- ►uoguelph.ca [PDF] HF Kramer, EB Taylor, CA Witczak, N Fujii, MF … - Diabetes, 2007 - Am Diabetes Assoc RESULTS—Immunoprecipitates of wild-type and CBD-mutant AS160 were incubated with biotinylated
calmodulin in the presence of Ca 2+ . Wild-type AS160, but not the CBD-mutant AS160, associated
with calmodulin. Next, we measured insulin- and contraction-stimulated glucose uptake in ... Cited by 16 - Related articles - BL Direct - All 4 versions
K Funai, GD Cartee - Journal of Applied Physiology, 2008 - Am Physiological Soc Akt substrate of 160 kDa (AS160), the most distal insulin signaling protein known to be important
for insulin-stimulated glucose transport, becomes phosphorylated with skeletal muscle
contraction. Akt, AMP-activated protein kinase (AMPK), and Ca 2+ /calmodulin-dependent ... Cited by 5 - Related articles - All 3 versions
- ►jbc.org JA Chavez, WG Roach, SR Keller, WS Lane, GE … - Journal of Biological …, 2008 - ASBMB Insulin increases glucose transport by stimulating the trafficking of intracellular GLUT4 to the
cell surface, a process known as GLUT4 translocation. A key protein in signaling this process
is AS160, a Rab GTPase-activating protein (GAP) whose activity appears to be ... Cited by 23 - Related articles - All 5 versions
EB Taylor, D An, HF Kramer, H Yu, NL Fujii, KSC … - Journal of Biological …, 2008 - ASBMB The Akt substrate of 160 kDa (AS160) is phosphorylated on Akt substrate (PAS) motifs in response
to insulin and contraction in skeletal muscle, regulating glucose uptake. Here we discovered
a dissociation between AS160 protein expression and apparent AS160 PAS ... Cited by 34 - Related articles - All 6 versions
- ►diabetesjournals.org K Funai, GD Cartee - Diabetes, 2009 - Am Diabetes Assoc OBJECTIVE Phosphorylation of two members of the TBC1 domain family of proteins, Akt substrate
of 160 kDa (AS160, also known as TBC1D4) and TBC1D1, has been implicated in the regulation
of glucose transport in skeletal muscle. Insulin-stimulated phosphorylation (measured ... Cited by 3 - Related articles - All 2 versions
K Funai, GG Schweitzer, N Sharma, M … - American Journal of …, 2009 - Am Physiological Soc A single exercise bout can increase insulin-independent glucose transport immediately postexercise
and insulin-dependent glucose transport (GT) for several hours postexercise. Akt substrate of
160 kDa (AS160) and TBC1D1 are paralog Rab GTPase-activating proteins that have ... Cited by 3 - Related articles - All 3 versions
DR Blair, K Funai, GG Schweitzer, GD … - American Journal of …, 2009 - Am Physiological Soc Contraction-stimulated glucose transport by skeletal muscle appears to be caused by the cumulative
effects of multiple inputs [potentially including AMP-activated protein kinase (AMPK), Ca 2+
flux, and force production], making it challenging to isolate the roles of these putative ... Cited by 3 - Related articles - All 3 versions
- ►physiology.org EB Arias, J Kim, K Funai, GD Cartee - American Journal of …, 2007 - Am Physiological Soc The main purpose of this study was to determine whether the increased glucose transport
(GT) found immediately postexercise (IPEX) or 4 h postexercise (4hPEX) is accompanied by
increased phosphorylation of Akt substrate of 160 kDa (AS160, a protein regulator of ... Cited by 18 - Related articles - BL Direct - All 7 versions
GD Cartee, JFP Wojtaszewski - Applied Physiology, Nutrition, …, 2007 - article.pubs.nrc-cnrc.gc.ca Abstract: Insulin and exercise, the most important physiological stimuli to increase glucose transport
in skeletal muscle, trigger a redistribution of GLUT4 glucose transporter proteins from the cell
interior to the cell surface, thereby increasing glucose transport capacity. The most distal ... Cited by 26 - Related articles - Cached - BL Direct - All 4 versions
JT Treebak, C Frøsig, C Pehmøller, S Chen, SJ … - Diabetologia, 2009 - Springer Page 1. ARTICLE Potential role of TBC1D4 in enhanced post-exercise insulin action in human
skeletal muscle JT Treebak & C. Frøsig & C. Pehmøller & S. Chen & SJ Maarbjerg & N. Brandt
& C. MacKintosh & JR Zierath & DG Hardie & B. Kiens & EA Richter & H. Pilegaard & ... Cited by 7 - Related articles - All 2 versions
