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Two Novel C-Terminus RUNX2 Mutations in Two Cleidocranial Dysplasia (CCD) Patients Impairing p53 Expression

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10336

2021

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West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature

Mediterranean journal of hematology and infectious diseases, 2019-05, Vol.11 (1), p.e2019033

2019

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Runx2 stimulates neoangiogenesis through the Runt domain in melanoma

Scientific reports, 2019-05, Vol.9 (1), p.8052-8052, Article 8052

2019

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Fisetin: An Integrated Approach to Identify a Strategy Promoting Osteogenesis

Frontiers in pharmacology, 2022-05, Vol.13, p.890693-890693

2022

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Dietary iron intake and anemia: food frequency questionnaire in patients with hereditary hemorrhagic telangiectasia

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-295, Article 295

2020

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Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression

Cells (Basel, Switzerland), 2024-02, Vol.13 (5), p.408

2024

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Syntheses, Structures, Second-Harmonic Generating, and Ferroelectric Properties of Tungsten Bronzes: A6M2M‘8O30 (A = Sr2+, Ba2+, or Pb2+; M = Ti4+, Zr4+, or Hf4+; M‘ = Nb5+ or Ta5+)

Chemistry of materials, 2004-09, Vol.16 (19), p.3616-3622

2004

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New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration

Cells (Basel, Switzerland), 2018-11, Vol.7 (11), p.220

2018

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Μηδὲν (ὑπ)εναντίον πράττειν: A Slogan of Pro-Roman Diplomacy after Pydna?

Axon (Venezia. Periodico), 2019-12 (2)

Gandini, Alberto

2019

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Μηδὲν (ὑπ)εναντίον πράττειν: uno slogan della diplomazia filoromana dopo Pidna?

Axon (Venezia. Periodico), 2019-12, Vol.3 (2)

Gandini, Alberto

2019

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A Potential Role of RUNX2- RUNT Domain in Modulating the Expression of Genes Involved in Bone Metastases: An In Vitro Study with Melanoma Cells

Cells (Basel, Switzerland), 2020-03, Vol.9 (3), p.751

2020

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Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes

Clinical endocrinology (Oxford), 2005-08, Vol.63 (2), p.146-151

2005

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D.S. XXX 8: un giudizio polibiano sulla diplomazia senatoria?

Dialogues d'histoire ancienne, 2013-11, Vol.S 9 (Supplement9), p.173-189

Gandini, Alberto

2013

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Expression of FBXW11 in normal and disease‐associated osteogenic cells

Journal of cellular and molecular medicine, 2023-06, Vol.27 (11), p.1580-1591

2023

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Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

Journal of bone and mineral research, 2012-03, Vol.27 (3), p.723-728

2012

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Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation

The journal of clinical endocrinology and metabolism, 2015-09, Vol.100 (9), p.E1234-E1241

2015

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RapidQ: A reader-free microfluidic platform for the quantitation of antibodies against the SARS-CoV-2 spike protein

Biomicrofluidics, 2022-03, Vol.16 (2), p.024105-024105

2022

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Removal of malaria-infected red blood cells using magnetic cell separators: A computational study

Applied mathematics and computation, 2012-02, Vol.218 (12), p.6841-6850

2012

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Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis

Genes & diseases, 2024-11, p.101449, Article 101449

2024

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Design of microfluidic channels for magnetic separation of malaria-infected red blood cells

Microfluidics and nanofluidics, 2016, Vol.20 (2), p.1, Article 41

2016

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A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect

Bone (New York, N.Y.), 2012-01, Vol.50 (1), p.343-349

2012

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Publisher Correction: Runx2 stimulates neoangiogenesis through the Runt domain in melanoma

Scientific reports, 2020-02, Vol.10 (1), p.2784-2784, Article 2784

2020

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THE PUZZLE OF TWO DIFFERENT SUB-MICROMETER TUNGSTEN-RICH DEPOSITS IN BULK YBCO: ONE ACTS AS PINNING CENTERS AND THE OTHER DOES NOT

AIP conference proceedings, 2010, Vol.1219 (1)

2010

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The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene

Journal of pediatric genetics (Birmingham, Ala.), 2014-03, Vol.3 (1), p.035-039

2014

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How and why discontinuous multiple-in-line-damage results in much higher Jc than continuous columnar pinning centres

Superconductor science & technology, 2006-07, Vol.19 (7), p.S575-S579

2006

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Two Novel C-Terminus RUNX2 Mutations in Two Cleidocranial Dysplasia (CCD) Patients Impairing p53 Expression

West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature

Runx2 stimulates neoangiogenesis through the Runt domain in melanoma

Fisetin: An Integrated Approach to Identify a Strategy Promoting Osteogenesis

Dietary iron intake and anemia: food frequency questionnaire in patients with hereditary hemorrhagic telangiectasia

Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression

Syntheses, Structures, Second-Harmonic Generating, and Ferroelectric Properties of Tungsten Bronzes: A6M2M‘8O30 (A = Sr2+, Ba2+, or Pb2+; M = Ti4+, Zr4+, or Hf4+; M‘ = Nb5+ or Ta5+)

New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration

Μηδὲν (ὑπ)εναντίον πράττειν: A Slogan of Pro-Roman Diplomacy after Pydna?

Μηδὲν (ὑπ)εναντίον πράττειν: uno slogan della diplomazia filoromana dopo Pidna?

A Potential Role of RUNX2- RUNT Domain in Modulating the Expression of Genes Involved in Bone Metastases: An In Vitro Study with Melanoma Cells

Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes

D.S. XXX 8: un giudizio polibiano sulla diplomazia senatoria?

Expression of FBXW11 in normal and disease‐associated osteogenic cells

Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation

RapidQ: A reader-free microfluidic platform for the quantitation of antibodies against the SARS-CoV-2 spike protein

Removal of malaria-infected red blood cells using magnetic cell separators: A computational study

Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis

Design of microfluidic channels for magnetic separation of malaria-infected red blood cells

A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect

Publisher Correction: Runx2 stimulates neoangiogenesis through the Runt domain in melanoma

THE PUZZLE OF TWO DIFFERENT SUB-MICROMETER TUNGSTEN-RICH DEPOSITS IN BULK YBCO: ONE ACTS AS PINNING CENTERS AND THE OTHER DOES NOT

The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene

How and why discontinuous multiple-in-line-damage results in much higher Jc than continuous columnar pinning centres

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