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JCI Insight
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March 2, 2021
Micro-dystrophin gene therapy prevents heart failure in an improved Duchenne muscular dystrophy cardiomyopathy mouse model
Zachary M Howard, Lisa E Dorn, Jeovanna Lowe, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 1, 1993
Evaluation of pulmonary systemic blood flow using ECG gated acquisition
J J de Lima, M F Botelho, J A Rafael, et al.
The Journal of Experimental Medicine
|
August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy
D S Chao, J R Gorospe, J E Brenman, et al.
European Journal of Nuclear Medicine
|
January 1, 1991
Ventilation and perfusion display in a single image
J J de Lima, M F Botelho, A M Pereira, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 2, 2012
Sustaining cardiac claudin-5 levels prevents functional hallmarks of cardiomyopathy in a muscular dystrophy mouse model
Dawn A Delfín, Ying Xu, Kevin E Schill, et al.
American Journal of Physiology. Cell Physiology
|
January 19, 2022
Myeloid mineralocorticoid receptors contribute to skeletal muscle repair in muscular dystrophy and acute muscle injury
Zachary M Howard, Neha Rastogi, Jeovanna Lowe, et al.
Cell
|
August 22, 1997
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
A E Deconinck, J A Rafael, J A Skinner, et al.
Proceedings. Biological Sciences
|
June 26, 2023
300 Million years of coral treaders (Insecta: Heteroptera: Hermatobatidae) back to the ocean in the phylogenetic context of Arthropoda
Yan-Hui Wang, Yun-Xia Luan, Jiu-Yang Luo, et al.
Frontiers in Physiology
|
March 18, 2021
Is Upregulation of Sarcolipin Beneficial or Detrimental to Muscle Function?
Naresh C Bal, Subash C Gupta, Meghna Pant, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
January 6, 2026
Inflammation in a severe model of dystrophic cardiomyopathy contains a high proportion of T cells that contribute to onset of pathology
Arden B Piepho, Swathy Krishna, Sarah L Sturgill, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 153) with videos related to
Sort By:
Page
of 16
JCI Insight
|
March 2, 2021
Micro-dystrophin gene therapy prevents heart failure in an improved Duchenne muscular dystrophy cardiomyopathy mouse model
Zachary M Howard, Lisa E Dorn, Jeovanna Lowe, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 1, 1993
Evaluation of pulmonary systemic blood flow using ECG gated acquisition
J J de Lima, M F Botelho, J A Rafael, et al.
The Journal of Experimental Medicine
|
August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy
D S Chao, J R Gorospe, J E Brenman, et al.
European Journal of Nuclear Medicine
|
January 1, 1991
Ventilation and perfusion display in a single image
J J de Lima, M F Botelho, A M Pereira, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 2, 2012
Sustaining cardiac claudin-5 levels prevents functional hallmarks of cardiomyopathy in a muscular dystrophy mouse model
Dawn A Delfín, Ying Xu, Kevin E Schill, et al.
American Journal of Physiology. Cell Physiology
|
January 19, 2022
Myeloid mineralocorticoid receptors contribute to skeletal muscle repair in muscular dystrophy and acute muscle injury
Zachary M Howard, Neha Rastogi, Jeovanna Lowe, et al.
Cell
|
August 22, 1997
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
A E Deconinck, J A Rafael, J A Skinner, et al.
Proceedings. Biological Sciences
|
June 26, 2023
300 Million years of coral treaders (Insecta: Heteroptera: Hermatobatidae) back to the ocean in the phylogenetic context of Arthropoda
Yan-Hui Wang, Yun-Xia Luan, Jiu-Yang Luo, et al.
Frontiers in Physiology
|
March 18, 2021
Is Upregulation of Sarcolipin Beneficial or Detrimental to Muscle Function?
Naresh C Bal, Subash C Gupta, Meghna Pant, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
January 6, 2026
Inflammation in a severe model of dystrophic cardiomyopathy contains a high proportion of T cells that contribute to onset of pathology
Arden B Piepho, Swathy Krishna, Sarah L Sturgill, et al.
Page
of 16