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A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations
Françoise Paris
,
Delphine Flatters
,
Sandrine Caburet
,
Bérangère Legois
,
Nadège Servant
et al.
Journal articles
hal-01758673v1
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A homozygous $FANCM$ mutation underlies a familial case of non-syndromic primary ovarian insufficiency
Baptiste Fouquet
,
Patrycja Pawlikowska
,
Sandrine Caburet
,
Céline Guigon
,
Marika Mäkinen
et al.
Journal articles
hal-02391886v1
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The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells
Adrien Georges
,
David L'Hôte
,
Anne Laure Todeschini
,
Aurelie A. Auguste
,
Bérangère Legois
et al.
Journal articles
hal-02118875v1
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A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors
Laurianne Bessière
,
Anne-Laure Todeschini
,
Aurelie A. Auguste
,
Sabine Sarnacki
,
Delphine Flatters
et al.
Journal articles
hal-02118885v1
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Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.
Aurélie Auguste
,
Laurianne Bessière
,
Anne-Laure Todeschini
,
Sandrine Caburet
,
Sabine Sarnacki
et al.
Journal articles
hal-01266741v1
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