Daniela Formicola
- Type
- Persona (Classe)
- Label
- Daniela Formicola (literal)
- Daniela Formicola (literal)
- Persona in rapporto
- Employment relationship with CNR of Daniela Formicola (Rapporto con CNR)
- Autore CNR di
- Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (Prodotto della ricerca)
- Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree. (Articolo in rivista) (Prodotto della ricerca)
- The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis (Articolo in rivista) (Prodotto della ricerca)
- Coautore
- Filomena Napolitano (Unità di personale esterno)
- Sara Magliocca (Unità di personale esterno)
- FERNANDO GIANFRANCESCO (Persona)
- ANNALISA FRATTINI (Persona)
- Giovanna Morello (Persona)
- Andrea Aloia (Persona)
- TERESA ESPOSITO (Unità di personale interno)
- Alessandra Mingione (Persona)
- Nome
- Daniela (literal)
- Cognome
- Formicola (literal)
- Afferisce a
Incoming links:
- Coautore
- FERNANDO GIANFRANCESCO (Persona)
- ANNALISA FRATTINI (Persona)
- Andrea Aloia (Persona)
- TERESA ESPOSITO (Unità di personale interno)
- Sara Magliocca (Unità di personale esterno)
- Filomena Napolitano (Unità di personale esterno)
- Giovanna Morello (Persona)
- Alessandra Mingione (Persona)
- Ha afferente
- Rapporto con persona
- Employment relationship with CNR of Daniela Formicola (Rapporto con CNR)
- Autore CNR
- Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- piR_015520 Belongs to Piwi-Associated RNAs Regulates Expression of the Human Melatonin Receptor 1A Gene (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A nonsynonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- The melatonin receptor 1a (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis (Articolo in rivista) (Prodotto della ricerca)
- Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree. (Articolo in rivista) (Prodotto della ricerca)
- Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Distinct disease phenotypes linked to different combinations of GAA mutations in a large late-onset GSDII sibship. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A non-synonymous TNFRSF11A variation increases NFkB activity and the severity of Paget's disease (Articolo in rivista) (Prodotto della ricerca)