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Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly.
Sandrine Vuillaumier-Barrot
,
Céline Bouchet-Séraphin
,
Malika Chelbi
,
Louise Devisme
,
Samuel Quentin
et al.
Journal articles
hal-01120423v1
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Naturally occurring melanomas in dogs as models for non-UV pathways of human melanomas.
Marc Gillard
,
Edouard Cadieu
,
Clotilde de Brito
,
Jérôme Abadie
,
Béatrice Vergier
et al.
Journal articles
istex
hal-01002709v1
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Autophagy inhibition cooperates with erlotinib to induce glioblastoma cell death.
Sandrine Eimer
,
Marc-Antoine Belaud-Rotureau
,
Kelly Airiau
,
Marie Jeanneteau
,
Elodie Laharanne
et al.
Journal articles
inserm-00589909v1
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MYD88 somatic mutation is a diagnostic criterion in primary cutaneous large B-cell lymphoma
Sarah Menguy
,
Audrey Gros
,
Anne Pham-Ledard
,
Maxime Battistella
,
Nicolas Ortonne
et al.
Journal articles
hal-01321411v1
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Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Clinical, Pathologic, and Molecular Study of 11 Cases Displaying a High Frequency of GNA11 Mutations, BAP1 Expression Loss, and a Predilection for the Scalp
Sebastian Costa
,
Michelle Byrne
,
Daniel Pissaloux
,
Veronique Haddad
,
Sandrine Paindavoine
et al.
Journal articles
hal-01255859v1
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Angioimmunoblastic T-cell lymphoma is the most common T-cell lymphoma in two distinct French information data sets
Laurence De Leval
,
Marie Parrens
,
Fabien Le Bras
,
Jean-Philippe Jais
,
Virginie Fataccioli
et al.
Journal articles
hal-01301144v1
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Long-term forest mapping from classification of MODIS time series: best practices
Jean-Philippe Denux
,
Emmanuelle Cano
,
Laurence Hubert-Moy
,
Marie Parrens
,
Véronique Cheret
et al.
Journal articles
hal-02420467v1
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ESM-1 expression in stromal cells is predictive of recurrence after radiofrequency ablation in early hepatocellular carcinoma
Marianne Ziol
,
Angela Sutton
,
Julien Caldéraro
,
Nathalie Barget
,
Mounir Aout
et al.
Journal articles
hal-02067507v1
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Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome)
Cécile Courdier
,
John Boudjarane
,
Valérie Malan
,
Christine Muti
,
Brian Sperelakis-Beedham
et al.
Journal articles
hal-04032330v1
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Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma.
Cécile Guichard
,
Giuliana Amaddeo
,
Sandrine Imbeaud
,
Yannick Ladeiro
,
Laura Pelletier
et al.
Journal articles
inserm-00719917v1
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