Agnès Noël
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Agnès Noël has a total of 1000 co-authors. Here are the top co-authors by number of shared publications:
Jean-Michel Foidart
83 shared publicationsSilvia Blacher
Laboratory of Tumor and Development Biology, GIGA-Cancer, Liège University, Liège, Belgium
66 shared publications- Nor Eddine Sounni
Cancer Metabolism and Tumor Microenvironment Laboratory, Interdisciplinary Group for Applied Genoproteomics, University of Liège
58 shared publications - Didier Cataldo
Laboratory of Tumour and Development Biology, GIGA-Cancer, University of Liege (ULiege), Liege, Belgium
42 shared publications Carine Munaut
40 shared publicationsFrancis Frankenne
Laboratory of Tumour and Development Biology, University of Liège, Tour de Pathologie (B23), Groupe Interdisciplinaire de Génoprotéomique Appliquée-Cancer (GIGA Cancer), Liège
27 shared publications
Latest Publications
- Open Access
- 4 November 2026
- Published by Springer Nature in Breast Cancer Research
An extracellular vesicle multiplexed immunoassay to profile the immune checkpoint landscape in plasmatic samples
- 4 November 2026
- Published by Springer Nature in Breast Cancer Research
Open AccessAn extracellular vesicle multiplexed immunoassay to profile the immune checkpoint landscape in plasmatic samples
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S5 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Clinical characteristics of patients included in statistical analyses
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S5 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Clinical characteristics of patients included in statistical analyses
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S1 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S1 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S1 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S1 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S8 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S8 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S8 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S8 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S7 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S7 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S7 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S7 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S2 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S2 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Table S2 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
- 1 June 2026
- Published by Rockefeller University Press in Journal of Experimental Medicine
- Vol. 223 (7)
Aquaporin-1 sustains lymphangiogenic responses in hyperosmotic inflammatory microenvironments
Intestinal lymphatic vessels are essential for dietary lipid absorption and immune cell trafficking. Villus lymphatic capillaries, lacteals, undergo continuous VEGF-C–dependent renewal to function in a hyperosmolar, inflammatory environment exposed to dietary and microbial by-products. To define mechanisms underlying this adaptation, we integrated new and published single-cell RNA-sequencing datasets of murine small intestinal lymphatic endothelial cells (LECs). Lacteal LECs resembled Ptx3+ immune-interacting LECs and were characterized by high expression of water channel AQP1. LEC-specific Aqp1 deletion reduced lacteal length, impaired lipid uptake, and limited weight gain on a high-fat diet, while mosaic deletion revealed a cell-autonomous requirement for AQP1 in LEC positioning at hyperosmolar tip regions. AQP1 promoted LEC migration under hyperosmotic stress by preserving cytoskeletal and junctional remodeling and alleviating osmotic stress–induced transcriptional programs. AQP1 was upregulated during inflammatory remodeling in lymphedema and lymphatic malformations, but not during embryonic lymphangiogenesis. These findings link lacteal regeneration to inflammatory lymphatic remodeling and highlight tissue osmolarity as a biophysical determinant of postnatal lymphangiogenesis.
- 1 June 2026
- Published by Rockefeller University Press in Journal of Experimental Medicine
- Vol. 223 (7)
Aquaporin-1 sustains lymphangiogenic responses in hyperosmotic inflammatory microenvironments
Intestinal lymphatic vessels are essential for dietary lipid absorption and immune cell trafficking. Villus lymphatic capillaries, lacteals, undergo continuous VEGF-C–dependent renewal to function in a hyperosmolar, inflammatory environment exposed to dietary and microbial by-products. To define mechanisms underlying this adaptation, we integrated new and published single-cell RNA-sequencing datasets of murine small intestinal lymphatic endothelial cells (LECs). Lacteal LECs resembled Ptx3+ immune-interacting LECs and were characterized by high expression of water channel AQP1. LEC-specific Aqp1 deletion reduced lacteal length, impaired lipid uptake, and limited weight gain on a high-fat diet, while mosaic deletion revealed a cell-autonomous requirement for AQP1 in LEC positioning at hyperosmolar tip regions. AQP1 promoted LEC migration under hyperosmotic stress by preserving cytoskeletal and junctional remodeling and alleviating osmotic stress–induced transcriptional programs. AQP1 was upregulated during inflammatory remodeling in lymphedema and lymphatic malformations, but not during embryonic lymphangiogenesis. These findings link lacteal regeneration to inflammatory lymphatic remodeling and highlight tissue osmolarity as a biophysical determinant of postnatal lymphangiogenesis.
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S6 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Comparison of the model performance after inclusion of continuous PET-derived features
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S6 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Comparison of the model performance after inclusion of continuous PET-derived features
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S3 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Clinical parameters 137 pPET+ and pPET-
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S3 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
Clinical parameters 137 pPET+ and pPET-
- Open Access
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Table S4 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
TUMOR UNIVARIATE and MULTIVARIATE ANALYSIS
- 1 June 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable S4 from Nonmetastatic Para-aortic Lymph Node Remodeling as a Predictor of Outcome in Locally Advanced Cervical Cancer
TUMOR UNIVARIATE and MULTIVARIATE ANALYSIS