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P S Hart

Showing results (31-40 of 52) with videos related to

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Archives of Oral Biology|April 5, 2001
Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfectaD Pallos, P S Hart, J R Cortelli, et al.
Journal of Dental Research|May 2, 2009
Phenotypic variation in FAM83H-associated amelogenesis imperfectaJ T Wright, S Frazier-Bowers, D Simmons, et al.
Cytogenetics and Cell Genetics|June 14, 2002
Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21Y Zhang, M C Gorry, P S Hart, et al.
Journal of Dental Research|October 26, 2005
MMP20 active-site mutation in hypomaturation amelogenesis imperfectaD Ozdemir, P S Hart, O H Ryu, et al.
Anesthesiology|April 1, 1995
Edrophonium increases mivacurium concentrations during constant mivacurium infusion, and large doses minimally antagonize paralysisP S Hart, P M Wright, R Brown, et al.
Human Mutation|July 12, 2002
Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndromeY Zhang, P S Hart, A J Moretti, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Archives of Oral Biology|April 5, 2001
Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfectaD Pallos, P S Hart, J R Cortelli, et al.
Journal of Dental Research|May 2, 2009
Phenotypic variation in FAM83H-associated amelogenesis imperfectaJ T Wright, S Frazier-Bowers, D Simmons, et al.
Cytogenetics and Cell Genetics|June 14, 2002
Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22-->p21Y Zhang, M C Gorry, P S Hart, et al.
Journal of Dental Research|October 26, 2005
MMP20 active-site mutation in hypomaturation amelogenesis imperfectaD Ozdemir, P S Hart, O H Ryu, et al.
Anesthesiology|April 1, 1995
Edrophonium increases mivacurium concentrations during constant mivacurium infusion, and large doses minimally antagonize paralysisP S Hart, P M Wright, R Brown, et al.
Human Mutation|July 12, 2002
Biochemical and mutational analyses of the cathepsin c gene (CTSC) in three North American families with Papillon Lefèvre syndromeY Zhang, P S Hart, A J Moretti, et al.
Gastroenterology|September 13, 2000
SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitisR H Pfützer, M M Barmada, A P Brunskill, et al.
Journal of Medical Genetics|December 14, 1999
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndromeT C Hart, P S Hart, D W Bowden, et al.
Journal of Medical Genetics|March 4, 2005
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaJ-W Kim, J P Simmer, T C Hart, et al.
Clinical Genetics|February 18, 2009
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfectaP S Hart, S Becerik, D Cogulu, et al.
Pageof 6