ライフサイエンスコーパス: mitoplast

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1 present in highly purified mitochondria and mitoplasts.

2 mbrane space and can be observed in isolated mitoplasts.

3 proteolysis in both intact mitochondria and mitoplasts.

4 ysical properties by directly patch clamping mitoplasts.

5 ained by a patch-clamp approach in rat liver mitoplasts.

6 d quantified the amount of tagged subunit in mitoplasts and holo-CI by non-native and native PAGE, re

7 loop connecting helices 2 and 3 of QPs3, in mitoplasts and submitochondrial particles.

8 ptibility of a C-terminal Myc epitope tag in mitoplasts but not intact mitochondria.

9 Our results indicate that the mitoplasts contain just 15-19% of the outer membrane mar

10 ll as the inner CPT-II, was localized in the mitoplast fraction.

11 itochondria and mouse liver mitochondria and mitoplast fractions derived from these preparations poss

12 Brain mitoplasts from 10-day BNF-treated rats and also purifie

13 10(-10) and 10(-8) M, respectively, whereas mitoplasts had lost the high affinity binding.

14 As tested with mitoplasts, holocytochromes c from a range of species we

15 detected by direct patch clamp recording of mitoplasts, increased O(2) consumption and decreased rea

16 ious subfractions of rat liver mitochondria (mitoplast, inner membrane, intermembrane, and matrix) as

17 ondrial membrane potential but was absent in mitoplasts lacking an outer mitochondrial membrane.

18 was susceptible to proteinase K digestion in mitoplasts (mitochondria with a disrupted outer membrane

19 In addition, the MCU mitoplast patch-clamp current (IMCU) was largely unaffec

20 ent fatty acid oxidation was retained in the mitoplasts, showing that they were physiologically intac

21 Patch clamp recordings in isolated mitoplasts suggest insertion into the inner mitochondria

22 e possibility that most of the mitochondrial/mitoplast TGase activity is due to TGase 2, the TGase is

23 The identity of the mitochondrial/mitoplast TGase(s) is not yet known.

24 tely 0.6 mM) is the same in mitochondria and mitoplasts, the same as that of AMPPNP, and is not alter

25 e c from cardiolipin-lacking mitochondria or mitoplasts under our standard experimental conditions wa

26 initively identify the channel, we use whole-mitoplast voltage-clamping, the technique that originall

27 n addition, the MCC activity of mouse kidney mitoplasts was unaffected by carboxyatractyloside, a kno

28 These mitoplasts were shown by electron microscopy to have the

29 IV activity in isolated mitochondria and in mitoplasts, whereas other ceramide species, sphingomyeli

30 e distinguished by chymotrypsin treatment of mitoplasts, which eliminates the action of Mg2+ but does

31 ryanodine receptor channel activity in heart mitoplasts with biophysical and pharmacological properti

32 en (Km approximately 1 nM), as were those of mitoplasts with broken outer membranes (Km approximately

33 upon short incubation of isolated fibroblast mitoplasts with dibutyryl cAMP and ATP, which also promo

34 Pretreatment of isolated mitoplasts with the anti-TbTim17 antibody inhibited impo

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