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Suzanne Hart

Showing results (21-30 of 37) with videos related to

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Human Mutation|June 4, 2008
A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP geneDianalee A McKnight, P Suzanne Hart, Thomas C Hart, et al.
Head & Face Medicine|February 3, 2007
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfectaMaria C L G Santos, P Suzanne Hart, Mukundhan Ramaswami, et al.
Journal of Periodontology|December 8, 2005
Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre SyndromeN Arzu Cagli, Sema S Hakki, Recep Dursun, et al.
JIMD Reports|February 23, 2013
Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C diseasePranoot Tanpaiboon, Jennifer L Sloan, Patrick F Callahan, et al.
Journal of Dental Education|April 9, 2008
Genetics and its implications for clinical dental practice and education: report of panel 3 of the Macy studyLynn Johnson, Robert J Genco, Caroline Damsky, et al.
American Journal of Human Genetics|February 28, 2002
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1Thomas C Hart, Yingze Zhang, Michael C Gorry, et al.
Bone|October 24, 2007
A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitroSun Jin Choi, In Sun Song, Ok Hee Ryu, et al.
The Journal of Biological Chemistry|February 25, 2005
Proteolysis of macrophage inflammatory protein-1alpha isoforms LD78beta and LD78alpha by neutrophil-derived serine proteasesOk Hee Ryu, Sun Jin Choi, Erhan Firatli, et al.
American Journal of Medical Genetics. Part A|March 3, 2012
Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading systemRafael Denadai, Cassio E Raposo-Amaral, Débora Bertola, et al.
Cells, Tissues, Organs|August 21, 2008
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4J Timothy Wright, Thomas C Hart, P Suzanne Hart, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Human Mutation|June 4, 2008
A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP geneDianalee A McKnight, P Suzanne Hart, Thomas C Hart, et al.
Head & Face Medicine|February 3, 2007
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfectaMaria C L G Santos, P Suzanne Hart, Mukundhan Ramaswami, et al.
Journal of Periodontology|December 8, 2005
Clinical, genetic, and biochemical findings in two siblings with Papillon-Lefèvre SyndromeN Arzu Cagli, Sema S Hakki, Recep Dursun, et al.
JIMD Reports|February 23, 2013
Noncompaction of the ventricular myocardium and hydrops fetalis in cobalamin C diseasePranoot Tanpaiboon, Jennifer L Sloan, Patrick F Callahan, et al.
Journal of Dental Education|April 9, 2008
Genetics and its implications for clinical dental practice and education: report of panel 3 of the Macy studyLynn Johnson, Robert J Genco, Caroline Damsky, et al.
American Journal of Human Genetics|February 28, 2002
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1Thomas C Hart, Yingze Zhang, Michael C Gorry, et al.
Bone|October 24, 2007
A 4 bp deletion mutation in DLX3 enhances osteoblastic differentiation and bone formation in vitroSun Jin Choi, In Sun Song, Ok Hee Ryu, et al.
The Journal of Biological Chemistry|February 25, 2005
Proteolysis of macrophage inflammatory protein-1alpha isoforms LD78beta and LD78alpha by neutrophil-derived serine proteasesOk Hee Ryu, Sun Jin Choi, Erhan Firatli, et al.
American Journal of Medical Genetics. Part A|March 3, 2012
Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading systemRafael Denadai, Cassio E Raposo-Amaral, Débora Bertola, et al.
Cells, Tissues, Organs|August 21, 2008
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4J Timothy Wright, Thomas C Hart, P Suzanne Hart, et al.
Pageof 4