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D J Watts

Showing results (41-50 of 54) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1994
Inhibitory effects of bisphosphonates on growth of amoebae of the cellular slime mold Dictyostelium discoideumM J Rogers, D J Watts, R G Russell, et al.
The Biochemical Journal|October 1, 1994
Incorporation of bisphosphonates into adenine nucleotides by amoebae of the cellular slime mould Dictyostelium discoideumM J Rogers, X Ji, R G Russell, et al.
Rhode Island Medical Journal (2013)|April 27, 2022
Differences in Work-Life Experiences of Physicians by Parenting Status, Gender, and Training Level During the COVID-19 PandemicC Paula Lewis-de Los Angeles, William Lewis-de Los Angeles, Shuba Kamath, et al.
Nature Genetics|March 23, 2004
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing proteinGiles D J Watts, Jill Wymer, Margaret J Kovach, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathySarju G Mehta, Giles D J Watts, Barbara McGillivray, et al.
Annals of Neurology|February 26, 2005
Mutant valosin-containing protein causes a novel type of frontotemporal dementiaRolf Schröder, Giles D J Watts, Sarju G Mehta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2007
APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)Sarju G Mehta, Giles D J Watts, Jennifer L Adamson, et al.
Human Genetics|October 26, 2005
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndromeGiles D J Watts, Sarju G Mehta, Chengfeng Zhao, et al.
Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, 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.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 1, 1994
Inhibitory effects of bisphosphonates on growth of amoebae of the cellular slime mold Dictyostelium discoideumM J Rogers, D J Watts, R G Russell, et al.
The Biochemical Journal|October 1, 1994
Incorporation of bisphosphonates into adenine nucleotides by amoebae of the cellular slime mould Dictyostelium discoideumM J Rogers, X Ji, R G Russell, et al.
Rhode Island Medical Journal (2013)|April 27, 2022
Differences in Work-Life Experiences of Physicians by Parenting Status, Gender, and Training Level During the COVID-19 PandemicC Paula Lewis-de Los Angeles, William Lewis-de Los Angeles, Shuba Kamath, et al.
Nature Genetics|March 23, 2004
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing proteinGiles D J Watts, Jill Wymer, Margaret J Kovach, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathySarju G Mehta, Giles D J Watts, Barbara McGillivray, et al.
Annals of Neurology|February 26, 2005
Mutant valosin-containing protein causes a novel type of frontotemporal dementiaRolf Schröder, Giles D J Watts, Sarju G Mehta, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2007
APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)Sarju G Mehta, Giles D J Watts, Jennifer L Adamson, et al.
Human Genetics|October 26, 2005
Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndromeGiles D J Watts, Sarju G Mehta, Chengfeng Zhao, et al.
Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, 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.
Pageof 6