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Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian Families

International journal of molecular sciences, 2021-03, Vol.22 (7), p.3625

2021

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A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model

Bone research, 2023-03, Vol.11 (1), p.16-16

2023

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Modulation of Endocannabinoid Tone in Osteoblastic Differentiation of MC3T3-E1 Cells and in Mouse Bone Tissue over Time

Cells (Basel, Switzerland), 2021-05, Vol.10 (5), p.1199

2021

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The two faces of giant cell tumor of bone

Cancer letters, 2020-10, Vol.489, p.1-8

2020

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The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Journal of bone and mineral research, 2020-08, Vol.35 (8), p.1387-1398

2020

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Profilin 1 deficiency drives mitotic defects and reduces genome stability

Communications biology, 2023-01, Vol.6 (1), p.9-9, Article 9

2023

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ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology

Journal of bone and mineral research, 2020-10, Vol.35 (10), p.1974-1980

2020

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The Osteoclast Traces the Route to Bone Tumors and Metastases

Frontiers in cell and developmental biology, 2022-05, Vol.10, p.886305-886305

2022

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The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences

Oncotarget, 2017-09, Vol.8 (38), p.63121-63131

2017

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The loss of Profilin 1 is associated with early-onset Paget's disease of bone degenerating into osteosarcoma

Bone Reports, 2020-10, Vol.13, p.100333, Article 100333

2020

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Zfp687 knock-in mouse model of Paget’s disease of bone exhibits increased bone marrow adiposity preceding bone remodelling alteration

Bone Reports, 2022-05, Vol.16, p.101197, Article 101197

2022

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A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model

骨研究（英文版）, 2023, Vol.11 (1), p.201-214

2023

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The loss of Profilin 1 is a driver of chromosome instability in osteosarcoma

Bone Reports, 2022-05, Vol.16, p.101183, Article 101183

2022

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Bilateral morphometric analysis of corneal sub-basal nerve plexus in patients undergoing unilateral cataract surgery: a preliminary in vivo confocal microscopy study

British journal of ophthalmology, 2021-02, Vol.105 (2), p.174

2021

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Rare Variants in Autophagy and Non-Autophagy Genes in Late-Onset Pompe Disease: Suggestions of Their Disease-Modifying Role in Two Italian Families

A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model

Modulation of Endocannabinoid Tone in Osteoblastic Differentiation of MC3T3-E1 Cells and in Mouse Bone Tissue over Time

The two faces of giant cell tumor of bone

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Profilin 1 deficiency drives mitotic defects and reduces genome stability

ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology

The Osteoclast Traces the Route to Bone Tumors and Metastases

The distinct clinical features of giant cell tumor of bone in pagetic and non-pagetic patients are associated with genetic, biochemical and histological differences

The loss of Profilin 1 is associated with early-onset Paget's disease of bone degenerating into osteosarcoma

Zfp687 knock-in mouse model of Paget’s disease of bone exhibits increased bone marrow adiposity preceding bone remodelling alteration

A mutation in the ZNF687 gene that is responsible for the severe form of Paget's disease of bone causes severely altered bone remodeling and promotes hepatocellular carcinoma onset in a knock-in mouse model

The loss of Profilin 1 is a driver of chromosome instability in osteosarcoma

Population Trends in Rates of Percutaneous Coronary Revascularization for Acute Coronary Syndromes Associated With the COVID-19 Outbreak

Bilateral morphometric analysis of corneal sub-basal nerve plexus in patients undergoing unilateral cataract surgery: a preliminary in vivo confocal microscopy study

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