ライフサイエンスコーパス: subclass

1 tested with high efficiency to targeted IgH subclass.

2 nation (CSR) of the IgH chain to the desired subclass.

3 IgG2 was the predominant anti-PEG IgG subclass.

4 e different pathogenicities according to IgG subclass.

5 ystemic candidiasis is influenced by its IgG subclass.

6 of endogenous IgG, especially from the IgG2 subclass.

7 erization of the isomeric lipids within each subclass.

8 IIIA due to afucosylated Fc glycans and IgG1 subclass.

9 a functional measure of ADCC as well as IgG subclasses.

10 dissecting the differences among human tumor subclasses.

11 composition changed with age across all IgG subclasses.

12 scular and respiratory diseases, including 7 subclasses.

13 to both human and M. mulatta IgG of varying subclasses.

14 response to treatment in different nephritis subclasses.

15 n of the connectivity patterns of inhibitory subclasses.

16 ain one member each of the PBC and MEIS/PREP subclasses.

17 t function at ion channels of distinct NMDAR subclasses.

18 ies with identical specificity but different subclasses.

19 defining therapeutically homogeneous patient subclasses.

20 are greater than observed for comparable IgG subclasses.

21 mmunoglobulin G1 and G4 were the predominant subclasses.

22 peline to classify HRGPs into 23 descriptive subclasses.

23 promoter and enhancer transcription response subclasses.

24 rmacokinetic properties of the corresponding subclasses.

25 , belong to different transcription response subclasses.

26 ent for individual fatty acids or fatty acid subclasses.

27 ion (ESI) efficiencies across the various PL subclasses.

28 ls carrying New Delhi metallo-beta-lactamase subclass 1 (NDM-1) can be monitored in real time by NMR

29 frequency of ESRD at 10 years increased from subclass 1A (2.4%) to 1E (66.9%) in the Mayo cohort and

30 periodontal condition, immunoglobulin (Ig)G subclasses against Porphyromonas gingivalis in individua

31 he ventral nerve cord can be subdivided into subclasses along the anterior-posterior (A-P) axis based

32 cium-dependent protein kinase C conventional subclass alpha/beta leading to reduced phosphorylation o

33 Allenes constitute an important subclass among these.

34 The distribution of iDSA IgG1-4 subclasses among the population was 75.2%, 44.0%, 28.0%,

35 type 2 diabetes in youths by antidepressant subclass and according to duration of use, cumulative do

36 theirreversible genomic selection of isotype/subclass and alterations in glycosylation.

37 cule; IgG4 was the most predominant antibody subclass and antibodies to rLinB-13 did not cross react

38 associations between antibody features (IgG subclass and antigen specificity) and effector function

39 at these time points, immunoglobulin G (IgG) subclass and C1q binding activity for donor-specific ant

40 murine backbones as either an IgG1 or IgG2a subclass and evaluated for binding to multiple F protein

41 ation, which, in turn, are determined by IgG subclass and Fc glycan composition within ICs.

42 ed regulation of anti-hemagglutinin (HA) IgG subclass and Fc glycans, with abundance of sialylated Fc

43 ition of hinge epitopes was dependent on IgG subclass and protease used to create the F(ab')2 targets

44 n the amino acid sequence of the various IgG subclasses and by the composition of the complex, Fc-ass

45 much faster rate than V region-identical IgG subclasses and IgA, consistent with an altered paratope.

46 e sera were analyzed to characterize all IgG subclasses and IgE antibody responses.

47 evaluated only a limited number of flavonoid subclasses and intake ranges, yielding inconsistent resu

48 rties compared with the IgG2, IgG3, and IgG4 subclasses and is the most exploited subclass in therape

49 ificant decrease of all immunoglobulins, IgG subclasses and pneumococcal polysaccharide antibodies.

50 ive, namely nanobodies against all mouse IgG subclasses and rabbit IgG.

51 etermine how the modified regimen alters IgG subclasses and serum opsonophagocytic activity (OPA).

52 Typbar-TCV induced multiple IgG subclasses and strong booster responses in all ages.

53 ated with polyunsaturated long complex lipid subclasses and the C16-C20 FFAs but directly associated

54 d to evaluate the relation between flavonoid subclasses and total flavonoid intakes and incidence of

55 FR slopes were significantly different among subclasses and, except for 1A, different from those in h

56 scence intensity (MFI), C1q-binding, and IgG subclass, and graft injury phenotype at the time of sera

57 (+) Th cell-dependent, dominated by the IgG1 subclass, and Id specific.

58 n fluorescence intensity, rarely of the IgG3 subclass, and often capable of binding C1q.

59 Here, we studied isotypes, immunoglobulin G subclasses, and apparent affinities of anti-FVIII autoan

60 ed for the presence of Ebola-GP specific IgG subclasses, and for their binding to FcgammaRs.

61 conclusion, AHAs specifically recognize IgG subclass- and protease-restricted hinge neoepitopes.

62 Yearly average intake of major flavonoid subclasses (anthocyanins, flavanones, flavan-3-ols, flav

63 Overall, proliferation subclasses are associated with a more aggressive phenoty

64 sceinated secondary Ab (2nd-Ab), whereas IgG subclasses are monitored with Fc-specific monoclonal who

65 that control the separation of neurons into subclasses are the mean and standard deviation (SD) of n

66 is upregulated across human medulloblastoma subclasses as well as in other varieties of pediatric br

67 e primary amino acid sequence of the various subclasses, as well as the structure and composition of

68 d on disease endotypes, which are phenotypic subclasses associated with specific mechanisms underlyin

69 with Kis of 6-15 microM or 36-84 microM for subclass B1 MBLs (IMP-1 and BcII, respectively), and 10-

70 n laryngeal gene mutations are found in both subclasses, better prognosis is strongly associated with

71 ds (FA), triacylglycerols or nutritional fat subclasses but significant differences between cultivars

72 tion of glioblastoma into distinct molecular subclasses, but mechanisms that regulate tumor subclass

73 dual increase of all immunoglobulins and IgG subclasses, but values were always significantly lower t

74 lung function associated with each flavonoid subclass, categorized into quartiles, in linear mixed-ef

75 ight have diverged in two or three different subclasses, channels, scramblases and dual-function chan

76 We identified 2 subclasses, characterized by adaptive or exhausted immun

77 The FIPs are organized into two subclasses (class I and class II) based on sequence and

78 olesterol) were 26-52 % higher in both stone subclasses compared to controls (p < 0.05 for all).

79 ponses against the antigen and different IgG subclasses compared with soluble antigen alone.

80 h small VLDL, IDL, and large LDL lipoprotein subclass components, while hsa-miR-885-5p levels associa

81 of the Fc-associated glycan structure and Ig subclass composition on the one hand and selective Fcgam

82 intraclonal versatility in Ig class and IgG subclass composition, with particular patterns of memory

83 Su(Hw) genomic sites separate into sequence subclasses comprised of combinations of modules, with su

84 imited data on total flavonoid and flavonoid-subclass consumption over a long period of time and the

85 n sequence and domain organization, and both subclasses contain a highly conserved Rab-binding domain

86 id cells and its differential binding of IgG subclasses controls the contributions of mast cells, bas

87 rent understanding of the molecular basis of subclass conversion that is often involved in GBM recurr

88 reporter response and GP-specific total IgG1 subclass correlated in the studied group of Ebola surviv

89 at a higher habitual intake of any flavonoid subclass decreases the risk of colorectal cancer.

90 The prevalence of IgG subclass deficiency (5% to 50%) and specific antibody de

91 evidence of immunodeficiency, including IgG subclass deficiency, impaired Ag-induced lymphocyte prol

92 The subclass-defining genes correspond to adaptive immunity

93 Gene expression data for the 100 subclass-defining genes were generated using a multiplex

94 one subclass had decreased expression of the subclass-defining genes.

95 sophils, neutrophils, and macrophages to IgG subclass-dependent anaphylaxis.

96 OPA, which we subsequently confirmed by IgG subclass depletion.

97 Class and subclass designations were stable.

98 Tumor subclasses differ according to the genotypes and phenoty

99 This subclass distribution is atypical for food allergies and

100 -35.9% to 11.3%) and shifted the lipoprotein subclass distribution toward smaller LDL size (-1.5%; 95

101 ional gene regulatory principle for neuronal subclass diversification may be conserved from nematodes

102 The establishment of spinal motor neuron subclass diversity is achieved through developmental pro

103 mer dielectrics within known generic polymer subclasses (e.g., polyurea, polythiourea, polyimide), an

104 s comprised of combinations of modules, with subclasses enriched for different chromatin features.

105 phologically distinct, echinoid (sea urchin) subclasses, Euechinoidea and Cidaroidea, which diverged

106 definition, higher intakes of all flavonoid subclasses except for flavan-3-ols were associated with

107 The exhausted immune response subclass expressed many genes regulated by transforming

108 firins, including those where beta- or gamma-subclass expression was suppressed.

109 phylogenetic hierarchical system of classes, subclasses, families, subfamilies and transport systems.

110 ut their systemic effects across lipoprotein subclasses, fatty acids, and circulating metabolites rem

111 registry, intakes of total flavonoids and 7 subclasses (flavanones, anthocyanins, flavan-3-ols, flav

112 Intakes of total flavonoids and subclasses (flavonols, flavones, flavanones, anthocyanin

113 higher habitual dietary intakes of flavonoid subclasses (flavonols, flavones, flavanones, flavan-3-ol

114 lyp Prevention Trial, a higher intake of one subclass, flavonols, was statistically significantly ass

115 Each class contains subclasses; for a rapidly growing number of these, conse

116 enols representative of the main classes and subclasses found in the diet.

117 e canonical Gi, but via the unique G-protein subclass Gz.

118 As previously, one subclass had decreased expression of the subclass-defini

119 It is the most abundant subclass, has a half-life as long as that of IgG2 and Ig

120 IgA subclasses have been linked to protection against respir

121 strikingly different affinities, these 3 IgG subclasses have been shown to enable induction of system

122 fferent IgG subclasses was only observed for subclasses having homologous F(ab')2 C termini (IgG1/3/4

123 2) especially if the HLA DSA was of the IgG3 subclass (HR, 2.28; P = 0.01).

124 , and we were able to assign to one of these subclasses hundreds of proteins whose subcellular locali

125 These results suggest IgG iDSA subclasses identify distinct phenotypes of kidney allogr

126 The IgG subclass identity for each variant was confirmed with DN

127 ciencies (including deficiencies of IgG with subclasses, IgA, and IgM; specific antibody deficiencies

128 ntly not known whether and how the human IgA subclasses IgA1 and IgA2 contribute to the clinical stat

129 inant anti-RhD IgG Abs of the four different subclasses (IgG1-4) with and without core fucose (i.e.,

130 In contrast to other IgG subclasses, IgG3 is highly polymorphic and usually conta

131 s a structure-based rationale for this Nudix subclass in degrading protein-conjugated ADP-ribose, inc

132 IgG4, the least represented human IgG subclass in serum, is an intriguing antibody with unique

133 nd IgG4 subclasses and is the most exploited subclass in therapeutic antibodies.

134 city, MFI level, C1q-binding status, and IgG subclasses in a Cox survival model revealed IgG3 iDSA an

135 s was used to detect hapten-specific IgG 1-4 subclasses in patient plasma.

136 Identifying the subclasses in real time has theranostic implications, gi

137 The inducibility of different isoflavonoid subclasses in seedlings with Rhizopus varied per species

138 ealth of structural information for the IgG1 subclass, including complexes with Fcgamma receptors, an

139 All hypofucosylated anti-RhD IgGs of all IgG subclasses indeed showed enhanced binding affinity for i

140 In mice, the IgG subclass induced after Ag encounter can reflect the natu

141 ined the relation between habitual flavonoid subclass intakes and incidence of ED.

142 n between total flavonoid or other flavonoid subclass intakes and incident CHD.

143 Total flavonoid and subclass intakes were calculated from food-frequency que

144 iation between total flavonoid and flavonoid subclass intakes with incident CHD in a biracial and geo

145 ontaining gangliosides and other polar lipid subclasses is further purified by C18 solid-phase extrac

146 fference in transcriptional response between subclasses is the local chromatin environment.

147 mn onto the poles of the white dwarf, a star subclass known as AM Herculis.

148 mphocyte phenotype, and serum immunoglobulin subclass levels were evaluated.

149 rculating metabolites, including lipoprotein subclasses, lipids, fatty acids, amino acids, small mole

150 clear AURKA can be recruited by Forkhead box subclass M1 (FOXM1) as a co-factor to transactivate FOXM

151 on of gp120, in particular the IgG1 and IgG3 subclass mediating antibody-dependent cell-mediated cyto

152 e maintenance and is the most prevalent GPCR subclass mutated in human cancers, but to date, no drugs

153 shows hybrid features of different supernova subclasses, namely a light curve that is typical of norm

154 ed two well-differentiated, nonproliferation subclasses, namely periportal-type (wild-type beta-caten

155 n ARO/CYCs can further be separated into two subclasses: "nonreducing" ARO/CYCs, which act on nonredu

156 ependently associated with mortality in this subclass (odds ratio = 4.1; CI95 = 1.4-12.0; P = 0.011).

157 In conclusion, we identified a new subclass of ALK-negative ALCL characterized by aberrant

158 grase (IN) inhibitors (MINIs) are a distinct subclass of allosteric IN inhibitors.

159 zation of RCL1 with the layer 1 interlaminar subclass of astrocytes found exclusively in higher-order

160 P2X7 receptors (Rs) constitute a subclass of ATP-sensitive ionotropic receptors (P2X1-P2X

161 zonia aromatic heterocycles are an important subclass of aza-heterocyles as they are the structural m

162 A subclass of bacterial phytochromes (BphPs) utilizes heme

163 chamigrene sesquiterpenes constitute a large subclass of bromocyclohexane-containing natural products

164 sult from an additional yet-to-be-identified subclass of dopamine neurons.

165 Exosomes are a subclass of extracellular vesicles involved in intercell

166 Thus, a subclass of FKBP prolyl isomerase enzymes is recruited t

167 elaborate enzymatic biofuel cells (EBFCs), a subclass of fuel cells in which enzymes replace the conv

168 apparent affinities for each isotype and IgG subclass of FVIII-specific antibodies without the need f

169 Interestingly, a subclass of h-ChCs exhibits calretinin (CR) expression,

170 TLF-1 is a subclass of high density lipoprotein particles defined b

171 igated, optimized, and characterized a novel subclass of host defense peptide (HDP) mimics based on a

172 stability, leading to the formation of a new subclass of human ribosomal ultrafine anaphase bridges.

173 Immunoglobulin G1 (IgG1), a subclass of human serum antibodies, is the most widely u

174 (DIPs), comprising nine paralogs of another subclass of Ig-containing proteins, are expressed in a c

175 strate that 21 paralogs of the Dpr family, a subclass of immunoglobulin (Ig)-domain containing protei

176 nital disorders of autophagy' as an emerging subclass of inborn errors of metabolism by using the exa

177 repeats) family proteins constitute a major subclass of ISG proteins and are characterized by multip

178 that D3 receptor expression defines a novel subclass of layer 5 glutamatergic pyramidal cell in mous

179 ithms with applicability limited to a narrow subclass of materials.

180 important for the aggressive phenotype of a subclass of medulloblastomas in children.

181 zeolitic imidazolate frameworks (ZIFs) are a subclass of metal-organic frameworks (MOFs) amenable to

182 Zeolitic imidazolate frameworks (ZIFs), a subclass of metal-organic frameworks (MOFs) built with t

183 Of special interest is the subclass of metal-organic frameworks (MOFs) with pore ap

184 Plants contain a distinct subclass of minor H1 variants that are induced by drough

185 A subclass of miRNAs, termed mirtrons, derives from short

186 t, as well as selected applications for this subclass of MOFs, will be discussed.

187 cation channel that is expressed on a major subclass of nociceptors and is found in many orofacial t

188 pecificity of different members of the PTP4A subclass of phosphatases.

189 cal, physical and biological sciences, are a subclass of polyoxometalates and usually self-assemble i

190 -organic frameworks (MOFs) are emerging as a subclass of porous materials that can have a transformat

191 Ionic metal-organic frameworks (MOFs) are a subclass of porous materials that have the ability to in

192 rizing current injections, are enhanced by a subclass of potassium conductances that are recruited at

193 utations in SPOP define a distinct molecular subclass of prostate cancer.

194 n array of hybrid compounds from which a new subclass of receptor-selective antagonists was identifie

195 noncoding ribonucleic acids (lncRNAs) are a subclass of regulatory noncoding ribonucleic acids for w

196 Super-enhancers are an emerging subclass of regulatory regions controlling cell identity

197 with five subtypes named M1-M5) are a unique subclass of RGCs with axons that project directly to man

198 Thiopeptides are a subclass of ribosomally synthesized and posttranslationa

199 is governed by ADP-ribosyltransferases and a subclass of sirtuins (writers), is sensed by proteins th

200 provide compelling evidence that a specific subclass of sulfate groups, and not the overall charge o

201 AP1, a member of the neuronal calcium sensor subclass of the calmodulin superfamily, confers Ca(2+)-s

202 pected roles of type I DNA topoisomerases, a subclass of these enzymes, in regulating gene expression

203 P2-dependent NHEJ in the formation of a rare subclass of translocations associated previously with th

204 Moreover, a subclass of weak non-canonical terminators was identifie

205 acter aerogenes, and would seem to suggest a subclass of Zn(2+)-specific transporters among the clust

206 ied the levels of anti-PEG IgM and different subclasses of anti-PEG IgG (IgG1-4) in both contemporary

207 , indicates that myelin profiles on distinct subclasses of axons might be determined by diverse mecha

208 the basis of the N-substituent, three major subclasses of carbonate monomers were synthesized (N-ary

209 We investigated the association between IgG subclasses of circulating anti-human HLA antibodies and

210 We characterize 16 recurrent subclasses of complex SV (cxSV), revealing that: (1) cxS

211 expression profiling has identified 2 major subclasses of diffuse large B-cell lymphoma (DLBCL).

212 crement of 2.8 microg/m(3)) and with several subclasses of disease.

213 istinct immunoglobulin (Ig) isotypes and IgG subclasses of factor VIII (FVIII)-specific antibodies ar

214 focus on the current knowledge for the main subclasses of flavonoids, including anthocyanins, flavon

215 avone and flavonol glycosides, two important subclasses of flavonoids.

216 Identification of subclasses of GABAergic cells (up to 15 in the cerebral

217 (HS), which are representatives of two major subclasses of glycosaminoglycans.

218 decrease in FcgammaRI affinity to all three subclasses of IgGs.

219 tivated K(+) channels (SK, KCa 2) are unique subclasses of K(+) channels that are regulated by Ca(2+)

220 te RNA stability and translation on specific subclasses of mRNAs.

221 The ability to target subclasses of neurons with defined connectivity is cruci

222 1 is required for the generation of specific subclasses of neurons within the lateral hypothalamic ar

223 layer-specific piriform genes mark different subclasses of neurons, which project to distinct target

224 l-B displays high inhibitory selectivity for subclasses of NMDARs that contain the functionally impor

225 ss averages of these complexes into discrete subclasses of particles helped reduce human bias.

226 re, we review how genetic alterations define subclasses of patients with acute leukemias, myelodyspla

227 ing seven (n=13), six (n=12) and five (n=14) subclasses of polyphenol.

228 tify successfully the transcription response subclasses of promoters and enhancers from two different

229 analysis revealed two functionally distinct subclasses of release sites differing by over 60-fold in

230 Transcripts from multiple classes and subclasses of repetitive elements (LINEs, endogenous ret

231 EP neurons are differentially innervated by subclasses of striatal and pallidal neurons.

232 s nephropathy (MN), and define two molecular subclasses of this disease.

233 of treatments that target discrete molecular subclasses of tumours.

234 Thus, activation of specific subclasses of voltage- and/or calcium-gated potassium ch

235 Here, we evaluate the influence of IgG subclass on antimannan antibody-mediated protection.

236 arly delineating parkinsonian disorders into subclasses on the basis of molecular mechanisms with wel

237 is related to an intrinsic property of this subclass or only the allergen specificity.

238 bclasses, but mechanisms that regulate tumor subclass phenotypes are only now emerging.

239 We investigated whether different flavonoid subclasses present in the habitual diet were associated

240 ns to Ab immune complexes was affected by Ab subclass, presentation, opsonization density, Fc fucosyl

241 o be the main determinant of the type of IgG subclass produced.

242 ects of pravastatin treatment on lipoprotein subclass profiles and fatty acids.

243 their effects on metabolite and lipoprotein subclass profiles.

244 ltaneously provides fine-grained lipoprotein subclass profiling and quantification of circulating fat

245 o-localization defines two distinct neuronal subclasses projecting either to the contralateral cortex

246 Overall, our catalog of neuronal subclasses provides new understanding of hypothalamic or

247 differing from the non-prognostic laryngeal subclasses reported by The Cancer Genome Atlas (TCGA).

248 The new periportal-type subclass represented 29% of all HCCs; expressed a hepato

249 Group A-specific immunoglobulin G (IgG) subclass response was characterized using an enzyme-link

250 The predominant IgG subclass response, regardless of vaccine, was IgG1.

251 explored the diversity of protease- and IgG subclass-restricted AHAs and their potential as immunolo

252 ipal component analysis integrating iDSA IgG subclasses revealed aABMR was mainly driven by IgG3 iDSA

253 ell known plagiopyleans; (8) validity of the subclass Rhynchostomatia is supported, and (9) the syste

254 Gallstone subclasses shared enhanced cholesterol synthesis.

255 days postinfection, and isotyping of the Ig subclass showed that the total IgG response switched fro

256 The human IgG1 antibody subclass shows distinct properties compared with the IgG

257 ific IgE and sIgE/Total IgE ratio), (ii) IgG-subclasses (sIgG1, sIgG4 including SIgE/IgG4 ratio), (ii

258 Subclass specific IgG glycosylation profile was analyzed

259 variant was confirmed with DNA sequence and subclass-specific antibodies.

260 ng of therapeutic antibodies, as well as for subclass-specific biomarker discovery in clinical IgG sa

261 s in the form of Hox proteins to co-activate subclass-specific effector genes in post-mitotic motor n

262 e sialic acid derivatization method to allow subclass-specific MALDI-TOF-MS analysis of tryptic IgG g

263 of a neuron class, but is also required for subclass-specific traits expressed along the A-P axis.

264 anism necessary for motor neurons to acquire subclass-specific traits in the nematode Caenorhabditis

265 rn between reported flavonoids compounds and subclass studied.

266 efficient generation of murine bsAbs for all subclasses studied (mouse IgG1, IgG2a and IgG2b; rat IgG

267 hese data indicate that individual precursor subclasses synchronously produce functionally different

268 ata regarding C1q binding antibodies and IgG subclass testing.

269 ain-infiltrating monocytes as a myeloid-cell subclass that contributes to neuroinflammation and morbi

270 ithin the class of open channels, there is a subclass that is not permeable to ions.

271 GP-specific IgG1 is by far the seroprevalent subclass that retained and even enhanced its presence in

272 -hinge antibodies (AHAs) are an autoantibody subclass that, following proteolytic cleavage, recognize

273 These alterations can be grouped into major subclasses that include ABL-class fusions involving ABL1

274 s the diversification of neuron classes into subclasses that share large sets of features but differ

275 vival within the germinal center B-cell-like subclass; the centrocyte subtype had a superior prognosi

276 ay predispose to SPOP mutant prostate cancer subclass through a hormone dependent DNA damage response

277 ay predispose to SPOP mutant prostate cancer subclass through a hormone-dependent DNA damage response

278 The presence of FVIII-specific IgG subclass titer >/=1:40 antibodies was significantly asso

279 Therefore, individual IgG subclasses to a single Ag can provide different levels o

280 er are regulated differently in clock neuron subclasses to support their specific functions.

281 udy subjects (n = 168) were allocated to the subclasses using computer-assisted image analysis and mi

282 Three IgG subclass variants of M1g1 were constructed: M1g2, M1g3,

283 Allocation to this subclass was independently associated with mortality (od

284 ion; the prevalence of other GP-specific IgG subclasses was considerably reduced over time.

285 ated F(ab')2 fragments of all four human IgG subclasses was determined.

286 ncoding CIDRalpha1.4 and CIDRalpha1.5 domain subclasses was higher in patients with severe disease (P

287 ty for F(ab')2s generated from different IgG subclasses was only observed for subclasses having homol

288 SNRIs-the most commonly used antidepressant subclass-was associated with an increased risk of type 2

289 cardiovascular disease risk factors, several subclasses were associated with reduced ED incidence, sp

290 Six polyphenol subclasses were identified.

291 Intakes of flavonoid subclasses were not associated with risk of colorectal c

292 th the exception of high-density lipoprotein subclasses, which displayed a more heterogeneous respons

293 ification of 145 ganglioside species from 19 subclasses, which represents the highest number of repor

294 The gene expression score identified this subclass with an area under the curve of 0.98 (95% confi

295 r data suggest the evolution of an Argonaute subclass with noncanonical specificity for a 5'-hydroxyl

296 -throughput purification of pyramidal neuron subclasses with deep profiling of spatiotemporal transcr

297 ributed in four splicing-mediated biogenesis subclasses, with 5'-tailed mirtrons as, by far, the domi

298 identified 924 unique lipids across 21 lipid subclasses, with dramatic alterations in the lipidome ac

299 tatin globally lowered levels of lipoprotein subclasses, with the exception of high-density lipoprote

300 nt reductive dehalogenases, constitute a new subclass within the nitro-FMN reductase superfamily.