ライフサイエンスコーパス: serine protease inhibitor

1 a-1 (apoptosis related) and reduced Clade-B (serine protease inhibitor).

2 ion movement, all of which were blocked by a serine protease inhibitor.

3 rigidity which may aid in its function as a serine protease inhibitor.

4 bited stoichiometrically by an electrophilic serine protease inhibitor.

5 Trypsin was strongly inhibited by serine protease inhibitor.

6 ypsin (AAT) is the most abundant circulating serine protease inhibitor.

7 ioactive peptide from the alpha1-antitrypsin serine protease inhibitor.

8 nd closely related Kunitz-type transmembrane serine protease inhibitors.

9 ignificant similarity to the Kazal family of serine protease inhibitors.

10 D34+ cells, but this effect was abrogated by serine protease inhibitors.

11 and EDTA but not by cysteine, aspartate, or serine protease inhibitors.

12 lytic effect of lactoferrin was prevented by serine protease inhibitors.

13 cular weight proteins classically defined as serine protease inhibitors.

14 unit can form the basis for a novel class of serine protease inhibitors.

15 ibited by a prostasin antibody, heparin, and serine protease inhibitors.

16 e a large and functionally diverse family of serine protease inhibitors.

17 y processing is inhibited by brefeldin A and serine protease inhibitors.

18 at in vitro it was sensitive to a profile of serine protease inhibitors.

19 design templates for engineering reversible serine protease inhibitors.

20 phil response was sensitive to inhibition by serine protease inhibitors.

21 the myxobacterial crocapeptins proved to be serine protease inhibitors.

22 ains and its high homology with other Kunitz serine protease inhibitors.

23 of Ca(+2) ions and exclusively inhibited by serine protease inhibitors.

24 ng new avenues for a systematic discovery of serine protease inhibitors.

25 MSO)/Ringer's solution, 300 KIU aprotinin (a serine protease inhibitor), 0.05% or 0.10% IL-1 receptor

26 Deletion of the gene that encodes serine protease inhibitor 1 (SPI-1) of rabbitpox virus a

27 T. gondii serine protease inhibitor 1 (TgPI1) is the most abundant

28 ajority of patients harbor a mutation in the serine protease inhibitor 1A (SERPINA1) gene leading to

29 onse element (GHRE) from the promoter of rat serine protease inhibitor 2.1, was found to contain Stat

30 nt components, lipocalin-2, metallothionein, serine protease inhibitor-2, transferrin, tissue inhibit

31 The serine protease inhibitor 2A (Spi2a) was highly up-regul

32 The function of serine protease inhibitor 2A (Spi2A) was studied in mous

33 ed, at least in part, by the upregulation of Serine protease inhibitor 2A (Spi2A), a potent inhibitor

34 Here we report that the gene encoding serine protease inhibitor 2A (Spi2A), an inhibitor of ly

35 sed expression of serum amyloid A (Saa3) and serine protease inhibitor 3n (Serpina3n).

36 sion of a novel member of the serpin family, Serine protease inhibitor 4 (Spn4), that we propose is i

37 However, if mineralization was blocked with serine protease inhibitor 4-(2-aminoethyl)benzenesulfony

38 st different protease classes were screened, serine protease inhibitor 4-(2-aminoethyl)benzenesulfony

39 in the presence or absence of cell-permeant serine protease inhibitors 4-(2-aminoethyl)-benzenesulfo

40 with either a protease mixture, or specific serine protease inhibitors 4-(2-Aminoethyl)benzenesulfon

41 studies were designed to examine the role of serine protease inhibitor 6 (SPI-6) in limiting granzyme

42 Serine protease inhibitor 6 (SPI-6), also called Serpinb

43 We show in this study that although serine protease inhibitor 6 (Spi6) is required to protec

44 ression of GrB and its endogenous inhibitor, serine protease inhibitor 6 (Spi6) upon activation.

45 By using mice deficient in Serine Protease Inhibitor 6 (Spi6), we show that by inhi

46 Using mice deficient in serine protease inhibitor 6 (Spi6), we show that Spi6 pr

47 honuclear neutrophils from mice deficient in serine protease inhibitor 6, a weak intracellular NE inh

48 r, mice overexpressing the inhibitor of GZB, serine protease inhibitor 6, are also resistant to toler

49 demonstrated that constitutive expression of serine protease inhibitor 9 (PI-9) on hPB-MSCs and bone

50 ected human alveolar macrophages (AMs) found serine protease inhibitor 9 (PI-9) to be the most promin

51 Serine protease inhibitors abrogated both CPE and collag

52 issue factor pathway inhibitor-2 (TFPI-2), a serine protease inhibitor abundant in the extra cellular

53 The overexpressed human serine protease inhibitor accumulated in lung cells and

54 Incubation of hepatocytes with the serine protease inhibitor AEBSF reduced the death respon

55 mechanism of action of this novel series of serine protease inhibitors against the HCMV deltaAla pro

56 The use of these serine protease inhibitors allows observations as to the

57 ase-3 (PR3), we determined the effect of the serine protease inhibitor alpha-1 antitrypsin (AAT) on I

58 everity can be dampened by administration of serine protease inhibitor alpha-1 antitrysin (AAT).(2)

59 One such protein is the serine protease inhibitor alpha-1-antichymotrypsin (ACT)

60 -c) and IgE-tp interact with polymers of the serine protease inhibitor alpha-1-antitrypsin (A1AT).

61 o have anti-inflammatory properties, and the serine protease inhibitors alpha-1-antitrypsin and alpha

62 caused by the Z mutation (Glu342Lys) in the serine protease inhibitor alpha1-antitrypsin (alpha1AT),

63 Treatment with the serine protease inhibitor alpha1-antitrypsin decreased s

64 M-DEX including, in addition to TIGR/MYOC, a serine protease inhibitor (alpha1-antichymotrypsin), a n

65 Elafin is an endogenous serine protease inhibitor and is transcriptionally down-

66 f the MBP cleavage site within L1 as well as serine protease inhibitors and an L1 peptide containing

67 Serine protease inhibitors and an S456A or an E431A poin

68 The addition of selected serine protease inhibitors and anti-human elastase Ab ma

69 essing resistance to inhibition by canonical serine protease inhibitors and in cleaving these inhibit

70 y human and mouse neutrophils was blocked by serine protease inhibitors and was impaired in infected

71 S intercerebralis major Peptide C (PMP-C), a serine protease inhibitor, and that the EGF-CFC domains

72 Serine proteases, serine protease inhibitors, and protease-activated recep

73 ferential regulation of serine proteases and serine protease inhibitors, and the identification of tr

74 2 or ALLN but was partially sensitive to the serine protease inhibitor APMSF.

75 Consistent with these results, the serine protease inhibitor aprotinin reproduced the effec

76 (aminocaproic acid and tranexamic acid), the serine protease inhibitor aprotinin, or no antibleeding

77 kinase plasminogen activator inhibitor-1 and serine protease inhibitor aprotinin.

78 ll carcinoma antigen-2 (SCCA-2/serpinb3a), a serine protease-inhibitor, are overexpressed in the airw

79 carbamoyl triazole TCMDC-134379 (1), a known serine protease inhibitor, as an excellent starting poin

80 i2A) was studied in mouse TH2 cells, and the serine protease inhibitor B3 (SERPINB3) and SERPINB4 gen

81 Protease nexin-1 (PN-1) is a serine protease inhibitor belonging to the serpin superf

82 SCO0762, a serine-protease inhibitor belonging to the Streptomyces

83 The reversible serine protease inhibitor, benzamidine, inhibited VesB a

84 ultiple human and murine cell lines and that serine protease inhibitors block Xps-mediated rounding a

85 A serine protease inhibitor blocked peptide and oligosacch

86 Both cell-permeant serine protease inhibitors blocked amylase secretion in

87 ine protease inhibitors, but not aspartic or serine protease inhibitors, blocked antibody-drug conjug

88 prior therapy (from the Retreatment with HCV Serine Protease Inhibitor Boceprevir and PegIntron/Rebet

89 naive patients) and the Retreatment With HCV Serine Protease Inhibitor Boceprevir and Pegintron/Rebet

90 A serine protease inhibitor but not inhibitors of cysteine

91 modulators of tumorigenesis/metastasis from serine protease inhibitors but also strengthens the func

92 of EKsolCorin was inhibited by trypsin-like serine protease inhibitors but not inhibitors of chymotr

93 This generation was sensitive to serine protease inhibitors but not to other classes of i

94 s treated with soy bean trypsin inhibitor, a serine protease inhibitor, but this inhibition is overco

95 ate by the C. parvum lysate was inhibited by serine protease inhibitors, by the specific furin inhibi

96 in inhibition, which is in contrast to other serine protease inhibitors (camostat mesylate and aproti

97 Serine protease inhibitors can block the gelatinase acti

98 those of the previously characterized fungal serine protease inhibitors, cnispin from Clitocybe nebul

99 animals they are known to act as kinase and serine protease inhibitors controlling cell growth and d

100 nzyme: aiPLA(2) activity is inhibited by the serine protease inhibitor, diethyl p-nitrophenyl phospha

101 In contrast, the serine protease inhibitor does not affect TRAIL-induced

102 s not inhibited significantly by Pefabloc (a serine protease inhibitor), EDTA (a metalloprotease inhi

103 alphavbeta(3) antibodies, RGD-peptide, and a serine protease inhibitor effectively blocked plasmin-in

104 native state dynamics of the small globular serine protease inhibitor eglin c has been studied in a

105 nanosecond time scale dynamics of the small serine protease inhibitor eglin c have been studied by N

106 ine mutations were introduced into the small serine protease inhibitor eglin c, and the (15)N and (2)

107 Because CI2 is a homologue of the serine protease inhibitor eglin c, which has already bee

108 The serine protease inhibitor, elafin, is a critical compone

109 Maspin, a noninhibitory serine protease inhibitor, exerts multifaceted tumor-sup

110 atic secretory trypsin inhibitor (PSTI) is a serine protease inhibitor, expressed in gut mucosa, whos

111 ng pathway and alpha1-antitrypsin protein (a serine protease inhibitor) expression and downregulation

112 StcE does not digest other serine protease inhibitors, extracellular matrix protein

113 umin and OVAY, OVAX belongs to the ovalbumin serine protease inhibitor family (ov-serpin).

114 nd protein expression of maspin, a member of serine protease inhibitor family and an epithelial cell

115 It is of interest that a member of the serine protease inhibitor family is concomitantly induce

116 , functional APC levels are regulated by the serine protease inhibitor family of proteins including a

117 SerpinB2, a member of the serine protease inhibitor family, is expressed by macrop

118 esterase inhibitor (C1-INH), a member of the serine protease inhibitor family.

119 Bikunin is a serine protease inhibitor found in human amniotic fluid,

120 Ecotin is a dimeric serine protease inhibitor from Escherichia coli which bi

121 creases once the expression of a Kunitz-type serine protease inhibitor from the American dog tick (De

122 eased the selectivity of ShPI-1, a versatile serine protease inhibitor from the sea anemone Stichodac

123 ibed a family of 14 Kazal-like extracellular serine protease inhibitors from P. infestans.

124 and structural similarities to extracellular serine protease inhibitors from the nematode Ascaris.

125 rotease activity by targeted deletion of the serine protease inhibitor gene Spink5 each increases inf

126 Matriptase and its cognate, Kunitz-type serine protease inhibitor, HAI-1, comprise a newly chara

127 SPINT2 encodes the transmembrane serine protease inhibitor HAI2 (placental bikunin), and

128 ine-alpha-methylpyrrolidine-5,5-trans-lactam serine protease inhibitors has been developed as antivir

129 reported discovery in 1994, maspin (mammary serine protease inhibitor) has been characterized as a c

130 ore, C1INH, in addition to its function as a serine protease inhibitor, has a novel anti-inflammatory

131 on in the absence of the cognate Kunitz-type serine protease inhibitors, hepatocyte growth factor act

132 (Although aprotinin is a serine protease inhibitor, here we use the term antifibr

133 rotein (IalphaIp) functions as an endogenous serine protease inhibitor in human plasma, and IalphaIp

134 nhibitor protein (IalphaIp) is an endogenous serine protease inhibitor in human plasma.

135 likely that induction of both IRF-1 and the serine protease inhibitor in response to infection by M.

136 nents of the Toll and JAK/STAT pathways, and serine protease inhibitors in both social and solitary b

137 alpha inhibitor proteins serve as endogenous serine protease inhibitors in human plasma.

138 guishing cospin from other beta-trefoil-fold serine protease inhibitors in which beta4-beta5 or beta5

139 Treatment with FUT-175 (10 mg/kg), a potent serine protease inhibitor, increased survival after I-R,

140 parison of the LTI sequence with other known serine protease inhibitors indicates that LTI is a membe

141 5B polymerase inhibitor, and GS-9256, an NS3 serine protease inhibitor, individually have activity ag

142 he problem of identifying sites of potential serine protease inhibitor interactions on the surface of

143 iruses upregulates a cellular protein called serine protease inhibitor Kazal (SPIK).

144 inogen (PRSS1), anionic trypsinogen (PRSS2), serine protease inhibitor Kazal 1 (SPINK1), cystic fibro

145 static associations between filaggrin (FLG), serine protease inhibitor Kazal-type 5 (SPINK5), and thy

146 tly, we identified SPINK5, which encodes the serine protease inhibitor Kazal-type 5 protein (LEKTI),

147 The loss-of-function mutations of serine protease inhibitor, Kazal type 1 (SPINK1) gene ar

148 In a preliminary study, we found serine protease inhibitor, Kazal type 1 (SPINK1) mutatio

149 static function of a five-domain Kunitz-type serine protease inhibitor (KPI) from the tick Dermacento

150 These genes included that encoding the serine protease inhibitor Kunitz type 1 (Spint1), which

151 RWJ-50353, a serine protease inhibitor, led to reduced pigment deposi

152 Deficiency in the serine protease inhibitor LEKTI is the etiological origi

153 SPINK5, encoding the putative multi-domain serine protease inhibitor LEKTI, was recently identified

154 rated in SPINK5-deficient mice that lack the serine protease inhibitor LEKTI.

155 the SPINK5 gene, which encodes a multidomain serine protease inhibitor (LEKTI) predominantly expresse

156 e inhibition of protease activity by using a serine protease inhibitor leupeptin or two structurally

157 derivatives in disease states with elevated serine protease inhibitor levels.

158 Vaspin (visceral adipose tissue-derived serine protease inhibitor) levels increase with hyperins

159 c alpha-amylase inhibitor CM2 (Tri a 29.02), serine protease inhibitor-like allergen (Tri a 39), and

160 The variant is located in the gene encoding serine protease inhibitor, low levels of which are assoc

161 f lamellar bodies; SPINK5, which encodes the serine protease inhibitor lymphoepithelial Kazal-type tr

162 We have targeted the Mammary Serine Protease Inhibitor (maspin) (SERPINB5) tumor supp

163 Mammary serine protease inhibitor (Maspin) represents an importa

164 g domains it also contains several "serpin" (serine protease inhibitor) motifs.

165 We found that a serine protease inhibitor, N-tosyl-L-lysine chloromethyl

166 Maspin is a unique serine protease inhibitor of which the down-regulation i

167 Naturally-occurring serine protease inhibitors of the Bowman-Birk family exe

168 thora infestans, secrete a diverse family of serine protease inhibitors of the Kazal family.

169 The suicide inhibitory mechanism of serine protease inhibitors of the serpin superfamily dep

170 Therefore we examined the effects of serine protease inhibitors on skin pigmentation and foun

171 onic acids include biochemically significant serine protease inhibitors, one of which is the clinical

172 eatments of C57/BL6J-betaENaC-Tg mice with a serine protease inhibitor ONO-3403, a derivative of camo

173 Maspin is a mammary serine protease inhibitor or serpin with tumor suppressi

174 Penetration was prevented by addition of serine protease inhibitors or a chicken monoclonal antib

175 of CDCP1 with unique anti-CDCP1 antibodies, serine protease inhibitors or genetic modulation of the

176 Serine protease inhibitors, or serpins, are paradigms fo

177 PI10) is a member of the ovalbumin family of serine protease inhibitors (ov-serpin) that is expressed

178 This serine protease inhibitor participates in the regulation

179 The serine protease inhibitors phenylmethylsulfonyl fluoride

180 This degradation was inhibited by serine protease inhibitors phenylmethylsulfonyl fluoride

181 ivity of BRS1 can be strongly inhibited by a serine protease inhibitor, phenylmethylsulfonyl fluoride

182 translational processing is inhibited by the serine protease inhibitor, phenylmethylsulfonyl fluoride

183 sive activities of CDCP1 by upregulating the serine protease inhibitor plasminogen activator inhibito

184 urthermore, stable transfection of a related serine protease inhibitor, plasminogen activator inhibit

185 This was suppressed by serine protease inhibitors (PMSF, Pefabloc SC), but not

186 This activity could not be inhibited by a serine protease inhibitor, PMSF, but could be inhibited

187 In summation, novel and potent trypsin-like serine protease inhibitors possessing a unique mode of b

188 inogen activator and urokinase, as well as a serine protease inhibitor, PP5.

189 alpha1-Antitrypsin is a serine protease inhibitor produced in the liver that is

190 n alpha1-antitrypsin (hAAT), the major serum serine-protease inhibitor, prolongs islet graft survival

191 Here, we identify the serine protease inhibitor protease nexin 1 (PN1) as a ne

192 d Western blotting analyses, revealed that a serine protease inhibitor, protease nexin-1 (PN-1), was

193 ctor, interleukin 1 receptor antagonist, and serine protease inhibitor protein 1, and the phosphoryla

194 The serpin family of serine protease inhibitors provides a well-defined struc

195 A serine protease inhibitor reduced saliva-mediated enhanc

196 Inhibition of HGFA activity with serine protease inhibitors reduced ureteric bud branchin

197 Although aprotinin, a serine protease inhibitor, reduces blood loss in patient

198 Serpins (serine protease inhibitors) regulate some innate immune

199 activated receptor 2 activation by synthetic serine protease inhibitors requires keratinocyte-melanoc

200 inogen activator inhibitor type 2 (PAI-2), a serine protease inhibitor, resulted in NLRP3- and ASC (a

201 alpha(1)-Antitrypsin is a serine protease inhibitor secreted by hepatocytes.

202 ficantly increased neurogenesis, whereas the serine protease inhibitor, secretory leukocyte protease

203 neutrophil apoptosis and efferocytosis in a serine-protease inhibitor-sensitive manner.

204 The human serine protease inhibitor (serpin) alpha-1 antitrypsin (

205 Many members of the serine protease inhibitor (serpin) family are activated

206 The serine protease inhibitor (serpin) family can readily fo

207 at secreted proteins Fibronectin 1 (FN1) and serine protease inhibitor (serpin) family E member 2 (SE

208 rcinoma antigen 1 (SCCA1) is a member of the serine protease inhibitor (serpin) family of proteins, w

209 We have identified a member of the serine protease inhibitor (serpin) family which is highl

210 elium-derived factor (PEDF), a member of the serine protease inhibitor (serpin) family, is a survival

211 Maspin, a member of the serine protease inhibitor (serpin) family, is a tumor su

212 inhibitor type-1 (PAI-1) is a member of the serine protease inhibitor (serpin) family.

213 The human serine protease inhibitor (serpin) gene cluster at 14q32

214 The human serine protease inhibitor (serpin) gene cluster at 14q32

215 The human serine protease inhibitor (serpin) gene cluster at 14q32

216 1AT, gene symbol PI) resides in a cluster of serine protease inhibitor (serpin) genes on chromosome 1

217 ine residues important for inhibition by the serine protease inhibitor (serpin) heparin cofactor II (

218 ogen activator inhibitor type 1 (PAI-1) is a serine protease inhibitor (serpin) in which the reactive

219 igment epithelium-derived factor (PEDF) is a serine protease inhibitor (serpin) protein with well est

220 Maspin is a member of the serine protease inhibitor (serpin) superfamily and displ

221 Point mutations cause members of the serine protease inhibitor (serpin) superfamily to underg

222 Maspin is a non-inhibitory serine protease inhibitor (serpin) that influences many

223 Maspin is a novel serine protease inhibitor (serpin) with tumor suppressiv

224 Maspin is a novel serine protease inhibitor (serpin) with tumor suppressiv

225 Maspin, a serine protease inhibitor (serpin), can suppress tumor g

226 Maspin, a novel serine protease inhibitor (serpin), suppresses the growt

227 xamined the unique relationship of maspin, a serine protease inhibitor (serpin), that plays a critica

228 Expression of two serine protease inhibitors [Serpina1a (alpha1-antitrypsi

229 , we observed a compensatory increase in the serine protease inhibitor Serpina3n in mouse models of M

230 Elevated levels of the serine protease inhibitors SERPINB3 and SERPINB4 are see

231 rand in a manner similar to that observed in serine protease inhibitors serpins.

232 Serine protease inhibitors (serpins) are a superfamily o

233 The native form of serine protease inhibitors (serpins) is kinetically trap

234 nomodulating genes with sequence homology to serine protease inhibitors (serpins) that possess antiap

235 mmatory properties with sequence homology to serine protease inhibitors (serpins).

236 arks of such cascades is their regulation by serine protease inhibitors (serpins).

237 rpin superfamily proteins, most of which are serine protease inhibitors, share an unusual mechanism r

238 presence of phenylmethylsulfonyl fluoride (a serine protease inhibitor) showed an increased autolysin

239 vel bifunctional metallocarboxypeptidase and serine protease inhibitor (SmCI) isolated from the tenta

240 we show that soymilk and the soybean-derived serine protease inhibitors soybean trypsin inhibitor and

241 Previously, we showed that maspin, a serine protease inhibitor, specifically inhibits PC-asso

242 Serine protease inhibitor (Spi) 2A, an anti-apoptotic cy

243 ort that memory cells express high levels of serine protease inhibitor (Spi) 6, an inhibitor of the e

244 A novel filarial serine protease inhibitor (SPI) from the human parasitic

245 This study has focused on the novel role of serine protease inhibitor (SPI) in the escape of MSCs fr

246 F), exhibits sequence homology to a poxvirus serine protease inhibitor, SPI-1, as well as to another

247 hese data suggest that in the absence of the serine protease inhibitor spink5, there is an abnormal i

248 Serine protease inhibitors (SPIs) regulate protease-medi

249 not efficiently inhibited by broad spectrum serine protease inhibitors, suggesting that the enzyme c

250 face-associated, and secreted protein in the serine protease inhibitor superfamily.

251 echanism of disease caused by mutants of the serine protease inhibitor superfamily.

252 at serpin5 (Spn5), a largely uncharacterized serine protease inhibitor, suppresses the melanization p

253 Maspin, a novel serine protease inhibitor, suppresses tumor progression

254 Serine protease inhibitors, termed serpins, are key regu

255 l)-benzenesulfonyl fluoride hydrochloride, a serine protease inhibitor that blocks activating transcr

256 -2-phenylethyl chloromethyl ketone (TPCK), a serine protease inhibitor that blocks IkappaBalpha degra

257 Chymostatin, a serine protease inhibitor that does not prevent the acti

258 tor-1 (HAI-1) is a Kunitz-type transmembrane serine protease inhibitor that forms inhibitor complexes

259 k to c-Myc-induced death processes, AEBSF, a serine protease inhibitor that inhibits apoptosis by c-M

260 athway inhibitor-2 (TFPI-2) is a Kunitz-type serine protease inhibitor that inhibits plasmin, trypsin

261 CHFI is considered a canonical serine protease inhibitor that interacts with FXIIa thro

262 1 is an epithelial Kunitz-type transmembrane serine protease inhibitor that is encoded by the SPINT1

263 The HE4 gene encodes for a putative serine protease inhibitor that is upregulated in human a

264 (HAI-1) is a membrane-associated Kunitz-type serine protease inhibitor that regulates cell surface an

265 vator inhibitor-1 (HAI-1) is a transmembrane serine protease inhibitor that regulates the conversion

266 e domains and likely functions as a secreted serine protease inhibitor that targets two distinct prot

267 intact IRF-1 correlated with induction of a serine protease inhibitor that was able to significantly

268 Serine protease inhibitors that block CIAP1 cleavage inh

269 be common to a large class of tight-binding serine protease inhibitors that mimic good substrates.

270 ratory post hoc analyses using data from the Serine Protease Inhibitor Therapy 2 (SPRINT-2) study (tr

271 Previously untreated patients (from the Serine Protease Inhibitor Therapy 2 [SPRINT-2] trial) an

272 strate the clinical potential for this novel serine protease inhibitor to prevent GVD in solid organ

273 pithelial cells require both the caspase and serine protease inhibitors to efficiently prevent apopto

274 We have characterized a Kazal family serine protease inhibitor, Toxoplasma gondii protease in

275 y the pan-caspase inhibitor zVAD-fmk and the serine protease inhibitor TPCK, but not the caspase-3 in

276 d the thermodynamics of binding of the Kazal serine protease inhibitor, turkey ovomucoid third domain

277 ied the functions of the Arabidopsis UNUSUAL SERINE PROTEASE INHIBITOR (UPI) gene, which encodes an 8

278 at alpha-1 antitrypsin (AAT; Prolastin-C), a serine protease inhibitor used for the treatment of AAT

279 otease TMPRSS2, but Zhou et al. found that a serine protease inhibitor was more protective than a cat

280 esign and synthesis of a novel iodine-labile serine protease inhibitor was realized by the use of an

281 SerpinA3N, a serine protease inhibitor, was upregulated in the dorsal

282 Finally, using selective serine protease inhibitors, we determined that PR3 activ

283 r efforts toward a second generation HCV NS3 serine protease inhibitor were directed at improving the

284 The serine protease inhibitors were able to block killing by

285 The resulting potent serine protease inhibitors were designed from lead molec

286 ked by metalloproteinase inhibitors, whereas serine protease inhibitors were ineffective.

287 The NS3/4A serine protease inhibitors were the first of these to be

288 Maspin is a tumor-suppressor serpin (serine protease inhibitor), which inhibits cell invasion

289 SLPI is a secreted serine protease inhibitor, which is overexpressed in a n

290 th inter-alpha-inhibitor (IalphaI), a potent serine protease inhibitor, which may be immobilized via

291 t this cascade is regulated by a serpin-type serine protease inhibitor, which plays an essential role

292 n G suppressed HIV infection of macrophages, serine protease inhibitors, which are exuded from the bl

293 ay glands express Kunitz-type and non-Kunitz serine protease inhibitors, which might prevent proteoly

294 t the kinetic characterization of a class of serine protease inhibitors whose potencies and selectivi

295 Cospin (PIC1) from Coprinopsis cinerea is a serine protease inhibitor with biochemical properties si

296 Maspin is a novel serine protease inhibitor with tumor suppressive activit

297 pentapeptide 2 are alpha-ketoamide-type HCV serine protease inhibitors with modest potency.

298 A combinatorial library of 400 serine protease inhibitors with the general structure Cb

299 Coapplication of serine protease inhibitors with the superbase normalized

300 odulating, and tissue-protective circulating serine-protease inhibitor, with levels that increase dur