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Volumn 28, Issue 8, 2011, Pages 743-746

Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest

Author keywords

Azoospermia; Meiotic arrest; Polymorphism; UBR2

Indexed keywords

ADULT; ARTICLE; AZOOSPERMIA; CELL CYCLE ARREST; CLINICAL ARTICLE; CONTROL GROUP; CONTROLLED STUDY; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; GENOTYPE; HUMAN; JAPANESE; MALE; MEIOSIS; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; UBR2 GENE;

EID: 80755138385     PISSN: 10580468     EISSN: 15737330     Source Type: Journal    
DOI: 10.1007/s10815-011-9576-y     Document Type: Article
Times cited : (9)

References (26)
  • 1
    • 0029088061 scopus 로고
    • Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
    • Reijo R, Lee TY, Salo P, Alagappan R, Brown LG, Rosenberg M, et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet. 1995; 10: 383-93.
    • (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
  • 3
    • 0032727618 scopus 로고    scopus 로고
    • An azoospermic man with a de novo point mutation in the Ychromosomal gene USP9Y
    • Sun C, Skaletsky H, Birren B, Devon K, Tang Z, Silber S, et al. An azoospermic man with a de novo point mutation in the Ychromosomal gene USP9Y. Nat Genet. 1999; 23: 429-32.
    • (1999) Nat Genet , vol.23 , pp. 429-432
    • Sun, C.1    Skaletsky, H.2    Birren, B.3    Devon, K.4    Tang, Z.5    Silber, S.6
  • 4
    • 0036798824 scopus 로고    scopus 로고
    • Genetic dissection of mammalian fertility pathways
    • Matzuk MM, Lamb DJ. Genetic dissection of mammalian fertility pathway. Nat Med. 2002; 8 suppl 1: S41-9. (Pubitemid 35175933)
    • (2002) Nature Medicine , vol.8 , Issue.10 SUPPL.
    • Matzuk, M.M.1    Lamb, D.J.2
  • 5
    • 0344983426 scopus 로고    scopus 로고
    • Azoospermia in patients heterozygous for a mutation in SYCP3
    • DOI 10.1016/S0140-6736(03)14845-3
    • Miyamoto T, Hasuike S, Yogev L, Maduro MR, Ishikawa M, Westphal H, et al. Azoospermia in patients heterozygous for a mutation in SYCP3. Lancet. 2003; 362: 1714-9. (Pubitemid 37468322)
    • (2003) Lancet , vol.362 , Issue.9397 , pp. 1714-1719
    • Miyamoto, T.1    Hasuike, S.2    Yogev, L.3    Maduro, M.R.4    Ishikawa, M.5    Westphal, H.6    Lamb, D.J.7
  • 6
    • 33745255403 scopus 로고    scopus 로고
    • Protamines and male infertility
    • DOI 10.1093/humupd/dml009
    • Oliva R. Protamines and male infertility. Hum Reprod Update. 2006; 12: 417-35. (Pubitemid 43923415)
    • (2006) Human Reproduction Update , vol.12 , Issue.4 , pp. 417-435
    • Oliva, R.1
  • 9
    • 33751357550 scopus 로고    scopus 로고
    • Non-invasive genetic diagnosis of male infertility using spermatozoal RNA: KLHL 10 mutations in oligozoospermic patients impair homodimerization
    • DOI 10.1093/hmg/ddl417
    • Yatsenko AN, Roy A, Chen R, Ma L, Murthy LJ, Yan W, et al. Non-invasive genetic diagnosis of male infertility using spermatozoa RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization. Hum Mol Genet. 2006; 15: 3411-9. (Pubitemid 44811593)
    • (2006) Human Molecular Genetics , vol.15 , Issue.23 , pp. 3411-3419
    • Yatsenko, A.N.1    Roy, A.2    Chen, R.3    Ma, L.4    Murthy, L.J.5    Yan, W.6    Lamb, D.J.7    Matzuk, M.M.8
  • 10
    • 0035682067 scopus 로고    scopus 로고
    • Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo- or azoospermia
    • DOI 10.1023/A:1013117123244
    • Yao G, Chen G, Pan T. Study of microdeletions in the Y chromosome of infertilemen with idiopathic oligo- or azoospermia. J Assist Reprod Genet. 2001; 18: 612-6. (Pubitemid 34056735)
    • (2001) Journal of Assisted Reproduction and Genetics , vol.18 , Issue.11 , pp. 612-616
    • Yao, G.1    Chen, G.2    Pan, T.3
  • 11
    • 77957562653 scopus 로고    scopus 로고
    • BCL2 Ala43Thr is a functional variant associated with protection against azoospermia in a Han-Chinese population
    • Ma J, Lu HY, Xia YK, Dong HB, Gu AH, Li ZY, et al. BCL2 Ala43Thr is a functional variant associated with protection against azoospermia in a Han-Chinese population. Biol Reprod. 2010; 83: 656-62.
    • (2010) Biol Reprod , vol.83 , pp. 656-662
    • Ma, J.1    Lu, H.Y.2    Xia, Y.K.3    Dong, H.B.4    Gu, A.H.5    Li, Z.Y.6
  • 12
    • 77956096988 scopus 로고    scopus 로고
    • The role of endothelial nitric oxide synthase (eNOS) T-786C G894T and 4a/b gene polymorphisms in the risk of idiopathic male infertility
    • Safarinejad MR, Shafiei N, Safarinejad S. The role of endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms in the risk of idiopathic male infertility. Mol Reprod Dev. 2010; 77: 720-7.
    • (2010) Mol Reprod Dev , vol.77 , pp. 720-727
    • Safarinejad, M.R.1    Shafiei, N.2    Safarinejad, S.3
  • 13
    • 0037178719 scopus 로고    scopus 로고
    • Segregating sister genomes: The molecular biology of chromosome separation
    • DOI 10.1126/science.1074757
    • Nasmyth K. Segregating sister genomes: the molecular biology of chromosome separation. Science. 2002; 297: 559-65. (Pubitemid 34815333)
    • (2002) Science , vol.297 , Issue.5581 , pp. 559-565
    • Nasmyth, K.1
  • 14
    • 0032037422 scopus 로고    scopus 로고
    • The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis
    • Yoshida K, Kondoh G, Matsuda Y, Habu T, Nishimune Y, Morita T. The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis. Mol Cell. 1998; 1: 707-18. (Pubitemid 128379248)
    • (1998) Molecular Cell , vol.1 , Issue.5 , pp. 707-718
    • Yoshida, K.1    Kondoh, G.2    Matsuda, Y.3    Habu, T.4    Nishimune, Y.5    Morita, T.6
  • 17
    • 0033638183 scopus 로고    scopus 로고
    • Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11
    • Baudat F, Manova K, Yuen JP, Jasin M, Keeney S. Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. Mol Cell. 2000; 6: 989-98.
    • (2000) Mol Cell , vol.6 , pp. 989-998
    • Baudat, F.1    Manova, K.2    Yuen, J.P.3    Jasin, M.4    Keeney, S.5
  • 19
    • 0033634652 scopus 로고    scopus 로고
    • The mouse Spo11 gene is required formeiotic chromosome synapsis
    • Romanienko PJ, Camerini-Otero RD. The mouse Spo11 gene is required formeiotic chromosome synapsis.Mol Cell. 2000; 6: 975-87.
    • (2000) Mol Cell , vol.6 , pp. 975-987
    • Romanienko, P.J.1    Camerini-Otero, R.D.2
  • 20
    • 0033975302 scopus 로고    scopus 로고
    • The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility
    • Yuan L, Liu JG, Zhao J, Brundell E, Daneholt B, Hoog C. The murine SCP3 gene is required for synaptonemal complex assembly, chromosome synapsis, and male fertility. Mol Cell. 2000; 5: 73-83. (Pubitemid 30105437)
    • (2000) Molecular Cell , vol.5 , Issue.1 , pp. 73-83
    • Yuan, L.1    Liu, J.-G.2    Zhao, J.3    Brundell, E.4    Daneholt, B.5    Hoog, C.6
  • 22
    • 27844440989 scopus 로고    scopus 로고
    • A histone H3 methyltransferase controls epigenetic events required for meiotic prophase
    • DOI 10.1038/nature04112, PII N04112
    • Hayashi K, Yoshida K, Matsui Y. A histone H3 methyltransferase controls epigenetic events required for meiotic prophase. Nature. 2005; 438: 374-8. (Pubitemid 41643955)
    • (2005) Nature , vol.438 , Issue.7066 , pp. 374-378
    • Hayashi, K.1    Yoshida, K.2    Matsui, Y.3
  • 24
    • 0346783290 scopus 로고    scopus 로고
    • The Hop2 protein has a direct role in promoting interhomolog interactions during mouse meiosis
    • DOI 10.1016/S1534-5807(03)00369-1, PII S1534580703003691
    • Petukhova GV, Romanienko PJ, Camerini-Otero RD. The Hop2 protein has a direct role in promoting interhomolog interactions during mouse meiosis. Dev Cell. 2003; 5: 927-36. (Pubitemid 37527692)
    • (2003) Developmental Cell , vol.5 , Issue.6 , pp. 927-936
    • Petukhova, G.V.1    Romanienko, P.J.2    Camerini-Otero, R.D.3
  • 26
    • 76649112438 scopus 로고    scopus 로고
    • UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination
    • An JY, Kim EA, Jiang Y, Zakrzewska A, Kim DE, Lee MJ, et al. UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination. Proc Natl Acad Sci USA. 2010; 107: 1912-7.
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 1912-1917
    • An, J.Y.1    Kim, E.A.2    Jiang, Y.3    Zakrzewska, A.4    Kim, D.E.5    Lee, M.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.