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Michael P Whyte

Showing results (51-60 of 165) with videos related to

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Molecular Genetics and Metabolism|February 22, 2002
Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasiaSteven Mumm, Jonathan Jones, Patrick Finnegan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 7, 2024
Skeletal fluorosis: an uncommon cause, yet a rescue treatment?Julia Rose R Shariff, Khine Mon Swe, Neil Binkley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 8, 2006
Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosisSteven Mumm, Deborah Wenkert, Xiafang Zhang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 5, 2011
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligandMichael P Whyte, William G Totty, Deborah V Novack, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 26, 2010
Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disordersMichael P Whyte, Lydia G Kempa, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 2, 2011
Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1Michael P Whyte, Deborah Wenkert, Jennifer L Demertzis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 26, 2013
Acute severe hypercalcemia after traumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failureMichael P Whyte, Rattana Leelawattana, William R Reinus, et al.
Bone|January 11, 2020
Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANKSean J Iwamoto, Micol S Rothman, Shenghui Duan, et al.
Genomics|November 10, 2004
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPaseM Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
JBMR Plus|April 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6Michael P Whyte, Steven Mumm, Jonathan C Baker, et al.
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
Molecular Genetics and Metabolism|February 22, 2002
Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasiaSteven Mumm, Jonathan Jones, Patrick Finnegan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 7, 2024
Skeletal fluorosis: an uncommon cause, yet a rescue treatment?Julia Rose R Shariff, Khine Mon Swe, Neil Binkley, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 8, 2006
Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosisSteven Mumm, Deborah Wenkert, Xiafang Zhang, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 5, 2011
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligandMichael P Whyte, William G Totty, Deborah V Novack, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 26, 2010
Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disordersMichael P Whyte, Lydia G Kempa, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 2, 2011
Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1Michael P Whyte, Deborah Wenkert, Jennifer L Demertzis, et al.
The Journal of Clinical Endocrinology and Metabolism|September 26, 2013
Acute severe hypercalcemia after traumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failureMichael P Whyte, Rattana Leelawattana, William R Reinus, et al.
Bone|January 11, 2020
Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANKSean J Iwamoto, Micol S Rothman, Shenghui Duan, et al.
Genomics|November 10, 2004
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPaseM Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
JBMR Plus|April 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6Michael P Whyte, Steven Mumm, Jonathan C Baker, et al.
Pageof 17