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P Bianco

Showing results (181-190 of 186) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 10, 2002
Phenotypic effects of biglycan deficiency are linked to collagen fibril abnormalities, are synergized by decorin deficiency, and mimic Ehlers-Danlos-like changes in bone and other connective tissuesA Corsi, T Xu, X D Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1993
Structure and molecular regulation of bone matrix proteinsP G Robey, N S Fedarko, T E Hefferan, et al.
Cell|October 16, 1999
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnoverK Holmbeck, P Bianco, J Caterina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 29, 2013
Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risksL C Rossetti, I Szurkalo, C P Radic, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of boneP Bianco, M Riminucci, A Majolagbe, et al.
Nature Genetics|September 10, 1998
Targeted disruption of the biglycan gene leads to an osteoporosis-like phenotype in miceT Xu, P Bianco, L W Fisher, et al.
Pageof 19

Showing results (181-190 of 186) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 186 results.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 10, 2002
Phenotypic effects of biglycan deficiency are linked to collagen fibril abnormalities, are synergized by decorin deficiency, and mimic Ehlers-Danlos-like changes in bone and other connective tissuesA Corsi, T Xu, X D Chen, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1993
Structure and molecular regulation of bone matrix proteinsP G Robey, N S Fedarko, T E Hefferan, et al.
Cell|October 16, 1999
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnoverK Holmbeck, P Bianco, J Caterina, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 29, 2013
Factor VIII genotype characterization of haemophilia A affected patients with transient and permanent inhibitors: a comprehensive Argentine study of inhibitor risksL C Rossetti, I Szurkalo, C P Radic, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 26, 2000
Mutations of the GNAS1 gene, stromal cell dysfunction, and osteomalacic changes in non-McCune-Albright fibrous dysplasia of boneP Bianco, M Riminucci, A Majolagbe, et al.
Nature Genetics|September 10, 1998
Targeted disruption of the biglycan gene leads to an osteoporosis-like phenotype in miceT Xu, P Bianco, L W Fisher, et al.
Pageof 19