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J Hocking

Showing results (101-110 of 163) with videos related to

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European Journal of Human Genetics : EJHG|January 12, 2012
Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal womenAlison Gartland, Kristen K Skarratt, Lynne J Hocking, et al.
Leukemia|December 1, 2016
Circulating tumour DNA analysis demonstrates spatial mutational heterogeneity that coincides with disease relapse in myelomaS Mithraprabhu, T Khong, M Ramachandran, et al.
Oecologia|November 22, 2014
Abundance and phenology patterns of two pond-breeding salamanders determine species interactions in natural populationsThomas L Anderson, Daniel J Hocking, Christopher A Conner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 14, 2005
Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descentGavin J A Lucas, Lynne J Hocking, Anna Daroszewska, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2016
Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohortToni-Kim Clarke, Jana Obsteter, Lynsey S Hall, et al.
Plos One|February 23, 2017
Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin studyOliver van Hecke, Lynne J Hocking, Nicola Torrance, et al.
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.
Bone Marrow Transplantation|March 21, 2017
Adverse impact of high donor CD3+ cell dose on outcome following tandem auto-NMA allogeneic transplantation for high-risk myelomaA P Nair, P Walker, A Kalff, 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.
Translational Psychiatry|July 1, 2015
Major depressive disorder and current psychological distress moderate the effect of polygenic risk for obesity on body mass indexT-K Clarke, L S Hall, A M Fernandez-Pujals, et al.
Pageof 17

Showing results (101-110 of 163) with videos related to

Sort By:
Pageof 17
European Journal of Human Genetics : EJHG|January 12, 2012
Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal womenAlison Gartland, Kristen K Skarratt, Lynne J Hocking, et al.
Leukemia|December 1, 2016
Circulating tumour DNA analysis demonstrates spatial mutational heterogeneity that coincides with disease relapse in myelomaS Mithraprabhu, T Khong, M Ramachandran, et al.
Oecologia|November 22, 2014
Abundance and phenology patterns of two pond-breeding salamanders determine species interactions in natural populationsThomas L Anderson, Daniel J Hocking, Christopher A Conner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 14, 2005
Ubiquitin-associated domain mutations of SQSTM1 in Paget's disease of bone: evidence for a founder effect in patients of British descentGavin J A Lucas, Lynne J Hocking, Anna Daroszewska, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 3, 2016
Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohortToni-Kim Clarke, Jana Obsteter, Lynsey S Hall, et al.
Plos One|February 23, 2017
Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin studyOliver van Hecke, Lynne J Hocking, Nicola Torrance, et al.
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.
Bone Marrow Transplantation|March 21, 2017
Adverse impact of high donor CD3+ cell dose on outcome following tandem auto-NMA allogeneic transplantation for high-risk myelomaA P Nair, P Walker, A Kalff, 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.
Translational Psychiatry|July 1, 2015
Major depressive disorder and current psychological distress moderate the effect of polygenic risk for obesity on body mass indexT-K Clarke, L S Hall, A M Fernandez-Pujals, et al.
Pageof 17