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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+/- mice
Sisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Nano Letters
|
June 15, 2012
A facile, one-step nanocarbon functionalization for biomedical applications
Magdalena 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 imperfecta
Elena 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 imperfecta
Elena 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 mutations
Aileen 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 bone
Kit 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 imperfecta
Wayne 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 imperfecta
Cristina Panaroni, Roberta Gioia, Anna Lupi, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 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+/- mice
Sisi Liu, Emmanouil Saloustros, Edward L Mertz, et al.
Nano Letters
|
June 15, 2012
A facile, one-step nanocarbon functionalization for biomedical applications
Magdalena 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 imperfecta
Elena 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 imperfecta
Elena 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 mutations
Aileen 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 bone
Kit 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 imperfecta
Wayne 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 imperfecta
Cristina Panaroni, Roberta Gioia, Anna Lupi, et al.
Page
of 2