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1. Modelling human diabetes ex vivo: a glance at maturity onset diabetes of the young.

4. TheEIF4EBP1gene encoding 4EBP1 is transcriptionally upregulated by MYC and linked to shorter survival in medulloblastoma

5. A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression

6. EXTH-46. SCHLAFEN11 IS A POWERFUL BIOMARKER OF CHEMOSENSITIVITY IN MEDULLOBLASTOMAS

7. In Vivo Medulloblastoma Modeling

8. SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation

10. An autocrine ActivinB mechanism drives TGFβ/Activin signaling in Group 3 medulloblastoma

12. Epigenetic upregulation of Schlafen11 renders WNT- and SHH-activated medulloblastomas sensitive to cisplatin

13. An FGFR3/MYC positive feedback loop provides new opportunities for targeted therapies in bladder cancers

22. Clonally Expanded T Cells Reveal Immunogenicity of Rhabdoid Tumors

23. An autocrine ActivinB mechanism drives TGF β/Activin signaling in Group 3 medulloblastoma

25. Immune responses in genomically simple SWI/SNF–deficient cancers.

26. Aberrant ERBB4-SRC Signaling as a Hallmark of Group 4 Medulloblastoma Revealed by Integrative Phosphoproteomic Profiling

27. NRL and CRX Define Photoreceptor Identity and Reveal Subgroup-Specific Dependencies in Medulloblastoma

28. An FGFR 3/ MYC positive feedback loop provides new opportunities for targeted therapies in bladder cancers

29. CSIG-15. PROTEOMIC AND PHOSPHOPROTEOMIC ANALYSIS OF HUMAN MEDULLOBLASTOMA REVEALS DISTINCT ACTIVATED PATHWAYS BETWEEN SUBGROUPS

31. MEDU-24. INSTRUMENTAL ROLE OF THE PHOTORECEPTOR PROGRAM IN GROUP 3 MEDULLOBLASTOMA THROUGH THE TRANSCRIPTION FACTOR NRL

32. RAF proteins exert both specific and compensatory functions during tumour progression of NRAS-driven melanoma

33. Transforming growth factor [Beta]-inducible independent binding of SMAD to the Smad7 promoter

34. Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies

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