Citations for
1LHX8, NOBOX, SOHLH1, SOHLH2
Transcription factors SOHLH1 and SOHLH2 coordinate oocyte differentiation without affecting meiosis I.
Shin YH, Ren Y, Suzuki H, Golnoski KJ, Ahn HW, Mico V, Rajkovic A.
J Clin Invest. Jun 1;127(6):2106-2117. doi: 10.1172/JCI90281. Epub 2017 May 15. 2017
2ARGFX, DPRX, DUXA, DUXB, NOBOX, TPRX1
Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos.
Madissoon E, Jouhilahti EM, Vesterlund L, Töhönen V, Krjutškov K, Petropoulos S, Einarsdottir E, Linnarsson S, Lanner F, Månsson R, Hovatta O, Bürglin TR, Katayama S, Kere J.
Sci Rep 6:28995. doi: 10.1038/srep28995. Erratum in: Sci Rep. 2016 Sep 02;6:32053. 2016
3DAZL, FIGLA, NOBOX, STRA8, TAF4B
TAF4b Regulates Oocyte-Specific Genes Essential for Meiosis.
Grive KJ, Gustafson EA, Seymour KA, Baddoo M, Schorl C, Golnoski K, Rajkovic A, Brodsky AS, Freiman RN
PLoS Genet. Jun 24;12(6):e1006128. doi: 10.1371/journal.pgen.1006128. 2016
4GDF9, NOBOX
GDF9 is transiently expressed in oocytes before follicle formation in the human fetal ovary and is regulated by a novel NOBOX transcript
Bayne RA, Kinnell HL, Coutts SM, He J, Childs AJ, Anderson RA.
PLoS One. Mar 19;10(3):e0119819. doi: 10.1371/journal.pone.0119819. 2015
5FIGLA, LHX8, NOBOX, SOHLH1, SOHLH2
Transcription factors in the maintenance and survival of primordial follicles
Lim EJ, Choi Y.
Clin Exp Reprod Med. Dec;39(4):127-31. doi: 10.5653/cerm.2012.39.4.127. Epub 2012 Dec 31. 2012
6NOBOX, POF5
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, Touraine P, Binart N.
Hum Mutat 32(10):1108-13. doi: 10.1002/humu.21543. Epub 2011 Sep 9. 2011
7NOBOX
Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown.
Lechowska A, Bilinski S, Choi Y, Shin Y, Kloc M, Rajkovic A.
J Assist Reprod Genet 28(7):583-9. doi: 10.1007/s10815-011-9553-5. Epub 2011 Mar 3. 2011
8NOBOX, PADI6
The oocyte-specific transcription factor, Nobox, regulates the expression of Pad6, a peptidylarginine deiminase in the oocyte.
Choi M, Lee OH, Jeon S, Park M, Lee DR, Ko JJ, Yoon TK, Rajkovic A, Choi Y.
FEBS Lett 584(16):3629-34. doi: 10.1016/j.febslet.2010.07.037. Epub 2010 Jul 24. Erratum in: FEBS Lett. 2010 Nov 5;584(21):4490. 2010
9NOBOX
Oogenesis specific genes (Nobox, Oct4, Bmp15, Gdf9, Oogenesin1 and Oogenesin2) are differentially expressed during natural and gonadotropin-induced mouse follicular development.
Monti M, Redi C.
Mol Reprod Dev 76(10):994-1003. doi: 10.1002/mrd.21059. 2009
10NOBOX, POF5
Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure.
Qin Y, Shi Y, Zhao Y, Carson SA, Simpson JL, Chen ZJ.
Fertil Steril 91(4 Suppl):1507-9. doi: 10.1016/j.fertnstert.2008.08.020. Epub 2008 Oct 17. 2009
11CNTNAP2, DEL7QO, NOBOX
A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea.
Rossi E, Verri AP, Patricelli MG, Destefani V, Ricca I, Vetro A, Ciccone R, Giorda R, Toniolo D, Maraschio P, Zuffardi O.
Eur J Med Genet 51(6):631-8. Epub 2008 Jul 16. 2008
12NOBOX
NOBOX Homeobox Mutation Causes Premature Ovarian Failure.
Qin Y, Choi Y, Zhao H, Simpson JL, Chen ZJ, Rajkovic A.
Am J Hum Genet 81(3):576-81. Epub 2007 Jul 10. 2007
13NOBOX
cDNA cloning and expression of the human NOBOX gene in oocytes and ovarian follicles.
Huntriss J, Hinkins M, Picton HM.
Mol Hum Reprod 12(5):283-9. Epub 2006 Apr 5. 2006
14NOBOX
NOBOX deficiency disrupts early folliculogenesis and oocyte-specific gene expression.
Rajkovic A, Pangas SA, Ballow D, Suzumori N, Matzuk MM.
Science 305(5687):1157-9. 2004
15NOBOX
Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes.
Suzumori N, Yan C, Matzuk MM, Rajkovic A.
Mech Dev 111(1-2):137-41. 2002