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Alan Boyde

Showing results (61-70 of 70) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 7, 2010
Optimal bone strength and mineralization requires the type 2 iodothyronine deiodinase in osteoblastsJ H Duncan Bassett, Alan Boyde, Peter G T Howell, et al.
Molecular Endocrinology (Baltimore, Md.)|October 13, 2007
A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidismJ H Duncan Bassett, Allan J Williams, Elaine Murphy, et al.
Endocrinology|May 29, 2015
Thyrostimulin Regulates Osteoblastic Bone Formation During Early Skeletal DevelopmentJ H Duncan Bassett, Anne van der Spek, John G Logan, et al.
Plos Genetics|August 10, 2012
Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strengthJ H Duncan Bassett, Apostolos Gogakos, Jacqueline K White, et al.
Bone|April 19, 2011
The relationship between the chemistry and biological activity of the bisphosphonatesFrank H Ebetino, Anne-Marie L Hogan, Shuting Sun, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 14, 2011
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imagingAngelo Karunaratne, Christopher R Esapa, Jennifer Hiller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 27, 2011
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutationChristopher T Esapa, Tertius A Hough, Sarah Testori, et al.
Nature Communications|January 21, 2021
Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature Communications|May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain MalformationLong Guo, Débora Romeo Bertola, Asako Takanohashi, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Proceedings of the National Academy of Sciences of the United States of America|April 7, 2010
Optimal bone strength and mineralization requires the type 2 iodothyronine deiodinase in osteoblastsJ H Duncan Bassett, Alan Boyde, Peter G T Howell, et al.
Molecular Endocrinology (Baltimore, Md.)|October 13, 2007
A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidismJ H Duncan Bassett, Allan J Williams, Elaine Murphy, et al.
Endocrinology|May 29, 2015
Thyrostimulin Regulates Osteoblastic Bone Formation During Early Skeletal DevelopmentJ H Duncan Bassett, Anne van der Spek, John G Logan, et al.
Plos Genetics|August 10, 2012
Rapid-throughput skeletal phenotyping of 100 knockout mice identifies 9 new genes that determine bone strengthJ H Duncan Bassett, Apostolos Gogakos, Jacqueline K White, et al.
Bone|April 19, 2011
The relationship between the chemistry and biological activity of the bisphosphonatesFrank H Ebetino, Anne-Marie L Hogan, Shuting Sun, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 14, 2011
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imagingAngelo Karunaratne, Christopher R Esapa, Jennifer Hiller, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 27, 2011
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutationChristopher T Esapa, Tertius A Hough, Sarah Testori, et al.
Nature Communications|January 21, 2021
Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature Communications|May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
American Journal of Human Genetics|April 16, 2019
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain MalformationLong Guo, Débora Romeo Bertola, Asako Takanohashi, et al.
Pageof 7