ライフサイエンスコーパス: J

1 J Climate, 23: 1696-1718, 2010), as a stand-alone criter

2 J Gerontol A Biol Sci Med Sci.

3 (J Nucl Cardiol 2020).

4 J-Lat cells exhibited successful engraftment in several

5 J., Biddiscombe, S.

6 J., Corbett, S., Ewing, S.

7 ees (-11.74 kJ/mol) andDeltaS degrees (-8.08 J/K.mol) led to the most excellent stability at 100 degr

8 C-H bonds indicated by the corresponding (1)J(CH) coupling constants.

9 the two competing allylic C-H bonds (Delta(1)J(CH)) and the C-H activation barriers (DeltaDeltaG(*))

10 elationship between the difference in the (1)J(CH) coupling constants of the two competing allylic C-

11 curvature constant (51 +/- 11 vs. 52 +/- 10 J P(max) (-1) , P = 0.733) of the power-duration relatio

12 emented by diagnostic coupling constants (1h)J(NH...F(-)) give insight into how multiple H bonds to f

13 a 1.5-second on/off cycle (total energy 7.2 J/cm(2)).

14 at and squirrel monkey and the genetic DBA/2 J mouse model) with distinct durations of IOP elevation.

15 (+) cells were illuminated at a fluence of 2 J/cm(2) with a near-infrared light (830 nm) transmitted

16 erimental ones, critical for the case of (2) J(CH) .

17 vering nonarcing, nonbarotraumatic 6 ms, 200 J direct current IRE applications via a custom nondeflec

18 h as the gill slits [Huysseune et al., 2009, J.

19 igh areal energy and power densities of 1.24 J cm(-2) and 75.5 mW cm(-2) , respectively, and can be c

20 3 s) and reduced-fluence PDT (light dose, 25 J/cm2; dose rate, 600 mW/cm2; wavelength, 689 nm PDT app

21 hormetic UVC irradiation (two pulses of 0.3 J/cm(2)), showed significantly less degradation of vitam

22 based on comparison of DFT-calculated (2,3) J(CH) values with experimental ones, critical for the ca

23 guration selection also works well using (3) J(CH) values predicted from a semi-empirical Karplus-bas

24 nly photobiomodulation (890 nm, 80 Hz, 0.324 J/cm(2), and 0.001 W/cm(2)).

25 m-packaged and flashed with 2.1, 4.2 and 8.4 J/cm(2).

26 d with 830 nm light (180 s; 25 mW/cm(2); 4.5 J/cm(2)) using a light-emitting diode array (Quantum Dev

27 between standard-fluence PDT (light dose, 50 J/cm2; dose rate, 600 mW/cm2; wavelength, 689 nm PDT app

28 ese neurons in adult male and female C57BL/6 J mice undergoing a voluntary chronic intermittent ethan

29 C57Bl/6 J mice were fed chow or the GAN diet rich in saturated f

30 omuscular sections from adult female C57BL/6 J mice were incubated in normoglycemic (NG, 5 mM) or hyp

31 Male C57BL/6 J mice were randomly divided into three groups and gavag

32 precedented discharged energy density of 5.7 J cm(-3) far outperforming the best reported flexible di

33 of energy density (1000; 3000; 5000 and 7000 J g(-1)) compared to two pasteurization techniques (70 d

34 CYTO specimens were UV-sterilized (8 J/cm(2)) and monomer extracted in growth medium (1, 3 or

35 with an interfacial fatigue threshold of 800 J m(-2), because the fatigue-crack propagation at the in

36 e interleukin-15 (IL-15) superagonist N-803 (J.

37 erage high angle grain boundary energy (0.87 J/m(2)).

38 diating area: 5 cm(2), energy delivered: 896 J, time average intensity: 0.88 W/cm(2)).

39 A J-shaped relationship of body mass index (BMI) with seve

40 concentrations, this oxidized form adopts a J-elongated, flexible conformation, not circular or twis

41 h localized Stage II/III periodontitis and a J-shaped association was suggestive for BMI.

42 d the physical mode of interaction between a J-domain and an Hsp70, the structural and dynamic conseq

43 T antigen was previously shown to contain a J domain; however, this the first known example of the a

44 We developed a J-aggregate-based Forster-resonance energy-transfer (FRE

45 rikingly, Ubqln4 engages the J proteins in a J-domain-independent manner, in contrast to the previous

46 We observed a J-shaped association between alcohol intake and all-caus

47 of myocardial infarction (MI), reflecting a J- or U-shaped relationship.

48 All-cause mortality showed a J-shaped association with BMI, with the lowest mortality

49 vational analysis of our cohorts suggested a J-shaped association between DBP and MI.

50 We find that a J( pai) = 5/2(-) spin assignment is needed to explain th

51 @C(60) displays a doublet structure due to a J-coupling of magnitude 77.5 +/- 0.2 mHz at 340 K betwee

52 ong 6916 patients with COVID-19, there was a J-shaped association between BMI and risk for death, eve

53 Overall, BMI demonstrated a "J-Shaped" risk profile with elevated risks for overall g

54 e to tobacco carcinogens and inflammation, A/J mice were intranasally treated with the tobacco carcin

55 l-dC in genomic DNA isolated from lungs of A/J mice exposed whole-body to environmental cigarette smo

56 t and growth over time in the lungs of the A/J mice.

57 Vaccination studies in the A/J mouse model showed that the human vaccine protected ag

58 and complement B. anthracis Sterne in the A/J mouse model.

59 pathway controls a timely juvenile-to-adult (J/A) transition.

60 Jonckers et al. ( J.

61 nes, originally proposed by Murakami et al. (J.

62 atch-up vaccination campaigns (Grais et al., J.

63 Avian leukosis virus subgroup J (ALV-J) is an important concern for the poultry industry.

64 Replication of ALV-J depends on a functional cellular receptor, the chicken

65 Am J Obstet Gynecol.

66 s issue of the Journal, DeVilbiss et al. (Am J Epidemiol.

67 t issue of the Journal, DeVilbiss et al. (Am J Epidemiol.

68 his issue of the Journal, Baranyi et al. (Am J Epidemiol.

69 his issue of the Journal, Elbogen et al. (Am J Epidemiol.

70 The accompanying paper by Rudolph et al. (Am J Epidemiol.

71 DeVilbiss et al. (Am J Epidemiol.

72 r accompanying paper, Schildcrout et al. (Am J Epidemiol.

73 The article by Prentice et al. (Am J Epidemiol.

74 rent issue of the Journal, Torres et al. (Am J Epidemiol.

75 Masarwa et al. (Am J Epidemiol.

76 ctives on 3 findings of DeVilbiss et al. (Am J Epidemiol.

77 Blackburn (Am J Epidemiol.

78 As noted by Galea and Hernan (Am J Epidemiol.

79 ata analysis or systems science modeling (Am J Epidemiol.

80 Risch (Am J Epidemiol.

81 In the article by Chen and VanderWeele (Am J Epidemiol.

82 zed to 25 degrees C (V(cmax25 degrees C) and J(max25 degrees C) , respectively) were estimated based

83 reased the activation energy for V(cmax) and J(max) (E(aV) and E(aJ) , respectively) and the thermal

84 We found that only 73/183 (40%) V, D and J human genes were shared between the reference germline

85 in which reversible switching between H- and J-aggregates can be induced for multiple cycles simply b

86 irpins H(C) and H(D), the templates I'/I and J'/J, and the RNA polymerase (RNAp)/NTPs machinery.

87 ation parameters (i.e., V(cmax) , J(max) and J(max) :V(cmax) ratio) are sensitive to temperature and

88 Although reconstruction of V and J genes is a well-studied problem, the more challenging

89 investigate whether shared SHMs in the V and J segments of the BCR can be leveraged along with the ju

90 Here we identify apolipoprotein J (ApoJ) as a novel hepatokine targeting muscle glucose

91 roductivity and exp(H), while the asymptotic J(CO2) response on the silty clay arose from a net negat

92 specific cochaperones, in particular class B J-domain proteins and a heat shock protein 110 (Hsp110)-

93 (B6xA/J)F1 and (B6xNOD)F1 HER2 transgenic mice received Ad/E2T

94 show that acetylated histone H3 (AcH3), base J and a kinetochore factor co-localise in each chromosom

95 Upon binding a recombination centre-based J(H), RAG scans upstream chromatin via loop extrusion, p

96 Here we examine, using male C57BL6/J mice and patch-clamp electrophysiology, how chronic hi

97 Juglandaceae (Juglans regia, J. cathayensis, J. hindsii, J. microcarpa, J. nigra, J. sigillata and Pt

98 ment by day 42 in C57BL/6J and day 28 in CBA/J mice, respectively.

99 which comprised 11 distinct CDK groups (CDKA-J) with CDKB being the most widely distributed CDK prote

100 binding domain, similar to type II cellular J proteins.

101 lectron microscopy (cryo-EM) to characterize J-C bound to RIIbeta, the major PKA regulatory (R) subun

102 mical limitation parameters (i.e., V(cmax) , J(max) and J(max) :V(cmax) ratio) are sensitive to tempe

103 functions as a virally encoded cochaperone (J-protein/Hsp40) functioning together with its Hsc70 par

104 Consequently, J represents a spectroscopic observable that distnguishe

105 ows the magnetic exchange coupling constant, J(Gd-rad), for the gadolinium compounds in this series t

106 ere, we identify MCJ (Methylation-Controlled J protein) as a target for non-alcoholic steatohepatitis

107 tations with an effective exchange coupling (J(eff) ) of 2.5 meV, whereas trimers and longer peripent

108 ultaneous increase of short-circuit current (J(sc) ) and fill factor (FF), displaying the state-of-th

109 C)) but increases the short circuit current (J(SC)) and fill factor (FF) such that the resulting powe

110 ecombination center composed of RAG-bound (D)J gene segments.

111 V(D)J analysis shows clonally expanded T cells, indicating t

112 rearranged variable regions comprised of V(D)J gene segments miss a significant fraction (27-53% and

113 enes regulating B cell proliferation and V(D)J mutation (CARD11, TNFAIP3, CCND3, ID3, BTG2, and KLHL6

114 Antibody V(D)J mutations conferred pathogenicity by causing the antig

115 with B cell diversification such as the V(D)J rearrangement process.

116 mmon ancestor and share the same initial V(D)J rearrangement, but their B cell receptor (BCR) sequenc

117 stribution, ignoring the complexities of V(D)J rearrangement.

118 Replacement of V(D)J recombinase targets at two different mouse Vbeta gene

119 1 with a nucleolar marker, and increased V(D)J recombination activity.

120 G1 is a negative regulatory mechanism in V(D)J recombination and identify regions of the RAG1 N-termi

121 Degradation of RAD21 eliminated all V(D)J recombination and interactions associated with RAG sca

122 anisms that might contribute to aberrant V(D)J recombination and the development of lymphoid tumors.

123 V(D)J recombination assembles and diversifies Ig and T cell

124 Restricted V(D)J recombination during fetal development was postulated

125 , since the classical 12/23 rule for the V(D)J recombination fails to explain the V(DD)J recombinatio

126 The RAG endonuclease initiates Igh locus V(D)J recombination in progenitor (pro)-B cells(1).

127 V(D)J recombination is initiated by the recombination-activa

128 At most AgR loci, V(D)J recombination is regulated so that only one allele ass

129 , with subsequent feedback inhibition of V(D)J recombination on the other allele.

130 This process called V(D)J recombination that involves the RAG recombinase bindin

131 t are assembled in developing B cells by V(D)J recombination(1).

132 ires the participation of all V genes in V(D)J recombination(16), which depends on contraction of the

133 that, owing to junctional biases during V(D)J recombination, appear much more frequently than predic

134 RAG2, a late evolutionary addition in V(D)J recombination, appears to enforce the sharp kinks and

135 Nuclear processes, such as V(D)J recombination, are orchestrated by the three-dimension

136 n RAG1-RAG2 recombinase, which initiates V(D)J recombination, we find that the active site is reconfi

137 To identify mechanisms that regulate V(D)J recombination, we used proximity-dependent biotin iden

138 inconsequential variant of the canonical V(D)J recombination.

139 to facilitate or to impose a barrier to V(D)J recombination.

140 hypermutation levels and in features of V(D)J recombination.

141 ing how these dynamic mechanisms control V(D)J recombination.

142 al to quantitatively capture kinetics in V(D)J recombination.

143 formed a deep sequencing analysis of the V(D)J regions of VH and VLK genes, demonstrating the high ab

144 high-throughput assay that analyses both V(D)J segment usage and somatic hypermutation profiles, we e

145 R) loci by variable (diversity) joining (V[D]J) recombination.

146 ociation in the BKS.Cg-Dock7(m) +/+ Lepr(db)/J mouse model of obesity and diabetes, known to have abn

147 viruses had increased lethality in the DBA2/J mouse model.

148 The V(DD)J recombination is currently viewed as an aberrant and i

149 an genomes, thus demonstrating that the V(DD)J recombination is not a "bug" but an important feature

150 (D)J recombination fails to explain the V(DD)J recombination, the molecular mechanism of tandem D-D f

151 talline lipid bilayers using two-dimensional J-resolved NMR spectroscopy.

152 Dinnes J, Deeks JJ, Adriano A, et al.

153 Deeks JJ, Dinnes J, Takwoingi Y, et al.

154 A DP4/J-DP4/DP4+ tandem suggested 3 as the most likely structu

155 maintain constant applied electrical energy (J) or total charge flux (C/m(2)).

156 considered a defining feature of enhancers [J.

157 ted by the antioxidant N-acetylcysteine (Eur J Neurosci.

158 ly, we compare the triplet-triplet exchange (J) for tetracene dimers, bipentacene, a subunit of the b

159 Experimental J(HF) values were used to identify the two fluoroketone

160 typologies of public health care facilities [J.

161 , respectively) and the thermal optimum for J(max) .

162 ggregated, and the leader of the task force (J.D.S.) merged the material into a cohesive draft.

163 Single-dye-loaded nanoparticles form J-aggregates because of the high dye-loading (50 wt %),

164 CF(3)-substituted BODIPY, known for forming J-type aggregates, was also encapsulated as an H-dimer.

165 py, we investigated 10 papyri fragments from J.-F.

166 cally H(4) TPPS(2-) dissolved in water, from J- to an H-aggregation was induced by strong electrostat

167 n example of the acquisition of a functional J-like protein by a virus and suggests that HSV has take

168 -pseudopteroxazole, pseudopterosin A-F and G-J aglycones, and (+)-heritonin.

169 Thus, RSP geometry (J-shape versus C-shape), but not stiffness or height, af

170 P., Granadeiro J.

171 (Juglans regia, J. cathayensis, J. hindsii, J. microcarpa, J. nigra, J. sigillata and Pterocarya ste

172 However, J(max) :V(cmax) ratio decreased significantly with warmi

173 Illuminated J-V measurements under catalytic conditions show that th

174 ing the polar transformation method in Image J software (National Institutes of Health, Bethesda, MD)

175 ing plasma cells that express immunoglobulin J-which also accrue concurrently across diverse organs.

176 ) facet of beta-NiOOH previously examined in J.

177 ble contractions in several gene families in J. hindsii, including disease resistance-related wall-as

178 We found linear increases in J(CO2) on an alluvial sandy loam and a lowland clay soil

179 lid-state NMR (SSNMR) experiments, including J-resolved SiH coupling and quantitative (29)Si measurem

180 LIN-29 dose sensitivities of the individual J/A transition events help to ensure their temporal orde

181 r to yeast Pam18, TbPam27 requires an intact J-domain to function.

182 d state of strontium-73 must differ from its J (pai) = 1/2(-) mirror bromine-73.

183 ins H(C) and H(D), the templates I'/I and J'/J, and the RNA polymerase (RNAp)/NTPs machinery.

184 l were associated with an IGLJ3*02 junction (J) gene, confirming the high restriction of VJ region us

185 most 40 years ago when one of the authors (K.J.H.) published an organized system to quantify the accu

186 nal-binding protein for immunoglobulin kappa J region (RBPJkappa).

187 Timal RJ, Kooiman J, Sijpkens YWJ, et al.

188 Fernando, and Kristen J.

189 on from a single limiting factor, the linear J(CO2) response on the sandy loam was reinforced by posi

190 The value of ln J versus E(1/2) is linear for both PC and dark current,

191 ComponentsRECOMMENDED CITATION STYLE:Pozo, M.J., Albrectsen, B.R., Bejarano, E.R., de la Pena, E., He

192 Graham DY, Canaan Y, Maher J, et al.

193 a second linear-response (SLR) TDDFT method [J.

194 Michael J Fox Foundation for Parkinson's Research.

195 Disney and Michael J.

196 , J. cathayensis, J. hindsii, J. microcarpa, J. nigra, J. sigillata and Pterocarya stenoptera) produc

197 te, labelled by their total angular momentum J and parity pai.

198 ed with the effective total angular momentum J(eff) = 1/2 Mott state remains robust against Ru doping

199 we report on the measurement of (15)N-(15)N J-couplings of (15)N His37-labeled full length M2 (M2FL)

200 ile costly punishment (Helbing et al. in New J Phys 12:083005, 2010) presents one such method, the co

201 yensis, J. hindsii, J. microcarpa, J. nigra, J. sigillata and Pterocarya stenoptera) produced using B

202 of DBP, we found no evidence for a nonlinear J- or U-shaped relationship between DBP and adverse CVD

203 and mutated TrkB knock-in mice (Ntrk2tm1Ddg/J) with impaired BDNF signaling were chronically exposed

204 exchange activity of Sse1, and the action of J-proteins are all needed for Ubr1-mediated quality cont

205 , the structural and dynamic consequences of J-domain action once bound and how Hsp70s discriminate a

206 Exchange-split energy gaps of J and 3J separate a singlet from a triplet and a singlet

207 Measured relative intensities of J = 1-0 rotational transition lines yield vibrational-le

208 s for 1-Dy through 4-Dy and the magnitude of J(Gd-rad) for the corresponding gadolinium derivatives t

209 ether, our data points to a two-step mode of J-domain action, a recognition stage followed by a mecha

210 s taken advantage of the adaptable nature of J proteins to evolve a multifunctional cochaperone that

211 s taken advantage of the adaptable nature of J proteins to evolve a multifunctional cochaperone that

212 dependent and exhibit approximate overlap of J versus E response for d = 14-60 nm.

213 ups U4 and U5a, and an overrepresentation of J (30%) similar to the pre-Roman remains, also excavated

214 sity studies of Gujjars from Jammu region of J&K and Ladakhi population based on a battery of autosom

215 We identified the trajectory of J(CO2) responses and feedbacks from other resources, pla

216 While controlling for velocity, use of J-shaped versus C-shaped RSPs resulted in greater stance

217 entified CO(2) as the dominant limitation on J(CO2) on the clay soil.

218 es with unilateral TTAs are prescribed C- or J-shaped RSPs with a manufacturer-recommended stiffness

219 dependence of the loop-closure probability, J, to a statistical-mechanical theory of DNA looping pro

220 compared to an earlier reported procedure ( J.

221 quential addition of acetylene to propargyl (J.

222 In this context, Salicornia ramosissima J.

223 RBP-J represses, while NFATc1 activates miR182 expression th

224 Inhibition of miR182 by RBP-J servers as a critical mechanism that limits TNF-induce

225 y a novel regulatory network mediated by RBP-J/NFATc1-miR182 in TNF-induced osteoclastogenesis and in

226 This network includes negative regulator RBP-J and positive regulators, NFATc1 and miR182, of osteocl

227 study, we demonstrate that FCRL4 recognizes J chain-linked systemic IgA in the absence of heat aggre

228 outgroup within Juglandaceae (Juglans regia, J. cathayensis, J. hindsii, J. microcarpa, J. nigra, J.

229 the Max Cure Foundation, the Richard "Rick" J.

230 RNase J enzymes are metallohydrolases that are involved in RNA

231 ures of two Staphylococcus epidermidis RNase J paralogs, RNase J1 and RNase J2.

232 However, little is known of how RNase J paralogs differ in expression and activity.

233 ions suggest that multiple interacting RNase J paralogs could provide a strategy for functional impro

234 The catalytic activity of RNase J is regulated by multiple mechanisms which include olig

235 he American Heart Association and the Robert J.

236 he American Heart Association and the Robert J.

237 he American Heart Association and the Robert J.

238 ssociation, in collaboration with the Robert J.

239 ered about 890-920 MHz, the maximum Youden's J index is 81.5%.

240 Two masked reading center graders (N.S., J.S.) independently and blindly performed manual segment

241 Chiarito M, Sanz-Sanchez J, Cannata F, et al.

242 Non-significant J-shaped curves were found in sub-analyses of subjects w

243 by the non-orthologous euglenozoan-specific J-protein TbPam27.

244 ictors were trained using 19 tissue-specific J. regia transcriptomes aligned to the genomes.

245 associated with maternal fructose and SSB + J consumption at 6 postnatal months.

246 nificant after adjustment for maternal SSB + J intake (B = -0.05; 95% CI = -0.10, 0.00; P = 0.07), wh

247 .10, 0.00; P = 0.07), whereas maternal SSB + J intake was significant in the same model (B = -0.29; 9

248 g fructose, and 2.5 +/- 2.6 servings SSBs + J, and reported 6.9 +/- 2.1 breastfeedings per day at 1

249 mN/tex, or sigma(f) ~ 22 MPa) and stiffest (J = 300 mN/tex, or E ~ 320 MPa) self-healing polymers ab

250 st genome, X174, requires the more stringent J protein packaging guide.

251 Avian leukosis virus subgroup J (ALV-J) is an important concern for the poultry indust

252 omain and STI1 motif (1-2) of Ubqln4 support J protein binding, essential for SV40 infection.

253 Numerical simulations of a two-band t-J model reveal that the THz oscillations originate from

254 ynchronously around the Triassic-Jurassic (T-J) boundary (201 Ma).

255 the carbon cycle perturbations around the T-J boundary.

256 indicated that ICP22 contains an N-terminal J domain and a C-terminal substrate binding domain, simi

257 e.g., Black and Tan BRachyury T(+)Itpr3(tf)/J (BTBR) mice, we revealed that increased excitability o

258 The J-coupling increases in magnitude with increasing temper

259 The J-domain also alters several biochemical properties of t

260 ates to an equilibrium quantity known as the J factor that is widely used to characterize DNA bending

261 action of the Hsc70 "uncoating ATPase." The J- and PTEN-like domain-containing proteins, auxilin 1 (

262 se-associated motor (PAM) which contains the J-protein Pam18.

263 Strikingly, Ubqln4 engages the J proteins in a J-domain-independent manner, in contrast

264 y updated with an anonymized patient ID, the J-CKD-DB will be a dynamic registry of Japanese CKD pati

265 As the genome size increases, the J protein's length and charge decreases.

266 strychnine as a proof of concept, makes the J-based CASE-3D analysis a viable option for the applica

267 indicate that the invariant aspartate of the J-domain perturbs a conserved intramolecular Hsp70 netwo

268 etween warming and rainfall reduction on the J(max25 degrees C) to V(cmax25 degrees C) ratio were not

269 is experiments revealed that in solution the J-form interacts with negatively charged liposomes and w

270 rdized exchangeable information storage, the J-CKD-DB succeeded to efficiently collect clinical data

271 While strong evidence indicates that the J-form is the structure bound to aPLs, which conformatio

272 ere remarkably insensitive in terms of their J(max25 degrees C) and V(cmax25 degrees C) when grown at

273 Using this J-aggregate-based FRET method, dye-core-polymer-shell na

274 o-B cell lines(9), which undergo robust D-to-J(H) but little V(H)-to-DJ(H) rearrangements, presumably

275 pt for reecombination centre-located DQ52-to-J(H) joining, in which synapsis occurs by diffusion(2).

276 oxylation (V(cmax) ) and electron-transport (J(max) ) capacities with increasing elevation were predi

277 lation, V(cmax) , and of electron transport, J(max) ) was reduced in warm-grown seedlings, correlatin

278 regulated by a heterodimeric complex of two J-domain proteins (JDPs), Pam18 and Pam16.

279 (11)C-UCB-J ((R)-1-((3-((11)C-methyl-(11)C)pyridin-4-yl)methyl)-4-

280 onal V (T) was slightly higher for (11)C-UCB-J, but BP (ND) was higher for (18)F-SynVesT-1, though th

281 For (11)C-UCB-J, COD yielded 3.7% +/- 5.2% differences in V (T) compar

282 f (18)F-SynVesT-1 and compare with (11)C-UCB-J.

283 of the clinically used compounds [(11)C]UCB-J and [(11)C]PHNO.

284 , CUDs showed significantly lower [(11)C]UCB-J BP(ND) in the hippocampus (~10%, p = 0.008, effect siz

285 d structural brain measures using [(11)C]UCB-J positron emission tomography in 18 patients with schiz

286 [(11)C]UCB-J V(T) was significantly lower in the frontal and anteri

287 ron emission tomography (PET) and [(11)C]UCB-J, a radioligand for the synaptic vesicle glycoprotein 2

288 awley rats using western blotting, [(3)H]UCB-J autoradiography and immunostaining with confocal micro

289 cer, an (18)F-labeled difluoro-analog of UCB-J ((18)F-SynVesT-1, also known as (18)F-SDM-8), which di

290 Presently, with the upcoming J-EPoCH high repetition rate laser at Osaka University,

291 ncluding GmCCA1a, which directly upregulates J/GmELF3a to modulate flowering time.

292 , 274-275 (1967)] and GRA 95205, a ureilite [J.

293 max) was 3.8-10.7% faster when athletes used J-shaped versus C-shaped RSP models (p < 0.05), but was

294 nce average vGRFs were less asymmetric using J-shaped versus C-shaped RSPs (p < 0.05).

295 The V-J reverted germline configuration of ZIKV-116 preferenti

296 Evans NR, Wall J, To B, et al.

297 s generated by replacing the indigenous X174 J gene with that of G4.

298 n the level of plaque formation without X174 J gene complementation.

299 termined by using the DeLong test and Youden J statistic, respectively.

300 Zhu J, Yu X, Zheng Y, et al.