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P Whyte

Showing results (411-420 of 454) with videos related to

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Bone|March 4, 2015
Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patientsMichael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasiaK N Fedde, L Blair, J Silverstein, et al.
Bone|July 31, 2024
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorderMichael P Whyte, Robert S Weinstein, Paul H Phillips, et al.
Cell Reports|February 9, 2018
AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein SelectivityCaroline M Gorvin, Angela Rogers, Benoit Hastoy, et al.
Journal of Dental Research|February 27, 2015
Periodontal Defects in the A116T Knock-in Murine Model of OdontohypophosphatasiaB L Foster, C R Sheen, N E Hatch, et al.
The Journal of Clinical Investigation|May 29, 1998
Insulin-like growth factor system abnormalities in hepatitis C-associated osteosclerosis. Potential insights into increasing bone mass in adultsS Khosla, A A Hassoun, B K Baker, et al.
Bone|April 17, 2020
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)Michael P Whyte, Philippe M Campeau, William H McAlister, et al.
Human Molecular Genetics|August 10, 2012
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosisPhilippe M Campeau, James T Lu, Gautam Sule, et al.
Bone|January 20, 2019
Absence of an osteopetrosis phenotype in IKBKG (NEMO) mutation-positive women: A case-control studyMorten Frost, Michaela Tencerova, Christina M Andreasen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 12, 2021
Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked HypophosphatemiaAgnès Linglart, Erik A Imel, Michael P Whyte, et al.
Pageof 46

Showing results (411-420 of 454) with videos related to

Sort By:
Pageof 46
Bone|March 4, 2015
Hypophosphatasia: validation and expansion of the clinical nosology for children from 25 years experience with 173 pediatric patientsMichael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasiaK N Fedde, L Blair, J Silverstein, et al.
Bone|July 31, 2024
Transmembrane protein 53 craniotubular dysplasia (OMIM # 619727): The skeletal disease and consequent blindness of this new disorderMichael P Whyte, Robert S Weinstein, Paul H Phillips, et al.
Cell Reports|February 9, 2018
AP2σ Mutations Impair Calcium-Sensing Receptor Trafficking and Signaling, and Show an Endosomal Pathway to Spatially Direct G-Protein SelectivityCaroline M Gorvin, Angela Rogers, Benoit Hastoy, et al.
Journal of Dental Research|February 27, 2015
Periodontal Defects in the A116T Knock-in Murine Model of OdontohypophosphatasiaB L Foster, C R Sheen, N E Hatch, et al.
The Journal of Clinical Investigation|May 29, 1998
Insulin-like growth factor system abnormalities in hepatitis C-associated osteosclerosis. Potential insights into increasing bone mass in adultsS Khosla, A A Hassoun, B K Baker, et al.
Bone|April 17, 2020
Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)Michael P Whyte, Philippe M Campeau, William H McAlister, et al.
Human Molecular Genetics|August 10, 2012
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosisPhilippe M Campeau, James T Lu, Gautam Sule, et al.
Bone|January 20, 2019
Absence of an osteopetrosis phenotype in IKBKG (NEMO) mutation-positive women: A case-control studyMorten Frost, Michaela Tencerova, Christina M Andreasen, et al.
The Journal of Clinical Endocrinology and Metabolism|October 12, 2021
Sustained Efficacy and Safety of Burosumab, a Monoclonal Antibody to FGF23, in Children With X-Linked HypophosphatemiaAgnès Linglart, Erik A Imel, Michael P Whyte, et al.
Pageof 46