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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 l insight into the interaction mechanisms of leucine-rich repeat proteins.
6 oll-Interleukin1 Receptor-nucleotide binding-Leucine-rich repeat) protein.
7 tor TLR8, and the inflammasome protein NAcht leucine-rich repeat protein 1 (NALP1).
8 LRR1) (cullin2 RING ubiquitin ligase complex/leucine-rich repeat protein 1) complex as the E3 ligase
9 stem [thioester-containing protein 1 (TEP1), leucine-rich repeat protein 1, and Anopheles Plasmodium-
10 iated with variants of NALP1, encoding NACHT leucine-rich repeat protein 1.
11 otein 1, and Anopheles Plasmodium-responsive leucine-rich repeat protein 1] prevented melanization of
12                         Nuclear localization leucine-rich-repeat protein 1 (NLRP1) is a key regulator
13 show that a molecular platform [NALP1 (NAcht leucine-rich-repeat protein 1) inflammasome] consisting
14  a candidate gene NALP1, which encodes NACHT leucine-rich-repeat protein 1, a regulator of the innate
15 nes for vitiligo have been identified, NACHT-leucine-rich-repeat protein-1 (NALP1), part of the infla
16  (NSD1), and a lysine demethylase, F-box and leucine-rich repeat protein 11 (FBXL11).
17 he EMT inducer Twist1 by enhancing F-box and leucine-rich repeat protein 14 (FBXL14)-mediated polyubi
18         Here, we show that Fbxl17 (F-box and leucine-rich repeat protein 17) targets Sufu for proteol
19  sarcomere proteins, we identified F-box and leucine-rich repeat protein 22 (Fbxl22).
20 ulators, casein kinase 1 (CKI) and F-box and leucine-rich repeat protein 3 (FBXL3), modulate the stab
21 hesis that the nucleotide-binding domain and leucine-rich repeat protein 3 (NLRP3) inflammasome, an i
22  is capable of triggering NLRP3 (NLR-family, leucine-rich repeat protein 3) inflammasome activation a
23 lex that contains cullin 1 and the F-box and leucine-rich repeat protein 4 (FbxL4).
24     The hemerythrin-like domain of F-box and leucine-rich repeat protein 5 (FBXL5), an E3 ubiquitin l
25 resistance genes encoding nucleotide binding-leucine rich repeat proteins and genes encoding pentatri
26     Lgi4 encodes a secreted and glycosylated leucine-rich repeat protein and is expressed in Schwann
27  proteins interacted with nucleotide binding-leucine-rich repeat proteins and effector proteins, sugg
28                                    The small leucine-rich repeat proteins and proteoglycans (SLRPs) f
29 ose for F-box factors, ubiquitin conjugases, Leucine-rich repeat proteins, and metabolic enzymes, and
30      Several NLR (nucleotide-binding domain, leucine-rich repeat) proteins are implicated in the form
31              NLR (nucleotide-binding domain, leucine-rich repeat) proteins are intracellular regulato
32     Human placental RNase inhibitor (hRI), a leucine-rich repeat protein, binds the blood vessel-indu
33 bspA gene encoding a cell surface associated leucine-rich repeat protein (BspA) involved in adhesion
34 surface-associated, as well as the secreted, leucine-rich-repeat protein (BspA) of this bacterium hav
35  to a portion of the Tannerella forsythensis leucine-rich repeat protein, BspA, which is mediated by
36 munity in jawless vertebrates is mediated by leucine-rich repeat proteins called "variable lymphocyte
37 multi-PDZ (PSD-95, Discs-large and ZO-1) and leucine-rich-repeat protein, cause aberrant cell shapes
38 rice gene Xa1, encoding a nucleotide-binding leucine-rich repeat protein, confers resistance against
39 enes encoding coiled-coil nucleotide-binding leucine-rich repeat proteins designated CNL3 and CNL13.
40         Surprisingly, a single transmembrane leucine-rich repeat protein, DMA-1, plays a major role i
41 sed this coiled-coil nucleotide-binding site leucine-rich repeat protein-encoding gene as a model for
42 te that reovirus binds Nogo receptor NgR1, a leucine-rich repeat protein expressed in the CNS, to inf
43 roteins of the immunoglobulin, cadherin, and leucine-rich repeat protein families, as well as secrete
44 C1 is a member of the SDS22+ subclass of the leucine-rich repeat protein family and as such is likely
45 chain 1 (LC1) polypeptide is a member of the leucine-rich repeat protein family and binds at or near
46 peats of a sequence that assigns them to the leucine-rich repeat protein family.
47 a membrane-localized nucleotide binding site/leucine-rich repeat protein from Arabidopsis thaliana, a
48                        We show that LeSHY, a leucine-rich repeat protein from pollen, and LeSTIG1, a
49 d loss-of-function analyses implicate LTL, a leucine-rich repeat protein, in the regulation of wing g
50 rc1e as a nucleotide-binding oligomerization-leucine-rich repeat protein involved in the detection an
51                                      YopM, a leucine-rich repeat protein, is a critical virulence fac
52 of nucleotide-binding oligomerization domain-leucine-rich repeat proteins, is critical in such a resp
53 usly unrecognized role for the transmembrane leucine-rich repeat protein Lapsyn in regulating mng dev
54 nst degeneration and indicate a role for the leucine-rich repeat protein LINGO-1 and related classes
55               These results suggest that the leucine-rich repeat protein LrrA plays a role in the att
56                    The gene lrrA, encoding a leucine-rich repeat protein, LrrA, that contains eight c
57       The aberrant nuclear localization of a leucine-rich repeat protein might result in additional p
58 association of the nucleotide-binding domain leucine-rich repeat protein Monarch-1 with heat shock pr
59 trins G1 and G2, which are known to bind the leucine-rich repeat proteins netrin G ligand (NGL)-1 and
60 hibit caspase-1 activation by the NLR family leucine-rich repeat protein (NLRP)1 and NLRP3 inflammaso
61                Nucleotide binding domain and leucine-rich repeat proteins (NLRs) are important recept
62                    Nucleotide-binding domain leucine-rich repeat proteins (NLRs) play a key role in i
63                The nucleotide-binding domain leucine-rich repeat proteins (NLRs) represent the major
64                           Nucleotide-binding leucine-rich repeat proteins (NLRs) serve as intracellul
65 s in the expansion of nucleotide-binding and leucine-rich-repeat proteins (NLRs), the major disease-r
66 e TLRs and cytosolic nucleotide binding site/leucine-rich repeat proteins Nod1 and Nod2 in epithelial
67               Pleckstrin homology domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a
68       We show that the phosphatase PH domain leucine-rich repeat protein phosphatase (PHLPP) downstre
69  we show that the pleckstrin homology domain leucine-rich repeat protein phosphatase (PHLPP) suppress
70 ge decrease of protein phosphatase PH domain leucine-rich repeat protein phosphatase (PHLPP) was foun
71 mily of protein phosphatases named PH domain leucine-rich repeat protein phosphatase (PHLPP) whose me
72 n this study, we demonstrated that PH domain leucine-rich repeat protein phosphatase (PHLPP), a novel
73 we identify a protein phosphatase, PH domain leucine-rich repeat protein phosphatase (PHLPP), that sp
74 otif phosphatase, pleckstrin homology domain leucine-rich repeat protein phosphatase (PHLPP).
75 we identified pleckstrin homology domain and leucine-rich repeat protein phosphatase 1 (PHLPP1) as a
76               The pleckstrin homology domain leucine-rich repeat protein phosphatase 1 (PHLPP1) diffe
77 tion of two splice variants of PH domain and Leucine-rich repeat Protein Phosphatase 1 (PHLPP1), PHLP
78                            PHLPP1 (PH domain leucine-rich repeat protein phosphatase 1) is a protein-
79                            PHLPP2 (PH domain leucine-rich repeat protein phosphatase 2) terminates Ak
80 co-localization of Akt and PHLPP1 (PH domain leucine-rich repeat protein phosphatase isoform 1), a Se
81 ery of the PHLPP (pleckstrin homology domain leucine-rich repeat protein phosphatase) family of Ser/T
82 tase PHLPP1 (pleckstrin homology (PH) domain leucine-rich repeat protein phosphatase) to Akt.
83                                The PH domain leucine-rich repeat protein phosphatase, PHLPP, plays a
84 red a novel phosphatase PHLPP, for PH domain leucine-rich repeat protein phosphatase, which terminate
85 on of Akt through pleckstrin homology domain leucine-rich repeats protein phosphatase (PHLPP) 2.
86                                    PH domain leucine-rich-repeats protein phosphatase (PHLPP) is a fa
87 tion of the translation of the PH domain and leucine-rich repeat protein phosphatases 1 (PHLPP1), a p
88 or 1 (NHERF1) and pleckstrin-homology domain leucine-rich repeat protein phosphatases 1 (PHLPP1).
89      We tested the effect of the novel small leucine-rich repeat protein podocan on SMC migration and
90 c map of the entire folding landscape of the leucine-rich repeat protein, pp32 (Anp32), obtained by c
91 r matrix component proline/arginine-rich end leucine-rich repeat protein (PRELP) is a novel antibacte
92 lar complex with the nucleotide binding site-leucine rich repeats protein Prf.
93  complex, composed of the nucleotide-binding leucine-rich repeats protein Prf and the protein kinase
94 in can be identified in virulence-associated leucine-rich repeat proteins produced by Salmonella typh
95 in depolymerizing factor (PtADF) and a novel leucine-rich repeat protein (PtLRR).
96 y or signaling functions and include S/D4, a leucine-rich repeat protein, S/D1, a LIM-domain protein,
97 dulin have different developmental stage and leucine-rich repeat protein specific functions in the re
98                             The role(s) of a leucine-rich repeat protein subfamily in the regulation
99                        YopM, a member of the leucine-rich repeat protein superfamily, is an effector
100 1.2 encodes a coiled-coil nucleotide-binding leucine-rich repeat protein that in addition to potato a
101 ive leucine-rich repeat 1 (APL1), encoding a leucine-rich repeat protein that is similar to molecules
102 psis thaliana CLAVATA2 (CLV2) gene encodes a leucine-rich repeat protein that regulates the developme
103   SLRPs belong to the group of extracellular leucine-rich repeat proteins that are flanked at both en
104     Variable lymphocyte receptors (VLRs) are leucine-rich repeat proteins that mediate adaptive immun
105 tomes, the lampreys and hagfish, instead use leucine-rich repeat proteins to construct variable lymph
106 e assigned the name of Hal (heme-acquisition leucine-rich repeat protein) to BAS0520.
107 , the polypeptide was designated T. pallidum leucine-rich repeat protein (TpLRR).
108 identified the ODA7 gene product as a 58-kDa leucine-rich repeat protein unrelated to outer row dynei
109                       FLOR1, which encodes a leucine-rich repeat protein, was induced in the early in
110 s a common structural feature found in other leucine-rich repeat proteins, we have defined characteri
111 g member of the Lrig family of transmembrane leucine-rich repeat proteins, which also includes Lrig2
112 structure reveals a bent solenoid typical of leucine-rich repeat proteins with an amino-terminal pock
113 multigene family encoding nucleotide-binding leucine-rich repeat proteins with Toll/interleukin-1 rec
114           Here we identify a brain-specific, leucine-rich-repeat protein with high affinity for solub
115    Finally, we show that inactivation of the leucine-rich repeat protein ZYG-11 produces meiotic and

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