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Volumn 13, Issue SUPPL. 3, 1998, Pages 76-88

Genetic contribution to male infertility

Author keywords

Chromosomes; Microdeletions; Spermatogenesis; Y chromosome

Indexed keywords

AUTOSOME; CELL MATURATION; CHROMOSOME ABERRATION; CONFERENCE PAPER; GENETIC DISORDER; GENETIC PREDISPOSITION; GENOME; GERM CELL; HUMAN; MALE; MALE INFERTILITY; SCREENING; SPERMATOGENESIS; Y CHROMOSOME;

EID: 18144433816     PISSN: 02681161     EISSN: None     Source Type: Journal    
DOI: 10.1093/humrep/13.suppl_3.76     Document Type: Conference Paper
Times cited : (38)

References (43)
  • 1
    • 0023921510 scopus 로고
    • Y-autosome translocations and mosaicism in the etiology of 45,X maleness: Assignment of fertility factor to distal Yq11
    • Andersson, M., Page, D.C., Pettay, D. et al. (1988) Y-autosome translocations and mosaicism in the etiology of 45,X maleness: assignment of fertility factor to distal Yq11. Hum. Genet., 79, 2-7.
    • (1988) Hum. Genet. , vol.79 , pp. 2-7
    • Andersson, M.1    Page, D.C.2    Pettay, D.3
  • 2
    • 0022589841 scopus 로고
    • X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallman syndrome: Linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome
    • Ballabio, A., Parenti, G., Tippett, P. et al. (1986) X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallman syndrome: linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosome. Hum. Genet., 72, 237-240.
    • (1986) Hum. Genet. , vol.72 , pp. 237-240
    • Ballabio, A.1    Parenti, G.2    Tippett, P.3
  • 3
    • 0023944147 scopus 로고
    • Sperm chromosome complements in a 47,XYY man
    • Benet, J. and Martin, R.H. (1988) Sperm chromosome complements in a 47,XYY man. Hum. Genet., 78, 313-315.
    • (1988) Hum. Genet. , vol.78 , pp. 313-315
    • Benet, J.1    Martin, R.H.2
  • 4
    • 0018407084 scopus 로고
    • The chromosomal basis of human infertility
    • Chandley, A.C. (1979) The chromosomal basis of human infertility. Br. Med. Bull., 35, 181-186.
    • (1979) Br. Med. Bull. , vol.35 , pp. 181-186
    • Chandley, A.C.1
  • 5
    • 0021669928 scopus 로고
    • Infertility and chromosome abnormality
    • Chandley, A.C. (1984) Infertility and chromosome abnormality. Oxford Rev. Reprod. Biol., 6, 1-46.
    • (1984) Oxford Rev. Reprod. Biol. , vol.6 , pp. 1-46
    • Chandley, A.C.1
  • 6
    • 0006350117 scopus 로고
    • Meiotic studies and fertility in human translocations
    • Chandley, A.C. (1988) Meiotic studies and fertility in human translocations. Prog. Top. Cytogenet., 8, 361-382.
    • (1988) Prog. Top. Cytogenet. , vol.8 , pp. 361-382
    • Chandley, A.C.1
  • 7
    • 0023273754 scopus 로고
    • Towards an objective evaluation of signs and symptoms in male infertility
    • Comhaire, F.H., de Kretser, D., Farley T.M.M. et al. (1987) Towards an objective evaluation of signs and symptoms in male infertility. Int. J. Androl., 7 (Suppl.) 3-9.
    • (1987) Int. J. Androl. , vol.7 , Issue.SUPPL. , pp. 3-9
    • Comhaire, F.H.1    De Kretser, D.2    Farley, T.M.M.3
  • 8
    • 0029923501 scopus 로고    scopus 로고
    • A murine homologue of the human DAZ gene is autosomal and expressed only in male and female gonads
    • Cooke, H.J., Lee, M., Kerr, S. et al. (1996) A murine homologue of the human DAZ gene is autosomal and expressed only in male and female gonads. Hum. Mol. Genet., 5, 513-516.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 513-516
    • Cooke, H.J.1    Lee, M.2    Kerr, S.3
  • 9
    • 0028158533 scopus 로고
    • Achievement of meiosis in XXY germ cells: Study of 543 sperm karyotypes from an XY/XXY mosaic patient
    • Cozzi, J., Chevret, E., Rousseaux, S. et al. (1994) Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient. Hum. Genet., 93, 32-34.
    • (1994) Hum. Genet. , vol.93 , pp. 32-34
    • Cozzi, J.1    Chevret, E.2    Rousseaux, S.3
  • 10
    • 0031053390 scopus 로고    scopus 로고
    • A human candidate spermatogenesis gene, RBMl, is conserved and amplified on the marsupial Y chromosome
    • Delbridge, M.L., Harry, J.L., Toder, R. et al. (1997) A human candidate spermatogenesis gene, RBMl, is conserved and amplified on the marsupial Y chromosome. Nature Genet., 15, 131-136.
    • (1997) Nature Genet. , vol.15 , pp. 131-136
    • Delbridge, M.L.1    Harry, J.L.2    Toder, R.3
  • 11
    • 0029900958 scopus 로고    scopus 로고
    • Meiotic cell cycle requirement for a fly homologue of a human Deleted in Azoospermia
    • Eberhart, C.G., Maines, J.Z. and Wasserman, S.A. (1996) Meiotic cell cycle requirement for a fly homologue of a human Deleted in Azoospermia. Nature, 381, 783-785.
    • (1996) Nature , vol.381 , pp. 783-785
    • Eberhart, C.G.1    Maines, J.Z.2    Wasserman, S.A.3
  • 12
    • 0030015975 scopus 로고    scopus 로고
    • An RBM homologue maps to the mouse Y chromosome and is expressed in germ cells
    • Elliot, D.J., Ma, K., Kerr, S. et al. (1996) An RBM homologue maps to the mouse Y chromosome and is expressed in germ cells. Hum. Mol. Genet., 5, 869-874.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 869-874
    • Elliot, D.J.1    Ma, K.2    Kerr, S.3
  • 13
    • 12644310287 scopus 로고    scopus 로고
    • Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm
    • Elliot, D.J., Millar, M.R., O'Ghene, K. et al. (1997) Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm. Proc. Natl. Acad. Sci. USA, 94, 3848-3853.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 3848-3853
    • Elliot, D.J.1    Millar, M.R.2    O'Ghene, K.3
  • 14
    • 0028334369 scopus 로고
    • Genital tract function in men with Noonan syndrome
    • Elsawi, M., Pryor, J.P., Klufio, G. et al. (1994) Genital tract function in men with Noonan syndrome. J. Med. Genet., 31, 468-470.
    • (1994) J. Med. Genet. , vol.31 , pp. 468-470
    • Elsawi, M.1    Pryor, J.P.2    Klufio, G.3
  • 15
    • 0014931984 scopus 로고
    • XY spermatocytes in an XYY male
    • Evans, E.P., Ford, C.E., Chaganti, R.S.K. et al. (1970) XY spermatocytes in an XYY male. Lancet, i, 719-720.
    • (1970) Lancet , vol.1 , pp. 719-720
    • Evans, E.P.1    Ford, C.E.2    Chaganti, R.S.K.3
  • 16
    • 0020079261 scopus 로고
    • Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly
    • Faed, M.J.W., Lamont, M.A., Baxby, K. et al. (1982) Cytogenetic and histological studies of testicular biopsies from subfertile men with chromosome anomaly. J. Med. Genet., 19, 49-54.
    • (1982) J. Med. Genet. , vol.19 , pp. 49-54
    • Faed, M.J.W.1    Lamont, M.A.2    Baxby, K.3
  • 17
    • 0022908388 scopus 로고
    • Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XYt(19;22) and 46,XY,t(17;21)
    • Gabriel-Robez, O., Ratomponirina, C., Dutrillaux, B. et al. (1986) Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XYt(19;22) and 46,XY,t(17;21). Cytogenetics, 43, 154-160.
    • (1986) Cytogenetics , vol.43 , pp. 154-160
    • Gabriel-Robez, O.1    Ratomponirina, C.2    Dutrillaux, B.3
  • 19
    • 0015014003 scopus 로고
    • Fluorescent evidence for spermatocytes with two Y chromosomes in an XYY male
    • Hulten, M.A., and Pearson, P.L. (1971) Fluorescent evidence for spermatocytes with two Y chromosomes in an XYY male. Ann. Hum. Genet., 34, 273-276.
    • (1971) Ann. Hum. Genet. , vol.34 , pp. 273-276
    • Hulten, M.A.1    Pearson, P.L.2
  • 20
    • 0019945729 scopus 로고
    • The use of surface spreading in the pachtene analysis of a human t(Y; 17) reciprocal translocation
    • Laurent, C., Chandley, A.C. Dutrillaux, B. et al. (1982) The use of surface spreading in the pachtene analysis of a human t(Y; 17) reciprocal translocation. Cytogenet. Cell Genet., 33, 312-318.
    • (1982) Cytogenet. Cell Genet. , vol.33 , pp. 312-318
    • Laurent, C.1    Chandley, A.C.2    Dutrillaux, B.3
  • 21
    • 0021685229 scopus 로고
    • Studies on chiasma frequency and distribution in two infertile men carrying reciprocal translocations; one with a t(9; 10) karyotype and one with a t(Y;10) karyotype
    • Laurie, D.A., Palmer, R.W. and Hulten, M.A. (1984) Studies on chiasma frequency and distribution in two infertile men carrying reciprocal translocations; one with a t(9; 10) karyotype and one with a t(Y;10) karyotype. Hum. Genet., 68, 235-247.
    • (1984) Hum. Genet. , vol.68 , pp. 235-247
    • Laurie, D.A.1    Palmer, R.W.2    Hulten, M.A.3
  • 22
    • 0015253206 scopus 로고
    • The role of X-chromosome inactivation during spermatogenesis
    • Lifschytz, E. and Lindsley, D.L. (1972) The role of X-chromosome inactivation during spermatogenesis. Proc.Natl. Acad. Sci. USA, 69, 182-186.
    • (1972) Proc.Natl. Acad. Sci. USA , vol.69 , pp. 182-186
    • Lifschytz, E.1    Lindsley, D.L.2
  • 23
    • 0028128358 scopus 로고
    • Case-control study of whether subfertility in men is familial
    • Lilford, R., Jones, A.M., Bishop, D.T. et al. (1994) Case-control study of whether subfertility in men is familial. Br. Med. J., 309, 570-573.
    • (1994) Br. Med. J. , vol.309 , pp. 570-573
    • Lilford, R.1    Jones, A.M.2    Bishop, D.T.3
  • 24
    • 0013984380 scopus 로고
    • Autosomal translocations causing male sterility and viable aneuploidy in the mouse
    • Lyon, M.F. and Meredith, R. (1966) Autosomal translocations causing male sterility and viable aneuploidy in the mouse. Cytogenetics, 5, 335-354.
    • (1966) Cytogenetics , vol.5 , pp. 335-354
    • Lyon, M.F.1    Meredith, R.2
  • 25
    • 0026849360 scopus 로고
    • Towards the molecular localisation of the AZF locus: Mapping of microdeletions 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 microdeletions 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
  • 26
    • 0027715823 scopus 로고
    • A Y chromosome gene family with RNA-binding protein homology:candidate for the azoospermia factor AZF controlling human spermatogenesis
    • Ma, K., Inglis, J., Sharkey, et al. (1993) A Y chromosome gene family with RNA-binding protein homology:candidate for the azoospermia factor AZF controlling human spermatogenesis. Cell, 75, 1287-1295.
    • (1993) Cell , vol.75 , pp. 1287-1295
    • Ma, K.1    Inglis, J.2    Sharkey3
  • 27
    • 0027511117 scopus 로고
    • Sex chromosomes, recombination, and chromatin conformation
    • McKee, B.D. and Handel, M.A. (1993) Sex chromosomes, recombination, and chromatin conformation. Chromosoma, 102, 71-80.
    • (1993) Chromosoma , vol.102 , pp. 71-80
    • McKee, B.D.1    Handel, M.A.2
  • 28
    • 0027438374 scopus 로고
    • Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens
    • Osborne, L.R., Lynch, M., Middleton, P.O. et al. (1993) Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens. Hum. Mol. Genet., 2, 1605-1609.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 1605-1609
    • Osborne, L.R.1    Lynch, M.2    Middleton, P.O.3
  • 29
    • 0031050740 scopus 로고    scopus 로고
    • Microdeletions in the Y chromosome of infertile men
    • Pryor, J.L., Kent-First, M., Muallem, A. et al. (1997) Microdeletions in the Y chromosome of infertile men. N. Engl. J. Med., 336, 534-539.
    • (1997) N. Engl. J. Med. , vol.336 , pp. 534-539
    • Pryor, J.L.1    Kent-First, M.2    Muallem, A.3
  • 30
    • 0023775790 scopus 로고
    • Meiotic analysis of two human reciprocal X-autosome translocations
    • Quack, B., Speed, R.M., Luciani, J.M. et al. (1988) Meiotic analysis of two human reciprocal X-autosome translocations. Cytogenet. Cell Genet., 48, 43-47.
    • (1988) Cytogenet. Cell Genet. , vol.48 , pp. 43-47
    • Quack, B.1    Speed, R.M.2    Luciani, J.M.3
  • 31
    • 0030253042 scopus 로고    scopus 로고
    • Polymerase chain reaction screening for Y chromosome microdeletions: A first step towards the diagnosis of genetically-determined spermatogenic failure in men
    • Qureshi, S., Ross, A.R., Ma, K. et al. (1996) Polymerase chain reaction screening for Y chromosome microdeletions: a first step towards the diagnosis of genetically-determined spermatogenic failure in men. Mol. Hum. Reprod., 2, 775-779.
    • (1996) Mol. Hum. Reprod. , vol.2 , pp. 775-779
    • Qureshi, S.1    Ross, A.R.2    Ma, K.3
  • 32
    • 0029088061 scopus 로고
    • Diverse spermatogenic 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 spermatogenic 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
  • 33
    • 0029871858 scopus 로고    scopus 로고
    • Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome
    • Reijo, R., Alagappan, R.K., Patrizio, P. et al. (1996) Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome. Lancet, 347, 1290-1293.
    • (1996) Lancet , vol.347 , pp. 1290-1293
    • Reijo, R.1    Alagappan, R.K.2    Patrizio, P.3
  • 34
    • 0030292382 scopus 로고    scopus 로고
    • The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, then repeatedly amplified and pruned
    • Saxena, R., Brown, L.G., Hawkins, T.T. et al. (1996) The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, then repeatedly amplified and pruned. Nature Genet.,14, 292-299.
    • (1996) Nature Genet. , vol.14 , pp. 292-299
    • Saxena, R.1    Brown, L.G.2    Hawkins, T.T.3
  • 35
    • 0029032452 scopus 로고
    • Comparative mapping of YRRM-and TSPY-related cosmids in man and hominoid apes
    • Schempp, W., Binkele, A., Arnemann, J. et al. (1995) Comparative mapping of YRRM-and TSPY-related cosmids in man and hominoid apes. Chromosome Res., 3, 227-234.
    • (1995) Chromosome Res. , vol.3 , pp. 227-234
    • Schempp, W.1    Binkele, A.2    Arnemann, J.3
  • 37
    • 34548197866 scopus 로고
    • Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome
    • Shapiro, L.J. (1985) Steroid sulfatase deficiency and the genetics of the short arm of the human X chromosome. Adv. Genet., 23, 331-381.
    • (1985) Adv. Genet. , vol.23 , pp. 331-381
    • Shapiro, L.J.1
  • 38
    • 0015594564 scopus 로고
    • Quantification of human seminiferous epithelium. II. Histological studies in eight 47,XYY men
    • Skakkebaek, N.E., Hulten, M., Jacobsen, P. et al. (1973) Quantification of human seminiferous epithelium. II. Histological studies in eight 47,XYY men. J. Reprod. Fertil., 32, 391-401.
    • (1973) J. Reprod. Fertil. , vol.32 , pp. 391-401
    • Skakkebaek, N.E.1    Hulten, M.2    Jacobsen, P.3
  • 39
    • 0025836026 scopus 로고
    • Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man
    • Speed, R.M., Faed, M.J.W., Batstone, P.J. et al. (1991) Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man. Hum. Genet., 87, 416-420.
    • (1991) Hum. Genet. , vol.87 , pp. 416-420
    • Speed, R.M.1    Faed, M.J.W.2    Batstone, P.J.3
  • 40
    • 0017119580 scopus 로고
    • Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
    • 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.
    • (1976) Hum. Genet. , vol.34 , pp. 119-124
    • Tiepolo, L.1    Zuffardi, O.2
  • 41
    • 0022530702 scopus 로고
    • A deletion map of the human Y chromosome based on DNA hybridization
    • Vergnaud, G., Page, D.C., Simmler, M.-C. et al. (1986) A deletion map of the human Y chromosome based on DNA hybridization. Am. J. Hum. Genet., 38, 109-124.
    • (1986) Am. J. Hum. Genet. , vol.38 , pp. 109-124
    • Vergnaud, G.1    Page, D.C.2    Simmler, M.-C.3
  • 42
    • 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
  • 43
    • 0029842285 scopus 로고    scopus 로고
    • The human autosomal gene DAZLA: Testis specificity and a candidate for male infertility
    • 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., 5, 2013-2017.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 2013-2017
    • Yen, P.H.1    Chai, N.N.2    Salido, E.C.3


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