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Circulation
|
July 20, 2005
Epidermal growth factor receptor blockade mediates smooth muscle cell apoptosis and improves survival in rats with pulmonary hypertension
Sandra L Merklinger, Peter L Jones, Eliana C Martinez, et al.
Disease Models & Mechanisms
|
April 7, 2026
Transgenic mouse models for investigating human DUX4 expression during development and its roles in FSHD pathophysiology
Yosuke Hiramuki, Charis L Himeda, Peter L Jones, et al.
Neuromuscular Disorders : NMD
|
February 6, 2017
Large family cohorts of lymphoblastoid cells provide a new cellular model for investigating facioscapulohumeral muscular dystrophy
Takako I Jones, Charis L Himeda, Daniel P Perez, et al.
International Journal of Clinical and Experimental Pathology
|
May 22, 2010
Testing the effects of FSHD candidate gene expression in vertebrate muscle development
Ryan D Wuebbles, Steven W Long, Meredith L Hanel, et al.
Tissue Engineering. Part A
|
May 15, 2014
Engineering de novo assembly of fetal pulmonary organoids
Mark J Mondrinos, Peter L Jones, Christine M Finck, et al.
Bioscience Reports
|
November 13, 2010
A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
Steven W Long, Jenny Y Y Ooi, Peter M Yau, et al.
The Journal of Biological Chemistry
|
July 29, 2003
Platelet-derived growth factor-BB-mediated activation of Akt suppresses smooth muscle-specific gene expression through inhibition of mitogen-activated protein kinase and redistribution of serum response factor
Nihal Kaplan-Albuquerque, Chrystelle Garat, Christina Desseva, et al.
The Journal of Heart Valve Disease
|
October 3, 2002
Thymosin beta4 regulation, expression and function in aortic valve interstitial cells
Quan-Yi Li, Peter L Jones, Robert P Lafferty, et al.
Journal of Cell Science
|
March 11, 2010
Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites
Qian Liu, Takako Iida Jones, Vivian W Tang, et al.
Human Molecular Genetics
|
February 10, 2024
Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy
Andreia M Nunes, Monique M Ramirez, Enrique Garcia-Collazo, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Circulation
|
July 20, 2005
Epidermal growth factor receptor blockade mediates smooth muscle cell apoptosis and improves survival in rats with pulmonary hypertension
Sandra L Merklinger, Peter L Jones, Eliana C Martinez, et al.
Disease Models & Mechanisms
|
April 7, 2026
Transgenic mouse models for investigating human DUX4 expression during development and its roles in FSHD pathophysiology
Yosuke Hiramuki, Charis L Himeda, Peter L Jones, et al.
Neuromuscular Disorders : NMD
|
February 6, 2017
Large family cohorts of lymphoblastoid cells provide a new cellular model for investigating facioscapulohumeral muscular dystrophy
Takako I Jones, Charis L Himeda, Daniel P Perez, et al.
International Journal of Clinical and Experimental Pathology
|
May 22, 2010
Testing the effects of FSHD candidate gene expression in vertebrate muscle development
Ryan D Wuebbles, Steven W Long, Meredith L Hanel, et al.
Tissue Engineering. Part A
|
May 15, 2014
Engineering de novo assembly of fetal pulmonary organoids
Mark J Mondrinos, Peter L Jones, Christine M Finck, et al.
Bioscience Reports
|
November 13, 2010
A brain-derived MeCP2 complex supports a role for MeCP2 in RNA processing
Steven W Long, Jenny Y Y Ooi, Peter M Yau, et al.
The Journal of Biological Chemistry
|
July 29, 2003
Platelet-derived growth factor-BB-mediated activation of Akt suppresses smooth muscle-specific gene expression through inhibition of mitogen-activated protein kinase and redistribution of serum response factor
Nihal Kaplan-Albuquerque, Chrystelle Garat, Christina Desseva, et al.
The Journal of Heart Valve Disease
|
October 3, 2002
Thymosin beta4 regulation, expression and function in aortic valve interstitial cells
Quan-Yi Li, Peter L Jones, Robert P Lafferty, et al.
Journal of Cell Science
|
March 11, 2010
Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites
Qian Liu, Takako Iida Jones, Vivian W Tang, et al.
Human Molecular Genetics
|
February 10, 2024
Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy
Andreia M Nunes, Monique M Ramirez, Enrique Garcia-Collazo, et al.
Page
of 8