Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of “protective” and “risk” factors E Pedrini, I Jennes, M Tremosini, A Milanesi, M Mordenti, A Parra, ... JBJS 93 (24), 2294-2302, 2011 | 153 | 2011 |
Heparan sulfate in skeletal development, growth, and pathology: the case of hereditary multiple exostoses J Huegel, F Sgariglia, M Enomoto‐Iwamoto, E Koyama, JP Dormans, ... Developmental Dynamics 242 (9), 1021-1032, 2013 | 90 | 2013 |
Perichondrium phenotype and border function are regulated by Ext1 and heparan sulfate in developing long bones: a mechanism likely deranged in Hereditary Multiple Exostoses J Huegel, C Mundy, F Sgariglia, P Nygren, PC Billings, Y Yamaguchi, ... Developmental biology 377 (1), 100-112, 2013 | 74 | 2013 |
Heparanase stimulates chondrogenesis and is up-regulated in human ectopic cartilage: a mechanism possibly involved in hereditary multiple exostoses J Huegel, M Enomoto-Iwamoto, F Sgariglia, E Koyama, M Pacifici The American journal of pathology 185 (6), 1676-1685, 2015 | 51 | 2015 |
Genetic models of osteochondroma onset and neoplastic progression: evidence for mechanisms alternative to EXT genes inactivation M Zuntini, E Pedrini, A Parra, F Sgariglia, FV Gentile, M Pandolfi, ... Oncogene 29 (26), 3827-3834, 2010 | 50 | 2010 |
MicroRNA profiling of multiple osteochondromas: identification of disease‐specific and normal cartilage signatures M Zuntini, M Salvatore, E Pedrini, A Parra, F Sgariglia, A Magrelli, ... Clinical genetics 78 (6), 507-516, 2010 | 47 | 2010 |
Epiphyseal abnormalities, trabecular bone loss and articular chondrocyte hypertrophy develop in the long bones of postnatal Ext1-deficient mice F Sgariglia, ME Candela, J Huegel, O Jacenko, E Koyama, Y Yamaguchi, ... Bone 57 (1), 220-231, 2013 | 38 | 2013 |
Unsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice S Sinha, C Mundy, T Bechtold, F Sgariglia, MM Ibrahim, PC Billings, ... PLoS Genetics 13 (4), e1006742, 2017 | 35 | 2017 |
Loss of β-catenin induces multifocal periosteal chondroma-like masses in mice L Cantley, C Saunders, M Guttenberg, ME Candela, Y Ohta, R Yasuhara, ... The American Journal of Pathology 182 (3), 917-927, 2013 | 25 | 2013 |
HhAntag, a hedgehog signaling antagonist, suppresses chondrogenesis and modulates canonical and non‐canonical BMP signaling C Mundy, A Bello, F Sgariglia, E Koyama, M Pacifici Journal of cellular physiology 231 (5), 1033-1044, 2016 | 22 | 2016 |
The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in hereditary multiple exostoses: insights into pathogenesis F Sgariglia, E Pedrini, JP Bradfield, TR Bhatti, P D'Adamo, JP Dormans, ... Bone 72, 123-127, 2015 | 12 | 2015 |
Previously unsuspected defects in the cranial base of a mouse model of Hereditary Multiple Exostoses F Sgariglia, P Billings, H Um, K Jones, E Koyama, M Pacifici JOURNAL OF BONE AND MINERAL RESEARCH 29, S386-S386, 2014 | | 2014 |
Postnatal Ablation of Ext1 in Cartilage Induces Ectopic Hypertrophy of Articular Chondrocytes and Loss of Bone Volume in Primary Spongiosa. F Sgariglia, ME Candela, J Huegel, O Jacenko, E Koyama, Y Yamaguchi, ... JOURNAL OF BONE AND MINERAL RESEARCH 28, 2013 | | 2013 |
Type I collagen molecular map lends insights into the domain structure of the fibril and the genotype-phenotype relationship for some collagen mutations J San Antonio, A Persikov, A Forlino, J Marini, P Byers, F Glorieux, A Lund, ... Book of abstracts-XXXII Congress of the International Union of Leather …, 2013 | | 2013 |
Loss of β-Catenin Induces Multifocal Periosteal Chondroma-Like Masses in Mice | | |