Suchergebnisse - "Mansini, Adrian P"

PubPharm (10)

1

Myeloid differentiation factor-2/LY96, a potential predictive biomarker of metastasis and poor outcomes in prostate cancer : clinical implications as a potential therapeutic target

enthalten in: Oncogene | 2024

von Ferrari, M. | Jimenez-Uribe, A. | Wang, L. | +7

UpdateOf: Res Sq. 2023 Jun 09;:. - PMID 37333086

2

Anti-S100A4 Antibody Therapy Is Efficient in Treating Aggressive Prostate Cancer and Reversing Immunosuppression : Serum and Biopsy S100A4 as a Clinical Predictor

enthalten in: Molecular cancer therapeutics | 2020

von Ganaie, A. | Mansini, A. | Hussain, T. | +11

3

Identifying and treating ROBO1-ve /DOCK1+ve prostate cancer : An aggressive cancer subtype prevalent in African American patients

enthalten in: The Prostate | 2020

von Ferrari, M. | Ganaie, A. | Shabenah, A. | +10

4

COMMD3:BMI1 Fusion and COMMD3 Protein Regulate C-MYC Transcription : Novel Therapeutic Target for Metastatic Prostate Cancer

enthalten in: Molecular cancer therapeutics | 2019

von Umbreen, S. | Banday, M. | Jamroze, A. | +10

5

The Chemosensory Function of Primary Cilia Regulates Cholangiocyte Migration, Invasion, and Tumor Growth

enthalten in: Hepatology (Baltimore, Md.) | 2019

von Mansini, A. | Peixoto, E. | Jin, S. | +2

6

MicroRNA (miR)-433 and miR-22 dysregulations induce histone-deacetylase-6 overexpression and ciliary loss in cholangiocarcinoma

enthalten in: Hepatology (Baltimore, Md.) | 2018

von Mansini, A. | Lorenzo Pisarello, M. | Thelen, K. | +10

CommentIn: AME Med J. 2018 Oct;3:. - PMID 30506034

7

The cholangiocyte primary cilium in health and disease

enthalten in: Biochimica et biophysica acta. Molecular basis of disease | 2018

von Mansini, A. | Peixoto, E. | Thelen, K. | +3

8

Hemoglobin Woodville associated with double point mutation in the gene of glucose-6-phosphate dehydrogenase

enthalten in: Medicina | 2015

von Mansini, A. | Fernández, D. | Aguirre, F. | +5

9

A new β(0) frameshift mutation, HBB : c.44delT (p.Leu14ArgfsX5), identified in an Argentinean family associated with secondary genetic modifiers of β-thalassemia

enthalten in: Hemoglobin | 2014

von Pepe, C. | Eberle, S. | Chaves, A. | +11

10

Mutation characterization in the GATA-1 gene in patients with Down's Syndrome diagnosed with transient abnormal myelopoiesis or acute megakaryoblastic leukemia

enthalten in: Archivos argentinos de pediatria | 2013

von Mansini, A. | Rubio, P. | Rossi, J. | +5

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