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1 nriched, truncated NRG1 protein resistant to proteolytic processing.
2  GTPase OPA1, whose activity is regulated by proteolytic processing.
3 l flexibility may thus change the pattern of proteolytic processing.
4 ndolysosomal compartments and its subsequent proteolytic processing.
5 onstrating E-cad overexpression and specific proteolytic processing.
6 oteins and activated by the inflammasome via proteolytic processing.
7 sing RNAi that TC10alpha is required for TUG proteolytic processing.
8 play altered gamma-secretase-dependent Notch proteolytic processing.
9 upling entry into the endocytic pathway with proteolytic processing.
10 post-translation modifications, isoforms and proteolytic processing.
11 ocally in tissues and is itself regulated by proteolytic processing.
12 ms, but there is little information on TWEAK proteolytic processing.
13 452) is essential for the initiation of DSPP proteolytic processing.
14  terminus and 65 kDa carboxy terminus, after proteolytic processing.
15 e availability of APP for secretase-mediated proteolytic processing.
16  endoplasmic reticulum (ER) to the Golgi for proteolytic processing.
17 es many important signaling proteins through proteolytic processing.
18 tase (RT) instability as well as inefficient proteolytic processing.
19  alpha- and betaB-subunit mRNA, protein, and proteolytic processing.
20  protein while retaining similar kinetics of proteolytic processing.
21  that these mutant proteins were impaired in proteolytic processing.
22 via inhibition of CA-SP1 cleavage during Gag proteolytic processing.
23  rhomboid family protease required for SREBP proteolytic processing.
24  1 and a type 2 orientation are generated by proteolytic processing.
25  the secreted precursor protein, DfsB, after proteolytic processing.
26 he channel from entering a state that allows proteolytic processing.
27 without affecting its Golgi localization and proteolytic processing.
28 are fully concealed and independent of their proteolytic processing.
29 ting in AMIGO2 silencing and changes in PTK7 proteolytic processing.
30  is activated during ageing and mediates APP proteolytic processing.
31 n destruction complex by gingipain-dependent proteolytic processing.
32 SIRT2 deletion increased TUG acetylation and proteolytic processing.
33 ation status of beta-catenin but resulted in proteolytic processing.
34 s to facilitate LC-MS/MS characterization of proteolytic processing, a major form of posttranslationa
35 ubunits are modified post-translationally by proteolytic processing, acetylation, and/or ubiquitylati
36 isive role in controlling the outcome of APP proteolytic processing and Abeta generation.
37         The presented DISC1 mechanism of APP proteolytic processing and Abeta peptide generation, whi
38 n type III NRG1 that disrupt intramembranous proteolytic processing and abolish intracellular domain
39 enzyme that is internalized and subjected to proteolytic processing and activation in lysosomes.
40 CIRL in the GPS domain inhibit intracellular proteolytic processing and also result in the absence of
41 s of lacritin is multifunctional by dose and proteolytic processing and appears to play a key role in
42 P combination enhances mature glycosylation, proteolytic processing and cell-surface expression of al
43 -GX sPLA2 is a substrate for furin and PCSK6 proteolytic processing and define a novel mechanism for
44 iquitination is associated with irreversible proteolytic processing and inactivation of Bag6.
45                          This is followed by proteolytic processing and mobilization of the transcrip
46 e absence of Hh, Cos2 and Kif7 contribute to proteolytic processing and silencing of the Hh-regulated
47                  However, the location(s) of proteolytic processing and subsequent secretion of APP f
48  virulence activity of AvrRPS4 requires both proteolytic processing and the KRVY motif at the N-termi
49 wnstream target genes through the control of proteolytic processing and the transcriptional activatio
50 the inner membrane before the FtsH-dependent proteolytic processing and translocation of the toxic tR
51 mal degradation pathway and autophagy on the proteolytic processing and turnover of C99.
52 the expanded PolyQ region can be produced by proteolytic processing and/or aberrant splicing.
53 ar those that perturbed particle production, proteolytic processing, and particle-associated IN level
54 udy the biosynthesis, cell-surface delivery, proteolytic processing, and release of soluble EGFR liga
55 atures of Env involved in protein stability, proteolytic processing, and virus assembly and entry, th
56 ment LG3 is generated at increased levels by proteolytic processing as long as 3 days after ischemia.
57 oteinases as being primarily responsible for proteolytic processing (as opposed to degradation) durin
58 the viral fusion (F) protein, which requires proteolytic processing at a basic cleavage site in order
59 ose bioactivity is closely regulated through proteolytic processing at its C terminus.
60                                              Proteolytic processing at N- and C-terminal sites of the
61  We demonstrate that native BB0323 undergoes proteolytic processing at the C-terminus, at a site afte
62         Chymotrypsin zymogen is activated by proteolytic processing at the N terminus, resulting in s
63 th both nucleocapsid and matrix domains, and proteolytic processing at the spacer peptide 1|nucleocap
64 oid precursor protein (APP) with consecutive proteolytic processing: beta-secretase, followed by gamm
65 one or together with YXXPhi, did not prevent proteolytic processing but increased cell surface expres
66 ts suggest a direct relationship between APP proteolytic processing, but not amyloid-beta, in GSK-3be
67 in the lymphovascular embolus, E-cad and its proteolytic processing by calpain and other proteases ha
68  demonstrate that TREM2 undergoes sequential proteolytic processing by ectodomain shedding and intram
69 t a 25-kDa fragment, probably resulting from proteolytic processing by eta-secretase.
70 o assessed the affect of lattice assembly on proteolytic processing by exogenous PR.
71 nimum of two events are required for fusion, proteolytic processing by furin-like proteases and expos
72  are synthesized as proproteins that undergo proteolytic processing by furin/subtilisin proprotein co
73 myloid precursor protein (APP) is subject to proteolytic processing by gamma-secretase within neurona
74 n shedding by alpha-secretase and subsequent proteolytic processing by gamma-secretase.
75          Structural changes in DeltaGag upon proteolytic processing by HIV-1 protease, monitored by N
76                                              Proteolytic processing by matrix metalloproteinase-20 (M
77 fensins protects the mature peptides against proteolytic processing by MMP-7.
78 y deleted, provided that the requirement for proteolytic processing by PLP1 was offset by an alternat
79 le-pass transmembrane protein that undergoes proteolytic processing by secretases to generate the pat
80                           In addition to the proteolytic processing by secretases, APP is also metabo
81 epatitis C virus (HCV) core protein requires proteolytic processing by two host proteases: signal pep
82 ene expression levels and post-translational proteolytic processing can be controlled.
83 inding consistent with P. gingivalis-induced proteolytic processing causing the increase in TCF/LEF p
84      Since changes in lectican abundance and proteolytic processing did not accompany the synaptic pr
85 for insulin enhancement of SREBP-1c mRNA and proteolytic processing diverge after mTORC1.
86  we showed that regulation of FANCC involved proteolytic processing during apoptosis.
87 inent yet previously uncharacterized role of proteolytic processing during platelet storage.
88  an unanticipated role of IN for polyprotein proteolytic processing during virion morphogenesis.
89             Post-translational modification, proteolytic processing, endocytosis and membrane traffic
90 erated on the expressed IgG1 Fc by utilizing proteolytic processing enzymes in the yeast secretory pa
91               We demonstrate that this novel proteolytic processing event depends on a two-step casca
92          PKA is known to be required for the proteolytic processing event that generates the represso
93 thways and physiologic processes to specific proteolytic processing events is a major challenge in si
94                                          The proteolytic processing events of the alpha and gamma sub
95 ination cycling specifically regulates later proteolytic processing events required for destruction o
96 proteases in Giardia have been implicated in proteolytic processing events that enable the continuanc
97 DD8 is translated as a precursor protein and proteolytic processing exposes a C-terminal glycine requ
98 otch with membrane-anchored ligands triggers proteolytic processing, first by Adam10 and then preseni
99  the context of a polyprotein that undergoes proteolytic processing for NS5 maturation.
100 ins than in controls, while genes related to proteolytic processing (for example, LGMN, CTSZ) were hy
101         Site-specific mutagenesis to prevent proteolytic processing generated a full-length enzyme th
102                                     Although proteolytic processing goes to completion, the rate of c
103  peptide derived from VGF (non-acronymic) by proteolytic processing, has been shown to modulate energ
104 49) and His(151) to asparagine decreased APP proteolytic processing, impaired APP endoplasmic reticul
105 -mediated shedding and highlight the role of proteolytic processing in prion disease.
106          Toll-like receptor (TLR) 9 requires proteolytic processing in the endolysosome to initiate s
107 for p38 MAPK phosphorylation fail to undergo proteolytic processing in the Golgi apparatus and drive
108  redistribution toward the basolateral side, proteolytic processing in the membranes, and excretion i
109  a requirement for Taspase 1-dependent TFIIA proteolytic processing in the mouse testis to enable TRF
110 xpressed and is subject to posttranslational proteolytic processing in the retina, brain, and kidney.
111 t evidence that chemerin undergoes extensive proteolytic processing in vivo, underlining the importan
112 at most mutations do not disrupt expression, proteolytic processing, incorporation into virus, or rec
113  at several levels, including transcription, proteolytic processing, inhibition of enzymatic function
114                                              Proteolytic processing inside producing cells is a novel
115 cate that annexin A1 externalization and its proteolytic processing into a chemotactic peptide repres
116  cytokines lack a signal peptide and require proteolytic processing into an active molecule.
117 disease, has a complex biology that includes proteolytic processing into potentially toxic fragments,
118 orm of DMP1 is an inactive precursor and its proteolytic processing is an activation step essential t
119          Together, our data demonstrate that proteolytic processing is an important event that allows
120                                              Proteolytic processing is dispensable for hydrolytic sul
121  Taken together, our data indicate that TLR3 proteolytic processing is essential for its function, an
122 e we introduce a molecular probe, which upon proteolytic processing is retained at the site of enzyme
123 eavage of the transit peptide and additional proteolytic processing, mature HMR, which begins from Ly
124 sibility that targeting aberrant splicing or proteolytic processing may present attractive therapeuti
125                      Therefore, the two-step proteolytic processing may represent a regulatory mechan
126         Tal(2009) and Tal(901-1) can undergo proteolytic processing mid-protein at the glycine-rich s
127 ddition to changes in PrPC glycosylation and proteolytic processing, net reductions in PrPC occur in
128 sponsive transcription factor PacC, and PacC proteolytic processing occurred normally during calcium
129                                              Proteolytic processing of 38-kDa CTGF occurs during corn
130 n C (SP-C) by alveolar type 2 cells requires proteolytic processing of a 21-kDa propeptide (proSP-C21
131 We show that transcript abundance as well as proteolytic processing of a borrelial protein required f
132 Pg/NIaPro, NIb, and CP, all derived from the proteolytic processing of a large polyprotein, and an ad
133                                              Proteolytic processing of alpha2delta then permits volta
134  beta-Amyloid peptides (Abeta), derived from proteolytic processing of amyloid precursor protein (APP
135 myloid beta (Abeta) peptide derived from the proteolytic processing of amyloid precursor protein (APP
136                                              Proteolytic processing of amyloid precursor protein (APP
137                                              Proteolytic processing of amyloid precursor protein (APP
138            We report the novel regulation of proteolytic processing of amyloid precursor protein (APP
139 embrane aspartyl protease that catalyzes the proteolytic processing of APP and other plasma membrane
140 This sequestration significantly delayed the proteolytic processing of APP by secretases and the prot
141 ral and dynamic features are critical in the proteolytic processing of APP by the gamma-secretase enz
142         Here, we investigated expression and proteolytic processing of APP during differentiation of
143 proteins is required for the P2X7R-dependent proteolytic processing of APP leading to sAPPalpha relea
144                                              Proteolytic processing of ataxin-7 by caspase-7 generate
145                               IFN-stimulated proteolytic processing of ATF6 and ERK1/2-mediated phosp
146                            IFN-gamma-induced proteolytic processing of ATF6 and phosphorylation of C/
147 nduced expression of DAPK1 IFN-gamma-induced proteolytic processing of ATF6 and phosphorylation of C/
148                          Importantly, active proteolytic processing of AtMCP2d proteins dependent on
149                                 In addition, proteolytic processing of cadherin extracellular and cyt
150 causing altered febrile responses, increased proteolytic processing of caspase-1, and more rapid infl
151         In cells, F1L inhibits apoptosis and proteolytic processing of caspases induced by overexpres
152  I3C directly inhibits the elastase-mediated proteolytic processing of CD40, which alters downstream
153                SPPL2A deficiency blocked the proteolytic processing of CD74 MHC II invariant chain in
154 n, and DNA replication and reveal widespread proteolytic processing of cellular proteins to generate
155 s a polytopic membrane protein that inhibits proteolytic processing of CREB3L1 (cAMP response element
156                                              Proteolytic processing of CTGF in HCF cultures, normal a
157             This study addresses the role of proteolytic processing of CTGF in human corneal fibrobla
158           In addition to liver, the enhanced proteolytic processing of CtsB was also observed in brai
159                                              Proteolytic processing of defensins is a critical mode o
160 t D213A substitution effectively blocked the proteolytic processing of DMP1 in vivo.
161 13A-Tg mice) to test the hypothesis that the proteolytic processing of DMP1 is an activation step ess
162             These findings indicate that the proteolytic processing of DMP1 is essential to the forma
163 t D452A substitution effectively blocked the proteolytic processing of DSPP in vivo.
164              These results indicate that the proteolytic processing of DSPP is an activation step ess
165                          We believe that the proteolytic processing of DSPP is an essential activatio
166 ere we report that phosphorylation-regulated proteolytic processing of EIN2 triggers its endoplasmic
167  to lymphatic vessels stimulated release and proteolytic processing of endothelium-derived Reelin.
168                                              Proteolytic processing of epithelial sodium channel (ENa
169             This is an intriguing cue, since proteolytic processing of extracellular matrix macromole
170 ly on ameloblast-ameloblast interactions and proteolytic processing of extracellular matrix proteins
171 dent ubiquitination in controlling the later proteolytic processing of G protein-coupled receptors, w
172                         We hypothesized that proteolytic processing of gammaENaC occurs in the human
173 a function, we find that cilia formation and proteolytic processing of Gli3 are disrupted in C2cd3 mu
174  of Hh signaling, is down-regulated, and the proteolytic processing of Gli3 is compromised.
175  we had provided evidence of tissue-specific proteolytic processing of histone H3 in White Leghorn ch
176 ells exhibited markers of lysosomal-mediated proteolytic processing of histones and were progressivel
177 dition, A3G and Mov10 overexpression reduced proteolytic processing of HIV-1 Gag.
178 edly, T124N/T174I IN substitutions inhibited proteolytic processing of HIV-1 polyproteins Gag and Gag
179                         Our understanding of proteolytic processing of Htt has thus far focused on th
180                                              Proteolytic processing of human host cell factor 1 (HCF-
181 regulated in large part by the extracellular proteolytic processing of hyaluronan-bound proteoglycan.
182 ediated knockout of caspase b, which acts by proteolytic processing of il1beta, results in increased
183  activate the inflammasome complex and drive proteolytic processing of inflammatory cytokines; howeve
184 ermed "inflammasomes," which are involved in proteolytic processing of interleukin-1beta (IL-1beta) a
185 ote T cell activation was due to inefficient proteolytic processing of internalized ICs.
186 ng through the other branches of the UPR, or proteolytic processing of its close homolog ATF6beta or
187 cum AMB-1, was recently shown to promote the proteolytic processing of itself and two other biominera
188 ode of growth is associated with an abnormal proteolytic processing of L1 and N-cadherin, two ADAM10
189                           Heat shock-induced proteolytic processing of Lsb1 is crucial for prion main
190  impaired lysosomal acidification, decreased proteolytic processing of lysosomal enzymes, reduced deg
191 trostudies showing that FAP mediates ordered proteolytic processing of matrix metalloproteinase (MMP)
192                           Post-translational proteolytic processing of mature chemokines is a key, ye
193                            We show here that proteolytic processing of Msb2p was induced by underglyc
194 SP1-specific antibodies shown to inhibit the proteolytic processing of MSP1 that occurs at invasion.
195 roteolysis of APP, BACE1 participates in the proteolytic processing of neuregulin 1 (NRG1) and influe
196  abnormalities, and pcd mice display altered proteolytic processing of Nna1 interacting proteins.
197 ubsequent study suggested that site-specific proteolytic processing of Nrf1 by the proteasome yields
198                         Here we investigated proteolytic processing of NRG1 type III and demonstrate
199 ression and the subcellular distribution and proteolytic processing of NRG1-IVNV isoforms were also d
200 aracterized the synaptic consequences of the proteolytic processing of Nrxns in cultured hippocampal
201 min-related protein 1) at Ser637 and altered proteolytic processing of OPA1 (optic atrophy 1).
202                                              Proteolytic processing of PKCalpha by calcium-activated
203    Recently, we showed that calpain-mediated proteolytic processing of PKCalpha in ischemic myocardiu
204 ic function, we address the relevance of the proteolytic processing of presynaptic neurexins (Nrxns)
205 e that mature L-SMase arises from C-terminal proteolytic processing of pro-aSMase and suggest that im
206 or activation of Met signaling that bypasses proteolytic processing of pro-HGF.
207 nt molecular protein complex which initiates proteolytic processing of pro-IL-1beta and pro-IL-18 int
208 scription whereas inflammasomes regulate the proteolytic processing of pro-IL-1beta.
209 d profound effects on MHC-I presentation and proteolytic processing of proinsulin.
210  Nalpha acetylation, protein maturation, and proteolytic processing of proteins in human platelets.
211 m open reading frame repression requires the proteolytic processing of PTEF by PfCalpain.
212 drive the amyloid cascade in AD and that the proteolytic processing of RanBP9 may be an attractive th
213 valent modification in controlling the later proteolytic processing of receptors.
214 h is essential for viral replication through proteolytic processing of RNA replicase machinery.
215               Adenovirus maturation involves proteolytic processing of seven precursor proteins.
216           Adenovirus assembly concludes with proteolytic processing of several capsid and core protei
217 amily of endosomal proteases is required for proteolytic processing of several viruses during entry i
218 these studies, it has become recognized that proteolytic processing of signaling molecules by certain
219 n collagen fibril assembly is the C-terminal proteolytic processing of soluble procollagen precursors
220 CMV infection was also found to increase the proteolytic processing of SREBP-2, a transcription facto
221  notion that proper vacuolar trafficking and proteolytic processing of storage proteins require endom
222                                              Proteolytic processing of synaptic adhesion components c
223                  Interestingly, the observed proteolytic processing of Tal(2009) and Tal(901-1) facil
224    Because cathepsins are known to influence proteolytic processing of Tg in vivo, we examined in thi
225 tural dimer, 3,3'-diindolylmethane, disrupts proteolytic processing of the 50-kDa cyclin E into the l
226  effects of elastase on receptor activation, proteolytic processing of the adhesion protein ICAM-1, N
227                    Abeta is generated by the proteolytic processing of the amyloid precursor protein
228 in Alzheimer's disease (AD), is generated by proteolytic processing of the amyloid precursor protein
229        There is compelling evidence that the proteolytic processing of the amyloid precursor protein
230  Alzheimer's disease (AD) is associated with proteolytic processing of the amyloid precursor protein
231                                              Proteolytic processing of the amyloid precursor protein
232                                              Proteolytic processing of the amyloid-beta precursor pro
233 re in that its maturation requires extensive proteolytic processing of the astrovirus capsid protein
234                 Maturation of HAstV requires proteolytic processing of the astrovirus CP both inside
235 gene and represent products of intracellular proteolytic processing of the CIRL precursor.
236 ease expressed during enamel maturation, and proteolytic processing of the enamel matrix by KLK4 is c
237 pitope presentation at a step other than the proteolytic processing of the epitope.
238                                              Proteolytic processing of the flavivirus polyprotein is
239 hybridization and immunostaining and confirm proteolytic processing of the FRFamide precursor by mass
240  that in skeletal muscle, insulin stimulates proteolytic processing of the GLUT4 retention protein, T
241                                  Apparently, proteolytic processing of the HIV-1 Env precursor decrea
242                                  Remarkably, proteolytic processing of the HIV-1 Env precursor result
243                                              Proteolytic processing of the laminin-gamma2 chain is a
244            When L2 expression was repressed, proteolytic processing of the major core proteins and th
245                         We have demonstrated proteolytic processing of the matrix proteoglycan, versi
246 , insulin rapidly and selectively stimulates proteolytic processing of the nascent SREBP-1c by enhanc
247                                              Proteolytic processing of the nuclear factor (NF)-kappaB
248                                              Proteolytic processing of the pigment cell-specific Mela
249  but there was no change in the abundance or proteolytic processing of the prominent lecticans brevic
250                                              Proteolytic processing of the protein leads to a number
251 how cleavage might activate membrane fusion, proteolytic processing of the SARS-CoV S protein remains
252 tern blot analysis revealed an age-dependent proteolytic processing of the TGFBIp N terminus resultin
253 omplex array of glycosylation substrates and proteolytic processing of the transcription factor host
254                                              Proteolytic processing of the viral nonstructural polypr
255 inhibitor and exhibit a significant delay in proteolytic processing of the viral replicase polyprotei
256 ctivate KLKs because of gingipain K-mediated proteolytic processing of the zymogenic proform of KLK13
257 ation of collagen metabolism by uPA-mediated proteolytic processing of transforming growth factor (TG
258                Immunoblots demonstrated that proteolytic processing of TRAP5b and the cytoskeletal pr
259   To determine whether peptides derived from proteolytic processing of VGF participate in nociceptive
260 ivity of endosomal proteases or delaying the proteolytic processing of virions.
261                                              Proteolytic processing of von Willebrand factor (VWF) by
262 uggest that FVIII plays a role in regulating proteolytic processing of VWF by ADAMTS13 under shear st
263  to the trans-Golgi network (TGN) to prevent proteolytic processing or by directing newly produced Ab
264  variations are not caused by differences in proteolytic processing or degrees of phosphorylation or
265  processed by TDP2 unless they first undergo proteolytic processing or denaturation.
266 signaling proteins IKKbeta and IKKgamma, the proteolytic processing p105 and p100 and NF-kappaB DNA b
267 cell culture model to investigate huntingtin proteolytic processing; previous studies of these cells
268   Contrary, in PNS glia, but not in neurons, proteolytic processing produced a two-chain SorCS2 isofo
269 at axonal entry and secretion of APP and its proteolytic processing products traverse different pathw
270 ined with the appropriate enzymes to analyze proteolytic processing rates in the presence or absence
271                     Here we demonstrate that proteolytic processing regulates the biological activity
272                                   Subsequent proteolytic processing releases the toxic compound insid
273  that Sonic hedgehog (Shh) is solubilized by proteolytic processing (shedding) of lipidated peptide t
274 eavage fragments produced by pathogen-driven proteolytic processing should be further characterized t
275  without altering cell surface expression or proteolytic processing significantly.
276                                     Multiple proteolytic processing sites in Glass bottom boat (Gbb),
277   We demonstrate that HERV-K ENV undergoes a proteolytic processing step and triggers membrane fusion
278 w that PmpD undergoes an infection-dependent proteolytic processing step late in the growth cycle tha
279 w here that Fat is subject to a constitutive proteolytic processing, such that most or all cell surfa
280  hundreds of peptides in different levels of proteolytic processing that may provide a range of biolo
281        In the cell, monomeric gp12 undergoes proteolytic processing that releases the C-terminal doma
282 r knowledge, the first example of tail fiber proteolytic processing that results in a heterogeneous p
283 e site of protein VI that profoundly impacts proteolytic processing, the generation of infectious par
284 this study, we demonstrate that, after hTLR7 proteolytic processing, the liberated amino (N)-terminal
285                                            A proteolytic processing then transforms the proenzyme int
286 cked Gli3 phosphorylation and its subsequent proteolytic processing, thereby abrogating its ability t
287 Da proenzyme and then undergoes biosynthetic proteolytic processing to active approximately 30 kDa LO
288                Whether TLR3 requires similar proteolytic processing to become competent for signaling
289                 Nrf1 was reported to require proteolytic processing to enter the nucleus [3].
290 LOX protein and then undergoes extracellular proteolytic processing to form approximately 30 kDa LOX
291 s constitutively active and does not require proteolytic processing to function.
292 ssibility to the aqueous environment undergo proteolytic processing to generate active neuropeptides
293 ized the necessity of appropriate C-terminal proteolytic processing to generate the likely physiologi
294 rmore, both increased CAMP secretion and its proteolytic processing to LL-37 are required for antimic
295 ly transcription factors and prevents Ci/Gli proteolytic processing to repressor forms.
296                                         This proteolytic processing, unusually extensive for an envel
297 hereas certain NLRs trigger their subsequent proteolytic processing via caspase 1.
298  A1 during secondary necrosis coincided with proteolytic processing within its unique N-terminal doma
299    Activation of TLR9 for signaling requires proteolytic processing within the ectodomain by endosome
300 sm of aSMase maturation involving C-terminal proteolytic processing within, or in close proximity to,

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