ライフサイエンスコーパス: subfamily

1 hylases, including the Jumonji C (JmjC) KDM5 subfamily.

2 step in the evolutionary history of the RfaH subfamily.

3 functional diversity of this ABC transporter subfamily.

4 lovirus genus of the human Betaherpesvirinae subfamily.

5 appear to be conserved within the kinesin-5 subfamily.

6 redominantly metabolized by the CYP3A enzyme subfamily.

7 nsin-like B, the less-studied plant expansin subfamily.

8 itional characterization of this ion channel subfamily.

9 o acquire a better understanding of this AQP subfamily.

10 ion gene network is conserved throughout the subfamily.

11 of tuning responses within any discrete HsOr subfamily.

12 t underlie the functional properties of this subfamily.

13 und in TRPV1, a TRP channel from a different subfamily.

14 into the diversity of the kappa-carrageenase subfamily.

15 e GluD ionotropic glutamate receptor (iGluR) subfamily.

16 es (adult, larva) of major groups within the subfamily.

17 three to the TPS-e/f, and four to the TPS-b subfamilies.

18 ntially utilized particular Vbeta and Valpha subfamilies.

19 erent RCARs, which can be divided into three subfamilies.

20 carried out across discrete odorant receptor subfamilies.

21 BAM2 is the ancestral member of one of these subfamilies.

22 Transition rates differed between Lamiaceae subfamilies.

23 -clustered delta and clustered protocadherin subfamilies.

24 fied them into conserved and phylum-specific subfamilies.

25 Arabidopsis BAM genes fall into two distinct subfamilies.

26 ruses that is not found in other herpesvirus subfamilies.

27 ity, not only within, but also between aGPCR subfamilies.

28 homeobox genes can be classified into eleven subfamilies.

29 er the core clock component nuclear receptor subfamily 1 group D member 1 (NR1D1, also called Rev-erb

30 BACKGROUND & AIMS: The nuclear receptor subfamily 1 group H member 4 (NR1H4 or farnesoid X recep

31 The nuclear receptor subfamily 1, group H, members 2 and 3 (also known as liv

32 ABSTRACT: Inward rectifier K(+) channel subfamily 2 (Kir2) channels primarily maintain the norma

33 Inward rectifier K(+) channel subfamily 2 (Kir2) channels primarily maintain the resti

34 A and protein expression of nuclear receptor subfamily 2 group F member 6, whereas the PSA-lacking NC

35 , we show that inward rectifier K(+) channel subfamily 2 isoform 1 (Kir2.1) currents non-linearly cou

36 The purple sea urchin genome encodes 10 IL17 subfamilies (35 genes) and 2 IL17 receptors.

37 GH5 subfamily 4 (GH5_4) is one of the largest, with known ac

38 nscription of c-fos and the nuclear receptor subfamily 4 (Nr4a) genes Nr4a1-3 in the hippocampus thro

39 s of transient receptor potential melastatin subfamily 4 (TRPM4), intracellular introduction of TRPM4

40 d by transient receptor potential melastatin subfamily 4 channels via type 2 inositol 1,4,5-trisphosp

41 signature genes, including nuclear receptor subfamily 4 group A member 1 (NR4A1) and ATP-binding cas

42 erol efflux by inducing ATP-binding cassette subfamily A member 1 (ABCA1) and ABCG1.

43 with fewer C alleles at ATP-binding cassette subfamily A member 1 (ABCA1) rs2246293 (beta = -0.6 mg/d

44 D3-24-hydroxylase (cytochrome P450 family 24 subfamily A member 1) mRNA expression is up-regulated by

45 mber 1 (CYP2E1) and cytochrome P450 family 1 subfamily A member 2 (CYP1A2) that convert acetaminophen

46 The voltage-gated potassium channel subfamily A member 3 (Kv1.3) dominantly expresses on T c

47 denosine triphosphate (ATP)-binding cassette subfamily A member 4 (ABCA4) gene and who met the follow

48 ciations related to Cytochrome P450 Family 2 Subfamily A Member 6 (CYP2A6), we investigated the human

49 ceptor transient receptor potential channel, subfamily A, member 1 and may thus induce energy expendi

50 transient receptor potential cation channel, subfamily A, member 1) have been implicated in itch.

51 By contrast, ATP-binding cassette, subfamily A, member 1-dependent efflux was reduced after

52 transient receptor potential cation channel subfamily A, receptor 1 (TRPA1); TRPV4; transient recept

53 ted, actin-dependent regulator of chromatin, subfamily a-like 1), and COL7A1 (collagen type VII alpha

54 xpression of aldehyde dehydrogenase family 1 subfamily A1 (Aldh1a1).

55 We uncovered a conserved AGO subfamily absent in angiosperms.

56 superfamily: expansion or contraction of OR subfamilies accompanies major changes in habitat and lif

57 genome, but only the human-specific L1HS-Ta subfamily acts as an endogenous mutagen in modern humans

58 ons of African lizard species in the reptile subfamily Agaminae (a relatively young, Neogene radiatio

59 during the evolution of a single staphylinid subfamily, Aleocharinae.

60 -1 and other members of the GABA transporter subfamily all contain an extra amino acid residue at or

61 Three subfamilies and 16 tribes (as previously delimited) were

62 cal system of classes, subclasses, families, subfamilies and transport systems.

63 With 87 genera representing all subfamilies and tribes of Rosaceae and six of the other

64 is conserved only in two genera of the beta-subfamily and absent in alpha- and gamma-herpesviruses.

65 s an RNA helicase belonging to the Ski2-like subfamily and an essential component of spliceosome.

66 enes belong to a previously undescribed Toll subfamily and that members of this subfamily exhibit str

67 se to vernalization is widespread within the subfamily and that the genetic basis of this trait is co

68 their regulatory proteins identified the Rac subfamily and the Rac-specific guanine nucleotide exchan

69 g the commelinid orders, among the five palm subfamilies, and among tribes of the subfamily Coryphoid

70 This monophyly can be divided into four subfamilies, and each can be traced to ancestral members

71 130 nM, >700-fold selectivity over other GRK subfamilies, and no detectable inhibition of ROCK1.

72 NOMPC is the founding member of the TRPN subfamily, and is thought to be gated by tethering of it

73 rkably few evolutionary studies of the whole subfamily, and only one genome sequence has been publish

74 m cold responsiveness around the base of the subfamily, and that a set of more ancient pathways enabl

75 ing functional characterizations of distinct subfamily architectures using SPARCLE: Subfamily Protein

76 eae, although species belonging to different subfamilies are characterized by distinct allergen subse

77 Most of these subfamilies are conserved throughout echinoderms.

78 Two IL17 subfamilies are sequentially strongly upregulated and at

79 are described, and the compositions of other subfamilies are updated based on new findings from the l

80 e-gated potassium channels of the KCNQ (Kv7) subfamily are essential for control of cellular excitabi

81 new evidence that Eph receptors in the same subfamily are not simply interchangeable but are functio

82 to generate knockouts of the LC3 and GABARAP subfamilies as well as all six Atg8 family members in He

83 ons with MED25 are specific for the ETV1/4/5 subfamily as other ETS factors display weaker binding.

84 , we engineered cells lacking genes for each subfamily as well as all six mammalian ATG8s.

85 Pseudomonas phage LKA1 of the subfamily Autographivirinae encodes a tailspike protein

86 bosome-associated complex and stress-seventy subfamily B chaperones.

87 y ribosome-associated complex-stress-seventy subfamily B couples translation rate to the unfolded pro

88 alpha-hydroxylase (cytochrome P450 family 27 subfamily B member 1), and there is no detectable 1alpha

89 d reduced ABC subfamily G member 5/8 and ABC subfamily B member 11 transporter expression in comparis

90 These studies identified DnaJ homolog subfamily B member 9 (DNAJB9) as a highly sampled protei

91 ein (adenosine triphosphate-binding cassette subfamily B, member 1 [ABCB1]) and breast cancer resista

92 atic induction of cytochrome P450, family 7, subfamily b, polypeptide 1 (CYP7B1) and results in incre

93 onsidered part of the pro-apoptotic Bax-like subfamily, but no studies have yet been performed in neu

94 tested the cis-regulatory activity of 69 TE subfamilies by luciferase reporter assays, spanning all

95 e that exerts activities beyond the original subfamily by interacting with multiple receptors.

96 transient receptor potential cation channel subfamily C 3 (TRPC3).

97 The subfamily C ATP-binding cassette (ABCC) transporters med

98 37S ribosomal protein 1/ATP-binding cassette subfamily C member 1 (MRP1/ABCC1) and the PI3/AKT pathwa

99 biallelic mutations in DNAJC21 (DNAJ homolog subfamily C member 21).

100 transient receptor potential cation channel, subfamily C, member 6 (TRPC6) gene encoding a nonselecti

101 transient receptor potential cation channel, subfamily C, member 6 (TRPC6), consistent with cardiac e

102 ked to a mutation in an ATP Binding Cassette subfamily C2 (ABCC2) gene that functions as a Cry1Fa rec

103 abled classification of the evasins into two subfamilies: C8 evasins share a conserved set of eight C

104 t and lifestyle; independent selection on OR subfamilies can permit local adaptation or conserved che

105 ynthases, and those belonging to the TPS-e/f subfamily catalyzed the formation of precursors of kaura

106 Siglec-8 is a CD33 subfamily cell-surface receptor selectively expressed on

107 The subfamily Chrysopinae includes 97% of the species divers

108 s were further characterized regarding their subfamily classification, distribution along the genomes

109 ry history of the cosmopolitan diving beetle subfamily Colymbetinae, the majority of which are found

110 The Lmod subfamily comprises three somewhat divergent isoforms ex

111 The LIV-1 subfamily, containing nine out of the 14 human ZIP prote

112 teriviridae, Coronaviridae (divided into the subfamilies Coronavirinae and Torovirinae), Roniviridae,

113 ve palm subfamilies, and among tribes of the subfamily Coryphoideae.

114 The young age of the subfamily, coupled with the high number of independent l

115 Based on these results, three new subfamilies-Cymarioideae, Peronematoideae, and Premnoide

116 ted, actin-dependent regulator of chromatin, subfamily d, member 1) as a novel target gene of miR-7.

117 ted, actin-dependent regulator of chromatin, subfamily D, member 2), also known as BAF60b (BRG1/Brahm

118 aper explores the phylogeny of the delphacid subfamily Delphacinae based on nuclear ribosomal and mit

119 ationships among included representatives of subfamily Deltocephalinae.

120 These emerging Vss subfamilies displayed a higher functional avidity for th

121 he Evacanthinae, a highly diverse leafhopper subfamily distributed worldwide, were explored by analys

122 ineage of land plants, suggesting that these subfamilies diverged prior to the origin of land plants.

123 basal expression of cytochrome P450 family 2 subfamily E member 1 (CYP2E1) and cytochrome P450 family

124 number of tandem repeat-Alu (SINE-VNTR-Alu), subfamily-E retrotransposon (SVA-E) inserted into CASP8

125 amma clustered Pcdh isoforms illustrate that subfamilies encode specificity in distinct ways through

126 The TPS-b subfamily encompassed genes coding for enzymes involved

127 coside hydrolase family 5 (GH5) members into subfamilies enhances the prediction of substrate specifi

128 s), with fourteen receptors divided into two subfamilies - EphAs and EphBs.

129 AviRTE subfamilies exhibit 83-99% nucleotide identity between g

130 ibed Toll subfamily and that members of this subfamily exhibit striped expression (as seen in Triboli

131 Protein subfamily functional classifications have more than doub

132 imer adenosine triphosphate binding cassette subfamily G member 5/8 (ABCG5/G8).

133 reased hepatic inflammation, and reduced ABC subfamily G member 5/8 and ABC subfamily B member 11 tra

134 ein (adenosine triphosphate-binding cassette subfamily G, member 2 [ABCG2]).

135 domain potassium (K2P) channels of the TREK subfamily generate 'leak' currents that regulate neurona

136 Among the 51 described GH5 subfamilies, subfamily GH5_26 contains members that display either en

137 madillo crown-group, representing a distinct subfamily (Glyptodontinae) within family Chlamyphoridae.

138 The Rac subfamily GTPases act downstream of the GEFs; CED-10/Rac

139 tide-gated (HCN) and voltage-gated potassium subfamily H (KCNH) channels by plasma membrane component

140 as the majority of them, except those of AP2 subfamily, had no intron.

141 d distinct regulation mechanisms among NEDD4 subfamily HECTs and proved useful for modulating therape

142 lexity of host plant use in the Lepidopteran subfamily Heliothinae suggest that architecture may not

143 volves two transporters of the PIB-1-ATPases subfamily: HMA6 at the chloroplast envelope and HMA8 in

144 The PP2Ac of the subfamily I (StPP2Ac1, 2a and 2b) were suggested to be i

145 ng lysine acetyl transferases are members of subfamily I of the bromodomain phylogenetic tree.

146 elected one of the catalytic subunits of the subfamily I, StPP2Ac2b, to develop transgenic plants ove

147 genes were identified and divided into four subfamilies, i.e., ERF (ethylene responsive factor), DRE

148 K-J1, a selective inhibitor of the KDM6/KDM5 subfamilies, identify critical residues for binding of t

149 erent tissues and the expression of DREB/ERF subfamilies in B. distachyon, wheat and rice under abiot

150 ork defines unique roles for GABARAP and LC3 subfamilies in macroautophagy and selective autophagy an

151 2268 full-length Platy-1 elements across 62 subfamilies in the common marmoset genome.

152 Members of the APOBEC3 subfamily in humans (APOBEC3A, APOBEC3B, APOBEC3C, APOBE

153 fore therapy (thereafter called emerging Vss subfamilies) in responding patients, with a predominant

154 The Alphaherpesvirinae subfamily includes HSV types 1 and 2 and the sequence-di

155 The ABCC transporter subfamily includes pumps, the long and short multidrug r

156 r DNA-binding autoinhibition in the ETV1/4/5 subfamily involving a network of intramolecular interact

157 wn, and the binding specificity of the CPEB2 subfamily is a matter of debate.

158 A third IL17 subfamily is activated in adult immune cells indicating

159 erly Sensitive (SOS)2, a member of the SnRK3 subfamily, is a critical mediator of the response to sal

160 or 21 (FGF21), a member of the endocrine FGF subfamily, is expressed in thymic stromal cells along wi

161 ies showed that Pcdh ectodomains from gammaB-subfamily isoforms formed cis dimers, whereas gammaA iso

162 pathophysiological role of potassium channel subfamily K member 3 (KCNK3) in PAH is unclear.

163 V VP24 (rVP24) interactions with three NPI-1 subfamily KPNAs (KPNA1, KPNA5, and KPNA6).

164 Hsp90beta subfamily lacks the dual lysine motif and the extracellu

165 (transient receptor potential cation channel subfamily M member 7) regulates gene expression and stre

166 transient receptor potential cation channel subfamily M member 8 (TRPM8(EGFPf/+)) locus in the 3 bra

167 transient receptor potential cation channel, subfamily M, member 7 (TRPM7)-dependent magnesium entry,

168 transient receptor potential cation channel subfamily M, member 8 (TRPM8); and nerve growth factor (

169 ctive transient receptor potential vanilloid subfamily member 6 (TRPV6) channels play a critical role

170 titutions were introduced into RGS10, an R12 subfamily member.

171 indicating that the transcription of SAUR19 subfamily members are influenced by this hormone signali

172 tion of the Atg8 family and identify GABARAP subfamily members as primary contributors to PINK1/Parki

173 of cattle, and like many Alphaherpesvirinae subfamily members establishes latency in sensory neurons

174 sion of the TREK (TWIK-related K(+) channel) subfamily members of K2P channels often overlaps in neur

175 re converted to those typically found in R12 subfamily members, and the reverse substitutions were in

176 Like many Alphaherpesvirinae subfamily members, bovine herpesvirus 1 (BoHV-1) express

177 east characterized of the three human SULT1C subfamily members.

178 ription of hypocotyl growth-promoting SAUR19 subfamily members.

179 CYP2C8, an important member of this subfamily, metabolizes the anticancer drug paclitaxel, c

180 The braconid parasitoid wasp subfamily Microgastrinae is perhaps the most species-ric

181 ntially other lineages within the widespread subfamily Murinae, may play a role in the spread of GALV

182 l avidity for their cognate antigen than Vss subfamilies not amplified upon anti-PD-1 therapy and cou

183 te-specific OR enrichment and distinctive OR subfamily odorant response profiles, our findings sugges

184 We also identified 13 gene subfamilies of FXYDs and propose a revised, phylogeny-ba

185 f the endoglucanases revealed three distinct subfamilies of glycoside hydrolase family 5 (GH5).

186 Each of the three subfamilies of herpesviruses (alpha, beta, and gamma) en

187 nt protein UL37 is conserved among all three subfamilies of herpesviruses.

188 ulted in ligands of representatives of three subfamilies of human bromodomains with favorable ligand

189 ional kainate receptors (KARs), one of three subfamilies of ionotropic glutamate receptors, as well a

190 eable or, at best, different variants of two subfamilies of pointed-end capping proteins.

191 Among the 20 subfamilies of protein receptor tyrosine kinases (RTKs),

192 on with structure and conjugation of various subfamilies of push-pull nitrogen bases: nitriles, azole

193 b2 are single members of the CPEB1 and CPEB2 subfamilies of the CPEB proteins, respectively.

194 ACHT (named for NAIP, CIIA, HET-E, and TEP1) subfamilies of the STAND NTPases, we analyzed the phylog

195 rogastrinae is perhaps the most species-rich subfamily of animals on Earth.

196 XBAT35 belongs to a subfamily of Arabidopsis (Arabidopsis thaliana) RING-typ

197 ALG-5 belongs to the AGO subfamily of Argonautes that includes ALG-1 and ALG-2, b

198 IKE (LRL) transcription factor (TF) [11, 12] subfamily of basic loop helix (bHLH) proteins by compari

199 The subfamily of beta2 integrins is implicated in macrophage

200 of human PcdhgammaB3, a member of the gamma subfamily of clustered Pcdhs.

201 nships: a poaeamide analogue and a molecular subfamily of cyclic lipopeptides, bananamides 1, 2 and 3

202 The IL-20 subfamily of cytokines has been reported to act at epith

203 The Ded1/DDX3 subfamily of DEAD-box proteins is of particular interest

204 of the ovarian tumor domain (OTU)-containing subfamily of deubiquitinating enzymes.

205 Dynemicin A is a member of a subfamily of enediyne antitumour antibiotics characteriz

206 the only known specific inhibitors of the Gq subfamily of G proteins; however, no synthetic route has

207 In this study, we reveal that a subfamily of GGDEF enzymes synthesizes the asymmetric si

208 y provided evidence that GlyA1 defines a new subfamily of GH3 proteins with a novel permuted domain t

209 ia (DRG) express kainate receptors (KARs), a subfamily of glutamate receptors that modulate neurite o

210 ins (GBPs) are an interferon (IFN)-inducible subfamily of guanosine triphosphatases (GTPases) with we

211 one of 19 members of the chemokine receptor subfamily of human class A G-protein-coupled receptors.

212 -related transient receptor potential (TRPM) subfamily of ion channels.

213 P24) involves its interaction with the NPI-1 subfamily of karyopherin alpha (KPNA) nuclear transporte

214 analysis indicate that StnA represents a new subfamily of lipolytic enzymes with the specific binding

215 Here, we uncover a novel role for a subfamily of MAP4 kinases consisting of MAP4K4, Traf2- a

216 that in ants such as H. saltator, the 9-exon subfamily of odorant receptors (HsOrs) responds to CHCs,

217 Here we functionally characterize a subfamily of odorant receptors (Ors) with a nine-exon ge

218 enes in a clade of 180 ORs within the 9-exon subfamily of ORs are expressed exclusively in females an

219 2 (ALA2) and the related ALA1 in the type IV subfamily of P-type ATPases as key components of antivir

220 The protein phosphatase 2A (PP2A) subfamily of phosphatases, PP2A, PP4, and PP6, are multi

221 atic swapping of pre-existing variation in a subfamily of plant CLE peptide hormones leads to a synth

222 placed unambiguously into the Bax-like Bcl-2 subfamily of pro-apoptotic proteins.

223 The DLG-MAGUK subfamily of proteins plays a role on the recycling and

224 Rem2 is a member of the RGK subfamily of RAS small GTPases.

225 Eph receptors belong to a subfamily of receptor tyrosine kinases that are activate

226 Although the R4 subfamily of RGS proteins generally accepts both Galphai

227 Both RGS7 and RGS9-2 belong to the R7 subfamily of RGS proteins that form macromolecular compl

228 Previous studies have identified p90 subfamily of ribosomal S6 kinase (p90RSK) family kinases

229 The TAM (Tyro3, Axl, Mer) subfamily of RTKs in particular feature in a variety of

230 Since the Sema3 subfamily of signaling molecules plays diverse roles in

231 se-DNA binding (CHD) Type III proteins are a subfamily of SWI2/SNF2 proteins that control nucleosome

232 EaDAcT belongs to a small, plant-specific subfamily of the membrane bound O-acyltransferases (MBOA

233 Here, we identify a subfamily of these proteins as cyclopropanoid cyclopropy

234 y, the Soluble NSF-Attachment Protein (SNAP) subfamily of TPR containing proteins is characterized.

235 reveal a general architecture for this major subfamily of TRP channels and a well-defined calcium-bin

236 timulated K(+) channel (TRAAK) form the TREK subfamily of two-pore-domain K(+) (K2P) channels.

237 acteriaceae and related Actinobacteria, this subfamily of type IA topoisomerase may be required for m

238 gamma-Pcdh trans interface, and suggest that subfamily- or isoform-specific cis-interactions may play

239 d member of the genus Protoparvovirus in the subfamily Parvovirinae.

240 ch was used to investigate the role of a PLS-subfamily pentatricopeptide repeat protein, Mitochondria

241 the three enzymes belonging to the class II subfamily (PI3K-C2alpha, beta and gamma) are the least i

242 Cytochrome P450 enzymes of the CYP720B subfamily play a central role in the biosynthesis of dit

243 tophagosome-lysosome fusion, whereas the LC3 subfamily plays a less prominent role in these processes

244 Grasses of subfamily Pooideae, including several important crops, s

245 are primarily tropical, but one major clade, subfamily Pooideae, radiated extensively within temperat

246 We find that the GABARAP subfamily promotes PLEKHM1 recruitment and governs autop

247 tinct subfamily architectures using SPARCLE: Subfamily Protein Architecture Labeling Engine.

248 Sequence-derived contact information for the subfamilies proves sufficient to assemble accurate struc

249 MYB proteins have been classified into four subfamilies: R2R3-MYB, R1/2-MYB, 3R-MYB, and 4R-MYB.

250 Our subfamily reconstruction and phylogenetic analyses suppo

251 R7 subfamily RGS proteins are stabilized by the G-protein s

252 r of G protein signaling) proteins of the R7 subfamily (RGS6, -7, -9, and -11) are highly expressed i

253 aq/11 subunits as substrates, the R7 and R12 subfamilies select against Galphaq/11.

254 s has six PEX11 isoforms which fall into two subfamilies, similar to those found in monocots and dico

255 tissues 1 (RIT1) is a disease-associated RAS subfamily small guanosine triphosphatase (GTPase).

256 The core is flanked by subfamily-specific extensions of idiosyncratic function.

257 Here, we define the function of the subfamily-specific extensions of the human DEAD-box prot

258 3) is mediated by kinases of the class I PAK subfamily, specifically 1) exposing cells to four struct

259 shuttling dynamics of the Arabidopsis SRSF1 subfamily (SR30, SR34, SR34a, and SR34b) under control o

260 Among the 51 described GH5 subfamilies, subfamily GH5_26 contains members that disp

261 sentatives of other heterotrimeric G protein subfamilies, such as Galphai1, Galphao, Galphas, and Gal

262 cket, particularly for GPCRs within a single subfamily, such as the nine adrenergic receptors.

263 Thr as the catalytic residue in certain BPH subfamilies, suggest a proteolytic function for BPH dist

264 ivate more than one member of the respective subfamily supporting their evolutionary relationship and

265 iogeographical and ecological origin of this subfamily, testing whether they originated in dry biomes

266 We define two Cas13a protein subfamilies that can operate in parallel for RNA detecti

267 subunit DPY-21 define a Jumonji demethylase subfamily that converts H4K20me2 to H4K20me1 in worms an

268 dues, lys-270 and lys-277, in the Hsp90alpha subfamily that determine the extracellular Hsp90alpha fu

269 PIWIL3 is an Argonaute protein of the PIWI subfamily that is mainly expressed in the germline and t

270 The subfamily Thaumetopoeinae consists of approximately 100

271 ty between receptor-ligand pairs within each subfamily, the functional relevance of which is not defi

272 Within the hydrophobe-amphiphile efflux subfamily, these resistance-nodulation-cell division pro

273 nt residue contact networks of the LacI/GalR subfamilies to design and experimentally validate an all

274 he largest time-calibrated phylogeny for the subfamily to date, reconstructed ancestral states for ge

275 presence or absence in flours depends on the subfamily to which the plant belongs.

276 Two-pore channels (TPCs) comprise a subfamily (TPC1-3) of eukaryotic voltage- and ligand-gat

277 eceptor potential channel 4 of the vanilloid subfamily (TRPV4) is activated by a diverse range of mol

278 served amplification of Melan-A-specific Vss subfamilies undetectable before therapy (thereafter call

279 [transient receptor potential cation channel subfamily V member 1 (TRPV1) expressing C-fibres] or onl

280 transient receptor potential cation channel subfamily V member 1 (TRPV1) or vanilloid receptor 1 is

281 transient receptor potential cation channel subfamily V member 1 (TRPV1)-sensitive or TRPV1-resistan

282 Transient receptor potential cation channel, subfamily V, member 4 (TRPV4) is widely expressed in the

283 transient receptor potential cation channel subfamily V, receptor 1 (TRPV1)-substance P nociceptive

284 Across taxonomic subfamilies, variations in intelligence (G) are sometime

285 Stachel peptides derived from aGPCRs of subfamily VI (GPR110/ADGRF1, GPR116/ADGRF5) and subfamil

286 mple, the Stachel-derived peptide of GPR110 (subfamily VI) can activate GPR64 and GPR126 (both subfam

287 family VI (GPR110/ADGRF1, GPR116/ADGRF5) and subfamily VIII (GPR64/ADGRG2, GPR126/ADGRG6) are able to

288 mily VI) can activate GPR64 and GPR126 (both subfamily VIII).

289 tem in Escherichia coli Members of the TPS-c subfamily were characterized as copalyl diphosphate (dit

290 Members of the kinesin-5 subfamily were initially described as unidirectional plu

291 a P-type PPR and a member of a small PPR-DYW subfamily, were shown to interact in yeast.

292 t vertebrates can be classified into 13 gene subfamilies, which do not always correspond to the estab

293 ifies a peptide hormone family into multiple subfamilies, which exert distinct activities by exclusiv

294 members of the SMALL AUXIN UP RNA19 (SAUR19) subfamily, which promote cell expansion, are repressed b

295 monstrate that DCA can differentiate between subfamilies with different binding modes within one larg

296 phylinidae), a vast and ecologically diverse subfamily with numerous morphologically and behaviourall

297 between Caryophyllales families, and between subfamilies within the Amaranthaceae, suggested that the

298 The three subfamilies within the RCAR family showed different sens

299 rotein (CPII), represents a new and distinct subfamily within the broad superfamily of previously stu

300 the immunity-associated leucine-rich repeat subfamily XII genes, heritable mutations were recovered