ライフサイエンスコーパス: Ca concentration

1 cts of several PLB mutants, as a function of Ca concentration.

2 also be affected by changes in intracellular Ca concentration.

3 d that it is only detectable at low external Ca concentration.

4 (NCX) is determined by Vm as well as Na and Ca concentrations.

5 a was distributed contained a relatively low Ca++ concentration.

6 bited parallel changes in intracellular-free Ca(++) concentration.

7 are linear (r > 0.999) over a wide range of CA concentrations (5-400 pmol).

8 sCAX1 gene reduces cytosolic and apoplastic Ca concentrations, affecting plasma membrane structure a

9 unitary conductance (gamma) to physiological Ca concentration and compare it to barium ion (Ba) condu

10 onditions, with relatively subtle changes in CA concentration and molecular crowding influencing self

11 A recently completed model of Ca concentration and movements in the cardiac cell diadi

12 Measurements using different CA concentrations and HgCl(2) indicated that liposome P(

13 There was no effect of treatment on S-Ca concentrations and no incidence of hypercalcemia (S-C

14 , the diadic cleft, with respect to calcium (Ca) concentration and movement.

15 Ca++ thus reveal heterogeneity in luminal ER Ca++ concentration and permit observation of receptor- a

16 d cells, a finding consistent with very high Ca++ concentrations (approximately 10(-5)-10(-3) M Ca++

17 ccurately not only the PLB effects on K(Ca) (Ca concentration at half-maximal activity) of the Ca-ATP

18 ABSTRACT: The intracellular Ca concentration ([Ca(2+) ]i ) must be sufficently low i

19 ity is regulated by changes in intracellular Ca concentration ([Ca(2+)]i).

20 -induced changes in intramitochondrial total Ca concentration ([Ca](mito)) obtained by x-ray microana

21 this although accurate measurement of stable Ca concentrations coupled with precise half-life data ar

22 its effects by influencing the local luminal Ca concentration-dependent gating of the Ca-release chan

23 xchange alone is unlikely to raise cytosolic Ca concentration enough to directly activate the myofila

24 Changes in intracellular calcium (Ca) concentration following synaptic and suprathreshold

25 It was prevented by Ca++ concentrations greater than 50 mM, but was not alte

26 We found that sedimentary Ca concentrations had been declining steadily for 900 y

27 at past and future changes in available soil Ca concentrations have important and previously unrecogn

28 ncentrations, lower apoplastic and cytosolic Ca concentrations, higher membrane leakage, and Ca accum

29 h the action potential duration and the peak Ca concentration in the cell can exhibit well known peri

30 pulse voltammetry (DPV) varies linearly with CA concentration in the range 1x10(-7)-3x10(-3) M.

31 label from [3H]IAA increased with increasing Ca concentration in the receiver up to 5 to 10 millimola

32 Similarly, OEA induced a rise in Ca(+) concentration in wild-type but not TRPV1-deficient

33 Although calcium (Ca) concentration in cellular compartments has been sugg

34 In the batch experiment, Ca concentrations increase until calcite saturation is r

35 rp had higher total tissue and water-soluble Ca concentrations, lower apoplastic and cytosolic Ca con

36 sumption of ATP and the increase in cellular Ca concentration may result in mitochondrial Ca (mCa) ov

37 Exposure to high Ca concentrations may influence the development of low-t

38 The effects of CA concentration, molecular crowding, and the conformati

39 33 mmol/L, pH = 7.4, 37 degrees C) yielded a Ca concentration of (0.65 +/- 0.02) mmol/L and PO(4) of

40 erroelectric transition is observed around a Ca concentration of approximately 1/8, where a new pseud

41 g CRUs, which helps to maintain the local SR Ca concentration of the firing CRUs above a critical lev

42 sions in genomes, have allele-specific shoot Ca concentration phenotypes compared with their segregat

43 significance using a large database of shoot Ca concentration phenotypes of Arabidopsis thaliana.

44 psis gene identifiers tagged to robust shoot Ca concentration phenotypes, 21 mapped to 27 B. rapa eQT

45 ynaptic activity that produced intracellular Ca++ concentration spikes that were measured by indo-1-b

46 After a sudden imposed drop in Ca concentration, the effect of recoverin switched off w

47 has been previously shown to contain similar Ca concentrations to wild-type (WT) plants, but lower ox

48 tions, and preparations exposed to different Ca concentrations was estimated by electron microscopy.

49 Under air-excluded conditions Ca concentrations were controlled by dicalcium silicate

50 eal doses (0.25, 1.0, and 4.0 mg/kg), plasma CAS concentrations were assayed by high-performance liqu