ライフサイエンスコーパス: leucine-rich repeat protein

1 odulator of NF-kappaB activation, which is a leucine-rich repeat protein.

2 n kinase, and Prf, a nucleotide binding site-leucine-rich repeat protein.

3 Arabidopsis gene ORE9/MAX2 encodes an F-box leucine-rich repeat protein.

4 ncodes a coiled-coil-nucleotide binding site-leucine-rich repeat protein.

5 de unrelated (34.8%) nucleotide binding site leucine rich repeat proteins.

6 l insight into the interaction mechanisms of leucine-rich repeat proteins.

7 oll-Interleukin1 Receptor-nucleotide binding-Leucine-rich repeat) protein.

8 tor TLR8, and the inflammasome protein NAcht leucine-rich repeat protein 1 (NALP1).

9 LRR1) (cullin2 RING ubiquitin ligase complex/leucine-rich repeat protein 1) complex as the E3 ligase

10 stem [thioester-containing protein 1 (TEP1), leucine-rich repeat protein 1, and Anopheles Plasmodium-

11 iated with variants of NALP1, encoding NACHT leucine-rich repeat protein 1.

12 otein 1, and Anopheles Plasmodium-responsive leucine-rich repeat protein 1] prevented melanization of

13 Nuclear localization leucine-rich-repeat protein 1 (NLRP1) is a key regulator

14 show that a molecular platform [NALP1 (NAcht leucine-rich-repeat protein 1) inflammasome] consisting

15 a candidate gene NALP1, which encodes NACHT leucine-rich-repeat protein 1, a regulator of the innate

16 nes for vitiligo have been identified, NACHT-leucine-rich-repeat protein-1 (NALP1), part of the infla

17 (NSD1), and a lysine demethylase, F-box and leucine-rich repeat protein 11 (FBXL11).

18 he EMT inducer Twist1 by enhancing F-box and leucine-rich repeat protein 14 (FBXL14)-mediated polyubi

19 F-box and leucine-rich repeat protein 16 (FBXL16) is a poorly stud

20 Here, we show that Fbxl17 (F-box and leucine-rich repeat protein 17) targets Sufu for proteol

21 ein 3 (FBXO3; proinflammatory) and F-box and leucine-rich repeat protein 2 (FBXL2; anti-inflammatory

22 ISLR2 (immunoglobulin superfamily containing leucine-rich repeat protein 2) and STRA6 (stimulated by

23 sarcomere proteins, we identified F-box and leucine-rich repeat protein 22 (Fbxl22).

24 ulators, casein kinase 1 (CKI) and F-box and leucine-rich repeat protein 3 (FBXL3), modulate the stab

25 hesis that the nucleotide-binding domain and leucine-rich repeat protein 3 (NLRP3) inflammasome, an i

26 is capable of triggering NLRP3 (NLR-family, leucine-rich repeat protein 3) inflammasome activation a

27 protein A repetitions predominant (GARP) and leucine-rich repeat protein 33 (LRRC33).

28 lex that contains cullin 1 and the F-box and leucine-rich repeat protein 4 (FbxL4).

29 The hemerythrin-like domain of F-box and leucine-rich repeat protein 5 (FBXL5), an E3 ubiquitin l

30 resistance genes encoding nucleotide binding-leucine rich repeat proteins and genes encoding pentatri

31 Lgi4 encodes a secreted and glycosylated leucine-rich repeat protein and is expressed in Schwann

32 proteins interacted with nucleotide binding-leucine-rich repeat proteins and effector proteins, sugg

33 The small leucine-rich repeat proteins and proteoglycans (SLRPs) f

34 ose for F-box factors, ubiquitin conjugases, Leucine-rich repeat proteins, and metabolic enzymes, and

35 Several NLR (nucleotide-binding domain, leucine-rich repeat) proteins are implicated in the form

36 NLR (nucleotide-binding domain, leucine-rich repeat) proteins are intracellular regulato

37 ns, immunoglobulin superfamily proteins, and leucine-rich repeat proteins, as well as their associate

38 Human placental RNase inhibitor (hRI), a leucine-rich repeat protein, binds the blood vessel-indu

39 bspA gene encoding a cell surface associated leucine-rich repeat protein (BspA) involved in adhesion

40 surface-associated, as well as the secreted, leucine-rich-repeat protein (BspA) of this bacterium hav

41 to a portion of the Tannerella forsythensis leucine-rich repeat protein, BspA, which is mediated by

42 munity in jawless vertebrates is mediated by leucine-rich repeat proteins called "variable lymphocyte

43 multi-PDZ (PSD-95, Discs-large and ZO-1) and leucine-rich-repeat protein, cause aberrant cell shapes

44 s a coiled-coil, nucleotide-binding site and leucine-rich repeat protein (CNL).

45 rice gene Xa1, encoding a nucleotide-binding leucine-rich repeat protein, confers resistance against

46 enes encoding coiled-coil nucleotide-binding leucine-rich repeat proteins designated CNL3 and CNL13.

47 Surprisingly, a single transmembrane leucine-rich repeat protein, DMA-1, plays a major role i

48 sed this coiled-coil nucleotide-binding site leucine-rich repeat protein-encoding gene as a model for

49 te that reovirus binds Nogo receptor NgR1, a leucine-rich repeat protein expressed in the CNS, to inf

50 roteins of the immunoglobulin, cadherin, and leucine-rich repeat protein families, as well as secrete

51 C1 is a member of the SDS22+ subclass of the leucine-rich repeat protein family and as such is likely

52 chain 1 (LC1) polypeptide is a member of the leucine-rich repeat protein family and binds at or near

53 peats of a sequence that assigns them to the leucine-rich repeat protein family.

54 a membrane-localized nucleotide binding site/leucine-rich repeat protein from Arabidopsis thaliana, a

55 We show that LeSHY, a leucine-rich repeat protein from pollen, and LeSTIG1, a

56 d loss-of-function analyses implicate LTL, a leucine-rich repeat protein, in the regulation of wing g

57 rc1e as a nucleotide-binding oligomerization-leucine-rich repeat protein involved in the detection an

58 YopM, a leucine-rich repeat protein, is a critical virulence fac

59 ard protein, often a nucleotide-binding site-leucine-rich repeat protein, is activated by interaction

60 of nucleotide-binding oligomerization domain-leucine-rich repeat proteins, is critical in such a resp

61 usly unrecognized role for the transmembrane leucine-rich repeat protein Lapsyn in regulating mng dev

62 nst degeneration and indicate a role for the leucine-rich repeat protein LINGO-1 and related classes

63 These results suggest that the leucine-rich repeat protein LrrA plays a role in the att

64 The gene lrrA, encoding a leucine-rich repeat protein, LrrA, that contains eight c

65 rod bipolar cell terminals is regulated by a leucine-rich repeat protein, LRRTM4.

66 tly or indirectly by NLR (Nucleotide-binding Leucine-rich Repeat) proteins, many of which "guard" the

67 The aberrant nuclear localization of a leucine-rich repeat protein might result in additional p

68 association of the nucleotide-binding domain leucine-rich repeat protein Monarch-1 with heat shock pr

69 trins G1 and G2, which are known to bind the leucine-rich repeat proteins netrin G ligand (NGL)-1 and

70 ty of the rice nucleotide-binding domain and leucine-rich repeat protein (NLR) immune receptor Pik, w

71 Ptr1 candidates to eight nucleotide-binding leucine-rich repeat protein (NLR)-encoding genes.

72 hibit caspase-1 activation by the NLR family leucine-rich repeat protein (NLRP)1 and NLRP3 inflammaso

73 Nucleotide binding domain and leucine-rich repeat proteins (NLRs) are important recept

74 Nucleotide-binding domain leucine-rich repeat proteins (NLRs) play a key role in i

75 The nucleotide-binding domain leucine-rich repeat proteins (NLRs) represent the major

76 Nucleotide-binding leucine-rich repeat proteins (NLRs) serve as intracellul

77 sistance (R) genes encode nucleotide-binding leucine-rich repeat proteins (NLRs), but many have been

78 une receptors, primarily nucleotide-binding, leucine-rich repeat proteins (NLRs), detect pathogen eff

79 s in the expansion of nucleotide-binding and leucine-rich-repeat proteins (NLRs), the major disease-r

80 e TLRs and cytosolic nucleotide binding site/leucine-rich repeat proteins Nod1 and Nod2 in epithelial

81 Pleckstrin homology domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a

82 We find PHLPP2 (PH domain and leucine rich repeat protein phosphatase 2), recently ide

83 We show that the phosphatase PH domain leucine-rich repeat protein phosphatase (PHLPP) downstre

84 we show that the pleckstrin homology domain leucine-rich repeat protein phosphatase (PHLPP) suppress

85 ge decrease of protein phosphatase PH domain leucine-rich repeat protein phosphatase (PHLPP) was foun

86 mily of protein phosphatases named PH domain leucine-rich repeat protein phosphatase (PHLPP) whose me

87 n this study, we demonstrated that PH domain leucine-rich repeat protein phosphatase (PHLPP), a novel

88 we identify a protein phosphatase, PH domain leucine-rich repeat protein phosphatase (PHLPP), that sp

89 otif phosphatase, pleckstrin homology domain leucine-rich repeat protein phosphatase (PHLPP).

90 we identified pleckstrin homology domain and leucine-rich repeat protein phosphatase 1 (PHLPP1) as a

91 The pleckstrin homology domain leucine-rich repeat protein phosphatase 1 (PHLPP1) diffe

92 that deletion of the gene encoding PH domain Leucine-rich repeat Protein Phosphatase 1 (PHLPP1) prote

93 Pleckstrin homology (PH) domain and leucine-rich repeat protein phosphatase 1 (Phlpp1) regul

94 tion of two splice variants of PH domain and Leucine-rich repeat Protein Phosphatase 1 (PHLPP1), PHLP

95 PHLPP1 (PH domain leucine-rich repeat protein phosphatase 1) is a protein-

96 PHLPP2 (PH domain leucine-rich repeat protein phosphatase 2) terminates Ak

97 co-localization of Akt and PHLPP1 (PH domain leucine-rich repeat protein phosphatase isoform 1), a Se

98 ery of the PHLPP (pleckstrin homology domain leucine-rich repeat protein phosphatase) family of Ser/T

99 tase PHLPP1 (pleckstrin homology (PH) domain leucine-rich repeat protein phosphatase) to Akt.

100 The PH domain leucine-rich repeat protein phosphatase, PHLPP, plays a

101 red a novel phosphatase PHLPP, for PH domain leucine-rich repeat protein phosphatase, which terminate

102 on of Akt through pleckstrin homology domain leucine-rich repeats protein phosphatase (PHLPP) 2.

103 PH domain leucine-rich-repeats protein phosphatase (PHLPP) is a fa

104 tion of the translation of the PH domain and leucine-rich repeat protein phosphatases 1 (PHLPP1), a p

105 or 1 (NHERF1) and pleckstrin-homology domain leucine-rich repeat protein phosphatases 1 (PHLPP1).

106 We tested the effect of the novel small leucine-rich repeat protein podocan on SMC migration and

107 c map of the entire folding landscape of the leucine-rich repeat protein, pp32 (Anp32), obtained by c

108 r matrix component proline/arginine-rich end leucine-rich repeat protein (PRELP) is a novel antibacte

109 lar complex with the nucleotide binding site-leucine rich repeats protein Prf.

110 complex, composed of the nucleotide-binding leucine-rich repeats protein Prf and the protein kinase

111 in can be identified in virulence-associated leucine-rich repeat proteins produced by Salmonella typh

112 in depolymerizing factor (PtADF) and a novel leucine-rich repeat protein (PtLRR).

113 iled multi-genome-derived nucleotide-binding leucine-rich repeat protein repertoire involved in disea

114 y or signaling functions and include S/D4, a leucine-rich repeat protein, S/D1, a LIM-domain protein,

115 dulin have different developmental stage and leucine-rich repeat protein specific functions in the re

116 The role(s) of a leucine-rich repeat protein subfamily in the regulation

117 YopM, a member of the leucine-rich repeat protein superfamily, is an effector

118 1.2 encodes a coiled-coil nucleotide-binding leucine-rich repeat protein that in addition to potato a

119 r47 encodes a coiled-coil nucleotide-binding leucine-rich repeat protein that is both necessary and s

120 ive leucine-rich repeat 1 (APL1), encoding a leucine-rich repeat protein that is similar to molecules

121 psis thaliana CLAVATA2 (CLV2) gene encodes a leucine-rich repeat protein that regulates the developme

122 SLRPs belong to the group of extracellular leucine-rich repeat proteins that are flanked at both en

123 Variable lymphocyte receptors (VLRs) are leucine-rich repeat proteins that mediate adaptive immun

124 al helper NLR (nucleotide-binding domain and leucine-rich repeat) proteins that execute immune respon

125 tomes, the lampreys and hagfish, instead use leucine-rich repeat proteins to construct variable lymph

126 e assigned the name of Hal (heme-acquisition leucine-rich repeat protein) to BAS0520.

127 , the polypeptide was designated T. pallidum leucine-rich repeat protein (TpLRR).

128 identified the ODA7 gene product as a 58-kDa leucine-rich repeat protein unrelated to outer row dynei

129 FLOR1, which encodes a leucine-rich repeat protein, was induced in the early in

130 s a common structural feature found in other leucine-rich repeat proteins, we have defined characteri

131 g member of the Lrig family of transmembrane leucine-rich repeat proteins, which also includes Lrig2

132 structure reveals a bent solenoid typical of leucine-rich repeat proteins with an amino-terminal pock

133 multigene family encoding nucleotide-binding leucine-rich repeat proteins with Toll/interleukin-1 rec

134 Here we identify a brain-specific, leucine-rich-repeat protein with high affinity for solub

135 Finally, we show that inactivation of the leucine-rich repeat protein ZYG-11 produces meiotic and