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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 14, 2012
Hexa-D-arginine treatment increases 7B2•PC2 activity in hyp-mouse osteoblasts and rescues the HYP phenotype
Baozhi Yuan, Jian Q Feng, Stephen Bowman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 9, 2014
FGF23 is endogenously phosphorylated in bone cells
Iris Lindberg, Hong Weng Pang, Joseph P Stains, et al.
Nature Structural Biology
|
June 10, 2003
The crystal structure of the proprotein processing proteinase furin explains its stringent specificity
Stefan Henrich, Angus Cameron, Gleb P Bourenkov, et al.
Plos Pathogens
|
August 11, 2017
Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy
Elizaveta Katorcha, Natallia Makarava, Young Jin Lee, et al.
Molecular Pharmacology
|
December 17, 2008
Synthetic small-molecule prohormone convertase 2 inhibitors
Dorota Kowalska, Jin Liu, Jon R Appel, et al.
Biological Chemistry
|
July 20, 2010
Effects of magnesium ions on recombinant human furin: selective activation of hydrolytic activity upon substrates derived from virus envelope glycoprotein
Mario A Izidoro, Diego M Assis, Vitor Oliveira, et al.
Endocrinology
|
May 10, 2005
Strain-dependent influences on the hypothalamo-pituitary-adrenal axis profoundly affect the 7B2 and PC2 null phenotypes
Juan R Peinado, Virginie Laurent, Sang-Nam Lee, et al.
The Journal of Biological Chemistry
|
November 23, 2012
The neuroendocrine protein 7B2 suppresses the aggregation of neurodegenerative disease-related proteins
Michael Helwig, Akina Hoshino, Casey Berridge, et al.
Endocrinology
|
March 4, 2022
The G209R mutant mouse as a model for human PCSK1 polyendocrinopathy
Manita Shakya, Surbhi Gahlot, Nicolle K Martin, et al.
Endocrinology
|
May 16, 2014
Defective transport of the obesity mutant PC1/3 N222D contributes to loss of function
Yogikala Prabhu, Elias H Blanco, Ming Liu, et al.
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of 10
Search research articles
Search
Showing results (61-70 of 96) with videos related to
Sort By:
Page
of 10
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 14, 2012
Hexa-D-arginine treatment increases 7B2•PC2 activity in hyp-mouse osteoblasts and rescues the HYP phenotype
Baozhi Yuan, Jian Q Feng, Stephen Bowman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 9, 2014
FGF23 is endogenously phosphorylated in bone cells
Iris Lindberg, Hong Weng Pang, Joseph P Stains, et al.
Nature Structural Biology
|
June 10, 2003
The crystal structure of the proprotein processing proteinase furin explains its stringent specificity
Stefan Henrich, Angus Cameron, Gleb P Bourenkov, et al.
Plos Pathogens
|
August 11, 2017
Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy
Elizaveta Katorcha, Natallia Makarava, Young Jin Lee, et al.
Molecular Pharmacology
|
December 17, 2008
Synthetic small-molecule prohormone convertase 2 inhibitors
Dorota Kowalska, Jin Liu, Jon R Appel, et al.
Biological Chemistry
|
July 20, 2010
Effects of magnesium ions on recombinant human furin: selective activation of hydrolytic activity upon substrates derived from virus envelope glycoprotein
Mario A Izidoro, Diego M Assis, Vitor Oliveira, et al.
Endocrinology
|
May 10, 2005
Strain-dependent influences on the hypothalamo-pituitary-adrenal axis profoundly affect the 7B2 and PC2 null phenotypes
Juan R Peinado, Virginie Laurent, Sang-Nam Lee, et al.
The Journal of Biological Chemistry
|
November 23, 2012
The neuroendocrine protein 7B2 suppresses the aggregation of neurodegenerative disease-related proteins
Michael Helwig, Akina Hoshino, Casey Berridge, et al.
Endocrinology
|
March 4, 2022
The G209R mutant mouse as a model for human PCSK1 polyendocrinopathy
Manita Shakya, Surbhi Gahlot, Nicolle K Martin, et al.
Endocrinology
|
May 16, 2014
Defective transport of the obesity mutant PC1/3 N222D contributes to loss of function
Yogikala Prabhu, Elias H Blanco, Ming Liu, et al.
Page
of 10