Detalhe da pesquisa
1.
Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysis.
FASEB J
; 34(1): 571-587, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31914586
2.
Homozygous hypomorphic BRCA2 variant in primary ovarian insufficiency without cancer or Fanconi anaemia trait.
J Med Genet
; 2020 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32482800
3.
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes.
Clin Genet
; 98(3): 293-298, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32613604
4.
Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.
Hum Mol Genet
; 24(23): 6687-98, 2015 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26362254
5.
Mutant cohesin in premature ovarian failure.
N Engl J Med
; 370(10): 943-949, 2014 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24597867
6.
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.
Clin Endocrinol (Oxf)
; 87(5): 539-544, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28708305
7.
STAG3 is a strong candidate gene for male infertility.
Hum Mol Genet
; 23(13): 3421-31, 2014 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24608227
8.
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes.
BMC Cancer
; 15: 251, 2015 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25884336
9.
Forkhead transcription factors: key players in health and disease.
Trends Genet
; 27(6): 224-32, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21507500
10.
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.
Hum Mol Genet
; 20(13): 2642-50, 2011 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21505076
11.
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.
Hum Mol Genet
; 20(9): 1673-86, 2011 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21289058
12.
Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?
FASEB J
; 24(2): 346-56, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19762556
13.
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.
Hum Mol Genet
; 17(20): 3118-27, 2008 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18635577
14.
[STAG3 in premature ovarian failure]. / Mutation de STAG3 - Une nouvelle cause d'insuffisance ovarienne prématurée.
Med Sci (Paris)
; 31(2): 129-31, 2015 Feb.
Artigo
em Francês
| MEDLINE | ID: mdl-25744256
15.
A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1.
Elife
; 92020 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32845237
16.
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
EBioMedicine
; 42: 524-531, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31000419
17.
The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways.
Proteomics
; 8(15): 3118-23, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18604817
18.
Natural and molecular history of prolactinoma: insights from a Prlr-/- mouse model.
Oncotarget
; 9(5): 6144-6155, 2018 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29464061
19.
A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome.
Eur J Endocrinol
; 176(5): K9-K14, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28348023
20.
A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.
Elife
; 62017 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29231814