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Caburet, Sandrine
73  Ergebnisse:
Personensuche X
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1

A missense in HSF2BP causing primary ovarian insufficiency ..:

Felipe-Medina, Natalia ; Caburet, Sandrine ; Sánchez-Sáez, Fernando...
eLife.  9 (2020)  - p. , 2020
Link: https://doi.org/10.7554/..
 
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2

An exome‐wide exploration of cases of primary ovarian insuf..:

Alvarez‐Mora, Maria Isabel ; Todeschini, Anne‐Laure ; Caburet, Sandrine...
Clinical Genetics.  98 (2020)  3 - p. 293-298 , 2020
Link: https://doi.org/10.1111/..
 
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3

A truncating MEIOB mutation responsible for familial primar..:

Caburet, Sandrine ; Todeschini, Anne-Laure ; Petrillo, Cynthia...
EBioMedicine.  42 (2019)  - p. 524-531 , 2019
Link: https://doi.org/10.1016/..
 
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4

Conventional and unconventional interactions of the transcr..:

Penrad‐Mobayed, May ; Perrin, Caroline ; Herman, Laetitia...
The FASEB Journal.  34 (2019)  1 - p. 571-587 , 2019
Link: https://doi.org/10.1096/..
 
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5

A novel variant of DHH in a familial case of 46,XY disorder..:

Paris, Francoise ; Flatters, Delphine ; Caburet, Sandrine...
Clinical Endocrinology.  87 (2017)  5 - p. 539-544 , 2017
Link: https://doi.org/10.1111/..
 
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6

Natural and molecular history of prolactinoma: insights fro..:

Bernard, Valérie ; Villa, Chiara ; Auguste, Aurélie...
Oncotarget.  9 (2017)  5 - p. 6144-6155 , 2017
Link: https://doi.org/10.18632..
 
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7

A homozygous FANCM mutation underlies a familial case of no..:

Fouquet, Baptiste ; Pawlikowska, Patrycja ; Caburet, Sandrine...
eLife.  6 (2017)  - p. , 2017
Link: https://doi.org/10.7554/..
 
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8

Molecular analyses of juvenile granulosa cell tumors bearin..:

Auguste, Aurélie ; Bessière, Laurianne ; Todeschini, Anne-Laure...
Human Molecular Genetics.  24 (2015)  23 - p. 6687-6698 , 2015
Link: https://doi.org/10.1093/..
 
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9

Combined comparative genomic hybridization and transcriptom..:

Caburet, Sandrine ; Anttonen, Mikko ; Todeschini, Anne-Laure...
BMC Cancer.  15 (2015)  1 - p. , 2015
Link: https://doi.org/10.1186/..
 
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10

STAG3 is a strong candidate gene for male infertility:

Llano, Elena ; Gomez-H, Laura ; García-Tuñón, Ignacio...
Human Molecular Genetics.  23 (2014)  13 - p. 3421-3431 , 2014
Link: https://doi.org/10.1093/..
 
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11

Genome-Wide Linkage in a Highly Consanguineous Pedigree Rev..:

Caburet, Sandrine ; Zavadakova, Petra ; Ben-Neriah, Ziva...
PLoS ONE.  7 (2012)  3 - p. e33412 , 2012
Link: https://doi.org/10.1371/..
 
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12

The transcription factor FOXL2: At the crossroads of ovaria..:

Caburet, Sandrine ; Georges, Adrien ; L'Hôte, David...
Molecular and Cellular Endocrinology.  356 (2012)  1-2 - p. 55-64 , 2012
Link: https://doi.org/10.1016/..
 
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13

Transcription factor FOXL2 protects granulosa cells from st..:

Benayoun, Bérénice A. ; Georges, Adrien B. ; L'Hôte, David...
Human Molecular Genetics.  20 (2011)  9 - p. 1673-1686 , 2011
Link: https://doi.org/10.1093/..
 
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14

Forkhead transcription factors: key players in health and d..:

Benayoun, Bérénice A. ; Caburet, Sandrine ; Veitia, Reiner A.
Trends in Genetics.  27 (2011)  6 - p. 224-232 , 2011
Link: https://doi.org/10.1016/..
 
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15

Functional Exploration of the Adult Ovarian Granulosa Cell ..:

Benayoun, Bérénice A. ; Caburet, Sandrine ; Dipietromaria, Aurélie...
PLoS ONE.  5 (2010)  1 - p. e8789 , 2010
Link: https://doi.org/10.1371/..
 
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