Sandrine Caburet
Sandrine Caburet
Université Paris Diderot
Email verificata su ijm.fr
Titolo
Citata da
Citata da
Anno
Forkhead transcription factors: key players in health and disease
BA Benayoun, S Caburet, RA Veitia
Trends in Genetics 27 (6), 224-232, 2011
2422011
Eucaryotic genome evolution through the spontaneous duplication of large chromosomal segments
R Koszul, S Caburet, B Dujon, G Fischer
The EMBO journal 23 (1), 234-243, 2004
2182004
Mutant cohesin in premature ovarian failure
S Caburet, VA Arboleda, E Llano, PA Overbeek, JL Barbero, K Oka, ...
New England Journal of Medicine 370 (10), 943-949, 2014
1982014
Human ribosomal RNA gene arrays display a broad range of palindromic structures
S Caburet, C Conti, C Schurra, R Lebofsky, SJ Edelstein, A Bensimon
Genome research 15 (8), 1079-1085, 2005
1352005
A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation
S Caburet, A Demarez, L Moumne, M Fellous, E De Baere, RA Veitia
Journal of medical genetics 41 (12), 932-936, 2004
1102004
Generic binding sites, generic DNA‐binding domains: where does specific promoter recognition come from?
AB Georges, BA Benayoun, S Caburet, RA Veitia
The FASEB Journal 24 (2), 346-356, 2010
972010
Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase
BA Benayoun, AB Georges, D l'Hôte, N Andersson, A Dipietromaria, ...
Human molecular genetics 20 (9), 1673-1686, 2011
842011
Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p. Cys134Trp (c. 402C> G)
BA Benayoun, S Caburet, A Dipietromaria, A Georges, B d'Haene, ...
PloS one 5 (1), e8789, 2010
732010
The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology
S Caburet, A Georges, D L’Hôte, AL Todeschini, BA Benayoun, RA Veitia
Molecular and cellular endocrinology 356 (1-2), 55-64, 2012
722012
The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles
BA Benayoun, S Caburet, A Dipietromaria, M Bailly-Bechet, F Batista, ...
Human molecular genetics 17 (20), 3118-3127, 2008
632008
STAG3 is a strong candidate gene for male infertility
E Llano, L Gomez-H, I García-Tuñón, M Sánchez-Martín, S Caburet, ...
Human molecular genetics 23 (13), 3421-3431, 2014
542014
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure
S Caburet, P Zavadakova, Z Ben-Neriah, K Bouhali, A Dipietromaria, ...
PLoS One 7 (3), e33412, 2012
432012
Coding repeats and evolutionary “agility”
S Caburet, J Cocquet, D Vaiman, RA Veitia
Bioessays 27 (6), 581-587, 2005
422005
A non‐sense MCM9 mutation in a familial case of primary ovarian insufficiency
F Fauchereau, S Shalev, E Chervinsky, R Beck‐Fruchter, B Legois, ...
Clinical Genetics 89 (5), 603-607, 2016
392016
Combing the genome for genomic instability
S Caburet, C Conti, A Bensimon
TRENDS in Biotechnology 20 (8), 344-350, 2002
362002
Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes
S Caburet, M Anttonen, AL Todeschini, L Unkila-Kallio, D Mestivier, ...
BMC cancer 15 (1), 1-11, 2015
302015
Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads
A Auguste, L Bessière, AL Todeschini, S Caburet, S Sarnacki, J Prat, ...
Human molecular genetics 24 (23), 6687-6698, 2015
292015
Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.
E De Baere, S Copelli, S Caburet, P Laissue, D Beysen, S Christin-Maitre, ...
Pediatric endocrinology reviews: PER 2 (4), 653-660, 2005
292005
Molecular combing
C Conti, S Caburet, C Schurra, A Bensimon
Current protocols in Cytometry 16 (1), 8.10. 1-8.10. 23, 2001
292001
The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2
M Elzaiat, AL Todeschini, S Caburet, RA Veitia
Clinical genetics 91 (2), 173-182, 2017
282017
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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