NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis
- PMID: 24620032
- DOI: 10.1093/jmcb/mju006
NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis
Similar articles
-
Genetics of early mammalian folliculogenesis.Cell Mol Life Sci. 2006 Mar;63(5):579-90. doi: 10.1007/s00018-005-5394-7. Cell Mol Life Sci. 2006. PMID: 16416028 Free PMC article. Review.
-
Stage-specific mice ovarian somatic cell is involved in primordial folliculogenesis.Front Biosci (Elite Ed). 2011 Jun 1;3(3):1025-33. doi: 10.2741/E308. Front Biosci (Elite Ed). 2011. PMID: 21622111
-
The NOBOX protein becomes undetectable in developmentally competent antral and ovulated oocytes.Int J Dev Biol. 2013;57(1):35-9. doi: 10.1387/ijdb.120125mz. Int J Dev Biol. 2013. PMID: 23585350
-
Minireview: roles of the forkhead transcription factor FOXL2 in granulosa cell biology and pathology.Endocrinology. 2011 Apr;152(4):1199-208. doi: 10.1210/en.2010-1041. Epub 2011 Jan 19. Endocrinology. 2011. PMID: 21248146 Free PMC article. Review.
-
NOBOX does right for the follicle reserve: insights into premature ovarian failure.J Assist Reprod Genet. 2011 Jul;28(7):567-8. doi: 10.1007/s10815-011-9615-8. J Assist Reprod Genet. 2011. PMID: 21822584 Free PMC article. No abstract available.
Cited by
-
Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation.J Clin Endocrinol Metab. 2017 Jan 1;102(1):93-99. doi: 10.1210/jc.2016-2749. J Clin Endocrinol Metab. 2017. PMID: 27754803 Free PMC article.
-
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation.Dev Biol. 2016 Aug 1;416(1):200-211. doi: 10.1016/j.ydbio.2016.05.022. Epub 2016 May 19. Dev Biol. 2016. PMID: 27212026 Free PMC article.
-
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.Mol Genet Genomic Med. 2021 Oct;9(10):e1776. doi: 10.1002/mgg3.1776. Epub 2021 Sep 4. Mol Genet Genomic Med. 2021. PMID: 34480423 Free PMC article.
-
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.EMBO Mol Med. 2017 Oct;9(10):1379-1397. doi: 10.15252/emmm.201607376. EMBO Mol Med. 2017. PMID: 28754744 Free PMC article.
-
Screening of premature ovarian insufficiency associated genes in Hungarian patients with next generation sequencing.BMC Med Genomics. 2024 Apr 22;17(1):98. doi: 10.1186/s12920-024-01873-z. BMC Med Genomics. 2024. PMID: 38649916 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources