Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sandhya, Ramani"'
Autor:
Sandhya Ramani Sattiraju, Abdulrahman Jama, Abdullah A. Alshudukhi, Nicholas Edward Townsend, Daniel Reynold Miranda, Rebecca R Reese, Andrew A. Voss, Hongmei Ren
Publikováno v:
Physiological Reports, Vol 8, Iss 20, Pp n/a-n/a (2020)
Abstract Mutations in lipin1 are suggested to be a common cause of massive rhabdomyolysis episodes in children; however, the molecular mechanisms involved in the regulation of myofiber death caused by the absence of lipin1 are not fully understood. L
Externí odkaz:
https://doaj.org/article/92233ddff242487596a705e98a099c9c
Autor:
Nicholas Edward Townsend, Sandhya Ramani Sattiraju, Andrew A. Voss, Daniel R. Miranda, Rebecca R Reese, Abdullah A. Alshudukhi, Abdulrahman Jama, Hongmei Ren
Publikováno v:
Physiological Reports, Vol 8, Iss 20, Pp n/a-n/a (2020)
Physiological Reports
Physiological Reports
Mutations in lipin1 are suggested to be a common cause of massive rhabdomyolysis episodes in children; however, the molecular mechanisms involved in the regulation of myofiber death caused by the absence of lipin1 are not fully understood. Loss of me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f16f5c85910712d667eb3490f1bf8bc8
https://doaj.org/article/92233ddff242487596a705e98a099c9c
https://doaj.org/article/92233ddff242487596a705e98a099c9c
Autor:
Sattiraju, Sandhya Ramani
Mutations in lipin1 are suggested to be a common cause of massive rhabdomyolysis episodes in children, however, the molecular mechanism involved in the regulation of myofiber death by lipin1 is not known. In this study, we utilized the skeletal muscl
Publikováno v:
Journal of the Royal Asiatic Society of Sri Lanka, 1993 Jan 01. 38, 127-140.
Externí odkaz:
https://www.jstor.org/stable/23731076