ライフサイエンスコーパス: porter

1 a mitochondrial targeting nanocarrier (MITO-Porter).

2 ely) by molecular motors, which act as cargo porters.

3 pothesis, uncoupling protein is a pure anion porter and does not transport protons; rather it is desi

4 Using electron microscopy (EM), K. R. Porter and his laboratory defined the SR, the unique jun

5 ependent of role or working location, and in porters and cleaners (2.06 [1.34-3.15]).

6 This porter appears to be specific for glycine betaine, since

7 stigating the structure and function of this porter because it is a member of a large gene family in

8 tructure' by Myron C. Ledbetter and Keith R. Porter by summarizing the very limited knowledge of plan

9 A malate-phosphate anti-porter DctA is regulated by RpoN and AsIII, and is requi

10 Transport by this porter did not require sodium ion and could be driven on

11 The AsIII/H(+) anti-porters encoded by acr3-1 and acr3-2 are required for ma

12 ither to the left or right side of the nose (Porter et al.) or to the inside or outside of the mouth

13 ransport and release mechanism for the sugar porter family of proteins.

14 e morpholino oligonucleotides using the Endo-Porter formula (Gene-Tools, LLC, Philomath, OR), with de

15 n, and membrane localization of one of these porters found in sugar beet (Beta vulgaris L.).

16 utamate:gamma-amino butyric acid (GABA) anti-porter (GadC) to expel GABA in exchange for extracellula

17 ycine betaine uptake system (glycine betaine porter I), uptake in this vesicle system was dependent o

18 The novel Kaya-Porter identity framework deconstructs the entity of emi

19 ven glycine betaine permease glycine betaine porter II (Gbu) is functional.

20 derstood, but the role of Acr3 and DctA anti-porters in AsIII oxidation and its regulation is unexpec

21 otif, instead of like conventional substrate porters in the 12-TM motif.

22 ntered and value-based system built upon the Porter model of value-based health care.

23 l model and extracellularly in the substrate porter model.

24 By comparing many different sugar porter models and scrutinizing their sequence, we have b

25 cally by the permeation of intrinsic "proton-porter" molecules.

26 Porter Novelli survey data were collected from adolescen

27 the structural features and dynamics of this portering process and analysed the associated binding st

28 synthesis of the decarboxylase and the anti-porter proteins.

29 The Aliso Canyon (Porter Ranch), California, natural gas blowout lasted 11

30 SLC7A11 codes for a cysteine-glutamate anti-porter regulating levels of the antioxidant glutathione,

31 rminal MFS folds prevails for metazoan sugar porters, revealing evolutionary conflicts between foldab

32 To paraphrase Cole Porter's famous 1926 song, "What is this thing called pa

33 Sugar porters (SPs) represent the largest group of secondary-a

34 Sugar Transport Proteins (STPs) are Sugar Porters (SPs) that mediate proton-driven cellular uptake

35 n than when using attributes obtained by the Porter stemmer algorithm (AUC in 0.86-0.93 range).

36 anchors our complementary investigations of porter structure and function using site-directed and ra

37 Because only a few sugar porter structures have been determined, mechanistic mode

38 g, to predict structures of the entire sugar porter superfamily in each state of the transport cycle.

39 le, which are conserved throughout the sugar porter superfamily.

40 n of output bit-string probabilities and the Porter-Thomas distribution.

41 They expand the roster of such porters to encompass one with a complex organic substrat

42 W., Rodriguez, F., Rigali, E., Weitzman, S., Porter, V., Rubbi, L., Morselli, M., Pellegrini, M., Fia

43 but is a low affinity Na+/H+ and K+/H+ anti-porter with a Km of 22.4 and 82.2 mm for Na+ and K+, res