Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sonia Ciarmatori"'
Autor:
Burkhard Tönshoff, Burkhardt Schütt, Ulrike Hügel, Daniela Kiepe, Ludger Ständker, Andreas Hoeflich, Sonia Ciarmatori, Jun Oh, Anke Van Der Pas
Publikováno v:
Endocrinology. 149:4901-4911
The IGF/IGF binding protein (IGFBP) system is an important component in the hormonal regulation of longitudinal growth. Evidence from in vitro studies indicates that IGFBPs may have IGF-independent effects. We analyzed the biological activity of inta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d92e0d64367539bf78a6febe4cf41ea6
https://doi.org/10.1210/en.2007-1395
https://doi.org/10.1210/en.2007-1395
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 290:E363-E371
The growth plate is an important target tissue for insulin-like growth factors (IGFs), but little is known about the regulation of the IGF system during the developmental sequence of chondrocytes. We therefore examined the expression profile of IGF s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69bbb1a9331c3d98bcf718d2cdf07ea8
https://doi.org/10.1152/ajpendo.00363.2005
https://doi.org/10.1152/ajpendo.00363.2005
Publikováno v:
Pediatric Nephrology. 20:279-289
Disturbances of the somatotropic hormone axis play an important pathogenic role in growth retardation and catabolism in children with chronic renal failure (CRF). The apparent discrepancy between normal or elevated growth hormone (GH) levels and dimi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe74cad16f9d77cf9dd6ddae8ab3aba5
https://doi.org/10.1007/s00467-005-1821-0
https://doi.org/10.1007/s00467-005-1821-0
Autor:
Massimo Zeviani, Roberto Marconi, Patricio Fernandez, Alessandro Filla, Alexandre Dürr, Bertrand Fontaine, Andrea Ballabio, Marina Mora, Sonia Ciarmatori, Sergio Cocozza, Giorgio Casari, Maurizio De Fusco, Giuseppe De Michele
Publikováno v:
Cell. 93(6):973-983
Hereditary spastic paraplegia (HSP) is characterized by progressive weakness and spasticity of the lower limbs due to degeneration of corticospinal axons. We found that patients from a chromosome 16q24.3–linked HSP family are homozygous for a 9.5 k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec689a0c881659b6d019d0c258ea544
Autor:
Nicoletta Malgaretti, Salvador Martinez, Ombretta Pozzoli, G. Giacomo Consalez, Alessandro Bosetti, Anna Corradi, Marco Bianchi, Sonia Ciarmatori, Maddalena Panigada
Publikováno v:
Journal of Biological Chemistry. 272:17632-17639
Several genetic factors have been proven to contribute to the specification of the metencephalic-mesencephalic territory, a process that sets the developmental foundation for prospective morphogenesis of the cerebellum and mesencephalon. However, evi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19edaa54b2fe4da272c2cc42522cf8ee
https://doi.org/10.1074/jbc.272.28.17632
https://doi.org/10.1074/jbc.272.28.17632
Publikováno v:
Journal of molecular endocrinology. 38(4)
Since IGF-I is an important chondrocyte growth factor, we sought to examine the intracellular mechanisms by which it exerts two of its pivotal effects, stimulation of proliferation and differentiation. We used the mesenchymal chondrogenic cell line R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d0d61ed1995b1f362e57ea4c19f0e9d
https://pubmed.ncbi.nlm.nih.gov/17446238
https://pubmed.ncbi.nlm.nih.gov/17446238
Publikováno v:
Endocrinology. 146(7)
The bioactivity of IGF-I in the cellular microenvironment is modulated by both inhibitory and stimulatory IGF binding proteins (IGFBPs), whose production is partially under control of IGF-I. However, little is known on the IGF-mediated regulation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf03f362cceb462bf212dc9a5e0030b4
https://pubmed.ncbi.nlm.nih.gov/15845624
https://pubmed.ncbi.nlm.nih.gov/15845624
Autor:
Carla Navone, Milvia Cecconi, Michele Sacco, Gianpaolo Grumieri, Cristina Curcio, Alberto Bettinelli, Augusto Rosini, Giuseppe Ruffa, Giovanna Leozappa, Silvana Tedeschi, Aldo Claris Appiani, Sonia Ciarmatori, Giorgio Casari, Layla Cesareo, Silvana Binda, Marie Louise Syren, Bruno Mercuri
Publikováno v:
Scopus-Elsevier
Limited phenotypic variability has been reported in patients with Bartter syndrome type I, with mutations in the Na-K-2Cl cotransporter gene (BSC). The diagnosis of this hereditary renal tubular disorder is usually made in the antenatal-neonatal peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87154dfac900b9bb58571ee6a2de01bc
https://pubmed.ncbi.nlm.nih.gov/10975303
https://pubmed.ncbi.nlm.nih.gov/10975303
Autor:
Silvana Tedeschi, Sonia Ciarmatori, Giorgio Casari, Clementina Isimbaldi, Maurizio Bevilacqua, Velella Righini, Layla Cesareo, Enrico Zammarchi, Roberto Rusconi, Alberto Bettinelli, Maria Alice Donati, Rosanna Garavaglia
Publikováno v:
Pediatric research. 46(2)
Gitelman disease was diagnosed in two unrelated children with hypokalemic metabolic alkalosis and growth failure (a boy and a girl aged 7 mo and 9.5 y, respectively, at clinical presentation) on the basis of mutations detected in the gene encoding th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c4bf5a2c58627111e74d3bb30bd95f8
https://pubmed.ncbi.nlm.nih.gov/10447120
https://pubmed.ncbi.nlm.nih.gov/10447120
Autor:
Sonia Ciarmatori, Michela Bossolasco, Carol L. Stayton, Nicoletta Malgaretti, G.Giacomo Gonzalez, Anna Corradi
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f76791d26804531fc2e87e341697e891
