메뉴 건너뛰기




Volumn 3, Issue 7, 1997, Pages 549-554

On the origin and frequency of Y chromosome deletions responsible for severe male infertility

Author keywords

Deletions; Meiosis; Mosaicism; Oligozoospermia; Post fertilization deletions

Indexed keywords

ARTICLE; CHROMOSOME DELETION; GENETICS; HUMAN; MALE; OLIGOSPERMIA; Y CHROMOSOME;

EID: 0031181517     PISSN: 13609947     EISSN: None     Source Type: Journal    
DOI: 10.1093/molehr/3.7.549     Document Type: Article
Times cited : (65)

References (65)
  • 1
    • 0030011808 scopus 로고    scopus 로고
    • Report of the Second International Workshop on Y Chromosome Mapping, 1995
    • Affara, N., Bishop, C., Brown, W. et al. (1996) Report of the Second International Workshop on Y Chromosome Mapping, 1995. Cytogenet. Cell Genet., 73, 33-76.
    • (1996) Cytogenet. Cell Genet. , vol.73 , pp. 33-76
    • Affara, N.1    Bishop, C.2    Brown, W.3
  • 2
    • 0031568328 scopus 로고    scopus 로고
    • Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo
    • Aoki, F., Worrad, D.M. and Schultz, R.M. (1997) Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo Dev. Biol., 181, 296-307.
    • (1997) Dev. Biol. , vol.181 , pp. 296-307
    • Aoki, F.1    Worrad, D.M.2    Schultz, R.M.3
  • 3
    • 0029099989 scopus 로고
    • Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
    • Baker, S.M. et al. (1995) Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell, 82, 309-319.
    • (1995) Cell , vol.82 , pp. 309-319
    • Baker, S.M.1
  • 4
    • 8944232867 scopus 로고    scopus 로고
    • Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
    • Baker, S.M., Plug, A.W., Prolla, T.A. et al. (1996) Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nature Genet., 13, 336-342.
    • (1996) Nature Genet. , vol.13 , pp. 336-342
    • Baker, S.M.1    Plug, A.W.2    Prolla, T.A.3
  • 5
    • 84971791311 scopus 로고
    • Transmission ratios at the T-locus in the mouse inter and intra-male heterogeneity
    • Braden, A.W.H. and Wieler, H. (1964) Transmission ratios at the T-locus in the mouse inter and intra-male heterogeneity. J. Biol. Sci., 17, 921-934.
    • (1964) J. Biol. Sci. , vol.17 , pp. 921-934
    • Braden, A.W.H.1    Wieler, H.2
  • 6
    • 0028281589 scopus 로고
    • Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy
    • Bunyan, D.J., Robinson, D.O., Collins, A.L. et al. (1994) Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy. Hum. Genet., 93, 541-544.
    • (1994) Hum. Genet. , vol.93 , pp. 541-544
    • Bunyan, D.J.1    Robinson, D.O.2    Collins, A.L.3
  • 7
    • 0023341383 scopus 로고
    • Gene conversion, recombination nodules, and the initiation of meiotic synapsis
    • Carpenter, A.T.C. (1987) Gene conversion, recombination nodules, and the initiation of meiotic synapsis. BioEssays, 6, 232-236.
    • (1987) BioEssays , vol.6 , pp. 232-236
    • Carpenter, A.T.C.1
  • 10
    • 0006350117 scopus 로고
    • Meiotic studies and fertility in human translocation carriers
    • Daniel, A. (ed), Alan R.Liss, New York
    • Chandley, A.C. (1988) Meiotic studies and fertility in human translocation carriers. In Daniel, A. (ed), The Cytogenetics of Mammalian Autosomal Rearrangements. Alan R.Liss, New York, pp. 361-382.
    • (1988) The Cytogenetics of Mammalian Autosomal Rearrangements , pp. 361-382
    • Chandley, A.C.1
  • 11
    • 0028059593 scopus 로고
    • Human male fertility - Y-linked genes and spermatogenesis
    • Chandley, A.C. and Cooke, H.J. (1994) Human male fertility - Y-linked genes and spermatogenesis. Hum. Mol. Genet., 3, 1449-1452.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1449-1452
    • Chandley, A.C.1    Cooke, H.J.2
  • 12
    • 10144238527 scopus 로고    scopus 로고
    • Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DNF3 gene POU3F4
    • de Kok, Y.J.M., Vossenaar, E.R., Cremers, C.W.R.J. et al. (1996) Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DNF3 gene POU3F4. Hum. Mol. Genet., 5, 1229-1235.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1229-1235
    • Kok, Y.J.M.1    Vossenaar, E.R.2    Cremers, C.W.R.J.3
  • 13
    • 0029295123 scopus 로고    scopus 로고
    • The origin of genetic defects in the human and their detection in the preimplantation embryo
    • Delhanty, J.D.A. and Handyside, A.H. (1996) The origin of genetic defects in the human and their detection in the preimplantation embryo. Hum. Reprod. Update, 1, 201-215.
    • (1996) Hum. Reprod. Update , vol.1 , pp. 201-215
    • Delhanty, J.D.A.1    Handyside, A.H.2
  • 14
    • 0020341574 scopus 로고
    • The transition from maternal to embryonic control in 2-cell mouse embryos
    • Flach, G., Johnson, M.H., Braude, P.R. et al. (1982) The transition from maternal to embryonic control in 2-cell mouse embryos. EMBO J., 6, 681-686.
    • (1982) EMBO J. , vol.6 , pp. 681-686
    • Flach, G.1    Johnson, M.H.2    Braude, P.R.3
  • 15
    • 0019444653 scopus 로고
    • XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocystes of the mouse (Mus musculus)
    • Forejt, J., Gregorova, S. and Goetz, P. (1981) XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocystes of the mouse (Mus musculus). Chromosoma, 82, 41.
    • (1981) Chromosoma , vol.82 , pp. 41
    • Forejt, J.1    Gregorova, S.2    Goetz, P.3
  • 16
    • 0027089750 scopus 로고
    • Identification of a second pseudoautosomal region near the Xq and Yq telomeres
    • Freije, D., Helms, C., Watson, M.S. and Donis-Keller, H. (1992) Identification of a second pseudoautosomal region near the Xq and Yq telomeres. Science, 258, 1784-1787.
    • (1992) Science , vol.258 , pp. 1784-1787
    • Freije, D.1    Helms, C.2    Watson, M.S.3    Donis-Keller, H.4
  • 17
    • 0029962236 scopus 로고    scopus 로고
    • Expression of the recombinase-activating gene (Rag-1) in murine early embryogensis
    • Hayakawa, S., Togichi, M , Chishima, F. et al. (1996) Expression of the recombinase-activating gene (Rag-1) in murine early embryogensis. Immunol. Cell Biol., 74, 52-56.
    • (1996) Immunol. Cell Biol. , vol.74 , pp. 52-56
    • Hayakawa, S.1    Togichi, M.2    Chishima, F.3
  • 18
    • 0028364565 scopus 로고
    • Complex gene conversion events in germline mutation at human minisatellites
    • Jeffreys, A.J., Tamaki, K., MacLeod, A. et al. (1994) Complex gene conversion events in germline mutation at human minisatellites. Nature Genet., 6, 136-145.
    • (1994) Nature Genet. , vol.6 , pp. 136-145
    • Jeffreys, A.J.1    Tamaki, K.2    MacLeod, A.3
  • 19
    • 0029147621 scopus 로고
    • The IL-9 receptor gene (IL9R): Genomic structure, chromosomal localization in the pseudioautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter and 18pter
    • Kermoum, A., Van Roost, E., Arden, K.C. et al (1995) The IL-9 receptor gene (IL9R): genomic structure, chromosomal localization in the pseudioautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter and 18pter. Genomics. 29, 371-382.
    • (1995) Genomics. , vol.29 , pp. 371-382
    • Kermoum, A.1    Van Roost, E.2    Arden, K.C.3
  • 20
    • 0030036032 scopus 로고    scopus 로고
    • Infertility in intracytoplasmic-sperm-injection-derived sons
    • Kent-First, M.G., Kol, S., Muallem, A. et al. (1996a) Infertility in intracytoplasmic-sperm-injection-derived sons. Lancet, 348, 332.
    • (1996) Lancet , vol.348 , pp. 332
    • Kent-First, M.G.1    Kol, S.2    Muallem, A.3
  • 21
    • 0030323575 scopus 로고    scopus 로고
    • The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmic sperm injection and their infertile fathers
    • Kent-First, M.G., Kol, S., Muallem, A. et al. (1996b) The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmic sperm injection and their infertile fathers. Mol. Hum. Reprod., 2, 943-950.
    • (1996) Mol. Hum. Reprod. , vol.2 , pp. 943-950
    • Kent-First, M.G.1    Kol, S.2    Muallem, A.3
  • 22
    • 0028114292 scopus 로고
    • PCR analysis of the Y chromosome long arm in azoospermic patients: Evidence for a second locus required for spermatogenesis
    • Kobayashi, K., Mizuno, K., Hida, A. et al. (1994) PCR analysis of the Y chromosome long arm in azoospermic patients: evidence for a second locus required for spermatogenesis. Hum. Mol. Genet., 3, 1965-1967.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1965-1967
    • Kobayashi, K.1    Mizuno, K.2    Hida, A.3
  • 23
    • 0030973347 scopus 로고    scopus 로고
    • Microdeletions of the Y chromosome and intracytoplasmic sperm injection (ICSI): From gene to clinic
    • in press
    • Kremer, J.A.M., Tuerlings, J H.A.M., Meulem, E.J.H. et al (1997) Microdeletions of the Y chromosome and intracytoplasmic sperm injection (ICSI): from gene to clinic. Hum. Reprod., 12, in press.
    • (1997) Hum. Reprod. , vol.12
    • Kremer, J.A.M.1    Tuerlings, J.H.A.M.2    Meulem, E.J.H.3
  • 24
    • 0028091740 scopus 로고
    • Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,Xyq-karyotyoe
    • Lahn, B.T., Ma, N., Breg, W.R. et al. (1994) Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,Xyq-karyotyoe. Nature Genet, 8, 243-250.
    • (1994) Nature Genet , vol.8 , pp. 243-250
    • Lahn, B.T.1    Ma, N.2    Breg, W.R.3
  • 26
    • 0015253206 scopus 로고
    • The role of X-chromosome inactivation during spermiogenesis
    • Lifschytz, E. and Lindsley, D.L. (1972) The role of X-chromosome inactivation during spermiogenesis. Proc. Natl. Acad. Sci., 69, 182.
    • (1972) Proc. Natl. Acad. Sci. , vol.69 , pp. 182
    • Lifschytz, E.1    Lindsley, D.L.2
  • 27
    • 9344253898 scopus 로고    scopus 로고
    • Rothmund-Thomson syndrome in siblings: Evidence for in vivo acquired mosaicism
    • Lindor, N.M., Devries, E.M.G., Michels, V.V et al. (1996) Rothmund-Thomson syndrome in siblings: evidence for in vivo acquired mosaicism. Clin Genet., 49, 124-129.
    • (1996) Clin Genet. , vol.49 , pp. 124-129
    • Lindor, N.M.1    Devries, E.M.G.2    Michels, V.V.3
  • 28
    • 0026849360 scopus 로고
    • Towards the molecular localisation of the AZF locus: Mapping of deletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome
    • Ma, K., Sharkey, A., Kirsch, S. et al. (1992) Towards the molecular localisation of the AZF locus: Mapping of deletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome. Hum. Mol. Genet., 1, 29-33.
    • (1992) Hum. Mol. Genet. , vol.1 , pp. 29-33
    • Ma, K.1    Sharkey, A.2    Kirsch, S.3
  • 29
    • 0027715823 scopus 로고
    • A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis
    • Ma, K., Inglis, J.D., Sharkey, A. et al. (1993) A Y chromosome gene family with RNA-binding protein homology: candidates for the azoospermia factor AZF controlling human spermatogenesis. Cell, 75, 1287-1295.
    • (1993) Cell , vol.75 , pp. 1287-1295
    • Ma, K.1    Inglis, J.D.2    Sharkey, A.3
  • 30
    • 0027417793 scopus 로고
    • The control in cis of the position and the amount of the ARG meiotic double-strand break of Saccharomyces cerevisiae
    • Massey, B. and Nicholas, A. (1993) The control in cis of the position and the amount of the ARG meiotic double-strand break of Saccharomyces cerevisiae. EMBO J., 12, 1459-1466.
    • (1993) EMBO J. , vol.12 , pp. 1459-1466
    • Massey, B.1    Nicholas, A.2
  • 31
    • 0031037973 scopus 로고    scopus 로고
    • Expression of DAZ, an azoospermia factor candidate in human spermatogenesis
    • Menke, D.B., Mutter, G.L. and Page, D.C. (1997) Expression of DAZ, an azoospermia factor candidate in human spermatogenesis. Am. J. Hum. Genet., 60, 237-241.
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 237-241
    • Menke, D.B.1    Mutter, G.L.2    Page, D.C.3
  • 32
    • 0028087883 scopus 로고
    • Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism
    • Monckton, D.G., Neumann, R., Guram, T. et al. (1994) Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism. Nature Genet., 8, 162-170.
    • (1994) Nature Genet. , vol.8 , pp. 162-170
    • Monckton, D.G.1    Neumann, R.2    Guram, T.3
  • 33
    • 0023119242 scopus 로고
    • Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryonic development
    • Monk, M., Roubelik, M and Lehnert, S. (1987) Temporal and regional changes in DNA methylation in the embryonic, extraembryonic and germ cell lineages during mouse embryonic development. Development, 99, 371-382.
    • (1987) Development , vol.99 , pp. 371-382
    • Monk, M.1    Roubelik, M.2    Lehnert, S.3
  • 34
    • 0030914159 scopus 로고    scopus 로고
    • Azoospermic men with deletion of the DAZ cluster are capable of completing spermatogenesis: Fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection
    • Mulhall, J.P., Reijo, R., Alagappan, R. et al (1997) Azoospermic men with deletion of the DAZ cluster are capable of completing spermatogenesis: fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection. Hum. Reprod., 12, 503-508.
    • (1997) Hum. Reprod. , vol.12 , pp. 503-508
    • Mulhall, J.P.1    Reijo, R.2    Alagappan, R.3
  • 35
    • 0030955751 scopus 로고    scopus 로고
    • Treatment-related chromosome abnormalities in human embryos
    • Munné, S., Magli, C., Adler, A. et al. (1997) Treatment-related chromosome abnormalities in human embryos. Hum. Reprod., 12, 780-784.
    • (1997) Hum. Reprod. , vol.12 , pp. 780-784
    • Munné, S.1    Magli, C.2    Adler, A.3
  • 36
    • 0031109738 scopus 로고    scopus 로고
    • In situ hybridization shows that DAZLA expression in mouse testis is restricted to premeiotic stages IV-VI of spermatogenesisis
    • in press
    • Niedeberger, C., Agulnik, A., Cho, Y. et al. (1997) In situ hybridization shows that DAZLA expression in mouse testis is restricted to premeiotic stages IV-VI of spermatogenesisis. Mammalian Genome, in press.
    • (1997) Mammalian Genome
    • Niedeberger, C.1    Agulnik, A.2    Cho, Y.3
  • 37
    • 0029081376 scopus 로고
    • Regulation of gene expression at the beginning of mammalian development
    • Nothias, J.Y., Majumder, S., Kaneko, K.J. and DePamplis, M.L. (1995) Regulation of gene expression at the beginning of mammalian development. J. Biol. Chem., 270, 22077-22080.
    • (1995) J. Biol. Chem. , vol.270 , pp. 22077-22080
    • Nothias, J.Y.1    Majumder, S.2    Kaneko, K.J.3    DePamplis, M.L.4
  • 38
    • 0000095291 scopus 로고
    • Duration of spermatogenesis in the mouse
    • Oakberg, E.F. (1957) Duration of spermatogenesis in the mouse. Nature, 180, 1137-1139.
    • (1957) Nature , vol.180 , pp. 1137-1139
    • Oakberg, E.F.1
  • 39
    • 77049264222 scopus 로고
    • A description of spermiogenesis in the mouse and timing of the stages of the cycle of the seminiferous epithelium
    • Oakberg, E.F. (1956) A description of spermiogenesis in the mouse and timing of the stages of the cycle of the seminiferous epithelium. Am. J. Anat., 99, 391-413..
    • (1956) Am. J. Anat. , vol.99 , pp. 391-413
    • Oakberg, E.F.1
  • 41
    • 0027959928 scopus 로고
    • Oct-4 transcription factor is differentially expressed in the mouse embryo during establishment of the first two extraembryonic cell lineages involved in implantation
    • Palmieri et al. (1994) Oct-4 transcription factor is differentially expressed in the mouse embryo during establishment of the first two extraembryonic cell lineages involved in implantation. Dev. Biol., 166, 259-267.
    • (1994) Dev. Biol. , vol.166 , pp. 259-267
    • Palmieri1
  • 42
    • 0029871858 scopus 로고    scopus 로고
    • Severe oligozoospermia resulting from deletions of azoospermia factor gene on the Y chromosome
    • Reijo, R., Alagappan, R.K., Patrizio, P. et al. (1996) Severe oligozoospermia resulting from deletions of azoospermia factor gene on the Y chromosome. Lancet, 347, 1290-1293.
    • (1996) Lancet , vol.347 , pp. 1290-1293
    • Reijo, R.1    Alagappan, R.K.2    Patrizio, P.3
  • 43
    • 0029088061 scopus 로고
    • Diverse spermatogenetic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
    • Reijo, R., Lee, T-Y., Salo, P. et al. (1995) Diverse spermatogenetic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nature Genet., 10, 383-393.
    • (1995) Nature Genet. , vol.10 , pp. 383-393
    • Reijo, R.1    Lee, T.-Y.2    Salo, P.3
  • 44
    • 0029111463 scopus 로고
    • MSH2 deficient mice are viable and susceptible to lymphoid tumours
    • Reitmar, A.H., Schmits, R., Ewel, A. et al (1995) MSH2 deficient mice are viable and susceptible to lymphoid tumours. Nature Genet., 11, 64-70.
    • (1995) Nature Genet. , vol.11 , pp. 64-70
    • Reitmar, A.H.1    Schmits, R.2    Ewel, A.3
  • 45
    • 0027288903 scopus 로고
    • The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm
    • Reyneirs, E., Vits, L., De Boulle, K. et al. (1993) The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm. Nature Genet., 4, 143-146.
    • (1993) Nature Genet. , vol.4 , pp. 143-146
    • Reyneirs, E.1    Vits, L.2    De Boulle, K.3
  • 47
    • 13844311600 scopus 로고
    • Developmental anomalies derived from exposure of zygotes and first cleavage embryos to mutagens
    • Rutledge, J.C., Generoso, W.M., Shourbajid, A. et al. (1992) Developmental anomalies derived from exposure of zygotes and first cleavage embryos to mutagens. Mutat. Res., 296, 166-177.
    • (1992) Mutat. Res. , vol.296 , pp. 166-177
    • Rutledge, J.C.1    Generoso, W.M.2    Shourbajid, A.3
  • 48
    • 0030292382 scopus 로고    scopus 로고
    • The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned
    • Saxena, R., Brown, L.G., Hawkins, T. et al. (1996) The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nature Genet., 14, 292-300.
    • (1996) Nature Genet. , vol.14 , pp. 292-300
    • Saxena, R.1    Brown, L.G.2    Hawkins, T.3
  • 49
    • 0025924380 scopus 로고
    • A poly(dA.dT) tract is a component of the recombination initiation site at the ARG4 locus in Saccharomyces cerevisiae
    • Schultes, N.P. and Szostak, J.W. (1991) A poly(dA.dT) tract is a component of the recombination initiation site at the ARG4 locus in Saccharomyces cerevisiae. Mol. Cell Biol., 11, 322-328.
    • (1991) Mol. Cell Biol. , vol.11 , pp. 322-328
    • Schultes, N.P.1    Szostak, J.W.2
  • 50
    • 0031569890 scopus 로고    scopus 로고
    • Gene sequence, localization and evolutionary conservation of DAZLA, a candidate male sterility gene
    • in press
    • Seboun, E., Barbaux, S., Bourgeon, T. et al. (1997) Gene sequence, localization and evolutionary conservation of DAZLA, a candidate male sterility gene. Genomics, in press.
    • (1997) Genomics
    • Seboun, E.1    Barbaux, S.2    Bourgeon, T.3
  • 51
    • 0029803595 scopus 로고    scopus 로고
    • A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad
    • Shan, Z., Hirschmann, P., Seebacher, T. et al. (1996) A SPGY copy homologous to the mouse gene Dazla and the Drosophila gene boule is autosomal and expressed only in the human male gonad. Hum. Mol. Genet., 5, 2005-2011.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 2005-2011
    • Shan, Z.1    Hirschmann, P.2    Seebacher, T.3
  • 52
    • 0000095291 scopus 로고
    • Duration of spermatogenesis in the mouse
    • Sirlin, J.L. and Edwards, R.G. (1957) Duration of spermatogenesis in the mouse. Nature, 180, 1137-1139.
    • (1957) Nature , vol.180 , pp. 1137-1139
    • Sirlin, J.L.1    Edwards, R.G.2
  • 53
    • 0003037504 scopus 로고
    • The labelling of mammalian spermatozoa with radioactive tracers
    • Sirlin, J.L. and Edwards, R.G. (1958). The labelling of mammalian spermatozoa with radioactive tracers. J. Exp. Zool., 137, 363-387.
    • (1958) J. Exp. Zool. , vol.137 , pp. 363-387
    • Sirlin, J.L.1    Edwards, R.G.2
  • 54
    • 0024338584 scopus 로고
    • Nucleic acid synthesis and development of human male pronucleus
    • Tesarik, J. and Kopecny, V. (1989) Nucleic acid synthesis and development of human male pronucleus. J. Reprod. Fertil., 86, 549-558.
    • (1989) J. Reprod. Fertil. , vol.86 , pp. 549-558
    • Tesarik, J.1    Kopecny, V.2
  • 55
    • 0025173629 scopus 로고
    • Assembly of the nucleolar precursdor bodies in human male pronuclei is correlated with an early RNA synthetic activity
    • Tesarik, J. and Kopecny, V. (1990) Assembly of the nucleolar precursdor bodies in human male pronuclei is correlated with an early RNA synthetic activity. Exp. Cell Res., 191, 153-156.
    • (1990) Exp. Cell Res. , vol.191 , pp. 153-156
    • Tesarik, J.1    Kopecny, V.2
  • 57
    • 0017119580 scopus 로고
    • Localisation of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
    • Tiepolo, L. and Zuffardi, O. (1976) Localisation of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Genet., 34, 119-124.
    • (1976) Hum. Genet. , vol.34 , pp. 119-124
    • Tiepolo, L.1    Zuffardi, O.2
  • 58
    • 0030634920 scopus 로고    scopus 로고
    • Absence of DAZ gene mutations in cases of non-obstructed azoospermia
    • Vereb, M., Agulnik, A.I., Houston, J.T. et al. (1997) Absence of DAZ gene mutations in cases of non-obstructed azoospermia. Mol. Hum. Reprod., 3, 55-59.
    • (1997) Mol. Hum. Reprod. , vol.3 , pp. 55-59
    • Vereb, M.1    Agulnik, A.I.2    Houston, J.T.3
  • 59
    • 0028847432 scopus 로고
    • Genetic aspects of artificial fertilization
    • Vogt, P.H. (1995) Genetic aspects of artificial fertilization. Hum Reprod., 10 (Suppl. 1), 128-137.
    • (1995) Hum Reprod. , vol.10 , Issue.1 SUPPL. , pp. 128-137
    • Vogt, P.H.1
  • 60
    • 0007272350 scopus 로고    scopus 로고
    • Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
    • Vogt, P.H., Edelmann, A., Kirsch, S. et al. (1996) Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum. Mol. Genet., 5, 933-943.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 933-943
    • Vogt, P.H.1    Edelmann, A.2    Kirsch, S.3
  • 61
    • 0029872174 scopus 로고    scopus 로고
    • Telomerase activity in human germline and embryonic tissues and cells
    • Wright, W.E., Piatyszek, M.A., Rainey, W.E. et al. (1996) Telomerase activity in human germline and embryonic tissues and cells. Dev. Genet., 18, 173-179.
    • (1996) Dev. Genet. , vol.18 , pp. 173-179
    • Wright, W.E.1    Piatyszek, M.A.2    Rainey, W.E.3
  • 62
    • 0019901038 scopus 로고
    • Human chromosome 2 rod/ring mosaicism: Probable origin by prezygotic breakage and intrachromosomal exchange
    • Wyandt, H.E., Kasprzak, R., Lamb, A. et al. (1982) Human chromosome 2 rod/ring mosaicism: probable origin by prezygotic breakage and intrachromosomal exchange. Cytogenet. Cell Genet., 33, 222-231.
    • (1982) Cytogenet. Cell Genet. , vol.33 , pp. 222-231
    • Wyandt, H.E.1    Kasprzak, R.2    Lamb, A.3
  • 63
    • 0029842285 scopus 로고    scopus 로고
    • The human autosomal gene DAZLA: Testis specificity and a candidate for male infertility
    • in press
    • Yen, P.H., Chai, N.N. and Salido, E.C. (1996) The human autosomal gene DAZLA: testis specificity and a candidate for male infertility. Hum. Mol. Genet., in press.
    • (1996) Hum. Mol. Genet.
    • Yen, P.H.1    Chai, N.N.2    Salido, E.C.3
  • 64
    • 0025280088 scopus 로고
    • Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
    • Yen, P.H. et al. (1990) Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements. Cell, 61, 603-610.
    • (1990) Cell , vol.61 , pp. 603-610
    • Yen, P.H.1
  • 65
    • 0029865895 scopus 로고    scopus 로고
    • Germline regulatory element of oct-4 specific for the totipotent cycle of embryonal cells
    • Yeom, Y.I., Fuhrmann, G., Ovvitt, C.E. et al (1996) Germline regulatory element of oct-4 specific for the totipotent cycle of embryonal cells. Development, 122, 881-894.
    • (1996) Development , vol.122 , pp. 881-894
    • Yeom, Y.I.1    Fuhrmann, G.2    Ovvitt, C.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.