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Volumn 103, Issue 2, 2015, Pages 548-553.e5

Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency

Author keywords

Primary ovarian insufficiency; SOHLH1; variant screening

Indexed keywords

SPERMATOGENESIS AND OOGENESIS SPECIFIC BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; SOHLH1 PROTEIN, HUMAN;

EID: 84923264798     PISSN: 00150282     EISSN: 15565653     Source Type: Journal    
DOI: 10.1016/j.fertnstert.2014.11.011     Document Type: Article
Times cited : (28)

References (45)
  • 1
    • 40749100654 scopus 로고    scopus 로고
    • Primary ovarian insufficiency: A more accurate term for premature ovarian failure
    • C.K. Welt Primary ovarian insufficiency: a more accurate term for premature ovarian failure Clin Endocrinol (Oxf) 68 2008 499 509
    • (2008) Clin Endocrinol (Oxf) , vol.68 , pp. 499-509
    • Welt, C.K.1
  • 2
    • 59749096464 scopus 로고    scopus 로고
    • Clinical practice. Primary ovarian insufficiency
    • L.M. Nelson Clinical practice. Primary ovarian insufficiency N Engl J Med 360 2009 606 614
    • (2009) N Engl J Med , vol.360 , pp. 606-614
    • Nelson, L.M.1
  • 4
    • 67649970424 scopus 로고    scopus 로고
    • Aetiology of premature ovarian failure
    • S. Vujovic Aetiology of premature ovarian failure Menopause Int 15 2009 72 75
    • (2009) Menopause Int , vol.15 , pp. 72-75
    • Vujovic, S.1
  • 5
    • 84863573475 scopus 로고    scopus 로고
    • Cytogenetic analysis of 531 Chinese women with premature ovarian failure
    • X. Jiao, C. Qin, J. Li, Y. Qin, X. Gao, and B. Zhang Cytogenetic analysis of 531 Chinese women with premature ovarian failure Hum Reprod 27 2012 2201 2207
    • (2012) Hum Reprod , vol.27 , pp. 2201-2207
    • Jiao, X.1    Qin, C.2    Li, J.3    Qin, Y.4    Gao, X.5    Zhang, B.6
  • 7
    • 39149108084 scopus 로고    scopus 로고
    • Recent advances in the study of genes involved in non-syndromic premature ovarian failure
    • P. Laissue, G. Vinci, R.A. Veitia, and M. Fellous Recent advances in the study of genes involved in non-syndromic premature ovarian failure Mol Cell Endocrinol 282 2008 101 111
    • (2008) Mol Cell Endocrinol , vol.282 , pp. 101-111
    • Laissue, P.1    Vinci, G.2    Veitia, R.A.3    Fellous, M.4
  • 8
    • 78649576457 scopus 로고    scopus 로고
    • Genes involved in human premature ovarian failure
    • L. Persani, R. Rossetti, and C. Cacciatore Genes involved in human premature ovarian failure J Mol Endocrinol 45 2010 257 279
    • (2010) J Mol Endocrinol , vol.45 , pp. 257-279
    • Persani, L.1    Rossetti, R.2    Cacciatore, C.3
  • 9
    • 77956617098 scopus 로고    scopus 로고
    • Primary ovarian insufficiency
    • M. De Vos, P. Devroey, and B.C. Fauser Primary ovarian insufficiency Lancet 376 2010 911 921
    • (2010) Lancet , vol.376 , pp. 911-921
    • De Vos, M.1    Devroey, P.2    Fauser, B.C.3
  • 10
    • 68549117062 scopus 로고    scopus 로고
    • Molecular mechanisms underlying the activation of mammalian primordial follicles
    • D. Adhikari, and K. Liu Molecular mechanisms underlying the activation of mammalian primordial follicles Endocr Rev 30 2009 438 464
    • (2009) Endocr Rev , vol.30 , pp. 438-464
    • Adhikari, D.1    Liu, K.2
  • 11
    • 0036798824 scopus 로고    scopus 로고
    • Genetic dissection of mammalian fertility pathways
    • M.M. Matzuk, and D.J. Lamb Genetic dissection of mammalian fertility pathways Nat Cell Biol Suppl. 2002 S41 S49
    • (2002) Nat Cell Biol , pp. S41-S49
    • Matzuk, M.M.1    Lamb, D.J.2
  • 12
    • 84859632100 scopus 로고    scopus 로고
    • Oogenesis: Transcriptional regulators and mouse models
    • K. Jagarlamudi, and A. Rajkovic Oogenesis: transcriptional regulators and mouse models Mol Cell Endocrinol 356 2012 31 39
    • (2012) Mol Cell Endocrinol , vol.356 , pp. 31-39
    • Jagarlamudi, K.1    Rajkovic, A.2
  • 13
    • 84855811865 scopus 로고    scopus 로고
    • ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure
    • Y. Qin, M. Sun, L. You, D. Wei, J. Sun, and X. Liang ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure Orphanet J Rare Dis 7 2012 5
    • (2012) Orphanet J Rare Dis , vol.7 , pp. 5
    • Qin, Y.1    Sun, M.2    You, L.3    Wei, D.4    Sun, J.5    Liang, X.6
  • 14
    • 84867018612 scopus 로고    scopus 로고
    • The CC-allele of the PvuII polymorphic variant in intron 1 of the alpha-estrogen receptor gene is significantly more prevalent among infertile women at risk of premature ovarian aging
    • N. M'Rabet, R. Moffat, S. Helbling, A. Kaech, H. Zhang, and C. de Geyter The CC-allele of the PvuII polymorphic variant in intron 1 of the alpha-estrogen receptor gene is significantly more prevalent among infertile women at risk of premature ovarian aging Fertil Steril 98 2012 965 972.e1-5
    • (2012) Fertil Steril , vol.98 , pp. 965e1-972e5
    • M'Rabet, N.1    Moffat, R.2    Helbling, S.3    Kaech, A.4    Zhang, H.5    De Geyter, C.6
  • 15
    • 84871413400 scopus 로고    scopus 로고
    • Estrogen receptor alpha gene (ESR1) polymorphisms associated with idiopathic premature ovarian failure in Chinese women
    • L. Liu, R. Tan, Y. Cui, J. Liu, and J. Wu Estrogen receptor alpha gene (ESR1) polymorphisms associated with idiopathic premature ovarian failure in Chinese women Gynecol Endocrinol 29 2013 182 185
    • (2013) Gynecol Endocrinol , vol.29 , pp. 182-185
    • Liu, L.1    Tan, R.2    Cui, Y.3    Liu, J.4    Wu, J.5
  • 17
    • 67650508076 scopus 로고    scopus 로고
    • Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
    • P. Laissue, B. Lakhal, B.A. Benayoun, A. Dipietromaria, R. Braham, and H. Elghezal Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 J Med Genet 46 2009 455 457
    • (2009) J Med Genet , vol.46 , pp. 455-457
    • Laissue, P.1    Lakhal, B.2    Benayoun, B.A.3    Dipietromaria, A.4    Braham, R.5    Elghezal, H.6
  • 18
    • 75749098036 scopus 로고    scopus 로고
    • A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome
    • F.J. Correa, A.B. Tavares, R.W. Pereira, and M.S. Abrao A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome Fertil Steril 93 2010 1006.e3 1006.e6
    • (2010) Fertil Steril , vol.93 , pp. 1006e3-1006e6
    • Correa, F.J.1    Tavares, A.B.2    Pereira, R.W.3    Abrao, M.S.4
  • 19
    • 77949454237 scopus 로고    scopus 로고
    • Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure
    • F. Ni, Q. Wen, B. Wang, S. Zhou, J. Wang, and Y. Mu Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure Gynecol Endocrinol 26 2010 246 249
    • (2010) Gynecol Endocrinol , vol.26 , pp. 246-249
    • Ni, F.1    Wen, Q.2    Wang, B.3    Zhou, S.4    Wang, J.5    Mu, Y.6
  • 22
    • 80053023062 scopus 로고    scopus 로고
    • Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort
    • J. Bouilly, A. Bachelot, I. Broutin, P. Touraine, and N. Binart Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort Hum Mutat 32 2011 1108 1113
    • (2011) Hum Mutat , vol.32 , pp. 1108-1113
    • Bouilly, J.1    Bachelot, A.2    Broutin, I.3    Touraine, P.4    Binart, N.5
  • 23
    • 45449120985 scopus 로고    scopus 로고
    • Transcription factor FIGLA is mutated in patients with premature ovarian failure
    • H. Zhao, Z.J. Chen, Y. Qin, Y. Shi, S. Wang, and Y. Choi Transcription factor FIGLA is mutated in patients with premature ovarian failure Am J Hum Genet 82 2008 1342 1348
    • (2008) Am J Hum Genet , vol.82 , pp. 1342-1348
    • Zhao, H.1    Chen, Z.J.2    Qin, Y.3    Shi, Y.4    Wang, S.5    Choi, Y.6
  • 24
    • 69149097964 scopus 로고    scopus 로고
    • Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure
    • B. Wang, L. Li, F. Ni, J. Song, J. Wang, and Y. Mu Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure Mol Hum Reprod 15 2009 557 562
    • (2009) Mol Hum Reprod , vol.15 , pp. 557-562
    • Wang, B.1    Li, L.2    Ni, F.3    Song, J.4    Wang, J.5    Mu, Y.6
  • 25
    • 79951605768 scopus 로고    scopus 로고
    • New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients
    • J. Wang, B. Wang, J. Song, P. Suo, F. Ni, and B. Chen New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients Reprod Biomed Online 22 2011 312 316
    • (2011) Reprod Biomed Online , vol.22 , pp. 312-316
    • Wang, J.1    Wang, B.2    Song, J.3    Suo, P.4    Ni, F.5    Chen, B.6
  • 27
    • 84866353260 scopus 로고    scopus 로고
    • Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure
    • B. Lakhal, S. Ben-Hadj-Khalifa, N. Bouali, P. Philipert, F. Audran, and R. Braham Mutational screening of SF1 and WNT4 in Tunisian women with premature ovarian failure Gene 509 2012 298 301
    • (2012) Gene , vol.509 , pp. 298-301
    • Lakhal, B.1    Ben-Hadj-Khalifa, S.2    Bouali, N.3    Philipert, P.4    Audran, F.5    Braham, R.6
  • 28
    • 84873279263 scopus 로고    scopus 로고
    • NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency
    • P. Philibert, F. Paris, B. Lakhal, F. Audran, L. Gaspari, and A. Saad NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency Fertil Steril 99 2013 484 489
    • (2013) Fertil Steril , vol.99 , pp. 484-489
    • Philibert, P.1    Paris, F.2    Lakhal, B.3    Audran, F.4    Gaspari, L.5    Saad, A.6
  • 29
    • 84884488195 scopus 로고    scopus 로고
    • Novel NR5A1 missense mutation in premature ovarian failure: Detection in Han chinese indicates causation in different ethnic groups
    • X. Jiao, Y. Qin, G. Li, S. Zhao, L. You, and J. Ma Novel NR5A1 missense mutation in premature ovarian failure: detection in Han chinese indicates causation in different ethnic groups PLoS One 8 2013 e74759
    • (2013) PLoS One , vol.8 , pp. e74759
    • Jiao, X.1    Qin, Y.2    Li, G.3    Zhao, S.4    You, L.5    Ma, J.6
  • 30
    • 84897129902 scopus 로고    scopus 로고
    • Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure
    • Y. Qin, X. Jiao, R. Dalgleish, S. Vujovic, J. Li, and J.L. Simpson Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure Fertil Steril 101 2014 1104 1109.e6
    • (2014) Fertil Steril , vol.101 , pp. 1104-1109e6
    • Qin, Y.1    Jiao, X.2    Dalgleish, R.3    Vujovic, S.4    Li, J.5    Simpson, J.L.6
  • 31
    • 33646486836 scopus 로고    scopus 로고
    • Sohlh1 is essential for spermatogonial differentiation
    • D. Ballow, M.L. Meistrich, M. Matzuk, and A. Rajkovic Sohlh1 is essential for spermatogonial differentiation Dev Biol 294 2006 161 167
    • (2006) Dev Biol , vol.294 , pp. 161-167
    • Ballow, D.1    Meistrich, M.L.2    Matzuk, M.3    Rajkovic, A.4
  • 32
    • 77954126153 scopus 로고    scopus 로고
    • Mutations in SOHLH1 gene associate with nonobstructive azoospermia
    • Y. Choi, S. Jeon, M. Choi, M.H. Lee, M. Park, and D.R. Lee Mutations in SOHLH1 gene associate with nonobstructive azoospermia Hum Mutat 31 2010 788 793
    • (2010) Hum Mutat , vol.31 , pp. 788-793
    • Choi, Y.1    Jeon, S.2    Choi, M.3    Lee, M.H.4    Park, M.5    Lee, D.R.6
  • 34
    • 33847196759 scopus 로고    scopus 로고
    • Candidate genes for premature ovarian failure
    • N. Suzumori, S.A. Pangas, and A. Rajkovic Candidate genes for premature ovarian failure Curr Med Chem 14 2007 353 357
    • (2007) Curr Med Chem , vol.14 , pp. 353-357
    • Suzumori, N.1    Pangas, S.A.2    Rajkovic, A.3
  • 35
    • 4043141372 scopus 로고    scopus 로고
    • An overview of the basic helix-loop-helix proteins
    • S. Jones An overview of the basic helix-loop-helix proteins Genome Biol 5 2004 226
    • (2004) Genome Biol , vol.5 , pp. 226
    • Jones, S.1
  • 37
    • 84355162807 scopus 로고    scopus 로고
    • SOHLH1 and SOHLH2 coordinate spermatogonial differentiation
    • H. Suzuki, H.W. Ahn, T. Chu, W. Bowden, K. Gassei, and K. Orwig SOHLH1 and SOHLH2 coordinate spermatogonial differentiation Dev Biol 361 2012 301 312
    • (2012) Dev Biol , vol.361 , pp. 301-312
    • Suzuki, H.1    Ahn, H.W.2    Chu, T.3    Bowden, W.4    Gassei, K.5    Orwig, K.6
  • 38
    • 84861207250 scopus 로고    scopus 로고
    • SOHLH1 and SOHLH2 control Kit expression during postnatal male germ cell development
    • F. Barrios, D. Filipponi, F. Campolo, M. Gori, F. Bramucci, and M. Pellegrini SOHLH1 and SOHLH2 control Kit expression during postnatal male germ cell development J Cell Sci 125 2012 1455 1464
    • (2012) J Cell Sci , vol.125 , pp. 1455-1464
    • Barrios, F.1    Filipponi, D.2    Campolo, F.3    Gori, M.4    Bramucci, F.5    Pellegrini, M.6
  • 39
    • 56749112423 scopus 로고    scopus 로고
    • Germ cell-specific transcriptional regulator sohlh2 is essential for early mouse folliculogenesis and oocyte-specific gene expression
    • Y. Choi, D. Yuan, and A. Rajkovic Germ cell-specific transcriptional regulator sohlh2 is essential for early mouse folliculogenesis and oocyte-specific gene expression Biol Reprod 79 2008 1176 1182
    • (2008) Biol Reprod , vol.79 , pp. 1176-1182
    • Choi, Y.1    Yuan, D.2    Rajkovic, A.3
  • 40
    • 84864339913 scopus 로고    scopus 로고
    • Differentially expressed plasma microRNAs in premature ovarian failure patients and the potential regulatory function of mir-23a in granulosa cell apoptosis
    • X. Yang, Y. Zhou, S. Peng, L. Wu, H.Y. Lin, and S. Wang Differentially expressed plasma microRNAs in premature ovarian failure patients and the potential regulatory function of mir-23a in granulosa cell apoptosis Reproduction 144 2012 235 244
    • (2012) Reproduction , vol.144 , pp. 235-244
    • Yang, X.1    Zhou, Y.2    Peng, S.3    Wu, L.4    Lin, H.Y.5    Wang, S.6
  • 41
    • 84870564116 scopus 로고    scopus 로고
    • Association of miR-146aC>G, miR-196a2T>C, and miR-499A>G polymorphisms with risk of premature ovarian failure in Korean women
    • H. Rah, Y.J. Jeon, S.H. Shim, S.H. Cha, D.H. Choi, and H. Kwon Association of miR-146aC>G, miR-196a2T>C, and miR-499A>G polymorphisms with risk of premature ovarian failure in Korean women Reprod Sci 20 2013 60 68
    • (2013) Reprod Sci , vol.20 , pp. 60-68
    • Rah, H.1    Jeon, Y.J.2    Shim, S.H.3    Cha, S.H.4    Choi, D.H.5    Kwon, H.6
  • 42
    • 84875170985 scopus 로고    scopus 로고
    • MicroRNA-181a suppresses mouse granulosa cell proliferation by targeting activin receptor IIA
    • Q. Zhang, H. Sun, Y. Jiang, L. Ding, S. Wu, and T. Fang MicroRNA-181a suppresses mouse granulosa cell proliferation by targeting activin receptor IIA PLoS One 8 2013 e59667
    • (2013) PLoS One , vol.8 , pp. e59667
    • Zhang, Q.1    Sun, H.2    Jiang, Y.3    Ding, L.4    Wu, S.5    Fang, T.6
  • 43
    • 80052181929 scopus 로고    scopus 로고
    • Mir-290-295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects
    • L.A. Medeiros, L.M. Dennis, M.E. Gill, H. Houbaviy, S. Markoulaki, and D. Fu Mir-290-295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects Proc Natl Acad Sci U S A 108 2011 14163 14168
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 14163-14168
    • Medeiros, L.A.1    Dennis, L.M.2    Gill, M.E.3    Houbaviy, H.4    Markoulaki, S.5    Fu, D.6
  • 44
    • 79952134938 scopus 로고    scopus 로고
    • A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease
    • P. Brest, P. Lapaquette, M. Souidi, K. Lebrigand, A. Cesaro, and V. Vouret-Craviari A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease Nat Genet 43 2011 242 245
    • (2011) Nat Genet , vol.43 , pp. 242-245
    • Brest, P.1    Lapaquette, P.2    Souidi, M.3    Lebrigand, K.4    Cesaro, A.5    Vouret-Craviari, V.6
  • 45
    • 0032452410 scopus 로고    scopus 로고
    • The frequency of an inactivating point mutation (566C→T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry
    • M. Jiang, K. Aittomaki, C. Nilsson, P. Pakarinen, A. Iitia, and T. Torresani The frequency of an inactivating point mutation (566C→T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry J Clin Endocrinol Metab 83 1998 4338 4343
    • (1998) J Clin Endocrinol Metab , vol.83 , pp. 4338-4343
    • Jiang, M.1    Aittomaki, K.2    Nilsson, C.3    Pakarinen, P.4    Iitia, A.5    Torresani, T.6


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