ライフサイエンスコーパス: preterminal

1 onset of terminal decline (28%) and rates of preterminal (32%) and terminal decline (19%).

2 orating the tips of short appendages on fine preterminal and terminal axons; 2) tiny, round varicosit

3 loss of distal conducting airways, including preterminal and terminal bronchioles (pre-TBs/TBs), unde

4 ces on the onset of terminal decline and the preterminal and terminal components of the cognitive tra

5 h the onset of terminal decline and rates of preterminal and terminal decline (ie, nonlinear decline)

6 h the onset of terminal decline and rates of preterminal and terminal decline.

7 n the onset of terminal decline and rates of preterminal and terminal decline.

8 PHA-L-immunoreactive (IR) fibers showing preterminal and terminal-like arborization that containe

9 diately prior to the euthanasia of moribund (preterminal) animals).

10 mbedded in an extensive granular matrix, (2) preterminal arrays of "axonal reticulum" derived from th

11 ough an opioid mechanism, possibly acting by preterminal autoinhibition of NTS projections to the pPV

12 (SC) processes arising from somata along the preterminal axon cover almost all of these synapses.

13 vation of alpha4beta2-like nAChRs present in preterminal axon segments and/or in presynaptic terminal

14 very few side-branches were found along the preterminal axon throughout the developmental period stu

15 the incidence of axonal side branches on the preterminal axon within the confines of the geniculate.

16 t in myelinating Schwann cells that wrap the preterminal axon, nestin is not detected in the terminal

17 ed postsynaptically, although immunoreactive preterminal axonal segments were also frequently encount

18 ERbeta-ir was in preterminal axons and axon terminals, associated with cl

19 lect vesicles or with the plasmalemma within preterminal axons and axon terminals.

20 opathy characterized by dramatic swelling of preterminal axons and nerve terminals by the accumulatio

21 opsin labeling was confined to unmyelinated preterminal axons and small terminals that formed asymme

22 ABApre-sensory synapses, suggesting that the preterminal axons of GABApre neurons compete for access

23 dritic shafts and, less frequently, glia and preterminal axons were also identified.

24 r compartments, including spines, dendrites, preterminal axons, axon terminals, and glia; however, qu

25 Model simulations of real preterminal-branch tree structures confirmed that short

26 and lengths of nonreconstructed terminal and preterminal branches and the numbers and locations of ax

27 urones, and the topological structure of the preterminal branches of the primary sensory ending.

28 tribution of axon terminals, in terminal and preterminal branching, and in varicosity density.

29 We identify 502 terminal and preterminal cell types, mapping most single-cell transcr

30 ts show for the first time that terminal and preterminal corticospinal axon branches increase in comp

31 cies do not provide evidence for a model of "preterminal differentiation" of HIV-specific CD8(+) T ce

32 and is essential for progression through its preterminal end stage.

33 ow that GFP(+) cells from Bmi1(GFP) mice are preterminal enteroendocrine cells and we identify CD69(+

34 iatum in cocaine fatalities with and without preterminal excited delirium as compared to drug-free an

35 trastructural analysis of the injected giant preterminal further showed a reduced number of docked sy

36 Our studies confirm that preterminal gasping during ventricular fibrillation incr

37 Metabolomic shifts in these preterminal groups also revealed consistent disturbances

38 ter metabolic disruption was observed in the preterminal groups than all of the other post-irradiatio

39 ic illness and is not associated solely with preterminal hospitalizations.

40 Indeed, preterminal injection of a specific antibody against squ

41 lagen XIII is particularly important for the preterminal integrity, and when absent, destabilization

42 nal has at least two major determinants: the preterminal internodal shortening and axonal slow K chan

43 nt changes to our understanding and study of preterminal kidney failure.

44 tion of sentence comprehension, and finally, preterminal mutism and dementia.

45 ptively adjust therapy to devices to support preterminal patients with end-stage disease, it is recog

46 For 4 preterminal patients, observation was preferred.

47 pathway appears to be representative of the preterminal phenotype, confirming the results of our pre

48 ly predictor for health decline leading to a preterminal phenotype.

49 me patients, decline followed by a prolonged preterminal plateau at very low functional levels.

50 KYNA also blocked the activity of preterminal/presynaptic alpha7 nAChRs in hippocampal neu

51 ral vector for replication, we constructed a preterminal protein (pTP) deletion mutant adenovirus typ

52 t an adenovirus type 5 (Ad5) mutant with the preterminal protein (pTP) gene deleted can provide helpe

53 An adenovirus type 5 mutant deleted for the preterminal protein (pTP) gene was constructed using cel

54 hal in-frame insertion mutant alleles of the preterminal protein (pTP) gene were constructed with cel

55 Of particular interest is the Ad preterminal protein (pTP), which binds alone or in compl

56 ar matrix (NM) through the interaction of Ad preterminal protein (pTP).

57 Preterminal protein directly binds to the cellular trans

58 cipitation of POU with individual domains of preterminal protein expressed by in vitro translation in

59 trate that coexpression of the adenoviral E2-preterminal protein from the vector or in trans stabiliz

60 competent viruses carrying a deletion of the preterminal protein gene.

61 Partial proteolysis of preterminal protein in the presence or absence of POU ho

62 Adenovirus preterminal protein interacts with three of the four pro

63 ndent on the ionic strength, suggesting that preterminal protein may undergo a sodium chloride-induce

64 tidomain structure and that interaction with preterminal protein takes place with non-contiguous regi

65 The accessibility of sites in free preterminal protein to cleavage by trypsin was strongly

66 OU homeodomain contacts a number of sites on preterminal protein to induce a conformational change wh

67 t many sites accessible to proteases in free preterminal protein were resistant to cleavage in the pr

68 , coexpressing adenoviral DNA polymerase and preterminal protein, converted plasmid DNA into replicat

69 olymerase transfers dCMP onto the adenovirus preterminal protein, to which it is tightly bound.

70 ovirus DNA replication involves the incoming preterminal protein-adenovirus DNA polymerase heterodime

71 ndicated that POU contacts multiple sites on preterminal protein.

72 tamate release onto DMV neurons by acting at preterminal receptors in slices from intact mice, but fa

73 ptide injection into the squid giant synapse preterminal results in a decrease in transmitter release

74 ve trunk but developed dysmyelination of the preterminal segment associated with denervation processe

75 t on remaining miniature IPSCs, suggesting a preterminal site of glycine receptors (GlyRs).

76 acterize and validate metabolomic changes in preterminal stage (immediately prior to death) samples c

77 cted pre-exposure, post-exposure, and at the preterminal stage of nonhuman primates (NHPs that did no

78 ndin correlated in peripheral blood with the preterminal stage.

79 ysis revealed the presence of 5-HT axons and preterminals throughout the PAG, and in particular, in i