Suchergebnisse - "Pasmant, Eric"

PubPharm (9)

1

NF1 alterations in cancers : therapeutic implications in precision medicine

enthalten in: Expert opinion on investigational drugs | 2023

von Giraud, J. | Bièche, I. | Pasmant, �. | +1

2

VEGF and VEGFR family members are expressed by neoplastic cells of NF1-associated tumors and may play an oncogenic role in malignant peripheral nerve sheath tumor growth through an autocrine loop

enthalten in: Annals of diagnostic pathology | 2022

von Bonsang, B. | Maksimovic, L. | Maille, P. | +7

3

BRAF inhibitor resistance of melanoma cells triggers increased susceptibility to natural killer cell-mediated lysis

enthalten in: Journal for immunotherapy of cancer | 2020

von Frazao, A. | Rethacker, L. | Jeudy, G. | +9

ErratumIn: J Immunother Cancer. 2021 Aug;9(8):. - PMID 34373259

4

Phosphorylation of Merlin by Aurora A kinase appears necessary for mitotic progression

enthalten in: The Journal of biological chemistry | 2019

von Mandati, V. | Del Maestro, L. | Dingli, F. | +9

5

Shifting the Balance of Activating and Inhibitory Natural Killer Receptor Ligands on BRAFV600E Melanoma Lines with Vemurafenib

enthalten in: Cancer immunology research | 2017

von Frazao, A. | Colombo, M. | Fourmentraux-Neves, E. | +14

6

Copy number variants and rasopathies : germline KRAS duplication in a patient with syndrome including pigmentation abnormalities

enthalten in: Orphanet journal of rare diseases | 2016

von Gilbert-Dussardier, B. | Briand-Suleau, A. | Laurendeau, I. | +6

7

Dual mTORC1/2 inhibition induces anti-proliferative effect in NF1-associated plexiform neurofibroma and malignant peripheral nerve sheath tumor cells

enthalten in: Oncotarget | 2016

von Varin, J. | Poulain, L. | Hivelin, M. | +9

8

Immunohistochemistry versus next-generation sequencing for the routine detection of BRAF V600E mutation in melanomas

enthalten in: Human pathology | 2014

von Just, P. | Audebourg, A. | Pasmant, E. | +7

CommentOn: Hum Pathol. 2014 Mar;45(3):464-72. - PMID 24529329

9

Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway : genotype-phenotype relationships and overlap with Costello syndrome

enthalten in: Journal of medical genetics | 2007

von Nava, C. | Hanna, N. | Michot, C. | +18

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