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Elke Piters

Showing results (11-20 of 16) with videos related to

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Bone|October 10, 2012
Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosisEveline Boudin, Elke Piters, Igor Fijalkowski, et al.
Bone|May 24, 2011
Identification of the first deletion in the LRP5 gene in a patient with autosomal dominant osteopetrosis type IAlessandra Pangrazio, Eveline Boudin, Elke Piters, et al.
Genetic Testing|December 17, 2008
A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian originChong Ae Kim, Rachel Honjo, Débora Bertola, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 28, 2010
A new familial sclerosing bone dysplasiaEliane Chouery, Alessandra Pangrazio, Annalisa Frattini, et al.
Human Mutation|June 29, 2010
First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin functionElke Piters, Cavit Culha, Martiene Moester, et al.
The Journal of Biological Chemistry|April 8, 2011
Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator functionOlivier Leupin, Elke Piters, Christine Halleux, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Bone|October 10, 2012
Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosisEveline Boudin, Elke Piters, Igor Fijalkowski, et al.
Bone|May 24, 2011
Identification of the first deletion in the LRP5 gene in a patient with autosomal dominant osteopetrosis type IAlessandra Pangrazio, Eveline Boudin, Elke Piters, et al.
Genetic Testing|December 17, 2008
A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian originChong Ae Kim, Rachel Honjo, Débora Bertola, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 28, 2010
A new familial sclerosing bone dysplasiaEliane Chouery, Alessandra Pangrazio, Annalisa Frattini, et al.
Human Mutation|June 29, 2010
First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin functionElke Piters, Cavit Culha, Martiene Moester, et al.
The Journal of Biological Chemistry|April 8, 2011
Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator functionOlivier Leupin, Elke Piters, Christine Halleux, et al.
Pageof 2