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N-acetylcysteine treatment ameliorates the skeletal phenotype of a mouse model of diastrophic dysplasia

Human molecular genetics, 2015-10, Vol.24 (19), p.5570-5580

2015

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Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta: A New Target for Osteogenesis Imperfecta Pharmacological Therapy

Stem cells (Dayton, Ohio), 2012-07, Vol.30 (7), p.1465-1476

2012

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Collagen Fibril Structure Is Affected by Collagen Concentration and Decorin

Biomacromolecules, 2007-07, Vol.8 (7), p.2087-2091

2007

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Mapping of SPARC/BM-40/Osteonectin-binding Sites on Fibrillar Collagens

The Journal of biological chemistry, 2008-07, Vol.283 (28), p.19551-19560

2008

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Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue

PloS one, 2013-03, Vol.8 (3), p.e58792-e58792

2013

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Identifying the structure of the active sites of human recombinant prolidase

European biophysics journal, 2010-05, Vol.39 (6), p.935-945

2010

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XXV Meeting THE ITALIAN SOCIETY FOR THE STUDY OF CONNECTIVE TISSUES (SISC)

European journal of histochemistry, 2009-06, Vol.49 (3), p.313

2009

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Fibromodulin Interactions with Type I and II Collagens

Connective Tissue Research, 2007-01, Vol.48 (3), p.141-148

2007

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Glycosaminoglycans show a specific periodic interaction with type I collagen fibrils

Journal of structural biology, 2008-10, Vol.164 (1), p.134-139

2008

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Mapping Hsp47 binding site(s) using CNBr peptides derived from type I and type II collagen

Protein science, 2003-08, Vol.12 (8), p.1792-1800

2003

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Molecular stability of chemically modified collagen triple helices

FEBS letters, 2003-07, Vol.547 (1), p.170-176

2003

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Human recombinant prolidase from eukaryotic and prokaryotic sources

The FEBS journal, 2006-12, Vol.273 (23), p.5466-5478

2006

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Extracellular matrix structure and nano-mechanics determine megakaryocyte function

Blood, 2011-10, Vol.118 (16), p.4449-4453

2011

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Altered Signaling in the G1 Phase Deregulates Chondrocyte Growth in a Mouse Model With Proteoglycan Undersulfation

Journal of cellular biochemistry, 2014-10, Vol.115 (10), p.1779-1786

2014

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The effect of treatment on urinary glycosylated lysine a marker of extracellular matrix integrity and lysosome function in mucopolysaccharidosis types I, II, IV and VI patients

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S63-S63

2018

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Lack of prolidase causes a bone phenotype both in human and in mouse

Bone (New York, N.Y.), 2015-03, Vol.72, p.53-64

2015

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Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling

Matrix biology, 2010-07, Vol.29 (6), p.453-460

2010

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A Mn(II)–Mn(II) center in human prolidase

Biochimica et biophysica acta, 2013-01, Vol.1834 (1), p.197-204

2013

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Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies

The FEBS journal, 2006-12, Vol.273 (23), p.5466-5478

2006

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A Mn(II)aMn(II) center in human prolidase

Biochimica et biophysica acta. Proteins and proteomics, 2013-01, Vol.1834 (1), p.197-204

2013

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In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation

Biochemical journal, 2006-09, Vol.398 (3), p.509-514

2006

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quantitative and qualitative method for direct 2-DE analysis of murine cartilage

Proteomics (Weinheim), 2007-11, Vol.7 (21), p.4003-4007

2007

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Pre-column derivatisation method for the measurement of glycosylated hydroxylysines of collagenous proteins

Journal of chromatography. B, Biomedical sciences and applications, 1997-12, Vol.703 (1), p.267-272

1997

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XXV Meeting THE ITALIAN SOCIETY FOR THE STUDY OF CONNECTIVE TISSUES (SISC)

European journal of histochemistry, 2005-07, Vol.49 (3), p.313

2005

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Confocal microscopy study of decorin binding to collagen fibrils

Matrix biology, 2008-12, Vol.27, p.56-56

2008

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N-acetylcysteine treatment ameliorates the skeletal phenotype of a mouse model of diastrophic dysplasia

Impaired Osteoblastogenesis in a Murine Model of Dominant Osteogenesis Imperfecta: A New Target for Osteogenesis Imperfecta Pharmacological Therapy

Collagen Fibril Structure Is Affected by Collagen Concentration and Decorin

Mapping of SPARC/BM-40/Osteonectin-binding Sites on Fibrillar Collagens

Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue

Identifying the structure of the active sites of human recombinant prolidase

XXV Meeting THE ITALIAN SOCIETY FOR THE STUDY OF CONNECTIVE TISSUES (SISC)

Fibromodulin Interactions with Type I and II Collagens

Glycosaminoglycans show a specific periodic interaction with type I collagen fibrils

Mapping Hsp47 binding site(s) using CNBr peptides derived from type I and type II collagen

Molecular stability of chemically modified collagen triple helices

Human recombinant prolidase from eukaryotic and prokaryotic sources

Extracellular matrix structure and nano-mechanics determine megakaryocyte function

Altered Signaling in the G1 Phase Deregulates Chondrocyte Growth in a Mouse Model With Proteoglycan Undersulfation

The effect of treatment on urinary glycosylated lysine a marker of extracellular matrix integrity and lysosome function in mucopolysaccharidosis types I, II, IV and VI patients

Lack of prolidase causes a bone phenotype both in human and in mouse

Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling

A Mn(II)–Mn(II) center in human prolidase

Human recombinant prolidase from eukaryotic and prokaryotic sources. Expression, purification, characterization and long-term stability studies

A Mn(II)aMn(II) center in human prolidase

In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation

quantitative and qualitative method for direct 2-DE analysis of murine cartilage

Pre-column derivatisation method for the measurement of glycosylated hydroxylysines of collagenous proteins

XXV Meeting THE ITALIAN SOCIETY FOR THE STUDY OF CONNECTIVE TISSUES (SISC)

Confocal microscopy study of decorin binding to collagen fibrils

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