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1 hat the effect of sAnk1 is less than that of sarcolipin.
2 m (SERCA1a) and is controlled by the protein sarcolipin.
3 rt by generating a mouse model deficient for sarcolipin.
4 pite the absence of SR Ca(2+) pump regulator sarcolipin.
5  homology in its TM amino acid sequence with sarcolipin, a small protein inhibitor of the sarco(endo)
6         In its monomeric form, we found that sarcolipin adopts a helical conformation, with a compute
7 proteins of the calcium ATPase SERCA, namely sarcolipin and phospholamban, in explicit lipid bilayers
8 ia increased expression of SERCA uncouplers, sarcolipin and/or neuronatin, under chow-fed and HFD-fed
9 placing the SERCA inhibitors, phospholamban, sarcolipin, and myoregulin.
10 se to isoproterenol stimulation, implicating sarcolipin as a mediator of beta-adrenergic responses in
11 CA within the first transport cycle, whereas sarcolipin did not.
12                               The absence of sarcolipin does not modify the expression level of other
13 timulating hormone (TSH) are responsible for sarcolipin expression or FAO stimulation; rather, thyroi
14          These changes, along with increased sarcolipin expression, provide evidence for the recruitm
15 uorescence analysis confirmed the absence of sarcolipin in normal left ventricles and its marked upre
16 tably by phospholamban in cardiac muscle and sarcolipin in skeletal muscle.
17 vestigated the physiological significance of sarcolipin in the heart by generating a mouse model defi
18 ssociated with beta-adrenergic signaling and sarcolipin in the left ventricles of patients with isola
19                    Our study documented that sarcolipin is a key regulator of SERCA2a in atria.
20                                              Sarcolipin is a novel regulator of cardiac sarcoplasmic
21 late Na(+) ,K(+) -ATPase, and phospholamban, sarcolipin, myoregulin and DWORF, which regulate the sar
22                                          The sarcolipin-null mice do not show any developmental abnor
23                      Furthermore, atria from sarcolipin-null mice showed a blunted response to isopro
24 e evaluated the effects of phospholamban and sarcolipin on calcium translocation and ATP hydrolysis b
25 tylleucine and the integral membrane protein sarcolipin oriented in lipid bicelles.
26               However, how phospholamban and sarcolipin regulate SERCA is not fully understood.
27     An important finding is that ablation of sarcolipin resulted in an increase in atrial Ca2+ transi
28 ies revealed that, in the atria, ablation of sarcolipin resulted in an increase in the affinity of th
29                     This suggests that, like sarcolipin, sAnk1 interacts with SERCA1 at least in part
30 e have detected directly the interactions of sarcolipin (SLN) and the sarcoplasmic reticulum Ca-ATPas
31                      Phospholamban (PLN) and sarcolipin (SLN) are two single-pass membrane proteins t
32 vity is modulated by phospholamban (PLB) and sarcolipin (SLN) in cardiac and skeletal muscle.
33                                  The role of sarcolipin (SLN) in cardiac physiology was critically ev
34                                              Sarcolipin (SLN) is a 31 amino acid integral membrane pr
35                                              Sarcolipin (SLN) is a novel regulator of sarcoplasmic re
36                                              Sarcolipin (SLN) is a regulatory peptide present in sarc
37                                              Sarcolipin (SLN) is an inhibitor of the sarco/endoplasmi
38                                              Sarcolipin (SLN) is an integral membrane protein that is
39 ic reticulum Ca(2+)-ATPase (SERCA)-inhibitor sarcolipin (SLN) is up-regulated >70-fold in nebulin kno
40                                              Sarcolipin (SLN), a 31 amino acid integral membrane prot
41                            Here we show that sarcolipin (Sln), a newly identified regulator of the sa
42                        SERCA is regulated by sarcolipin (SLN), a single-pass membrane protein that un
43                      We recently showed that sarcolipin (SLN), an uncoupler of the sarco(endo)plasmic
44 spholamban (PLB), an affinity modulator, and sarcolipin (SLN), an uncoupler.
45 ic genes [natriuretic peptide type A (Nppa), sarcolipin (Sln), and myosin light polypeptide 4 (Myl4)]
46 onal similarity with phospholamban (PLN) and sarcolipin (SLN), which inhibit SERCA, the membrane pump
47 in 1 (UCP1)-based) and skeletal muscle (i.e. sarcolipin (SLN)-based) thermogenesis processes play imp
48 ost well-known being phospholamban (PLN) and sarcolipin (SLN).
49 mbrane domain in a manner similar to that of sarcolipin (SLN).
50 al membrane proteins phospholamban (PLN) and sarcolipin (SLN).
51 s of SERCA activity, phospholamban (PLB) and sarcolipin (SLN).
52 al membrane proteins phospholamban (PLN) and sarcolipin (SLN).
53 e coding region of the atrial-specific gene, Sarcolipin (SLN).
54  the unrestrained simulations, the resulting sarcolipin structures are in agreement with distances an
55 ty as well as gene expression of SERCA1a and sarcolipin, we found an age-related increase in all thre
56 osomes containing SERCA and phospholamban or sarcolipin were adsorbed to a solid-supported membrane a
57 culum Ca2+ ATPase (SERCA) regulatory protein sarcolipin, which is predominantly expressed in normal a
58 onment of a small membrane-embedded protein, sarcolipin, which regulates the sarcoplasmic reticulum C
59  skeletal-muscle adaptive thermogenic marker sarcolipin, with an associated increase in fatty acid ox