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Stuart H Ralston

Showing results (191-200 of 275) with videos related to

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Human Molecular Genetics|October 11, 2002
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseLynne 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|October 20, 2005
Polymorphisms of the CLCN7 gene are associated with BMD in womenUlrika Pettersson, Omar M E Albagha, Max Mirolo, et al.
Acta Ophthalmologica|May 19, 2021
Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic reviewSanne Treurniet, Pia Burger, Ebba A E Ghyczy, et al.
Biochimica Et Biophysica Acta|March 20, 2014
Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and functionAlice Goode, Jed E Long, Barry Shaw, et al.
Stroke|October 6, 2016
Cerebral Small Vessel Disease Burden Is Increased in Systemic Lupus ErythematosusStewart J Wiseman, Mark E Bastin, Charlotte L Jardine, et al.
Plos Genetics|February 6, 2008
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfectaThomas S Lisse, Frank Thiele, Helmut Fuchs, et al.
Bone|October 4, 2005
Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of boneGavin J A Lucas, Sarju G Mehta, Lynne J Hocking, et al.
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.
Lancet (London, England)|November 12, 2020
Long-term cardiovascular safety of febuxostat compared with allopurinol in patients with gout (FAST): a multicentre, prospective, randomised, open-label, non-inferiority trialIsla S Mackenzie, Ian Ford, George Nuki, 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.
Pageof 28

Showing results (191-200 of 275) with videos related to

Sort By:
Pageof 28
Human Molecular Genetics|October 11, 2002
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseLynne 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|October 20, 2005
Polymorphisms of the CLCN7 gene are associated with BMD in womenUlrika Pettersson, Omar M E Albagha, Max Mirolo, et al.
Acta Ophthalmologica|May 19, 2021
Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic reviewSanne Treurniet, Pia Burger, Ebba A E Ghyczy, et al.
Biochimica Et Biophysica Acta|March 20, 2014
Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and functionAlice Goode, Jed E Long, Barry Shaw, et al.
Stroke|October 6, 2016
Cerebral Small Vessel Disease Burden Is Increased in Systemic Lupus ErythematosusStewart J Wiseman, Mark E Bastin, Charlotte L Jardine, et al.
Plos Genetics|February 6, 2008
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfectaThomas S Lisse, Frank Thiele, Helmut Fuchs, et al.
Bone|October 4, 2005
Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of boneGavin J A Lucas, Sarju G Mehta, Lynne J Hocking, et al.
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.
Lancet (London, England)|November 12, 2020
Long-term cardiovascular safety of febuxostat compared with allopurinol in patients with gout (FAST): a multicentre, prospective, randomised, open-label, non-inferiority trialIsla S Mackenzie, Ian Ford, George Nuki, 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.
Pageof 28