Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Tahseen Mozaffar"'
Autor:
Sameer B. Shah, Ranjan Gupta, Jeffery D. Kocsis, Justin P. Chan, James Clune, Tahseen Mozaffar, Samuel R. Ward, Oswald Steward
Publikováno v:
Muscle & Nerve. 61:390-395
INTRODUCTION After traumatic nerve injury, neuromuscular junction remodeling plays a key role in determining functional outcomes. Immunohistochemical analyses of denervated muscle biopsies may provide valuable prognostic data regarding clinical outco
Publikováno v:
BMC neurology, vol 22, iss 1
Background Proper evaluation of ocular fundi is an integral part of neurological examination. Unfortunately, neurology residents are increasingly uncomfortable performing fundoscopy and interpreting findings because of diminishing skills and lack of
Autor:
Therese T. Cristal, Rodolfo Rios, Gerald Coulis, Adam K. Savage, Tahseen Mozaffar, Brandon S. Hughes, Scott Q. Harper, Jenna M. Kastenschmidt, Rachel E. Ayer, Archis A. Deshpande, S. Armando Villalta, Ali H. Mannaa, Richard M. Locksley, Rayan Yahia, Philip K. Farahat, Carlee R. Giesige, Phillip Pham
Publikováno v:
Cell reports, vol 35, iss 2
Cell reports
Cell Reports, Vol 35, Iss 2, Pp 108997-(2021)
Cell reports
Cell Reports, Vol 35, Iss 2, Pp 108997-(2021)
SUMMARY Despite the well-accepted view that chronic inflammation contributes to the pathogenesis of Duchenne muscular dystrophy (DMD), the function and regulation of eosinophils remain an unclear facet of type II innate immunity in dystrophic muscle.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93634d2ee96482c107503c688e1e7242
https://escholarship.org/uc/item/57k699x2
https://escholarship.org/uc/item/57k699x2
Autor:
Conrad C. Weihl, Tahseen Mozaffar, Michael Hunter, Matthew Wicklund, Chad Heatwole, Nicholas E. Johnson, Jeffrey Statland
Publikováno v:
Muscle & Nerve. 60:419-424
Introduction Limb-girdle muscular dystrophy (LGMD) consists of over 30 genetic conditions with varying clinical phenotypes primarily affecting pelvic girdle, shoulder girdle, and other proximal limb muscles. Studies focusing on the physical, mental,
Autor:
Carlee R. Giesige, Adam K. Savage, Phillip Pham, Rayan Yahia, Richard M. Locksley, S. Armando Villalta, Rodolfo Rios, Ali H. Mannaa, Tahseen Mozaffar, Rachel E. Ayer, Gerald Coulis, Jenna M. Kastenschmidt, Scott Q. Harper
Publikováno v:
SSRN Electronic Journal.
Chronic muscle inflammation contributes to the pathogenesis of Duchenne muscular dystrophy (DMD), a lethal muscle disorder attributed to dystrophin gene mutations. However, the function and regulation of eosinophilia, an unappreciated facet of type I
Autor:
Jenna M. Kastenschmidt, Kyle L. Ellefsen, Ali H. Mannaa, Jesse J. Giebel, Rayan Yahia, Rachel E. Ayer, Phillip Pham, Rodolfo Rios, Sylvia A. Vetrone, Tahseen Mozaffar, S. Armando Villalta
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology
Frontiers in Physiology
Skeletal muscle injury provokes a regenerative response, characterized by the de novo generation of myofibers that are distinguished by central nucleation and re-expression of developmentally restricted genes. In addition to these characteristics, my
Publikováno v:
Experimental Neurology. 271:84-94
The secreted protein desert hedgehog (dhh) controls the formation of the nerve perineurium during development and is a key component of Schwann cells that ensures peripheral nerve survival. We postulated that dhh may play a critical role in maintaini
Autor:
Tahseen Mozaffar, Namita Goyal
Publikováno v:
Current Treatment Options in Neurology. 20
The purpose of this review is to update the audience on the recent progress in the treatment of idiopathic inflammatory myopathies, highlighting a myriad of treatment trials aimed at slowing down progression of muscle weakness and/or skin involvement
Autor:
Hal Landy, Robin H. Lachmann, Marie Wencel, Crista Walters, Manisha Kak, Priya S. Kishnani, Matt Appleby, Vincenzo Libri, Laura E. Case, Tahseen Mozaffar
Publikováno v:
Molecular Genetics and Metabolism. 126:S85-S86
Disease progression in Pompe Disease, a lysosomal storage disorder, occurs despite enzyme replacement therapy ERT, and is characterized by cytoplasmic accumulation of glycogen, presumably due to rupture or seepage of glycogen from lysosomes, defects
Autor:
Angèle Nalbandian, Agnesa Avanesian, Tahseen Mozaffar, Kwang-Mook Jung, Christopher Nguyen, Virginia Kimonis, Daniele Piomelli, Katrina J. Llewellyn
Publikováno v:
Llewellyn, Katrina J; Nalbandian, Angèle; Jung, Kwang-Mook; Nguyen, Christopher; Avanesian, Agnesa; Mozaffar, Tahseen; et al.(2014). Lipid-enriched diet rescues lethality and slows down progression in a murine model of VCP-associated disease. Human Molecular Genetics, 23(5), 1333-1344. doi: 10.1093/hmg/ddt523. UC Irvine: Institute for Clinical and Translational Science. Retrieved from: http://www.escholarship.org/uc/item/0cv5910p
Valosin-containing protein (VCP)-associated disease caused by mutations in the VCP gene includes combinations of a phenotypically heterogeneous group of disorders such as hereditary inclusion body myopathy, Paget's disease of bone, frontotemporal dem