Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Whyte

Showing results (401-410 of 454) with videos related to

Pageof 46
Sort By:
American Journal of Medical Genetics. Part A|October 14, 2005
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?Carrie L Heike, Michael L Cunningham, Robert D Steiner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Nature Genetics|December 30, 1999
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisA E Hughes, S H Ralston, J Marken, 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.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 23, 2008
Changes in vascular and cardiac function after prolonged strenuous exercise in humansEllen A Dawson, Greg P Whyte, Mark A Black, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancyJesse E Otero, Gary S Gottesman, William H McAlister, et al.
International Journal of Food Microbiology|July 30, 2004
Occurrence of Campylobacter in retail foods in IrelandP Whyte, K McGill, D Cowley, et al.
Human Molecular Genetics|December 14, 2001
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneE Cleiren, O Bénichou, E Van Hul, et al.
The New England Journal of Medicine|January 11, 2002
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasiaEileen M Shore, Jaimo Ahn, Suzanne Jan de Beur, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 19, 2007
Enzyme replacement therapy for murine hypophosphatasiaJosé Luis Millán, Sonoko Narisawa, Isabelle Lemire, et al.
Pageof 46

Showing results (401-410 of 454) with videos related to

Sort By:
Pageof 46
American Journal of Medical Genetics. Part A|October 14, 2005
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?Carrie L Heike, Michael L Cunningham, Robert D Steiner, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 13, 2014
Rapid skeletal turnover in a radiographic mimic of osteopetrosisMichael P Whyte, Katherine L Madson, Steven Mumm, et al.
Nature Genetics|December 30, 1999
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisA E Hughes, S H Ralston, J Marken, 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.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 23, 2008
Changes in vascular and cardiac function after prolonged strenuous exercise in humansEllen A Dawson, Greg P Whyte, Mark A Black, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 14, 2012
Severe skeletal toxicity from protracted etidronate therapy for generalized arterial calcification of infancyJesse E Otero, Gary S Gottesman, William H McAlister, et al.
International Journal of Food Microbiology|July 30, 2004
Occurrence of Campylobacter in retail foods in IrelandP Whyte, K McGill, D Cowley, et al.
Human Molecular Genetics|December 14, 2001
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneE Cleiren, O Bénichou, E Van Hul, et al.
The New England Journal of Medicine|January 11, 2002
Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasiaEileen M Shore, Jaimo Ahn, Suzanne Jan de Beur, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 19, 2007
Enzyme replacement therapy for murine hypophosphatasiaJosé Luis Millán, Sonoko Narisawa, Isabelle Lemire, et al.
Pageof 46