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C Hart

Showing results (801-810 of 1,012) with videos related to

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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.
The Journal of Pharmacology and Experimental Therapeutics|October 15, 2005
Improved bioavailability of the mGlu2/3 receptor agonist LY354740 using a prodrug strategy: in vivo pharmacology of LY544344Linda M Rorick-Kehn, Everett J Perkins, Karen M Knitowski, 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.
Journal of Periodontology|March 15, 2018
Gingival Epithelial Cell Expression of Macrophage Inflammatory Protein-1α Induced by Interleukin-1β and LipopolysaccharideOk H Ryu, Sun J Choi, Ana Maria G Linares, et al.
Journal of Health, Population, and Nutrition|August 16, 2001
Influence of placental malaria infection and maternal hypergammaglobulinaemia on materno-foetal transfer of measles and tetanus antibodies in a rural west African populationB J Okoko, L H Wesuperuma, M O Ota, et al.
Molecular Urology|February 24, 2001
Overview consensus statement. Fifth International Conference on Neoadjuvant Hormonal Therapy for Prostate CancerM B Garnick, W R Fair, D Bostwick, et al.
Journal of Periodontology|August 3, 2007
Gingival epithelial cell expression of macrophage inflammatory protein-1alpha induced by interleukin-1beta and lipopolysaccharideOk H Ryu, Sun J Choi, Ana Maria G Linares, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 11, 2011
Local RNA translation at the synapse and in diseaseLiqun Liu-Yesucevitz, Gary J Bassell, Aaron D Gitler, 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.
Neurology|June 15, 2007
Neurological findings in aminoacylase 1 deficiencyJ O Sass, H Olbrich, V Mohr, et al.
Pageof 102

Showing results (801-810 of 1,012) with videos related to

Sort By:
Pageof 102
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.
The Journal of Pharmacology and Experimental Therapeutics|October 15, 2005
Improved bioavailability of the mGlu2/3 receptor agonist LY354740 using a prodrug strategy: in vivo pharmacology of LY544344Linda M Rorick-Kehn, Everett J Perkins, Karen M Knitowski, 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.
Journal of Periodontology|March 15, 2018
Gingival Epithelial Cell Expression of Macrophage Inflammatory Protein-1α Induced by Interleukin-1β and LipopolysaccharideOk H Ryu, Sun J Choi, Ana Maria G Linares, et al.
Journal of Health, Population, and Nutrition|August 16, 2001
Influence of placental malaria infection and maternal hypergammaglobulinaemia on materno-foetal transfer of measles and tetanus antibodies in a rural west African populationB J Okoko, L H Wesuperuma, M O Ota, et al.
Molecular Urology|February 24, 2001
Overview consensus statement. Fifth International Conference on Neoadjuvant Hormonal Therapy for Prostate CancerM B Garnick, W R Fair, D Bostwick, et al.
Journal of Periodontology|August 3, 2007
Gingival epithelial cell expression of macrophage inflammatory protein-1alpha induced by interleukin-1beta and lipopolysaccharideOk H Ryu, Sun J Choi, Ana Maria G Linares, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 11, 2011
Local RNA translation at the synapse and in diseaseLiqun Liu-Yesucevitz, Gary J Bassell, Aaron D Gitler, 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.
Neurology|June 15, 2007
Neurological findings in aminoacylase 1 deficiencyJ O Sass, H Olbrich, V Mohr, et al.
Pageof 102