ライフサイエンスコーパス: arginine

1 les measured to date and are more basic than arginine.

2 ting that protection from colitis requires l-arginine.

3 , augment the ISCs function in response to L-arginine.

4 inverse of FBF reserve to N(G)-monomethyl-L-arginine.

5 cellular programming requires extracellular arginine.

6 from 0.723 and 0.640 to 0.734 and 0.643 for arginine.

7 ecific helix of the vWF A1 domain, via three arginines.

8 We found PRMT6 to methylate CRAF at arginine 100, interfering with its RAS/RAF binding poten

9 ) with moderate certainty; for air stimulus, arginine (2.22; 1.45-2.99), potassium + hydroxyapatite (

10 that PRMT5 catalyzes methylation of YBX1 at arginine 205 (YBX1-R205me2), an event that is critical f

11 MoHMT1 catalyses the di-methylation of arginine 247, 251, 261 and 271 residues of MoSNP1, a U1

12 We identify arginine-49 as a key residue that forms a salt bridge to

13 l amounts (5-8 mg/g), as well as proline and arginine (~5 mg/g).

14 ) catalyzes symmetric dimethylation (SDM) of arginine, a posttranslational modification involved in o

15 Strikingly, in extracellular arginine absence, both cell types display flexibility as

16 gested that Tempranillo blanco behaved as an arginine accumulator variety.

17 Introducing the cleavable arginine-alanine peptide into the NAc attenuated express

18 Arginine also decreased protein-carbonyl levels across a

19 Here we add that arginine also directly impacts bacterial virulence.

20 onds and pai-stacking interactions involving arginine and aromatic residues.

21 herefore aimed to develop a method to detect arginine and determine its delta(15)N value (delta(15)N(

22 m sized fluorescent capsules based on poly-L-arginine and dextran sulfate for targeting the kidney vi

23 ation, we converted each of these lysines to arginine and found that replacing two of these residues,

24 ; 10(7) copies per cell)(6,7) and their high arginine and lysine content has led to the hypothesis th

25 terized protein methylation events encompass arginine and lysine N-methylation, and only a few cases

26 chets/d) of either a formula enriched with l-arginine and omega-3 (n-3) fatty and ribonucleic acids (

27 herapy drugs cisplatin and doxorubicin alter arginine and polyamine metabolites.

28 erturbation in metabolic pathways related to arginine and proline metabolism as well as TCA cycle was

29 as low as 50 nM, can covalently transacylate arginine and serine residues in GSTP and cross-link them

30 bind in the open state to positively charged arginines and lysines between the intracellular ends of

31 The production of amino acids, like arginine, and other N-rich compounds corresponded with g

32 conserved epitopes, including two conserved arginines, are shared by the class 5 adhesins.

33 20 amino acids, three of them-leucine (Leu), arginine (Arg), and serine (Ser)-are encoded by six diff

34 bstrate dUMP in the N3-ionized form using an arginine, Arg199, in Mtb.

35 and simultaneously cross-linking to another arginine (Arg45) located across the carbohydrate-binding

36 unds bind galectin-8N by engaging its unique arginine (Arg59) and simultaneously cross-linking to ano

37 ivate it, with the latter cutting within the arginine-arginine site.

38 f an asparagine, imply the use of the distal arginine as a catalytic base.

39 tains amlodipine, indapamide and perindopril arginine as active ingredients which might have induced

40 ium Pseudomonas putida KT2440, identifying L-arginine as the main one causing a significant increase

41 Thus, an increased availability of l-arginine as well as altered intestinal microbiota and me

42 We demonstrate that arginine, as its N-acetyl isopropyl ester, is amenable t

43 Proteins composed exclusively of arginine-aspartic acid dipeptide repeats undergo length-

44 rains, except for replacement of lysine with arginine at 378th position of the cryptic epitope of a S

45 tation found, P542R (proline was replaced by arginine at aminoacid 542), affects the location of the

46 Mean acute C-peptide response to arginine at maximal glycemic potentiation did not signif

47 upported a critical role for substitution of arginine at position 207 (S207R) in mediating resistance

48 cancer, with small molecule inhibitors of an arginine-binding pocket of WDR5 (the 'WIN' site) showing

49 pathways (eg, branched chain amino acids and arginine biosynthesis) and virulence genes (eg, beta-tox

50 (100 and 300 mg/dL) followed by intravenous arginine bolus before and after 72-h glucose infusion.

51 60% (second clamp step) and by 62% following arginine (both P < 0.005) following 72-h glucose infusio

52 thine side chains were further modified into arginine by an abiotic chemical reaction, improving both

53 ide (NO(-)) is a member of RNS produced from arginine by inducible Nitric Oxide Synthase (iNOS) enzym

54 ed nominally significant increases in plasma arginine, citrulline, and glycine, with decreases in tot

55 istidine near motif IVa, reminiscent of the "arginine clamp" of RNA helicases.

56 eology, we demonstrate that droplets of poly-arginine coassembled with mono/polynucleotides have appr

57 Three of six arginine codons (CGU, CGC, and CGA) are decoded by two E

58 The majority of remaining N is from arginine, comprising 16 and 14% of collagen and plant pr

59 he peak of C. rodentium infection, increased arginine concentration in the colon correlated with down

60 een shown to co-precipitate with the C9orf72 arginine-containing dipeptide repeat proteins (R-DPRs),

61 as five arginines were analyzed, only three arginines could bind simultaneously with major-groove gu

62 ether with its postsynthesis modification to arginine, could have been the earliest basic amino acids

63 nt3a in the Paneth cell niche by exogenous L-arginine couples ISCs function and favours a model in wh

64 Arginine, cysteine and methionine have Generally Recogni

65 Protein arginine deiminase 4 (PAD4) facilitates the post-transla

66 Inhibition of protein arginine deiminase 4, an enzyme important for the releas

67 s also reduced by citrullination by peptidyl arginine deiminase 4, or digestion by serine proteases.

68 efficacy of arginine deprivation (pegylated arginine deiminase) and chemotherapy (cisplatin), offeri

69 iR-1291 effectively enhanced the efficacy of arginine deprivation (pegylated arginine deiminase) and

70 Effects of arginine deprivation on osteoclastogenesis are independe

71 rably sensitized ASS1-abundant L3.3 cells to arginine deprivation therapy.

72 -1291 was effective to sensitize PC cells to arginine deprivation treatment and chemotherapy through

73 kably, fractional excretions of 6 lysine and arginine-derived glycation free adducts were higher in p

74 4 binding through mutation of the C-terminal arginine did not impact the ability of several high-risk

75 and nonribosomal interfaces with analysis of arginine dihedral angles and structural (suite) classifi

76 In contrast, mutations in arginine display a severely altered conformation, static

77 75% hemoglobin-SS) were randomized to 1 of 3 arginine doses: (1) 100 mg/kg IV 3 times/day (TID); (2)

78 ncreased at discharge in subjects from all 3 arginine-dosing schemes; greatest increase occurred with

79 t DNA, and why replacement of residue 848 by arginine during RAG domestication led to suppression of

80 in the M(pro)C domain-swapping hinge and an arginine elsewhere forms early during folding, modulates

81 Pre-treatment with L-arginine enhances the ISCs pool and protects the gut in

82 her P-loop NTPases such as an alternative to arginine-finger-based catalysis.

83 d incorporation of key amino acids including arginine for nucleic acid complexation and cellular upta

84 of DyPs can be tuned to select aspartate or arginine for the rate enhancement of peroxide heterolysi

85 When arginine fork chemical recognition principles were appli

86 inine-guanine recognition, we found that the arginine fork geometry was more consistent with the expe

87 Nearly 30 years ago, a theoretical arginine fork model was posited to account for the speci

88 stence of a recurrent structural motif, the "arginine fork", that codifies arginine readout of cognat

89 he results revealed four distinct classes of arginine forks that we have defined using a rigorous but

90 These findings prompted us to search for arginine forks within experimental protein-RNA structure

91 effect of Arg1 deletion was reduced by an l-arginine-free diet, but rescued by simultaneous deletion

92 l activity for a T3SS effector and show that arginine-GlcNAcylation, once thought to be restricted to

93 investigations show that TNPO1 recognizes an arginine-glycine(-glycine) (RG/RGG)-rich region, whereas

94 matrix (ECM) proteins, and reveal tripeptide Arginine-Glycine-Aspartate (RGD) domains that bind and s

95 (68)Ga-labeled arginine-glycine-aspartate tripeptide sequence (RGD) PET

96 Gylated surface decorated with two different arginine-glycine-aspartic acid (RGD) peptides: one is cy

97 S with the high-affinity amino acid sequence arginine-glycine-aspartic acid-phenylalanine-cysteine (R

98 cretory responses from a glucose-potentiated arginine (GPA) test, insulin sensitivity from a hyperins

99 ptide repeat proteins (R-DPRs), poly-glycine arginine (GR) and poly-proline arginine (PR), and are pr

100 applied to existing structures with unusual arginine-guanine recognition, we found that the arginine

101 PTPN14 binds to a C-terminal arginine highly conserved in diverse HPV E7.

102 Specificity is mediated by a single arginine, highly conserved across most DUF1338 proteins.

103 n of ASS1 protein levels, miR-1291 perturbed arginine homeostasis and preferably sensitized ASS1-abun

104 To determine if arginine improves mitochondrial function, 12 children wi

105 of large condensates, signifying the role of arginine in driving proper RNA interaction.

106 tatic interaction between positively charged arginine in extracellular loop 2 (K210) and a negatively

107 co-cultured models to clarify the role of L-arginine in ISC function.

108 timulation or intraperitoneal injection of l-arginine in mice with deletion of interleukin (IL)12B, N

109 le of the distal heme residues aspartate and arginine in the heterolysis of peroxide to form the cata

110 +/- 5.6% for methionine to 69.0 +/- 5.8% for arginine in the zein group.

111 n 2 (VSD2) and that each of the three gating arginines in VSD2 reduces the activation threshold.

112 imethylarginine (ADMA) and N(G)-monomethyl-l-arginine, in tumor-bearing mice compared with control mi

113 , respectively, and 4) increased fasting and arginine-induced glucagon levels compared with control s

114 secretion in response to glucose-potentiated arginine-induced insulin secretion (GPAIS) challenge in

115 in the pancreas of mice with cerulean- or L-arginine-induced pancreatitis, and in an oncogenic Kras

116 Exogenously added arginine induces EHEC virulence gene expression in vitro

117 vironmental) and endogenous (biosynthetic) L-arginine influence biofilm formation by P. putida throug

118 xes have unveiled new details, including (i) arginine interactions with the phosphate backbone and th

119 Arginase 1 (Arg1), which converts l-arginine into ornithine and urea, exerts pleiotropic imm

120 es virulence gene expression in C. rodentium Arginine is an important modulator of the host immune re

121 We find that exogenous L-arginine is essential for ISCs proliferation and intesti

122 sporins such as cefotaxime, either lysine or arginine is sufficient for hydrolysis of ampicillin.

123 ifically after the basic residues lysine and arginine, is the predominant enzyme used for proteome di

124 We showed that TbUnc119 binds to a flagellar arginine kinase TbAK3 in a myristoylation-dependent mann

125 ea moiety constructed from N(omega)-methyl-l-arginine (l-NMA) by the multi-domain metalloenzyme SznF.

126 oxide synthase inhibitor N(G) -monomethyl-l-arginine (l-NMMA, 5 mg kg(-1) bolus & subsequent 50 mug

127 This study examined the ability of l-arginine, l-cysteine and l-methionine, to inhibit postha

128 astingly, increasing positive charge through arginine leads to enhanced condensation, speckle enlarge

129 ignificantly increased in VOE subjects after arginine-loading dose treatment.

130 e C9orf72 complex is negatively regulated by arginine, lysine, and histidine, the amino acids that PQ

131 veals a major amino acid profile composition-arginine, lysine, aspartic acid, alanine, threonine and

132 ) is an inborn error of cationic amino acid (arginine, lysine, ornithine) transport caused by biallel

133 hydrophobicity scheme nor one augmented with arginine/lysine-aromatic cation-pai interactions consist

134 a single active site, where it then uses an arginine/lysine-mediated hydrogen-bonding network to rep

135 metabolism, glutathione metabolism, and urea/arginine metabolism compared with controls.

136 Consequently, l-arginine metabolism may serve as a target for clinical i

137 amino acid metabolism (methionine, cysteine/arginine metabolism) in sucrose medium.

138 rescued by simultaneous deletion of other l-arginine-metabolizing enzymes, such as Arg2 or Nos2, dem

139 The NOS inhibitor N(G)-nitro-L-arginine methyl ester (L-NAME) administered after blast

140 nd mechanism of action of Mb on N(G)-Nitro-L-arginine Methyl Ester (L-NAME) and Deoxycorticosterone A

141 xide (NO) synthase inhibitor l-N (G)-nitro-l-arginine methyl ester, while iontophoresis of the NO don

142 ed protein modification catalyzed by Protein aRginine Methyl Transferases (PRMTs).

143 erface previously shown to bind a lysine and arginine methylated sequence of histone H3.

144 Arginine methylation has been recognized as a post-trans

145 uate the effect of type I PRMT inhibition on arginine methylation in normal human peripheral blood mo

146 Arginine methylation is an evolutionarily conserved prot

147 We found that arginine methylation might regulate the early-differenti

148 PRMT1 overexpression increased arginine methylation of HSPs of 70 kDa (HSP70); this met

149 ts highlight a novel role for PRMT7-mediated arginine methylation of RBP substrates, suggesting a reg

150 Our study shows that arginine methylation plays an essential role in accurate

151 T1), a key enzyme that catalyzes the protein arginine methylation process, particularly the isoform e

152 gluconeogenesis, enhancing its activity via arginine methylation, while no effects of PRMT1V1 were o

153 drug resistance and was dependent on protein arginine methylation.

154 eral chromatin decompaction and compete with arginine methylation.

155 CARM1 is a protein arginine methyltransferase (PRMT) that acts as a coactiv

156 ere, we identify that coactivator-associated arginine methyltransferase 1 (CARM1) methylates Pontin c

157 Protein arginine methyltransferase 1 (PRMT1) is a key regulator

158 Here, we show protein arginine methyltransferase 1 (PRMT1), a key enzyme that

159 Protein arginine methyltransferase 5 (PRMT5) catalyzes symmetric

160 Protein arginine methyltransferase 5 (PRMT5) catalyzes the symme

161 Here we demonstrate that protein arginine methyltransferase 5 (PRMT5) functions as an epi

162 The aberrant expression of protein arginine methyltransferase 5 (PRMT5) has been associated

163 Protein arginine methyltransferase 5 (PRMT5) is the major methyl

164 eraction between NF-kappaB, YBX1 and protein arginine methyltransferase 5 (PRMT5).

165 Protein arginine methyltransferase 6 (PRMT6) plays important rol

166 showed that the Arabidopsis thaliana protein arginine methyltransferase AtPRMT3 regulates pre-rRNA pr

167 The approach revealed protein arginine methyltransferase gene 5 (PRMT5) as an effectiv

168 The major Trypanosoma brucei protein arginine methyltransferase, TbPRMT1 enzyme (ENZ), requir

169 Protein arginine methyltransferase-5 (PRMT5) is overexpressed in

170 Protein arginine methyltransferases (PRMTs) regulate many physio

171 es aimed at blocking the activity of protein arginine methyltransferases (PRMTs), which catalyze the

172 found that a small molecule inhibitor of the arginine methyltransferases CARM1 and PRMT6 was able to

173 However, the resulting low arginine microenvironment also impairs chimeric antigen

174 T cells are susceptible to the low arginine microenvironment because of the low expression

175 ride, PP-O, PP-R, pentalsamonin, puractin-A, arginine-monascorubrin, purpurquinone-A, ankaflavin, pur

176 sequence containing a highly conserved twin-arginine motif.

177 Using this strategy we probed several lethal arginine mutants and found that they retain appreciable

178 maging animal models, we showed that protein arginine N-methyltransferase 6 (PRMT6) regulates aerobic

179 lance between host and pathogen responses to arginine occur during disease progression.

180 tion, little is known about the effects of L-arginine on intestinal stem cells (ISCs).

181 signaling pathway, mediates the effects of L-arginine on ISCs function.

182 t the beneficial effects of spermidine, or l-arginine, on gut immunity by promoting Treg cell develop

183 across fungi and reflects the polycistronic arginine operon in prokaryotes.

184 Mutation of H3K36 to arginine or alanine inhibits H3K27 methylation by PRC2 o

185 These effects were mimicked by free arginine or by a modified ZIP in which all but the argin

186 supplementation of the media with lysine and arginine or suboptimal temperature appears to delay bloc

187 Serum concentrations of arginine, ornithine, polyamines, and acetyl polyamines a

188 =6.1x10(-67)), nitric oxide bioavailability (arginine/ornithine + citrulline, +29%; P=2.8x10(-169)),

189 Moreover, SaNanK has a stacked arginine pair coordinated by negative residues critical

190 udy, we assessed whether kisspeptin (Kp) and arginine-phenylalanine (RF)-amide related peptide-3 (RFR

191 We propose that arginine plays a connecting role between cellular metabo

192 ids-processing enzymes, a positively charged arginine plays a key role by assisting with transition s

193 Rather, their contribution to global L-arginine pools appears to determine changes in c-di-GMP

194 poly-glycine arginine (GR) and poly-proline arginine (PR), and are protective in genetic modifier sc

195 their formation can be restored with select arginine precursors.

196 catalyze the formation of various methylated arginine products on a wide variety of cellular substrat

197 nalysis revealed up-regulated AA metabolism, arginine/proline metabolism, and branched-chain AA (BCAA

198 his increase in the concentration of colonic arginine promotes virulence gene expression in C. rodent

199 The twin-arginine protein transport (Tat pathway) is found in pro

200 Extracellular gating involves arginine protonation on the channel surface and correlat

201 do not readily interact with WT FUS, whereas arginine (R) mutants form mixed condensates with WT FUS.

202 We show that, relative to the CD32a arginine (R)-131 (CD32aR) variant, CD32aH more avidly bo

203 metry, we find that substitution of the FLVR arginine R377A does not cause a significant loss of phos

204 actions unique to the closed complex between arginines R55/R57 of eIF2alpha with mRNA, including the

205 al motif, the "arginine fork", that codifies arginine readout of cognate backbone and guanine nucleob

206 NrfA, and site-directed mutagenesis of this arginine reduced enzymatic activity to <3% of the WT lev

207 th all five intracellular lysines altered to arginines remains deubiquitinated and shows augmented tr

208 through mutation of the conserved C-terminal arginine rendered both HPV16 and HPV18 E7 unable to repr

209 An arginine residue at position 136 was found to be essenti

210 al cap of THIK-1 showed that mutation of the arginine residue at position 92, which is in the linker

211 Binding to Scap requires an arginine residue in exon 18 of SREBP2.

212 Here, we show that a highly conserved arginine residue in the C-terminal domain of diverse HPV

213 A hallmark of SH2 domains is the arginine residue in the conserved FLVR motif that forms

214 We find that the arginine residue in the FLVR motif does not directly con

215 strom resolution revealed the presence of an arginine residue in the region otherwise occupied by cal

216 synthetase (GshB) is glycosylated by NleB on arginine residue R256.

217 ral spectroscopy assays, we identified three arginine residues (Arg-97, Arg-277, and Arg-303) that ar

218 ified with hydroimidazolone modifications of arginine residues and products of their hydrolysis) by b

219 5) catalyzes the symmetric di-methylation of arginine residues in histones H3 and H4, marks that are

220 at interrupts the series of regularly spaced arginine residues in the S4 voltage sensor.

221 Additionally, mutations of arginine residues in the Sug(1-19) tag suggest that the

222 s, as well as by converting already-glycated arginine residues into citrulline.

223 uantitate changes in methylation of specific arginine residues on hnRNP-A1.

224 A competitive inhibitor rich in arginine residues reduced the number of enzymatic cleava

225 e measured the contributions of tyrosine and arginine residues to phase separation experimentally thr

226 ne or by a modified ZIP in which all but the arginine residues were replaced by alanine.

227 trates with N-acetyl glucosamine (GlcNAc) on arginine residues.

228 Systemic arginine restriction improves outcome in multiple murine

229 ronment because of the low expression of the arginine resynthesis enzymes argininosuccinate synthase

230 We show that PEs in serine-arginine-rich (SR) proteins, a family of 14 essential SF

231 d in cultured cells expressing either of two arginine-rich dipeptide repeats (R-DPRs), poly(GR) and p

232 ve splicing is pronounced in the serine- and arginine-rich intrinsically disordered domain; these dom

233 red acidic tracts and the positively charged arginine-rich region.

234 passing amino acids 2 to 8 of the N-proximal arginine-rich RNA binding motif.

235 A proline-arginine-rich sequence within the LCD binds to microtubu

236 Software to analyze arginine-RNA interactions has been made available to the

237 a key role for multivalent contacts through arginine's guanidinium ion.

238 h nominally significant increases in NAD(+), arginine, saturated long chain free fatty acids, diacylg

239 Arginine scarcity also dampens generation of IL-4 induce

240 The source of arginine sensed by C. rodentium is not dietary.

241 e show that in the presence of arginine, the arginine sensor ArgR, identified through this screen, di

242 ent degradation of Cactin, a coiled-coil and arginine-serine-rich domain-containing protein that regu

243 n, whereas TNPO3 recognizes a region rich in arginine-serine-tyrosine (RSY) residues.

244 This model predicted that a single arginine should form four complementary contacts with ne

245 between the incorporated nucleotide and the arginine side chain are broken, but the templating base

246 the methylation status and symmetry of each arginine side chain even in highly repetitive RGG amino

247 and the incoming dCTP hydrogen bonds with an arginine side chain of Rev1.

248 ial in the inner leaflet, ordered lysine and arginine side chains in the membrane interfacial regions

249 one MGO-glycation by protecting the reactive arginine sites, as well as by converting already-glycate

250 ism by which METTL2 identifies specific tRNA arginine species for m3C formation as well as the biolog

251 In addition, we show that a methionine-to-arginine substitution at residue 58 impairs Orf6 binding

252 in an SLC30A8 exon, encoding a tryptophan-to-arginine substitution that decreases SLC30A8 function, w

253 nalysis of the LLI sequence with alanine and arginine substitutions showed that its overall hydrophob

254 Here, a six-arginine-tailed anti-epidermal growth factor receptor (E

255 acute C-peptide and proinsulin responses to arginine that were positively correlated with peak MMTT

256 Here we show that in the presence of arginine, the arginine sensor ArgR, identified through t

257 n which these lysine residues are mutated to arginine, the inhibitory effect of RGFP966 on expansions

258 Arginine, the substrate for NO production, becomes acute

259 issue of Blood, Morris et al have shown that arginine therapy can improve mitochondrial function and

260 Arginine therapy increases mitochondrial activity and re

261 cers catabolize the semiessential amino acid arginine to drive cell proliferation.

262 n domain then rearranges the triply modified arginine to N(delta)-hydroxy-N(omega)-methyl-N(omega)-ni

263 ructure reveals that cGAS uses two conserved arginines to anchor to the nucleosome acidic patch.

264 f nutritional glucose and amino acids (e.g., arginine) to drive the synthesis of critical macromolecu

265 ementation of spermidine, or its precursor l-arginine, to assess the frequency and total numbers of r

266 Yeast cells with arginine-to-alanine mutations in the H4 basic patch (H4(

267 The mutation causes an arginine-to-glutamine (RQ) substitution within the first

268 d, a phenylalanine-to-alanine (FtoA), and an arginine-to-lysine (RtoK) mutant of Ddx4 IDR.

269 The twin-arginine translocation (Tat) pathway transports folded p

270 Congruently, a mutant deficient in arginine transport (DeltaartP) had decreased virulence g

271 take of glycation free adducts by lysine and arginine transporter proteins in patients with early GFR

272 In mammals, a subset of arginine tRNA isoacceptors are methylated in the anticod

273 rate that mutations in a neuronally enriched arginine tRNA, n-Tr20, increased seizure threshold and a

274 g 3 (DALRD3) protein to recognize particular arginine tRNAs destined for m3C modification.

275 DALRD3 protein in the targeting of distinct arginine tRNAs for m3C modification and suggest a crucia

276 he NTD forms insoluble aggregates through an arginine/tyrosine-rich sequence reminiscent of low-compl

277 on on nucleophilic side chains, particularly arginines, under metabolic stress conditions.

278 rofiling of mutant cells highlighted purine, arginine/urea cycle and glutamate metabolisms as the mos

279 Histone H3.3 glycine 34 to arginine/valine (G34R/V) mutations drive deadly gliomas

280 Treatment with IV 1-deamino-8-D-arginine vasopressin (0.4 ug/kg) + platelet transfusion

281 Arginine vasopressin (AVP) and its type-2 receptor (V2R)

282 ) concentration of the "social" neuropeptide arginine vasopressin (AVP) is significantly lower in ped

283 The neuropeptide arginine vasopressin (AVP) plays significant roles in ma

284 sed that a self-assembling lipidized peptide arginine vasopressin (AVP) receptor agonist, that had no

285 Treatment with 1-deamino-8-D-arginine vasopressin + platelet transfusion was not asso

286 sotocin or isotocin, homologues of mammalian arginine vasopressin and oxytocin that are broadly impli

287 al hemorrhage studies, adjunct 1-deamino-8-D-arginine vasopressin showed no benefit in limiting hemat

288 sses of peptidergic neurons in the SCN: AVP (arginine vasopressin) and VIP (vasoactive intestinal pol

289 , but the latter conferred responsiveness to arginine-vasopressin (an inhibitory PKC-dependent respon

290 s RXFP3-mediated inhibition of oxytocin- and arginine-vasopressin-synthesizing paraventricular nucleu

291 In fishes, arginine vasotocin (AVT) expression is related to social

292 neurons express galanin and the nonapeptides arginine-vasotocin or isotocin, homologues of mammalian

293 t systems to the response to environmental L-arginine was also studied.

294 Arginine was beneficial for air stimulus, and strontium

295 idine, phenylalanine, lysine, tryptophan and arginine were the monitored AAs in wort and finished bee

296 Although loops with as many as five arginines were analyzed, only three arginines could bind

297 itrulline (co-product of NO synthesis from L-arginine), which were affected by NOS inhibitors confirm

298 Substituting arginine with lysine in synthetic and natural speckle-as

299 ing in GluA2 subunits replacing glutamine to arginine, with the percent inhibition being lower and IC

300 requires a distinct sequence and spacing of arginines within a specific beta2-beta3 hairpin loop tha