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Volumn 6, Issue 2, 2014, Pages 175-177

NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis

Author keywords

[No Author keywords available]

Indexed keywords

FORKHEAD TRANSCRIPTION FACTOR; FORKHEAD TRANSCRIPTION FACTOR 2; HOMEODOMAIN PROTEIN; NEWBORN OOGENESIS HOMEOBOX; UNCLASSIFIED DRUG; FOXL2 PROTEIN, HUMAN; NOBOX PROTEIN, HUMAN; PROTEIN BINDING; TRANSCRIPTION FACTOR;

EID: 84899684696     PISSN: 16742788     EISSN: 17594685     Source Type: Journal    
DOI: 10.1093/jmcb/mju006     Document Type: Letter
Times cited : (20)

References (10)
  • 1
    • 53349176609 scopus 로고    scopus 로고
    • The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
    • Benayoun, B.A., Caburet, S., Dipietromaria, A., et al. (2008). The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles. Hum. Mol. Genet. 17, 3118-3127.
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 3118-3127
    • Benayoun, B.A.1    Caburet, S.2    Dipietromaria, A.3
  • 2
    • 59749101082 scopus 로고    scopus 로고
    • FOXL2 mutations and genomic rearrangements in BPES
    • Beysen, D., De, P.A., and De, B.E. (2009). FOXL2 mutations and genomic rearrangements in BPES. Hum. Mutat. 30, 158-169.
    • (2009) Hum. Mutat. , vol.30 , pp. 158-169
    • Beysen, D.1    De, P.A.2    De, B.E.3
  • 3
    • 80053023062 scopus 로고    scopus 로고
    • Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort
    • Bouilly, J., Bachelot, A., Broutin, I., et al. (2011). Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort. Hum. Mutat. 32, 1108-1113.
    • (2011) Hum. Mutat. , vol.32 , pp. 1108-1113
    • Bouilly, J.1    Bachelot, A.2    Broutin, I.3
  • 4
    • 33845971561 scopus 로고    scopus 로고
    • Characterization of NOBOX DNA binding specificity and its regulation of Gdf9 and Pou5f1 promoters
    • Choi, Y., and Rajkovic, A. (2006). Characterization of NOBOX DNA binding specificity and its regulation of Gdf9 and Pou5f1 promoters. J. Biol. Chem. 281, 35747-35756.
    • (2006) J. Biol. Chem. , vol.281 , pp. 35747-35756
    • Choi, Y.1    Rajkovic, A.2
  • 5
    • 0038297111 scopus 로고    scopus 로고
    • Joint regulation of the MAP1B promoter by HNF3beta/Foxa2 and Engrailed is the result of a highly conserved mechanism for direct interaction of homeoproteins and Fox transcription factors
    • Foucher, I., Montesinos, M.L., Volovitch, M., et al. (2003). Joint regulation of the MAP1B promoter by HNF3beta/Foxa2 and Engrailed is the result of a highly conserved mechanism for direct interaction of homeoproteins and Fox transcription factors. Development 130, 1867-1876.
    • (2003) Development , vol.130 , pp. 1867-1876
    • Foucher, I.1    Montesinos, M.L.2    Volovitch, M.3
  • 6
    • 39149117672 scopus 로고    scopus 로고
    • The mutations and potential targets of the forkhead transcription factor FOXL2
    • Moumne, L., Batista, F., Benayoun, B.A., et al. (2008). The mutations and potential targets of the forkhead transcription factor FOXL2. Mol. Cell. Endocrinol. 282, 2-11.
    • (2008) Mol. Cell. Endocrinol. , vol.282 , pp. 2-11
    • Moumne, L.1    Batista, F.2    Benayoun, B.A.3
  • 7
    • 34548288054 scopus 로고    scopus 로고
    • NOBOX homeobox mutation causes premature ovarian failure
    • Qin, Y., Choi, Y., Zhao, H., et al. (2007). NOBOX homeobox mutation causes premature ovarian failure. Am. J. Hum. Genet. 81, 576-581.
    • (2007) Am. J. Hum. Genet. , vol.81 , pp. 576-581
    • Qin, Y.1    Choi, Y.2    Zhao, H.3
  • 8
    • 4143068997 scopus 로고    scopus 로고
    • NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression
    • Rajkovic, A., Pangas, S.A., Ballow, D., et al. (2004). NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression. Science 305, 1157-1159.
    • (2004) Science , vol.305 , pp. 1157-1159
    • Rajkovic, A.1    Pangas, S.A.2    Ballow, D.3
  • 9
    • 1342327343 scopus 로고    scopus 로고
    • The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
    • Schmidt, D., Ovitt, C.E., Anlag, K., et al. (2004). The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance. Development 131, 933-942.
    • (2004) Development , vol.131 , pp. 933-942
    • Schmidt, D.1    Ovitt, C.E.2    Anlag, K.3
  • 10
    • 2942750361 scopus 로고    scopus 로고
    • Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development
    • Uda, M., Ottolenghi, C., Crisponi, L., et al. (2004). Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. Hum. Mol. Genet. 13, 1171-1181.
    • (2004) Hum. Mol. Genet. , vol.13 , pp. 1171-1181
    • Uda, M.1    Ottolenghi, C.2    Crisponi, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.