ライフサイエンスコーパス: type A

1 is uncommon for conventional photocatalysis (type A).

2 eritoneal administration of Rhesus rotavirus type A.

3 er the implicated pruno yielded C. botulinum type A.

4 type B, but this region was absent from PhV1 type A.

5 rmed the presence of Clostridium perfringens type A.

6 d by about 2 and 8 K when compared with wild-type A(1)-receptor and A(1)R-Y288A(7.53) (a folding-defi

7 -G279S(7.44) (73 +/- 23 kJ/mol) than in wild-type A(1)R (135 +/- 4 kJ/mol) or in A(1)R-Y288A(7.53) (1

8 lexes formed between D(1)-receptors and wild-type A(1)R or A(1)R-G279S(7.44) by coimmunoprecipitation

9 -G279S(7.44) than in those coexpressing wild-type A(1)R.

10 moting guanine nucleotide exchange than wild-type A(1)R.

11 94), followed by type C (22% [21 of 94]) and type A (20% [19 of 94]).

12 Forty-nine percent corresponded to type A, 26% corresponded to type C, and 18.3% correspond

13 Molecular dynamics simulations of the wild-type A(3)R in complex with both agonists, combined with

14 D independently of sentinel dissection type (type A: 4.3 cm [3.5-5.6 cm] versus 3.3 cm [2.9-3.7 cm],

15 Toxin type A accounted for half of outbreaks, and these outbre

16 features of the defibrillators, although the type A and B defibrillators accounted for a significantl

17 Since type A and B subspecies are closely related, we hypothes

18 Three pairs of NGLs based on the blood group type A and B trisaccharides, with three different lipid

19 ously, we profiled the antibody responses in type A and B tularemia cases in the United States using

20 tar is at the dividing line between stars of type A and B, and we measure the dayside temperature of

21 ts, including the two master variants of DWV-type A and B-was used.

22 ness against type B was greater than against type A and greater than the IIV3 effectiveness against t

23 rst effective therapy for patients with MoCD type A and has a favourable safety profile.

24 otensin type 1 receptor (AT1R), endothelin-1 type A and natural polyreactive Abs-did not increase sig

25 Four patients had type A and nine had type B dissection.

26 genotypes of a novel virus, designated PhV1 type A and PhV1 type B.

27 heir thymic precursors (IELps) include PD-1+ type A and Tbet+ type B populations, which differ in the

28 rties of CBM_E1 are at the interface between type A and type B CBMs.

29 In young mice, both type A and type B IELps had an S1PR1+ and alpha4beta7+ e

30 was started in neonates diagnosed with MoCD (type A and type B) following a standardised protocol.

31 t an unprecedented 'double K-turn' module in type A and type M archaeal RPR variants.

32 evolution or introduction of high-titre RSV type-A and B infections that seeded HiT clades in the su

33 RSV type-A and B infections were most closely related to RSV

34 is genetic element into strain G27 (hpEurope/type-A and cagPAI type-A) was sufficient to generate the

35 to two different H. pylori types, termed pre-type-A and pre-type-B, which consequently evolved to cag

36 type-B, which consequently evolved to cagPAI type-A and type-B, respectively; importantly, all multi-

37 s divided hpEurope into two groups: hpEurope/type-A and type-B.

38 We also characterized two types (A and B) of muscarinic acetylcholine receptors (m

39 rapidly and severely than illness caused by types A and B botulinum neurotoxin.

40 F. tularensis Types A and B form poor biofilms, but F. tularensis muta

41 enzyme, acid sphingomyelinase, required for types A and B Niemann-Pick disease.

42 ed more than 2,000 confirmations for each of types A and B over the study period.

43 and have been linked to Niemann-Pick disease types A and B.

44 was increased for type AB and decreased for types A and B.

45 dwarfed by, seasonal epidemics of influenza types A and B.

46 y promote biofilm formation by F. tularensis Types A and B.

47 Budding yeast cells exist in two mating types, a and alpha, which use peptide pheromones to comm

48 The sample titres between RSV types-A and B were not significantly different.

49 , Ciona robusta (formerly Ciona intestinalis type A) and C. intestinalis (formerly Ciona intestinalis

50 tularensis: F. tularensis subsp. tularensis (type A) and F. tularensis subsp. holarctica (type B).

51 Nine patients had acute, 2 had chronic type A, and 3 had chronic type B aortic dissections befo

52 se, which is mutated in Niemann Pick disease type A, and beta galactosidase-1, which is mutated in GM

53 onic anhydrase, Sushi, Von Willebrand factor type A, and chitin binding, were identified from all the

54 , serotonin type 3, gamma-amminobutyric acid type A, and glycine receptors are major players of human

55 ydrolase 109 (GH109) that is active on blood type A-antigen, along with a new subfamily of glycoside

56 gnosis is urgently needed for acute Stanford type A aortic dissection (AAAD) patients due to its high

57 en, diagnostic tools and management of acute type A aortic dissection (ATAAD) have undergone substant

58 s an association between admission for acute type A aortic dissection (ATAAD) to the University of Mi

59 dicare beneficiaries diagnosed with an acute type A aortic dissection between 1999 and 2014 who (1) w

60 egionalizing the surgical treatment of acute type A aortic dissection in the United States.

61 dissection is close to the remaining risk of type A aortic dissection in this population, which under

62 nched endograft during follow-up after acute type A aortic dissection open repair.

63 The classification proposed that type A aortic dissection should be surgically repaired i

64 tic root diameter prior to or at the time of type A aortic dissection tended to be smaller in patient

65 99 and 2014, 40.5% of patients with an acute type A aortic dissection were transferred, and 51.9% rec

66 substantially reduced in patients with acute type A aortic dissection who were rerouted to high-volum

67 ed forty-one patients (13%) had AAS: 125 had type A aortic dissection, 53 had type B aortic dissectio

68 phylactic aortic root surgery, 5 experienced type A aortic dissection, and 12 died (noncardiovascular

69 sely affects outcomes in patients with acute type A aortic dissection, but reliable quantitative data

70 ied from cardiogenic shock on day 50 after a type A aortic dissection, not related to treatment.

71 ying surgery to transfer patients with acute type A aortic dissection-a catastrophic disease that req

72 Acute type A aortic dissections are often treated with prosthe

73 Three type A aortic dissections occurred in this population du

74 zing care at high-volume hospitals for acute type A aortic dissections will lower mortality.

75 pt abundance of a clade of the CK-responsive type-A Arabidopsis response regulator (ARR) genes increa

76 t as selective autophagy receptors to target type-A ARR cargos for autophagic degradation, demonstrat

77 Type-A ARR proteins were degraded by autophagy in an AUT

78 autophagic vesicles, have elevated levels of type-A ARR proteins, and are hyposensitive to cytokinin.

79 EXO70D family members interacted with type-A ARR proteins, likely in a phosphorylation-depende

80 sensitivity through autophagic regulation of type-A ARR proteins.

81 The Arabidopsis type-A response regulators (type-A ARR) are negative regulators of cytokinin signali

82 Disruption of both type-A ARRs and EXO70D1,2,3 compromised survival in carb

83 3 mutants exhibited compromised targeting of type-A ARRs to autophagic vesicles, have elevated levels

84 of cytokinin-regulated genes, including the type-A ARRs, although it does not impair the cytokinin i

85 es not impair the cytokinin induction of the type-A ARRs.

86 rved aspartate in the receiver domain of the type-A ARRs.

87 open surgical repair is optimal for treating type A (ascending aorta) AAS, whereas thoracic endovascu

88 d clustering analysis identified 3 molecular types (A, B, and C) that reliably predicted recurrence.

89 ite detection of botulinum neurotoxin (BoNT) types A, B, and E in complex matrixes, which is innovati

90 Toxin types A, B, E, and F were identified as the causative ag

91 Of the four main blood types, A, B, AB, and O, only O can be given to any patie

92 inally, an oxyR mutant is less fit than wild-type A. baumannii during infection of the murine lung.

93 drogen peroxide (H(2)O(2)) killing than wild-type A. baumannii However, mumR, which encodes the trans

94 ection of minute amounts of BoNTs, primarily type A (BoNT-A), has useful long-lasting muscle relaxati

95 combinant derivative of Botulinum neurotoxin Type A (BoNT/A).

96 ns (considered a single transcriptional cell type), a broad mean FR distribution is achieved through

97 We propose that transmission of DWV type A by Varroa mites occurs in a non-propagative manne

98 ion of two previously unidentified structure types: a C2-symmetric M(II)4L6 assembly with meridionall

99 -2,3 linkage in H1 subtype viruses; the wild-type A/California/07/2009 isolate, like most circulating

100 Modular cellulases contain non-catalytic type A carbohydrate-binding modules (CBMs) that specific

101 Although type A CBMs play a critical role in cellulose recycling,

102 with an N-terminal GFP domain, revealed that type A CBMs possess the ability to recognize different c

103 e ligand interacting platform illustrate how type A CBMs target their appended plant cell wall-degrad

104 th the beta-strands, is a typical feature of type A CBMs, although the expected affinity for bacteria

105 Recombinantly produced wild-type A-chain and mutant B-chains were combined efficient

106 available experimental LLPS data on the wild-type, a charge-scrambled, a phenylalanine-to-alanine (Ft

107 assimilation capacity of canopies with wild type, a Chl-deficient mutant (Y11y11), and 67 other muta

108 therapeutic effects that depended on muscle type, a combination of neurotrophic factors may optimall

109 biased transcriptional profiling of all cell types, a complementary method to isolate and sequence sp

110 and resiliency of fibroblasts make this cell type a conventional tool for basic research.

111 Eight patients with type A disease rapidly improved under treatment and conv

112 By typing a disease term of interest, the user can identify

113 ic root diameter was <50 mm, risk for proven type A dissection (0.4 events/1,000 patient-years) and r

114 lications, in-hospital mortality, retrograde type A dissection and follow-up mortality appeared lower

115 Depending on seizure type, a diverse range of therapies are available, includ

116 hat VWF interacts with C3b through its three type A domains and initiates AP activation, although ass

117 Two varieties of dsRBD exist: canonical Type A dsRBDs interact with dsRNA, while non-canonical T

118 h increased glomerular endothelin-1 receptor type A (Ednra) expression and increased circulating endo

119 The endothelin receptor type A (EDNRA) signaling pathway is essential for the es

120 ry-mesh electrode arrangement was applied in Type A electrospray system, and for Type B, an additiona

121 Diffuse midline gliomas and posterior fossa type A ependymomas contain the recurrent histone H3 lysi

122 tein-coupled receptors - endothelin receptor type A (ET(A)) and endothelin receptor type B (ET(B)) -

123 s attenuated by blocking endothelin receptor type A (ETAR) and/or endothelin receptor type B (ETBR).

124 s are usually insignificant when compared to type A (experimental) uncertainties.

125 ability during intracellular infections with type A F. tularensis.

126 lethal in IL-6 (-/-) mice than it is in wild-type, a finding associated with diminished neutrophil re

127 e noncovalent interactions between component types, a finding that may aid the rational design of fun

128 ays from the original CNV: 1) progression to type A, followed by RPE erosion and subretinal hyperrefl

129 Sporulation is critical for C. perfringens type A food poisoning since spores contribute to transmi

130 ion in SM101, a derivative of C. perfringens type A food-poisoning strain NCTC8798.

131 NLS residues were mutated to alanine using a type A full-genome cDNA clone, and the virus progeny was

132 Hyperpolarizing inhibition mediated by type A GABA (GABAA) receptors is dependent on chloride e

133 GluA1 synaptic levels after 48 h blockade of type A GABA receptor (GABAA R)-mediated inhibition with

134 wards motoneurons and is required to recruit type A GABA receptors (GABA(A)Rs) at inhibitory neuromus

135 is primarily mediated by chloride-permeable Type A GABA receptors.

136 We identified type-A GABA receptors (GABA(A)Rs) in inhibitory synapses

137 BRB2, coding for the gamma-aminobutyric acid type A (GABA(A) ) receptor subunit beta2.

138 Similar to the widely used GABA receptor type A (GABA(A)) antagonist picrotoxinin, TETS has been

139 Gabazine, a gamma-aminobutyric acid type A (GABA(A)) receptor antagonist, has previously bee

140 ent responses of the gamma-aminobutyric acid type A (GABA(A)) receptor.

141 units comprising the gamma-aminobutyric acid type A (GABA(A)) receptor.

142 sitive modulation of gamma-aminobutyric acid type A (GABA(A)) receptors to dampen neuronal activity i

143 ovo mutations in the gamma-aminobutyric acid type A (GABAA ) receptor beta3 subunit gene GABRB3 and o

144 between the EC50 for activation of the GABA type A (GABAA) receptor by the transmitter GABA and basa

145 While gamma amino-butyric acid Type A (GABAA) receptors are the primary molecular targe

146 tasis maintenance of gamma-aminobutyric acid type A (GABAA) receptors dictates their function in cont

147 r affinity for brain gamma-aminobutyric acid type A (GABAA) receptors.

148 Type A gamma-aminobutyric acid (GABA(A)) receptors are p

149 erpolarizing synaptic inhibition mediated by type A gamma-aminobutyric acid (GABAA) receptors, which

150 Type-A gamma-aminobutyric (GABA(A)) receptors are ligand

151 rase gene designated csaA (capsule synthesis type a gene A).

152 In addition, in the absence of filamin, type-A glutamate receptor subunits are lacking at the po

153 Compared to wild-type, a growth-defective yeast PCNA mutant (DD41,42AA) s

154 A validated human infection model with wild-type A(H1N1)pdm09 was reported previously.

155 inclusion in the annual influenza vaccine: a type A:H1N1 virus, a type A:H3N2 virus, and one or two t

156 al influenza vaccine: a type A:H1N1 virus, a type A:H3N2 virus, and one or two type B viruses.

157 al descent, such as in the case of influenza type A hemagglutinin.

158 tion that recapitulates critical features of type A hepatitis in humans.

159 f 2 cases of invasive Haemophilus influenzae type a (Hia) disease in Italy.

160 were classified according to OCT patterns as type A (high reflectivity with optical shadowing), type

161 in (15) N-amino acid-fed mutants versus wild-type, a higher percentage of (15) N remained in roots in

162 This increase was more prominent in type A ICs than in type B ICs.

163 tent phenotype, while this was restricted to type A IELps in adults.

164 d fibrosis on spectral-domain OCT slices, as type A if located underneath the RPE, as type B if locat

165 The QAV was type A in 32% and type B in 32% (Hurwitz and Roberts cla

166 can be understood as follows: for species of type A, in environments of type B, nonadaptive radiation

167 gyrophilic grain disease); FTLD-TDP (55 nine type A including one with motor neuron disease, 27 type

168 structure-sequence conservation analysis for type A influenza.

169 testes, p53R172H was expressed in gonocytes, type A, Int, B spermatogonia as well as in pre-Sertoli c

170 H(+) secretion in type A intercalated cells (A-ICs) is regulated by apical

171 secretion is mediated by highly specialized type A intercalated cells (A-ICs), which contain vacuola

172 polysaccharidosis IIIA or Sanfilippo disease type A is a progressive neurodegenerative disorder prese

173 Type A is usually caused by recessive pathogenic variant

174 A 78-year-old, personality type A, lady with a history of pseudo-exfoliative glauco

175 Type A lesions were higher in attenuation than the thyro

176 y injecting adenoviruses expressing CaM-wild type, a loss-of-function CaM mutation, CaM (1-4), and a

177 agnostic product ions (M) resulted mainly in type A (M - DMA) and B fragment ions (M - HO-B(N(CH3)2)2

178 scence, infected cell types included CD68(+) type A (macrophage-like) synoviocytes and CD44(+) type B

179 Surprisingly, in all three cell types, a majority of Gag peptides derived from p15 rathe

180 mical probes useful to selectively report on type-A MCPs activity in complex media.

181 we further identified the scavenger receptor type A member I (SR-AI) to be a macrophage-specific rece

182 eroxidase is, by sequence analysis, a hybrid type A member of class I heme peroxidases [TcAPx-cytochr

183 contrast agent solution (perflutren protein-type A microspheres) was injected via the nephrostomy tu

184 BMs representative of the known diversity of type A modules.

185 mphoma (DLBCL) of the activated B-cell (ABC) type, a molecular subtype characterized by adverse outco

186 Depending on the reaction type, a molybdenum-based monoaryloxide pyrrolide or chlo

187 ferentiated culture consists of various cell types, a mucociliary clearance system, and tight junctio

188 e olfactory learning in adult flies requires type A muscarinic acetylcholine receptors (mAChR-A), par

189 ctrum to adults, including a shift away from type A mutations and toward longer N-regions, consistent

190 Type A neurons increased their discharge rates across co

191 is type IV (ML4) (TRPML1-F408), Niemann-Pick type A (NPA) and Fabry disease.

192 microglia activation in Niemann-Pick disease type A (NPA).

193 ed three specific genes [natriuretic peptide type A (Nppa), sarcolipin (Sln), and myosin light polype

194 tural determinants governing selectivity for type-A of the M14A MCP family.

195 albumin) now follow, with no broad bands for type A or B species that dominated at 1 atm.

196 iciently and made a more robust biofilm than Type A or B strains, but loss of O-antigen or capsule-li

197 Only patients with type A or O blood were included in the primary analysis,

198 imary analysis included 20,858 patients with type A or O blood.

199 athogen modifies its flagellin with either a type A or type B O-linked glycosylation system, which ha

200 urned to almost normal concentrations in all type A patients within 2 days, and remained normal for u

201 Furthermore, compared with the wild type, a permanently negative phototactic mutant required

202 Posterior fossa type A (PFA) ependymoma is a lethal pediatric brain tumo

203 Posterior fossa type A (PFA) ependymomas exhibit very low H3K27 methylat

204 porcine alveolar macrophages (PAMs) and wild-type A. pleuropneumoniae (5b WT) or an Adh-deletion stra

205 nol substrates has been developed to produce type A polycyclic polyprenylated acylphloroglucinol (PPA

206 the enantioselective total syntheses of the type A PPAPs (-)-nemorosone and (-)-6-epi-garcimultiflor

207 ontaining Ephs and ephrins by different cell types, a process requiring endosomal sorting complex req

208 Clinical distinction of type A (progressive myoclonus epilepsy) and type B (deme

209 on retinal densitometry to distinguish cone types, a prohibitively slow process.

210 xtrasynaptic alpha-5 gamma-aminobutyric acid type A receptor (alpha5-GABAAR) regulates neuronal excit

211 es reported a central role of the endothelin type A receptor (ETAR) in tumor progression leading to t

212 tensin type 1 receptor (AT1R) and endothelin type A receptor (ETAR) is associated with allograft reje

213 acious modulators of gamma-aminobutyric acid type A receptor (GABA(A)) receptor function.

214 for the slow type of gamma-aminobutyric acid type A receptor (GABA(A)R) could have potent anesthetic

215 ive allosteric modulators (PAMs) of the GABA-type A receptor (GABA(A)R).

216 The gamma-aminobutyric acid type A receptor (GABAA-R) is a major inhibitory neurorec

217 show reduced surface gamma-aminobutyric acid type A receptor (GABAAR) levels and impaired GABAAR-medi

218 Two predominant genes, ephrin type A receptor 6 (EPHA6) and folliculin (FLCN), with mu

219 uncta and dendritic spine formation via GABA type A receptor activation and voltage-gated calcium cha

220 ts developed anti-AT1R and/or antiendothelin type A receptor antibodies (non-HLAabs group), 9 did not

221 or antibodies (anti-AT1R) and antiendothelin type A receptor antibodies associated with the clinical

222 of the alpha(2)beta(3)gamma(2) GABA receptor type A receptor at the so-called T6' ring, wherein five

223 sin II type-1 receptor and anti-endothelin-1 type A receptor autoantibodies are associated with an in

224 iotensin II type-1 receptor and endothelin-1 type A receptor autoantibodies pre-LT, and year 1 post-L

225 5 subunit-containing gamma-aminobutyric acid type A receptor function improve cognitive performance.

226 and impaired spinal gamma-aminobutyric acid type A receptor function, indicative of spinal inhibitor

227 tivation and modulation of the human 5-HT(3) type A receptor has been based only on macroscopic curre

228 sists despite either gamma-aminobutyric acid type A receptor or N-methyl-D-aspartate receptor inhibit

229 A5, GABRG3, encoding gamma-aminobutyric acid type A receptor subunits (beta3, alpha5, gamma3).

230 ntly increased by blockade of the endothelin type A receptor with ABT-627 (0.116 +/- 0.006 mM vs. 0.1

231 injection treatments that inhibited the Edn type a receptor, Edn type b receptor, angiotensin type 1

232 , angiotensin-II type 1 receptor, endothelin type A receptor, lamin B1, BPI fold-containing family B

233 ted protein 1 light chain 3 alpha (LC3)/GABA type A receptor-associated protein (GABARAP) comprises a

234 activating kinases 1/2 (ULK1/ULK2), and GABA type A receptor-associated proteins (GABARAPs), but inte

235 Here, we demonstrate that the ephrin type-A receptor 2 (EphA2) is an oral epithelial cell PRR

236 The receptor tyrosine kinase ephrin type-A receptor 2 (EphA2) was identified as a SOCS2-inte

237 unctional siRNA screen, we identified Ephrin type-A receptor 2 (EPHA2), an oncogenic cell-surface rec

238 esis and DNA repair including, EPHA2 (ephrin type-A receptor 2), FHL2 (four and a half LIM domains pr

239 s or function of the tyrosine kinase, ephrin type-A receptor 4 (EphA4), has been suggested as a poten

240 Alpha-5 gamma-aminobutyric acid type A receptors (alpha5-GABAARs) are located extrasynap

241 ective modulation of gamma-aminobutyric acid type A receptors (GABA(A)R) is considered to exert fewer

242 and pharmacology of gamma-aminobutyric acid type A receptors (GABA(A)Rs) are of great physiological

243 GABA type A receptors (GABA(A)Rs) mediate fast synaptic inhib

244 e main modulators of gamma-aminobutyric acid type A receptors (GABA(A)Rs), which are the ligand-gated

245 ffects being mediated by the ionotropic GABA type A receptors (GABA(A)Rs).

246 ceptors (nAChRs) and gamma-aminobutyric acid type A receptors (GABAARs) are members of the pentameric

247 The gamma2 subunit of GABA type A receptors (GABAARs) is thought to be subject to p

248 Extrasynaptic gamma-aminobutyric acid type A receptors (GABAARs),which contribute generalized

249 5 subunit-containing gamma-aminobutyric acid type A receptors are novel targets for pharmacologic tre

250 tein Gephyrin and of gamma-aminobutyric acid type A receptors at inhibitory neuronal synapses is crit

251 5 subunit-containing gamma-aminobutyric acid type A receptors attenuated cognitive deficits after tra

252 5 subunit-containing gamma-aminobutyric acid type A receptors attenuated deficits in long-term potent

253 5 subunit-containing gamma-aminobutyric acid type A receptors would improve cognitive performance aft

254 reversed following blockade of GABAARs (GABA Type A receptors), but not GABABRs (GABA Type B receptor

255 5 subunit-containing gamma-aminobutyric acid type A receptors, 30 minutes before undergoing behaviora

256 oral, positive allosteric modulator of GABA type A receptors, is effective and safe for the treatmen

257 5 subunit-containing gamma-aminobutyric acid type A receptors.

258 In any given cell type a relatively few active L1 loci contribute to the '

259 In order to study this tumor type, a reliable model system exhibiting the molecular f

260 The Arabidopsis type-A response regulators (type-A ARR) are negative reg

261 For detection of HPV types, a Roche Linear Array test was performed.

262 ordingly, Deltacpa and DeltapfoA mutants, in type A (S13) or type C (CN3685) backgrounds, were unable

263 For wild type, a sensitive stomatal response to increasing VPD wa

264 For each cancer type, a set of "known" target genes was obtained and equ

265 of BT3686 showed that the enzyme displayed a type A seven-bladed beta-propeller fold.

266 ting the notion that gamma-aminobutyric acid type A signaling can also initiate ictogenesis.

267 lation, we demonstrate that undifferentiated type A spermatogonia are the cells that activate NOTCH s

268 We conclude that antigens from the type A strain Schu S4 are suitable for detection of anti

269 of 1,741 different proteins derived from the type A strain Schu S4.

270 nt Francisella tularensis subsp. tularensis (type A) strain Schu S4 in hypervesiculating E. coli cell

271 Despite there being no type A strains in Spain, we confirmed the responses agai

272 C. perfringens type A strains producing C. perfringens enterotoxin (CPE

273 is mostly conserved between influenza virus type A strains.

274 These results define universal for type A structured regions that could be important for vi

275 h3-null mutant plants were crossed with wild-type A. thaliana.

276 ntified two main types of pulmonary LFs: (1) type A, the predominant type in GOLD stages I-II COPD an

277 aling receptor, natriuretic peptide receptor type A, to the clearance receptor, nprc, was increased a

278 sure of haploid yeast cells, carrying mating type "a," to "alpha pheromone" stimulates polarized grow

279 Across 17 cancer types, a total of 648 significant diagnoses correlated d

280 monitors to fuel divergence from two reactor types: a traditional light-water reactor and an advanced

281 t lacks the keto group at C-8 and hence is a type A trichothecene.

282 Using two representative sample types, a triglyceride mixture and dissolved organic matt

283 ABSTRACT: The type A trimeric intracellular cation channel (TRIC-A) is

284 Compared with Type A, Type B system has smaller droplet size and veloc

285 The recurrent type A, type D, and type B mutations require 1, 2, and 3

286 three different enterotypes, referred as "P-type", "A-type "and "F-type" which were highly abundant

287 n this study, we exposed Varroa mites to DWV type A via feeding on artificially infected honey bees.

288 e innate immunity defense, removes influenza type A virus (IAV) through interaction with hemagglutini

289 natal and adult mice infected with influenza type A virus.

290 ariable overall contributions from influenza type A viruses across seasons, but relatively stable con

291 e demonstrate that the von Willebrand factor type A (VWA) domain within the cleaved CLCA1 N-terminal

292 Forkhead-associated (FHA) and von Willebrand type A (vWA) domains are involved in several phosphoryla

293 consists primarily of von Willebrand factor type A (VWA) domains, protein-protein interaction module

294 main together with its von Willebrand domain type A (VWA).

295 into strain G27 (hpEurope/type-A and cagPAI type-A) was sufficient to generate the multi-cagA genoty

296 (German Registry for Acute Aortic Dissection Type A) who underwent surgery between 2006 and 2010, of

297 pe C FGL (17/47 eyes); and 3) persistence of type A with development of a flat, fibroatrophic lesion

298 in Type B system is more stable than that in Type A with its smaller root mean square velocity.

299 ced metal-organic framework materials of the type A(x)Fe(2)(bdp)(3) (A = Na(+), K(+); bdp(2-) = 1,4-b

300 tra where all possible backbone fragment ion types (a/x, b/y, and c/z) are typically observed.