ライフサイエンスコーパス: BAP

1 BAP binding was affected by the conformation of the ATPa

2 BAP but not BLA increased unconditioned port-entries, wh

3 BAP encoded an approximately 54-kDa protein with an N-te

4 BAP stimulated the ATPase activity of BiP when added alo

5 BAP was ubiquitously expressed but showed the highest le

6 BAP-135, which exhibits no detectable homology to known

7 BAP/TFII-I is a substrate for Btk in vitro and is hyperp

8 BAP/TFII-I, a protein implicated in transcriptional regu

9 each of the paced groups (RAP, 8%; LAP, 20%; BAP, 26%) compared with patients who did not receive pos

10 F in the three groups (NAP = 33%; RAP = 29%; BAP = 37%; p > 0.7).

11 Experimental measurements show that a BAP evoked by current injection at the soma causes calci

12 All abnormal BAP and CTX concentrations fell within the elevated ( ge

13 differentiation at a level similar to adult-BAP differentiation.

14 a low adipogenic capacity compared to adult-BAPs when maintained in a traditional adipogenic cocktai

15 s hiPSC-BAPs display similarities with adult-BAPs, it opens new opportunities to develop alternative

16 Interestingly, BLA and BAP inactivation produced dissociable effects.

17 Btk and BAP-135 exist in a complex before B cell antigen recepto

18 high (> or = 100 nmol/mmol creatinine), and BAP as low (< 146 U/L) or high (> or = 146 U/L).

19 that the step sizes of both M10(Full)LZ and BAP-M10(1-979)HMM are widely distributed on single actin

20 e sensitivities and specificities of OIA and BAP culture (both performed and interpreted in the offic

21 in Chicago, the sensitivities of the OIA and BAP culture were 79% and 72%, respectively (P<.001), whi

22 go, the overall sensitivities of the OIA and BAP culture were 84% and 78%, respectively (P<.001), whi

23 onnecticut, the sensitivities of the OIA and BAP culture were 94% and 89%, respectively (P=.004), whi

24 Low concentrations of osteocalcin and BAP suggested reduced bone formation, and low TRAP level

25 Patients in the RAP and BAP groups were continuously paced at a rate of 100 puls

26 er ml (LIM broth) with subculture to another BAP and the costs associated with the GPGB.

27 Pt-oxidizing enzyme, which was proven to be BAP by N terminus protein sequencing.

28 drogen peroxide (H2O2), 6-benzylaminopurine (BAP) and calcium chloride (CaCl2) could induce tolerance

29 city to the aromatic CK 6-benzylaminopurine (BAP) and that fast posttranscriptional and/or posttransl

30 (DMBQ) or the cytokinin 6-benzylaminopurine (BAP).

31 tryptic soy agar plate with 5% sheep blood (BAP) and a 3-ml tube of Todd-Hewitt broth supplemented w

32 engagement; in response to BCR crosslinking, BAP-135 is transiently phosphorylated on tyrosine.

33 signal sequence and a transmembrane domain, (BAP-TM) was efficiently biotinylated by endogenous bioti

34 al transcription factor II-I), which encodes BAP-135, a target for Bruton's tyrosine kinase.

35 iction of developmental potential by the Erm-BAP-dependent mechanism functionally distinguishes inter

36 , these data led us to conclude that the Erm-BAP-dependent mechanism stably restricts the development

37 can also be provided by synaptically-evoked BAPs.

38 ormation derived from synaptically-generated BAPs can indicate synapse location and can subsequently

39 hiPSC-BAPs expressed the molecular identity of adult-UCP1 expr

40 As hiPSC-BAPs display similarities with adult-BAPs, it opens new

41 However, hiPSC-BAPs display a low adipogenic capacity compared to adult

42 acid and EGF were required to promote hiPSCs-BAP differentiation at a level similar to adult-BAP diff

43 pression of the cell proliferation inhibitor BAP 37, which was associated with their less activated g

44 Low molecular mass BAP sequences are less likely to be broken down by diges

45 al and electrophysiological model to measure BAP-induced voltage and calcium signals in spines after

46 we identified the role of proteins mediating BAP-induced ethylene production, METHIONINE SYNTHASE1 an

47 sin-X without artificial dimerization motif (BAP-M10(1-979)HMM).

48 oratory's interpretation of a combination of BAP culture and Todd-Hewitt broth (THB) culture of trans

49 o understand the physiologic consequences of BAP/TFII-I tyrosine phosphorylation following B cell rec

50 Btk-dependent phosphorylation of BAP-135 is abolished by mutations that impair activation

51 Phosphorylation of BAP/TFII-I by Btk may link engagement of receptors such

52 r sites for Btk-dependent phosphorylation of BAP/TFII-I in vivo.

53 ene (BAP) on the accumulation and removal of BAP-DNA adducts in skin, lung, and liver.

54 The dual roles of BAP and BON genes in repressing defense responses mediat

55 omain of Btk comprises the principal site of BAP-135 binding.

56 were used to locate the predominant sites of BAP/TFII-I phosphorylation by Btk in vitro.

57 On BAP, sensitivity was 96.0% with induced growth.

58 h from BMHA and 95.9% with induced growth on BAP.

59 An algorithm using beta-hemolysis on BAP, lactose reaction on eosin-methylene blue or MacConk

60 (RAP), left atrial (LAP) or biatrial pacing (BAP) for 72 h after surgery.

61 ight atrial pacing (RAP) or biatrial pacing (BAP).

62 hich incorporates a biotin acceptor peptide (BAP) between an N-terminal signal sequence and a transme

63 re we report that a biotin acceptor peptide (BAP) substrate for Escherichia coli biotin holoenzyme sy

64 d to the bacterial biotin acceptor peptides (BAP) varies among different mammalian cell types and can

65 erous low molecular mass bioactive peptides (BAPs) can be generated during the hydrolysis of bovine m

66 ties including the broader autism phenotype (BAP) [2, 3].

67 Studies of this broad autism phenotype (BAP) may provide a potentially important complementary a

68 nd serum bone-specific alkaline phosphatase (BAP) were measured.

69 e (Ntx) and serum bone alkaline phosphatase (BAP) were obtained in 1,824 bisphosphonate-treated patie

70 id hormone (PTH), bone alkaline phosphatase (BAP), and C-telopeptide (CTX) in youth infected with hum

71 sing Ab's against bone alkaline phosphatase (BAP), CD3, and CD20, respectively, in 12 premenopausal w

72 ocalcin, bone-specific alkaline phosphatase (BAP), procollagen I carboxy-terminal propeptide, and tar

73 hich encodes bacterial alkaline phosphatase (BAP).

74 f urine plated onto blood (blood agar plate [BAP]), colistin-nalidixic acid (CNA), and MacConkey agar

75 eading organisms on sheep blood agar plates (BAP), having typical gram-negative rod plate morphology,

76 d from growth on BMHA and blood agar plates (BAP), with and without cefoxitin disk induction.

77 stral basolateral (BLA) and basal posterior (BAP)- as they provide a major source of glutamatergic in

78 The backpropagating action potential (BAP) is hypothesised to provide distance-dependent infor

79 d products, and biomass-associated products (BAP).

80 d source of brown/brite adipose progenitors (BAPs).

81 We now describe a protein, BAP-135, that is associated with Btk in B cells and is a

82 entified a mammalian BiP-associated protein, BAP, using a yeast two-hybrid screen that shared low hom

83 Bronchial allergen provocations (BAP) were repeated at weeks 1, 2, 4, and 8.

84 Outcomes included change in TRP, PTH, BAP, and CTX from baseline to week 12 by TDF/noTDF; and

85 Highly purified BAP catalyzed Pt oxidation with specific activities of 6

86 ronic topical application of benzo[a]pyrene (BAP) on the accumulation and removal of BAP-DNA adducts

87 s and the ABA response, whereas in the root, BAP rapidly and strongly up-regulates the majority of pr

88 Serum BAP posttreatment was negatively related to percentage c

89 In the shoot, BAP up-regulates the abundance of proteins involved in a

90 A and fibroblast growth factor-2 signaling (BAP treatment).

91 reticulum (ER)-associated co-chaperone SIL1/BAP were identified to be the major cause of MSS.

92 Age- and sex-specific BAP and CTX concentrations of at least the 97th percenti

93 toward the 14-3-3 protein and BCR substrate, BAP-1.

94 Surprisingly, BAP catalyzes the oxidation of Pt to phosphate and molec

95 Our results confirm that BAP treated hESC (ESCd) lack a mesoderm signature and ar

96 We demonstrate that BAP predominantly regulates proteins involved in carbohy

97 Together, these data demonstrate that BAP serves as a nucleotide exchange factor for BiP and p

98 mmunofluorescence staining demonstrated that BAP co-localized with GRP94 in the endoplasmic reticulum

99 Furthermore, we found that BAP treatment affects endogenous hormonal homeostasis, a

100 rements of hormone metabolites, showing that BAP increases ABA levels in the shoot and 1-aminocyclopr

101 on mutagenesis studies strongly suggest that BAP is the only enzyme involved in the phoA-dependent pa

102 en together, these observations suggest that BAP-135 may reside downstream of Btk in a signaling path

103 characteristic of the syndrome [6-9] and the BAP [10, 11], we examined whether neural sensitivity to

104 Tumors expressing the BAP-TM have high sensitivity for magnetic resonance and

105 mplex associates either with Osa to form the BAP complex or with Bap170 and Bap180 to form the PBAP c

106 d electron microscopy (EM) structures of the BAP variant of ClpB that binds the protease ClpP, clearl

107 offices, the OIA was more sensitive than the BAP culture.

108 We also identified that the BAP chromatin-remodeling complex probably functions coop

109 Thus, the BAP genes function as general negative regulators of PCD

110 individuals with autism and parents with the BAP differed from controls on measures of social cogniti

111 This BAP-TM allows noninvasive real-time imaging of any cell

112 Thus, BAP is a unique Pt-dependent, H2-evolving hydrogenase.

113 increased in T. versicolor roots exposed to BAP, but not DMBQ or maize root exudates.

114 also increased in L. muraria in response to BAP treatment.

115 IDASE2, in the early root growth response to BAP.

116 rasting shoot and root proteome responses to BAP.

117 from a c-fos promoter relative to wild-type BAP/TFII-I in transfected COS-7 cells, consistent with t

118 t always need to be routinely confirmed with BAP cultures.

119 Animals were treated with BAP at 10, 25, or 50 nMol topically once or twice per we

120 djacent helix-loop-helix-like repeats within BAP/TFII-I.