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Geoff C Nicholson

Showing results (21-30 of 26) with videos related to

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Plos One|August 23, 2012
Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivationNigel A Morrison, Alexandre A Stephens, Motomi Osato, et al.
The Journal of Clinical Investigation|January 7, 2010
Oncostatin M promotes bone formation independently of resorption when signaling through leukemia inhibitory factor receptor in miceEmma C Walker, Narelle E McGregor, Ingrid J Poulton, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 5, 2004
Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequencesLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 2019
The Cost of Osteoporosis, Osteopenia, and Associated Fractures in Australia in 2017Gemma Tatangelo, Jennifer Watts, Karen Lim, et al.
Nature Genetics|May 4, 2010
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of boneOmar M E Albagha, Micaela R Visconti, Nerea Alonso, et al.
Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Plos One|August 23, 2012
Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivationNigel A Morrison, Alexandre A Stephens, Motomi Osato, et al.
The Journal of Clinical Investigation|January 7, 2010
Oncostatin M promotes bone formation independently of resorption when signaling through leukemia inhibitory factor receptor in miceEmma C Walker, Narelle E McGregor, Ingrid J Poulton, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 5, 2004
Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequencesLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 2019
The Cost of Osteoporosis, Osteopenia, and Associated Fractures in Australia in 2017Gemma Tatangelo, Jennifer Watts, Karen Lim, et al.
Nature Genetics|May 4, 2010
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of boneOmar M E Albagha, Micaela R Visconti, Nerea Alonso, et al.
Nature Genetics|May 31, 2011
Genome-wide association identifies three new susceptibility loci for Paget's disease of boneOmar M E Albagha, Sachin E Wani, Micaela R Visconti, et al.
Pageof 3