Marie‐Ambre Monet

Université Claude Bernard Lyon 1 FR

0000-0002-7778-4216

Publications

197

Citations

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i10-Index

0.6

2yr Mean Cite

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Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar

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Publication & Citation Trends

Publications

0 total

Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance OA

Gabriel Thérizols, Zeina Bash-Imam, Baptiste Panthu, C. Machon, A. Vincent - Nature Communications, 2022

Cited by 36 Semantic Scholar

ZEB1‐mediated melanoma cell plasticity enhances resistance to MAPK inhibitors OA

G. Richard, S. Dalle, Marie Monet, Maud Ligier, A. Boespflug - EMBO Molecular Medicine, 2016

Cited by 120 Semantic Scholar

A NASP (N1/N2)-Related Protein, Sim3, Binds CENP-A and Is Required for Its Deposition at Fission Yeast Centromeres OA

Elaine M. Dunleavy, A. Pidoux, Marie Monet, C. Bonilla, William A. Richardson - Molecules and Cells, 2007

Cited by 110 Semantic Scholar

function in vivo

Marie Monet, V. Domenga, Barbara Lemaire, Celine Souilhol, C. Babinet - Unknown Venue, 2007

Cited by 7 Semantic Scholar

The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo. OA

Marie Monet, V. Domenga, Barbara Lemaire, Celine Souilhol, Francina Langa - Human Molecular Genetics, 2007

Cited by 108 Semantic Scholar

Nas transgenic mouse line allows visualization of Notch pathway activity in vivo OA

Celine Souilhol, Sarah Cormier, Marie Monet, S. Vandormael-Pournin, A. Joutel - Genesis, 2006

Cited by 41 Semantic Scholar

Notch3 is required for arterial identity and maturation of vascular smooth muscle cells. OA

V. Domenga, Peggy Fardoux, P. Lacombe, Marie Monet, J. Maciazek - Genes & Development, 2004

Cited by 536 Semantic Scholar

Notch 3 is required for arterial identity and maturation of vascular smooth muscle cells

V. Domenga, Peggy Fardoux, P. Lacombe, Marie Monet, J. Maciazek - Unknown Venue, 2004

Cited by 63 Semantic Scholar

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway. OA

A. Joutel, Marie Monet, V. Domenga, F. Riant, E. Tournier-Lasserve - American Journal of Human Genetics, 2004

Cited by 164 Semantic Scholar

Research Topics

RNA modifications and cancer (3) Liver Disease Diagnosis and Treatment (2) RNA and protein synthesis mechanisms (2) RNA Research and Splicing (2) Neuroblastoma Research and Treatments (2)

Affiliations

Université Claude Bernard Lyon 1

FR 2025 - 2016

Centre National de la Recherche Scientifique

FR 2025 - 2016

Inserm

FR 2025 - 2016

Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement

FR 2024 - 2024

Hospices Civils de Lyon

FR 2024 - 2021

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Marie‐Ambre Monet

Publication & Citation Trends

Publications

Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance OA

ZEB1‐mediated melanoma cell plasticity enhances resistance to MAPK inhibitors OA

A NASP (N1/N2)-Related Protein, Sim3, Binds CENP-A and Is Required for Its Deposition at Fission Yeast Centromeres OA

function in vivo

The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo. OA

Nas transgenic mouse line allows visualization of Notch pathway activity in vivo OA

Notch3 is required for arterial identity and maturation of vascular smooth muscle cells. OA

Notch 3 is required for arterial identity and maturation of vascular smooth muscle cells

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway. OA

Research Topics

Affiliations

External Profiles

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