메뉴 건너뛰기




Volumn 103, Issue 1, 2015, Pages 214-219

Copy number variation associated with meiotic arrest in idiopathic male infertility

Author keywords

Azoospermia; Copy number variation; Genetics; Human

Indexed keywords

LONG UNTRANSLATED RNA; CELL CYCLE PROTEIN;

EID: 84924370716     PISSN: 00150282     EISSN: 15565653     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2014.09.030     Document Type: Article
Times cited : (34)

References (59)
  • 1
    • 22144441746 scopus 로고    scopus 로고
    • Men in Australia Telephone Survey (MATeS): A national survey of the reproductive health and concerns of middle-aged and older Australian men
    • Holden CA, McLachlan RI, Pitts M, Cumming R, Wittert G, Agius PA, et al. Men in Australia Telephone Survey (MATeS): a national survey of the reproductive health and concerns of middle-aged and older Australian men. Lancet 2005;366:218-24.
    • (2005) Lancet , vol.366 , pp. 218-224
    • Holden, C.A.1    McLachlan, R.I.2    Pitts, M.3    Cumming, R.4    Wittert, G.5    Agius, P.A.6
  • 2
    • 77749240212 scopus 로고    scopus 로고
    • Clinical review: State of the art for genetic testing of infertile men
    • McLachlan RI, O'Bryan MK. Clinical review: state of the art for genetic testing of infertile men. J Clin Endocrinol Metab 2010;95:1013-24.
    • (2010) J Clin Endocrinol Metab , vol.95 , pp. 1013-1024
    • McLachlan, R.I.1    O'Bryan, M.K.2
  • 3
    • 85030399939 scopus 로고    scopus 로고
    • Clinical management of male infertility
    • McLachlan R, editor South Dartmouth, MA: MDTEXT.COM
    • Baker C, Barak S. Clinical management of male infertility. In: McLachlan R, editor. Endocrinology of male reproduction. South Dartmouth, MA: MDTEXT.COM; 2012.
    • (2012) Endocrinology of Male Reproduction
    • Baker, C.1    Barak, S.2
  • 4
    • 84874411690 scopus 로고    scopus 로고
    • The genetics of male fertility - from basic science to clinical evaluation
    • Pastuszak AW, Lamb DJ. The genetics of male fertility - from basic science to clinical evaluation. J Androl 2012;33:1075-84.
    • (2012) J Androl , vol.33 , pp. 1075-1084
    • Pastuszak, A.W.1    Lamb, D.J.2
  • 5
    • 33845665444 scopus 로고    scopus 로고
    • Histological evaluation of the human testis - approaches to optimizing the clinical value of the assessment: Mini review
    • McLachlan RI, Rajpert-De Meyts E, Hoei-Hansen CE, de Kretser DM, Skakkebaek NE. Histological evaluation of the human testis - approaches to optimizing the clinical value of the assessment: mini review. Hum Reprod 2007;22:2-16.
    • (2007) Hum Reprod , vol.22 , pp. 2-16
    • McLachlan, R.I.1    Rajpert-De Meyts, E.2    Hoei-Hansen, C.E.3    De Kretser, D.M.4    Skakkebaek, N.E.5
  • 7
    • 33751329250 scopus 로고    scopus 로고
    • Global variation in copy number in the human genome
    • Redon R. Global variation in copy number in the human genome. Nature 2006;444:444-54.
    • (2006) Nature , vol.444 , pp. 444-454
    • Redon, R.1
  • 8
    • 77950461601 scopus 로고    scopus 로고
    • Origins and functional impact of copy number variation in the human genome
    • Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, et al. Origins and functional impact of copy number variation in the human genome. Nature 2010;464:704-12.
    • (2010) Nature , vol.464 , pp. 704-712
    • Conrad, D.F.1    Pinto, D.2    Redon, R.3    Feuk, L.4    Gokcumen, O.5    Zhang, Y.6
  • 10
    • 33846978695 scopus 로고    scopus 로고
    • Relative impact of nucleotide and copy number variation on gene expression phenotypes
    • Stranger BE. Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science 2007;315:848-53.
    • (2007) Science , vol.315 , pp. 848-853
    • Stranger, B.E.1
  • 11
    • 34347353237 scopus 로고    scopus 로고
    • Copy-number variation and association studies of human disease
    • McCarroll SA, Altshuler DM. Copy-number variation and association studies of human disease. Nat Genet 2007;39:37-42.
    • (2007) Nat Genet , vol.39 , pp. 37-42
    • McCarroll, S.A.1    Altshuler, D.M.2
  • 12
    • 77956628767 scopus 로고    scopus 로고
    • Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
    • Mefford HC, Muhle H, Ostertag P, von Spiczak S, Buysse K, Baker C, et al. Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet 2010;6:e1000962.
    • (2010) PLoS Genet , vol.6 , pp. e1000962
    • Mefford, H.C.1    Muhle, H.2    Ostertag, P.3    Von Spiczak, S.4    Buysse, K.5    Baker, C.6
  • 13
    • 84860741138 scopus 로고    scopus 로고
    • Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
    • O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012;485:246-50.
    • (2012) Nature , vol.485 , pp. 246-250
    • O'Roak, B.J.1    Vives, L.2    Girirajan, S.3    Karakoc, E.4    Krumm, N.5    Coe, B.P.6
  • 15
    • 79952333478 scopus 로고    scopus 로고
    • Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis
    • White S, Ohnesorg T, Notini A, Roeszler K, Hewitt J, Daggag H, et al. Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis. PLoS One 2011;6:e17793.
    • (2011) PLoS One , vol.6 , pp. e17793
    • White, S.1    Ohnesorg, T.2    Notini, A.3    Roeszler, K.4    Hewitt, J.5    Daggag, H.6
  • 16
    • 79955782135 scopus 로고    scopus 로고
    • Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome
    • Tüttelmann F, Simoni M, Kliesch S, Ledig S, Dworniczak B, Wieacker P, et al. Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome. PLoS One 2011;6:e19426.
    • (2011) PLoS One , vol.6 , pp. e19426
    • Tüttelmann, F.1    Simoni, M.2    Kliesch, S.3    Ledig, S.4    Dworniczak, B.5    Wieacker, P.6
  • 18
    • 33744456276 scopus 로고    scopus 로고
    • Degl'Innocenti S. Y chromosome and male infertility: Update, 2006
    • Krausz C, Degl'Innocenti S. Y chromosome and male infertility: update, 2006. Front Biosci 2006;11:3049-61.
    • (2006) Front Biosci , vol.11 , pp. 3049-3061
    • Krausz, C.1
  • 20
    • 33745446478 scopus 로고    scopus 로고
    • Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
    • Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, et al. Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest. J Hum Genet 2006;51:533-40.
    • (2006) J Hum Genet , vol.51 , pp. 533-540
    • Sato, H.1    Miyamoto, T.2    Yogev, L.3    Namiki, M.4    Koh, E.5    Hayashi, H.6
  • 21
    • 84867015532 scopus 로고    scopus 로고
    • Genetic variants in the ETV5 gene in fertile and infertile men with nonobstructive azoospermia associated with Sertoli cell only syndrome
    • O'Bryan MK, Grealy A, Stahl PJ, Schlegel PN, McLachlan RI, Jamsai D. Genetic variants in the ETV5 gene in fertile and infertile men with nonobstructive azoospermia associated with Sertoli cell only syndrome. Fertil Steril 2012;98:827-35.
    • (2012) Fertil Steril , vol.98 , pp. 827-835
    • O'Bryan, M.K.1    Grealy, A.2    Stahl, P.J.3    Schlegel, P.N.4    McLachlan, R.I.5    Jamsai, D.6
  • 23
    • 40749162839 scopus 로고    scopus 로고
    • Estimation and assessment of raw copy numbers at the single locus level
    • Bengtsson H, Irizarry R, Carvalho B, Speed TP. Estimation and assessment of raw copy numbers at the single locus level. Bioinformatics 2008;24:759-67.
    • (2008) Bioinformatics , vol.24 , pp. 759-767
    • Bengtsson, H.1    Irizarry, R.2    Carvalho, B.3    Speed, T.P.4
  • 24
    • 3042824616 scopus 로고    scopus 로고
    • Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses
    • White SJ, Vink GR, Kriek M, Wuyts W, Schouten J, Bakker B, et al. Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostoses. Hum Mutat 2004;24:86-92.
    • (2004) Hum Mutat , vol.24 , pp. 86-92
    • White, S.J.1    Vink, G.R.2    Kriek, M.3    Wuyts, W.4    Schouten, J.5    Bakker, B.6
  • 25
    • 16644383298 scopus 로고    scopus 로고
    • Detecting copy number changes in genomic DNA: MAPH and MLPA
    • White SJ, Breuning MH, den Dunnen JT. Detecting copy number changes in genomic DNA: MAPH and MLPA. Methods Cell Biol 2004;75:751-68.
    • (2004) Methods Cell Biol , vol.75 , pp. 751-768
    • White, S.J.1    Breuning, M.H.2    Den Dunnen, J.T.3
  • 26
    • 45249099559 scopus 로고    scopus 로고
    • Characterization of gametogenetin 1 (GGN1) and its potential role in male fertility through the interaction with the ion channel regulator, cysteine-rich secretory protein 2 (CRISP2) in the sperm tail
    • Jamsai D, Bianco DM, Smith SJ, Merriner DJ, Ly-Huynh JD, Herlihy A, et al. Characterization of gametogenetin 1 (GGN1) and its potential role in male fertility through the interaction with the ion channel regulator, cysteine-rich secretory protein 2 (CRISP2) in the sperm tail. Reproduction 2008;135:751-9.
    • (2008) Reproduction , vol.135 , pp. 751-759
    • Jamsai, D.1    Bianco, D.M.2    Smith, S.J.3    Merriner, D.J.4    Ly-Huynh, J.D.5    Herlihy, A.6
  • 27
    • 81455139473 scopus 로고    scopus 로고
    • GGN1 in the testis and ovary and its variance within the Australian fertile and infertile male population
    • Jamsai D, Sarraj MA, Merriner DJ, Drummond AE, Jones KT, McLachlan RI, et al. GGN1 in the testis and ovary and its variance within the Australian fertile and infertile male population. Int J Androl 2010;34:624-32.
    • (2010) Int J Androl , vol.34 , pp. 624-632
    • Jamsai, D.1    Sarraj, M.A.2    Merriner, D.J.3    Drummond, A.E.4    Jones, K.T.5    McLachlan, R.I.6
  • 28
    • 45749142102 scopus 로고    scopus 로고
    • Intramanchette transport during primate spermiogenesis: Expression of dynein, myosin Va, motor recruiter myosin Va, VIIa-Rab27a/b interacting protein, and Rab27b in the manchette during human and monkey spermiogenesis
    • Hayasaka S, Terada Y, Suzuki K, Murakawa H, Tachibana I, Sankai T, et al. Intramanchette transport during primate spermiogenesis: expression of dynein, myosin Va, motor recruiter myosin Va, VIIa-Rab27a/b interacting protein, and Rab27b in the manchette during human and monkey spermiogenesis. Asian J Androl 2008;10:561-8.
    • (2008) Asian J Androl , vol.10 , pp. 561-568
    • Hayasaka, S.1    Terada, Y.2    Suzuki, K.3    Murakawa, H.4    Tachibana, I.5    Sankai, T.6
  • 29
    • 0034962275 scopus 로고    scopus 로고
    • Spermatid manchette: Plugging proteins to zero into the sperm tail
    • Kierszenbaum AL. Spermatid manchette: plugging proteins to zero into the sperm tail. Mol Reprod Dev 2001;59:347-9.
    • (2001) Mol Reprod Dev , vol.59 , pp. 347-349
    • Kierszenbaum, A.L.1
  • 31
    • 33749026932 scopus 로고    scopus 로고
    • NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation
    • Kim S, Burette A, Chung HS, Kwon S-K, Woo J, Lee HW, et al. NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation. Nat Neurosci 2006;9:1294-301.
    • (2006) Nat Neurosci , vol.9 , pp. 1294-1301
    • Kim, S.1    Burette, A.2    Chung, H.S.3    Kwon, S.-K.4    Woo, J.5    Lee, H.W.6
  • 32
    • 0344442833 scopus 로고    scopus 로고
    • The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons
    • Lin J, Ho W, Gurney A, Rosenthal A. The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons. Nat Neurosci 2003;6:1270-6.
    • (2003) Nat Neurosci , vol.6 , pp. 1270-1276
    • Lin, J.1    Ho, W.2    Gurney, A.3    Rosenthal, A.4
  • 33
  • 34
    • 0030721027 scopus 로고    scopus 로고
    • HSP70-2 is required for desynapsis of synaptonemal complexes during meiotic prophase in juvenile and adult mouse spermatocytes
    • Dix DJ, Allen JW, Collins BW, Poorman-Allen P, Mori C, Blizard DR, et al. HSP70-2 is required for desynapsis of synaptonemal complexes during meiotic prophase in juvenile and adult mouse spermatocytes. Development 1997;124:4595-603.
    • (1997) Development , vol.124 , pp. 4595-4603
    • Dix, D.J.1    Allen, J.W.2    Collins, B.W.3    Poorman-Allen, P.4    Mori, C.5    Blizard, D.R.6
  • 35
    • 38649127832 scopus 로고    scopus 로고
    • Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L
    • La Salle S, Oakes CC, Oakes CC, Neaga OR, Bourc'his D, Bestor TH, et al. Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L. BMC Dev Biol 2007;7:104.
    • (2007) BMC Dev Biol , vol.7 , pp. 104
    • La Salle, S.1    Oakes, C.C.2    Oakes, C.C.3    Neaga, O.R.4    Bourc'His, D.5    Bestor, T.H.6
  • 36
    • 4544223707 scopus 로고    scopus 로고
    • Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
    • Bourc'his D, Bestor TH. Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L. Nature 2004;431:96-9.
    • (2004) Nature , vol.431 , pp. 96-99
    • Bourc'His, D.1    Bestor, T.H.2
  • 37
    • 0029099989 scopus 로고
    • Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
    • Baker SM, Bronner CE, Zhang L, Plug AW, Robatzek M, Warren G, et al. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell 1995;82:309-19.
    • (1995) Cell , vol.82 , pp. 309-319
    • Baker, S.M.1    Bronner, C.E.2    Zhang, L.3    Plug, A.W.4    Robatzek, M.5    Warren, G.6
  • 39
    • 0038813659 scopus 로고    scopus 로고
    • Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis
    • Crackower MA, Kolas NK, Noguchi J, Sarao R, Sarao R, Kikuchi K, et al. Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis. Science 2003;300:1291-5.
    • (2003) Science , vol.300 , pp. 1291-1295
    • Crackower, M.A.1    Kolas, N.K.2    Noguchi, J.3    Sarao, R.4    Sarao, R.5    Kikuchi, K.6
  • 40
    • 18844446130 scopus 로고    scopus 로고
    • RNA helicases: Regulators of differentiation
    • Abdelhaleem M. RNA helicases: regulators of differentiation. Clin Biochem 2005;38:499-503.
    • (2005) Clin Biochem , vol.38 , pp. 499-503
    • Abdelhaleem, M.1
  • 42
    • 0032564457 scopus 로고    scopus 로고
    • Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse
    • Watson ML, Zinn AR, Inoue N, Hess KD, Cobb J, Handel MA, et al. Identification of morc (microrchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse. Proc Natl Acad Sci U S A 1998;95:14361-6.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 14361-14366
    • Watson, M.L.1    Zinn, A.R.2    Inoue, N.3    Hess, K.D.4    Cobb, J.5    Handel, M.A.6
  • 44
    • 10744220744 scopus 로고    scopus 로고
    • Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites
    • Desnos C, Schonn J-S, Huet S, Tran VS, El-Amraoui A, Raposo G, et al. Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites. J Cell Biol 2003;163:559-70.
    • (2003) J Cell Biol , vol.163 , pp. 559-570
    • Desnos, C.1    Schonn, J.-S.2    Huet, S.3    Tran, V.S.4    El-Amraoui, A.5    Raposo, G.6
  • 45
    • 1842580500 scopus 로고    scopus 로고
    • The actin-based motor myosin Va is a component of the acroplaxome, an acrosome-nuclear envelope junctional plate, and of manchette-associated vesicles
    • Kierszenbaum AL, Rivkin E, Tres LL. The actin-based motor myosin Va is a component of the acroplaxome, an acrosome-nuclear envelope junctional plate, and of manchette-associated vesicles. Cytogenet Genome Res 2003;103:337-44.
    • (2003) Cytogenet Genome Res , vol.103 , pp. 337-344
    • Kierszenbaum, A.L.1    Rivkin, E.2    Tres, L.L.3
  • 46
    • 1942476757 scopus 로고    scopus 로고
    • The acroplaxome is the docking site of golgi-derived myosin Va/Rab27a/bcontaining proacrosomal vesicles in wild-type and Hrb mutant mouse spermatids
    • Kierszenbaum AL, Tres LL, Rivkin E, Kang-Decker N, van Deursen JM. The acroplaxome is the docking site of golgi-derived myosin Va/Rab27a/bcontaining proacrosomal vesicles in wild-type and Hrb mutant mouse spermatids. Biol Reprod 2004;70:1400-10.
    • (2004) Biol Reprod , vol.70 , pp. 1400-1410
    • Kierszenbaum, A.L.1    Tres, L.L.2    Rivkin, E.3    Kang-Decker, N.4    Van Deursen, J.M.5
  • 47
    • 79953858658 scopus 로고    scopus 로고
    • No-nonsense functions for long noncoding RNAs
    • Nagano T, Fraser P. No-nonsense functions for long noncoding RNAs. Cell 2011;145:178-81.
    • (2011) Cell , vol.145 , pp. 178-181
    • Nagano, T.1    Fraser, P.2
  • 48
    • 79957840356 scopus 로고    scopus 로고
    • Long noncoding RNAs and human disease
    • Wapinski O, Chang HY. Long noncoding RNAs and human disease. Trends Cell Biol 2011;21:354-61.
    • (2011) Trends Cell Biol , vol.21 , pp. 354-361
    • Wapinski, O.1    Chang, H.Y.2
  • 49
    • 84861222896 scopus 로고    scopus 로고
    • The long non-coding RNA, MHM, plays a role in chicken embryonic development, including gonadogenesis
    • Roeszler KN, Itman C, Sinclair AH, Smith CA. The long non-coding RNA, MHM, plays a role in chicken embryonic development, including gonadogenesis. Dev Biol 2012;366:317-26.
    • (2012) Dev Biol , vol.366 , pp. 317-326
    • Roeszler, K.N.1    Itman, C.2    Sinclair, A.H.3    Smith, C.A.4
  • 50
    • 84885404224 scopus 로고    scopus 로고
    • Long non-coding RNA expression profiling of mouse testis during postnatal development
    • Sun J, Lin Y, Wu J. Long non-coding RNA expression profiling of mouse testis during postnatal development. PLoS One 2013;8:e75750.
    • (2013) PLoS One , vol.8 , pp. e75750
    • Sun, J.1    Lin, Y.2    Wu, J.3
  • 51
    • 67650960831 scopus 로고    scopus 로고
    • The NGL family of leucine-rich repeat-containing synaptic adhesion molecules
    • Woo J, Kwon S-K, Kim E. The NGL family of leucine-rich repeat-containing synaptic adhesion molecules. Mol Cell Neurosci 2009;42:1-10.
    • (2009) Mol Cell Neurosci , vol.42 , pp. 1-10
    • Woo, J.1    Kwon, S.-K.2    Kim, E.3
  • 52
    • 84862972357 scopus 로고    scopus 로고
    • Whirlin interacts with espin and modulates its actin-regulatory function: An insight into the mechanism of Usher syndrome type II
    • Wang L, Zou J, Shen Z, Song E, Yang J. Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II. Hum Mol Genet 2012;21:692-710.
    • (2012) Hum Mol Genet , vol.21 , pp. 692-710
    • Wang, L.1    Zou, J.2    Shen, Z.3    Song, E.4    Yang, J.5
  • 53
    • 0043168114 scopus 로고    scopus 로고
    • Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
    • Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, et al. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nat Genet 2003;34:421-8.
    • (2003) Nat Genet , vol.34 , pp. 421-428
    • Mburu, P.1    Mustapha, M.2    Varela, A.3    Weil, D.4    El-Amraoui, A.5    Holme, R.H.6
  • 54
    • 34250366660 scopus 로고    scopus 로고
    • The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development
    • Mogensen MM, Rzadzinska A, Steel KP. The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development. Cell Motil Cytoskeleton 2007;64:496-508.
    • (2007) Cell Motil Cytoskeleton , vol.64 , pp. 496-508
    • Mogensen, M.M.1    Rzadzinska, A.2    Steel, K.P.3
  • 55
    • 33947148611 scopus 로고    scopus 로고
    • A novel gene for Usher syndrome type 2: Mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss
    • Ebermann I, Scholl H, Charbel Issa P, Becirovic E, Lamprecht J, Jurklies B, et al. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss. Hum Genet 2007;121:203-11.
    • (2007) Hum Genet , vol.121 , pp. 203-211
    • Ebermann, I.1    Scholl, H.2    Charbel Issa, P.3    Becirovic, E.4    Lamprecht, J.5    Jurklies, B.6
  • 56
    • 0034076573 scopus 로고    scopus 로고
    • Repression of hspA2 messenger RNA in human testes with abnormal spermatogenesis
    • Son W-Y, Han C-T, Hwang S-H, Lee J-H, Kim S, Kim YC. Repression of hspA2 messenger RNA in human testes with abnormal spermatogenesis. Fertil Steril 2000;73:1138-44.
    • (2000) Fertil Steril , vol.73 , pp. 1138-1144
    • Son, W.-Y.1    Han, C.-T.2    Hwang, S.-H.3    Lee, J.-H.4    Kim, S.5    Kim, Y.C.6
  • 58
    • 77956840942 scopus 로고    scopus 로고
    • Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis
    • Terribas E, Bonache S, Garcia-Arevalo M, Sanchez J, Franco E, Bassas L, et al. Changes in the expression profile of the meiosis-involved mismatch repair genes in impaired human spermatogenesis. J Androl 2010;31:346-57.
    • (2010) J Androl , vol.31 , pp. 346-357
    • Terribas, E.1    Bonache, S.2    Garcia-Arevalo, M.3    Sanchez, J.4    Franco, E.5    Bassas, L.6
  • 59
    • 0035199033 scopus 로고    scopus 로고
    • Decreased expression of the heat shock protein hsp70-2 is associated with the pathogenesis of male infertility
    • Feng HL, Sandlow JI, Sparks AET. Decreased expression of the heat shock protein hsp70-2 is associated with the pathogenesis of male infertility. Fertil Steril 2001;76:1136-9.
    • (2001) Fertil Steril , vol.76 , pp. 1136-1139
    • Feng, H.L.1    Sandlow, J.I.2    Sparks, A.E.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.