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Bryan M Reid

Showing results (1-10 of 6) with videos related to

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The Review of Scientific Instruments|July 2, 2009
Method for analyzing E x B probe spectra from Hall thruster plumesRohit Shastry, Richard R Hofer, Bryan M Reid, et al.
Connective Tissue Research|August 27, 2014
Ameloblast transcriptome changes from secretory to maturation stagesJames P Simmer, Amelia S Richardson, Shih-Kai Wang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|December 3, 2014
Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutationCurtis R Herzog, Bryan M Reid, Figen Seymen, et al.
Human Molecular Genetics|December 6, 2013
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfectaShih-Kai Wang, Murim Choi, Amelia S Richardson, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The Review of Scientific Instruments|July 2, 2009
Method for analyzing E x B probe spectra from Hall thruster plumesRohit Shastry, Richard R Hofer, Bryan M Reid, et al.
Connective Tissue Research|August 27, 2014
Ameloblast transcriptome changes from secretory to maturation stagesJames P Simmer, Amelia S Richardson, Shih-Kai Wang, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|December 3, 2014
Hypomaturation amelogenesis imperfecta caused by a novel SLC24A4 mutationCurtis R Herzog, Bryan M Reid, Figen Seymen, et al.
Human Molecular Genetics|December 6, 2013
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfectaShih-Kai Wang, Murim Choi, Amelia S Richardson, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
Pageof 1