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Showing results (521-530 of 852) with videos related to

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Journal of Neuromuscular Diseases|September 13, 2021
Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular DystrophyR Quinlivan, B Messer, P Murphy, et al.
Physiological Reports|April 30, 2019
Cardiac-specific ablation of glutaredoxin 3 leads to cardiac hypertrophy and heart failureJimmonique Donelson, Qiongling Wang, Tanner O Monroe, 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.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
The Journal of Experimental Medicine|April 2, 2020
Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathwayHeeseog Kang, Smita Jha, Aleksandra Ivovic, et al.
Journal of Clinical Pharmacology|February 27, 2007
Pharmacokinetics and safety of golimumab, a fully human anti-TNF-alpha monoclonal antibody, in subjects with rheumatoid arthritisHonghui Zhou, Haishan Jang, Roy M Fleischmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfectaWayne A Cabral, Aileen M Barnes, Adebowale Adeyemo, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 2020
Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasiaWayne A Cabral, Nadja Fratzl-Zelman, MaryAnn Weis, et al.
Elife|February 28, 2016
Tumor microenvironment derived exosomes pleiotropically modulate cancer cell metabolismHongyun Zhao, Lifeng Yang, Joelle Baddour, et al.
Pageof 86

Showing results (521-530 of 852) with videos related to

Sort By:
Pageof 86
Journal of Neuromuscular Diseases|September 13, 2021
Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular DystrophyR Quinlivan, B Messer, P Murphy, et al.
Physiological Reports|April 30, 2019
Cardiac-specific ablation of glutaredoxin 3 leads to cardiac hypertrophy and heart failureJimmonique Donelson, Qiongling Wang, Tanner O Monroe, 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.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
The Journal of Experimental Medicine|April 2, 2020
Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathwayHeeseog Kang, Smita Jha, Aleksandra Ivovic, et al.
Journal of Clinical Pharmacology|February 27, 2007
Pharmacokinetics and safety of golimumab, a fully human anti-TNF-alpha monoclonal antibody, in subjects with rheumatoid arthritisHonghui Zhou, Haishan Jang, Roy M Fleischmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 28, 2012
A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfectaWayne A Cabral, Aileen M Barnes, Adebowale Adeyemo, et al.
Neurology|January 28, 2012
GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsyP Striano, Y G Weber, M R Toliat, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 2020
Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasiaWayne A Cabral, Nadja Fratzl-Zelman, MaryAnn Weis, et al.
Elife|February 28, 2016
Tumor microenvironment derived exosomes pleiotropically modulate cancer cell metabolismHongyun Zhao, Lifeng Yang, Joelle Baddour, et al.
Pageof 86