Results 251 to 260 of about 40,807 (310)

A GSK-3/TSC2/mTOR pathway regulates glucose uptake and GLUT1 glucose transporter expression

, 2008
Carolyn L. Buller, Robert D. Loberg, Ming‐Hui Fan, Qihong Zhu, James L. Park, Eileen Vesely, Ken Inoki, Kun‐Liang Guan, Frank C. Brosius   +8 more
openalex   +2 more sources

The prospect of novel orphan therapeutic protocol for TSC2/PKD1 contiguous gene syndrome: a case report. [PDF]

BMC Nephrol
Agavriloaei BD, Costache RC, Babici RG, Racoviță S, Dodi G, Covic AC, Mititiuc IL.   +6 more
europepmc   +1 more source

Conditional and domain‐specific inactivation of the Tsc2 gene in neural progenitor cells [PDF]

, 2013
Cary Fu, Kevin C. Ess
openalex   +1 more source

Prenatal Diagnosis and Management of Tuberous Sclerosis Complex with Cardiac Rhabdomyoma: A Case Report Highlighting the Role of Sirolimus and Postnatal Complications. [PDF]

Diagnostics (Basel)
Rodríguez-Torres DA, Arenas-Estala J, Sánchez-Cortés RG, Dávila-Escamilla IV, Nieto-Sanjuanero A, López-Uriarte GA.   +5 more
europepmc   +1 more source

Tuberous Sclerosis Complex: A Case Series from a Romanian Genetics Center and a Review of the Literature. [PDF]

J Clin Med
Jurca AA, Hodisan R, Jurca AD, Severin E, Jurca S, Trandafir A, Ilias T, Vesa C, Jurca CM.   +8 more
europepmc   +1 more source

Unraveling the Binding Mode of TSC2-Rheb through Protein Docking and Simulations. [PDF]

Biochemistry
Pape BF, Parate S, Eriksson LA, Jha V.
europepmc   +1 more source

Role of Extracellular Vesicles in TSC Renal Cystogenesis. [PDF]

Int J Mol Sci
Zahedi K, Morgan M, Prieto B, Brooks M, Howard TA, Barone S, Bissler JJ, Argyropoulos C, Soleimani M.   +8 more
europepmc   +1 more source

mTOR signaling in skeletal development and disease [PDF]

, 2018
Chen, Jianquan, Long, Fanxin
core   +1 more source

Exceptional Response in a Patient with mRCC Through Precision-Guided Treatment Involving Immunotherapy Rechallenge with Temsirolimus and Bevacizumab. [PDF]

J Immunother Precis Oncol
Adibi A, Tokat ÜM, Aydın E, Özgü E, Bilgiç ŞN, Babacan NA, Tutar O, Kurzrock R, Demiray M.   +8 more
europepmc   +1 more source

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.

American Journal of Human Genetics, 2017
Jae Seok Lim, Ramu Gopalappa, Se Hoon Kim, S. Ramakrishna, M. Lee, Woo-il Kim, Junho Kim, Sang Min Park, Junehawk Lee, Jung-Hwa Oh, H. Kim, Chang-Hwan Park, Joon Soo Lee, Sangwoo Kim, Dong Seok Kim, J. Han, Hoon-Chul Kang, H. Kim, Jeong Ho Lee   +18 more
semanticscholar   +1 more source