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The American Journal of Pathology
|
July 25, 2016
Major Action of Endogenous Lysyl Oxidase in Clear Cell Renal Cell Carcinoma Progression and Collagen Stiffness Revealed by Primary Cell Cultures
Vitalba Di Stefano, Barbara Torsello, Cristina Bianchi, et al.
Oncotarget
|
January 27, 2018
The glucose and lipid metabolism reprogramming is grade-dependent in clear cell renal cell carcinoma primary cultures and is targetable to modulate cell viability and proliferation
Cristina Bianchi, Chiara Meregalli, Silvia Bombelli, et al.
Plos One
|
July 23, 2013
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism
Maria Carla Proverbio, Eleonora Mangano, Alessandra Gessi, et al.
Journal for Immunotherapy of Cancer
|
September 1, 2025
Regulatory polymorphisms of <i>MSH6</i>, <i>MSH2</i>, <i>FBXO11,</i> and <i>PPP1R21</i> genes affect survival of patients with immunotherapy-treated lung cancer
Martina Esposito, Sara Noci, Francesca Minnai, et al.
Genome Biology
|
November 1, 2013
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Alberto Magi, Lorenzo Tattini, Ingrid Cifola, et al.
Cancers
|
January 8, 2023
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, et al.
Cancer Cell International
|
June 26, 2024
Breast cancer patient-derived organoids for the investigation of patient-specific tumour evolution
Serena Mazzucchelli, Lorena Signati, Letizia Messa, et al.
Oncotarget
|
June 6, 2015
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns
Ingrid Cifola, Marta Lionetti, Eva Pinatel, et al.
Nature Communications
|
May 4, 2026
5'tRNA-derived fragments modulate β-cell homeostasis and islet macrophage activation in type 2 diabetes
Cristina Cosentino, Rémy Klein, Véronique Menoud, et al.
Frontiers in Genetics
|
January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population
Ferdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
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of 4
Search research articles
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Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
The American Journal of Pathology
|
July 25, 2016
Major Action of Endogenous Lysyl Oxidase in Clear Cell Renal Cell Carcinoma Progression and Collagen Stiffness Revealed by Primary Cell Cultures
Vitalba Di Stefano, Barbara Torsello, Cristina Bianchi, et al.
Oncotarget
|
January 27, 2018
The glucose and lipid metabolism reprogramming is grade-dependent in clear cell renal cell carcinoma primary cultures and is targetable to modulate cell viability and proliferation
Cristina Bianchi, Chiara Meregalli, Silvia Bombelli, et al.
Plos One
|
July 23, 2013
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism
Maria Carla Proverbio, Eleonora Mangano, Alessandra Gessi, et al.
Journal for Immunotherapy of Cancer
|
September 1, 2025
Regulatory polymorphisms of <i>MSH6</i>, <i>MSH2</i>, <i>FBXO11,</i> and <i>PPP1R21</i> genes affect survival of patients with immunotherapy-treated lung cancer
Martina Esposito, Sara Noci, Francesca Minnai, et al.
Genome Biology
|
November 1, 2013
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Alberto Magi, Lorenzo Tattini, Ingrid Cifola, et al.
Cancers
|
January 8, 2023
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
Rosina Paterra, Paola Bettinaglio, Arianna Borghi, et al.
Cancer Cell International
|
June 26, 2024
Breast cancer patient-derived organoids for the investigation of patient-specific tumour evolution
Serena Mazzucchelli, Lorena Signati, Letizia Messa, et al.
Oncotarget
|
June 6, 2015
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns
Ingrid Cifola, Marta Lionetti, Eva Pinatel, et al.
Nature Communications
|
May 4, 2026
5'tRNA-derived fragments modulate β-cell homeostasis and islet macrophage activation in type 2 diabetes
Cristina Cosentino, Rémy Klein, Véronique Menoud, et al.
Frontiers in Genetics
|
January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population
Ferdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
Page
of 4