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1  with autologous dendritic cells pulsed with Id protein.
2 : muscle regulatory factors, E proteins, and Id proteins.
3 y another class of HLH proteins known as the Id proteins.
4  dependency on the unlimited availability of Id proteins.
5 el transcriptional activity of the mammalian Id proteins.
6 eins MyoD and E12, and not at all with other Id proteins.
7  interplay between gammaherpesvirus RTAs and ID proteins.
8 ele, leading to an overall reduced dosage of Id proteins.
9 n emphasis on the known requirements for the ID proteins.
10 sarcomas coordinately overexpressed USP1 and ID proteins.
11 ergistic activity of Gata4 and Nkx2.5 by the Id proteins.
12 trolled in part by intrinsically disordered (ID) proteins.
13 6) V1V2, V2 HS, V3, and gp41 immunodominant (ID) proteins.
14  characteristic of intrinsically disordered (ID) proteins.
15      However, Usp1 deficiency did not impact Id protein abundance in effector T cells or alter effect
16                                              Id proteins act as negative regulators of bHLH transcrip
17                               E proteins and Id proteins also function to inhibit or promote cell pro
18 dimer partners-the Inhibitor of DNA-binding (ID) proteins-also exists.
19  proliferation and enhanced the secretion of Id protein and cytokines by myeloma cells.
20 dritic cells (DCs) pulsed with tumor-derived Id protein and now report on 35 patients treated using t
21  indicating that myeloma cells could process Id protein and present Id peptides in the context of the
22   Myozap is a recent addition to the list of ID proteins and has been implicated in serum-response fa
23 he G1 progression and apoptosis functions of Id proteins and hint at a common mechanism for this fami
24  those in the corresponding positions of the Id proteins and MyoD.
25 /2 (Id-1/2) by catalyzing phosphorylation of Id proteins and recruiting TRAF-6.
26  responses, suggesting a mechanism involving Id protein- and E protein-mediated survival and differen
27 atio of E-box transcription factors to their Id protein antagonists.
28                                              Id proteins antagonize basic helix-loop-helix proteins,
29                                              Id proteins are a class of dominant-negative antagonists
30                                          The Id proteins are a family of related mammalian helix-loop
31                                              Id proteins are believed to block expression of muscle-s
32                                              Id proteins are dominant negative regulators of basic he
33                                   Therefore, Id proteins are good candidates for regulating Math1 in
34                                              Id proteins are helix-loop-helix (HLH) transcriptional f
35                                              Id proteins are helix-loop-helix transcription factors t
36                                              Id proteins are inhibitors of basic helix-loop-helix tra
37                                              Id proteins are known negative regulators of E-box prote
38                                              Id proteins are known to play important roles in the pro
39                                              ID proteins are master regulators of stemness and anchor
40                                              Id proteins are negative regulators of basic helix-loop-
41 ng near a specific set of 170 genes encoding ID proteins are significantly enriched for association w
42        The helix-loop-helix (HLH)-containing Id proteins are trans-acting negative regulators of DNA
43                           The E proteins and Id proteins are, respectively, the positive and negative
44 hibitors of differentiation and DNA binding (Id) proteins are known to negatively regulate many bHLH
45 es encoding cardiomyocyte intercalated disc (ID) proteins are more enriched for associations with QT
46                    Inhibitor of DNA binding (ID) proteins are transcriptional targets of TGF-beta1 an
47  transcription factors and their inhibitors, Id proteins, are important regulators of both CD4(+) and
48                        This study identifies Id proteins as negative regulators of T cell specificati
49 , including modulation of DNA binding by the Id proteins, association with the transcriptional modula
50 th adaptive and innate-like requirements for ID proteins at distinct checkpoints during iNKT cell dev
51 en receptor and/or cytokine signaling, the E-Id protein axis modulates the activities of the PI3K-AKT
52    It is now well established that the E and Id protein axis regulates multiple steps in lymphocyte d
53 previous observations, we propose that the E-Id protein axis specifies innate and adaptive lymphoid c
54                                              Id proteins belong to a class of nuclear transcription f
55                                          The Id proteins belong to a family of nuclear HLH proteins l
56                                              Id proteins bind basic helix-loop-helix transcription fa
57                    Inhibitor of DNA binding (Id) proteins bind to and inhibit the function of basic h
58                   Inhibitors of DNA binding (ID) proteins block E-protein DNA binding in common lymph
59                    In addition, the OLIG and ID proteins both interacted with the E2A proteins E12 an
60 ctivities of E proteins and their antagonist Id proteins, but how these factors regulate early T cell
61           Induction of phospho-Smad1/5/8 and Id protein by BMP4 was also reduced in female hPASMCs.
62 s effector RBPSuh (CSL), GATA-3, E2A/HEB and Id proteins, c-Myb, TCF-1, and members of the Runx, Ets,
63 NA-binding domain, all four of the mammalian Id proteins can activate GAL4-dependent transcription.
64                                              Id proteins can also act as positive regulators of cell
65 ants and in vivo overexpression to show that Id proteins can differentially inhibit the activities of
66 mechanism by which autophagic degradation of Id proteins can regulate cell differentiation.
67    Inhibitor of differentiation/DNA binding (Id) proteins comprise a class of helix-loop-helix transc
68                                          TCR Id protein conjugated to keyhole limpet hemocyanin (KLH)
69 insight into the mechanisms by which E2A and Id proteins control cell growth.
70 n factors and their negative regulators, the Id proteins, control the development of iNKT sublineages
71 E proteins and their natural inhibitors, the Id proteins, control the timing of differentiation and t
72                                              Id proteins coordinate cell growth and differentiation p
73                          In mammalian cells, Id proteins coordinate proliferation and differentiation
74                      The presence of several Id proteins could reflect simple redundancy in function,
75 suggest that pharmacological inactivation of ID proteins could serve as a therapeutic strategy.
76               Our results demonstrate a new, Id protein-dependent, molecular mechanism of Notch1 repr
77 knockdown in osteosarcoma cells precipitated ID protein destabilization, cell-cycle arrest, and osteo
78 nisms that control the balance between E and Id proteins during DC subset specification remain unknow
79 insight into the dynamic regulation of E and Id proteins during this process.
80 of lineage-specific transcription factors by Id proteins enables the self-renewal response to LIF/STA
81  rate (FDR) of 5%, we had identified 28 such ID protein-encoding genes.
82  in myoblasts (a) decreased the level of the Id proteins, even in a culture in growth medium, and (b)
83 on of tumor-specific Ags or patient-specific Id protein expression.
84                  We show that the Drosophila Id protein Extra macrochaetae (Emc) also affects develop
85 ins to activate them, with expression of the Id protein Extramacrochaetae (Emc), which antagonizes bH
86 ifier screen in Drosophila, we show that the Id protein Extramacrochaetae enables growth by suppressi
87                                          The ID protein family is a critical transcriptional regulato
88 e the degradation of all four members of the ID protein family, suggesting an evolutionarily conserve
89  by members of the inhibitor of DNA binding (Id) protein family.
90                   Together, Cbfa1, p204, and Id proteins form a regulatory circuit and act in concert
91                              In contrast, an Id protein-FrC conjugate boosted both Id-specific and Fr
92  the depletion of CD4+ T cells converted the Id protein-FrC conjugate vaccine into an inhibitor.
93 sponses; yet, these were cross-reactive with Id proteins from other patient's tumors.
94 ific immune response detecting tumor-derived Id proteins from the original tumor and from all tumor v
95 unized 2 healthy human stem-cell donors with Id proteins from their recipients.
96                                              ID proteins function as antagonists of the E protein tra
97                                          The Id proteins function as dominant negative inhibitors of
98 d identifiers, such as UniProt, ChEBI and GO IDs, protein, gene and complex names or synonyms.
99                   Enforced overexpression of Id proteins has previously been shown to promote the cel
100 ese studies show that the entire ensemble of Id proteins has the ability to interact with E47, identi
101 esults are consistent with the idea that the Id proteins have a transcriptional activity when present
102 s a "hot spot" for heart disease, as several ID proteins have been found mutated in cardiomyopathy.
103        As negative regulators of E proteins, Id proteins have been implicated in lymphocyte developme
104                                          The Id proteins have been reported generally to function as
105 bers of the helix-loop-helix (HLH) family of Id proteins have demonstrated roles in the regulation of
106                                              ID-proteins have been implicated in the control of diffe
107 oteins and their functional antagonists, the ID proteins, have significant roles in normal hematopoie
108  in clinical studies of Id vaccination using Id proteins.However, Id protein is laborious and time-co
109                                              Id proteins (Id1 to Id4) are helix-loop-helix transcript
110                        Dimerization of three Id proteins (Id1, Id2, and Id3) with the four class A E
111 tivities of the MyoD and E47 proteins by the Id proteins: Id1, Id2, and Id3.
112                  Consistent with the role of Id proteins, Id2 prevents activation of p57Kip2 expressi
113  consequence of (i) binding and sequestering Id proteins, (ii) accelerating their ubiquitination and
114 quamous cell carcinoma of the head and neck, Id protein immunoreactivity was observed in the majority
115 nd in knockout mice implicate E proteins and ID proteins in a wide variety of diseases, belying the n
116                         The participation of Id proteins in advanced human malignancy, where they are
117 ht to determine the functional role of these Id proteins in BMP-induced osteoblast differentiation.
118             p204 overcame this inhibition by Id proteins in consequence of (i) binding and sequesteri
119   We found that lentiviral overexpression of ID proteins in cord blood HSCs biases myeloerythroid com
120                  The divergent regulation of Id proteins in distinct hypoxic cells may explain some o
121  steroid hormone receptors in particular and ID proteins in general can have multiple functionally di
122 e discuss the function and regulation of the Id proteins in lymphocyte development.
123 training factor of the oncogenic activity of Id proteins in neural tumors.
124                 Depletion of Cdh1 stabilizes Id proteins in neurons, whereas Id2 D-box mutants are im
125 usly identified the major binding partner of Id proteins in pluripotent cells as the basic helix-loop
126 s directly interact with previously reported ID proteins in six known pathways essential for cognitiv
127 stem cells is the constitutive expression of ID proteins in the former and inducible expression in th
128 oteasomes, and (iii) decreasing the level of Id proteins in the nucleus by increasing their transloca
129                       (ii) p204 bound to the Id proteins in vitro and in vivo.
130 which bind to the helix-loop-helix domain of Id proteins in vitro and in vivo.
131 tablished that inhibitor of differentiation (Id) proteins, including Id1, Id2, and Id3, associate wit
132                    Inhibitor of DNA binding (Id) proteins, including Id1-4, are transcriptional regul
133 can induce the degradation of all four human ID proteins, indicating that the interplay between gamma
134                                              Id proteins inhibit differentiation by HLH-mediated hete
135 ous or ectopic inhibitor of differentiation (Id) proteins inhibited the differentiation of P19 cells
136 ression in mesenchymal stem cells stabilized ID proteins, inhibited osteoblastic differentiation, and
137 of Id vaccination using Id proteins.However, Id protein is laborious and time-consuming to produce.
138 ion of the Id-specific memory B cells by the Id protein is largely independent of the FcgammaRIIB and
139                     Although upregulation of Id proteins is associated with a broad spectrum of tumor
140  interplay between gammaherpesvirus RTAs and ID proteins is evolutionarily conserved.
141  hypoxic, but it is unknown if expression of Id proteins is regulated in hypoxic cells.
142  transcription factors and their inhibitors, Id proteins, is important for the myeloid-versus-lymphoi
143                          Expression of other ID proteins like N-cadherin, desmoplakin, connexin-43, a
144                         We also predict that ID proteins may act as restriction factors of the lytic
145 s and suggest that deregulated expression of Id proteins may be an epigenetic mechanism to silence ex
146                                              Id proteins may control cell differentiation by interfer
147 on of protein-protein interactions involving ID proteins may therefore be possible through the target
148        However, it remains unknown how E and Id proteins mechanistically enforce and maintain the nai
149 ture and myelinating oligodendrocytes via an ID protein-mediated negative regulation and may serve as
150                              DCs pulsed with Id proteins modified to include foreign constant regions
151                       Users may query by PDB ID, protein name, function and Enzyme Classification num
152 s queries based on contributing site, target ID, protein name, sequence, status and other data.
153 at E47 interacts with the entire ensemble of Id proteins, namely, Id1, Id2, Id3, and Id4.
154                                              Id proteins negatively regulate the dimerization, DNA bi
155                                              Id protein not only failed to boost the response, but pe
156 dium, and (b) overcame the inhibition by the Id proteins of MyoD- and E47 dependent transcription and
157 ition of p204 overcame the inhibition by the Id proteins of the binding of MyoD and E47 to DNA in vit
158 ulated that demonstrates dominant effects of Id proteins on different aspects of cellular growth.
159                    Of the four characterized Id proteins, only Id2 is found in the nucleus of Sertoli
160              Since the identification of the Id proteins over a decade ago, a great many cell cycle a
161 uctural features underlying the functions of ID proteins/peptides by conventional methods, such as X-
162                    Intrinsically disordered (ID) proteins/peptides are considered equally important f
163                                        Thus, Id proteins play a central and evolutionarily conserved
164                We hypothesized that BMP4 and Id proteins play a role in the expansion and differentia
165                                          The Id proteins play an important role in proliferation, dif
166                                          The Id proteins play an important role in proliferation, dif
167                                              Id proteins play important roles in osteogenic different
168                    Inhibitor of DNA binding (Id) proteins play important roles in regulating cardiac
169 iption factors and their natural inhibitors, Id proteins, play critical and complex roles during lymp
170                               However, which Id protein plays a physiologic role during lymphocyte de
171                   Accordingly, Id4 and other Id proteins promote elimination of Ascl1 protein in NSC
172          Thus, we provide insight into E and Id protein regulation of iNKT cell proliferation and dif
173                                    Idiotype (Id) protein, secreted by myeloma cells, is a tumor-speci
174 how the folding of intrinsically disordered (ID) protein sequences, in particular, and population shi
175                                     Although Id-protein-specific T-cell responses have been reported
176                             Mechanistically, Id proteins specify cardiac cell fate by repressing two
177 at the deubiquitinating enzyme USP1 promotes ID protein stability and stem cell-like characteristics
178 eterodimers in a manner similar to MISTI and Id proteins, suggesting a possible transcriptional inhib
179 an inhibitor of differentiation/DNA binding (Id) proteins that comprise a class of helix-loop-helix f
180 on is prevented by Inhibitor of DNA-binding (Id) proteins that interfere with DNA binding by master r
181                                              Id proteins, the inhibitors of E2A, have opposite effect
182 plained experimental observations related to Id proteins; the speed of response varies with the initi
183                                          The Id proteins thus display a signature range of interactio
184 , we explore relationships of E proteins and ID proteins to a variety of disease processes and highli
185 ese activities are related to the ability of Id proteins to antagonize E proteins and other transcrip
186 on can be functionally replaced by fusion of Id proteins to SAP-1, whereby the Id moiety then acts to
187 apitulate those physiologically propelled by Id proteins to support normal development.
188 y expressed E2A or inhibitor of DNA binding (Id) proteins to activate or inhibit transcription, respe
189 pression levels of Inhibitor of DNA binding (ID) proteins to ask whether lineage priming affects self
190 ation affects the inhibitory activity of the Id proteins towards the TCFs.
191 e demonstrated a potent inhibitory effect of ID proteins upon CLOCK-BMAL1 transactivation of clock ge
192                                              Id protein vaccination has demonstrated clinical activit
193 s equivalent or superior to that afforded by Id protein vaccination.
194 ection than a traditional lymphoma idiotype (Id) protein vaccine, and in combination with chemotherap
195 al antibody, whereas the response to soluble Id protein was dependent on MHC class II.
196                                  Recombinant Id protein was manufactured and covalently linked with k
197 s expressed in T-BET(+) NKT1 cells, and both Id proteins were required for the formation of this subl
198                                     All four ID proteins were significantly increased in Mecp2-defici
199 ther ILCs, iNKT cells constitutively express ID proteins, which antagonize the E protein transcriptio
200      Studies involving ectopic expression of Id proteins, which inhibit E2A as well as other basic he
201                            Overexpression of Id proteins within a variety of cell types has been show

 
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