戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 kinase activity but it is independent of its sterile alpha motif.
2 mCystin, that contains ankyrin repeats and a sterile alpha motif.
3  cortactin SH3 domain-binding peptides and a sterile alpha motif.
4 d in the p63 carboxyl-terminal region with a sterile alpha-motif.
5 ruitment, highlighting the essential role of Sterile Alpha Motifs.
6                              Tnk1 contains a sterile alpha motif, a tyrosine kinase catalytic domain,
7 ymerases, we have detected new HhH motifs in sterile alpha motif and barrier-to-autointegration facto
8  difference may be due to degradation of the sterile alpha motif and HD domain 1 (SAMHD1) host restri
9 the homologs that are best studied are human sterile alpha motif and HD domain-containing protein 1 (
10                                              Sterile alpha motif and HD domain-containing protein 1 (
11                                              Sterile alpha motif and HD domain-containing protein 1 (
12                                              Sterile alpha motif and HD domain-containing protein 1 (
13                                          The sterile alpha motif and HD domain-containing protein 1 (
14                                              Sterile alpha motif and HD domain-containing protein 1 (
15                                      SAMHD1 (sterile alpha motif and HD domain-containing protein 1)
16                                              Sterile alpha motif and HD domain-containing protein-1 (
17                 The HIV-1 restriction factor sterile alpha motif and HD domain-containing protein-1 (
18                                          The sterile alpha motif and HD domain-containing protein-1 (
19                                              Sterile alpha motif and HD-domain containing protein 1 (
20                                        Human sterile alpha motif and HD-domain-containing protein 1 (
21                                      SAMHD1 (sterile alpha motif and histidine (H) aspartate (D) doma
22 h results from the cellular dNTP hydrolyzing sterile alpha motif and histidine aspartic domain contai
23                                              Sterile alpha motif and histidine-aspartate (HD) domain-
24                                              Sterile alpha motif and histidine-aspartate (HD) domain-
25                      In humans, mutations in sterile alpha motif and histidine-aspartate domain-conta
26                                We found that sterile alpha motif and histidine-aspartate domain-conta
27                                              Sterile alpha motif and histidine-aspartate domain-conta
28                                              Sterile alpha motif and histidine-aspartic acid domain-c
29  demonstrate that HPV16 replication converts sterile alpha motif and histidine-aspartic domain HD-con
30            We have demonstrated that SAMHD1 (sterile alpha motif and histidine-aspartic domain HD-con
31 e triphosphate triphosphohydrolase (dNTPase) sterile alpha motif and histidine/aspartic domain-contai
32 ctor in stressful conditions, the MAP3K ZAK (Sterile alpha motif and leucine zipper-containing kinase
33 es an autoinhibitory interaction between the sterile alpha motif and Rho-GAP domains of DLC1.
34  Odin, contains several ankyrin repeats, two sterile alpha motifs and a phosphotyrosine binding domai
35 ), TRIF-related adapter molecule (TRAM), and sterile alpha motifs and beta-catenin/armadillo repeats
36 d identity with TANK1 in the ankyrin repeat, sterile alpha-motif, and PARP catalytic domains but has
37 ed tRNA-binding domain of Tric1 and Tric2, a sterile-alpha-motif at the C-terminal end of the protein
38  degeneration upon knockdown of Sarm1 [SARM (sterile alpha-motif-containing and armadillo-motif conta
39 ure of DprA consists of the association of a sterile alpha motif domain and a Rossmann fold and that
40                                              Sterile alpha motif domain and HD domain-containing prot
41 gainst atherosclerosis by directly targeting Sterile Alpha Motif Domain Containing 1 (Samd1), a predi
42 is mediated through sequential activation of sterile alpha motif domain containing 4 (Samd4), mammali
43             We found that ankyrin repeat and sterile alpha motif domain containing 4B (ANKS4B) locali
44                                              Sterile alpha motif domain containing 7 (SAMD7) is a com
45 e, using proteomic strategies, we identified sterile alpha motif domain containing 9 (SAMD9), an inte
46 nse mutation (c.2640C>A, p.His880Gln) in the sterile alpha motif domain containing 9-like gene (SAMD9
47                                              Sterile alpha motif domain containing protein 4 (Samd4)
48                        Here we show that the sterile alpha motif domain of rat Shank3/ProSAP2, a mast
49  is similar to the ssRNA-binding site of the sterile alpha motif domain of the Saccharomyces cerevisi
50 embrane domains, multiple ankyrin repeats, a sterile alpha motif domain, and a potential PDZ-binding
51                                              Sterile alpha motif domain- and HD domain-containing pro
52                                        Human sterile alpha motif domain-containing 9 (SAMD9) protein
53                                              Sterile alpha motif domain-containing protein 9 (SAMD9)
54 o identify de novo heterozygous mutations in sterile alpha motif domain-containing protein 9 (SAMD9,
55 tant allele demonstrated that egt2 encodes a STERILE ALPHA MOTIF domain-containing protein.
56          This pentaloop is recognized by the sterile alpha motif domain-containing ZCCHC14 protein, w
57 would yield a protein lacking the N-terminal sterile alpha motif domain.
58  associates constitutively via an N-terminal sterile-alpha motif domain with Ste11, and this interact
59 expression of the dominant-negative Scm-SAM (sterile alpha motif) domain both affected the binding pa
60                                     The Sam (sterile alpha motif) domain from the lipid phosphatase S
61                          The yeast Vts1 SAM (sterile alpha motif) domain is a member of a new class o
62                                     Yan SAM (sterile alpha motif) domain mutations preventing polymer
63 iddleman of seventy-eight signaling), a SAM (sterile alpha motif) domain-containing cofactor that req
64 anslocation, which fuses the N-terminal SAM (sterile alpha-motif) domain of the ETV6 (or TEL) transcr
65   Deletion of the C-terminal coiled-coil and sterile alpha motif domains abolished neurabin I dimeriz
66 nkyrin repeats, a single SH3 domain, and two sterile alpha motif domains followed by a long proline-r
67                                         SAM (sterile alpha motif) domains are protein-protein interac
68              We further show that SARM1 SAM (sterile alpha motif) domains form an octamer essential f
69         By deleting exon 13 (which encodes a sterile alpha motif) from the Trp73 gene, we selectively
70                 The HIV-1 restriction factor sterile alpha-motif/histidine-aspartate domain-containin
71  with the p63alpha carboxyl terminus and its sterile alpha-motif, including the apobec-1-binding prot
72 , we have characterized a membrane-targeting sterile alpha motif-like domain in the amino terminus of
73 enerates a C-terminal domain that contains a sterile-alpha-motif-like domain.
74     Domain deletion analysis showed that the sterile alpha-motif of Mst50 but not the Ras-association
75 dies previously revealed that the N-terminal sterile alpha motif (or SAM) domain of SMSr drives self-
76     In contrast, mutation of either the SAM (sterile alpha motif) or TIR (Toll-interleukin-1 receptor
77 n, which is structurally similar to the SAM (sterile alpha motif) protein-protein interaction domain,
78 s), Eph receptors are unique in possessing a sterile alpha motif (SAM domain) at their C-terminal end
79 atalytic domain flanked by an amino-terminal sterile alpha motif (SAM) and a carboxyl-terminal START
80 -binding activity of ZCCHC14 requires both a sterile alpha motif (SAM) and a downstream unstructured
81 m has an extended C terminus consisting of a sterile alpha motif (SAM) and an extreme C terminus, it
82                                              Sterile alpha motif (SAM) and histidine-aspartic (HD) do
83                                              Sterile alpha motif (SAM) and histidine/aspartate (HD)-c
84 also generated MST11 mutant alleles with the sterile alpha motif (SAM) and Ras-association (RA) domai
85                                              Sterile alpha motif (SAM) and Src homology-3 (SH3) domai
86             Our prior work revealed that the sterile alpha motif (SAM) domain 14 (Samd14) gene increa
87 it of tankyrase, comprising the polymerizing sterile alpha motif (SAM) domain and its adjacent cataly
88               Interestingly, deletion of the sterile alpha motif (SAM) domain at the N terminus drama
89                                          The sterile alpha motif (SAM) domain is a protein interactio
90                                          The sterile alpha motif (SAM) domain is a protein module fou
91                                          The sterile alpha motif (SAM) domain of the ephrin receptor
92  an intron of Samd14 (Samd14-Enh) encoding a sterile alpha motif (SAM) domain protein.
93       aveugle encodes a small protein with a sterile alpha motif (SAM) domain that can physically int
94          The C terminus of Shank3 contains a sterile alpha motif (SAM) domain that is essential for i
95 own that tankyrase 1 polymerizes through its sterile alpha motif (SAM) domain to assemble large prote
96 13, Tyr-128, and Tyr-145, "3Y") as well as a sterile alpha motif (SAM) domain whose function is uncle
97 give rise to amino acid substitutions in the sterile alpha motif (SAM) domain, and are predicted to a
98 teraction, which requires the Scm C-terminal sterile alpha motif (SAM) domain, is crucial for the eff
99 adjacent region near the alpha9-helix in the sterile alpha motif (SAM) domain.
100 ala)via conserved residues in the C-terminal Sterile Alpha Motif (SAM) domain.
101 eptor ligation as mediated by the N-terminal sterile alpha motif (SAM) domain.
102 DGK family members, delta and eta, contain a sterile alpha motif (SAM) domain.
103 he highly conserved leucine 920 in the EphA4 sterile alpha motif (SAM) domain.
104                                              Sterile alpha motif (Sam) domains are protein interactio
105 tructures of the polymerizing TNKS and TNKS2 sterile alpha motif (SAM) domains, revealing versatile h
106 ed by malignant brain tumor domain (MBT) and sterile alpha motif (SAM) domains.
107                                  A conserved Sterile Alpha Motif (SAM) in the Polycomb Repressive Com
108 isrupting the polymerization activity of the sterile alpha motif (SAM) of the PcG protein Polyhomeoti
109 mical studies have shown that the N-terminal sterile alpha motif (SAM) of Yan is able to self associa
110 lex-drive condensate formation through their sterile alpha motif (SAM) oligomerization domains.
111 olling Ph function through modulation of its sterile alpha motif (SAM) polymerization leading to the
112  N-terminal KH domains, whereas a C-terminal sterile alpha motif (SAM) self-polymerizes in vitro and
113  encoded by ubc2 shows localized homology to Sterile Alpha Motif (SAM), Ras Association (RA) and Src
114 cruited to activated EphA2 via a heterotypic sterile alpha motif (SAM)-SAM domain interaction, leadin
115 structure of SHD2 identifies the domain as a sterile alpha-motif (SAM) domain and shows a propensity
116 rm::Polo interaction in vivo, we show that a sterile alpha-motif (SAM) domain located at the C termin
117                                          The sterile alpha-motif (SAM) domain of Mst50 was essential
118 ion of Dlx3 is abrogated by mutations in the sterile alpha-motif (SAM) domain of p63 that are associa
119  we identify and characterize the Drosophila sterile alpha-motif (SAM) domain-containing protein Cask
120 res functional integrity of its intraluminal sterile alpha-motif (SAM) domain.
121                                  Hundreds of sterile alpha-motif (SAM) domains have predicted structu
122 ure of n-NafY reveals that it belongs to the sterile alpha-motif (SAM) family of domains, which are f
123  TEL1, self-associates through an N-terminal sterile alpha-motif (SAM), leading to speculation that Y
124 roteins contain a characteristic RNA-binding sterile-alpha motif (SAM) domain and a conserved but unc
125                                It contains a sterile-alpha motif (SAM) domain, 3 phosphotyrosine moti
126 tudies, several mutations in the cytoplasmic sterile-alpha-motif (SAM) domain of human EPHA2 on chrom
127 ted by the binding of zinc to the C-terminal sterile-alpha-motif (SAM) domain of Shank3.

 
Page Top