Suchergebnisse - "Venuto, Santina"

PubPharm (17)

1

circPVT1 and PVT1/AKT3 show a role in cell proliferation, apoptosis, and tumor subtype-definition in small cell lung cancer

enthalten in: Genes, chromosomes & cancer | 2023

von Tolomeo, D. | Traversa, D. | Venuto, S. | +33

2

Advancements in Focal Amplification Detection in Tumor/Liquid Biopsies and Emerging Clinical Applications

enthalten in: Genes | 2023

von Arshadi, A. | Tolomeo, D. | Venuto, S. | +1

3

IGFBP-6 Network in Chronic Inflammatory Airway Diseases and Lung Tumor Progression

enthalten in: International journal of molecular sciences | 2023

von Venuto, S. | Coda, A. | González-Pérez, R. | +5

4

circPVT1 and PVT1/AKT3 show a role in cell proliferation, apoptosis, and tumor subtype‐definition in small cell lung cancer

enthalten in: Genes, Chromosomes and Cancer | 2023

von Tolomeo, D. | Traversa, D. | Venuto, S. | +33

5

Differential and divergent activity of insulin-like growth factor binding protein 6 in platinum-sensitive versus platinum-resistant high-grade serous ovarian carcinoma cell lines

enthalten in: Oncology letters | 2022

von Piscazzi, A. | Condelli, V. | Crispo, F. | +9

6

IGFBP-6 : At the Crossroads of Immunity, Tissue Repair and Fibrosis

enthalten in: International journal of molecular sciences | 2022

von Liso, A. | Venuto, S. | Coda, A. | +3

7

IGFBP-6/sonic hedgehog/TLR4 signalling axis drives bone marrow fibrotic transformation in primary myelofibrosis

enthalten in: Aging | 2021

von Longhitano, L. | Tibullo, D. | Vicario, N. | +14

8

Genetic Perturbation of Pyruvate Dehydrogenase Kinase 1 Modulates Growth, Angiogenesis and Metabolic Pathways in Ovarian Cancer Xenografts

enthalten in: Cells | 2021

von Venturoli, C. | Piga, I. | Curtarello, M. | +6

9

Correction : A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2020

von Cuvertino, S. | Hartill, V. | Colyer, A. | +32

ErratumFor: Genet Med. 2020 May;22(5):867-877. - PMID 31949313

10

A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2020

von Cuvertino, S. | Hartill, V. | Colyer, A. | +32

ErratumIn: Genet Med. 2020 Mar 23;:. - PMID 32203228