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Edward L Mertz

Showing results (11-20 of 18) with videos related to

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Human Molecular Genetics|August 7, 2015
Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- miceSisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Nano Letters|June 15, 2012
A facile, one-step nanocarbon functionalization for biomedical applicationsMagdalena Swierczewska, Ki Young Choi, Edward L Mertz, et al.
The Journal of Biological Chemistry|December 13, 2007
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfectaElena Makareeva, Edward L Mertz, Natalia V Kuznetsova, et al.
Plos One|July 11, 2018
Substitutions for arginine at position 780 in triple helical domain of the α1(I) chain alter folding of the type I procollagen molecule and cause osteogenesis imperfectaElena Makareeva, Guoli Sun, Lynn S Mirigian, et al.
Human Mutation|May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutationsAileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 28, 2010
Alternate protein kinase A activity identifies a unique population of stromal cells in adult boneKit Man Tsang, Matthew F Starost, Maria Nesterova, et al.
Plos Genetics|June 27, 2014
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaWayne A Cabral, Irina Perdivara, MaryAnn Weis, et al.
Blood|May 6, 2009
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfectaCristina Panaroni, Roberta Gioia, Anna Lupi, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Human Molecular Genetics|August 7, 2015
Haploinsufficiency for either one of the type-II regulatory subunits of protein kinase A improves the bone phenotype of Prkar1a+/- miceSisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Nano Letters|June 15, 2012
A facile, one-step nanocarbon functionalization for biomedical applicationsMagdalena Swierczewska, Ki Young Choi, Edward L Mertz, et al.
The Journal of Biological Chemistry|December 13, 2007
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfectaElena Makareeva, Edward L Mertz, Natalia V Kuznetsova, et al.
Plos One|July 11, 2018
Substitutions for arginine at position 780 in triple helical domain of the α1(I) chain alter folding of the type I procollagen molecule and cause osteogenesis imperfectaElena Makareeva, Guoli Sun, Lynn S Mirigian, et al.
Human Mutation|May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutationsAileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 28, 2010
Alternate protein kinase A activity identifies a unique population of stromal cells in adult boneKit Man Tsang, Matthew F Starost, Maria Nesterova, et al.
Plos Genetics|June 27, 2014
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaWayne A Cabral, Irina Perdivara, MaryAnn Weis, et al.
Blood|May 6, 2009
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfectaCristina Panaroni, Roberta Gioia, Anna Lupi, et al.
Pageof 2