ライフサイエンスコーパス: phospho-

1 -phosphocholine/1,2-dimyristoyl-sn-glycero-3-phospho- (1'-rac-glycerol)/cholesterol lipid bilayers us

2 -hexadecyl-2-(11Z-octadecenoyl)-sn-glycero-3-phospho-(1'-myo-inositol), in which the sn-1 position co

3 ly charged 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (POPG), or a POPC/POPG mixture

4 ta segment in LPPG (1-palmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt)) micelles show e

5 ids, POPG (1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt)), POPS (1-palmit

6 12:0PC:diC12:0PG [1,2-dilauroyl-sn-glycero-3-phospho-(1'-rac-glycerol)] liposomes were investigated u

7 phosphocholine, 1,2-dipalmitoyl-sn-glycero-3-phospho-(1'-rac-glycerol)] units.

8 rol) and Phos (1,2-dipalmitoyl-sn-glycerol-3-phospho-(1'rac-glycerol)) via disulfide bond formation.

9 er sulfate from adenosine 3'-phosphophate 5'-phospho-[35S]sulfate ([35S]PAPS) to the 3-OH position of

10 pho-AKT staining was associated with that of phospho (active)-mTOR in 27 of 31 (87%) ovarian tumors,

11 factor-alpha (6.4+/-1.3-fold) and increased phospho-(active) EGFR (5.9+/-1.1-fold), phospho-(active)

12 ased phospho-(active) EGFR (5.9+/-1.1-fold), phospho-(active) ErbB2 (2.3+/-0.2-fold), and phospho-(ac

13 phospho-(active) ErbB2 (2.3+/-0.2-fold), and phospho-(active) extracellular signal-regulated kinase (

14 differences in the RNA-binding properties of phospho- and dephosphoPKR.

15 izing enzymes it is able to increase overall phospho- and glycolipid synthesis.

16 resolving acidic phosphopeptides from other phospho- and non-phosphopeptides.

17 By comparing the levels of phospho- and nonphosphopeptides, the in vivo phosphoryla

18 These fractions, rich in phospho- and sphingolipids, were strongly antiproliferat

19 libraries using these scaffolds yielded >50 phospho- and target-specific mAbs against 70% of target

20 Both phospho- and total SGK1 increased 2 to 7 days after band

21 d the overlap in chemical properties between phospho- and unmodified peptides, it is likely that the

22 n cell proliferation (PCNA, Ki-67, cyclin A, phospho- cdc2, p21Waf, p27Kip) was transient ( approxima

23 The developed strategy enriches phospho- content from biological samples like phosvitin

24 sphorylation with formation of GalNAcbeta1-4(phospho-)GlcNAc.

25 creatine and accumulation of the precursor (phospho-)guanidinoacetate (P-GA).

26 Activated (phospho-) JNK colocalizes with FAK in focal adhesions of

27 of coenzyme F 420 involves the coupling of 2-phospho- l-lactate (LP) to 7,8-didemethyl-8-hydroxy-5-de

28 ensation requires an initial activation of 2-phospho- l-lactate through a pyrophosphate linkage to GM

29 -L 5', coding for the nucleocapsid, unknown, phospho-, matrix, fusion, hemagglutinin-neuraminidase, a

30 tion and to maintain a high level of active (phospho-) mitogen-activated protein kinases (MAPKs).

31 The enriched phospho- moieties are analyzed by matrix-assisted laser

32 Neither phospho- nor dephospho-KEPI inhibits protein phosphatase

33 -RCN and inhibited by high concentrations of phospho- or dephospho-RCN.

34 sphingosine 1-phosphate, or other sphingo-, phospho-, or glycerolipids tested.

35 wo viral polypeptides, the large (L) and the phospho- (P) proteins.

36 Morphine-induced phospho- (P-)GSK3beta was reduced 5 min after reperfusio

37 Rabies virus (RabV) phospho (P) protein, which is largely responsible for an

38 Activated phospho (p)-(Tyr416)-SRC was detected in the majority of

39 LX4032-resistant (PPRM) cell lines show dual phospho (p)-ERK and p-AKT upregulation, and their growth

40 ithelial cells showed enhanced expression of phospho (p)-mTOR in HIV-1 transgenic mice (Tgs).

41 IHC was performed for p53, p21, and phospho (p)-p38 mitogen-activated protein kinase (MAPK)

42 PI3K, phospho (p)-PKB, and PAK were co-localized to the site o

43 utable to its abnormal association with more phospho (P)-serine-type 1 insulin receptor substrate (IR

44 signaling in vivo, increasing the levels of phospho (P)-SMAD1 and decreasing P-SMAD3.

45 PA buffer and subjected to Western blot with phospho (p)-specific antibodies against p-JNK and p-c-Ju

46 We describe the synthesis of 3'-phospho-(para-nitrophenyl) oligonucleotides (3'-pNP DNAs

47 lly interpreted the exomes and quantitative (phospho-)proteomes of five ovarian cancer cell lines and

48 sponses in quantitative gene expression and (phospho-)proteomics data sets.

49 enzyme 11 (MRE11)-dependent accumulation of (phospho-)replication protein A (RPA)-coated ssDNA.

50 otidase had no effect on ATP/ADP/UTP-induced phospho- rylation of AMPK, indicating that AMPK activati

51 rnating animals, reduction of immunoreactive phospho (S473)-Akt was noted throughout the brain.

52 IX that accommodates an amphipathic helix in phospho (Ser-133) KID.

53 ecognize full-length CREB.CBP complexes in a phospho-(Ser(133))-dependent manner demonstrates that th

54 recruitment of CBP and RNA polymerase II to phospho-(Ser-133) CREB, attenuates transcriptional induc

55 A polymerase II to be recruited to CREB in a phospho-(Ser-133)-dependent manner.

56 body recognizing the Akt phosphomotif (alpha-phospho-[Ser/Thr] Akt substrate [PAS]), and PAS immunore

57 ver, and this repression was relieved by the phospho (Ser133) KID-dependent recruitment of p300 histo

58 KID stimulates transcription via a phospho (Ser133)-dependent interaction with the coactiva

59 Basal phospho-(Ser40)-TH levels did not differ between groups

60 to D-amphetamine (0.5 and 5.0 mg/kg, i.p.), phospho-(Ser40)-TH was selectively decreased in NAc of F