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Pierre Moffatt

Showing results (41-50 of 59) with videos related to

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Calcified Tissue International|January 28, 2016
Osteogenesis Imperfecta Type VI in Individuals from Northern CanadaLeanne Ward, Ghalib Bardai, Pierre Moffatt, et al.
Bone|November 28, 2017
Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in miceFrank Rauch, Yeqing Geng, Lisa Lamplugh, et al.
Scientific Reports|April 25, 2017
Interactions of AMTN, ODAM and SCPPPQ1 proteins of a specialized basal lamina that attaches epithelial cells to tooth mineralAurélien Fouillen, Juliana Dos Santos Neves, Charline Mary, et al.
Calcified Tissue International|October 20, 2015
Osteogenesis Imperfecta Type I Caused by COL1A1 DeletionsGhalib Bardai, Emmanuelle Lemyre, Pierre Moffatt, et al.
Bone|April 15, 2015
The effect of SERPINF1 in-frame mutations in osteogenesis imperfecta type VIHadil Al-Jallad, Telma Palomo, Peter Roughley, et al.
Bone|April 3, 2022
Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variantKarissa Ludwig, Leanne M Ward, Nasrin Khan, et al.
Bone|July 11, 2014
Skeletal characteristics associated with homozygous and heterozygous WNT1 mutationsTelma Palomo, Hadil Al-Jallad, Pierre Moffatt, et al.
The Journal of Biological Chemistry|October 24, 2007
Osteocrin is a specific ligand of the natriuretic Peptide clearance receptor that modulates bone growthPierre Moffatt, Gethin Thomas, Karine Sellin, et al.
The Journal of Biological Chemistry|October 3, 2003
Osteocrin, a novel bone-specific secreted protein that modulates the osteoblast phenotypeGethin Thomas, Pierre Moffatt, Patrick Salois, et al.
Human Molecular Genetics|September 13, 2014
A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in childrenSomayyeh Fahiminiya, Hadil Al-Jallad, Jacek Majewski, et al.
Pageof 6

Showing results (41-50 of 59) with videos related to

Sort By:
Pageof 6
Calcified Tissue International|January 28, 2016
Osteogenesis Imperfecta Type VI in Individuals from Northern CanadaLeanne Ward, Ghalib Bardai, Pierre Moffatt, et al.
Bone|November 28, 2017
Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in miceFrank Rauch, Yeqing Geng, Lisa Lamplugh, et al.
Scientific Reports|April 25, 2017
Interactions of AMTN, ODAM and SCPPPQ1 proteins of a specialized basal lamina that attaches epithelial cells to tooth mineralAurélien Fouillen, Juliana Dos Santos Neves, Charline Mary, et al.
Calcified Tissue International|October 20, 2015
Osteogenesis Imperfecta Type I Caused by COL1A1 DeletionsGhalib Bardai, Emmanuelle Lemyre, Pierre Moffatt, et al.
Bone|April 15, 2015
The effect of SERPINF1 in-frame mutations in osteogenesis imperfecta type VIHadil Al-Jallad, Telma Palomo, Peter Roughley, et al.
Bone|April 3, 2022
Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variantKarissa Ludwig, Leanne M Ward, Nasrin Khan, et al.
Bone|July 11, 2014
Skeletal characteristics associated with homozygous and heterozygous WNT1 mutationsTelma Palomo, Hadil Al-Jallad, Pierre Moffatt, et al.
The Journal of Biological Chemistry|October 24, 2007
Osteocrin is a specific ligand of the natriuretic Peptide clearance receptor that modulates bone growthPierre Moffatt, Gethin Thomas, Karine Sellin, et al.
The Journal of Biological Chemistry|October 3, 2003
Osteocrin, a novel bone-specific secreted protein that modulates the osteoblast phenotypeGethin Thomas, Pierre Moffatt, Patrick Salois, et al.
Human Molecular Genetics|September 13, 2014
A polyadenylation site variant causes transcript-specific BMP1 deficiency and frequent fractures in childrenSomayyeh Fahiminiya, Hadil Al-Jallad, Jacek Majewski, et al.
Pageof 6