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1 ic peptides by inhibiting their breakdown by neprilysin.
2 ting vascular remodeling but are degraded by neprilysin.
3  exhibited specificity for ECE-2 compared to neprilysin.
4 erting enzyme, insulin-degrading enzyme, and neprilysin.
5 lysin inhibitor, attenuated these effects of neprilysin.
6 nhibit both the renin-angiotensin system and neprilysin.
7 ta (Abeta), and the Abeta-degrading protease neprilysin.
8 substrate, and pathophysiological aspects of neprilysin.
9 arget, we used inducible drivers to modulate neprilysin 1 (Nep1) and dAbeta expression in adult DPM n
10 ched for an interaction between Amnesiac and Neprilysin 1 (Nep1), a fly neprilysin involved in memory
11 functional relationship between Amnesiac and Neprilysin 1 (Nep1), a membrane peptidase involved in me
12 data reveal a functional interaction between neprilysin 1 and amyloid peptide, suggesting that nepril
13 lysin 1 and amyloid peptide, suggesting that neprilysin 1 degrades amyloid peptide.
14 we show that an increase in the level of the neprilysin 1 peptidase overcomes memory deficits induced
15                One gain was observed for the Neprilysin-1 (Nep1) gene, which has evolved a unique exp
16    Of particular interest is the NEP homolog neprilysin 2 (NEP2), which is thiorphan/phosphoramidon-s
17 tions, Abeta1-40 (20 muM) was incubated with neprilysin (300 ng/ml), an endopeptidase known to hydrol
18 opeptidase related in amino acid sequence to neprilysin, a mammalian cell-surface peptidase involved
19  is important to determine whether increased neprilysin activity also diminishes the levels of pathog
20  beta1 antagonist bisoprolol inhibited renal neprilysin activity and increased circulation NP levels
21  explore whether substances that can elevate neprilysin activity could be a rational option for treat
22 ed that RF-RDN significantly inhibited renal neprilysin activity in SHR and WKY with HF.
23                                        Islet neprilysin activity was inhibited or up-regulated using
24 l nerves on kidney function attenuates renal neprilysin activity, augments circulating NP levels, red
25  is mediated, at least in part, by decreased neprilysin activity.
26 ion of insulin-like peptides is regulated by neprilysin activity.
27 rs individually and found that inhibition of neprilysin alone could enhance enkephalin responses to t
28 al development, was found to also target the neprilysin, aminopeptidase, and dipeptidylpeptidase clan
29                 Now we studied the effect of neprilysin, an Abeta-degrading enzyme, on development of
30               We sought to determine whether neprilysin, an amyloid-degrading enzyme, is present in i
31 ding enzyme, endothelin-converting enzyme-1, neprilysin and alpha-secretase.
32 ning proved that Phe(3) is a key residue for neprilysin and aminopeptidase N (AP-N) ectoenkephalinase
33  combining NP degradation inhibition through neprilysin and angiotensin receptor blockade, has led to
34 wo of the three angiotensin-forming enzymes (neprilysin and endopeptidase 24.15) also contribute to t
35               Angiotensin-converting enzyme, neprilysin and endothelin-converting enzyme function as
36 in strongly decreased tissue availability of neprilysin and impaired enzymatic activity.
37  and spatial relationships between decreased neprilysin and increased cell growth.
38 m roles for endothelin-converting enzyme and neprilysin and indicate that reductions in these enzymes
39 tein, and its degradation by enzymes such as neprilysin and insulin degrading enzyme.
40 t was independent of mRNA/protein changes in neprilysin and insulin-degrading enzyme and, instead, ma
41  closely similar sites as wild-type Abeta by neprilysin and insulin-degrading enzyme, the two most wi
42 dation of Abeta peptides within microglia by neprilysin and related enzymes is dramatically enhanced
43 s revealed a global myocardial response, and neprilysin and the STAT family as key regulators of intr
44 pted us to search for an interaction between neprilysins and Drosophila Abeta (dAbeta), a cleavage pr
45          The high functional conservation of neprilysins and their substrates renders the characteriz
46 three enzymes: neutral endopeptidases 24.11 (neprilysin) and 24.15 and prolyl-endopeptidase 24.26.
47 by isolation of the enzyme that degrades it (neprilysin) and its inhibitors.
48 I and Ang-(1-7), together with cardiac ACE2, neprilysin, Ang II type 1 receptor (AT1), and mas recept
49 10 muM) were used to inhibit the activity of neprilysin, angiotensin-converting enzyme, or aminopepti
50  there has been no direct demonstration that neprilysin antagonizes the deposition of amyloid-beta in
51                                              Neprilysins are also required in the MB, reflecting the
52                                              Neprilysins are endopeptidases known to degrade a number
53 gical target for Nep1.SIGNIFICANCE STATEMENT Neprilysins are endopeptidases known to degrade a number
54 use Drosophila melanogaster to study whether neprilysins are involved in memory.
55 RNA interference, we show here that all four neprilysins are involved in middle-term and long-term me
56                                              Neprilysins are Type II metalloproteinases known to degr
57                                              Neprilysins are type II metalloproteinases known to degr
58   Finally, we provide evidence about soluble neprilysin as a biomarker surrogate in patients with hea
59               We next highlight the value of neprilysin as a biotarget and weigh the clinical benefit
60  suggest that the recombinant brain-targeted neprilysin, ASN12, may be an effective treatment for AD
61  an increase in the Abeta-degrading protease neprilysin at the cell surface and a concomitant increas
62 (2, 4-dinitrophenyl) is also a substrate for neprilysin, but is hydrolyzed 10-fold more efficiently b
63                   Treatment with recombinant neprilysin, but not enzymatically inactive neprilysin, r
64 nificant regional association with BACE1 and neprilysin, but not PSD95 that regionally associated wit
65  genetically engineered form of the protease neprilysin completely arrest amyloid deposition in an ag
66                                       Median neprilysin concentration in 1,069 patients was 0.642 ng/
67     In age-adjusted Cox regression analyses, neprilysin concentrations were significantly associated
68                                              Neprilysin contributes to free fatty acid (FFA)-induced
69                   This finding suggests that neprilysin could facilitate neuroreplacement therapy wit
70                                  In summary, neprilysin decreases islet amyloid deposition by inhibit
71 proves learning and memory deficits, whereas neprilysin deficiency aggravates the behavioral phenotyp
72 ely, angiotensin-(1-2) enhanced GSIS in both neprilysin-deficient and wild-type islets.
73                                           In neprilysin-deficient mouse islets, angiotensin-(1-7) and
74  under nonpathological conditions, mammalian neprilysins degrade amyloid peptide to ensure memory for
75 er, a more widely expressed islet peptidase, neprilysin, degrades angiotensin-(1-7) into several pept
76 at the mechanism for protection conferred by neprilysin deletion involves prevention of reduced calci
77 lysin on plaques and oligomers suggests that neprilysin-dependent degradation of Abeta affects plaque
78 proach to test the alternate hypothesis that neprilysin depletion increases chronic hypoxic pulmonary
79 eficient mouse islets, angiotensin-(1-7) and neprilysin-derived degradation products angiotensin-(1-4
80 odel of ECE-2 using the crystal structure of neprilysin (EC 3.4.24.11) as a template.
81                 The fly genome contains five neprilysin-encoding genes, four of which are expressed i
82                       In Drosophila, several neprilysins expressed in the brain are required for midd
83           We previously showed that all four neprilysins expressed in the Drosophila brain are involv
84                 Functional studies involving neprilysin-expressing vascular endothelial cells demonst
85            Concomitant phenotypes of altered neprilysin expression included impaired food intake, red
86                             CG4721 encodes a neprilysin family metalloprotease that is highly up-regu
87                    Kell is classified in the neprilysin family of zinc endopeptidases, and XK has str
88 re not conserved in the other members of the neprilysin family, and based on the hypothesis that one
89 nase CD10/neutral endopeptidase 24.11 ([NEP] neprilysin) functions as part of a regulatory loop to co
90                                         Four neprilysin genes are expressed in adult Drosophila Using
91                                      Loss of neprilysin had no effect on baseline airway or alveolar
92                            The endopeptidase neprilysin has been successfully used to reduce the accu
93                                              Neprilysin has recently been implicated as a major extra
94  apparent structural similarities, ECE-1 and neprilysin have been considered to differ significantly
95 drug classes, namely inhibitors of DPP IV or neprilysin, have been developed.
96       Natriuretic peptides are substrates of neprilysin; hence, B-type natriuretic peptide (BNP) conc
97 CAP peptide is cleaved by the human membrane neprilysin hNEP, we searched for an interaction between
98 A screen for corresponding substrates of the neprilysin identified distinct peptides that regulate in
99 pinephrine, angiotensin II, aldosterone, and neprilysin) impair insulin sensitivity and contribute to
100 utations in MME encoding the metalloprotease neprilysin in 19 index case subjects diagnosed with axon
101 o assess the presence of circulating soluble neprilysin in a real-life cohort of HF patients and corr
102 d cardiomyocytes confirmed the importance of neprilysin in ameliorating PAO accumulation.
103 und zinc-metallopeptidase that is related to neprilysin in amino acid sequence.
104 ion of STAT1 and CASP3 and downregulation of neprilysin in both zones, suggesting r-I/R induced intri
105 Overexpression of the Abeta-degrading enzyme neprilysin in brains of human amyloid precursor protein
106 n beta-secretase activity and a reduction of neprilysin in female mice compared to males; this sugges
107                Identification of circulating neprilysin in HF patients and the positive association o
108  findings suggest that targeting the role of neprilysin in IAPP fibril assembly, in addition to IAPP
109    Importantly, adenoviral overexpression of neprilysin in islets cultured without FFA reproduces the
110        These data further support a role for neprilysin in regulating cerebral amyloid deposition and
111  suggesting the sustained elevation of islet neprilysin in these mice was a compensatory mechanism ai
112                                              Neprilysins in particular are the major amyloid-beta pep
113      Together, our data establish a role for neprilysins in two specific memory phases and further sh
114 rading enzymes (insulin-degrading enzyme and neprilysin) in APP/CCL2 and APP mice were indistinguisha
115                                              Neprilysin increased the number of neurospheres that for
116 romoting carcinogenesis, decreased levels of neprilysin increases inflammation and neuroendocrine cel
117 2 (angiotensin-converting enzyme 2) and NEP (neprilysin) induce the alternative, and potentially reno
118 ss spectrometry, which failed to demonstrate neprilysin-induced cleavage.
119 and signaling, whereas exogenous recombinant neprilysin inhibited signaling.
120                         Angiotensin receptor-neprilysin inhibition (ARNI) improves mortality among pa
121                         Angiotensin receptor neprilysin inhibition (ARNI) therapy provided incrementa
122                                     Although neprilysin inhibition appeared to have greater effects o
123                      These data suggest that neprilysin inhibition attenuates the risk of hyperkalemi
124                        (Angiotensin Receptor-Neprilysin Inhibition in Chagas Cardiomyopathy With Redu
125 odel, and data from the Angiotensin Receptor Neprilysin Inhibition in Heart Failure With Preserved Ej
126 We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure
127  results, and further suggest the benefit of neprilysin inhibition may be partially mediated by incre
128                        Lastly, the impact of neprilysin inhibition on mid-regional pro-ANP (MR-proANP
129                                  Angiotensin-neprilysin inhibition prevents the clinical progression
130                                        Thus, neprilysin inhibition reduces hypertension, ultimately l
131                    Recently, the addition of neprilysin inhibition to angiotensin receptor blockade h
132                    Analysis of the effect of neprilysin inhibition was 1 of 12 pre-specified subgroup
133  comparison, NT-proBNP is not a substrate of neprilysin inhibition, and thus may lead to less clinica
134                                    Following neprilysin inhibition, islet amyloid deposition and beta
135  chronic hypoxic pulmonary hypertension with neprilysin inhibition.
136 retic peptide (BNP) concentrations rise with neprilysin inhibition.
137                         Angiotensin receptor-neprilysin inhibitor (ARNI) prescription in the United S
138                 Angiotensin receptor blocker-neprilysin inhibitor (ARNi) therapy improves the prognos
139 betes status, age, sex, angiotensin receptor neprilysin inhibitor (ARNI) treatment, New York Heart As
140 in receptor blocker, or angiotensin receptor-neprilysin inhibitor (ARNI) use decreased over time, and
141 receptor blocker (ARB), angiotensin receptor-neprilysin inhibitor (ARNI), beta-blocker, and mineraloc
142 CZ696, a first-in-class angiotensin receptor neprilysin inhibitor (ARNI), in patients with this disor
143          Beta-blockers, angiotensin receptor-neprilysin inhibitor (ARNI), mineralocorticoid receptor
144 sin receptor blocker (valsartan [VAL]) and a neprilysin inhibitor (sacubitril [SAC]), was shown to be
145 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor + beta-blocker + mineralocorticoid
146 combined angiotensin receptor antagonist and neprilysin inhibitor addresses 2 of the pathophysiologic
147                         Angiotensin receptor-neprilysin inhibitor appeared to consistently reduce the
148                                          The neprilysin inhibitor component of LCZ696, LBQ657, inhibi
149 ptor antagonist in 30%, angiotensin receptor-neprilysin inhibitor in 2%, and ivabradine in 2%.
150                  We compared the angiotensin-neprilysin inhibitor LCZ696 (400 mg daily) with the angi
151 l size suggest that the angiotensin receptor neprilysin inhibitor LCZ696 may reduce this measure of m
152 NT) trial, in which the angiotensin receptor neprilysin inhibitor LCZ696 reduced markers of heart fai
153         We compared the angiotensin receptor-neprilysin inhibitor LCZ696 with enalapril in patients w
154 re (HF) treated with an angiotensin receptor neprilysin inhibitor lived longer without being hospital
155                         Angiotensin receptor neprilysin inhibitor measure performance was significant
156  cardiac hypertrophy than either stand-alone neprilysin inhibitor or angiotensin receptor blocker.
157 blocker, or any dose of angiotensin receptor neprilysin inhibitor plus any dose of mineralocorticoid
158 giotensin receptor blocker valsartan and the neprilysin inhibitor prodrug sacubitril in a 1:1 ratio i
159 stigated the biological effects of ARNi with neprilysin inhibitor sacubitril and angiotensin receptor
160                     The angiotensin receptor neprilysin inhibitor sacubitril/valsartan (LCZ696) reduc
161                     The angiotensin receptor neprilysin inhibitor sacubitril/valsartan was associated
162  in Heart Failure), the angiotensin receptor neprilysin inhibitor sacubitril/valsartan was more effec
163 d that a new angiotensin receptor antagonist-neprilysin inhibitor was superior to an angiotensin-conv
164 reases in NT-proBNP following the use of the neprilysin inhibitor were extremely rare.
165 ospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With an Angiotensin-Converting Enzy
166 ospective Comparison of Angiotensin Receptor-Neprilysin Inhibitor With Angiotensin Converting Enzyme
167 ospective comparison of angiotensin receptor neprilysin inhibitor with angiotensin receptor blocker o
168 on treatment with ARNI (angiotensin receptor/neprilysin inhibitor) therapy or left ventricular assist
169 ive Comparison of ARNI (angiotensin-receptor-neprilysin inhibitor) with ACEI (angiotensin-converting
170  medication (angiotensin II receptor blocker neprilysin inhibitor).
171 ortality when comparing angiotensin receptor-neprilysin inhibitor+BB+mineralocorticoid receptor antag
172 nhibitor or ARB+BB, and angiotensin receptor-neprilysin inhibitor+BB+mineralocorticoid receptor antag
173 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor, 20% on mineralocorticoid receptor
174 tensin receptor blocker/angiotensin receptor-neprilysin inhibitor, and 50 mg of mineralocorticoid rec
175 a-blocker and one of an angiotensin receptor-neprilysin inhibitor, angiotensin-converting enzyme inhi
176                            Phosphoramidon, a neprilysin inhibitor, attenuated these effects of nepril
177 alsartan, a combination angiotensin receptor-neprilysin inhibitor, improves morbidity and mortality i
178 bines an angiotensin receptor blocker with a neprilysin inhibitor, is well tolerated, and represents
179 esized that angiotensin receptor blocker and neprilysin inhibitor, sacubitril/valsartan (Sac/Val, LCZ
180 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-
181 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] With ACEI [Angiotensin-Converting-
182 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ACEI [Angiotensin-Converting-
183 ive Comparison of ARNI [Angiotensin Receptor-Neprilysin Inhibitor] with ARB [Angiotensin Receptor Blo
184 ive Comparison of ARNI [angiotensin receptor/neprilysin inhibitor] With ARB [angiotensin-receptor blo
185  combination of angiotensin receptor blocker/neprilysin inhibitors (ARNi)+beta-blockers (BB)+sodium-g
186                         Angiotensin receptor neprilysin inhibitors (ARNi), beyond blocking angiotensi
187  antagonists (MRA), and angiotensin receptor-neprilysin inhibitors (ARNI), have not been studied in a
188        Combined angiotensin receptor blocker neprilysin inhibitors (ARNIs) have been associated with
189 tor antagonists [MRAs], angiotensin receptor-neprilysin inhibitors [ARNIs], and sodium/glucose cotran
190 acological therapy with angiotensin receptor-neprilysin inhibitors and device therapy deserves furthe
191 medications, especially angiotensin receptor-neprilysin inhibitors and sodium-glucose cotransporter-2
192 rrent use of angiotensin-(1-7) compounds and neprilysin inhibitors as therapies for diabetes.
193       Combined treatment with both SGLT2 and neprilysin inhibitors can be expected to yield substanti
194 ceptor antagonists, and angiotensin receptor-neprilysin inhibitors were used in 85.1%, 44.4%, 28.6%,
195 nhibitors and ANG (angiotensin) II blockers, neprilysin inhibitors, and aldosterone antagonists.
196 in system inhibitors or angiotensin receptor-neprilysin inhibitors, beta blockers, mineralocorticoid
197 and weigh the clinical benefits of synthetic neprilysin inhibitors, either alone or in combination wi
198 cular pathways causing angioedema induced by neprilysin inhibitors, that is, sacubitril, are unclear,
199 inical data from investigations of synthetic neprilysin inhibitors.
200 nhibitors but insensitive to proteasomal and neprilysin inhibitors.
201 n patients treated with angiotensin receptor-neprilysin inhibitors.
202 's disease (AD) markers, synaptophysin, APP, neprilysin, insulin-degrading enzyme and transthyretin i
203 including the endothelin-converting enzymes, neprilysin, insulin-degrading enzyme, and plasmin.
204 ween Amnesiac and Neprilysin 1 (Nep1), a fly neprilysin involved in memory.
205                                              Neprilysin is a cell surface peptidase that catalyticall
206    Together, these findings demonstrate that neprilysin is a factor associated with islet amyloid acc
207                                              Neprilysin is a membrane-bound enzyme that breaks down n
208                                              Neprilysin is a metallopeptidase known to degrade amyloi
209                                              Neprilysin is a transmembrane metalloendopeptidase that
210                                      In sum, neprilysin is a versatile, veteran player returning yet
211                                              Neprilysin is a zinc-dependent endopeptidase.
212                                              Neprilysin is an endopeptidase that degrades vasoactive
213 ing live cell imaging, and that the protease neprilysin is involved in reduction of intraneuronal bet
214                                     Although neprilysin is known to degrade beta-amyloid, we observed
215 tan might cause cognitive impairment because neprilysin is one of several enzymes degrading amyloid-b
216                               This indicates neprilysin is the predominant peptidase responsible for
217 time that with prolonged FFA exposure, islet neprilysin is upregulated and this is associated with re
218 that require further research before soluble neprilysin is used clinically.
219 ctivity of an Abeta-degrading endopeptidase, neprilysin, is elevated in the brains of "enriched" mice
220 elevated in endothelin-converting enzyme and neprilysin knock-out mice, and inhibitors of these enzym
221  issue, a lentiviral vector expressing human neprilysin (Lenti-Nep) was tested in transgenic mouse mo
222                         Associations between neprilysin level and a composite endpoint that included
223         Lung-targeted strategies to increase neprilysin levels could have therapeutic benefits in the
224 eal-life cohort of HF patients and correlate neprilysin levels with outcomes.
225                                      Rather, neprilysin may act by reducing hIAPP fibrillogenesis, wh
226                      These data suggest that neprilysin may be protective against chronic hypoxic pul
227 l reduction of extracellular Abeta levels by neprilysin may facilitate development of HNPCs into neur
228 on and suggest that interventions to inhibit neprilysin may improve beta-cell function in obese human
229 le blood RNA expression of gene encoding for Neprilysin (MME) and miR-425 among blacks than whites.
230                              To determine if neprilysin modulated amyloid deposition by cleaving hIAP
231                                 In contrast, neprilysin mRNA and activity did not decrease in amyloid
232 t in islets, including beta-cells, and islet neprilysin mRNA and activity were found to decline with
233 e of the treatments had an effect on cardiac neprilysin mRNA.
234                                              Neprilysin (NEP) and angiotensin-converting enzyme (ACE)
235 t AD is with Abeta-degrading enzymes such as neprilysin (NEP) and insulin-degrading enzyme (IDE).
236 ression and execution of two endopeptidases, neprilysin (NEP) and insulin-degrading enzyme.
237                                              Neprilysin (NEP) appears to be the most potent Abeta pep
238 mily of Zn2+ metallopeptidases which include neprilysin (NEP) as prototype, has raised important ques
239 ression of insulin-degrading enzyme (IDE) or neprilysin (NEP) in neurons significantly reduces brain
240 creased expression of Abeta-degrading enzyme neprilysin (NEP) in primary neuronal cultures.
241 an ethyl ester prodrug of LBQ657, the active neprilysin (NEP) inhibitor, and a component of LCZ696 (s
242                            The endopeptidase neprilysin (NEP) is a major amyloid-beta (Abeta) degradi
243                                              Neprilysin (NEP) is a naturally occuring enzyme that bre
244                                              Neprilysin (NEP) is a zinc-dependent metalloprotease tha
245                                              Neprilysin (NEP) is an endopeptidase, which has an impor
246 s evidence that the Abeta-degrading protease neprilysin (NEP) is down-regulated in normal aging and L
247                                              Neprilysin (NEP) is one of the rate-limiting Abeta-degra
248                   The Abeta-degrading enzyme neprilysin (NEP) is the best known target of these inhib
249                                              Neprilysin (NEP) is the dominant Abeta peptide-degrading
250 icrovessels and the Abeta-degrading protease neprilysin (NEP) occurred 14-21 d after a substantial de
251 abolism in kidney homogenates, we identified neprilysin (NEP) to be a major source of renal Ang-(1-7)
252 tein and mRNA for the Abeta-degrading enzyme neprilysin (NEP) was found, whereas various Abeta-cleari
253                          Insulysin (IDE) and neprilysin (NEP) were found to be inactivated by oxidati
254     Angiotensin-converting enzyme 2 (ACE-2), neprilysin (NEP), and plasma kallikrein (KLKB1) cleave a
255 lin-derived peptides by proteases, including neprilysin (NEP).
256                                          The neprilysin (NEP)/endothelin-converting enzyme (ECE) fami
257  by two membrane-bound Zn-metallopeptidases, neprilysin (NEP, EC 3.4.24.11) and aminopeptidase N (APN
258  levels of the metallomembrane endopeptidase neprilysin, normal levels were maintained in the exercis
259                       After chronic hypoxia, neprilysin-null mice exhibited exaggerated pulmonary hyp
260                     Smooth muscle cells from neprilysin-null pulmonary arteries had increased prolife
261 This effect might result from degradation by neprilysin of endogenous Abeta produced and secreted by
262                   The differential effect of neprilysin on plaques and oligomers suggests that nepril
263 re resistant to a 1-h incubation with either neprilysin or insulin degrading enzyme, whereas the mono
264 al cyclic guanosine monophosphate content by neprilysin or phosphodiesterase 9 inhibition, and myocar
265      In mouse models of Alzheimer's disease, neprilysin overexpression improves learning and memory d
266                                              Neprilysin overexpression reduced soluble Abeta levels b
267 ion of the renin-angiotensin-aldosterone and neprilysin pathways, as well as the limitations of these
268 ux and GSIS, suggesting that upregulation of neprilysin per se mediates insulin secretory dysfunction
269 s a substrate specificity similar to that of neprilysin, preferring to cleave substrates at the amino
270                     These data indicate that neprilysin proteolytically inactivates fibroblast growth
271 hout exogenous Abeta1-40, the treatment with neprilysin reduced the number of developing colonies.
272         We previously showed that the enzyme neprilysin reduces islet amyloid deposition and thereby
273 omprehensive multivariable analyses, soluble neprilysin remained significantly associated with both t
274 mpared with controls, which was decreased by neprilysin replacement.
275                                              Neprilysin research has essentially focused on their rol
276  a specific inhibitor or adenovirus encoding neprilysin, respectively.
277 t neprilysin, but not enzymatically inactive neprilysin, resulted in a slight increase in basic fibro
278                                              Neprilysin's inability to prevent learning and memory de
279             To find out whether dAbeta was a neprilysin's target, we used inducible drivers to modula
280                 In this study, we found that neprilysin selectively controls endogenous opioid concen
281                          Genetic ablation of neprilysin specifically protects against FFA-induced imp
282 e rapid, comparable with that of other known neprilysin substrates.
283 t)Lu-DOTA-PP-F11N is less of a substrate for neprilysins than the other analogs, whereas intracellula
284    We previously characterized a recombinant neprilysin that contained a 38-amino acid brain-targetin
285  perineuronal net (PNN) and Mme encoding for Neprilysin, the enzyme degrading amyloid beta-peptides.
286 erted by esterases to LBQ657, which inhibits neprilysin, the enzyme responsible for the degradation o
287                   We previously demonstrated neprilysin to be present in pancreatic islets and now so
288 estion, we crossed hAPP transgenic mice with neprilysin transgenic mice and analyzed their offspring.
289                               This effect of neprilysin was associated with reduced amounts of the mo
290                          Circulating soluble neprilysin was measured with a modified sandwich immunoa
291 ving hIAPP, analysis of hIAPP incubated with neprilysin was performed by mass spectrometry, which fai
292                                              Neprilysin was present in islets, including beta-cells,
293 ed by 54 and 75%, respectively, whereas when neprilysin was up-regulated islet amyloid deposition and
294             Combined inhibition of SGLT2 and neprilysin was well-tolerated.
295                                ECE-1, unlike neprilysin, was found to have minimal activity against s
296                                              Neprilysin weakly but significantly correlated with age
297 rading enzymes, insulin degrading enzyme and neprilysin, were unchanged.
298 ding enzyme, the endogenous metallopeptidase neprilysin, which is fused to albumin to extend plasma h
299  HF patients and the positive association of neprilysin with cardiovascular mortality and morbidity f
300 not wild-type neurons show reduced levels of neprilysin with time in culture.

 
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