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E M Shore

Showing results (31-40 of 41) with videos related to

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Clinical Orthopaedics and Related Research|February 1, 1995
BMP-1 sublocalization on human chromosome 8. Molecular anatomy and orthopaedic implicationsE M Shore, A L Cook, G V Hahn, et al.
The Journal of Rheumatology|May 1, 1995
Mild expression of fibrodysplasia ossificans progressiva: a report of 3 casesH B Janoff, J A Tabas, E M Shore, et al.
Calcified Tissue International|August 12, 1999
Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressivaA S Virdi, E M Shore, R O Oreffo, et al.
Bone|November 11, 2009
GNAS-associated disorders of cutaneous ossification: two different clinical presentationsR J Schimmel, S G M A Pasmans, M Xu, et al.
Clinical Orthopaedics and Related Research|May 13, 1998
Embryonic overexpression of the c-Fos protooncogene. A murine stem cell chimera applicable to the study of fibrodysplasia ossificans progressiva in humansE A Olmsted, F H Gannon, Z Q Wang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
GNAS1 mutation and Cbfa1 misexpression in a child with severe congenital platelike osteoma cutisG L Yeh, S Mathur, A Wivel, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossificationM C Eddy, S M Jan De Beur, S M Yandow, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Calcified Tissue International|August 14, 1998
The human bone morphogenetic protein 4 (BMP-4) gene: molecular structure and transcriptional regulationE M Shore, M Xu, P B Shah, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Clinical Orthopaedics and Related Research|February 1, 1995
BMP-1 sublocalization on human chromosome 8. Molecular anatomy and orthopaedic implicationsE M Shore, A L Cook, G V Hahn, et al.
The Journal of Rheumatology|May 1, 1995
Mild expression of fibrodysplasia ossificans progressiva: a report of 3 casesH B Janoff, J A Tabas, E M Shore, et al.
Calcified Tissue International|August 12, 1999
Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressivaA S Virdi, E M Shore, R O Oreffo, et al.
Bone|November 11, 2009
GNAS-associated disorders of cutaneous ossification: two different clinical presentationsR J Schimmel, S G M A Pasmans, M Xu, et al.
Clinical Orthopaedics and Related Research|May 13, 1998
Embryonic overexpression of the c-Fos protooncogene. A murine stem cell chimera applicable to the study of fibrodysplasia ossificans progressiva in humansE A Olmsted, F H Gannon, Z Q Wang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
GNAS1 mutation and Cbfa1 misexpression in a child with severe congenital platelike osteoma cutisG L Yeh, S Mathur, A Wivel, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 25, 2000
Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossificationM C Eddy, S M Jan De Beur, S M Yandow, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Calcified Tissue International|August 14, 1998
The human bone morphogenetic protein 4 (BMP-4) gene: molecular structure and transcriptional regulationE M Shore, M Xu, P B Shah, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 5