고
    • Natural transmission of AZFb Y-chromosomal microdeletion from father to his three sons
    • H. Samli, M. Murat Samli, and M. Solak Natural transmission of AZFb Y-chromosomal microdeletion from father to his three sons Arch Androl 52 2006 423 426
    • (2006) Arch Androl , vol.52 , pp. 423-426
    • Samli, H.1    Murat Samli, M.2    Solak, M.3
  • 17
    • 0037967242 scopus 로고    scopus 로고
    • The male-specific region of the human y chromosome is a mosaic of discrete sequence classes
    • H. Skaletsky, T. Kuroda-Kawaguchi, P.J. Minx, H.S. Cordum, L. Hillier, and L.G. Brown The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes Nature 423 2003 825 837
    • (2003) Nature , vol.423 , pp. 825-837
    • Skaletsky, H.1    Kuroda-Kawaguchi, T.2    Minx, P.J.3    Cordum, H.S.4    Hillier, L.5    Brown, L.G.6
  • 18
    • 0036178949 scopus 로고    scopus 로고
    • A nomenclature system for the tree of human Y-chromosomal binary haplogroups
    • A nomenclature system for the tree of human Y-chromosomal binary haplogroups Genome Res 12 2002 339 348
    • (2002) Genome Res , vol.12 , pp. 339-348
  • 19
    • 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, and 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
  • 21
    • 2642530984 scopus 로고    scopus 로고
    • A family of human y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region
    • S. Repping, S.K. van Daalen, C.M. Korver, L.G. Brown, J.D. Marszalek, and J. Gianotten A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region Genomics 83 2004 1046 1052
    • (2004) Genomics , vol.83 , pp. 1046-1052
    • Repping, S.1    Van Daalen, S.K.2    Korver, C.M.3    Brown, L.G.4    Marszalek, J.D.5    Gianotten, J.6
  • 23
    • 0024340871 scopus 로고
    • Radioimmunoassay of testosterone not bound to sex-steroid-binding protein in plasma
    • H. Dechaud, H. Lejeune, M. Garoscio-Cholet, R. Mallein, and M. Pugeat Radioimmunoassay of testosterone not bound to sex-steroid-binding protein in plasma Clin Chem 35 1989 1609 1614
    • (1989) Clin Chem , vol.35 , pp. 1609-1614
    • Dechaud, H.1    Lejeune, H.2    Garoscio-Cholet, M.3    Mallein, R.4    Pugeat, M.5
  • 24
    • 0031024316 scopus 로고    scopus 로고
    • Screening for deletions of the y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia
    • M. Simoni, J. Gromoll, B. Dworniczak, C. Rolf, K. Abshagen, and A. Kamischke Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia Fertil Steril 67 1997 542 547
    • (1997) Fertil Steril , vol.67 , pp. 542-547
    • Simoni, M.1    Gromoll, J.2    Dworniczak, B.3    Rolf, C.4    Abshagen, K.5    Kamischke, A.6
  • 27
    • 0033032375 scopus 로고    scopus 로고
    • The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome
    • M.L. Delbridge, P.A. Lingenfelter, C.M. Disteche, and J.A. Graves The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome Nat Genet 22 1999 223 224
    • (1999) Nat Genet , vol.22 , pp. 223-224
    • Delbridge, M.L.1    Lingenfelter, P.A.2    Disteche, C.M.3    Graves, J.A.4
  • 29
    • 4143100211 scopus 로고    scopus 로고
    • Are sequence family variants useful for identifying deletions in the human y chromosome?
    • S. Repping, C.M. Korver, R.D. Oates, S. Silber, F. van der Veen, and D.C. Page Are sequence family variants useful for identifying deletions in the human Y chromosome? Am J Hum Genet 75 2004 514 517 author reply, 517-9
    • (2004) Am J Hum Genet , vol.75 , pp. 514-517
    • Repping, S.1    Korver, C.M.2    Oates, R.D.3    Silber, S.4    Van Der Veen, F.5    Page, D.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.