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Legois, Bérangère
34  results:
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1

A cellular model provides insights into the pathogenicity o..:

Herman, Laetitia ; Amo, Angélique ; Legois, Berangère...
British Journal of Cancer.  130 (2024)  9 - p. 1453-1462 , 2024
Link: https://doi.org/10.1038/..
 
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2

Genomic exploration of the targets of FOXL2 and ESR2 unveil..:

Herman, Laetitia ; Legois, Bérangère ; Todeschini, Anne‐Laure.
The FASEB Journal.  35 (2021)  4 - p. , 2021
Link: https://doi.org/10.1096/..
 
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3

DHH pathogenic variants involved in 46,XY disorders of sex ..:

Elzaiat, Maëva ; Flatters, Delphine ; Sierra-Díaz, Diana Carolina...
Human Genetics.  139 (2020)  11 - p. 1455-1470 , 2020
Link: https://doi.org/10.1007/..
 
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4

High-throughput Exploration of the Network Dependent on AKT..:

Elzaiat, Maëva ; Herman, Laetitia ; Legois, Bérangère...
Molecular & Cellular Proteomics.  18 (2019)  7 - p. 1307-1319 , 2019
Link: https://doi.org/10.1074/..
 
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5

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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6

High-throughput Exploration of the Network Dependent on AKT..:

Elzaiat, Maëva ; Herman, Laetitia ; Legois, Bérangère...
Molecular & Cellular Proteomics.  18 (2019)  7 - p. 1307-1319 , 2019
Link: https://doi.org/10.1074/..
 
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7

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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8

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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9

A Hot-spot of In-frame Duplications Activates the Oncoprote..:

Bessière, Laurianne ; Todeschini, Anne-Laure ; Auguste, Aurélie...
EBioMedicine.  2 (2015)  5 - p. 421-431 , 2015
Link: https://doi.org/10.1016/..
 
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10

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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11

The transcription factor FOXL2 mobilizes estrogen signaling..:

Georges, Adrien ; L'Hôte, David ; Todeschini, Anne Laure...
eLife.  3 (2014)  - p. , 2014
Link: https://doi.org/10.7554/..
 
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12

A truncating MEIOB mutation responsible for familial primar..:

Caburet, Sandrine ; Todeschini, Anne-Laure ; Petrillo, Cynthia...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ebiom.2019.03.075.  , 2019
Link: https://hal.science/hal-..
 
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13

A truncating MEIOB mutation responsible for familial primar..:

Caburet, Sandrine ; Todeschini, Anne-Laure ; Petrillo, Cynthia...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ebiom.2019.03.075.  , 2019
Link: https://hal.science/hal-..
 
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14

A truncating MEIOB mutation responsible for familial primar..:

Caburet, Sandrine ; Todeschini, Anne-Laure ; Petrillo, Cynthia...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ebiom.2019.03.075.  , 2019
Link: https://hal.science/hal-..
 
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15

A truncating MEIOB mutation responsible for familial primar..:

Caburet, Sandrine ; Todeschini, Anne-Laure ; Petrillo, Cynthia...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491878/.  , 2019
Link: http://www.ncbi.nlm.nih...
 
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