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Roberta Besio Selected Research

Prolidase Deficiency

3/2015Lack of prolidase causes a bone phenotype both in human and in mouse.
1/2013Kinetic and structural evidences on human prolidase pathological mutants suggest strategies for enzyme functional rescue.
1/2012Partial Rescue of Biochemical Parameters After Hematopoietic Stem Cell Transplantation in a Patient with Prolidase Deficiency Due to Two Novel PEPD Mutations.
9/2011Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis.
5/2010Identifying the structure of the active sites of human recombinant prolidase.

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Roberta Besio Research Topics

Disease

5Prolidase Deficiency
03/2015 - 05/2010
2Osteogenesis Imperfecta (Lobstein Disease)
07/2012 - 07/2009
1Genu Valgum
03/2015
1Microcephaly
03/2015
1Metabolic Bone Diseases (Osteopenia)
03/2015
1Hypertelorism
03/2015
1Crohn Disease (Crohn's Disease)
12/2013
1Inflammation
12/2013
1Shock
01/2013
1Developmental Bone Diseases (Bone Dysplasia)
07/2012
1Mental Retardation (Idiocy)
05/2010
1Respiratory Tract Infections (Respiratory Tract Infection)
05/2010

Drug/Important Bio-Agent (IBA)

5proline dipeptidase (prolidase)IBA
03/2015 - 05/2010
1Mutant Proteins (Protein, Mutant)IBA
03/2015
1Advanced Glycosylation End ProductsIBA
12/2013
1Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)IBA
12/2013
1Proteins (Proteins, Gene)IBA
01/2013
1CollagenIBA
07/2012
1Collagen Type I (Type I Collagen)IBA
07/2009
1Glycine (Aminoacetic Acid)FDA LinkGeneric
07/2009

Therapy/Procedure

1Hematopoietic Stem Cell Transplantation
01/2012
1Transplantation (Transplant Recipients)
07/2009