全文获取类型
收费全文 | 86篇 |
免费 | 7篇 |
专业分类
93篇 |
出版年
2022年 | 2篇 |
2017年 | 1篇 |
2016年 | 1篇 |
2015年 | 4篇 |
2014年 | 7篇 |
2013年 | 4篇 |
2012年 | 5篇 |
2011年 | 6篇 |
2010年 | 1篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2007年 | 1篇 |
2006年 | 3篇 |
2005年 | 3篇 |
2004年 | 7篇 |
2003年 | 5篇 |
2002年 | 5篇 |
2001年 | 1篇 |
2000年 | 2篇 |
1999年 | 2篇 |
1998年 | 1篇 |
1997年 | 5篇 |
1996年 | 5篇 |
1995年 | 1篇 |
1993年 | 3篇 |
1992年 | 1篇 |
1991年 | 3篇 |
1990年 | 4篇 |
1989年 | 2篇 |
1987年 | 1篇 |
1986年 | 2篇 |
1981年 | 1篇 |
排序方式: 共有93条查询结果,搜索用时 8 毫秒
11.
Xu GM González-Perrett S Essafi M Timpanaro GA Montalbetti N Arnaout MA Cantiello HF 《The Journal of biological chemistry》2003,278(3):1457-1462
Autosomal dominant polycystic kidney disease (ADPKD) is a prevalent genetic disorder largely caused by mutations in the PKD1 and PKD2 genes that encode the transmembrane proteins polycystin-1 and -2, respectively. Both proteins appear to be involved in the regulation of cell growth and maturation, but the precise mechanisms are not yet well defined. Polycystin-2 has recently been shown to function as a Ca(2+)-permeable, non-selective cation channel. Polycystin-2 interacts through its cytoplasmic carboxyl-terminal region with a coiled-coil motif in the cytoplasmic tail of polycystin-1 (P1CC). The functional consequences of this interaction on its channel activity, however, are unknown. In this report, we show that P1CC enhanced the channel activity of polycystin-2. R742X, a disease-causing polycystin-2 mutant lacking the polycystin-1 interacting region, fails to respond to P1CC. Also, P1CC containing a disease-causing mutation in its coiled-coil motif loses its stimulatory effect on wild-type polycystin-2 channel activity. The modulation of polycystin-2 channel activity by polycystin-1 may be important for the various biological processes mediated by this molecular complex. 相似文献
12.
Microtubules (MTs) are important cytoskeletal structures engaged in a number of specific cellular activities, including vesicular traffic, cell cyto-architecture and motility, cell division, and information processing within neuronal processes. MTs have also been implicated in higher neuronal functions, including memory and the emergence of "consciousness". How MTs handle and process electrical information, however, is heretofore unknown. Here we show new electrodynamic properties of MTs. Isolated, taxol-stabilized MTs behave as biomolecular transistors capable of amplifying electrical information. Electrical amplification by MTs can lead to the enhancement of dynamic information, and processivity in neurons can be conceptualized as an "ionic-based" transistor, which may affect, among other known functions, neuronal computational capabilities. 相似文献
13.
Nuclear ion channel activity is regulated by actin filaments 总被引:1,自引:0,他引:1
14.
15.
16.
María del Rocío Cantero Irina F. Velázquez Andrew J. Streets Albert C. M. Ong Horacio F. Cantiello 《The Journal of biological chemistry》2015,290(39):23888-23896
Polycystin-2 (PC2) is a TRP-type, Ca2+-permeable non-selective cation channel that plays an important role in Ca2+ signaling in renal and non-renal cells. The effect(s) of the cAMP pathway and kinase mediated phosphorylation of PC2 seem to be relevant to PC2 trafficking and its interaction with polycystin-1. However, the role of PC2 phosphorylation in channel function is still poorly defined. Here we reconstituted apical membranes of term human syncytiotrophoblast (hST), containing endogenous PC2 (PC2hst), and in vitro translated channel protein (PC2iv). Addition of the catalytic subunit of PKA increased by 566% the spontaneous PC2hst channel activity in the presence of ATP. Interestingly, 8-Br-cAMP also stimulated spontaneous PC2hst channel activity in the absence of the exogenous kinase. Either stimulation was inhibited by addition of alkaline phosphatase, which in turn, was reversed by the phosphatase inhibitor vanadate. Neither maneuver modified the single channel conductance but instead increased channel mean open time. PKA directly phosphorylated PC2, which increased the mean open time but not the single channel conductance of the channel. PKA phosphorylation did not modify either R742X truncated or S829A-mutant PC2iv channel function. The data indicate that the cAMP pathway regulates PC2-mediated cation transport in the hST. The relevant PKA site for PC2 channel regulation centers on a single residue serine 829, in the carboxyl terminus. 相似文献
17.
18.
Avner Priel Arnolt J. Ramos Jack A. Tuszynski Horacio F. Cantiello 《Journal of biological physics》2008,34(5):475-485
Microtubules (MTs) are important cytoskeletal superstructures implicated in neuronal morphology and function, which are involved
in vesicle trafficking, neurite formation and differentiation and other morphological changes. The structural and functional
properties of MTs depend on their high intrinsic charge density and functional regulation by the MT depolymerising properties
of changes in Ca2 + concentration. Recently, we reported on remarkable properties of isolated MTs, which behave as biomolecular transistors capable
of amplifying electrical signals (Priel et al., Biophys J 90:4639–4643, 2006). Here, we demonstrate that MT-bathing (cytoplasmic) Ca2 + concentrations modulate the electrodynamic properties of MTs. Electrical amplification by MTs was exponentially dependent
on the Ca2 + concentration between 10 − 7 and 10 − 2 M. However, the electrical connectivity (coupling) of MTs was optimal at a narrower window of Ca2 + concentrations. We observed that while raising bathing Ca2 + concentration increased electrical amplification by MTs, energy transfer was highest in the presence of ethylene glycol tetraacetic
acid (lowest Ca2 + concentration). Our data indicate that Ca2 + is an important modulator of electrical amplification by MTs, supporting the hypothesis that this divalent cation, which
adsorbs onto the polymer’s surface, plays an important role as a regulator of the electrical properties of MTs. The Ca2 + -dependent ability of MTs to modulate and amplify electrical signals may provide a novel means of cell signaling, likely contributing
to neuronal function. 相似文献
19.
Protein kinase A phosphorylation and G protein regulation of type II pneumocyte Na+ channels in lipid bilayers 总被引:1,自引:0,他引:1
20.