Molecular Genetics of Paget's Disease of Bone (Articolo in rivista)

Type

• Articolo in rivista (Classe)
• Prodotto della ricerca (Classe)

Label

• Molecular Genetics of Paget's Disease of Bone (Articolo in rivista) (literal)

Anno

• 2014-01-01T00:00:00+01:00 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi

• 10.1002/9780470015902.a0024396 (literal)

Alternative label

• Gennari L, Gianfrancesco F, Rendina D, Merlotti D (2014)
  Molecular Genetics of Paget's Disease of Bone
  in eLS John Wiley & Sons Ltd, Chichester
  (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

• Gennari L, Gianfrancesco F, Rendina D, Merlotti D (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url

• http://www.els.net/WileyCDA/ (literal)

Rivista

• eLS John Wiley & Sons Ltd, Chichester (Rivista)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni

• Department of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy Institute of Genetics and Biophysics Adriano Buzzati Traverso, National Research Council of Italy, Naples, Italy Department of Clinical and Experimental Medicine, Federico II University, Naples, Italy (literal)

Titolo

• Molecular Genetics of Paget's Disease of Bone (literal)

Abstract

• Paget's disease of bone (PDB) is a chronic disorder of bone metabolism, which typically results in enlarged and deformed bones in one or more regions of the skeleton. The aetiology of PDB has remained unknown for several decades, but either environmental or genetic factors have been implicated. The former mainly concern the presence of a slow-acting viral infection, a condition that may be present for many years before symptoms appear. However, there are also several data supporting a hereditary hypothesis, since in up to40%of patients the disease may appear in more than one family member. The genetic architecture of PDB is incompletely understood, but recent evidence suggests that the disease may be caused by a combination of rare variants in genes such as SQSTM1 (detected in up to 50% of familial cases of PDB) and more common variants (i.e. polymorphisms) in genes such as CSF1, TNFRSF11A, OPTN and TM7SF4. (literal)

Prodotto di

• Plasticità genomica: dal genoma ai sistemi biologici (SV.P13.003.001) (Modulo)
• Institute of genetics and biophysics \"Adriano Buzzati Traverso\" (IGB) (Istituto)

Autore CNR

• FERNANDO GIANFRANCESCO (Unità di personale interno)

Incoming links:

Autore CNR di

• FERNANDO GIANFRANCESCO (Unità di personale interno)

Prodotto

• Institute of genetics and biophysics \"Adriano Buzzati Traverso\" (IGB) (Istituto)
• Plasticità genomica: dal genoma ai sistemi biologici (SV.P13.003.001) (Modulo)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• eLS John Wiley & Sons Ltd, Chichester (Rivista)